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Archives Des Maladies Du Coeur Et Des Vaisseaux|December 1, 1994
[Demonstration of a fifth locus implicated in familial hypertrophic cardiomyopathies]C Hengstenberg, P Charron, R Isnard, et al.
Neuroscience|January 1, 1990
Neurons containing messenger RNA encoding glutamate decarboxylase in rat hypothalamus demonstrated by in situ hybridization, with special emphasis on cell groups in medial preoptic area, anterior hypothalamic area and dorsomedial hypothalamic nucleusH Okamura, M Abitbol, J F Julien, et al.
Iscience|March 23, 2026
Dual mechanisms of supporting cell regeneration in the neonatal mouse cochleaJulia M Abitbol, Maggie S Matern, Sara E Billings, et al.
Biochemical and Biophysical Research Communications|January 13, 2006
Genetic characterization of CHO production host DG44 and derivative recombinant cell linesM Derouazi, D Martinet, N Besuchet Schmutz, et al.
Nature Genetics|April 1, 1995
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12qM Vaxillaire, V Boccio, A Philippi, et al.
Medical and Pediatric Oncology|July 24, 2001
Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastomaM Lastowska, N Van Roy, N Bown, et al.
Human Molecular Genetics|September 1, 1993
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.
Human Mutation|March 1, 2000
Identification of novel PAX6 mutations in two families with bilateral aniridia. Mutations in brief no. 167. OnlineM Neuner-Jehle, F Munier, A Kobetz, et al.
Nature|October 10, 1991
Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive ratsP Hilbert, K Lindpaintner, J S Beckmann, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
Influence of specific regions in Lp82 calpain on protein stability, activity, and localization within lensH Ma, M Shih, C Fukiage, et al.
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