Breakefield XO - Search Results

1

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

2

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

3

Organization of the human monoamine oxidase genes and long-range physical mapping around them.

Chen ZY, Powell JF, Hsu YP, Breakefield XO, Craig IW. Chen ZY, et al. Among authors: breakefield xo. Genomics. 1992 Sep;14(1):75-82. doi: 10.1016/s0888-7543(05)80286-1. Genomics. 1992. PMID: 1427833

4

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease.

Levy ER, Powell JF, Buckle VJ, Hsu YP, Breakefield XO, Craig IW. Levy ER, et al. Among authors: breakefield xo. Genomics. 1989 Aug;5(2):368-70. doi: 10.1016/0888-7543(89)90072-4. Genomics. 1989. PMID: 2793188

5

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

6

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

7

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

8

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

9

Structure of the human gene for monoamine oxidase type A.

Chen ZY, Hotamisligil GS, Huang JK, Wen L, Ezzeddine D, Aydin-Muderrisoglu N, Powell JF, Huang RH, Breakefield XO, Craig I, et al. Chen ZY, et al. Among authors: breakefield xo. Nucleic Acids Res. 1991 Aug 25;19(16):4537-41. doi: 10.1093/nar/19.16.4537. Nucleic Acids Res. 1991. PMID: 1886775 Free PMC article.

10

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

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