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Wyszukujesz frazę ""Comparative Genomic Hybridization"" wg kryterium: Temat


Tytuł:
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and review.
Autorzy:
Pacot L; Fédération de Génétique et Médecine Génomique, Hôpital Cochin, DMU BioPhyGen, AP-HP, Centre-Université Paris Cité, Paris, France.; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.
Girish M; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Knight S; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Spurlock G; Cardiff University, Cardiff, Great Britain.
Varghese V; All Wales Medical Genomics Service, Cardiff, Great Britain.
Ye M; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.
Thomas N; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Pasmant E; Fédération de Génétique et Médecine Génomique, Hôpital Cochin, DMU BioPhyGen, AP-HP, Centre-Université Paris Cité, Paris, France. .; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France. .
Upadhyaya M; Division of Cancer and Genetics, Institute of Medical Genetics, Cardiff University, Heath Park, CF14 4XN, Cardiff, UK.
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Źródło:
BMC medical genomics [BMC Med Genomics] 2024 Mar 06; Vol. 17 (1), pp. 73. Date of Electronic Publication: 2024 Mar 06.
Typ publikacji:
Journal Article
MeSH Terms:
DNA Copy Number Variations*
Skin Neoplasms*
Humans ; Comparative Genomic Hybridization ; Genomics ; Phenotype
Czasopismo naukowe
Tytuł:
The first two whole mitochondrial genomes for the genus Dactylis species: assembly and comparative genomics analysis.
Autorzy:
Feng G; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Jiao Y; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Ma H; Grassland Research Institute, Chongqing Academy of Animal Science, Chongqing, 402460, China.
Bian H; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Nie G; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Huang L; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Xie Z; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
Ran Q; Grassland Research Institute, Chongqing Academy of Animal Science, Chongqing, 402460, China.
Fan W; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China.
He W; Grassland Research Institute, Chongqing Academy of Animal Science, Chongqing, 402460, China. .
Zhang X; College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, 611130, China. .
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Źródło:
BMC genomics [BMC Genomics] 2024 Mar 04; Vol. 25 (1), pp. 235. Date of Electronic Publication: 2024 Mar 04.
Typ publikacji:
Journal Article
MeSH Terms:
Genome, Mitochondrial*/genetics
Animals ; Dactylis ; Phylogeny ; Comparative Genomic Hybridization ; RNA, Ribosomal ; Genomics
Czasopismo naukowe
Tytuł:
Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study.
Autorzy:
Lo T; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kushima I; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Medical Genomics Center, Nagoya University Hospital, Nagoya, Japan.
Kimura H; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Aleksic B; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Okada T; Department of Developmental Disorders, National Institute of Mental Health, National Center of Neurology and Psychiatry, Nagoya, Japan.
Kato H; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Inada T; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Nawa Y; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Torii Y; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yamamoto M; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kimura R; Department of Anatomy and Developmental Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Funabiki Y; Department of Cognitive, Behavioral and Health Sciences, Graduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan.
Kosaka H; Department of Neuropsychiatry, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Numata S; Department of Psychiatry, Graduate School of Biomedical Science, Tokushima University, Tokushima, Japan.
Kasai K; Department of Neuropsychiatry, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.; International Research Center for Neurointelligence at University of Tokyo Institutes for Advanced Study, Tokyo, Japan.
Sasaki T; Laboratory of Health Education, Graduate School of Education, University of Tokyo, Tokyo, Japan.
Yokoyama S; Research Center for Child Mental Development, Kanazawa University, Ishikawa, Japan.
Munesue T; Research Center for Child Mental Development, Kanazawa University, Ishikawa, Japan.
Hashimoto R; Department of Pathology of Mental Diseases, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan.
Yasuda Y; Department of Pathology of Mental Diseases, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan.
Fujimoto M; Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Usami M; Department of Child and Adolescent Psychiatry, Kohnodai Hospital, National Center for Global Health and Medicine, Chiba, Japan.
Itokawa M; Schizophrenia Research Project, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.; Department of Psychiatry, Tokyo Metropolitan Matsuzawa Hospital, Tokyo, Japan.
Arai M; Schizophrenia Research Project, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Ohi K; Department of Psychiatry, Gifu University Graduate School of Medicine, Gifu, Japan.; Department of General Internal Medicine, Kanazawa Medical University, Ishikawa, Japan.
Someya T; Department of Psychiatry, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Watanabe Y; Department of Psychiatry, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Egawa J; Department of Psychiatry, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Takahashi T; Department of Neuropsychiatry, University of Toyama Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.; Research Center for Idling Brain Science, University of Toyama, Toyama, Japan.
Suzuki M; Department of Neuropsychiatry, University of Toyama Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.; Research Center for Idling Brain Science, University of Toyama, Toyama, Japan.
Yamasue H; Department of Psychiatry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Iwata N; Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan.
Ikeda M; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan.
Ozaki N; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Institute for Glyco-core Research, Nagoya University, Nagoya, Japan.
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Źródło:
Neuropsychopharmacology reports [Neuropsychopharmacol Rep] 2024 Mar; Vol. 44 (1), pp. 42-50. Date of Electronic Publication: 2023 Nov 01.
Typ publikacji:
Journal Article
MeSH Terms:
Autism Spectrum Disorder*/genetics
Schizophrenia*
Humans ; Case-Control Studies ; Comparative Genomic Hybridization ; DNA Copy Number Variations ; Genome-Wide Association Study ; Ubiquitin-Protein Ligases/genetics
Czasopismo naukowe
Tytuł:
Antenatal description of large 4q13.2q21.23 deletion and outcomes.
Autorzy:
Giguet-Valard AG; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
Thevenin C; Private Laboratory for Biological Tests - BIOLAB Martinique, Fort-de-France, France.
Dreux S; Pre-Natal Biochemistry Unit, Biochemistry-Hormonology Laboratory, Robert Debré Hospital, DMU Biogem AP-HP, Paris, France.
Decatrelle V; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
Juve ML; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
Yazza S; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
Adenet C; Radiology Department, University Hospital Center of Martinique, Fort-de-France, France.
Lesueur M; Genomic Laboratory, University Hospital of Necker, Paris, France.
Bouvagnet P; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
Gueneret M; Multidisciplinary Department for Antenatal Diagnosis/Rare Neurological and Neuromuscular Disorders, University Hospital Center of Martinique, Fort-de-France, France.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Feb; Vol. 12 (2), pp. e2397.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosome Disorders*/genetics
Chromosome Disorders*/diagnosis
Humans ; Female ; Pregnancy ; Comparative Genomic Hybridization ; Chromosome Aberrations ; Syndrome ; Fetal Growth Retardation/genetics
Czasopismo naukowe
Tytuł:
Recurrent human 16p11.2 microdeletions in type I Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome patients in Chinese Han population.
Autorzy:
Su K; The International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.; Shanghai Municipal Key Clinical Specialty, Shanghai, China.
Liu H; The International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.; Shanghai Municipal Key Clinical Specialty, Shanghai, China.
Ye X; Women's Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
Jin H; Women's Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
Xie Z; Women's Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
Yang C; Women's Hospital, School of Medicine, Zhejiang University, Zhejiang, China.
Zhou D; Bio-X Institutes of Shanghai Jiao Tong University, Shanghai, China.
Huang H; The International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, Fudan University, Shanghai, China.; Research Units of Embryo Original Diseases, Chinese Academy of Medical Sciences (No. 2019RU056), Shanghai, China.
Wu Y; Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, Fudan University, Shanghai, China.; Research Units of Embryo Original Diseases, Chinese Academy of Medical Sciences (No. 2019RU056), Shanghai, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2280. Date of Electronic Publication: 2023 Oct 03.
Typ publikacji:
Journal Article
MeSH Terms:
DNA Copy Number Variations*
46, XX Disorders of Sex Development*/genetics
Congenital Abnormalities*
Mullerian Ducts/*abnormalities
Humans ; Female ; Retrospective Studies ; Comparative Genomic Hybridization ; T-Box Domain Proteins/genetics
SCR Disease Name:
Mullerian aplasia
Czasopismo naukowe
Tytuł:
aCGH Analysis Reveals Novel Mutations Associated with Congenital Diaphragmatic Hernia Plus (CDH+).
Autorzy:
Schreiner, Yannick (AUTHOR)
Stoll, Teresa (AUTHOR)
Nowak, Oliver (AUTHOR)
Weis, Meike (AUTHOR)
Hetjens, Svetlana (AUTHOR)
Steck, Eric (AUTHOR)
Perez Ortiz, Alba (AUTHOR)
Rafat, Neysan (AUTHOR)
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Źródło:
Journal of Clinical Medicine. Oct2023, Vol. 12 Issue 19, p6111. 10p.
Czasopismo naukowe
Tytuł:
Assessing the Phenotype of a Homologous Recombination Deficiency Using High Resolution Array-Based Comparative Genome Hybridization in Ovarian Cancer.
Autorzy:
Magadeeva S; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Qian X; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Korff N; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Flörkemeier I; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Hedemann N; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Rogmans C; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Forster M; Institute of Clinical Molecular Biology, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Arnold N; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.; Institute of Clinical Molecular Biology, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Maass N; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Bauerschlag DO; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
Weimer JP; Department of Gynaecology and Obstetrics, Christian-Albrechts-University and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Dec 14; Vol. 24 (24). Date of Electronic Publication: 2023 Dec 14.
Typ publikacji:
Journal Article
MeSH Terms:
Homologous Recombination*
Ovarian Neoplasms*/pathology
Humans ; Female ; Retrospective Studies ; Comparative Genomic Hybridization ; Cicatrix/pathology ; Phenotype
Czasopismo naukowe
Tytuł:
Newly discovered genomic mutation patterns in radiation-induced small intestinal tumors of ApcMin/+ mice.
Autorzy:
Iizuka D; Department of Radiation Effects Research, Institute for Radiological Science, National Institutes for Quantum Science and Technology, Chiba, Japan.; Department of Experimental Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Sasatani M; Department of Experimental Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Ishikawa A; Department of Radiation Effects Research, Institute for Radiological Science, National Institutes for Quantum Science and Technology, Chiba, Japan.
Daino K; Department of Radiation Effects Research, Institute for Radiological Science, National Institutes for Quantum Science and Technology, Chiba, Japan.
Hirouchi T; Department of Radiobiology, Institute for Environmental Sciences, Rokkasho, Japan.
Kamiya K; Department of Experimental Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
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Źródło:
PloS one [PLoS One] 2023 Oct 12; Vol. 18 (10), pp. e0292643. Date of Electronic Publication: 2023 Oct 12 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenomatous Polyposis Coli*/genetics
Intestinal Neoplasms*/genetics
Intestinal Neoplasms*/pathology
Neoplasms, Radiation-Induced*/genetics
Mice ; Animals ; Genes, APC ; Comparative Genomic Hybridization ; Mutation ; Genomics
Czasopismo naukowe
Tytuł:
Difficult to Diagnose Cutaneous Melanoma in a Patient with BAP1 Tumor Predisposition Syndrome.
Autorzy:
Silva-Clavería F; Melanoma Unit, Department of Medical & Surgical Dermatology, University Hospital Virgen Macarena, Seville, Spain.
Álvarez-Muñoz A; Pathology Department, University Hospital Virgen Macarena, Seville, Spain.
Ferrándiz L; Melanoma Unit, Department of Medical & Surgical Dermatology, University Hospital Virgen Macarena, Seville, Spain.
Fernández-Orland A; Melanoma Unit, Department of Medical & Surgical Dermatology, University Hospital Virgen Macarena, Seville, Spain.
Conde-Martin AF; Pathology Department, University Hospital Virgen Macarena, Seville, Spain.
Moreno-Ramírez D; Melanoma Unit, Department of Medical & Surgical Dermatology, University Hospital Virgen Macarena, Seville, Spain.
Ríos-Martín JJ; Pathology Department, University Hospital Virgen Macarena, Seville, Spain.
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Źródło:
International journal of surgical pathology [Int J Surg Pathol] 2023 Oct; Vol. 31 (7), pp. 1398-1402. Date of Electronic Publication: 2023 Feb 19.
Typ publikacji:
Journal Article
MeSH Terms:
Melanoma*/diagnosis
Melanoma*/genetics
Melanoma*/metabolism
Skin Neoplasms*/diagnosis
Skin Neoplasms*/genetics
Skin Neoplasms*/metabolism
Nevus, Pigmented*/pathology
Neoplastic Syndromes, Hereditary*
Humans ; Comparative Genomic Hybridization ; In Situ Hybridization, Fluorescence ; Tumor Suppressor Proteins/genetics ; Ubiquitin Thiolesterase/genetics ; Melanoma, Cutaneous Malignant
Czasopismo naukowe
Tytuł:
Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions.
Autorzy:
Furukawa S; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kushima I; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Medical Genomics Center, Nagoya University Hospital, Nagoya, Japan.
Aleksic B; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Ozaki N; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.; Institute for Glyco-core Research, Nagoya University, Nagoya, Japan.
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Źródło:
Neuropsychopharmacology reports [Neuropsychopharmacol Rep] 2023 Sep; Vol. 43 (3), pp. 462-466. Date of Electronic Publication: 2023 Jun 01.
Typ publikacji:
Case Reports; Research Support, Non-U.S. Gov't
MeSH Terms:
Autism Spectrum Disorder*/diagnosis
Autism Spectrum Disorder*/genetics
Neurodevelopmental Disorders*
Intellectual Disability*
Male ; Female ; Humans ; Young Adult ; Adult ; Siblings ; DNA Copy Number Variations ; Comparative Genomic Hybridization
Raport
Tytuł:
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder.
Autorzy:
Cucinotta F; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.; IRCCS Centro Neurolesi 'Bonino Pulejo', Messina, Italy.
Lintas C; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy.
Tomaiuolo P; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.
Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.; Synlab Genetics, Bioggio, Switzerland.
Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Sacco R; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy.
Piras IS; Service for Neurodevelopmental Disorders & Laboratory of Molecular Psychiatry and Neurogenetics, University 'Campus Bio-Medico', Rome, Italy.; Neurogenomics Division, The Translational Genomics Research Institute, Phoenix, Arizona, USA.
Turriziani L; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.
Ricciardello A; Interdepartmental Program 'Autism 0-90', 'G. Martino' University Hospital of Messina, Messina, Italy.
Scattoni ML; Research Coordination and Support Service, Istituto Superiore di Sanità, Rome, Italy.
Persico AM; Child and Adolescent Neuropsychiatry Program, Modena University Hospital & Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Aug; Vol. 11 (8), pp. e2182. Date of Electronic Publication: 2023 Apr 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Autism Spectrum Disorder*/diagnosis
Autism Spectrum Disorder*/genetics
Autistic Disorder*
Child ; Humans ; Comparative Genomic Hybridization/methods ; Microarray Analysis ; DNA Copy Number Variations
Czasopismo naukowe
Tytuł:
The NIH Comparative Genomics Resource: addressing the promises and challenges of comparative genomics on human health.
Autorzy:
Bornstein K; The MITRE Corporation, 7525 Colshire Dr, McLean, VA, USA.
Gryan G; The MITRE Corporation, 7525 Colshire Dr, McLean, VA, USA.
Chang ES; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.
Marchler-Bauer A; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.
Schneider VA; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA. .
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Źródło:
BMC genomics [BMC Genomics] 2023 Sep 27; Vol. 24 (1), pp. 575. Date of Electronic Publication: 2023 Sep 27.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Genomics*
Algorithms*
United States ; Humans ; Comparative Genomic Hybridization ; Drug Delivery Systems ; National Institutes of Health (U.S.)
Czasopismo naukowe
Tytuł:
Comparative genomic analysis of two Arctic Pseudomonas strains reveals insights into the aerobic denitrification in cold environments.
Autorzy:
Hu YQ; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Zeng YX; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China. .; School of Oceanography, Shanghai Jiao Tong University, Shanghai, 200030, China. .
Du Y; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Zhao W; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Li HR; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Han W; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Hu T; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
Luo W; Key Laboratory for Polar Science, Polar Research Institute of China, Ministry of Natural Resources, Shanghai, 200136, China.
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Źródło:
BMC genomics [BMC Genomics] 2023 Sep 11; Vol. 24 (1), pp. 534. Date of Electronic Publication: 2023 Sep 11.
Typ publikacji:
Journal Article
MeSH Terms:
Denitrification*
Sewage*
Comparative Genomic Hybridization ; Genomics ; Nitrogen ; Pseudomonas/genetics
Czasopismo naukowe
Tytuł:
Multi-omics data provide insight into the adaptation of the glasshouse plant Rheum nobile to the alpine subnival zone.
Autorzy:
Li Y; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Niu Z; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Zhu M; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Wang Z; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Xu R; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Li M; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Zheng Z; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Lu Z; CAS Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla, Yunnan, 666303, China.
Dong C; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Hu H; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Yang Y; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Wu Y; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Wang D; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Yang J; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Zhang J; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Wan D; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China.
Abbott R; School of Biology, University of St Andrews, St Andrews, Fife, KY169TH, UK.
Liu J; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China. .; Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education & State Key Laboratory of Hydraulics & Mountain River Engineering, College of Life Sciences, Sichuan University, Chengdu, 610065, China. .
Yang Y; State Key Laboratory of Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou, 730000, China. .
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Źródło:
Communications biology [Commun Biol] 2023 Sep 04; Vol. 6 (1), pp. 906. Date of Electronic Publication: 2023 Sep 04.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Rheum*/genetics
Multiomics ; Acclimatization/genetics ; Comparative Genomic Hybridization ; Down-Regulation
Czasopismo naukowe
Tytuł:
Functional annotation and comparative genomics analysis of Balamuthia mandrillaris reveals potential virulence-related genes.
Autorzy:
Otero-Ruiz A; Programa de Doctorado en Ciencias Especialidad en Biotecnología, Departamento de Biotecnología y Ciencias Alimentarias, Instituto Tecnológico de Sonora, 85000, Ciudad Obregón, Sonora, Mexico.
Rodriguez-Anaya LZ; CONAHCYT-Instituto Tecnológico de Sonora, 85000, Ciudad Obregón, Sonora, Mexico. .
Lares-Villa F; Departamento de Ciencias Agronómicas y Veterinarias, Instituto Tecnológico de Sonora, 85000, Ciudad Obregón, Sonora, Mexico.
Lozano Aguirre Beltrán LF; Unidad de Análisis Bioinformáticos, Centro de Ciencias Genómicas de la Universidad Nacional Autónoma de México (UNAM), 62210, Cuernavaca, Morelos, Mexico.
Lares-Jiménez LF; Departamento de Ciencias Agronómicas y Veterinarias, Instituto Tecnológico de Sonora, 85000, Ciudad Obregón, Sonora, Mexico.
Gonzalez-Galaviz JR; CONAHCYT-Instituto Tecnológico de Sonora, 85000, Ciudad Obregón, Sonora, Mexico.
Cruz-Mendívil A; CONAHCYT-Instituto Politécnico Nacional, CIIDIR Unidad Sinaloa, 81101, Guasave, Sinaloa, Mexico.
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Źródło:
Scientific reports [Sci Rep] 2023 Aug 31; Vol. 13 (1), pp. 14318. Date of Electronic Publication: 2023 Aug 31.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Balamuthia mandrillaris*/genetics
Acanthamoeba*/genetics
Virulence/genetics ; Comparative Genomic Hybridization ; Genomics
Czasopismo naukowe
Tytuł:
A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome.
Autorzy:
Ben-Mahmoud A; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
Kishikawa S; Gene Engineering Division, RIKEN BioResource Research Center, Tsukuba, Japan.
Gupta V; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
Leach NT; Integrated Genetics, Laboratory Corporation of America Holdings, 3400 Computer Drive, Westborough, MA, 01581, USA.
Shen Y; Division of Genetics and Genomics at Boston Children's Hospital, Harvard Medical School, Boston, MA, 02114, USA.
Moldovan O; Medical Genetics Service, Pediatric Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.
Goel H; Hunter Genetics, Waratah, NSW, 2298, Australia.; University of Newcastle, Callaghan, NSW, 2308, Australia.
Hopper B; Forster Genetics-Hunter New England Local Health District, Forster, NSW, 2428, Australia.
Ranguin K; Department of Genetics, Reference Center for Rare Diseases of Developmental anomalies and polymalformative syndrome, CHU de Caen Normandie, Caen, France.
Gruchy N; Department of Genetics, Reference Center for Rare Diseases of Developmental anomalies and polymalformative syndrome, CHU de Caen Normandie, Caen, France.
Maas SM; Department of Human Genetics, Amsterdam University Medical Center, Amsterdam, the Netherlands.; Reproduction and Development Research Institute, University of Amsterdam, Amsterdam, the Netherlands.
Lacassie Y; Division of Genetics, Department of Pediatrics, Louisiana State University, New Orleans, LA, 70118, USA.
Kim SH; Molecular and Clinical Sciences Research Institute, St. George's, University of London, London, UK.
Kim WY; Department of Biological Sciences, Kent State University, Kent, OH, 44242, USA.
Quade BJ; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Morton CC; Departments of Obstetrics and Gynecology and of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 02115, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.; Manchester Centre for Audiology and Deafness, School of Health Sciences, University of Manchester, Manchester, UK.
Kim CH; Department of Biology, Chungnam National University, Daejeon, 34134, Korea.
Layman LC; Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, USA.; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA, USA.
Kim HG; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar. .; College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar. .
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Źródło:
Scientific reports [Sci Rep] 2023 Aug 10; Vol. 13 (1), pp. 12984. Date of Electronic Publication: 2023 Aug 10.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Intellectual Disability*/genetics
Kallmann Syndrome*/genetics
Humans ; Carrier Proteins/genetics ; Comparative Genomic Hybridization ; DNA Copy Number Variations ; Membrane Proteins/genetics ; Tetraspanins/genetics ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Genomic sequencing of fourteen bacillus thuringiensis isolates: insights into geographic variation and phylogenetic implications.
Autorzy:
Blackburn MB; Invasive Insect Biocontrol and Behavior Laboratory, USDA-ARS, Henry A Wallace Beltsville Agricultural Research Center, Beltsville, MD, 20705, USA. .
Sparks ME; Invasive Insect Biocontrol and Behavior Laboratory, USDA-ARS, Henry A Wallace Beltsville Agricultural Research Center, Beltsville, MD, 20705, USA.
Mishra R; Department of Entomology and Nematology, University of Florida, Gainesville, FL, 32611, USA.
Bonning BC; Department of Entomology and Nematology, University of Florida, Gainesville, FL, 32611, USA.
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Źródło:
BMC research notes [BMC Res Notes] 2023 Jul 04; Vol. 16 (1), pp. 134. Date of Electronic Publication: 2023 Jul 04.
Typ publikacji:
Journal Article
MeSH Terms:
Bacillus thuringiensis*/classification
Bacillus thuringiensis*/genetics
Genetic Variation*
Genome, Bacterial*/genetics
Phylogeny*
Comparative Genomic Hybridization ; Serogroup
Czasopismo naukowe
Tytuł:
Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study.
Autorzy:
Corallo D; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Zanon C; Bioinformatics Core Service, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Pantile M; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Tonini GP; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Zin A; Advanced Diagnostics and Target Discovery in Rare Pediatric Solid Tumors, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Francescato S; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Rossi B; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Trevisson E; Clinical Genetics Unit, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Pinato C; Clinical Genetics Unit, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Monferrer E; Pathology Department, Medical School, University of Valencia-INCLIVA, 46010 Valencia, Spain.
Noguera R; Pathology Department, Medical School, University of Valencia-INCLIVA, 46010 Valencia, Spain.
Aliño SF; Pharmacogenetics Unit, Instituto Investigación Sanitaria La Fe and Department Pharmacology, University of Valencia, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Herrero MJ; Pharmacogenetics Unit, Instituto Investigación Sanitaria La Fe and Department Pharmacology, University of Valencia, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Biffi A; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Viscardi E; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Aveic S; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.; Department of Dental Materials and Biomaterials Research, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
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Źródło:
Cells [Cells] 2021 Oct 09; Vol. 10 (10). Date of Electronic Publication: 2021 Oct 09.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Comparative Genomic Hybridization*
Exome Sequencing*
Neuroblastoma/*genetics
Child, Preschool ; Disease Progression ; Drug Resistance, Neoplasm/genetics ; Fatal Outcome ; Humans ; Immunophenotyping ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe

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