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Genetics and Molecular Research : GMR|May 27, 2017
SETD5 gene variant associated with mild intellectual disability - a case reportE Stur, L A Soares, I D Louro
Genetics and Molecular Research : GMR|July 11, 2017
Steroid metabolism gene polymorphisms and their implications on breast and ovarian cancer prognosisE V W Dos Santos, L N R Alves, I D Louro
Genetics and Molecular Research : GMR|August 6, 2013
Analysis of microsatellite instability and loss of heterozygosity in ovarian cancer: a study in the population of Espírito Santo, BrazilL N R Alves, E V Wolfgramm, A K de Castro Neto, et al.
Genetics and Molecular Research : GMR|July 16, 2016
HPRTYale proposed as a pathogenic variant for Lesch-Nyhan syndrome: a case reportE Stur, R S Reis, L P Agostini, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|August 7, 1999
The zinc finger protein GLI induces cellular sensitivity to the mTOR inhibitor rapamycinI D Louro, P McKie-Bell, H Gosnell, et al.
Genetics and Molecular Research : GMR|May 14, 2016
Molecular epidemiology of HFE gene polymorphic variants (C282Y, H63D and S65C) in the population of Espírito Santo, BrazilL N R Alves, E V W Santos, E Stur, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|October 1, 2019
Maternal polymorphisms in the FADS1 and FADS2 genes modify the association between PUFA ingestion and plasma concentrations of omega-3 polyunsaturated fatty acidsG Q Carvalho, M Pereira-Santos, L D Marcon, et al.
Genetics and Molecular Research : GMR|October 6, 2016
Comparative analysis of short tandem repeat data obtained by automated and gel electrophoresis techniquesU R Pagel, R S Reis, V P Carvalho, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 6, 2007
Analysis of Factor VIII polymorphic markers as a means for carrier detection in Brazilian families with haemophilia AF M de Carvalho, E de Vargas Wolfgramm, G G Paneto, et al.
Molecular Biology Reports|November 27, 2010
Cystic fibrosis Δf508 mutation screening in Brazilian women with altered fertilityG V F Brunoro, E V Wolfgramm, I D Louro, et al.
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