Sossey-Alaoui K - Search Results

1

Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation.

Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Friez MJ, et al. Hum Genet. 2000 Jan;106(1):36-9. doi: 10.1007/s004390051006. Hum Genet. 2000. PMID: 10982179

2

The HOPA gene dodecamer duplication is not a significant etiological factor in autism.

Michaelis RC, Copeland-Yates SA, Sossey-Alaoui K, Skinner C, Friez MJ, Longshore JW, Simensen RJ, Schroer RJ, Stevenson RE. Michaelis RC, et al. J Autism Dev Disord. 2000 Aug;30(4):355-8. doi: 10.1023/a:1005583517994. J Autism Dev Disord. 2000. PMID: 11039861

3

Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.

Sossey-Alaoui K, Hartung AJ, Guerrini R, Manchester DK, Posar A, Puche-Mira A, Andermann E, Dobyns WB, Srivastava AK. Sossey-Alaoui K, et al. Hum Mol Genet. 1998 Aug;7(8):1327-32. doi: 10.1093/hmg/7.8.1327. Hum Mol Genet. 1998. PMID: 9668176

4

Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel.

Sossey-Alaoui K, Lyon JA, Jones L, Abidi FE, Hartung AJ, Hane B, Schwartz CE, Stevenson RE, Srivastava AK. Sossey-Alaoui K, et al. Genomics. 1999 Sep 15;60(3):330-40. doi: 10.1006/geno.1999.5924. Genomics. 1999. PMID: 10493832

5

Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism.

Plank SM, Copeland-Yates SA, Sossey-Alaoui K, Bell JM, Schroer RJ, Skinner C, Michaelis RC. Plank SM, et al. Am J Med Genet. 2001 Jul 8;105(5):404-5. doi: 10.1002/ajmg.1432. Am J Med Genet. 2001. PMID: 11449390

6

DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX).

Sossey-Alaoui K, Srivastava AK. Sossey-Alaoui K, et al. Genomics. 1999 Feb 15;56(1):121-6. doi: 10.1006/geno.1998.5718. Genomics. 1999. PMID: 10036192

7

Absence of MeCP2 mutations in patients from the South Carolina autism project.

Lobo-Menendez F, Sossey-Alaoui K, Bell JM, Copeland-Yates SA, Plank SM, Sanford SO, Skinner C, Simensen RJ, Schroer RJ, Michaelis RC. Lobo-Menendez F, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):97-101. doi: 10.1002/ajmg.b.10016. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12555243

8

Integrated STS/YAC physical, genetic, and transcript map of human Xq21.3 to q23/q24 (DXS1203-DXS1059).

Srivastava AK, McMillan S, Jermak C, Shomaker M, Copeland-Yates SA, Sossey-Alaoui K, Mumm S, Schlessinger D, Nagaraja R. Srivastava AK, et al. Genomics. 1999 Jun 1;58(2):188-201. doi: 10.1006/geno.1999.5820. Genomics. 1999. PMID: 10366451

9

Characterization of FAM10A4, a member of the ST13 tumor suppressor gene family that maps to the 13q14.3 region associated with B-Cell leukemia, multiple myeloma, and prostate cancer.

Sossey-Alaoui K, Kitamura E, Head K, Cowell JK. Sossey-Alaoui K, et al. Genomics. 2002 Jul;80(1):5-7. doi: 10.1006/geno.2002.6792. Genomics. 2002. PMID: 12079276

10

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. Oncogene. 2000 Nov 23;19(50):5772-80. doi: 10.1038/sj.onc.1203978. Oncogene. 2000. PMID: 11126364

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