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Murat Bastepe

Showing results (1-10 of 88) with videos related to

Pageof 9
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Bone|September 11, 2017
GNAS mutations and heterotopic ossificationMurat Bastepe
Endocrine Development|February 9, 2013
Genetics and epigenetics of parathyroid hormone resistanceMurat Bastepe
The Journal of Clinical Endocrinology and Metabolism|July 19, 2018
A Gain-of-Function CASR Mutation Causing Hypocalcemia in a Recessive MannerMurat Bastepe
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 6, 2026
Gsα, Albright's hereditary osteodystrophy, and craniosynostosisMurat Bastepe
Current Genomics|May 5, 2009
The GNAS Locus: Quintessential Complex Gene Encoding Gsalpha, XLalphas, and other Imprinted TranscriptsMurat Bastepe
Advances in Experimental Medicine and Biology|April 1, 2008
The GNAS locus and pseudohypoparathyroidismMurat Bastepe
Reviews in Endocrine & Metabolic Disorders|March 28, 2008
Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulationMurat Bastepe, Harald Jüppner
Current Protocols in Human Genetics|October 7, 2015
Huntington Disease: Molecular Diagnostics ApproachMurat Bastepe, Winnie Xin
The New England Journal of Medicine|December 17, 2008
NHERF1 mutations and responsiveness of renal parathyroid hormoneClemens Bergwitz, Murat Bastepe
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Different mutations within or upstream of the GNAS locus cause distinct forms of pseudohypoparathyroidismHarald Jüppner, Murat Bastepe
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
Bone|September 11, 2017
GNAS mutations and heterotopic ossificationMurat Bastepe
Endocrine Development|February 9, 2013
Genetics and epigenetics of parathyroid hormone resistanceMurat Bastepe
The Journal of Clinical Endocrinology and Metabolism|July 19, 2018
A Gain-of-Function CASR Mutation Causing Hypocalcemia in a Recessive MannerMurat Bastepe
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 6, 2026
Gsα, Albright's hereditary osteodystrophy, and craniosynostosisMurat Bastepe
Current Genomics|May 5, 2009
The GNAS Locus: Quintessential Complex Gene Encoding Gsalpha, XLalphas, and other Imprinted TranscriptsMurat Bastepe
Advances in Experimental Medicine and Biology|April 1, 2008
The GNAS locus and pseudohypoparathyroidismMurat Bastepe
Reviews in Endocrine & Metabolic Disorders|March 28, 2008
Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulationMurat Bastepe, Harald Jüppner
Current Protocols in Human Genetics|October 7, 2015
Huntington Disease: Molecular Diagnostics ApproachMurat Bastepe, Winnie Xin
The New England Journal of Medicine|December 17, 2008
NHERF1 mutations and responsiveness of renal parathyroid hormoneClemens Bergwitz, Murat Bastepe
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Different mutations within or upstream of the GNAS locus cause distinct forms of pseudohypoparathyroidismHarald Jüppner, Murat Bastepe
Pageof 9