Heng HH - Search Results

1

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: heng hh. Genomics. 1994 Jan 1;19(1):183-5. doi: 10.1006/geno.1994.1039. Genomics. 1994. PMID: 7514565 No abstract available.

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. Among authors: heng hh. Genomics. 1995 Jul 1;28(1):84-91. doi: 10.1006/geno.1995.1109. Genomics. 1995. PMID: 7590751

3

Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase gene.

Marsden PA, Heng HH, Scherer SW, Stewart RJ, Hall AV, Shi XM, Tsui LC, Schappert KT. Marsden PA, et al. Among authors: heng hh. J Biol Chem. 1993 Aug 15;268(23):17478-88. J Biol Chem. 1993. PMID: 7688726 Free article.

4

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. Among authors: heng hh. Genomics. 1994 Oct;23(3):609-18. doi: 10.1006/geno.1994.1549. Genomics. 1994. PMID: 7851889

5

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. Cytogenet Cell Genet. 1994;66(2):135-8. doi: 10.1159/000133685. Cytogenet Cell Genet. 1994. PMID: 7904551

6

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. Genomics. 1993 Nov;18(2):429-31. doi: 10.1006/geno.1993.1491. Genomics. 1993. PMID: 8288250

7

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13.

Ali ST, Duncan AM, Schappert K, Heng HH, Tsui LC, Chow W, Robinson BH. Ali ST, et al. Among authors: heng hh. Genomics. 1993 Nov;18(2):435-9. doi: 10.1006/geno.1993.1493. Genomics. 1993. PMID: 8288251

8

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. Among authors: heng hh. Genomics. 1995 Sep 20;29(2):335-44. doi: 10.1006/geno.1995.9996. Genomics. 1995. PMID: 8666380

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: heng hh. Genomics. 1996 Sep 1;36(2):328-36. doi: 10.1006/geno.1996.0469. Genomics. 1996. PMID: 8812460 Free article.

10

Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q.

Scherer SW, Duvoisin RM, Kuhn R, Heng HH, Belloni E, Tsui LC. Scherer SW, et al. Among authors: heng hh. Genomics. 1996 Jan 15;31(2):230-3. doi: 10.1006/geno.1996.0036. Genomics. 1996. PMID: 8824806 Free article.

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