Breakefield XO - Search Results

1

The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene.

Slaugenhaupt SA, Blumenfeld A, Liebert CB, Mull J, Lucente DE, Monahan M, Breakefield XO, Maayan C, Parada L, Axelrod FB, et al. Slaugenhaupt SA, et al. Among authors: breakefield xo. Genomics. 1995 Feb 10;25(3):730-2. doi: 10.1016/0888-7543(95)80019-i. Genomics. 1995. PMID: 7759111

2

Exclusion of familial dysautonomia from more than 60% of the genome.

Blumenfeld A, Axelrod FB, Trofatter JA, Maayan C, Lucente DE, Slaugenhaupt SA, Liebert CB, Ozelius LJ, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: breakefield xo. J Med Genet. 1993 Jan;30(1):47-52. doi: 10.1136/jmg.30.1.47. J Med Genet. 1993. PMID: 8093738 Free PMC article.

3

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

Blumenfeld A, Slaugenhaupt SA, Axelrod FB, Lucente DE, Maayan C, Liebert CB, Ozelius LJ, Trofatter JA, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: breakefield xo. Nat Genet. 1993 Jun;4(2):160-4. doi: 10.1038/ng0693-160. Nat Genet. 1993. PMID: 8102296

4

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: breakefield xo. Somat Cell Mol Genet. 1995 Jan;21(1):83-8. doi: 10.1007/BF02255825. Somat Cell Mol Genet. 1995. PMID: 7541564

5

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: breakefield xo. Pain. 1996 Sep;67(1):135-139. doi: 10.1016/0304-3959(96)03113-2. Pain. 1996. PMID: 8895241

6

Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32-34.

Ozelius L, Schuback DE, Stefansson K, Slaugenhaupt S, Gusella JF, Breakefield XO. Ozelius L, et al. Among authors: breakefield xo. Hum Mol Genet. 1992 May;1(2):141. doi: 10.1093/hmg/1.2.141-a. Hum Mol Genet. 1992. PMID: 1284469 No abstract available.

7

Structural gene for beta-nerve growth factor not defective in familial dysautonomia.

Breakefield XO, Orloff G, Castiglione C, Coussens L, Axelrod FB, Ullrich A. Breakefield XO, et al. Proc Natl Acad Sci U S A. 1984 Jul;81(13):4213-6. doi: 10.1073/pnas.81.13.4213. Proc Natl Acad Sci U S A. 1984. PMID: 6330750 Free PMC article.

8

A genetic linkage map of human chromosome 9q.

Ozelius LJ, Kwiatkowski DJ, Schuback DE, Breakefield XO, Wexler NS, Gusella JF, Haines JL. Ozelius LJ, et al. Among authors: breakefield xo. Genomics. 1992 Nov;14(3):715-20. doi: 10.1016/s0888-7543(05)80173-9. Genomics. 1992. PMID: 1427899 Free article.

9

DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia.

Breakefield XO, Ozelius L, Bothwell MA, Chao MV, Axelrod F, Kramer PL, Kidd KK, Lanahan AA, Johnson DE, Ross AH, et al. Breakefield XO, et al. Mol Biol Med. 1986 Dec;3(6):483-94. Mol Biol Med. 1986. PMID: 2886891

10

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: breakefield xo. Genomics. 1999 Dec 15;62(3):377-84. doi: 10.1006/geno.1999.6039. Genomics. 1999. PMID: 10644435

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