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Blood|May 23, 2001
Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiencyA M Marinaki, E Escuredo, J A Duley, et al.
Molecular Pharmacology|November 28, 2001
Transcriptional mechanism of protein kinase C-induced isoform-specific expression of the gene for endothelin-converting enzyme-1 in human endothelial cellsH D Orzechowski, A Günther, S Menzel, et al.
Scientific Reports|October 12, 2019
Stateful Three-Input Logic with Memristive SwitchesA Siemon, R Drabinski, M J Schultis, et al.
Diabetes|December 1, 1995
Localization of MODY3 to a 5-cM region of human chromosome 12S Menzel, K Yamagata, J B Trabb, et al.
Nature|December 5, 1996
Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)K Yamagata, H Furuta, N Oda, et al.
Genomics|April 11, 2000
An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobinL Game, J Close, P Stephens, et al.
Diabetologia|June 1, 1996
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscleK Yamagata, J Takeda, S Menzel, et al.
Diabetes|May 1, 1995
Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDMM L Tsaur, S Menzel, F P Lai, et al.
Diabetes|November 1, 1996
Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12M M Byrne, J Sturis, S Menzel, et al.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2000
No evidence for linkage at candidate type 2 diabetes susceptibility loci on chromosomes 12 and 20 in United Kingdom CaucasiansT M Frayling, M I McCarthy, M Walker, et al.
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