Shalish C - Search Results

1

The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family.

Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Jacoby D, Penney J, Risch NJ, Fahn S, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: shalish c. Adv Neurol. 1998;78:93-105. Adv Neurol. 1998. PMID: 9750906 Review. No abstract available.

2

Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium.

Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: shalish c. Genome Res. 1997 May;7(5):483-94. doi: 10.1101/gr.7.5.483. Genome Res. 1997. PMID: 9149944 Free article.

3

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.

Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: shalish c. Nat Genet. 1997 Sep;17(1):40-8. doi: 10.1038/ng0997-40. Nat Genet. 1997. PMID: 9288096

4

The TOR1A (DYT1) gene family and its role in early onset torsion dystonia.

Ozelius LJ, Page CE, Klein C, Hewett JW, Mineta M, Leung J, Shalish C, Bressman SB, de Leon D, Brin MF, Fahn S, Corey DP, Breakefield XO. Ozelius LJ, et al. Among authors: shalish c. Genomics. 1999 Dec 15;62(3):377-84. doi: 10.1006/geno.1999.6039. Genomics. 1999. PMID: 10644435

5

Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat.

Ziefer P, Leung J, Razzano T, Shalish C, LeDoux MS, Lorden JF, Ozelius L, Breakefield XO, Standaert DG, Augood SJ. Ziefer P, et al. Among authors: shalish c. Brain Res Mol Brain Res. 2002 May 30;101(1-2):132-5. doi: 10.1016/s0169-328x(02)00176-6. Brain Res Mol Brain Res. 2002. PMID: 12007841

6

beta-Galactosidase gene mutations in patients with slowly progressive GM1 gangliosidosis.

Kaye EM, Shalish C, Livermore J, Taylor HA, Stevenson RE, Breakefield XO. Kaye EM, et al. Among authors: shalish c. J Child Neurol. 1997 Jun;12(4):242-7. doi: 10.1177/088307389701200404. J Child Neurol. 1997. PMID: 9203065 Review.

7

Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II.

Davar G, Shalish C, Blumenfeld A, Breakefield XO. Davar G, et al. Among authors: shalish c. Pain. 1996 Sep;67(1):135-139. doi: 10.1016/0304-3959(96)03113-2. Pain. 1996. PMID: 8895241

8

Relationship between platelet monoamine oxidase B activity and alleles at the MAOB locus.

Girmen AS, Baenziger J, Hotamisligil GS, Konradi C, Shalish C, Sullivan JL, Breakefield XO. Girmen AS, et al. Among authors: shalish c. J Neurochem. 1992 Dec;59(6):2063-6. doi: 10.1111/j.1471-4159.1992.tb10095.x. J Neurochem. 1992. PMID: 1431894

9

Mutational analysis of the human MAOA gene.

Tivol EA, Shalish C, Schuback DE, Hsu YP, Breakefield XO. Tivol EA, et al. Among authors: shalish c. Am J Med Genet. 1996 Feb 16;67(1):92-7. doi: 10.1002/(SICI)1096-8628(19960216)67:1<92::AID-AJMG16>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8678123

10

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

Sims KB, Lebo RV, Benson G, Shalish C, Schuback D, Chen ZY, Bruns G, Craig IW, Golbus MS, Breakefield XO. Sims KB, et al. Among authors: shalish c. Hum Mol Genet. 1992 May;1(2):83-9. doi: 10.1093/hmg/1.2.83. Hum Mol Genet. 1992. PMID: 1301161

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