Gusella JF - Search Results

1

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: gusella jf. Nat Genet. 1997 Sep;17(1):40-8. doi: 10.1038/ng0997-40. Nat Genet. 1997. PMID: 9288096

2

Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.

Kwiatkowski DJ, Ozelius L, Kramer PL, Perman S, Schuback DE, Gusella JF, Fahn S, Breakefield XO. Kwiatkowski DJ, et al. Among authors: gusella jf. Am J Hum Genet. 1991 Aug;49(2):366-71. Am J Hum Genet. 1991. PMID: 1867195 Free PMC article.

3

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: gusella jf. Genome Res. 1997 May;7(5):483-94. doi: 10.1101/gr.7.5.483. Genome Res. 1997. PMID: 9149944 Free article.

4

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: gusella jf. Adv Neurol. 1998;78:93-105. Adv Neurol. 1998. PMID: 9750906 Review. No abstract available.

5

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF, et al. Ozelius LJ, et al. Among authors: gusella jf. Am J Hum Genet. 1992 Mar;50(3):619-28. Am J Hum Genet. 1992. PMID: 1347197 Free PMC article.

6

Dinucleotide repeat polymorphism (D16S285) on human chromosome 16.

Konradi C, Ozelius L, Yan W, Gusella JF, Breakefield XO. Konradi C, et al. Among authors: gusella jf. Nucleic Acids Res. 1991 Oct 11;19(19):5449. doi: 10.1093/nar/19.19.5449. Nucleic Acids Res. 1991. PMID: 1923837 Free PMC article. No abstract available.

7

Identification of human chromosome 9 specific genes using exon amplification.

Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ. Church DM, et al. Among authors: gusella jf. Hum Mol Genet. 1993 Nov;2(11):1915-20. doi: 10.1093/hmg/2.11.1915. Hum Mol Genet. 1993. PMID: 7506603

8

Peripherin gene is linked to keratin 18 gene on human chromosome 12.

Blumenfeld A, Lucente DE, Trofatter JA, Lerner T, Slaugenhaupt SA, Liebert CB, Monahan M, Haines JL, Gusella JF, Breakefield XO, Parysek LM. Blumenfeld A, et al. Among authors: gusella jf. Somat Cell Mol Genet. 1995 Jan;21(1):83-8. doi: 10.1007/BF02255825. Somat Cell Mol Genet. 1995. PMID: 7541564

9

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p.

Ueki K, Rubio MP, Ramesh V, Correa KM, Rutter JL, von Deimling A, Buckler AJ, Gusella JF, Louis DN. Ueki K, et al. Among authors: gusella jf. Hum Mol Genet. 1994 Oct;3(10):1841-5. doi: 10.1093/hmg/3.10.1841. Hum Mol Genet. 1994. PMID: 7849711

10

Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.

Lerner TJ, Boustany RM, MacCormack K, Gleitsman J, Schlumpf K, Breakefield XO, Gusella JF, Haines JL. Lerner TJ, et al. Among authors: gusella jf. Am J Hum Genet. 1994 Jan;54(1):88-94. Am J Hum Genet. 1994. PMID: 8279474 Free PMC article.

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