Roe BA - Search Results

1

CYP3A variation and the evolution of salt-sensitivity variants.

Thompson EE, Kuttab-Boulos H, Witonsky D, Yang L, Roe BA, Di Rienzo A. Thompson EE, et al. Among authors: roe ba. Am J Hum Genet. 2004 Dec;75(6):1059-69. doi: 10.1086/426406. Epub 2004 Oct 18. Am J Hum Genet. 2004. PMID: 15492926 Free PMC article.

2

Comparative genomics analysis of human sequence variation in the UGT1A gene cluster.

Maitland ML, Grimsley C, Kuttab-Boulos H, Witonsky D, Kasza KE, Yang L, Roe BA, Di Rienzo A. Maitland ML, et al. Among authors: roe ba. Pharmacogenomics J. 2006 Jan-Feb;6(1):52-62. doi: 10.1038/sj.tpj.6500351. Pharmacogenomics J. 2006. PMID: 16314881

3

Sequence diversity and haplotype structure at the human CYP3A cluster.

Thompson EE, Kuttab-Boulos H, Yang L, Roe BA, Di Rienzo A. Thompson EE, et al. Among authors: roe ba. Pharmacogenomics J. 2006 Mar-Apr;6(2):105-14. doi: 10.1038/sj.tpj.6500347. Pharmacogenomics J. 2006. PMID: 16314882

4

The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor.

Pusch C, Hustert E, Pfeifer D, Südbeck P, Kist R, Roe B, Wang Z, Balling R, Blin N, Scherer G. Pusch C, et al. Hum Genet. 1998 Aug;103(2):115-23. doi: 10.1007/s004390050793. Hum Genet. 1998. PMID: 9760192

5

The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.

Gottlieb S, Emanuel BS, Driscoll DA, Sellinger B, Wang Z, Roe B, Budarf ML. Gottlieb S, et al. Am J Hum Genet. 1997 May;60(5):1194-201. Am J Hum Genet. 1997. PMID: 9150167 Free PMC article.

6

Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

Kurahashi H, Shaikh TH, Hu P, Roe BA, Emanuel BS, Budarf ML. Kurahashi H, et al. Among authors: roe ba. Hum Mol Genet. 2000 Jul 1;9(11):1665-70. doi: 10.1093/hmg/9.11.1665. Hum Mol Genet. 2000. PMID: 10861293

7

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.

Shaikh TH, Kurahashi H, Saitta SC, O'Hare AM, Hu P, Roe BA, Driscoll DA, McDonald-McGinn DM, Zackai EH, Budarf ML, Emanuel BS. Shaikh TH, et al. Among authors: roe ba. Hum Mol Genet. 2000 Mar 1;9(4):489-501. doi: 10.1093/hmg/9.4.489. Hum Mol Genet. 2000. PMID: 10699172

8

Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region.

Gong W, Emanuel BS, Galili N, Kim DH, Roe B, Driscoll DA, Budarf ML. Gong W, et al. Hum Mol Genet. 1997 Feb;6(2):267-76. doi: 10.1093/hmg/6.2.267. Hum Mol Genet. 1997. PMID: 9063747

9

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

Gong W, Emanuel BS, Collins J, Kim DH, Wang Z, Chen F, Zhang G, Roe B, Budarf ML. Gong W, et al. Hum Mol Genet. 1996 Jun;5(6):789-800. doi: 10.1093/hmg/5.6.789. Hum Mol Genet. 1996. PMID: 8776594

10

DNA structural properties of AF9 are similar to MLL and could act as recombination hot spots resulting in MLL/AF9 translocations and leukemogenesis.

Strissel PL, Strick R, Tomek RJ, Roe BA, Rowley JD, Zeleznik-Le NJ. Strissel PL, et al. Among authors: roe ba. Hum Mol Genet. 2000 Jul 1;9(11):1671-9. doi: 10.1093/hmg/9.11.1671. Hum Mol Genet. 2000. PMID: 10861294

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