From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Journal of the American Society of Nephrology : JASN 2017 May .
Heidet Laurence, Morinière Vincent, Henry Charline, De Tomasi Lara, Reilly Madeline Louise, Humbert Camille, Alibeu Olivier, Fourrage Cécile, Bole-Feysot Christine, Nitschké Patrick, Tores Frédéric, Bras Marc, Jeanpierre Marc, Pietrement Christine, Gaillard Dominique, Gonzales Marie, Novo Robert, Schaefer Elise, Roume Joëlle, Martinovic Jelena, Malan Valérie, Salomon Rémi, Saunier Sophie, Antignac Corinne, Jeanpierre Céci - Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thrombosis and haemostasis 2017 Feb .
Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari - MTHFR Gene Polymorphism-Mutations and Air Pollution as Risk Factors for Breast Cancer: A Metaprediction Study.
Nursing research 2017 Jan .
Gonzales Mildred C, Yu Pojui, Shiao S Pamela - The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer.
Clinical epigenetics 2017 9 26.
Savio Andrea J, Mrkonjic Miralem, Lemire Mathieu, Gallinger Steven, Knight Julia A, Bapat Bhar - MeQTL analysis of childhood obesity links epigenetics with a risk SNP rs17782313 near MC4R from meta-analysis.
Oncotarget 2016 Dec .
Tang Yuping, Jin Bo, Zhou Lingling, Lu Weife
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