Zobrazeno 1 - 10
of 180
pro vyhledávání: '"Family-based association test"'
Publikováno v:
Lipids in Health and Disease, Vol 17, Iss 1, Pp 1-7 (2018)
Abstract Background The serum lipid profile, including LDL-C level, is associated with hypertension which is the major cause of cerebrovascular disease (CVD) amounting 30% of global death rate. Previous work also demonstrated important roles of genet
Externí odkaz:
https://doaj.org/article/22a16b40e4604d4897b36a32ab1e6fe5
Publikováno v:
Kidney & Blood Pressure Research, Vol 41, Iss 1, Pp 18-28 (2016)
Background/Aims: Hypertension or persistent high blood pressure (BP) is a leading cause of death worldwide. Extensive evidence indicates that the thiazide-sensitive Na+-Cl- cotrans-porter (NCC) affects BP via regulation of renal sodium reabsorption.
Externí odkaz:
https://doaj.org/article/ee77ddc0d7f848219a521d1550d99efa
Publikováno v:
Proceedings of the National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, vol 117, iss 39
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, vol 117, iss 39
Significance The goal of genome-wide association studies is to identify meaningful relationships between genotypes and outcomes of interest. One challenge in the analysis of genetic data is that not all true statistical associations represent relevan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4826d021d4c67fdc2133fbc01679645
https://doi.org/10.1073/pnas.2007743117
https://doi.org/10.1073/pnas.2007743117
Publikováno v:
Indian Journal of Dermatology, Vol 52, Iss 1, Pp 21-26 (2007)
Background: The aim of this study was to investigate the role of FcgRIIB gene in susceptibility to systemic lupus erythematosus (SLE) using family-based association study and to examine possible interaction between the Ile225Thr (rs1050501, exon 5) p
Externí odkaz:
https://doaj.org/article/e7f6e526d991477d85ea83075dcfe9bc
Autor:
Erika Villa, Michael Escamilla, Robert Gonzalez, Juan Zavala, Javier Contreras, Regina Armas, Alfonso Ontiveros, Henriette Raventós, Suzanne Gonzalez, Albana M Dassori, Robin J. Leach, Humberto Nicolini, Alvaro Jerez, Mercedes Ramirez, Deborah Flores
Publikováno v:
Journal of Affective Disorders, Vol.186, pp.367-375
Kérwá
Universidad de Costa Rica
instacron:UCR
Kérwá
Universidad de Costa Rica
instacron:UCR
Background: Variations in circadian genes can impact biological rhythms. Given the rhythm disturbances that characterize bipolar disorder (BD), genes encoding components of molecular clocks are good candidate genes for the illness. Methods: A family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99e364d8e7507f3f9ae443b30231081
Akademický článek
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Publikováno v:
Lipids in Health and Disease
Lipids in Health and Disease, Vol 17, Iss 1, Pp 1-7 (2018)
Lipids in Health and Disease, Vol 17, Iss 1, Pp 1-7 (2018)
Background The serum lipid profile, including LDL-C level, is associated with hypertension which is the major cause of cerebrovascular disease (CVD) amounting 30% of global death rate. Previous work also demonstrated important roles of genetic varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cfa9c671c499e2957ae1563d1606098
https://pubmed.ncbi.nlm.nih.gov/29661184
https://pubmed.ncbi.nlm.nih.gov/29661184
Autor:
Li-Chun Xu, Zhen Ding, Rui Zhang, Qi Wang, Jia-Wei Hong, Zheng Li, Jun-Yu Shen, Xing Ge, Gang Chen
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Objective: Non-syndromic cleft of the lip and/or palate (NSCL/P) is one of the most common polygenic diseases. In this study, both case–control and family-based association study were used
Objective: Non-syndromic cleft of the lip and/or palate (NSCL/P) is one of the most common polygenic diseases. In this study, both case–control and family-based association study were used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f9256061233d4a0fefe60c066cd405
https://doi.org/10.1097/md.0000000000016170
https://doi.org/10.1097/md.0000000000016170
Autor:
Young Seok Ju, Hansoo Park, Jong Il Kim, Sung-Il Cho, Jung Eun Lee, Hyun-Jin Kim, Seung-Bok Lee, Joohon Sung, Yun Joo Yoo, Jeong-Sun Seo
Publikováno v:
Kidney International. 83(2):285-292
The estimated glomerular filtration rate is a well-known measure of renal function and is widely used to follow the course of disease. Although there have been several investigations establishing the genetic background contributing to renal function,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3076cb1fd2bb10448460d2915259309a
Autor:
Li, Ming, Li, Jingyun, He, Zihuai, Lu, Qing, Witte, John S, Macleod, Stewart L, Hobbs, Charlotte A, Cleves, Mario A, National Birth Defects Prevention Study
Publikováno v:
Genetic epidemiology, vol 40, iss 4
Family-based association studies are commonly used in genetic research because they can be robust to population stratification (PS). Recent advances in high-throughput genotyping technologies have produced a massive amount of genomic data in family-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::cbebd7f698fae8334b57168d6646262b
https://escholarship.org/uc/item/2f96j0kf
https://escholarship.org/uc/item/2f96j0kf
