Výsledky vyhľadávania - "HEREDITY"

When life began with fully acquired heredity: a non-standard hypothesis of evolutionary origins.

Autori: Cao Q Duan Y

Zdroj: Theory in biosciences = Theorie in den Biowissenschaften [Theory Biosci] 2025 Dec 05; Vol. 145 (1), pp. 3. Date of Electronic Publication: 2025 Dec 05.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Urban & Fischer Country of Publication: Germany NLM ID: 9708216 Publication Model: Electronic Cited Medium: Internet ISSN: 1611-7530 (Electronic) Linking ISSN: 14317613 NLM ISO Abbreviation: Theory Biosci Subsets: MEDLINE

Výrazy zo slovníka MeSH: Biological Evolution* , Heredity*, Selection, Genetic ; Phenotype ; Animals ; Models, Genetic ; Humans ; DNA/genetics

How critics of racial hereditarian research (mis)categorize empirical studies: Commentary on Bird et al. (2024).

Autori: León FR; Graduate School, Universidad San Ignacio de Loyola.

Zdroj: The American psychologist [Am Psychol] 2025 Jul-Aug; Vol. 80 (5), pp. 838-839.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: American Psychological Association Country of Publication: United States NLM ID: 0370521 Publication Model: Print Cited Medium: Internet ISSN: 1935-990X (Electronic) Linking ISSN: 0003066X NLM ISO Abbreviation: Am Psychol Subsets: MEDLINE

Výrazy zo slovníka MeSH: Racism* , Heredity* , Empirical Research*, Humans

Socio-economic status is a social construct with heritable components and genetic consequences.

Autori: Abdellaoui A Martin HC Kolk M a ďalší

Zdroj: Nature human behaviour [Nat Hum Behav] 2025 May; Vol. 9 (5), pp. 864-876. Date of Electronic Publication: 2025 Mar 26.

Spôsob vydávania: Journal Article; Review

Informácie o časopise: Publisher: Springer Nature Publishing Country of Publication: England NLM ID: 101697750 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2397-3374 (Electronic) Linking ISSN: 23973374 NLM ISO Abbreviation: Nat Hum Behav Subsets: MEDLINE

Výrazy zo slovníka MeSH: Social Class* , Heredity*, Humans ; Genomics

Freud, Heredity, and Genetics.

Autori: Tran The J Ansermet F

Zdroj: The Psychoanalytic quarterly [Psychoanal Q] 2025; Vol. 94 (4), pp. 723-766. Date of Electronic Publication: 2025 Nov 05.

Spôsob vydávania: Journal Article; Historical Article

Informácie o časopise: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 0226661 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2167-4086 (Electronic) Linking ISSN: 00332828 NLM ISO Abbreviation: Psychoanal Q Subsets: MEDLINE

Výrazy zo slovníka MeSH: Freudian Theory* , Psychoanalysis*/history , Mental Disorders*/genetics , Heredity*, Humans ; Genome-Wide Association Study ; History, 20th Century

Inbred rat heredity and sex affect oral oxycodone self-administration and augmented intake in long sessions: correlations with anxiety and novelty-seeking.

Autori: Sharp BM Leng S Huang J a ďalší

Zdroj: PloS one [PLoS One] 2025 Mar 10; Vol. 20 (3), pp. e0314777. Date of Electronic Publication: 2025 Mar 10 (Print Publication: 2025).

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

Výrazy zo slovníka MeSH: Oxycodone*/administration & dosage , Anxiety*/genetics , Exploratory Behavior*/drug effects , Heredity*, Animals ; Male ; Self Administration ; Female ; Rats ; Administration, Oral ; Sex Factors

Psychogenetic Features of Heredity and Pathology.

Autori: Spytska L; Department of Psychology and Pedagogy, Kyiv International University, Kyiv, Ukraine.

Zdroj: The Journal of nervous and mental disease [J Nerv Ment Dis] 2025 Feb 01; Vol. 213 (2), pp. 58-63. Date of Electronic Publication: 2025 Jan 10.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0375402 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1539-736X (Electronic) Linking ISSN: 00223018 NLM ISO Abbreviation: J Nerv Ment Dis Subsets: MEDLINE

Výrazy zo slovníka MeSH: Genetic Predisposition to Disease*/genetics , Heredity* , Mental Disorders*/genetics , Mental Disorders*/psychology , Mental Disorders*/pathology, Child ; Humans ; Autism Spectrum Disorder/genetics ; Autism Spectrum Disorder/psychology ; Gene-Environment Interaction ; Schizophrenia/genetics

High Diagnostic Yield of Genetic Screening in Autosomal Dominant Steroid-Resistant Nephrotic Syndrome: Predominance of INF2 and TRPC6 and Identification of a Novel Gene.

Autori: Azouaou L; Department of Nephrology, Chief of Hemodialysis Unit, CHU Hussein Dey, Algiers, Algeria.; Laboratory of Oxidative Stress, Kidney and Associated Complications Faculty of Medicine Algiers, University of Health Sciences, Algiers, Algeria.

Zdroj: Nephrology (Carlton, Vic.) [Nephrology (Carlton)] 2025 Dec; Vol. 30 (12), pp. e70152.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Blackwell Science Country of Publication: Australia NLM ID: 9615568 Publication Model: Print Cited Medium: Internet ISSN: 1440-1797 (Electronic) Linking ISSN: 13205358 NLM ISO Abbreviation: Nephrology (Carlton) Subsets: MEDLINE

Výrazy zo slovníka MeSH: TRPC6 Cation Channel*/genetics , Nephrotic Syndrome*/genetics , Nephrotic Syndrome*/diagnosis , Nephrotic Syndrome*/congenital , Genetic Testing*/methods , Mutation*, Humans ; Male ; Female ; Adult ; Child ; Adolescent ; Retrospective Studies ; Phenotype ; Young Adult ; Middle Aged ; Algeria/epidemiology ; Genetic Predisposition to Disease ; Child, Preschool ; Pedigree ; DNA Mutational Analysis ; Genetic Association Studies ; Actinin/genetics ; High-Throughput Nucleotide Sequencing ; Drug Resistance/genetics ; WT1 Proteins/genetics ; Predictive Value of Tests ; Heredity ; Formins

SCR Disease Name: Nephrotic syndrome, idiopathic, steroid-resistant

Child-parent cascade screening for familial hypercholesterolemia in Slovenia: Insights from the pilot program.

Autori: Šikonja J Kobale K Kafol J a ďalší

Zdroj: Atherosclerosis [Atherosclerosis] 2025 Dec; Vol. 411, pp. 120541. Date of Electronic Publication: 2025 Nov 17.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Elsevier Country of Publication: Ireland NLM ID: 0242543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1484 (Electronic) Linking ISSN: 00219150 NLM ISO Abbreviation: Atherosclerosis Subsets: MEDLINE

Výrazy zo slovníka MeSH: Hyperlipoproteinemia Type II*/genetics , Hyperlipoproteinemia Type II*/diagnosis , Hyperlipoproteinemia Type II*/epidemiology , Hyperlipoproteinemia Type II*/blood , Genetic Testing*/methods , Parents* , Mutation*, Humans ; Pilot Projects ; Slovenia/epidemiology ; Male ; Female ; Child ; Genetic Predisposition to Disease ; Child, Preschool ; Adult ; Prevalence ; Predictive Value of Tests ; Phenotype ; Pedigree ; Heredity ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/genetics ; Receptors, LDL/genetics

Synergic combination of the monogenic ANGPTL3 p.H343R variant and a polygenic predisposition in a family with hypobetalipoproteinemia.

Autori: Levy M Janin A Marmontel O a ďalší

Zdroj: Atherosclerosis [Atherosclerosis] 2025 Dec; Vol. 411, pp. 120569. Date of Electronic Publication: 2025 Nov 04.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Elsevier Country of Publication: Ireland NLM ID: 0242543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1484 (Electronic) Linking ISSN: 00219150 NLM ISO Abbreviation: Atherosclerosis Subsets: MEDLINE

Výrazy zo slovníka MeSH: Angiopoietin-like Proteins*/genetics , Angiopoietin-like Proteins*/metabolism , Multifactorial Inheritance* , Mutation, Missense* , Hypobetalipoproteinemias*/genetics , Hypobetalipoproteinemias*/blood , Hypobetalipoproteinemias*/diagnosis, Humans ; Angiopoietin-Like Protein 3/genetics ; Female ; Male ; Genetic Predisposition to Disease ; Pedigree ; Middle Aged ; Adult ; Phenotype ; Cholesterol, LDL/blood ; Heterozygote ; Heredity

Mendelian causes of early-onset emphysema: a review of the current literature.

Autori: Karabatic A van den Berge M Carroll TP a ďalší

Zdroj: European respiratory review : an official journal of the European Respiratory Society [Eur Respir Rev] 2025 Nov 12; Vol. 34 (178). Date of Electronic Publication: 2025 Nov 12 (Print Publication: 2025).

Spôsob vydávania: Journal Article; Review

Informácie o časopise: Publisher: European Respiratory Society Country of Publication: England NLM ID: 9111391 Publication Model: Electronic-Print Cited Medium: Internet ISSN: 1600-0617 (Electronic) Linking ISSN: 09059180 NLM ISO Abbreviation: Eur Respir Rev Subsets: MEDLINE

Výrazy zo slovníka MeSH: Pulmonary Emphysema*/genetics , Pulmonary Emphysema*/physiopathology , Pulmonary Emphysema*/diagnosis , Pulmonary Emphysema*/epidemiology , Mutation* , Lung*/physiopathology, Humans ; Genetic Predisposition to Disease ; Phenotype ; Risk Factors ; Age of Onset ; Heredity ; Pulmonary Disease, Chronic Obstructive/genetics ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Pulmonary Disease, Chronic Obstructive/diagnosis

The Somatic Impact on Inheritance and the Germline Control of the Soma.

Autori: Ishikawa S Schumacher B

Zdroj: Annual review of genetics [Annu Rev Genet] 2025 Nov; Vol. 59 (1), pp. 91-117. Date of Electronic Publication: 2025 Jul 16.

Spôsob vydávania: Journal Article; Review

Informácie o časopise: Publisher: Annual Reviews Country of Publication: United States NLM ID: 0117605 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1545-2948 (Electronic) Linking ISSN: 00664197 NLM ISO Abbreviation: Annu Rev Genet Subsets: MEDLINE

Výrazy zo slovníka MeSH: Germ Cells*/metabolism , Germ Cells*/physiology , Epigenesis, Genetic* , Inheritance Patterns*/genetics, Humans ; Animals ; Heredity ; Reproduction/genetics

Are children with familial type 1 diabetes from Kuwait different? Report on prevalence, clinical, biochemical, and immunological characteristics.

Autori: Al-Abdulrazzaq D Hudda MT Hussein DK a ďalší

Zdroj: Primary care diabetes [Prim Care Diabetes] 2025 Oct; Vol. 19 (5), pp. 533-539. Date of Electronic Publication: 2025 Jun 11.

Spôsob vydávania: Journal Article; Observational Study; Comparative Study

Informácie o časopise: Publisher: Elsevier Country of Publication: England NLM ID: 101463825 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0210 (Electronic) Linking ISSN: 18780210 NLM ISO Abbreviation: Prim Care Diabetes Subsets: MEDLINE

Výrazy zo slovníka MeSH: Diabetes Mellitus, Type 1*/epidemiology , Diabetes Mellitus, Type 1*/immunology , Diabetes Mellitus, Type 1*/genetics , Diabetes Mellitus, Type 1*/diagnosis , Diabetes Mellitus, Type 1*/blood, Humans ; Kuwait/epidemiology ; Prevalence ; Female ; Male ; Child ; Child, Preschool ; Phenotype ; Biomarkers/blood ; Registries ; Adolescent ; Genetic Predisposition to Disease ; Glycated Hemoglobin/metabolism ; Glycated Hemoglobin/analysis ; C-Peptide/blood ; Risk Factors ; Heredity ; Infant ; Blood Glucose/metabolism ; Age of Onset ; Age Factors

Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach.

Autori: Ylipää J Andersson T

Zdroj: Scandinavian cardiovascular journal : SCJ [Scand Cardiovasc J] 2024 Dec; Vol. 58 (1), pp. 2379356. Date of Electronic Publication: 2024 Jul 24.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Taylor & Francis Country of Publication: England NLM ID: 9708377 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1651-2006 (Electronic) Linking ISSN: 14017431 NLM ISO Abbreviation: Scand Cardiovasc J Subsets: MEDLINE

Výrazy zo slovníka MeSH: Cardiomyopathy, Dilated*/genetics , Cardiomyopathy, Dilated*/diagnosis , Pedigree* , Genetic Testing* , Genetic Predisposition to Disease* , Predictive Value of Tests* , Heredity* , Phenotype*, Humans ; Retrospective Studies ; Female ; Male ; Middle Aged ; Adult ; Echocardiography ; Medical History Taking ; Electrocardiography ; Time Factors ; Aged ; Risk Factors

SCR Disease Name: familial dilated cardiomyopathy

Positive genetic effect of hypertension family history on stroke: A cross Mendelian randomization study.

Autori: Chi X Zhang J Yin X

Zdroj: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association [J Stroke Cerebrovasc Dis] 2024 Oct; Vol. 33 (10), pp. 107901. Date of Electronic Publication: 2024 Aug 02.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Saunders Country of Publication: United States NLM ID: 9111633 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-8511 (Electronic) Linking ISSN: 10523057 NLM ISO Abbreviation: J Stroke Cerebrovasc Dis Subsets: MEDLINE

Výrazy zo slovníka MeSH: Mendelian Randomization Analysis* , Hypertension*/genetics , Hypertension*/epidemiology , Hypertension*/physiopathology , Hypertension*/diagnosis , Genetic Predisposition to Disease* , Genome-Wide Association Study* , Stroke*/genetics , Stroke*/diagnosis , Stroke*/epidemiology , Heredity*, Humans ; Risk Factors ; Risk Assessment ; Phenotype ; Pedigree ; Polymorphism, Single Nucleotide ; Blood Pressure/genetics ; Databases, Genetic

Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants.

Autori: Ishikawa T Kimoto H Seki A a ďalší

Zdroj: Cardiovascular research [Cardiovasc Res] 2025 Sep 29; Vol. 121 (11), pp. 1712-1721.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Oxford Journals Country of Publication: England NLM ID: 0077427 Publication Model: Print Cited Medium: Internet ISSN: 1755-3245 (Electronic) Linking ISSN: 00086363 NLM ISO Abbreviation: Cardiovasc Res Subsets: MEDLINE

Výrazy zo slovníka MeSH: Connectin*/genetics , Connectin*/metabolism , RNA Splice Sites* , RNA Splicing* , Cardiomyopathies*/genetics , Cardiomyopathies*/physiopathology , Cardiomyopathy, Dilated*/genetics , Cardiomyopathy, Dilated*/physiopathology , Mutation* , Cardiac Conduction System Disease*/genetics , Cardiac Conduction System Disease*/physiopathology , Arrhythmias, Cardiac*/genetics , Arrhythmias, Cardiac*/physiopathology, Humans ; Phenotype ; Male ; Pedigree ; Female ; Genetic Predisposition to Disease ; Middle Aged ; Myocytes, Cardiac/metabolism ; Myocytes, Cardiac/pathology ; Exome Sequencing ; Adult ; Aged ; Whole Genome Sequencing ; Action Potentials ; Cells, Cultured ; Induced Pluripotent Stem Cells/metabolism ; Heredity

A novel NOTCH1 nonsense variant in a bicuspid aortic valve family with intrafamilial clinical heterogeneity.

Autori: Chen Q Xu ZY Chi W a ďalší

Zdroj: BMC cardiovascular disorders [BMC Cardiovasc Disord] 2025 Sep 29; Vol. 25 (1), pp. 706. Date of Electronic Publication: 2025 Sep 29.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: BioMed Central Country of Publication: England NLM ID: 100968539 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2261 (Electronic) Linking ISSN: 14712261 NLM ISO Abbreviation: BMC Cardiovasc Disord Subsets: MEDLINE

Výrazy zo slovníka MeSH: Receptor, Notch1*/genetics , Bicuspid Aortic Valve Disease*/genetics , Bicuspid Aortic Valve Disease*/diagnostic imaging , Aortic Valve*/abnormalities , Aortic Valve*/diagnostic imaging , Heart Valve Diseases*/genetics , Heart Valve Diseases*/diagnostic imaging , Codon, Nonsense*, Humans ; Phenotype ; Pedigree ; Female ; Male ; Genetic Predisposition to Disease ; Adult ; Heredity ; Exome Sequencing ; Middle Aged ; China ; DNA Mutational Analysis

Plant Breeding and the Origins of Genetics.

Autori: Roll-Hansen N; Department of Philosophy, Classics, History of Art and Ideas, University of Oslo, Blidern, 0315 Oslo, Norway nils.roll-hansen@ifikk.uio.no.

Zdroj: Cold Spring Harbor perspectives in biology [Cold Spring Harb Perspect Biol] 2025 Sep 02; Vol. 17 (9). Date of Electronic Publication: 2025 Sep 02.

Spôsob vydávania: Historical Article; Journal Article

Informácie o časopise: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 101513680 Publication Model: Electronic Cited Medium: Internet ISSN: 1943-0264 (Electronic) Linking ISSN: 19430264 NLM ISO Abbreviation: Cold Spring Harb Perspect Biol Subsets: MEDLINE

Výrazy zo slovníka MeSH: Genetics*/history , Plant Breeding*/history , Plants*/genetics, Biological Evolution ; Genetics, Population/history ; Heredity ; History, 19th Century ; History, 20th Century ; Phenotype ; Selection, Genetic

Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene Mutation.

Autori: Santoro F D'Apolito M Ragnatela I a ďalší

Zdroj: Journal of cardiovascular electrophysiology [J Cardiovasc Electrophysiol] 2025 Sep; Vol. 36 (9), pp. 2132-2139. Date of Electronic Publication: 2025 Jun 23.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: Blackwell Country of Publication: United States NLM ID: 9010756 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-8167 (Electronic) Linking ISSN: 10453873 NLM ISO Abbreviation: J Cardiovasc Electrophysiol Subsets: MEDLINE

Výrazy zo slovníka MeSH: Brugada Syndrome*/genetics , Brugada Syndrome*/diagnosis , Brugada Syndrome*/physiopathology , Brugada Syndrome*/therapy , Caveolin 3*/genetics , G-Protein-Coupled Receptor Kinase 5*/genetics , Mutation, Missense* , Receptors, Adrenergic, beta-1*/genetics, Female ; Humans ; Male ; Middle Aged ; Action Potentials ; Defibrillators, Implantable ; DNA Mutational Analysis ; Electric Countershock/instrumentation ; Exome Sequencing ; Genetic Predisposition to Disease ; Heart Rate ; Heredity ; Pedigree ; Phenotype

Contribution and interaction of polygenic predisposition and family history of coronary heart disease in predicting cardiovascular risk.

Autori: Galimberti F Olmastroni E Casula M a ďalší

Zdroj: Atherosclerosis [Atherosclerosis] 2025 Sep; Vol. 408, pp. 120451. Date of Electronic Publication: 2025 Jul 17.

Spôsob vydávania: Journal Article; Research Support, Non-U.S. Gov't

Informácie o časopise: Publisher: Elsevier Country of Publication: Ireland NLM ID: 0242543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1484 (Electronic) Linking ISSN: 00219150 NLM ISO Abbreviation: Atherosclerosis Subsets: MEDLINE

Výrazy zo slovníka MeSH: Multifactorial Inheritance* , Coronary Disease*/genetics , Coronary Disease*/epidemiology , Coronary Disease*/diagnosis, Humans ; Female ; Male ; Middle Aged ; Genetic Predisposition to Disease ; Risk Assessment ; Aged ; United Kingdom/epidemiology ; Risk Factors ; Heredity ; Medical History Taking ; Adult ; Heart Disease Risk Factors

Glucose metabolism in heterozygous familial hypercholesterolemia with a founder effect and a high diabetes prevalence: a cross-sectional study.

Autori: González-Lleó AM Brito-Casillas Y Martín-Santana V a ďalší

Zdroj: Cardiovascular diabetology [Cardiovasc Diabetol] 2025 Aug 06; Vol. 24 (1), pp. 322. Date of Electronic Publication: 2025 Aug 06.

Spôsob vydávania: Journal Article

Informácie o časopise: Publisher: BioMed Central Country of Publication: England NLM ID: 101147637 Publication Model: Electronic Cited Medium: Internet ISSN: 1475-2840 (Electronic) Linking ISSN: 14752840 NLM ISO Abbreviation: Cardiovasc Diabetol Subsets: MEDLINE

Výrazy zo slovníka MeSH: Diabetes Mellitus, Type 2*/epidemiology , Diabetes Mellitus, Type 2*/diagnosis , Diabetes Mellitus, Type 2*/genetics , Diabetes Mellitus, Type 2*/blood , Receptors, LDL*/genetics , Hyperlipoproteinemia Type II*/genetics , Hyperlipoproteinemia Type II*/epidemiology , Hyperlipoproteinemia Type II*/diagnosis , Hyperlipoproteinemia Type II*/blood , Blood Glucose*/metabolism , Blood Glucose*/genetics , Mutation* , Founder Effect*, Humans ; Cross-Sectional Studies ; Male ; Female ; Prevalence ; Middle Aged ; Adult ; Genetic Predisposition to Disease ; Heterozygote ; Phenotype ; Biomarkers/blood ; Risk Factors ; Insulin Resistance/genetics ; Heredity ; Spain/epidemiology ; Risk Assessment ; Italy/epidemiology ; Aged