Showing results (6171-6180 of 7,441) with videos related to
Sort By:
Pageof 745
Nature Genetics|December 2, 2000
MAML1, a human homologue of Drosophila mastermind, is a transcriptional co-activator for NOTCH receptorsL Wu, J C Aster, S C Blacklow, et al.Nature Genetics|December 2, 2000
The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesityC Le Stunff, D Fallin, N J Schork, et al.Nature Genetics|November 4, 2000
Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunitI C Meij, J B Koenderink, H van Bokhoven, et al.Nature Genetics|November 4, 2000
Mutations in SDHC cause autosomal dominant paraganglioma, type 3S Niemann, U MüllerNature Genetics|November 4, 2000
Normal telomere lengths found in cloned cattleX C Tian, J Xu, X YangNature Genetics|November 4, 2000
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann diseaseK Janssens, R Gershoni-Baruch, N Guañabens, et al.Nature Genetics|November 4, 2000
Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorderW Vermeulen, E Bergmann, J Auriol, et al.Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.Nature Genetics|November 4, 2000
Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetesJ P Silva, M Köhler, C Graff, et al.Pageof 745