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Annals of the New York Academy of Sciences|August 21, 2015
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordanceAhmed Khattab, Tony Yuen, Sultan Al-Malki, et al.
Pituitary|August 3, 2024
Neuroendocrinology of boneSe-Min Kim, Farhath Sultana, Funda Korkmaz, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 2006
TNFalpha mediates the skeletal effects of thyroid-stimulating hormoneHidenori Hase, Takao Ando, Leslie Eldeiry, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyMaria I New, Moolamannil Abraham, Brian Gonzalez, et al.
Biochemical and Biophysical Research Communications|February 23, 2010
FSH-receptor isoforms and FSH-dependent gene transcription in human monocytes and osteoclastsLisa J Robinson, Irina Tourkova, Yujuan Wang, et al.
Current Osteoporosis Reports|December 9, 2009
Bone loss or lost bone: rationale and recommendations for the diagnosis and treatment of early postmenopausal bone lossMone Zaidi, Charles H Turner, Ernesto Canalis, et al.
Scientific Reports|October 18, 2017
Denervation-related alterations and biological activity of miRNAs contained in exosomes released by skeletal muscle fibersRita De Gasperi, Sayyed Hamidi, Lauren M Harlow, et al.
Experimental Physiology|May 13, 2022
Notch, Numb and Numb-like responses to exercise-induced muscle damage in human skeletal muscleMatthew P Bubak, Kevan Stout, Julia Tomtschik, et al.
Archives of Neurology|March 11, 2009
PGC-1alpha expression decreases in the Alzheimer disease brain as a function of dementiaWeiping Qin, Vahram Haroutunian, Pavel Katsel, et al.
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