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A survey of polypeptide deformylase function throughout the eubacterial lineage.
Mazel D, Coïc E, Blanchard S, Saurin W, Marlière P. Mazel D, et al. Among authors: blanchard s. J Mol Biol. 1997 Mar 14;266(5):939-49. doi: 10.1006/jmbi.1996.0835. J Mol Biol. 1997. PMID: 9086272
Cloning of the genes encoding two murine and human cochlear unconventional type I myosins.
Crozet F, el Amraoui A, Blanchard S, Lenoir M, Ripoll C, Vago P, Hamel C, Fizames C, Levi-Acobas F, Depétris D, Mattei MG, Weil D, Pujol R, Petit C. Crozet F, et al. Among authors: blanchard s. Genomics. 1997 Mar 1;40(2):332-41. doi: 10.1006/geno.1996.4526. Genomics. 1997. PMID: 9119401
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
Weil D, Küssel P, Blanchard S, Lévy G, Levi-Acobas F, Drira M, Ayadi H, Petit C. Weil D, et al. Among authors: blanchard s. Nat Genet. 1997 Jun;16(2):191-3. doi: 10.1038/ng0697-191. Nat Genet. 1997. PMID: 9171833
Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
Lévy G, Levi-Acobas F, Blanchard S, Gerber S, Larget-Piet D, Chenal V, Liu XZ, Newton V, Steel KP, Brown SD, Munnich A, Kaplan J, Petit C, Weil D. Lévy G, et al. Among authors: blanchard s. Hum Mol Genet. 1997 Jan;6(1):111-6. doi: 10.1093/hmg/6.1.111. Hum Mol Genet. 1997. PMID: 9002678
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).
Guilford P, Dodé C, Crozet F, Blanchard S, Chaïb H, Levilliers J, Levi-Acobas F, Weil D, Weissenbach J, Cohen D, et al. Guilford P, et al. Among authors: blanchard s. Genomics. 1995 Sep 1;29(1):163-9. doi: 10.1006/geno.1995.1227. Genomics. 1995. PMID: 8530067
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.
Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C. Hardelin JP, et al. Among authors: blanchard s. Hum Mol Genet. 1993 Apr;2(4):373-7. doi: 10.1093/hmg/2.4.373. Hum Mol Genet. 1993. PMID: 8504298
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C. Guilford P, et al. Among authors: blanchard s. Hum Mol Genet. 1994 Jun;3(6):989-93. doi: 10.1093/hmg/3.6.989. Hum Mol Genet. 1994. PMID: 7951250
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al. Weil D, et al. Among authors: blanchard s. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. Nature. 1995. PMID: 7870171
RNA sequence determinants for aminoglycoside binding to an A-site rRNA model oligonucleotide.
Recht MI, Fourmy D, Blanchard SC, Dahlquist KD, Puglisi JD. Recht MI, et al. Among authors: blanchard sc. J Mol Biol. 1996 Oct 4;262(4):421-36. doi: 10.1006/jmbi.1996.0526. J Mol Biol. 1996. PMID: 8893854
Upon chemical modification, the RNA oligonucleotide exhibits an accessibility pattern similar to that of 16 S rRNA in the 30 S subunit. ...Introduction into the oligonucleotide of base changes that are known to confer aminoglycoside resistance in 16 S rRNA re …
Upon chemical modification, the RNA oligonucleotide exhibits an accessibility pattern similar to that of 16 S rRNA in the 30 S
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