Barton N - Search Results

1

The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region.

Germino GG, Weinstat-Saslow D, Himmelbauer H, Gillespie GA, Somlo S, Wirth B, Barton N, Harris KL, Frischauf AM, Reeders ST. Germino GG, et al. Among authors: barton n. Genomics. 1992 May;13(1):144-51. doi: 10.1016/0888-7543(92)90214-d. Genomics. 1992. PMID: 1577479

2

Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.

Germino GG, Barton NJ, Lamb J, Higgs DR, Harris P, Xiao GH, Scherer G, Nakamura Y, Reeders ST. Germino GG, et al. Among authors: barton nj. Am J Hum Genet. 1990 May;46(5):925-33. Am J Hum Genet. 1990. PMID: 2339691 Free PMC article.

3

A long-range restriction map between the alpha-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus.

Harris PC, Barton NJ, Higgs DR, Reeders ST, Wilkie AO. Harris PC, et al. Among authors: barton nj. Genomics. 1990 Jun;7(2):195-206. doi: 10.1016/0888-7543(90)90541-2. Genomics. 1990. PMID: 2347584

4

Regional localization of the autosomal dominant polycystic kidney disease locus.

Reeders ST, Keith T, Green P, Germino GG, Barton NJ, Lehmann OJ, Brown VA, Phipps P, Morgan J, Bear JC, et al. Reeders ST, et al. Among authors: barton nj. Genomics. 1988 Aug;3(2):150-5. doi: 10.1016/0888-7543(88)90146-2. Genomics. 1988. PMID: 2906325

5

The molecular genetics of autosomal-dominant polycystic kidney disease of the PKD1 type.

Somlo S, Germino GG, Wirth B, Weinstat-Saslow D, Barton N, Gillespie GA, Frischauf AM, Reeders ST. Somlo S, et al. Among authors: barton n. Contrib Nephrol. 1992;97:101-9. doi: 10.1159/000421648. Contrib Nephrol. 1992. PMID: 1633710 Review. No abstract available.

6

A new human gene located in the PKD1 region of chromosome 16 is a functional homologue to ERV1 of yeast.

Lisowsky T, Weinstat-Saslow DL, Barton N, Reeders ST, Schneider MC. Lisowsky T, et al. Among authors: barton n. Genomics. 1995 Oct 10;29(3):690-7. doi: 10.1006/geno.1995.9950. Genomics. 1995. PMID: 8575761 Free article.

7

Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).

Snarey A, Thomas S, Schneider MC, Pound SE, Barton N, Wright AF, Somlo S, Germino GG, Harris PC, Reeders ST, et al. Snarey A, et al. Among authors: barton n. Am J Hum Genet. 1994 Aug;55(2):365-71. Am J Hum Genet. 1994. PMID: 8037213 Free PMC article.

8

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Wilkie AO, Buckle VJ, Harris PC, Lamb J, Barton NJ, Reeders ST, Lindenbaum RH, Nicholls RD, Barrow M, Bethlenfalvay NC, et al. Wilkie AO, et al. Among authors: barton nj. Am J Hum Genet. 1990 Jun;46(6):1112-26. Am J Hum Genet. 1990. PMID: 2339704 Free PMC article.

9

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

Lamb J, Wilkie AO, Harris PC, Buckle VJ, Lindenbaum RH, Barton NJ, Reeders ST, Weatherall DJ, Higgs DR. Lamb J, et al. Among authors: barton nj. Lancet. 1989 Oct 7;2(8667):819-24. doi: 10.1016/s0140-6736(89)92995-4. Lancet. 1989. PMID: 2477654

10

The N-ethylmaleimide-sensitive fusion protein and alpha-SNAP induce a conformational change in syntaxin.

Hanson PI, Otto H, Barton N, Jahn R. Hanson PI, et al. Among authors: barton n. J Biol Chem. 1995 Jul 14;270(28):16955-61. doi: 10.1074/jbc.270.28.16955. J Biol Chem. 1995. PMID: 7622514 Free article.

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