Roe B - Search Results

1

WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma.

Sossey-Alaoui K, Su G, Malaj E, Roe B, Cowell JK. Sossey-Alaoui K, et al. Among authors: roe b. Oncogene. 2002 Aug 29;21(38):5967-74. doi: 10.1038/sj.onc.1205734. Oncogene. 2002. PMID: 12185600

2

A transcription map of the minimally deleted region from 13q14 in B-cell chronic lymphocytic leukemia as defined by large scale sequencing of the 650 kb critical region.

Kitamura E, Su G, Sossey-Alaoui K, Malaj E, Lewis J, Pan HQ, Hawthorn L, Roe B, Cowell JK. Kitamura E, et al. Among authors: roe b. Oncogene. 2000 Nov 23;19(50):5772-80. doi: 10.1038/sj.onc.1203978. Oncogene. 2000. PMID: 11126364

3

A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells.

Chernova OB, Hunyadi A, Malaj E, Pan H, Crooks C, Roe B, Cowell JK. Chernova OB, et al. Among authors: roe b. Oncogene. 2001 Aug 30;20(38):5378-92. doi: 10.1038/sj.onc.1204694. Oncogene. 2001. PMID: 11536051

4

Chromosome evolution: the junction of mammalian chromosomes in the formation of mouse chromosome 10.

Pletcher MT, Roe BA, Chen F, Do T, Do A, Malaj E, Reeves RH. Pletcher MT, et al. Among authors: roe ba. Genome Res. 2000 Oct;10(10):1463-7. doi: 10.1101/gr.146600. Genome Res. 2000. PMID: 11042146 Free PMC article.

5

Transcript mapping in a 46-kb sequenced region at the core of 12q13.3 amplification in human cancers.

Elkahloun AG, Krizman DB, Wang Z, Hofmann TA, Roe B, Meltzer PS. Elkahloun AG, et al. Among authors: roe b. Genomics. 1997 Jun 1;42(2):295-301. doi: 10.1006/geno.1997.4727. Genomics. 1997. PMID: 9192850

6

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene.

Budarf ML, Collins J, Gong W, Roe B, Wang Z, Bailey LC, Sellinger B, Michaud D, Driscoll DA, Emanuel BS. Budarf ML, et al. Among authors: roe b. Nat Genet. 1995 Jul;10(3):269-78. doi: 10.1038/ng0795-269. Nat Genet. 1995. PMID: 7670464

7

The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers.

Tapia-Páez I, Kost-Alimova M, Hu P, Roe BA, Blennow E, Fedorova L, Imreh S, Dumanski JP. Tapia-Páez I, et al. Among authors: roe ba. Hum Genet. 2001 Aug;109(2):167-77. doi: 10.1007/s004390100560. Hum Genet. 2001. PMID: 11511922

8

Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.

Srivatsan ES, Chakrabarti R, Zainabadi K, Pack SD, Benyamini P, Mendonca MS, Yang PK, Kang K, Motamedi D, Sawicki MP, Zhuang Z, Jesudasan RA, Bengtsson U, Sun C, Roe BA, Stanbridge EJ, Wilczynski SP, Redpath JL. Srivatsan ES, et al. Oncogene. 2002 Aug 15;21(36):5631-42. doi: 10.1038/sj.onc.1205698. Oncogene. 2002. PMID: 12165862

9

The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking.

Zhang Q, Li W, Novak EK, Karim A, Mishra VS, Kingsmore SF, Roe BA, Suzuki T, Swank RT. Zhang Q, et al. Hum Mol Genet. 2002 Mar 15;11(6):697-706. doi: 10.1093/hmg/11.6.697. Hum Mol Genet. 2002. PMID: 11912185 Free PMC article.

10

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

Holmes SE, Riazi MA, Gong W, McDermid HE, Sellinger BT, Hua A, Chen F, Wang Z, Zhang G, Roe B, Gonzalez I, McDonald-McGinn DM, Zackai E, Emanuel BS, Budarf ML. Holmes SE, et al. Among authors: roe b. Hum Mol Genet. 1997 Mar;6(3):357-67. doi: 10.1093/hmg/6.3.357. Hum Mol Genet. 1997. PMID: 9147638

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