Adato A - Search Results

1

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Adato A, Weil D, Kalinski H, Pel-Or Y, Ayadi H, Petit C, Korostishevsky M, Bonne-Tamir B. Adato A, et al. Am J Hum Genet. 1997 Oct;61(4):813-21. doi: 10.1086/514899. Am J Hum Genet. 1997. PMID: 9382091 Free PMC article.

2

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.

Bonné-Tamir B, Nystuen A, Seroussi E, Kalinsky H, Kwitek-Black AE, Korostishevsky M, Adato A, Sheffield VC. Bonné-Tamir B, et al. Among authors: adato a. Am J Phys Anthropol. 1997 Oct;104(2):193-200. doi: 10.1002/(SICI)1096-8644(199710)104:2<193::AID-AJPA5>3.0.CO;2-#. Am J Phys Anthropol. 1997. PMID: 9386826

3

Deafness heterogeneity in a Druze isolate from the Middle East: novel OTOF and PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locus.

Adato A, Raskin L, Petit C, Bonne-Tamir B. Adato A, et al. Eur J Hum Genet. 2000 Jun;8(6):437-42. doi: 10.1038/sj.ejhg.5200489. Eur J Hum Genet. 2000. PMID: 10878664

4

Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.

Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Lainé S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C. Weil D, et al. Among authors: adato a. Hum Mol Genet. 2003 Mar 1;12(5):463-71. doi: 10.1093/hmg/ddg051. Hum Mol Genet. 2003. PMID: 12588794

5

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

Adato A, Kalinski H, Weil D, Chaib H, Korostishevsky M, Bonne-Tamir B. Adato A, et al. Am J Hum Genet. 1999 Jul;65(1):261-5. doi: 10.1086/302438. Am J Hum Genet. 1999. PMID: 10364543 Free PMC article. No abstract available.

6

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.

Adato A, Vreugde S, Joensuu T, Avidan N, Hamalainen R, Belenkiy O, Olender T, Bonne-Tamir B, Ben-Asher E, Espinos C, Millán JM, Lehesjoki AE, Flannery JG, Avraham KB, Pietrokovski S, Sankila EM, Beckmann JS, Lancet D. Adato A, et al. Eur J Hum Genet. 2002 Jun;10(6):339-50. doi: 10.1038/sj.ejhg.5200831. Eur J Hum Genet. 2002. PMID: 12080385

7

Interactions in the network of Usher syndrome type 1 proteins.

Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C. Adato A, et al. Hum Mol Genet. 2005 Feb 1;14(3):347-56. doi: 10.1093/hmg/ddi031. Epub 2004 Dec 8. Hum Mol Genet. 2005. PMID: 15590703

8

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.

Adato A, Lefèvre G, Delprat B, Michel V, Michalski N, Chardenoux S, Weil D, El-Amraoui A, Petit C. Adato A, et al. Hum Mol Genet. 2005 Dec 15;14(24):3921-32. doi: 10.1093/hmg/ddi416. Epub 2005 Nov 21. Hum Mol Genet. 2005. PMID: 16301217

9

Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families.

Adato A, Weston MD, Berry A, Kimberling WJ, Bonne-Tamir A. Adato A, et al. Hum Mutat. 2000 Apr;15(4):388. doi: 10.1002/(SICI)1098-1004(200004)15:4<388::AID-HUMU27>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10738000

10

GeneCards 2002: towards a complete, object-oriented, human gene compendium.

Safran M, Solomon I, Shmueli O, Lapidot M, Shen-Orr S, Adato A, Ben-Dor U, Esterman N, Rosen N, Peter I, Olender T, Chalifa-Caspi V, Lancet D. Safran M, et al. Among authors: adato a. Bioinformatics. 2002 Nov;18(11):1542-3. doi: 10.1093/bioinformatics/18.11.1542. Bioinformatics. 2002. PMID: 12424129

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