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Wyszukujesz frazę ""Heredity"" wg kryterium: Temat


Starter badań:

Tytuł :
Chicken embryo as a model in epigenetic research.
Autorzy :
Bednarczyk M; Department of Animal Biotechnology and Genetics, UTP University of Science and Technology, 85-084 Bydgoszcz, Poland. Electronic address: .
Dunislawska A; Department of Animal Biotechnology and Genetics, UTP University of Science and Technology, 85-084 Bydgoszcz, Poland.
Stadnicka K; Department of Animal Biotechnology and Genetics, UTP University of Science and Technology, 85-084 Bydgoszcz, Poland.
Grochowska E; Department of Animal Biotechnology and Genetics, UTP University of Science and Technology, 85-084 Bydgoszcz, Poland.
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Źródło :
Poultry science [Poult Sci] 2021 Jul; Vol. 100 (7), pp. 101164. Date of Electronic Publication: 2021 Mar 26.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Chickens*
Heredity*
Animals ; Chick Embryo ; DNA Methylation ; Embryonic Development ; Epigenesis, Genetic ; Phenotype
Czasopismo naukowe
Tytuł :
[Heredity and cancer].
Autorzy :
Docampo E; Services de Génétique Humaine et de Rhumatologie,CHU Liège, Belgique.
Martin M; Service de Génétique Humaine, CHU Liège, Belgique.
Gangolf M; Service des Informations médico-économiques,CHU Liège, Belgique.
Harvengt J; Service de Génétique Humaine, CHU Liège, Belgique.
Bulk S; Service de Génétique Humaine, CHU Liège, Belgique.
Segers K; Service de Génétique Humaine, CHU Liège, Belgique.
Leroi N; Service de Génétique Humaine, CHU Liège, Belgique.
Lete C; Service de Génétique Humaine, CHU Liège, Belgique.
Palmariciotti V; Service de Génétique Humaine, CHU Liège, Belgique.
Freire Chadrina V; Laboratoire de Génétique Humaine, GIGA, ULiège, Belgique.
Lambert F; Service de Génétique Humaine, CHU Liège, Belgique.
Bours V; Service de Génétique Humaine, CHU Liège et GIGA, ULiège; ERN GETURIS, Belgique.
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Transliterated Title :
Hérédité et cancer.
Źródło :
Revue medicale de Liege [Rev Med Liege] 2021 May; Vol. 76 (5-6), pp. 327-336.
Typ publikacji :
Journal Article
MeSH Terms :
Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis
Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics
Heredity*
Ovarian Neoplasms*
Child ; Female ; Genetic Predisposition to Disease ; Genetic Testing ; Humans
Czasopismo naukowe
Tytuł :
Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease.
Autorzy :
Durkie M; Sheffield Diagnostics Genetic Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
Chong J; Kidney Genetics Group, Academic Nephrology Unit, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Sheffield, UK.
Valluru MK; Kidney Genetics Group, Academic Nephrology Unit, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Sheffield, UK.
Harris PC; Division of Nephrology and Hypertension, Mayo Clinic and Foundation, Rochester, MN, USA.
Ong ACM; Kidney Genetics Group, Academic Nephrology Unit, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield Medical School, Sheffield, UK. .
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Źródło :
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2021 Apr; Vol. 23 (4), pp. 689-697. Date of Electronic Publication: 2020 Nov 10.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Heredity*
Polycystic Kidney, Autosomal Dominant*/diagnosis
Polycystic Kidney, Autosomal Dominant*/epidemiology
Polycystic Kidney, Autosomal Dominant*/genetics
Child ; Humans ; Infant ; Mutation ; TRPP Cation Channels/genetics ; Whole Exome Sequencing
Czasopismo naukowe
Tytuł :
Philipp Jolly and his 1913 "the heredity of psychosis": Homogeneity versus heterogeneity of familial transmission and an early look at Mendelian models for manic-depressive illness and dementia praecox.
Autorzy :
Kendler KS; Virginia Institute of Psychiatric and Behavioral Genetics, and Department of Psychiatry, Medical College of Virginia/Virginia Commonwealth University, Richmond, Virginia, USA.
Klee A; Valentino Drive, Kirstenhof, Cape Town, South Africa.
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Źródło :
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2021 Mar; Vol. 186 (2), pp. 90-100. Date of Electronic Publication: 2021 Jan 22.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Genetic Predisposition to Disease*
Heredity*
Bipolar Disorder/*genetics
Dementia/*genetics
Genetic Diseases, X-Linked/*genetics
Psychotic Disorders/*genetics
Bipolar Disorder/pathology ; Dementia/pathology ; Genetic Diseases, X-Linked/pathology ; Humans ; Mendelian Randomization Analysis ; Psychotic Disorders/pathology
SCR Disease Name :
Major Affective Disorder 2
Czasopismo naukowe
Tytuł :
Who's afraid of epigenetics? Habits, instincts, and Charles Darwin's evolutionary theory.
Autorzy :
Portera M; Dipartimento di Lettere e Filosofia, University of Florence, Firenze, Italy. .
Mandrioli M; Dipartimento di Scienze della Vita, University of Modena e Reggio Emilia, Modena, Italy.
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Źródło :
History and philosophy of the life sciences [Hist Philos Life Sci] 2021 Feb 10; Vol. 43 (1), pp. 20. Date of Electronic Publication: 2021 Feb 10.
Typ publikacji :
Biography; Historical Article; Journal Article
MeSH Terms :
Biological Evolution*
Epigenesis, Genetic*
Habits*
Heredity*
Selection, Genetic*
Epigenomics/*history
History, 19th Century
Personal Name as Subject :
Darwin C
Czasopismo naukowe
Tytuł :
[Concern about liver disease in children].
Autorzy :
Kuerbanjiang A; Department of Infectious Disease, Children's Hospital of Fudan University, Shanghai 201102, China.
Wang JS; Department of Infectious Disease, Children's Hospital of Fudan University, Shanghai 201102, China.
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Źródło :
Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology [Zhonghua Gan Zang Bing Za Zhi] 2021 Jan 20; Vol. 29 (1), pp. 5-8.
Typ publikacji :
Journal Article
MeSH Terms :
Heredity*
Liver Diseases*/diagnosis
Liver Diseases*/epidemiology
Child ; Disease Progression ; Humans ; Quality of Life
Czasopismo naukowe
Tytuł :
Hereditary Disorders of Cardiovascular Calcification.
Autorzy :
Rutsch F; Department of General Pediatrics, Muenster University Children's Hospital, Germany.
Buers I; Department of General Pediatrics, Muenster University Children's Hospital, Germany.
Nitschke Y; Department of General Pediatrics, Muenster University Children's Hospital, Germany.
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Źródło :
Arteriosclerosis, thrombosis, and vascular biology [Arterioscler Thromb Vasc Biol] 2021 Jan; Vol. 41 (1), pp. 35-47. Date of Electronic Publication: 2020 Nov 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Heredity*
Aortic Diseases/*genetics
Arteries/*metabolism
Dental Enamel Hypoplasia/*genetics
Metabolism, Inborn Errors/*genetics
Metacarpus/*abnormalities
Muscular Diseases/*genetics
Odontodysplasia/*genetics
Osteogenesis/*genetics
Osteoporosis/*genetics
Vascular Calcification/*genetics
Animals ; Aortic Diseases/complications ; Aortic Diseases/metabolism ; Arteries/pathology ; Dental Enamel Hypoplasia/complications ; Dental Enamel Hypoplasia/metabolism ; Gaucher Disease/complications ; Gaucher Disease/genetics ; Gaucher Disease/metabolism ; Genetic Predisposition to Disease ; Humans ; Metabolism, Inborn Errors/complications ; Metabolism, Inborn Errors/metabolism ; Metacarpus/metabolism ; Muscular Diseases/complications ; Muscular Diseases/metabolism ; Odontodysplasia/complications ; Odontodysplasia/metabolism ; Osteoporosis/complications ; Osteoporosis/metabolism ; Phenotype ; Risk Assessment ; Risk Factors ; Vascular Calcification/complications ; Vascular Calcification/metabolism ; Vascular Calcification/pathology
SCR Disease Name :
Singleton Merten syndrome
Czasopismo naukowe
Tytuł :
Transgenerational Inheritance: That Pathogen Gut Feeling.
Autorzy :
Rechavi O; Department of Neurobiology, Wise Faculty of Life Sciences and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel. Electronic address: .
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Źródło :
Current biology : CB [Curr Biol] 2020 Dec 21; Vol. 30 (24), pp. R1486-R1488.
Typ publikacji :
Journal Article; Comment
MeSH Terms :
Heredity*
Nematoda*/genetics
Animals ; Caenorhabditis elegans/genetics ; Inheritance Patterns/genetics ; RNA
Czasopismo naukowe
Tytuł :
Special Issue "Disentangling Mechanisms of Genomic Regulation of Cell Functions at the Gene Level".
Autorzy :
Binder H; IZBI, Interdisciplinary Centre for Bioinformatics, Universität Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.
Arakelyan A; Research Group of Bioinformatics, Institute of Molecular Biology NAS RA, 7 Hasratyan st, Yerevan 0014, Armenia.
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Źródło :
Genes [Genes (Basel)] 2020 Dec 07; Vol. 11 (12). Date of Electronic Publication: 2020 Dec 07.
Typ publikacji :
Editorial; Introductory Journal Article
MeSH Terms :
Genome, Human*
Genomics*
Heredity*
Animals ; Humans
Czasopismo naukowe
Tytuł :
Co-inherited novel SNPs of the LIPE gene associated with increased carcass dressing and decreased fat-tail weight in Awassi breed.
Autorzy :
Al-Thuwaini TM; Department of Animal Production, College of Agriculture, Al-Qasim Green University, Al-Qasim, Babil, 51001, Iraq. .
Al-Shuhaib MBS; Department of Animal Production, College of Agriculture, Al-Qasim Green University, Al-Qasim, Babil, 51001, Iraq.
Lepretre F; Plateau de genomique fonctionnelle et structurale, CHU Lille, University of Lille, Lille, France.
Mahdi ZA; Department of Animal Production, College of Agriculture, Al-Qasim Green University, Al-Qasim, Babil, 51001, Iraq.
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Źródło :
Tropical animal health and production [Trop Anim Health Prod] 2020 Nov; Vol. 52 (6), pp. 3631-3638. Date of Electronic Publication: 2020 Sep 17.
Typ publikacji :
Journal Article
MeSH Terms :
Heredity*
Polymorphism, Single Nucleotide*
Adipose Tissue/*metabolism
Lipoprotein Lipase/*genetics
Meat/*analysis
Sheep, Domestic/*physiology
Animals ; Iraq ; Linkage Disequilibrium ; Lipoprotein Lipase/metabolism ; Male ; Sheep, Domestic/metabolism
Czasopismo naukowe
Tytuł :
Revisiting Darwin's thoughts on environmentally induced heritable changes.
Autorzy :
Liu Y; Henan Institute of Science and Technology, Xinxiang 453003, China; Department of Medicine, University of Alberta, Edmonton T6G 2R3, Canada. Electronic address: .
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Źródło :
The Science of the total environment [Sci Total Environ] 2020 Oct 10; Vol. 738, pp. 139540. Date of Electronic Publication: 2020 May 20.
Typ publikacji :
Letter; Comment
MeSH Terms :
Heredity*
Biological Evolution ; Selection, Genetic
Opinia redakcyjna
Tytuł :
Pesticides and transgenerational inheritance of pathologies: Designing, analysing and reporting rodent studies.
Autorzy :
Plewis I; Social Statistics, School of Social Sciences, University of Manchester, Manchester, United Kingdom.
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Źródło :
PloS one [PLoS One] 2020 Oct 01; Vol. 15 (10), pp. e0228762. Date of Electronic Publication: 2020 Oct 01 (Print Publication: 2020).
Typ publikacji :
Journal Article
MeSH Terms :
Heredity*
Models, Statistical*
Rodentia*
Research Design/*standards
Animal Structures/drug effects ; Animal Structures/pathology ; Animals ; Humans ; Models, Animal ; Pesticides/adverse effects ; Public Health ; Sample Size ; Washington
Czasopismo naukowe
Tytuł :
Causal inference in genetic trio studies.
Autorzy :
Bates S; Department of Statistics, Stanford University, Stanford, CA 94305; .
Sesia M; Department of Data Sciences and Operations, Marshall School of Business, University of Southern California, Los Angeles, CA 90089.
Sabatti C; Department of Statistics, Stanford University, Stanford, CA 94305.; Department of Biomedical Data Science, Stanford University, Stanford, CA 94305.
Candès E; Department of Statistics, Stanford University, Stanford, CA 94305; .; Department of Mathematics, Stanford University, Stanford, CA 94305.
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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 Sep 29; Vol. 117 (39), pp. 24117-24126. Date of Electronic Publication: 2020 Sep 18.
Typ publikacji :
Comparative Study; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Genetic Association Studies*
Genetic Techniques*
Genetic Variation*
Heredity*
Phenotype*
Humans
Czasopismo naukowe
Tytuł :
The concepts of heredity and degeneration in the work of Jean-Martin Charcot.
Autorzy :
Walusinski O; Independent Researcher , Brou, France.
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Źródło :
Journal of the history of the neurosciences [J Hist Neurosci] 2020 Jul-Sep; Vol. 29 (3), pp. 299-324. Date of Electronic Publication: 2020 Feb 11.
Typ publikacji :
Biography; Historical Article; Journal Article; Portrait
MeSH Terms :
Heredity*
Nerve Degeneration*
Neurology/*history
France ; History, 19th Century ; History, 20th Century ; Humans
Personal Name as Subject :
Charcot J
Czasopismo naukowe
Tytuł :
A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene.
Autorzy :
Liu Y; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China; Department of Neurology, Suzhou Ninth People's Hospital, Suzhou 215200, China.
Huang S; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Yu L; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Li T; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Diao S; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Chen Z; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Zhou G; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Sheng X; Department of Neurology, Suzhou Ninth People's Hospital, Suzhou 215200, China.
Xu Y; Department of Neurology, Suzhou Ninth People's Hospital, Suzhou 215200, China. Electronic address: .
Fang Q; Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China. Electronic address: .
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Źródło :
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2021 Aug; Vol. 30 (8), pp. 105674. Date of Electronic Publication: 2021 Jun 10.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Mutation, Missense*
CADASIL/*genetics
Receptor, Notch3/*genetics
Adult ; Asian Continental Ancestry Group/genetics ; CADASIL/diagnosis ; CADASIL/ethnology ; China ; DNA Mutational Analysis ; Exons ; Female ; Genetic Predisposition to Disease ; Heredity ; Heterozygote ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Pedigree ; Phenotype
Czasopismo naukowe
Tytuł :
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.
Corporate Authors :
International Mismatch Repair Consortium
Źródło :
The Lancet. Oncology [Lancet Oncol] 2021 Jul; Vol. 22 (7), pp. 1014-1022. Date of Electronic Publication: 2021 Jun 07.
Typ publikacji :
Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene-Environment Interaction*
Residence Characteristics*
Colorectal Neoplasms, Hereditary Nonpolyposis/*epidemiology
Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics
Adult ; Age Factors ; Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis ; Female ; Genetic Predisposition to Disease ; Heredity ; Humans ; Male ; Middle Aged ; Pedigree ; Phenotype ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Sex Factors
Czasopismo naukowe
Tytuł :
Defective folate metabolism causes germline epigenetic instability and distinguishes Hira as a phenotype inheritance biomarker.
Autorzy :
Blake GET; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.; College of Medicine and Health, University of Exeter Medical School, Exeter, UK.
Zhao X; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.
Yung HW; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.
Burton GJ; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.
Ferguson-Smith AC; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.; Department of Genetics, University of Cambridge, Cambridge, UK.
Hamilton RS; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK.; Department of Genetics, University of Cambridge, Cambridge, UK.
Watson ED; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK. .; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK. .
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Źródło :
Nature communications [Nat Commun] 2021 Jun 17; Vol. 12 (1), pp. 3714. Date of Electronic Publication: 2021 Jun 17.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
DNA Methylation*
Cell Cycle Proteins/*metabolism
Ferredoxin-NADP Reductase/*genetics
Folic Acid/*metabolism
Germ Cells/*metabolism
Histone Chaperones/*metabolism
Inheritance Patterns/*genetics
Maternal Inheritance/*genetics
Transcription Factors/*metabolism
Animals ; Biomarkers/metabolism ; Cell Cycle Proteins/genetics ; Embryo, Mammalian/metabolism ; Epigenesis, Genetic ; Epigenomics ; Female ; Ferredoxin-NADP Reductase/metabolism ; Heredity ; Histone Chaperones/genetics ; Liver/metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Pedigree ; Phenotype ; Polymorphism, Single Nucleotide ; Spermatozoa/metabolism ; Transcription Factors/genetics ; Trophoblasts/metabolism ; Whole Genome Sequencing
Czasopismo naukowe
Tytuł :
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke.
Autorzy :
Bruno G; Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Ritelli M; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Di Pietro A; Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Cipriano L; Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Colombi M; Division of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Lus G; Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Puoti G; Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy. Electronic address: .
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Źródło :
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2021 Jun; Vol. 30 (6), pp. 105744. Date of Electronic Publication: 2021 Apr 01.
Typ publikacji :
Journal Article
MeSH Terms :
Genetic Heterogeneity*
Ischemic Stroke/*genetics
Methylenetetrahydrofolate Reductase (NADPH2)/*genetics
Multidrug Resistance-Associated Proteins/*genetics
Plasminogen Activator Inhibitor 1/*genetics
Pseudoxanthoma Elasticum/*genetics
Thrombophilia/*genetics
Adult ; Female ; Genetic Predisposition to Disease ; Heredity ; Humans ; Ischemic Stroke/blood ; Ischemic Stroke/diagnosis ; Male ; Pedigree ; Pseudoxanthoma Elasticum/complications ; Pseudoxanthoma Elasticum/diagnosis ; Risk Assessment ; Risk Factors ; Thrombophilia/blood ; Thrombophilia/complications ; Thrombophilia/diagnosis
Czasopismo naukowe
Tytuł :
Parental transgenerational epigenetic inheritance related to dietary crude oil exposure in Danio rerio .
Autorzy :
Bautista NM; Developmental Integrative Biology Research Group, Department of Biological Sciences, University of North Texas, 1155 Union Circle #305220, Denton, TX 76203-5017, USA .; Zoophysiology, Department of Bioscience, Aarhus University, C. F. Møllers Alle 3, Aarhus C 8000, Denmark.
Crespel A; Developmental Integrative Biology Research Group, Department of Biological Sciences, University of North Texas, 1155 Union Circle #305220, Denton, TX 76203-5017, USA.; Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK.
Crossley J; Developmental Integrative Biology Research Group, Department of Biological Sciences, University of North Texas, 1155 Union Circle #305220, Denton, TX 76203-5017, USA.
Padilla P; Developmental Integrative Biology Research Group, Department of Biological Sciences, University of North Texas, 1155 Union Circle #305220, Denton, TX 76203-5017, USA.
Burggren W; Developmental Integrative Biology Research Group, Department of Biological Sciences, University of North Texas, 1155 Union Circle #305220, Denton, TX 76203-5017, USA.
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Źródło :
The Journal of experimental biology [J Exp Biol] 2020 Aug 20; Vol. 223 (Pt 16). Date of Electronic Publication: 2020 Aug 20.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Heredity*
Petroleum*
Animals ; Epigenesis, Genetic ; Female ; Humans ; Male ; Paternal Exposure/adverse effects ; Zebrafish/genetics
Czasopismo naukowe

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