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European Journal of Clinical Investigation|October 1, 1988
Binding sites for atrial natriuretic peptide on platelets in patients with congestive cardiomyopathyT M Strom, J Weil, F Braun, et al.Gene|April 18, 2000
Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) geneK E White, B Lorenz, W E Evans, et al.Kidney International|December 12, 2001
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23K E White, G Carn, B Lorenz-Depiereux, et al.Molecular Endocrinology (Baltimore, Md.)|February 12, 1998
A transcriptional silencing domain in DAX-1 whose mutation causes adrenal hypoplasia congenitaE Lalli, B Bardoni, E Zazopoulos, et al.Human Molecular Genetics|November 18, 1998
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane proteinT M Strom, K Hörtnagel, S Hofmann, et al.Hormone Research|January 1, 1987
Plasma atrial natriuretic peptide levels in children with cardiac diseases: correlation with cGMP levels and haemodynamic parametersJ Weil, T M Strom, R Brangenberg, et al.Zeitschrift Fur Kardiologie|January 1, 1988
Influence of diurnal rhythm, posture and right atrial size on plasma atrial natriuretic peptide levelsJ Weil, T M Strom, J M Heim, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouseB Lorenz, C Migliaccio, P Lichtner, et al.Carcinogenesis|March 29, 2003
Allelic imbalance at intragenic markers of Tbx18 is a hallmark of murine osteosarcomaM Rosemann, V Kuosaite, M Nathrath, et al.Human Molecular Genetics|April 18, 1998
Spermine deficiency in Gy mice caused by deletion of the spermine synthase geneB Lorenz, F Francis, K Gempel, et al.Pageof 5