Shi XM - Search Results

1

Amplification of CFTR exon 9 sequences to multiple locations in the human genome.

Rozmahel R, Heng HH, Duncan AM, Shi XM, Rommens JM, Tsui LC. Rozmahel R, et al. Among authors: shi xm. Genomics. 1997 Nov 1;45(3):554-61. doi: 10.1006/geno.1997.4968. Genomics. 1997. PMID: 9367680

2

The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain.

O'Dowd BF, Scheideler MA, Nguyen T, Cheng R, Rasmussen JS, Marchese A, Zastawny R, Heng HH, Tsui LC, Shi X, et al. O'Dowd BF, et al. Genomics. 1995 Jul 1;28(1):84-91. doi: 10.1006/geno.1995.1109. Genomics. 1995. PMID: 7590751

3

Cloning of human genes encoding novel G protein-coupled receptors.

Marchese A, Docherty JM, Nguyen T, Heiber M, Cheng R, Heng HH, Tsui LC, Shi X, George SR, O'Dowd BF. Marchese A, et al. Genomics. 1994 Oct;23(3):609-18. doi: 10.1006/geno.1994.1549. Genomics. 1994. PMID: 7851889

4

Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors.

Marchese A, Heiber M, Nguyen T, Heng HH, Saldivia VR, Cheng R, Murphy PM, Tsui LC, Shi X, Gregor P, et al. Marchese A, et al. Genomics. 1995 Sep 20;29(2):335-44. doi: 10.1006/geno.1995.9996. Genomics. 1995. PMID: 8666380

5

Localization of the human gene for inducible nitric oxide synthase (NOS2) to chromosome 17q11.2-q12.

Marsden PA, Heng HH, Duff CL, Shi XM, Tsui LC, Hall AV. Marsden PA, et al. Among authors: shi xm. Genomics. 1994 Jan 1;19(1):183-5. doi: 10.1006/geno.1994.1039. Genomics. 1994. PMID: 7514565 No abstract available.

6

Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/KO15.

Heng HH, Shi XM, Scherer SW, Andrulis IL, Tsui LC. Heng HH, et al. Among authors: shi xm. Cytogenet Cell Genet. 1994;66(2):135-8. doi: 10.1159/000133685. Cytogenet Cell Genet. 1994. PMID: 7904551

7

Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locus.

Heng HH, Xie B, Shi XM, Tsui LC, Mahuran DJ. Heng HH, et al. Among authors: shi xm. Genomics. 1993 Nov;18(2):429-31. doi: 10.1006/geno.1993.1491. Genomics. 1993. PMID: 8288250

8

Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3.

Heng HH, Shi XM, Tsui LC. Heng HH, et al. Among authors: shi xm. Cytogenet Cell Genet. 1993;62(2-3):108-9. doi: 10.1159/000133451. Cytogenet Cell Genet. 1993. PMID: 8428507 Free article.

9

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC. Osborne LR, et al. Among authors: shi xm. Genomics. 1996 Sep 1;36(2):328-36. doi: 10.1006/geno.1996.0469. Genomics. 1996. PMID: 8812460 Free article.

10

Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21. 1 by fluorescence in situ hybridization.

Cohen D, Heng HH, Shi XM, McIntosh EM, Tsui LC, Pearlman RE. Cohen D, et al. Among authors: shi xm. Genomics. 1997 Feb 15;40(1):213-5. doi: 10.1006/geno.1996.4540. Genomics. 1997. PMID: 9070952 No abstract available.

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