Breakefield XO - Search Results

1

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.

Chen ZY, Battinelli EM, Fielder A, Bundey S, Sims K, Breakefield XO, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Nat Genet. 1993 Oct;5(2):180-3. doi: 10.1038/ng1093-180. Nat Genet. 1993. PMID: 8252044

2

Characterization of a mutation within the NDP gene in a family with a manifesting female carrier.

Chen ZY, Battinelli EM, Woodruff G, Young I, Breakefield XO, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Hum Mol Genet. 1993 Oct;2(10):1727-9. doi: 10.1093/hmg/2.10.1727. Hum Mol Genet. 1993. PMID: 8268931 No abstract available.

3

Norrie disease and MAO genes: nearest neighbors.

Chen ZY, Denney RM, Breakefield XO. Chen ZY, et al. Among authors: breakefield xo. Hum Mol Genet. 1995;4 Spec No:1729-37. doi: 10.1093/hmg/4.suppl_1.1729. Hum Mol Genet. 1995. PMID: 8541872 Review.

4

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp).

Battinelli EM, Boyd Y, Craig IW, Breakefield XO, Chen ZY. Battinelli EM, et al. Among authors: breakefield xo. Mamm Genome. 1996 Feb;7(2):93-7. doi: 10.1007/s003359900026. Mamm Genome. 1996. PMID: 8835523

5

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: breakefield xo. Hum Mol Genet. 1992 May;1(2):83-9. doi: 10.1093/hmg/1.2.83. Hum Mol Genet. 1992. PMID: 1301161

6

Isolation and characterization of a candidate gene for Norrie disease.

Chen ZY, Hendriks RW, Jobling MA, Powell JF, Breakefield XO, Sims KB, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Nat Genet. 1992 Jun;1(3):204-8. doi: 10.1038/ng0692-204. Nat Genet. 1992. PMID: 1303236

7

Mutations in the Norrie disease gene.

Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Among authors: breakefield xo. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181

8

Norrie disease gene: characterization of deletions and possible function.

Chen ZY, Battinelli EM, Hendriks RW, Powell JF, Middleton-Price H, Sims KB, Breakefield XO, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Genomics. 1993 May;16(2):533-5. doi: 10.1006/geno.1993.1224. Genomics. 1993. PMID: 8314592

9

Characterization of a YAC containing part or all of the Norrie disease locus.

Chen ZY, Sims KB, Coleman M, Donnai D, Monaco A, Breakefield XO, Davies KE, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Hum Mol Genet. 1992 Jun;1(3):161-4. doi: 10.1093/hmg/1.3.161. Hum Mol Genet. 1992. PMID: 1303171

10

Molecular genetics of the monoamine oxidases.

Hsu YP, Powell JF, Sims KB, Breakefield XO. Hsu YP, et al. Among authors: breakefield xo. J Neurochem. 1989 Jul;53(1):12-8. doi: 10.1111/j.1471-4159.1989.tb07289.x. J Neurochem. 1989. PMID: 2656914 Review. No abstract available.

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