Town M - Search Results

1

Genetic association of the serotonin transporter in pulmonary arterial hypertension.

Machado RD, Koehler R, Glissmeyer E, Veal C, Suntharalingam J, Kim M, Carlquist J, Town M, Elliott CG, Hoeper M, Fijalkowska A, Kurzyna M, Thomson JR, Gibbs SR, Wilkins MR, Seeger W, Morrell NW, Gruenig E, Trembath RC, Janssen B. Machado RD, et al. Among authors: town m. Am J Respir Crit Care Med. 2006 Apr 1;173(7):793-7. doi: 10.1164/rccm.200509-1365OC. Epub 2006 Jan 6. Am J Respir Crit Care Med. 2006. PMID: 16399993

2

Genome-wide scan for premature hypertension supports linkage to chromosome 2 in a large Kyrgyz family.

Kalmyrzaev B, Aldashev A, Khalmatov M, Polupanov A, Jumagulova A, Mamanova L, Wilkins MR, Town M. Kalmyrzaev B, et al. Among authors: town m. Hypertension. 2006 Nov;48(5):908-13. doi: 10.1161/01.HYP.0000244107.13957.2b. Epub 2006 Sep 25. Hypertension. 2006. PMID: 17000929

3

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.

Town M, Jean G, Cherqui S, Attard M, Forestier L, Whitmore SA, Callen DF, Gribouval O, Broyer M, Bates GP, van't Hoff W, Antignac C. Town M, et al. Nat Genet. 1998 Apr;18(4):319-24. doi: 10.1038/ng0498-319. Nat Genet. 1998. PMID: 9537412

4

Molecular analysis of cystinosis: probable Irish origin of the most common French Canadian mutation.

McGowan-Jordan J, Stoddard K, Podolsky L, Orrbine E, McLaine P, Town M, Goodyer P, MacKenzie A, Heick H. McGowan-Jordan J, et al. Among authors: town m. Eur J Hum Genet. 1999 Sep;7(6):671-8. doi: 10.1038/sj.ejhg.5200349. Eur J Hum Genet. 1999. PMID: 10482956

5

Genetic and other sources of variation in the activity of serum paraoxonase/diazoxonase in humans: consequences for risk from exposure to diazinon.

O'Leary KA, Edwards RJ, Town MM, Boobis AR. O'Leary KA, et al. Among authors: town mm. Pharmacogenet Genomics. 2005 Jan;15(1):51-60. doi: 10.1097/01213011-200501000-00008. Pharmacogenet Genomics. 2005. PMID: 15864126

6

Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assay.

Forestier L, Jean G, Attard M, Cherqui S, Lewis C, van't Hoff W, Broyer M, Town M, Antignac C. Forestier L, et al. Among authors: town m. Am J Hum Genet. 1999 Aug;65(2):353-9. doi: 10.1086/302509. Am J Hum Genet. 1999. PMID: 10417278 Free PMC article.

7

Immunolocalization of cystinosin, the protein defective in cystinosis.

Haq MR, Kalatzis V, Gubler MC, Town MM, Antignac C, Van't Hoff WG, Woolf AS. Haq MR, et al. Among authors: town mm. J Am Soc Nephrol. 2002 Aug;13(8):2046-51. doi: 10.1097/01.asn.0000022012.95680.ba. J Am Soc Nephrol. 2002. PMID: 12138135

8

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Jean G, Fuchshuber A, Town MM, Gribouval O, Schneider JA, Broyer M, van't Hoff W, Niaudet P, Antignac C. Jean G, et al. Among authors: town mm. Am J Hum Genet. 1996 Mar;58(3):535-43. Am J Hum Genet. 1996. PMID: 8644713 Free PMC article.

9

Clinical and molecular aspects of nephropathic cystinosis.

McDowell GA, Town MM, van't Hoff W, Gahl WA. McDowell GA, et al. Among authors: town mm. J Mol Med (Berl). 1998 Apr;76(5):295-302. doi: 10.1007/s001090050220. J Mol Med (Berl). 1998. PMID: 9587063 Review.

10

Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13.

McDowell G, Isogai T, Tanigami A, Hazelwood S, Ledbetter D, Polymeropoulos MH, Lichter-Konecki U, Konecki D, Town MM, Van't Hoff WV, Weissenbach J, Gahl WA. McDowell G, et al. Among authors: town mm. Biochem Mol Med. 1996 Aug;58(2):135-41. doi: 10.1006/bmme.1996.0041. Biochem Mol Med. 1996. PMID: 8812732

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