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Tytuł:
Identification of a De Novo Deletion by Using A-CGH Involving PLNAX2: An Interesting Candidate Gene in Psychomotor Developmental Delay.
Autorzy:
Falcone N; Department of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Napoli, Italy.; CEINGE-Biotecnologie Avanzate, Via G. Salvatore 486, 80145 Naples, Italy.
Ranieri A; CEINGE-Biotecnologie Avanzate, Via G. Salvatore 486, 80145 Naples, Italy.
Vitale A; Department of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Napoli, Italy.; CEINGE-Biotecnologie Avanzate, Via G. Salvatore 486, 80145 Naples, Italy.
Pastore L; Department of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Napoli, Italy.; CEINGE-Biotecnologie Avanzate, Via G. Salvatore 486, 80145 Naples, Italy.
Lombardo B; Department of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Napoli, Italy.; CEINGE-Biotecnologie Avanzate, Via G. Salvatore 486, 80145 Naples, Italy.
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Źródło:
Medicina (Kaunas, Lithuania) [Medicina (Kaunas)] 2022 Apr 08; Vol. 58 (4). Date of Electronic Publication: 2022 Apr 08.
Typ publikacji:
Case Reports
MeSH Terms:
Developmental Disabilities*/genetics
Gene Deletion*
Child ; Comparative Genomic Hybridization ; Humans ; Male ; Quality of Life
Raport
Szczegóły
Tytuł:
Approaches for Detection of Hepatitis B Virus Pre-S Gene Deletions and Pre-S Deleted Proteins and Their Application in Prediction of Higher Risk of Hepatocellular Carcinoma Development and Recurrence.
Autorzy:
Lin YT; Cancer Genome Research Center, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
Jeng LB; Organ Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.
Su IJ; Department of Biotechnology, Southern Taiwan University of Science and Technology, Tainan 710, Taiwan.
Teng CF; Organ Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.; Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404, Taiwan.; Research Center for Cancer Biology, China Medical University, Taichung 404, Taiwan.
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Źródło:
Viruses [Viruses] 2022 Feb 18; Vol. 14 (2). Date of Electronic Publication: 2022 Feb 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Gene Deletion*
Hepatitis B Surface Antigens/*genetics
Hepatitis B virus/*genetics
Hepatitis B, Chronic/*virology
Animals ; Base Sequence ; Biomarkers ; Carcinoma, Hepatocellular/etiology ; Carcinoma, Hepatocellular/pathology ; Disease Models, Animal ; Gene Expression Regulation, Viral ; Hepatitis B virus/physiology ; Hepatitis B, Chronic/complications ; High-Throughput Nucleotide Sequencing ; Humans ; Immunohistochemistry ; Liver Neoplasms/etiology ; Liver Neoplasms/pathology ; Neoplasm Recurrence, Local/etiology ; Neoplasm Recurrence, Local/pathology ; Prognosis ; Signal Transduction ; Virus Replication
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Consecutive deletions in a unique Uruguayan SARS-CoV-2 lineage evidence the genetic variability potential of accessory genes.
Autorzy:
Panzera Y; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Calleros L; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Goñi N; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Marandino A; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Techera C; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Grecco S; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Ramos N; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Frabasile S; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Tomás G; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Condon E; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
Cortinas MN; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Ramas V; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Coppola L; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Sorhouet C; Laboratorio de Biología Molecular, Mutualista Médica Uruguaya, Montevideo, Uruguay.
Mogdasy C; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Chiparelli H; Departamento de Laboratorios de Salud Pública, Centro Nacional de Referencia de Influenza y otros Virus Respiratorios, Ministerio de Salud Pública, Montevideo, Uruguay.
Arbiza J; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Delfraro A; Facultad de Ciencias, Sección Virología, Instituto de Biología e Instituto de Química Biológica, Universidad de la República, Montevideo, Uruguay.
Pérez R; Departamento de Biología Animal, Sección Genética Evolutiva, Instituto de Biología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
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Źródło:
PloS one [PLoS One] 2022 Feb 17; Vol. 17 (2), pp. e0263563. Date of Electronic Publication: 2022 Feb 17 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Lineage*
Gene Deletion*
Genome, Viral*
COVID-19/*virology
Open Reading Frames/*genetics
SARS-CoV-2/*genetics
Viral Proteins/*genetics
Adult ; Aged ; COVID-19/epidemiology ; COVID-19/genetics ; Child ; Female ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Middle Aged ; Phylogeny ; SARS-CoV-2/classification ; SARS-CoV-2/isolation & purification ; Uruguay/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Cas11 enables genome engineering in human cells with compact CRISPR-Cas3 systems.
Autorzy:
Tan R; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
Krueger RK; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
Gramelspacher MJ; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
Zhou X; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA.
Xiao Y; State Key Laboratory of Natural Medicines, Department of Pharmacology, China Pharmaceutical University, Nanjing, China.
Ke A; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.
Hou Z; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA. Electronic address: .
Zhang Y; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI, USA. Electronic address: .
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Źródło:
Molecular cell [Mol Cell] 2022 Feb 17; Vol. 82 (4), pp. 852-867.e5. Date of Electronic Publication: 2022 Jan 19.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
CRISPR-Cas Systems*
Clustered Regularly Interspaced Short Palindromic Repeats*
Gene Deletion*
Gene Editing*
Genome, Human*
Bacterial Proteins/*genetics
CRISPR-Associated Proteins/*genetics
Neisseria lactamica/*genetics
Bacterial Proteins/metabolism ; CRISPR-Associated Proteins/metabolism ; HEK293 Cells ; HeLa Cells ; Humans ; Neisseria lactamica/enzymology ; Ribonucleoproteins/genetics ; Ribonucleoproteins/metabolism
Czasopismo naukowe
Szczegóły
Tytuł:
Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience.
Autorzy:
Chen M; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Zhang M; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Chen L; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Lin N; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Wang Y; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Xu L; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Huang H; Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Medical Genetic Diagnosis and Therapy Center of Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China.
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Źródło:
Journal of clinical laboratory analysis [J Clin Lab Anal] 2022 Feb; Vol. 36 (2), pp. e24181. Date of Electronic Publication: 2021 Dec 23.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Multigene Family*
beta-Globins/*genetics
Adolescent ; Adult ; Child ; Child, Preschool ; China ; Female ; Genotype ; Humans ; Infant ; Male ; Phenotype ; Young Adult
Czasopismo naukowe
Szczegóły
Tytuł:
Long-read nanopore DNA sequencing can resolve complex intragenic duplication/deletion variants, providing information to enable preimplantation genetic diagnosis.
Autorzy:
Watson CM; North East and Yorkshire Genomics Laboratory Hub, Central Laboratory, St. James's University Hospital, Leeds, UK.; Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK.
Holliday DL; Department of Clinical Genetics, Leeds Teaching Hospitals NHS Trust, Chapel Allerton Hospital, Leeds, West Yorkshire, UK.
Crinnion LA; North East and Yorkshire Genomics Laboratory Hub, Central Laboratory, St. James's University Hospital, Leeds, UK.; Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK.
Bonthron DT; Leeds Institute of Medical Research, University of Leeds, St. James's University Hospital, Leeds, UK.; Department of Clinical Genetics, Leeds Teaching Hospitals NHS Trust, Chapel Allerton Hospital, Leeds, West Yorkshire, UK.
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Źródło:
Prenatal diagnosis [Prenat Diagn] 2022 Feb; Vol. 42 (2), pp. 226-232. Date of Electronic Publication: 2022 Jan 18.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Gene Deletion*
Gene Duplication*
Genetic Testing/*methods
Nanopore Sequencing/*methods
Preimplantation Diagnosis/*methods
Retinoblastoma/*diagnosis
Sequence Analysis, DNA/*methods
Female ; Genetic Markers ; Humans ; Infant ; Male ; Pregnancy ; Retinoblastoma/genetics ; Retinoblastoma Binding Proteins/genetics ; Ubiquitin-Protein Ligases/genetics
Czasopismo naukowe
Szczegóły
Tytuł:
A new KRT86 mutation in a Chinese family with monilethrix.
Autorzy:
Li XY; Department of Dermatology, West China Hospital of Sichuan University, Chengdu, China.
Wang S; Department of Dermatology, West China Hospital of Sichuan University, Chengdu, China.
Chen XM; Department of Dermatology, West China Hospital of Sichuan University, Chengdu, China.
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Źródło:
Clinical and experimental dermatology [Clin Exp Dermatol] 2022 Feb; Vol. 47 (2), pp. 461-463. Date of Electronic Publication: 2021 Nov 23.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Gene Deletion*
Keratins, Hair-Specific/*genetics
Keratins, Type II/*genetics
Monilethrix/*genetics
Asians ; Child, Preschool ; DNA Mutational Analysis ; Female ; Heterozygote ; Humans
Raport
Szczegóły
Tytuł:
Deletion in KRT75L4 linked to frizzle feather in Xiushui Yellow Chickens.
Autorzy:
Chen B; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Xi S; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.; Jiangxi Biotech Vocational College, Nanchang, Jiangxi, 330200, China.
El-Senousey HK; Department of Animal Production, Faculty of Agriculture, Cairo University, Giza, 12613, Egypt.
Zhou M; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Cheng D; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Chen K; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Wan L; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Xiong T; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Liao M; School of Foreign Languages, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Liu S; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
Mao H; College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi, 330045, China.
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Źródło:
Animal genetics [Anim Genet] 2022 Feb; Vol. 53 (1), pp. 101-107. Date of Electronic Publication: 2021 Dec 13.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Chickens/*physiology
Feathers/*anatomy & histology
Genome-Wide Association Study/*veterinary
Mutation, Missense/*physiology
Animals ; Chickens/genetics ; Feathers/growth & development
Czasopismo naukowe
Szczegóły
Tytuł:
Distinct effects on the secretion of MTRAP and AMA1 in Plasmodium yoelii following deletion of acylated pleckstrin homology domain-containing protein.
Autorzy:
Chaiyawong N; Program for Nurturing Global Leaders in Tropical and Emerging Communicable Diseases, Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.
Ishizaki T; Program for Nurturing Global Leaders in Tropical and Emerging Communicable Diseases, Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Laboratory for Molecular Infection Medicine Sweden, Department of Molecular Biology, Umeå University, Umeå 901 87, Sweden. Electronic address: .
Hakimi H; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843, United States.
Asada M; Program for Nurturing Global Leaders in Tropical and Emerging Communicable Diseases, Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Nishi 2-11, Obihiro, Hokkaido 080-0834, Japan. Electronic address: .
Yahata K; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan. Electronic address: .
Kaneko O; Program for Nurturing Global Leaders in Tropical and Emerging Communicable Diseases, Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan; Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan. Electronic address: .
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Źródło:
Parasitology international [Parasitol Int] 2022 Feb; Vol. 86, pp. 102479. Date of Electronic Publication: 2021 Oct 07.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Antigens, Protozoan/*genetics
Plasmodium yoelii/*genetics
Protozoan Proteins/*genetics
Acylation ; Antigens, Protozoan/metabolism ; Plasmodium yoelii/metabolism ; Protozoan Proteins/metabolism
Czasopismo naukowe
Szczegóły
Tytuł:
JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice.
Autorzy:
Rivellini C; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Porrello E; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Dina G; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Mrakic-Sposta S; Institute of Clinical Physiology National Research Council (IFC-CNR), Milan, Italy.
Vezzoli A; Institute of Clinical Physiology National Research Council (IFC-CNR), Milan, Italy.
Bacigaluppi M; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Gullotta GS; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Chaabane L; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Experimental Imaging Center (CIS), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Leocani L; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.; University Vita-Salute San Raffaele, Milan, Italy.
Marenna S; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Colombo E; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Farina C; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Newcombe J; NeuroResource, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, London, United Kingdom.
Nave KA; Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Göttingen, Germany.
Pardi R; Division of Immunology, Transplantation, and Infectious Disease, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Quattrini A; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Previtali SC; Institute of Experimental Neurology (INSPE), Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
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Źródło:
The Journal of clinical investigation [J Clin Invest] 2022 Feb 01; Vol. 132 (3).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
Aging/*metabolism
COP9 Signalosome Complex/*deficiency
Neurodegenerative Diseases/*metabolism
Oligodendroglia/*metabolism
Peptide Hydrolases/*deficiency
Aging/genetics ; Aging/pathology ; Animals ; COP9 Signalosome Complex/metabolism ; Inflammation/genetics ; Inflammation/metabolism ; Inflammation/pathology ; Mice ; Mice, Knockout ; Neurodegenerative Diseases/genetics ; Neurodegenerative Diseases/pathology ; Oligodendroglia/pathology ; Peptide Hydrolases/metabolism
Czasopismo naukowe
Szczegóły
Tytuł:
Plasmodium falciparum histidine-rich protein 2 and 3 genes deletion in global settings (2010-2021): a systematic review and meta-analysis.
Autorzy:
Jejaw Zeleke A; Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia. .
Hailu A; Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.; School of Medicine Addis, Ababa University, Addis Ababa, Ethiopia.
Bayih AG; Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Kefale M; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Amare AT; Department of Pediatrics, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Tegegne Y; Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Aemero M; Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
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Źródło:
Malaria journal [Malar J] 2022 Jan 29; Vol. 21 (1), pp. 26. Date of Electronic Publication: 2022 Jan 29.
Typ publikacji:
Journal Article; Meta-Analysis; Systematic Review
MeSH Terms:
Gene Deletion*
Antigens, Protozoan/*genetics
Malaria, Falciparum/*epidemiology
Plasmodium falciparum/*genetics
Protozoan Proteins/*genetics
Humans ; Prevalence
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The Deubiquitinase OTUB1 Is a Key Regulator of Energy Metabolism.
Autorzy:
Ruiz-Serrano A; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.
Boyle CN; Institute of Veterinary Physiology, University of Zurich, 8057 Zurich, Switzerland.
Monné Rodríguez JM; Laboratory for Animal Model Pathology (LAMP), Institute of Veterinary Pathology, University of Zurich, 8057 Zurich, Switzerland.
Günter J; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.; National Centre of Competence in Research 'Kidney.CH', 8057 Zurich, Switzerland.
Jucht AE; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.
Pfundstein S; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.
Bapst AM; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.
Lutz TA; Institute of Veterinary Physiology, University of Zurich, 8057 Zurich, Switzerland.
Wenger RH; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.; National Centre of Competence in Research 'Kidney.CH', 8057 Zurich, Switzerland.
Scholz CC; Institute of Physiology, University of Zurich, 8057 Zurich, Switzerland.; National Centre of Competence in Research 'Kidney.CH', 8057 Zurich, Switzerland.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Jan 28; Vol. 23 (3). Date of Electronic Publication: 2022 Jan 28.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Adenosine Triphosphate/*metabolism
Cysteine Endopeptidases/*genetics
Insulin/*administration & dosage
Insulin Resistance/*genetics
Mixed Function Oxygenases/*metabolism
Adenylate Kinase/metabolism ; Animals ; Blood Glucose ; Body Weight ; Cell Size ; Cells, Cultured ; Cysteine Endopeptidases/metabolism ; Energy Metabolism ; Fibroblasts/cytology ; Fibroblasts/drug effects ; Fibroblasts/metabolism ; Insulin/adverse effects ; Mice ; Phosphorylation ; Proto-Oncogene Proteins c-akt/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss.
Autorzy:
Stefanski HE; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Xing Y; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Nicholls J; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Jonart L; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Goren E; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Taylor PA; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Mills AA; Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, New York, United States of America.
Riddle M; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
McGrath J; Molecular Dermatology, St John's Institute of Dermatology, King's College, London, England.
Tolar J; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
Hollander GA; Department of Paediatrics, University of Oxford, Oxford, United Kingdom.; Department of Biomedicine, Basel University Children's Hospital, University of Basel, Basel, Switzerland.; Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Blazar BR; Division of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN, United States of America.
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Źródło:
PloS one [PLoS One] 2022 Jan 25; Vol. 17 (1), pp. e0261770. Date of Electronic Publication: 2022 Jan 25 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Gene Knockout Techniques*
Promoter Regions, Genetic*
Alopecia/*genetics
Forkhead Transcription Factors/*genetics
Thymus Gland/*growth & development
Trans-Activators/*deficiency
Alopecia/metabolism ; Animals ; Forkhead Transcription Factors/metabolism ; Mice ; Mice, Knockout ; Trans-Activators/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Heme A Synthase Deficiency Affects the Ability of Bacillus cereus to Adapt to a Nutrient-Limited Environment.
Autorzy:
Chateau A; Biology Department, Campus Jean-Henri Fabre, Avignon Université, INRAE, UMR SQPOV, 84914 Avignon, France.
Alpha-Bazin B; Département Médicaments et Technologies pour la Santé (DMTS), Université Paris Saclay, CEA, INRAE, SPI, 30200 Bagnols-sur-Cèze, France.
Armengaud J; Département Médicaments et Technologies pour la Santé (DMTS), Université Paris Saclay, CEA, INRAE, SPI, 30200 Bagnols-sur-Cèze, France.
Duport C; Biology Department, Campus Jean-Henri Fabre, Avignon Université, INRAE, UMR SQPOV, 84914 Avignon, France.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Jan 18; Vol. 23 (3). Date of Electronic Publication: 2022 Jan 18.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Deletion*
Bacillus cereus/*growth & development
Bacterial Proteins/*genetics
Cytochrome b Group/*genetics
Cytochrome c Group/*metabolism
Cytochromes a/*metabolism
Cytochromes a3/*metabolism
Membrane Proteins/*genetics
Bacillus cereus/genetics ; Bacillus cereus/metabolism ; Bacterial Proteins/metabolism ; Biofilms/growth & development ; Electron Transport Complex IV/metabolism ; Heme/analogs & derivatives ; Heme/metabolism ; Oxidative Stress ; Phenotype ; Proteomics ; Signal Transduction
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Intragenic NF1 deletions in sinonasal mucosal malignant melanoma.
Autorzy:
Riobello C; Department Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Centro de Investigación Biomédica en Red (CIBER-ONC), Oviedo, Spain.
Casanueva Muruais R; Department Otolaryngology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Suárez-Fernández L; Department Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Centro de Investigación Biomédica en Red (CIBER-ONC), Oviedo, Spain.
García-Marín R; Department Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Centro de Investigación Biomédica en Red (CIBER-ONC), Oviedo, Spain.
Cabal VN; Department Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Centro de Investigación Biomédica en Red (CIBER-ONC), Oviedo, Spain.
Blanco-Lorenzo V; Department Pathology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Franchi A; Department of Translational Research and of New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Laco J; The Fingerland Dept Pathology, Charles University Faculty of Medicine in Hradec Kralove, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
López F; Department Otolaryngology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Llorente JL; Department Otolaryngology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Hermsen MA; Department Head and Neck Cancer, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Centro de Investigación Biomédica en Red (CIBER-ONC), Oviedo, Spain.
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Źródło:
Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2022 Jan; Vol. 35 (1), pp. 88-96. Date of Electronic Publication: 2021 Oct 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
Biomarkers, Tumor/*genetics
Melanoma/*genetics
Neurofibromin 1/*genetics
Paranasal Sinus Neoplasms/*genetics
DNA Mutational Analysis ; Female ; Genetic Predisposition to Disease ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Melanoma/mortality ; Melanoma/secondary ; Melanoma/therapy ; Nasal Mucosa/pathology ; Paranasal Sinus Neoplasms/mortality ; Paranasal Sinus Neoplasms/pathology ; Paranasal Sinus Neoplasms/therapy ; Phenotype ; Prognosis
Czasopismo naukowe
Szczegóły
Tytuł:
The Effect of Dia2 Protein Deficiency on the Cell Cycle, Cell Size, and Recruitment of Ctf4 Protein in Saccharomyces cerevisiae .
Autorzy:
Ivanova A; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Atemin A; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Uzunova S; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Danovski G; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Aleksandrov R; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Stoynov S; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
Nedelcheva-Veleva M; Laboratory of Genomic Stability, Institute of Molecular Biology, Bulgarian Academy of Sciences, Acad. G., Bonchev Str. Bl.21, 1113 Sofia, Bulgaria.
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Źródło:
Molecules (Basel, Switzerland) [Molecules] 2021 Dec 24; Vol. 27 (1). Date of Electronic Publication: 2021 Dec 24.
Typ publikacji:
Journal Article
MeSH Terms:
Cell Size*
Gene Deletion*
Cell Cycle/*genetics
DNA-Binding Proteins/*metabolism
F-Box Proteins/*genetics
Saccharomyces cerevisiae/*physiology
Saccharomyces cerevisiae Proteins/*genetics
Saccharomyces cerevisiae Proteins/*metabolism
Chromatin/genetics ; Chromatin/metabolism ; Fluorescent Antibody Technique ; Microbial Viability ; Protein Binding ; Saccharomyces cerevisiae/cytology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Connexin 43 Gene Ablation Does Not Alter Human Pluripotent Stem Cell Germ Lineage Specification.
Autorzy:
Christopher GA; Division of BioMedical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL A1B 3V6, Canada.
Noort RJ; Division of BioMedical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL A1B 3V6, Canada.
Esseltine JL; Division of BioMedical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL A1B 3V6, Canada.
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Źródło:
Biomolecules [Biomolecules] 2021 Dec 22; Vol. 12 (1). Date of Electronic Publication: 2021 Dec 22.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
CRISPR-Cas Systems*
Cell Lineage*
Gene Deletion*
Connexin 43/*deficiency
Germ Layers/*metabolism
Induced Pluripotent Stem Cells/*metabolism
Connexin 43/metabolism ; Female ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Yeast Double Transporter Gene Deletion Library for Identification of Xenobiotic Carriers in Low or High Throughput.
Autorzy:
Almeida LD; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Silva ASF; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Mota DC; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Vasconcelos AA; Laboratory of Genomics and BioEnergy, Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Camargo AP; Laboratory of Genomics and BioEnergy, Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Pires GS; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Furlan M; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Freire HMRDC; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Klippel AH; School of Pharmaceutical Sciences, São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.
Silva SF; Chemistry Institute, São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.
Zanelli CF; School of Pharmaceutical Sciences, São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.
Carazzolle MF; Laboratory of Genomics and BioEnergy, Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Oliver SG; Cambridge Systems Biology Centre, University of Cambridgegrid.5335.0, Cambridge, United Kingdom.; Department of Biochemistry, University of Cambridgegrid.5335.0, Cambridge, United Kingdom.
Bilsland E; Synthetic Biology Laboratory, Department of Structural and Functional Biology, Institute of Biology, University of Campinas-UNICAMP, Campinas, São Paulo, Brazil.; Cambridge Systems Biology Centre, University of Cambridgegrid.5335.0, Cambridge, United Kingdom.; Department of Biochemistry, University of Cambridgegrid.5335.0, Cambridge, United Kingdom.
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Źródło:
MBio [mBio] 2021 Dec 21; Vol. 12 (6), pp. e0322121. Date of Electronic Publication: 2021 Dec 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
ATP-Binding Cassette Transporters/*genetics
Monosaccharide Transport Proteins/*genetics
Saccharomyces cerevisiae/*metabolism
Saccharomyces cerevisiae Proteins/*genetics
Xenobiotics/*metabolism
ATP-Binding Cassette Transporters/metabolism ; Antifungal Agents/metabolism ; Antifungal Agents/pharmacology ; Biological Transport ; Gene Library ; High-Throughput Screening Assays ; Monosaccharide Transport Proteins/metabolism ; Saccharomyces cerevisiae/drug effects ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae Proteins/metabolism ; Xenobiotics/pharmacology
Czasopismo naukowe
Szczegóły
Tytuł:
Deletions in VANGL1 are a risk factor for antibody-mediated kidney disease.
Autorzy:
Jiang SH; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.; Department of Renal Medicine, The Canberra Hospital, Canberra 2605, Australia.
Mercan S; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Department of Bioengineering, Kafkas University, Kars 36100, Turkey.
Papa I; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
Moldovan M; Centre for Population Health Research, University of South Australia, South Australian Health and Medical Research Institute (SAHMRI), Adelaide 5001, Australia.; Australian Institute of Health Innovation, Macquarie University, Sydney 2109, Australia.
Walters GD; Department of Renal Medicine, The Canberra Hospital, Canberra 2605, Australia.
Koina M; Department of Pathology, The Canberra Hospital, Canberra 2605, Australia.
Fadia M; Department of Pathology, The Canberra Hospital, Canberra 2605, Australia.
Stanley M; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
Lea-Henry T; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
Cook A; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
Ellyard J; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.
McMorran B; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
Sundaram M; Department of Renal Medicine, Royal Darwin Hospital, Northern Territory 0811, Australia.
Thomson R; Centre for Research in Mathematics and Data Science, School of Computer, Data and Mathematical Sciences, Western Sydney University, Parramatta 2150, NSW, Australia.
Canete PF; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.
Hoy W; Centre for Chronic Disease, Faculty of Health, The University of Queensland, Brisbane 4029, QLD, Australia.
Hutton H; Centre for Inflammatory Diseases, Monash University, Melbourne 3168, VIC, Australia.
Srivastava M; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.
McKeon K; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.
de la Rúa Figueroa I; University Hospital of Gran Canaria Dr. Negrin, Las Palmas 35010, Spain.
Cervera R; Department of Autoimmune Diseases, Hospital Clinic, Barcelona 08036, Spain.
Faria R; Unidade de Imunologia Clinica, Centro Hospitalar Unisersitario do Porto, Porto 4099-001, Portugal.
D'Alfonso S; Amedeo Avogadro University of East Piedmont 13100, Italy.
Gatto M; Department of Rheumatology, University of Padova, Italy.
Athanasopoulos V; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.
Field M; Australian Institute of Tropical Health and Medicine, James Cook University, Cairns 4870, QLD, Australia.
Mathews J; School of Population and Global Health, University of Melbourne, Melbourne 3053, Australia.
Cho E; Genome Informatics Laboratory, John Curtin School of Medical Research, Australian National University, Canberra 2601, Australia.
Andrews TD; Genome Informatics Laboratory, John Curtin School of Medical Research, Australian National University, Canberra 2601, Australia.
Kitching AR; Centre for Inflammatory Diseases, Monash University, Melbourne 3168, VIC, Australia.; Departments Nephrology and Paediatric Nephrology. Monash Health, Melbourne 3168, Australia.
Cook MC; Department of Immunology, The Canberra Hospital, Canberra 2605, Australia.
Riquelme MA; Department of Medical Genomics, GENYO. Centre for Genomics and Oncological Research: Pfizer/University of Granada/Andalusian Regional Government, Granada, 18016, Spain.
Bahlo M; Population Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne 3052, Australia.; Department of Medical Biology, The University of Melbourne, Parkville 3010 VIC, Australia.
Vinuesa CG; Department of Immunology and Infectious Disease, John Curtin School of Medical Research, Canberra, Australian National University, Canberra 2601, Australia.; Centre for Personalised Immunology, NHMRC Centre for Research Excellence, Australian National University, Canberra 2601, Australia.; China Australia Centre for Personalised Immunology, Renji Hospital Shanghai, JiaoTong University Shanghai 200001, China.; Francis Crick Institute, 1 Midland Rd, London NW1 1AT, UK.
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Źródło:
Cell reports. Medicine [Cell Rep Med] 2021 Dec 21; Vol. 2 (12), pp. 100475. Date of Electronic Publication: 2021 Dec 21 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
Antibodies/*adverse effects
Carrier Proteins/*genetics
Kidney Diseases/*pathology
Membrane Proteins/*genetics
Adult ; Aged ; Animals ; Biopsy ; Cohort Studies ; DNA Copy Number Variations/genetics ; Homozygote ; Humans ; Introns/genetics ; Kidney/metabolism ; Kidney/pathology ; Lupus Nephritis/genetics ; Membrane Proteins/deficiency ; Membrane Proteins/metabolism ; Mice, Inbred C57BL ; Mice, Knockout ; Middle Aged ; Risk Factors
Czasopismo naukowe
Szczegóły
Tytuł:
Nuclear NAD -biosynthetic enzyme NMNAT1 facilitates development and early survival of retinal neurons.
Autorzy:
Sokolov D; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.
Sechrest ER; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.
Wang Y; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.; Department of Biochemistry, One Medical Center Drive, West Virginia University, Morgantown, United States.
Nevin C; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.
Du J; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.; Department of Biochemistry, One Medical Center Drive, West Virginia University, Morgantown, United States.
Kolandaivelu S; Department of Ophthalmology and Visual Sciences, Eye Institute, One Medical Center Drive, West Virginia University, Morgantown, United States.; Department of Biochemistry, One Medical Center Drive, West Virginia University, Morgantown, United States.
Pokaż więcej
Źródło:
ELife [Elife] 2021 Dec 08; Vol. 10. Date of Electronic Publication: 2021 Dec 08.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Deletion*
Nicotinamide-Nucleotide Adenylyltransferase/*genetics
Photoreceptor Cells, Vertebrate/*enzymology
Retinal Degeneration/*enzymology
Retinal Neurons/*enzymology
Animals ; Female ; Male ; Mice ; Nicotinamide-Nucleotide Adenylyltransferase/deficiency ; Photoreceptor Cells, Vertebrate/pathology ; Retinal Degeneration/genetics ; Retinal Degeneration/pathology ; Retinal Neurons/pathology
Czasopismo naukowe
Szczegóły
Wyświetlanie 1-20 z 30950

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