Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kripa Asrani"'
Autor:
Semira Gonseth, Gary M. Shaw, Ritu Roy, Mark R. Segal, Kripa Asrani, Jasper Rine, Joseph Wiemels, Nicholas J. Marini
Publikováno v:
Epigenetics, Vol 14, Iss 2, Pp 198-213 (2019)
Cleft lip with or without cleft palate (CL/P) is a common human birth defect whose etiologies remain largely unknown. Several studies have demonstrated that periconceptional supplementation of folic acid can reduce risk of CL/P in offspring. In this
Externí odkaz:
https://doaj.org/article/a44c6ec8b0b940e9b45c59b522f17f40
Publikováno v:
Genetic Testing and Molecular Biomarkers
Aims: Archived newborn bloodspots are valuable sample collections for genetic and epigenetic disease research. However, they have often been stored for long periods of time, under less than ideal circumstances, and nucleic acid yields can be low, par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46bb13cd3cdf1bf61b2277485aab8814
http://europepmc.org/articles/PMC5568181
http://europepmc.org/articles/PMC5568181
Publikováno v:
American journal of medical genetics. Part A, vol 179, iss 7
American Journal of Medical Genetics. Part a
American Journal of Medical Genetics. Part a
Cleft lip with/without cleft palate (CLP) is a common craniofacial malformation with complex etiologies, reflecting both genetic and environmental factors. Most of the suspected genetic risk for CLP has yet to be identified. To further classify risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cb0c6b44986c9f313baa0790382abc5
https://escholarship.org/uc/item/4350z591
https://escholarship.org/uc/item/4350z591
Autor:
Mark R. Segal, Jasper Rine, Semira Gonseth, Gary M. Shaw, Ritu Roy, Nicholas J. Marini, Joseph L. Wiemels, Kripa Asrani
Publikováno v:
Epigenetics, vol 14, iss 2
Epigenetics
Epigenetics, vol. 14, no. 2, pp. 198-213
Epigenetics
Epigenetics, vol. 14, no. 2, pp. 198-213
Cleft lip with or without cleft palate (CL/P) is a common human birth defect whose etiologies remain largely unknown. Several studies have demonstrated that periconceptional supplementation of folic acid can reduce risk of CL/P in offspring. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b348783b2ac15eb951bce0d58b0772
https://escholarship.org/uc/item/1k0481c5
https://escholarship.org/uc/item/1k0481c5
Sequence Variation in Folate Pathway Genes and Risks of Human Cleft Lip with or without Cleft Palate
Autor:
Wei Yang, John S. Witte, Edward J. Lammer, Kripa Asrani, Jasper Rine, Gary M. Shaw, Nicholas J. Marini
Publikováno v:
American journal of medical genetics. Part A, vol 170, iss 11
Marini, Nicholas J; Yang, Wei; Asrani, Kripa; Witte, John S; Rine, Jasper; Lammer, Edward J; et al.(2016). Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate.. American journal of medical genetics. Part A, 170(11), 2777-2787. doi: 10.1002/ajmg.a.37874. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/4495s4tm
Marini, Nicholas J; Yang, Wei; Asrani, Kripa; Witte, John S; Rine, Jasper; Lammer, Edward J; et al.(2016). Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate.. American journal of medical genetics. Part A, 170(11), 2777-2787. doi: 10.1002/ajmg.a.37874. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/4495s4tm
In an effort to comprehensively interrogate genetic variation in the folate pathway for risk of cleft lip with or without cleft palate (CLP), we evaluated 504 common and rare variants in 35 folate-related genes in a panel of 330 infants with CLP and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6bae1b561579e35ae80c01685517c0b
https://europepmc.org/articles/PMC5634616/
https://europepmc.org/articles/PMC5634616/