Rezultati pretrage - Mohammad A. Abduljabbar
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Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability od Anne Raimondo, Ali Chakera, Soren K. Thomsen, Kevin Colclough, Amy Barrett, Elisa De Franco, Alisson Chatelas, Hüseyin Demirbilek, Teoman Akçay, Hussein Alawneh, Sarah E. Flanagan, Martijn van de Bunt, Andrew T. Hattersley, Anna L. Gloyn, Sian Ellard, Mohammad A. Abduljabbar, Mahmoud Alzyoud, Syed Aman, Louise Bath, Parijat De, Neeta Deshpande, Erdem Durmaz, Frank Eickmeier, Nancy Samir Elbarbary, Marc Fillion, Sujatha Jagadeesh, Melanie Kershaw, Waqas Khan, Wojciech Młynarski, Kathryn Noyes, Catherine Peters, Nick Shaw, Irina Tiron, Doğa Türkkahraman, Lesley Turner, Khadiga Eltonbary, Bilgin Yüksel
Izdano 2014Artigo
Alati za pretragu:
Povezani predmeti
Biology
Endocrinology
Gene
Genetics
Internal medicine
Medicine
Allele
Androgen
Biochemistry
Cholesterol side-chain cleavage enzyme
Congenital adrenal hyperplasia
Cytochrome P450
Dehydroepiandrosterone sulfate
Diabetes mellitus
Enzyme
Gene expression
Glucokinase
Hormone
Hyponatremia
Metabolism
Missense mutation
Mutant
Mutation
Phenotype
Pregnenolone
Steroid
Steroidogenic acute regulatory protein
Thermostability