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Plos One|March 17, 2015
Osteocytic protein expression response to doxercalciferol therapy in pediatric dialysis patientsRenata C Pereira, Harald Jüppner, Barbara Gales, et al.Endocrine Pathology|March 7, 2020
Immunohistochemicaf evidence of parathyroid hormone-related protein in human parathyroid tissuePer Hellman, Gunnel Bjerneroth, Claes Juhlin, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 12, 2020
A Novel GNAS Duplication Associated With Loss-of-Methylation Restricted to Exon A/B Causes Pseudohypoparathyroidism Type Ib (PHP1B)Monica Reyes, Masayo Kagami, Sayaka Kawashima, et al.The Journal of Clinical Endocrinology and Metabolism|July 26, 2013
Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal developmentNicolas Richard, Arnaud Molin, Nadia Coudray, et al.Bone|October 23, 2010
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)Murat Bastepe, Ozge Altug-Teber, Chhavi Agarwal, et al.European Journal of Endocrinology|June 12, 2010
Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type IbSerap Turan, Leyla Akin, Teoman Akcay, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 19, 2016
Prolonged Pharmacokinetic and Pharmacodynamic Actions of a Pegylated Parathyroid Hormone (1-34) Peptide FragmentJun Guo, Ashok Khatri, Akira Maeda, et al.The Journal of Clinical Endocrinology and Metabolism|May 7, 2010
Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cisSmitha Chillambhi, Serap Turan, Daw-Yang Hwang, et al.Molecular Endocrinology (Baltimore, Md.)|July 30, 2002
Receptor-mediated adenylyl cyclase activation through XLalpha(s), the extra-large variant of the stimulatory G protein alpha-subunitMurat Bastepe, Yasemin Gunes, Beatriz Perez-Villamil, et al.Nature Genetics|October 13, 2006
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasisBettina Lorenz-Depiereux, Murat Bastepe, Anna Benet-Pagès, et al.Pageof 49