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American Journal of Medical Genetics. Part A|December 2, 2017
Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1AKatia M Perez, Evon B Lee, Sachini Kahanda, et al.The Journal of Clinical Investigation|August 28, 2020
Selective pharmacological inhibition of the sodium-dependent phosphate cotransporter NPT2a promotes phosphate excretionValerie Clerin, Hiroshi Saito, Kevin J Filipski, et al.Bone|February 1, 2022
A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/BDevon Campbell, Monica Reyes, Sare Betul Kaygusuz, et al.Journal of Perinatal Medicine|March 8, 2006
Is the nausea and vomiting of early pregnancy really feto-protective?M Margaret Weigel, Monica Reyes, Maria Elena Caiza, et al.The Journal of Clinical Endocrinology and Metabolism|April 29, 2017
Early-Onset Obesity: Unrecognized First Evidence for GNAS Mutations and Methylation ChangesAnnette Grüters-Kieslich, Monica Reyes, Amita Sharma, et al.Proceedings of the National Academy of Sciences of the United States of America|April 13, 2012
Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism IbEduardo Fernández-Rebollo, Akira Maeda, Monica Reyes, et al.Proceedings of the National Academy of Sciences of the United States of America|April 18, 2025
Bidirectional disruption of GNAS transcripts causes broad methylation defects in pseudohypoparathyroidism type 1BYorihiro Iwasaki, Monica Reyes, Anna Ryabets-Lienhard, et al.JBMR Plus|October 9, 2023
Substantially Delayed Maturation of Growth Plate Chondrocytes in "Humanized" PTH1R Mice with the H223R Mutation of Jansen's DiseaseMonica Reyes, Damla Firat, Patrick Hanna, et al.Endocrinology|February 10, 2011
Transgenic overexpression of the extra-large Gsα variant XLαs enhances Gsα-mediated responses in the mouse renal proximal tubule in vivoZun Liu, Hiroko Segawa, Cumhur Aydin, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 20, 2015
Analysis of Multiple Families With Single Individuals Affected by Pseudohypoparathyroidism Type Ib (PHP1B) Reveals Only One Novel Maternally Inherited GNAS DeletionRieko Takatani, Angelo Molinaro, Giedre Grigelioniene, et al.Pageof 5