Bentley E - Search Results

1

Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Barton D, Jennings A, Fellows IW, Ponder MA, Ponder BA, Benjamin C, Harris R, et al. Maher ER, et al. Among authors: bentley e. J Neurol Sci. 1990 Dec;100(1-2):27-30. doi: 10.1016/0022-510x(90)90008-b. J Neurol Sci. 1990. PMID: 1982450

2

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.

Maher ER, Bentley E, Payne SJ, Latif F, Richards FM, Chiano M, Hosoe S, Yates JR, Linehan M, Barton DE, et al. Maher ER, et al. Among authors: bentley e. J Med Genet. 1992 Dec;29(12):902-5. doi: 10.1136/jmg.29.12.902. J Med Genet. 1992. PMID: 1362224 Free PMC article.

3

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Latif F, Lerman M, Zbar B, Affara NA, Ferguson-Smith MA. Maher ER, et al. Among authors: bentley e. Genomics. 1991 Aug;10(4):957-60. doi: 10.1016/0888-7543(91)90185-h. Genomics. 1991. PMID: 1680799

4

Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22.

Foster K, Crossey PA, Cairns P, Hetherington JW, Richards FM, Jones MH, Bentley E, Affara NA, Ferguson-Smith MA, Maher ER. Foster K, et al. Among authors: bentley e. Br J Cancer. 1994 Feb;69(2):230-4. doi: 10.1038/bjc.1994.44. Br J Cancer. 1994. PMID: 8297719 Free PMC article.

5

Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours.

Crossey PA, Foster K, Richards FM, Phipps ME, Latif F, Tory K, Jones MH, Bentley E, Kumar R, Lerman MI, et al. Crossey PA, et al. Among authors: bentley e. Hum Genet. 1994 Jan;93(1):53-8. doi: 10.1007/BF00218913. Hum Genet. 1994. PMID: 8270255

6

Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.

Sargent CA, Affara NA, Bentley E, Pelmear A, Bailey DM, Davey P, Dow D, Leversha M, Aplin H, Besley GT, et al. Sargent CA, et al. Among authors: bentley e. Hum Mol Genet. 1993 Feb;2(2):97-106. doi: 10.1093/hmg/2.2.97. Hum Mol Genet. 1993. PMID: 8499912

7

The identification of novel gene sequences of the human adult testis.

Affara NA, Bentley E, Davey P, Pelmear A, Jones MH. Affara NA, et al. Among authors: bentley e. Genomics. 1994 Jul 1;22(1):205-10. doi: 10.1006/geno.1994.1363. Genomics. 1994. PMID: 7959769

8

Fine mapping of 39 ESTs on human chromosome 6p23-p25.

Olavesen MG, Bentley E, Mason RV, Stephens RJ, Ragoussis J. Olavesen MG, et al. Among authors: bentley e. Genomics. 1997 Dec 1;46(2):303-6. doi: 10.1006/geno.1997.5032. Genomics. 1997. PMID: 9417921

9

A metabolomic comparison of urinary changes in type 2 diabetes in mouse, rat, and human.

Salek RM, Maguire ML, Bentley E, Rubtsov DV, Hough T, Cheeseman M, Nunez D, Sweatman BC, Haselden JN, Cox RD, Connor SC, Griffin JL. Salek RM, et al. Among authors: bentley e. Physiol Genomics. 2007 Apr 24;29(2):99-108. doi: 10.1152/physiolgenomics.00194.2006. Epub 2006 Dec 26. Physiol Genomics. 2007. PMID: 17190852

10

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.

McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, Smart N, Rutland P, Prescott N, Hopkins J, Bentley E, Shaw A, Roberts E, Mueller R, Jadeja S, Philip N, Nelson J, Francannet C, Perez-Aytes A, Megarbane A, Kerr B, Wainwright B, Woolf AS, Winter RM, Scambler PJ. McGregor L, et al. Among authors: bentley e. Nat Genet. 2003 Jun;34(2):203-8. doi: 10.1038/ng1142. Nat Genet. 2003. PMID: 12766769

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