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Tytuł :
A scalable unified framework of total and allele-specific counts for cis-QTL, fine-mapping, and prediction.
Autorzy :
Liang Y; Section of Genetic Medicine, The University of Chicago, Chicago, IL, USA. .
Aguet F; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Barbeira AN; Section of Genetic Medicine, The University of Chicago, Chicago, IL, USA.
Ardlie K; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Im HK; Section of Genetic Medicine, The University of Chicago, Chicago, IL, USA. .
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Źródło :
Nature communications [Nat Commun] 2021 Mar 03; Vol. 12 (1), pp. 1424. Date of Electronic Publication: 2021 Mar 03.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Alleles*
Quantitative Trait Loci*
Chromosome Mapping/*methods
Databases, Genetic ; Genome-Wide Association Study ; Human Genome Project ; Humans ; Models, Genetic ; Models, Statistical ; Regulatory Sequences, Nucleic Acid
Czasopismo naukowe
Tytuł :
CLIA Laboratory Testing for Facioscapulohumeral Dystrophy: A Retrospective Analysis.
Autorzy :
Rieken A; From the Departments of Pathology (A.R., A.D.B., S.A.M.) and Pediatrics and Neurology (A.R., K.D.M.), Carver College of Medicine, The University of Iowa, Iowa City.
Bossler AD; From the Departments of Pathology (A.R., A.D.B., S.A.M.) and Pediatrics and Neurology (A.R., K.D.M.), Carver College of Medicine, The University of Iowa, Iowa City.
Mathews KD; From the Departments of Pathology (A.R., A.D.B., S.A.M.) and Pediatrics and Neurology (A.R., K.D.M.), Carver College of Medicine, The University of Iowa, Iowa City.
Moore SA; From the Departments of Pathology (A.R., A.D.B., S.A.M.) and Pediatrics and Neurology (A.R., K.D.M.), Carver College of Medicine, The University of Iowa, Iowa City. .
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Źródło :
Neurology [Neurology] 2021 Feb 16; Vol. 96 (7), pp. e1054-e1062. Date of Electronic Publication: 2020 Dec 21.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Alleles*
Mutation*
Chromosomal Proteins, Non-Histone/*genetics
Muscular Dystrophy, Facioscapulohumeral/*diagnosis
DNA Methylation ; Diagnostic Tests, Routine ; Humans ; Muscular Dystrophy, Facioscapulohumeral/genetics ; Pathology, Molecular ; Phenotype
Czasopismo naukowe
Tytuł :
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma.
Autorzy :
Samur MK; Department of Data Science, Dana Farber Cancer Institute, Boston, MA, USA. .; Department of Biostatistics, Harvard T. H. Chan School of Public Health Boston, Boston, MA, USA. .; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. .
Fulciniti M; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Aktas Samur A; Department of Data Science, Dana Farber Cancer Institute, Boston, MA, USA.; Department of Biostatistics, Harvard T. H. Chan School of Public Health Boston, Boston, MA, USA.
Bazarbachi AH; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.; Department of Internal Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, New York, NY, USA.
Tai YT; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Prabhala R; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.; VA Boston Healthcare System, Boston, MA, USA.
Alonso A; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Sperling AS; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Campbell T; Bristol-Myers Squibb, San Francisco, CA, USA.
Petrocca F; Bluebird Bio, Cambridge, MA, USA.
Hege K; Bristol-Myers Squibb, San Francisco, CA, USA.
Kaiser S; Bristol-Myers Squibb, Seattle, WA, USA.
Loiseau HA; University Cancer Center of Toulouse Institut National de la Santé, Toulouse, France.
Anderson KC; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Munshi NC; Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. .; VA Boston Healthcare System, Boston, MA, USA. .
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Źródło :
Nature communications [Nat Commun] 2021 Feb 08; Vol. 12 (1), pp. 868. Date of Electronic Publication: 2021 Feb 08.
Typ publikacji :
Clinical Trial, Phase I; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Alleles*
Drug Resistance, Neoplasm*
Immunotherapy, Adoptive*
B-Cell Maturation Antigen/*genetics
Multiple Myeloma/*genetics
Multiple Myeloma/*therapy
Bone Marrow/pathology ; Humans ; Multiple Myeloma/immunology ; Tumor Microenvironment
Czasopismo naukowe
Tytuł :
Rapid Spread of Mutant Alleles in Worldwide SARS-CoV-2 Strains Revealed by Genome-Wide Single Nucleotide Polymorphism and Variation Analysis.
Autorzy :
Zhu Z; School of Life Sciences, Chongqing University, Chongqing, China.
Liu G; School of Life Sciences, Chongqing University, Chongqing, China.
Meng K; College of Veterinary Medicine, China Agricultural University, Beijing, China.
Yang L; Chongqing Occupational Disease Prevention Hospital, Chongqing, China.
Liu D; CAS Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Center for 25 Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, China.
Meng G; College of Veterinary Medicine, China Agricultural University, Beijing, China.
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Źródło :
Genome biology and evolution [Genome Biol Evol] 2021 Feb 03; Vol. 13 (2).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Alleles*
Mutation*
Polymorphism, Single Nucleotide*
COVID-19/*virology
SARS-CoV-2/*genetics
COVID-19/epidemiology ; Gene Frequency ; Genes, Viral ; Humans ; Linkage Disequilibrium
Czasopismo naukowe
Tytuł :
Characterizing allele- and haplotype-specific copy numbers in single cells with CHISEL.
Autorzy :
Zaccaria S; Department of Computer Science, Princeton University, Princeton, NJ, USA.
Raphael BJ; Department of Computer Science, Princeton University, Princeton, NJ, USA. .; Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA. .
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Źródło :
Nature biotechnology [Nat Biotechnol] 2021 Feb; Vol. 39 (2), pp. 207-214. Date of Electronic Publication: 2020 Sep 02.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Algorithms*
Alleles*
Evolution, Molecular*
Gene Dosage*
Haplotypes/*genetics
Breast Neoplasms/genetics ; Cell Line, Tumor ; DNA Copy Number Variations/genetics ; DNA, Neoplasm/genetics ; Female ; Genetic Heterogeneity ; Humans ; Single-Cell Analysis
Czasopismo naukowe
Tytuł :
The TRACE-Seq method tracks recombination alleles and identifies clonal reconstitution dynamics of gene targeted human hematopoietic stem cells.
Autorzy :
Sharma R; Department of Medicine, Division of Hematology, Cancer Institute, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, 94305, USA.
Dever DP; Department of Pediatrics, Stanford University, Stanford, CA, 94305, USA.
Lee CM; Department of Bioengineering, Rice University, Houston, TX, 77030, USA.
Azizi A; Department of Medicine, Division of Hematology, Cancer Institute, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, 94305, USA.
Pan Y; Department of Bioengineering, Rice University, Houston, TX, 77030, USA.
Camarena J; Department of Pediatrics, Stanford University, Stanford, CA, 94305, USA.
Köhnke T; Department of Medicine, Division of Hematology, Cancer Institute, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, 94305, USA.
Bao G; Department of Bioengineering, Rice University, Houston, TX, 77030, USA. .
Porteus MH; Department of Pediatrics, Stanford University, Stanford, CA, 94305, USA. .
Majeti R; Department of Medicine, Division of Hematology, Cancer Institute, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA, 94305, USA. .
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Źródło :
Nature communications [Nat Commun] 2021 Jan 20; Vol. 12 (1), pp. 472. Date of Electronic Publication: 2021 Jan 20.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Alleles*
Clone Cells*
Hematopoietic Stem Cells*
Recombination, Genetic*
Gene Targeting/*methods
Animals ; CRISPR-Cas Systems ; Clustered Regularly Interspaced Short Palindromic Repeats ; Female ; Gene Editing/methods ; Genetic Therapy/methods ; Humans ; Mice ; Mutation ; Targeted Gene Repair/methods
Czasopismo naukowe
Tytuł :
Vitamin D Receptor ( VDR ) Gene Polymorphism in Patients Diagnosed with Colorectal Cancer.
Autorzy :
Latacz M; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.; Faculty of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
Rozmus D; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
Fiedorowicz E; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
Snarska J; Department of General Surgery, Faculty of Medical Sciences, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
Jarmołowska B; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
Kordulewska N; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
Savelkoul H; Cell Biology and Immunology Group, Department of Animal Sciences, Wageningen University and Research, 6700 AH Wageningen, The Netherlands.
Cieślińska A; Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
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Źródło :
Nutrients [Nutrients] 2021 Jan 11; Vol. 13 (1). Date of Electronic Publication: 2021 Jan 11.
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Polymorphism, Single Nucleotide*
Colorectal Neoplasms/*genetics
Neoplasm Proteins/*genetics
Receptors, Calcitriol/*genetics
Aged ; Aged, 80 and over ; Female ; Humans ; Male ; Middle Aged ; Risk Factors
Czasopismo naukowe
Tytuł :
[Investigation of ABO allelic competition phenomena in a pedigree with Bw11 subtype].
Autorzy :
Feng C; Jiangsu Province Blood Center, Nanjing, Jiangsu 210042, China. .
Ren W
Cheng D
Gao J
Chen J
Li W
Xiao J
Liu T
Huang C
Chen Q
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 23-26.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
ABO Blood-Group System*/genetics
Alleles*
Female ; Genotype ; Humans ; Male ; Pedigree ; Phenotype
Czasopismo naukowe
Tytuł :
[Serological and molecular study of a novel B(A) allele with multiple missense mutations].
Autorzy :
Han B; Qingdao Blood Center, Shandong 266071, China. .
Zhang S
Zhu Y
Feng Z
Pang S
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 20-22.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
ABO Blood-Group System*/blood
ABO Blood-Group System*/genetics
Alleles*
Mutation, Missense*
Base Sequence ; Exons/genetics ; Humans ; Phenotype
Czasopismo naukowe
Tytuł :
[Molecular characterization of a recombination allele of ABO blood group].
Autorzy :
Hong X; Blood Center of Zhejiang Province, Zhejiang Provincial Key Laboratory of Blood Safety Research, Hangzhou, Zhejiang 310052, China. zfm00@ hotmail.com.
He Y
Chen S
Chen Y
Ying Y
Xu X
He J
Zhu F
Pokaż więcej
Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 15-19.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
ABO Blood-Group System*/genetics
Alleles*
Fucosyltransferases*/genetics
Recombination, Genetic*
Blood Grouping and Crossmatching ; Female ; Genotype ; Humans ; Phenotype
Czasopismo naukowe
Tytuł :
Relationship of PD-1 (PDCD1) and PD-L1 (CD274) Single Nucleotide Polymorphisms with Polycystic Ovary Syndrome.
Autorzy :
Han R; Department of Prenatal Diagnosis, Reproductive Medicine Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.; Department of Immunology, College of Basic Medicine, Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.; State Key Laboratory of Pathogenesis, Prevention, Treatment of Central Asian High incidence Diseases, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Gong X; Department of Reproductive Assistance, Center for Reproductive Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Zhu Y; Department of Reproductive Assistance, Center for Reproductive Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Liu X; Department of Prenatal Diagnosis, Reproductive Medicine Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Xia Y; Department of Prenatal Diagnosis, Reproductive Medicine Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Huang Y; Department of Immunology, College of Basic Medicine, Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Zhang M; Department of Reproductive Assistance, Center for Reproductive Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Zhang Y; Department of Immunology, College of Basic Medicine, Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
La X; Department of Reproductive Assistance, Center for Reproductive Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
Ding J; Department of Immunology, College of Basic Medicine, Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.; State Key Laboratory of Pathogenesis, Prevention, Treatment of Central Asian High incidence Diseases, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830011 Xinjiang, China.
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Źródło :
BioMed research international [Biomed Res Int] 2021 Jan 04; Vol. 2021, pp. 9596358. Date of Electronic Publication: 2021 Jan 04 (Print Publication: 2021).
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Polymorphism, Single Nucleotide*
B7-H1 Antigen/*genetics
Polycystic Ovary Syndrome/*genetics
Programmed Cell Death 1 Receptor/*genetics
Adult ; B7-H1 Antigen/blood ; Female ; Gene Frequency ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; Polycystic Ovary Syndrome/blood ; Programmed Cell Death 1 Receptor/blood ; Young Adult
Czasopismo naukowe
Tytuł :
Cartilage-Specific Cre Recombinase Transgenes/Alleles in the Mouse.
Autorzy :
Kanakis I; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Alhashmi M; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Liu K; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Keenan C; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Ramos Mucci L; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Poulet B; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Bou-Gharios G; Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK. .
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Źródło :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2021; Vol. 2245, pp. 23-38.
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Homologous Recombination*
Transgenes*
Cartilage, Articular/*metabolism
Integrases/*metabolism
Animals ; Gene Expression ; Gene Expression Regulation ; Gene Order ; Genetic Vectors/genetics ; Mice ; Mice, Transgenic ; Organ Specificity ; Promoter Regions, Genetic
Czasopismo naukowe
Tytuł :
Effect of APOE ε4 on multimodal brain connectomic traits: a persistent homology study.
Autorzy :
Li J; College of Automation, Harbin Engineering University, 145 Nantong Street, Harbin, 150001, Heilongjiang, China.
Bian C; College of Automation, Harbin Engineering University, 145 Nantong Street, Harbin, 150001, Heilongjiang, China.; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, B306 Richards Building, 3700 Hamilton Walk, Philadelphia, PA, 19104, USA.
Chen D; College of Automation, Harbin Engineering University, 145 Nantong Street, Harbin, 150001, Heilongjiang, China.
Meng X; School of Computer Information and Engineering, Changzhou Institute of Technology, Changzhou, 213032, China.
Luo H; College of Automation, Harbin Engineering University, 145 Nantong Street, Harbin, 150001, Heilongjiang, China.
Liang H; College of Automation, Harbin Engineering University, 145 Nantong Street, Harbin, 150001, Heilongjiang, China. .
Shen L; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, B306 Richards Building, 3700 Hamilton Walk, Philadelphia, PA, 19104, USA. .
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Corporate Authors :
Alzheimer’s Disease Neuroimaging Initiative
Źródło :
BMC bioinformatics [BMC Bioinformatics] 2020 Dec 28; Vol. 21 (Suppl 21), pp. 535. Date of Electronic Publication: 2020 Dec 28.
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Connectome*
Apolipoprotein E4/*genetics
Brain/*diagnostic imaging
Adult ; Aged ; Brain/physiopathology ; Diffusion Magnetic Resonance Imaging ; Female ; Heterozygote ; Humans ; Magnetic Resonance Imaging ; Male
Czasopismo naukowe
Tytuł :
Application of WES Towards Molecular Investigation of Congenital Cataracts: Identification of Novel Alleles and Genes in a Hospital-Based Cohort of South India.
Autorzy :
Kandaswamy DK; Department of Genetics, Dr. ALM Post Graduate Institute of Basic Medical Sciences, University of Madras, Tamil Nadu 600 113, India.; Institute of Developmental Genetics, Helmholtz Zentrum Munchen, D-85764 Munich, Germany.; School of Optometry and Vision Sciences, Cardiff University, Cardiff CF24 4HQ, UK.
Prakash MVS; Regional Institute of Ophthalmology, Government Eye Hospital, Egmore, Chennai 600 008, India.
Graw J; Institute of Developmental Genetics, Helmholtz Zentrum Munchen, D-85764 Munich, Germany.
Koller S; Institute of Medical Molecular Genetics, University of Zurich, CH-8952 Schlieren, Switzerland.
Magyar I; Institute of Medical Molecular Genetics, University of Zurich, CH-8952 Schlieren, Switzerland.
Tiwari A; Institute of Medical Molecular Genetics, University of Zurich, CH-8952 Schlieren, Switzerland.
Berger W; Institute of Medical Molecular Genetics, University of Zurich, CH-8952 Schlieren, Switzerland.; Zurich Center for Integrative Human Physiology, University of Zurich, 8057 Zurich, Switzerland.; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zurich, Switzerland.
Santhiya ST; Department of Genetics, Dr. ALM Post Graduate Institute of Basic Medical Sciences, University of Madras, Tamil Nadu 600 113, India.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2020 Dec 16; Vol. 21 (24). Date of Electronic Publication: 2020 Dec 16.
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Cataract/*genetics
Nuclear Receptor Coactivators/*genetics
Cataract/pathology ; Ephrin-A2/genetics ; Female ; Genetic Testing ; Humans ; Male ; Microtubule-Associated Proteins/genetics ; Mutation ; PAX6 Transcription Factor/genetics ; Pedigree ; Procollagen-Proline Dioxygenase/genetics ; Ribonucleoproteins/genetics ; Whole Genome Sequencing
Czasopismo naukowe
Tytuł :
Identifying potential germline variants from sequencing hematopoietic malignancies.
Autorzy :
Kraft IL; Section of Hematology/Oncology, Department of Medicine and The University of Chicago Comprehensive Cancer Center and.
Godley LA; Section of Hematology/Oncology, Department of Medicine and The University of Chicago Comprehensive Cancer Center and.; Department of Human Genetics, The University of Chicago, Chicago, IL.
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Źródło :
Hematology. American Society of Hematology. Education Program [Hematology Am Soc Hematol Educ Program] 2020 Dec 04; Vol. 2020 (1), pp. 219-227.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Alleles*
DNA Copy Number Variations*
Genetic Predisposition to Disease*
Germ-Line Mutation*
High-Throughput Nucleotide Sequencing*
Hematologic Neoplasms/*genetics
Aged ; Female ; Humans
Czasopismo naukowe
Tytuł :
Impact of HLA class I allele-level mismatch on viral infection within 100 days after cord blood transplantation.
Autorzy :
Iemura T; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Arai Y; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. .; Department of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan. .
Kanda J; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Kitawaki T; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Hishizawa M; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Kondo T; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Yamashita K; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Takaori-Kondo A; Department of Hematology and Oncology, Kyoto University, 54, Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
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Źródło :
Scientific reports [Sci Rep] 2020 Dec 03; Vol. 10 (1), pp. 21150. Date of Electronic Publication: 2020 Dec 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Alleles*
Cord Blood Stem Cell Transplantation/*adverse effects
Histocompatibility Antigens Class I/*genetics
Virus Diseases/*etiology
Virus Diseases/*genetics
Adult ; Aged ; Female ; Humans ; Incidence ; Male ; Middle Aged ; Multivariate Analysis ; Recurrence ; Risk Factors ; Treatment Outcome ; Virus Diseases/epidemiology ; Virus Diseases/mortality ; Young Adult
Czasopismo naukowe
Tytuł :
Probable HLA-mediated immunoediting of JAK2 V617F-driven oncogenesis.
Autorzy :
Ivanova M; Department of Clinical Immunology, University Hospital Alexandrovska, Medical University, Sofia, Bulgaria.
Tsvetkova G; Department of Clinical Hematology, University Hospital Alexandrovska, Medical University, Sofia, Bulgaria.
Lukanov T; Department of Clinical Immunology, University Hospital Alexandrovska, Medical University, Sofia, Bulgaria.
Stoimenov A; Laboratory of Transfusion Medicine, Sofiamed University Hospital, Sofia, Bulgaria.
Hadjiev E; Department of Clinical Hematology, University Hospital Alexandrovska, Medical University, Sofia, Bulgaria.
Shivarov V; Laboratory of Clinical Immunology, Sofiamed University Hospital, Sofia, Bulgaria; Department of Clinical Hematology, Sofiamed University Hospital, Sofia, Bulgaria; Department of Genetics, Faculty of Biology, St. Kliment Ohridski Sofia University, Sofia, Bulgaria. Electronic address: .
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Źródło :
Experimental hematology [Exp Hematol] 2020 Dec; Vol. 92, pp. 75-88.e10. Date of Electronic Publication: 2020 Oct 02.
Typ publikacji :
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Alleles*
Carcinogenesis*/genetics
Carcinogenesis*/immunology
Hematologic Neoplasms*/genetics
Hematologic Neoplasms*/immunology
Histocompatibility Antigens Class I*/genetics
Histocompatibility Antigens Class I*/immunology
Janus Kinase 2*/genetics
Janus Kinase 2*/immunology
Mutation, Missense*
Myeloproliferative Disorders*/genetics
Myeloproliferative Disorders*/immunology
Amino Acid Substitution ; Humans
Czasopismo naukowe
Tytuł :
Analysis of genomic distributions of SARS-CoV-2 reveals a dominant strain type with strong allelic associations.
Autorzy :
Yang HC; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan; .
Chen CH; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Wang JH; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Liao HC; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Yang CT; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Chen CW; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Lin YC; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.
Kao CH; Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.; Department of Statistics, Tamkang University, New Taipei City 251301, Taiwan.
Lu MJ; Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan.
Liao JC; Institute of Biological Chemistry, Academia Sinica, Taipei 11529, Taiwan .
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Źródło :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2020 Dec 01; Vol. 117 (48), pp. 30679-30686. Date of Electronic Publication: 2020 Nov 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Alleles*
Genome, Viral*
Genomics*
SARS-CoV-2/*genetics
Geography ; Humans ; Polymorphism, Single Nucleotide/genetics ; Time Factors
Czasopismo naukowe
Tytuł :
Discriminating between allele- and genotype-specific transmission ratio distortion.
Autorzy :
Casellas J; Departament de Ciència Animal i dels Aliments, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Id-Lahoucine S; Departament de Ciència Animal i dels Aliments, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.; Department of Animal Biosciences, Centre for Genetic Improvement of Livestock, University of Guelph, Guelph, ON, N1G 2W1, Canada.
Cánovas A; Department of Animal Biosciences, Centre for Genetic Improvement of Livestock, University of Guelph, Guelph, ON, N1G 2W1, Canada.
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Źródło :
Animal genetics [Anim Genet] 2020 Dec; Vol. 51 (6), pp. 847-854. Date of Electronic Publication: 2020 Sep 30.
Typ publikacji :
Journal Article
MeSH Terms :
Alleles*
Genotype*
Inheritance Patterns*
Models, Genetic*
Animals ; Cattle ; Female ; Heterozygote ; Male
Czasopismo naukowe
Tytuł :
Epidemiology, evolutionary origin, and malaria-induced positive selection effects of G6PD-deficient alleles in Chinese populations.
Autorzy :
Zheng Y; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Wang J; Reproductive Medicine Center, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Liang X; Department of Medical Genetics, Shantou University Medical College, Shantou, Guangdong, China.; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
Huang H; Department of Medical Genetics, Shantou University Medical College, Shantou, Guangdong, China.; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
Ma Y; School of Mathematics and Statistics, Hanshan Normal University, Chaozhou, Guangdong, China.
Lin L; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Wang C; Reproductive Medicine Center, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Zhan X; Department of Medical Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, Guangdong, China.
Yang L; Department of Medical Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, Guangdong, China.
Zha G; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Yang P; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Zou X; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Chen Z; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.
Chen X; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
Chen W; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
Liu X; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
Lin M; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, Guangdong Province, China.; Department of Medical Laboratory, Chaozhou People's Hospital Affiliated to Shantou University Medical College, Chaozhou, Guangdong, China.
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Źródło :
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Dec; Vol. 8 (12), pp. e1540. Date of Electronic Publication: 2020 Oct 31.
Typ publikacji :
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Alleles*
Evolution, Molecular*
Glucosephosphate Dehydrogenase Deficiency*/enzymology
Glucosephosphate Dehydrogenase Deficiency*/epidemiology
Glucosephosphate Dehydrogenase Deficiency*/genetics
Glucosephosphate Dehydrogenase Deficiency*/parasitology
Malaria*/enzymology
Malaria*/epidemiology
Malaria*/genetics
Mutation*
Glucosephosphate Dehydrogenase/*genetics
Asian Continental Ancestry Group ; China/epidemiology ; Humans ; Male ; Prevalence
Czasopismo naukowe

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