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Cis-regulatory elements are harbored in intron5 of the runx1 gene
(BIOMED CENTRAL, 2014)
Cis-regulatory elements are harbored in intron5 of the runx1 gene
(BIOMED CENTRAL, 2014)
Intron retention as an alternative splice variant of the rat urocortin 1 gene
(PERGAMON-ELSEVIER SCIENCE LTD,, 2006)
Novel intronic mutation of men1 gene causing familial isolated primary hyperparathyroidism
(ISSUED FOR THE ENDOCRINE SOCIETY BY THE WILLIAMS & WILKINS CO, 2004)
Polymorphisms in the rac1 gene are associated with hypertension risk factors in a chilean pediatric population
(OXFORD UNIV PRESS, 2014)
The GTPase Rac1 has been implicated in hypertension as a modulator of mineralocorticoid receptor activity. Our aim is to investigate the frequency of polymorphisms rs10951982 (intron 1, G > A) and rs836478 (intron 3, T > ...
Uncovering population structure in the Humboldt penguin (Spheniscus humboldti) along the Pacific coast at South America
(2019)
The upwelling hypothesis has been proposed to explain reduced or lack of population structure in seabird species specialized in food resources available at cold-water upwellings. However, population genetic structure may ...
A de novo unequal cross-over mutation between cyp11b1 and cyp11b2 genes causes familial hyperaldosteronism type i
(SPRINGER, 2011)
Familial hyperaldosteronism type I (FH-I) is an autosomal dominant disorder caused by an unequal cross-over of the gene encoding steroid 11 beta-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2), giving rise to a ...
Genomic Analysis On Subjects Exposed To Arsenic Identifies Genetic Risk Variants Associated With Bladder Cancer And Variants Under Recent Adaptive Selection
(2018)
INTRODUCTION AND OBJECTIVES: Only a small fraction of arsenic-exposed subjects is affected by malignant iseases. This suggests the existence of genetic risk factors influencing susceptibility to arseniasis and its consequences, ...