Browse Items (7 total)

Tags: 2020, animal-model, August 2020 List, Chanchlani R, Chronic kidney disease, d-receptor, d-resistant rickets, Department of Anatomy & Neurobiology, Department of Internal Medicine, hereditary hypophosphatemic rickets, hypocalcemia, hypophosphatemia, journalArticle, Kidney International Reports, Krishnappa V, mutations, Nemer L, Nemer P, NEOMED College of Medicine, NEOMED College of Medicine Student, phosphate, phosphorus, Prevention, Raina R, Safadi F, Sinha R, Sochett E, targeted ablation, Vitamin D, vitamin-d-deficiency, x-linked hypophosphatemia

Tags: 2022, cytochrome p450 1B1 (CYP1B1), demographics, mutations, primary congenital glaucoma.

Tags: 2019, aldosteronism, Amin Harshesh, apparent mineralocorticoid excess, congenital adrenal hyperplasia, Das Abhijit, Department of Internal Medicine, Disease, familial, familial hyperaldosteronism, features, Frontiers in pediatrics, Genes, Gordon syndrome, hyperaldosteronism, Krishnappa Vinod, Kusumi Kirsten, Liddle syndrome, mineralocorticoid excess, monogenic hypertension, mutations, Nair Nikhil R, NEOMED College of Graduate Studies Student, NEOMED College of Medicine, NEOMED College of Medicine Student, NEOMED Student Publications, Pediatrics, Prevalence, Radhakrishnan Yeshwanter, Raina Rupesh, September 2019 Update, stroke, update

Tags: 2009, bcs1l gene, complex, Cutis, defects, Dermatology, Disease, Journal Article or Conference Abstract Publication, Mirmirani P, Mostow E, mutations, Samimi S S

Tags: 2005, Bacteria, Bevins C L, Chu H T, expression, Feathers R W, Fellermann K, Ganz T, gene, human intestinal defensin, inflammatory bowel disease, Innate, Innate immunity, Intestine, Journal Article, Lima H, Linzmeier R, mechanisms, microflora, mutations, Nuding S, Peptides, Petras R E, Porter E, Proceedings of the National Academy of Sciences of the United States of America, Salzman N H, Schaeffeler E, Schwab M, Science & Technology - Other Topics, Shen B, Stange E F, Wehkamp J, Weichenthal M

Tags: 1998, alpha-hydroxylase, bile acid response element, Bile acid synthesis, Biochemistry & Molecular Biology, Chiang J Y L, cholesterol 7, Crestani M, cytochrome P450, elements, expression, factor coup-tf, Galli G, gene transcription and regulation, hormone receptor, Journal Article or Conference Abstract Publication, Journal of lipid research, Liver, messenger-rna, Metabolism, mutations, nuclear, promoter, rat, retinoic acid receptors, Sadeghpour A, Stroup D

Tags: 2007, cftr gene, congenital bilateral absence, Disease, Genetic Testing, Genetics & Heredity, Grody W W, Journal Article or Conference Abstract Publication, Lebo R V, males, messenger-rna, mutations, Polymorphism, repeat, Research & Experimental Medicine, Risk, vas-deferens