G Velasco, V Savarese, N Sandorfi, SA Jimenez… - Endocrine Practice, 2011 - AACE Submitted for publication June 21, 2010 Accepted for publication August 18, 2010 *Fellows. German Velasco is now affiliated with the Division of Endocrinology, Hawthorn Medical Associates, North Dartmouth, Massachusetts. From the 1Division of Endocrinology, ... Related articles
J Tornberg, GP Sykiotis, K Keefe… - Proceedings of the …, 2011 - National Acad Sciences Neuronal development is the result of a multitude of neural migrations, which require extensive cell-cell communication. These processes are modulated by extracellular matrix components, such as heparan sulfate (HS) polysaccharides. HS is molecularly complex ... Related articles - All 3 versions
RM Harris, J Weiss… - Endocrinology, 2011 - Endocrine Soc The genetic etiologies of male infertility remain largely unknown. To identify genes potentially involved in spermatogenesis and male infertility, we performed genome-wide mutagenesis in mice with N-ethyl-N-nitrosourea and identified a line with dominant hypogonadism and ...
A Cariboni, K Davidson, S Rakic… - Human Molecular …, 2011 - Oxford Univ Press Kallmann syndrome (KS) is a genetic disease characterized by hypogonadotropic hypogonadism and impaired sense of smell. The genetic causes underlying this syndrome are still largely unknown, but are thought to be due to a developmental defect in the migration of ... Cited by 1 - Related articles - All 4 versions
V Rochira, A Balestrieri, L Zirilli… - Endocrine …, 2011 - endocrine-abstracts.org Introduction: At puberty, the raise of serum estradiol (E 2 ) (after testosterone conversion) is needed to fuse ephiphyses and to complete bone maturation in boys. Owing to severe hypogonadism and very low circulating testosterone, adult men with congenital hypogonadotropic ... Cached
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