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JCI Insight|October 20, 2017
Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutationSarah A Howles, Fadil M Hannan, Caroline M Gorvin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 29, 2016
Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)Sian E Piret, Caroline M Gorvin, Alistair T Pagnamenta, et al.
The Journal of Clinical Endocrinology and Metabolism|August 3, 2012
Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomasPaul J Newey, M Andrew Nesbit, Andrew J Rimmer, et al.
The Journal of Biological Chemistry|February 27, 2004
Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndromeM Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
Microvascular Research|July 23, 2019
Quantitative assessment of the conjunctival microcirculation using a smartphone and slit-lamp biomicroscopePaul F Brennan, Andrew J McNeil, Min Jing, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|October 19, 2025
Topical mutant allele-specific siRNA delivery for treatment of Meesmann epithelial corneal dystrophy and elucidation of disease biomarkersAndrew McLain, Suzanne R Saffie-Siebert, Nadia Sukusu Nielsen, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2013
Whole-exome sequencing studies of nonfunctioning pituitary adenomasPaul J Newey, M Andrew Nesbit, Andrew J Rimmer, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|April 4, 2025
TGFBI R124H mutant allele silencing in granular corneal dystrophy type 2 using topical siRNA deliveryAndrew McLain, Amanda Kowalczyk, Paulina Baran-Rachwalska, et al.
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