Cargando…

Genetic Polymorphism of Human Y Chromosome and Risk Factors for Cardiovascular Diseases: A Study in WOBASZ Cohort

Genetic variants of Y chromosome predispose to hypertension in rodents, whereas in humans the evidence is conflicting. Our purpose was to study the distribution of a panel of Y chromosome markers in a cohort from a cross-sectional population-based study on the prevalence of cardiovascular risk facto...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kostrzewa, Grażyna, Broda, Grażyna, Konarzewska, Magdalena, Krajewki, Paweł, Płoski, Rafał
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723826/ https://www.ncbi.nlm.nih.gov/pubmed/23935855 http://dx.doi.org/10.1371/journal.pone.0068155

Ejemplares similares

Population Carrier Rates of Pathogenic ARSA Gene Mutations: Is Metachromatic Leukodystrophy Underdiagnosed?
por: Ługowska, Agnieszka, et al.
Publicado: (2011)

The Consumption of Nuts is Associated with Better Dietary and Lifestyle Patterns in Polish Adults: Results of WOBASZ and WOBASZ II Surveys
por: Witkowska, Anna M., et al.
Publicado: (2019)

Dietary Polyphenol Intake, but Not the Dietary Total Antioxidant Capacity, Is Inversely Related to Cardiovascular Disease in Postmenopausal Polish Women: Results of WOBASZ and WOBASZ II Studies
por: Witkowska, Anna M., et al.
Publicado: (2017)

Association between Variants on Chromosome 4q25, 16q22 and 1q21 and Atrial Fibrillation in the Polish Population
por: Kiliszek, Marek, et al.
Publicado: (2011)

Prevalence of cardiometabolic risk factors and selected cardiovascular diseases in hypertensive and normotensive participants in the adult Polish population: The WOBASZ II study
por: Niklas, Arkadiusz, et al.
Publicado: (2020)

Dietary Antioxidants, Quality of Nutrition and Cardiovascular Characteristics among Omnivores, Flexitarians and Vegetarians in Poland—The Results of Multicenter National Representative Survey WOBASZ
por: Kwaśniewska, Magdalena, et al.
Publicado: (2023)

Diabetic foot risk factors in type 2 diabetes patients: a cross-sectional case control study
por: Nehring, Piotr, et al.
Publicado: (2014)

Ten-Year Changes in the Prevalence and Socio-Demographic Determinants of Physical Activity among Polish Adults Aged 20 to 74 Years. Results of the National Multicenter Health Surveys WOBASZ (2003-2005) and WOBASZ II (2013-2014)
por: Kwaśniewska, Magdalena, et al.
Publicado: (2016)

Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
por: Stembalska, Agnieszka, et al.
Publicado: (2021)

Possible Association between Suicide Committed under Influence of Ethanol and a Variant in the AUTS2 Gene
por: Chojnicka, Izabela, et al.
Publicado: (2013)

Chronic kidney disease in Polish elderly population aged 75+: results of the WOBASZ Senior Survey
por: Zdrojewski, Łukasz, et al.
Publicado: (2016)

Prevalence, awareness, treatment and control of hypertension in the adult Polish population – Multi-center National Population Health Examination Surveys – WOBASZ studies
por: Niklas, Arkadiusz, et al.
Publicado: (2018)

Dietary Plant Sterols and Phytosterol-Enriched Margarines and Their Relationship with Cardiovascular Disease among Polish Men and Women: The WOBASZ II Cross-Sectional Study
por: Witkowska, Anna Maria, et al.
Publicado: (2022)

KIR2DS5 in the presence of HLA-C C2 protects against endometriosis
por: Nowak, Izabela, et al.
Publicado: (2015)

Filaggrin Gene Defects Are Independent Risk Factors for Atopic Asthma in a Polish Population: A Study in ECAP Cohort
por: Ponińska, Joanna, et al.
Publicado: (2011)

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes
por: Franaszczyk, Maria, et al.
Publicado: (2020)

Good performance of the criteria of American College of Medical Genetics and Genomics/Association for Molecular Pathology in prediction of pathogenicity of genetic variants causing thoracic aortic aneurysms and dissections
por: Ponińska, Joanna Kinga, et al.
Publicado: (2022)

Cytogenetic and genetic study of a Y-linked microsatellite polymorphism in Polish Black-and-White cattle breed
por: Parada, Rafał, et al.
Publicado: (2018)

Cardiovascular Disease Risk in Bears and Other Gay Men: A Descriptive Study from Poland
por: Mijas, Magdalena, et al.
Publicado: (2021)

The Role of Matrix Metalloproteinase-3 In the Development of Atherosclerosis and Cardiovascular Events
por: Magdalena, Krintus, et al.
Publicado: (2006)

Haplotype dependent association of rs7927894 (11q13.5) with atopic dermatitis and chronic allergic rhinitis: A study in ECAP cohort
por: Ponińska, Joanna Kinga, et al.
Publicado: (2017)

Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins—Diagnostic implications
por: Rydzanicz, Małgorzata, et al.
Publicado: (2020)

Aldosterone antagonist therapy and its relationship with inflammation, fibrosis, thrombosis, mineral-bone disorder and cardiovascular complications in peritoneal dialysis (PD) patients
por: Donderski, Rafał, et al.
Publicado: (2017)

Rules and Exceptions: The Role of Chromosomal ParB in DNA Segregation and Other Cellular Processes
por: Kawalek, Adam, et al.
Publicado: (2020)

Genetic polymorphism of Y-chromosome in Kazakh populations from Southern Kazakhstan
por: Ashirbekov, Yeldar, et al.
Publicado: (2023)

Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities
por: Szymańska, Edyta, et al.
Publicado: (2017)

The Genetic Basis of Graves' Disease
por: Płoski, Rafał, et al.
Publicado: (2011)

Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit
por: Goedbloed, Miriam, et al.
Publicado: (2009)

On the Forensic Use of Y-Chromosome Polymorphisms
por: de Knijff, Peter
Publicado: (2022)

Contemporary role of medical genetics in internal medicine
por: Saracyn, Marek, et al.
Publicado: (2013)

The Significance of VDR Genetic Polymorphisms in the Etiology of Preeclampsia in Pregnant Polish Women
por: Magiełda-Stola, Justyna, et al.
Publicado: (2021)

Rapid and effective response of the R222Q SCN5A to quinidine treatment in a patient with Purkinje-related ventricular arrhythmia and familial dilated cardiomyopathy: a case report
por: Zakrzewska-Koperska, Joanna, et al.
Publicado: (2018)

Circulating and Platelet MicroRNAs in Cardiovascular Risk Assessment and Antiplatelet Therapy Monitoring
por: Procyk, Grzegorz, et al.
Publicado: (2022)

Age at onset of obesity, transcription factor 7-like 2 (TCF7L2) rs7903146 polymorphism, adiponectin levels and the risk of type 2 diabetes in obese patients
por: Wrzosek, Małgorzata, et al.
Publicado: (2017)

Analysis of male specific region of the human Y chromosome sheds light on historical events in Nazi occupied eastern Poland
por: Diepenbroek, Marta, et al.
Publicado: (2018)

Endometriosis Is Associated with Functional Polymorphism in the Promoter of Heme Oxygenase 1 (HMOX1) Gene
por: Milewski, Łukasz, et al.
Publicado: (2021)

Does Inclusion of Education and Marital Status Improve SCORE Performance in Central and Eastern Europe and Former Soviet Union? Findings from MONICA and HAPIEE Cohorts
por: Vikhireva, Olga, et al.
Publicado: (2014)

Long-term Follow Up of a Boy with Unilateral Autosomal Dominant Polycystic Kidney Disease and Contralateral Renal Agenesis
por: Krzemień, Grażyna, et al.
Publicado: (2018)

Experiencing Stress among Different Professional Groups in the Context of Their Age
por: Bartkowiak, Grażyna, et al.
Publicado: (2022)

Academic Teachers about Their Productivity and a Sense of Well-Being in the Current COVID-19 Epidemic
por: Bartkowiak, Grażyna, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_t290l20uj4vk8ln8nl805d93sa