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British Journal of Clinical Pharmacology|October 26, 2018
Genetic approaches to metabolic bone diseasesFadil M Hannan, Paul J Newey, Michael P Whyte, et al.Human Genetics|April 1, 1993
Parathyroid hormone gene analysis in autosomal hypoparathyroidism using an intragenic tetranucleotide (AAAT)n polymorphismD B Parkinson, N J Shaw, R L Himsworth, et al.Nucleic Acids Research|September 12, 1989
Structure and methylation of the human calcitonin/alpha-CGRP geneP M Broad, A J Symes, R V Thakker, et al.Ophthalmic Plastic and Reconstructive Surgery|March 23, 2010
Eyelash resection procedure for severe, recurrent, or segmental cicatricial entropionAlbert Y Wu, Manoj M Thakker, Edward J Wladis, et al.Current Problems in Cardiology|April 10, 2022
Insight on the Etiologies of Chronically Elevated TroponinJimmy Hong, Khaled F Chatila, Jaison J John, et al.Human Molecular Genetics|February 5, 1999
Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's diseaseO Devuyst, P T Christie, P J Courtoy, et al.Expert Review of Gastroenterology & Hepatology|May 11, 2023
Novel fibro-inflammatory biomarkers associated with disease activity in patients with Crohn's diseaseM Pehrsson, M S Alexdóttir, M A Karsdal, et al.Kidney International|August 1, 2000
Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's diseaseT Igarashi, J Inatomi, T Ohara, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2005
A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challengesC P Burren, A Curley, P Christie, et al.Free Radical Biology & Medicine|May 27, 2005
JNK activation limits dendritic cell maturation in response to reactive oxygen species by the induction of apoptosisMatthew E Handley, Manish Thakker, Gabriele Pollara, et al.Pageof 107