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Wyszukujesz frazę ""Chromosomes, Human, Pair 3"" wg kryterium: Temat


Tytuł:
Efficient site-specific integration in CHO-K1 cells using CRISPR/Cas9-modified donors.
Autorzy:
Kheirandish MH; Medical Biotechnology Department, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Rahmani B; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.; Department of Biotechnology, Faculty of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
Zarei Jaliani H; Department of Medical Biotechnology, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Barkhordari F; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Mazlomi MA; Medical Biotechnology Department, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran. .
Davami F; Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran. .
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Źródło:
Molecular biology reports [Mol Biol Rep] 2023 Jul; Vol. 50 (7), pp. 5889-5899. Date of Electronic Publication: 2023 May 27.
Typ publikacji:
Journal Article
MeSH Terms:
CRISPR-Cas Systems*/genetics
Chromosomes, Human, Pair 3*
Animals ; Cricetinae ; Humans ; CHO Cells ; Clone Cells ; Cell Differentiation ; Cricetulus
Czasopismo naukowe
Tytuł:
EEG findings in a pediatric patient with 3q29 microdeletion syndrome.
Autorzy:
Sheikh IS; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Nascimento FA; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
Waite SR; Department of Pediatric Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Lam AD; Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, USA.
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Źródło:
Epileptic disorders : international epilepsy journal with videotape [Epileptic Disord] 2024 Feb; Vol. 26 (1), pp. 151-153. Date of Electronic Publication: 2023 Oct 03.
Typ publikacji:
Case Reports
MeSH Terms:
Chromosome Deletion*
Intellectual Disability*/genetics
Humans ; Child ; Developmental Disabilities/genetics ; Electroencephalography ; Phenotype ; Chromosomes, Human, Pair 3
SCR Disease Name:
Chromosome 3q29 Deletion Syndrome
Raport
Tytuł:
PRUNE1 (located on chromosome 1q21.3) promotes multiple myeloma with 1q21 Gain by enhancing the links between purine and mitochondrion.
Autorzy:
Xu J; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.; Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, China.
Wang Y; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.; Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, China.
Li P; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.; Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, China.
Chen C; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.; Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, China.
Jiang Z; Department of Hematology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, China.
Wang X; Department of Hematology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, China.
Liu P; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.; Cancer Center, Zhongshan Hospital, Fudan University, Shanghai, China.; Department of Hematology, Zhongshan Hospital (Xiamen), Fudan University, Xiamen, China.
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Źródło:
British journal of haematology [Br J Haematol] 2023 Nov; Vol. 203 (4), pp. 599-613. Date of Electronic Publication: 2023 Sep 04.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Multiple Myeloma*/therapy
Humans ; Chromatography, Liquid ; Chromosome Aberrations ; Chromosomes, Human, Pair 3 ; Prognosis ; Purines ; Tandem Mass Spectrometry
Czasopismo naukowe
Tytuł:
Evidence of cancer-linked rodent zoonoses from biophysical genomic variations.
Autorzy:
Alsufyani D; College of Sciences and Health Professions, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia. dani_.; King Abdullah International Medical Research Center, Jeddah, Saudi Arabia. dani_.
Lindesay J; Computational Physics Laboratory, Department of Physics, Howard University, 2355 Sixth Street NW, Washington, DC, USA.
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Źródło:
Scientific reports [Sci Rep] 2023 Aug 26; Vol. 13 (1), pp. 13969. Date of Electronic Publication: 2023 Aug 26.
Typ publikacji:
Journal Article
MeSH Terms:
Neoplasms*/genetics
Rodent Diseases*
Animals ; Humans ; Alleles ; Chromosomes, Human, Pair 3 ; Genomics ; Zoonoses ; Rodentia
Czasopismo naukowe
Tytuł:
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt.
Autorzy:
Pelgrims E; Department of Human Genetics, Catholic University Leuven, Leuven, Belgium.
Lynch SA; Department of Clinical Genetics, Children's University Hospital, Dublin, Republic of Ireland.
Hannes L; Department of Human Genetics, Catholic University Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Melotte C; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
Van Haeringen A; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Swillen A; Department of Human Genetics, Catholic University Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
Breckpot J; Department of Human Genetics, Catholic University Leuven, Leuven, Belgium.; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
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Źródło:
American journal of medical genetics. Part A [Am J Med Genet A] 2023 Jul; Vol. 191 (7), pp. 1889-1899. Date of Electronic Publication: 2023 May 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Developmental Disabilities*/genetics
Intellectual Disability*/genetics
Child ; Humans ; Chromosomes, Human, Pair 3 ; Face ; Phenotype ; Receptors, GABA-A/genetics ; Syndrome
Czasopismo naukowe
Tytuł:
Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome.
Autorzy:
Kopp J; Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Has C; Department of Dermatology, Faculty of Medicine, University Medical Center Freiburg, 79106 Freiburg, Germany.
Hotz A; Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Grünert SC; Department of General Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, University Medical Center Freiburg, 79106 Freiburg, Germany.
Fischer J; Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
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Źródło:
Genes [Genes (Basel)] 2021 Jul 29; Vol. 12 (8). Date of Electronic Publication: 2021 Jul 29.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 3*
Genes, Recessive*
Mutation*
1-Acylglycerol-3-Phosphate O-Acyltransferase/*genetics
Ichthyosiform Erythroderma, Congenital/*genetics
Lipid Metabolism, Inborn Errors/*genetics
Muscular Diseases/*genetics
Female ; Homozygote ; Humans ; Infant
SCR Disease Name:
Chanarin-Dorfman Syndrome
Czasopismo naukowe
Tytuł:
Human chromosome 3p21.3 carries TERT transcriptional regulators in pancreatic cancer.
Autorzy:
Yagyu T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.
Ohira T; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.; Chromosome Engineering Research Center, Tottori University, Yonago, Tottori, Japan.
Shimizu R; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.; Division of Urology, Department of Surgery, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Morimoto M; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Murakami Y; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Hanaki T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Kihara K; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Matsunaga T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Yamamoto M; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Tokuyasu N; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Sakamoto T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Fujiwara Y; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Kugoh H; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan. .; Chromosome Engineering Research Center, Tottori University, Yonago, Tottori, Japan. .
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Źródło:
Scientific reports [Sci Rep] 2021 Jul 28; Vol. 11 (1), pp. 15355. Date of Electronic Publication: 2021 Jul 28.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Loss of Heterozygosity*
Carcinogenesis/*genetics
Chimera/*genetics
Chromosomes, Human, Pair 3/*chemistry
Pancreatic Neoplasms/*genetics
Telomerase/*genetics
Animals ; Carcinogenesis/metabolism ; Carcinogenesis/pathology ; Cell Line, Tumor ; Cell Proliferation ; Chromosomes, Human, Pair 3/metabolism ; Gene Expression Regulation, Neoplastic ; Humans ; Mice ; Neoplasm Invasiveness ; Pancreatic Neoplasms/metabolism ; Pancreatic Neoplasms/pathology ; Promoter Regions, Genetic ; Telomerase/metabolism ; Transcription, Genetic
Czasopismo naukowe
Tytuł:
Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics.
Autorzy:
Horimoto ARVR; Department of Biostatistics, University of Washington, Seattle, WA, USA.
Xue D; Institute for Public Health Genetics, University of Washington, Seattle, WA, USA.
Thornton TA; Department of Biostatistics, University of Washington, Seattle, WA, USA.; Institute for Public Health Genetics, University of Washington, Seattle, WA, USA.
Blue EE; Institute for Public Health Genetics, University of Washington, Seattle, WA, USA. .; Division of Medical Genetics, University of Washington, BOX 357720, Seattle, WA, 98195-7720, USA. .
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Źródło:
Alzheimer's research & therapy [Alzheimers Res Ther] 2021 Jul 03; Vol. 13 (1), pp. 122. Date of Electronic Publication: 2021 Jul 03.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Alzheimer Disease*/epidemiology
Alzheimer Disease*/genetics
Chromosomes, Human, Pair 3*/genetics
Genome-Wide Association Study*
Caribbean Region ; Genetic Predisposition to Disease ; Hispanic or Latino/genetics ; Humans ; Polymorphism, Single Nucleotide ; White People/genetics ; American Indian or Alaska Native
Czasopismo naukowe
Tytuł:
Whole-genome analysis of recombinant inbred rice lines reveals a quantitative trait locus on chromosome 3 with genotype-by-environment interaction effects.
Autorzy:
Sakai T; Crop Evolution Laboratory, Kyoto University, Muko, Kyoto 617-0001, Japan.
Fujioka T; Iwate Agricultural Research Center, Kitakami, Iwate 024-0003, Japan.
Uemura T; Aomori Prefectural Industrial Technology Research Center Agricultural Research Institute, Kuroishi, Aomori 036-0522, Japan.
Saito S; Fukushima Agricultural Technology Centre, Koriyama, Fukushima 963-0531, Japan.
Terauchi R; Crop Evolution Laboratory, Kyoto University, Muko, Kyoto 617-0001, Japan.; Department of Genomics and Breeding, Iwate Biotechnology Research Center, Kitakami, Iwate 024-0003, Japan.
Abe A; Department of Genomics and Breeding, Iwate Biotechnology Research Center, Kitakami, Iwate 024-0003, Japan.
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Jun 01; Vol. 13 (6).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Quantitative Trait Loci*
Oryza*/genetics
Humans ; Chromosome Mapping/methods ; Gene-Environment Interaction ; Chromosomes, Human, Pair 3 ; Genotype ; Phenotype ; Crops, Agricultural/genetics
Czasopismo naukowe
Tytuł:
Coexistence of 3q29 microdeletion syndrome and Takayasu arteritis: A case report.
Autorzy:
Coşkun C; Department of Internal Medicine, Gazi University Faculty of Medicine, Ankara, Turkey.
Kardaş RC; Division of Rheumatology, Department of Internal Medicine, Gazi University Faculty of Medicine, Ankara, Turkey.
Küçük H; Division of Rheumatology, Department of Internal Medicine, Gazi University Faculty of Medicine, Ankara, Turkey.
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Źródło:
International journal of rheumatic diseases [Int J Rheum Dis] 2023 Apr; Vol. 26 (4), pp. 778-780. Date of Electronic Publication: 2022 Dec 11.
Typ publikacji:
Case Reports
MeSH Terms:
Takayasu Arteritis*/complications
Takayasu Arteritis*/diagnosis
Takayasu Arteritis*/genetics
Intellectual Disability*/diagnosis
Intellectual Disability*/genetics
Intellectual Disability*/complications
Female ; Humans ; Young Adult ; Adult ; Chromosomes, Human, Pair 3 ; Inflammation/complications
SCR Disease Name:
Chromosome 3q29 Deletion Syndrome
Raport
Tytuł:
A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes.
Autorzy:
Oliveira Junior AB; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; ICTP South American Institute for Fundamental Research, Instituto de Física Teórica, UNESP - 01140-070, São Paulo, SP, Brazil. Electronic address: .
Contessoto VG; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; Instituto de Biociências, Letras e Ciências Exatas, UNESP - Univ. Estadual Paulista, Departamento de Física, São José do Rio Preto, SP, Brazil. Electronic address: .
Mello MF; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; Chemical Engineering Department, Military Institute of Engineering, Rio de Janeiro, RJ, Brazil.
Onuchic JN; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; ICTP South American Institute for Fundamental Research, Instituto de Física Teórica, UNESP - 01140-070, São Paulo, SP, Brazil. Electronic address: .
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Źródło:
Journal of molecular biology [J Mol Biol] 2021 Mar 19; Vol. 433 (6), pp. 166700. Date of Electronic Publication: 2020 Nov 06.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Molecular Dynamics Simulation*
Software*
Chromatin/*chemistry
Chromosomes, Human, Pair 1/*chemistry
Chromosomes, Human, Pair 2/*chemistry
Chromosomes, Human, Pair 3/*chemistry
Chromosomes, Human, Pair 4/*chemistry
Animals ; Cell Line, Tumor ; Chromatin/metabolism ; Chromatin/ultrastructure ; Chromosomes, Human, Pair 1/metabolism ; Chromosomes, Human, Pair 1/ultrastructure ; Chromosomes, Human, Pair 2/metabolism ; Chromosomes, Human, Pair 2/ultrastructure ; Chromosomes, Human, Pair 3/metabolism ; Chromosomes, Human, Pair 3/ultrastructure ; Chromosomes, Human, Pair 4/metabolism ; Chromosomes, Human, Pair 4/ultrastructure ; Drosophila melanogaster/genetics ; Drosophila melanogaster/metabolism ; Humans ; Lymphocytes/cytology ; Lymphocytes/metabolism ; Saccharum/genetics ; Saccharum/metabolism ; Thermodynamics ; Triticum/genetics ; Triticum/metabolism
Czasopismo naukowe
Tytuł:
Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.
Autorzy:
Ali TM; Laboratório Igenomix, Laboratório de Genética E Medicina Reprodutiva, Sao Paulo, Sao Paulo, Brazil.
Mateu-Brull E; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain.
Balaguer N; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain.
Dantas C; Laboratório Igenomix, Laboratório de Genética E Medicina Reprodutiva, Sao Paulo, Sao Paulo, Brazil.
Borges HR; Clínica HR-Santa Rita do Passa Quatro, Sao Paulo, Brazil.
de Oliveira MQG; Clínica Nanu-Santa Rita do Passa Quatro, Sao Paulo, Brazil.
Rodrigo L; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain.
Campos-Galindo I; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain.
Navarro R; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain.
Milán M; IGENOMIX Lab S.L.U., Parque tecnológico, Ronda Narciso Monturiol, 11B, Edificios Europark, 46980, Paterna, Valencia, Spain. .
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Źródło:
European journal of medical research [Eur J Med Res] 2021 Jun 29; Vol. 26 (1), pp. 64. Date of Electronic Publication: 2021 Jun 29.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Cell-Free Nucleic Acids/*genetics
Chromosomes, Human, Pair 3/*genetics
Fetal Diseases/*genetics
Fetus/*metabolism
Trisomy/*genetics
Adult ; Biomarkers/blood ; Chromosomes, Human, Pair 3/metabolism ; DNA Copy Number Variations ; Female ; Fetal Diseases/diagnosis ; Fetal Diseases/metabolism ; Genetic Testing ; Humans ; Karyotyping ; Pregnancy ; Trisomy/diagnosis
SCR Disease Name:
Chromosome 3, trisomy 3q
Czasopismo naukowe
Tytuł:
An association between rs7635818 polymorphism located on chromosome 3p12.3 and the presence of abdominal aortic aneurysm.
Autorzy:
Rašiová M; Faculty of Medicine, Department of Angiology, East Slovak Institute of Cardiovascular Diseases, Šafárik University, Košice, Slovak Republic. .
Habalová V
Židzik J
Koščo M
Farkašová Ľ
Moščovič M
Hudák M
Javorský M
Tkáč I
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Źródło:
Physiological research [Physiol Res] 2021 Apr 30; Vol. 70 (2), pp. 193-201. Date of Electronic Publication: 2021 Mar 08.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 3*
Polymorphism, Single Nucleotide*
Aortic Aneurysm, Abdominal/*genetics
Aged ; Aortic Aneurysm, Abdominal/diagnostic imaging ; Aortic Aneurysm, Abdominal/ethnology ; Case-Control Studies ; Cross-Sectional Studies ; Czech Republic/epidemiology ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Phenotype ; Risk Assessment ; Risk Factors ; Severity of Illness Index ; White People/genetics
Czasopismo naukowe
Tytuł:
Genome and epigenome editing identify CCR9 and SLC6A20 as target genes at the 3p21.31 locus associated with severe COVID-19.
Autorzy:
Yao Y; School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.; Division of Hematology/Oncology, Boston Children's Hospital, Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Ye F; NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control & Prevention, Chinese Center for Disease Control and Prevention, China CDC, Beijing, China.
Li K; Children's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Xu P; Hematology Center of Cyrus Tang Medical Institute, Soochow University, Suzhou, China.
Tan W; NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control & Prevention, Chinese Center for Disease Control and Prevention, China CDC, Beijing, China.
Feng Q; School of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Rao S; Division of Hematology/Oncology, Boston Children's Hospital, Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. .
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Źródło:
Signal transduction and targeted therapy [Signal Transduct Target Ther] 2021 Feb 22; Vol. 6 (1), pp. 85. Date of Electronic Publication: 2021 Feb 22.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Epigenome*
Gene Editing*
Genetic Loci*
COVID-19/*genetics
Chromosomes, Human, Pair 3/*genetics
Membrane Transport Proteins/*genetics
Receptors, CCR/*genetics
SARS-CoV-2/*genetics
COVID-19/metabolism ; Cell Line ; Chromosomes, Human, Pair 3/metabolism ; Humans ; Membrane Transport Proteins/metabolism ; Receptors, CCR/metabolism ; SARS-CoV-2/metabolism ; Severity of Illness Index
Raport
Tytuł:
Screening and characterization of sex-specific sequences through 2b-RAD sequencing in American shad (Alosa sapidissima).
Autorzy:
Du J; Suzhou Fishseeds Bio-Technology, Suzhou, Jiangsu, China.; College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou, Zhejiang, China.
Liu Q; Suzhou Fishseeds Bio-Technology, Suzhou, Jiangsu, China.; Wisdom Lake Academy of Pharmacy, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu, China.
Zheng Y; Suzhou Health-Origin Bio-Technology, Suzhou, Jiangsu, China.
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Źródło:
PloS one [PLoS One] 2023 Mar 02; Vol. 18 (3), pp. e0282165. Date of Electronic Publication: 2023 Mar 02 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Fishes*
High-Throughput Nucleotide Sequencing*
Female ; Male ; Animals ; Humans ; Aquaculture ; China ; Chromosomes, Human, Pair 3
Czasopismo naukowe
Tytuł:
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.
Autorzy:
Serra G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy. .
Antona V; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Cimador M; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Collodoro G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Guida M; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Piro E; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Schierz IAM; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Verde V; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Giuffrè M; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Corsello G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
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Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2023 Feb 09; Vol. 49 (1), pp. 17. Date of Electronic Publication: 2023 Feb 09.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Trisomy*/diagnosis
Trisomy*/genetics
Abnormalities, Multiple*/diagnosis
Abnormalities, Multiple*/genetics
Pregnancy ; Infant, Newborn ; Female ; Humans ; Chromosomes, Human, Pair 3/genetics ; DNA
SCR Disease Name:
Partial Trisomy 3q Syndrome
Czasopismo naukowe
Tytuł:
Gene-by-gene screen of the unknown proteins encoded on Plasmodium falciparum chromosome 3.
Autorzy:
Kimmel J; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Schmitt M; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Sinner A; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Jansen PWTC; Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, 6525 GA Nijmegen, the Netherlands.
Mainye S; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Ramón-Zamorano G; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Toenhake CG; Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Radboud University, 6525 GA Nijmegen, the Netherlands.
Wichers-Misterek JS; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Cronshagen J; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Sabitzki R; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Mesén-Ramírez P; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Behrens HM; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany.
Bártfai R; Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Radboud University, 6525 GA Nijmegen, the Netherlands.
Spielmann T; Bernhard Nocht Institute for Tropical Medicine, Bernhard Nocht Str. 74, 20359 Hamburg, Germany. Electronic address: .
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Źródło:
Cell systems [Cell Syst] 2023 Jan 18; Vol. 14 (1), pp. 9-23.e7.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Plasmodium falciparum*/genetics
Malaria*
Humans ; Chromosomes, Human, Pair 3 ; Kinetochores ; Mitosis
Czasopismo naukowe
Tytuł:
Cytogenetic Abnormalities for Predicting the Risk of Metastases in Choroidal and Ciliary Body Melanoma.
Autorzy:
Chao AN; Department of Ophthalmology, Linkou Chang Gung Memorial Hospital, and College of Medicine, Chang Gung University, Taoyuan, Taiwan.; Department of Ophthalmology and Visual Sciences, Princess Margaret Cancer Centre, University Health Network, Ocular Oncology Service, University of Toronto, Toronto, Ontario, Canada.
Rose K; Department of Ophthalmology and Visual Sciences, Princess Margaret Cancer Centre, University Health Network, Ocular Oncology Service, University of Toronto, Toronto, Ontario, Canada.
Racher H; Department of Ophthalmology and Visual Sciences, Princess Margaret Cancer Centre, University Health Network, Ocular Oncology Service, University of Toronto, Toronto, Ontario, Canada.
Altomare F; Department of Ophthalmology and Visual Sciences, Princess Margaret Cancer Centre, University Health Network, Ocular Oncology Service, University of Toronto, Toronto, Ontario, Canada.
Krema H; Department of Ophthalmology and Visual Sciences, Princess Margaret Cancer Centre, University Health Network, Ocular Oncology Service, University of Toronto, Toronto, Ontario, Canada.
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Źródło:
Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2023 Jan 03; Vol. 64 (1), pp. 15.
Typ publikacji:
Journal Article
MeSH Terms:
Uveal Neoplasms*/genetics
Uveal Neoplasms*/pathology
Melanoma*/genetics
Melanoma*/pathology
Choroid Neoplasms*/genetics
Choroid Neoplasms*/pathology
Humans ; Ciliary Body/pathology ; Chromosome Deletion ; Monosomy ; Risk Factors ; Chromosomes, Human, Pair 3/genetics
SCR Disease Name:
Uveal melanoma
Czasopismo naukowe
Tytuł:
Uveal melanoma - testing of abnormalities of chromosome 3 and 8 in the Czech Republic.
Autorzy:
Matuskova V; Department of Ophthalmology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Hornackova P; Department of Ophthalmology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Uhmannova R; Department of Ophthalmology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Zlamalikova L; Department of Pathology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Liskova K; Department of Pathology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Uher M; Institute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Vlkova E; Department of Ophthalmology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.
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Źródło:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia [Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub] 2020 Dec; Vol. 164 (4), pp. 401-409. Date of Electronic Publication: 2019 Sep 23.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 3*
Chromosomes, Human, Pair 8*
Genetic Markers*
Melanoma/*genetics
Monosomy/*genetics
Uveal Neoplasms/*genetics
Aged ; Czech Republic ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Retrospective Studies
Czasopismo naukowe
Tytuł:
Chromosome 3p loss of heterozygosity and reduced expression of H3K36me3 correlate with longer relapse-free survival in sacral conventional chordoma.
Autorzy:
Zhu GG; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA; Department of Pathology, Cooper University Hospital, Cooper Medical School of Rowan University, Camden, NJ, 08003, USA.
Ramirez D; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA; Department of Pathology, Northwell Health, Great Neck, NY, 11021, USA.
Chen W; Department of Pathology, Washington DC VA Medical Center, Washington, DC, 20422, USA.
Lu C; Department of Genetics & Development, Columbia University Medical Center, New York, NY, 10032, USA.
Wang L; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Frosina D; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Jungbluth A; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Ntiamoah P; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Nafa K; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Boland PJ; Orthopaedic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Hameed MR; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. Electronic address: .
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Źródło:
Human pathology [Hum Pathol] 2020 Oct; Vol. 104, pp. 73-83. Date of Electronic Publication: 2020 Aug 12.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Chromosomes, Human, Pair 3*
DNA Methylation*
Loss of Heterozygosity*
Biomarkers, Tumor/*genetics
Chordoma/*genetics
Histone-Lysine N-Methyltransferase/*genetics
Sacrum/*pathology
Spinal Cord Neoplasms/*genetics
Adult ; Aged ; Aged, 80 and over ; Chordoma/mortality ; Chordoma/pathology ; Chordoma/therapy ; Disease Progression ; Female ; Humans ; Male ; Middle Aged ; Neoplasm Recurrence, Local ; Polymorphism, Single Nucleotide ; Progression-Free Survival ; Spinal Cord Neoplasms/mortality ; Spinal Cord Neoplasms/pathology ; Spinal Cord Neoplasms/therapy ; Time Factors ; Treatment Outcome ; Young Adult
Czasopismo naukowe

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