Showing results (41-50 of 2,608) with videos related to

Sort By:
Pageof 261
Pediatrics|February 4, 2003
Safety profile of frequent short courses of oral glucocorticoids in acute pediatric asthma: impact on bone metabolism, bone density, and adrenal functionFrancine M Ducharme, Gilles Chabot, Constantin Polychronakos, et al.
The Journal of Biological Chemistry|September 24, 2002
A common autoimmunity predisposing signal peptide variant of the cytotoxic T-lymphocyte antigen 4 results in inefficient glycosylation of the susceptibility alleleSuzana Anjos, Audrey Nguyen, Houria Ounissi-Benkalha, et al.
Diabetes|March 31, 2007
Toward further mapping of the association between the IL2RA locus and type 1 diabetesHui-Qi Qu, Alexander Montpetit, Bing Ge, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
The insulin-like growth factor-II receptor gene is associated with type 1 diabetes: evidence of a maternal effectJennifer A McCann, Yong Qin Xu, Rosalie Frechette, et al.
BMC Genomics|August 19, 2006
Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphismsHui-Qi Qu, Steve G Lawrence, Fan Guo, et al.
Health Education Research|July 21, 2009
Compensatory beliefs about glucose testing are associated with low adherence to treatment and poor metabolic control in adolescents with type 1 diabetesMarjorie A Rabiau, Bärbel Knäuper, Thien-Kim Nguyen, et al.
Molecular Immunology|November 30, 2006
No association of type 1 diabetes with a functional polymorphism of the LRAP geneHui-Qi Qu, Luc Marchand, Rosalie Fréchette, et al.
Diabetes/Metabolism Research and Reviews|August 7, 2012
Overexpression of ZAC impairs glucose-stimulated insulin translation and secretion in clonal pancreatic beta-cellsXiaoyu Du, Houria Ounissi-Benkalha, Merewyn K Loder, et al.
Human Genetics|July 4, 2013
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited diseaseDavid N Cooper, Michael Krawczak, Constantin Polychronakos, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 21, 2015
A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case seriesIsabelle Rousseau-Nepton, Minoru Okubo, Rosemarie Grabs, et al.
Pageof 261