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European Journal of Biochemistry|October 1, 1995
Chromosomal localisation, inducibility, tissue-specific expression and strain differences in three murine peroxisome-proliferator-activated-receptor genesP S Jones, R Savory, P Barratt, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 3, 1996
Fibroblast growth factor (FGF) homologous factors: new members of the FGF family implicated in nervous system developmentP M Smallwood, I Munoz-Sanjuan, P Tong, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 31, 2010
Asthma, asthma medications, and prostate cancer riskGianluca Severi, Laura Baglietto, David C Muller, et al.
Human Molecular Genetics|April 6, 2000
The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5aJ M Jones, J D Huang, V Mermall, et al.
Cytogenetic and Genome Research|November 20, 2002
Cloning, expression, and chromosomal localization of the mouse gene (Scgb3a1, alias Ugrp2) that encodes a member of the novel uteroglobin-related protein gene familyT Niimi, N G Copeland, D J Gilbert, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Chromosomal localization of the Ox-44 (CD53) leukocyte antigen gene in man and rodentsT Taguchi, A Bellacosa, J Y Zhou, et al.
Nature Genetics|August 1, 1992
The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouseC M Disteche, C I Brannan, A Larsen, et al.
Lancet (London, England)|April 8, 1995
Patterns of initial and acquired antituberculosis drug resistance in Karonga District, MalawiJ R Glynn, P A Jenkins, P E Fine, et al.
Genomics|June 11, 1992
Murine chromosomal location of four hepatocyte-enriched transcription factors: HNF-3 alpha, HNF-3 beta, HNF-3 gamma, and HNF-4K B Avraham, V R Prezioso, W S Chen, et al.
The British Journal of Ophthalmology|May 23, 2006
Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk geneM Tschernutter, S A Jenkins, N H Waseem, et al.
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