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The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 21, 2012
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomasS Lefebvre, F Borson-Chazot, N Boutry-Kryza, et al.
Human Molecular Genetics|November 13, 1998
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophyP Burlet, C Huber, S Bertrandy, et al.
Bioorganic & Medicinal Chemistry Letters|October 31, 2000
NMR line-broadening and transferred NOESY as a medicinal chemistry tool for studying inhibitors of the hepatitis C virus NS3 protease domainS R LaPlante, N Aubry, P R Bonneau, et al.
Journal Francais D'Ophtalmologie|August 4, 2006
[Prevalence of intraocular hypertension and glaucoma in a nonselected French population]A Bron, C Baudouin, J-P Nordmann, et al.
Journal of Cellular and Molecular Medicine|December 31, 2013
Cooperative role of endogenous leucotrienes and platelet-activating factor in ischaemia-reperfusion-mediated tissue injuryClaudia S Bitencourt, Valérie L Bessi, David N Huynh, et al.
Neurology|May 27, 2006
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36I Maystadt, M Zarhrate, D Leclair-Richard, et al.
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