Levi-Acobas F - Search Results

1

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.

Weil D, Levy G, Sahly I, Levi-Acobas F, Blanchard S, El-Amraoui A, Crozet F, Philippe H, Abitbol M, Petit C. Weil D, et al. Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3232-7. doi: 10.1073/pnas.93.8.3232. Proc Natl Acad Sci U S A. 1996. PMID: 8622919 Free PMC article.

2

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. Genomics. 1995 Sep 1;29(1):163-9. doi: 10.1006/geno.1995.1227. Genomics. 1995. PMID: 8530067

3

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. Hum Mol Genet. 1997 Jan;6(1):111-6. doi: 10.1093/hmg/6.1.111. Hum Mol Genet. 1997. PMID: 9002678

4

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. Genomics. 1997 Mar 1;40(2):332-41. doi: 10.1006/geno.1996.4526. Genomics. 1997. PMID: 9119401

5

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. Nat Genet. 1997 Jun;16(2):191-3. doi: 10.1038/ng0697-191. Nat Genet. 1997. PMID: 9171833

6

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.

Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Levi-Acobas F, Cruaud C, Le Merrer M, Mathieu M, König R, Vigneron J, Weissenbach J, Petit C, Weil D. Abdelhak S, et al. Hum Mol Genet. 1997 Dec;6(13):2247-55. doi: 10.1093/hmg/6.13.2247. Hum Mol Genet. 1997. PMID: 9361030

7

Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2).

Dodé C, Weil D, Levilliers J, Crozet F, Chaïb H, Levi-Acobas F, Guilford P, Petit C. Dodé C, et al. Genomics. 1998 Jan 1;47(1):125-30. doi: 10.1006/geno.1997.5081. Genomics. 1998. PMID: 9465305

8

Connexin 26 gene linked to a dominant deafness.

Denoyelle F, Lina-Granade G, Plauchu H, Bruzzone R, Chaïb H, Lévi-Acobas F, Weil D, Petit C. Denoyelle F, et al. Nature. 1998 May 28;393(6683):319-20. doi: 10.1038/30639. Nature. 1998. PMID: 9620796 No abstract available.

9

Evolution of abiotic cubane chemistries in a nucleic acid aptamer allows selective recognition of a malaria biomarker.

Cheung YW, Röthlisberger P, Mechaly AE, Weber P, Levi-Acobas F, Lo Y, Wong AWC, Kinghorn AB, Haouz A, Savage GP, Hollenstein M, Tanner JA. Cheung YW, et al. Among authors: levi acobas f. Proc Natl Acad Sci U S A. 2020 Jul 21;117(29):16790-16798. doi: 10.1073/pnas.2003267117. Epub 2020 Jul 6. Proc Natl Acad Sci U S A. 2020. PMID: 32631977 Free PMC article.

10

Interleukin 22 is a candidate gene for Tmevp3, a locus controlling Theiler's virus-induced neurological diseases.

Levillayer F, Mas M, Levi-Acobas F, Brahic M, Bureau JF. Levillayer F, et al. Genetics. 2007 Jul;176(3):1835-44. doi: 10.1534/genetics.107.073536. Epub 2007 May 4. Genetics. 2007. PMID: 17483407 Free PMC article.

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