Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Endocrinology|June 3, 2017
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic TherapyValerie N Babinsky, Fadil M Hannan, Reshma D Ramracheya, et al.
Scientific Reports|April 22, 2022
A novel algorithm for cardiovascular screening using conjunctival microcirculatory parameters and blood biomarkersAgnes Awuah, Julie S Moore, M Andrew Nesbit, et al.
Human Molecular Genetics|January 14, 2016
Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophyEdwin H A Allen, David G Courtney, Sarah D Atkinson, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2014
Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3)Angela Rogers, M Andrew Nesbit, Fadil M Hannan, et al.
Nephron. Physiology|June 24, 2009
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's diseaseFiona Wu, Anita A C Reed, Sian E Williams, et al.
BMJ Open|June 30, 2021
Evaluation of the IgG antibody response to SARS CoV-2 infection and performance of a lateral flow immunoassay: cross-sectional and longitudinal analysis over 11 monthsLouise J Robertson, Julie S Moore, Kevin Blighe, et al.
Human Molecular Genetics|March 17, 2012
Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesFadil M Hannan, M Andrew Nesbit, Chen Zhang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 27, 2011
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutationChristopher T Esapa, Tertius A Hough, Sarah Testori, et al.
Human Molecular Genetics|January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAsif Ali, Paul T Christie, Irina V Grigorieva, et al.
Human Molecular Genetics|June 18, 2015
Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effectsFadil M Hannan, Sarah A Howles, Angela Rogers, et al.
Pageof 8