Craig IW - Search Results

1

Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.

Shipley JM, Birdsall S, Clark J, Crew J, Gill S, Linehan M, Gnarra J, Fisher S, Craig IW, Cooper CS. Shipley JM, et al. Among authors: craig iw. Cytogenet Cell Genet. 1995;71(3):280-4. doi: 10.1159/000134127. Cytogenet Cell Genet. 1995. PMID: 7587394

2

Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.

Weterman MA, Wilbrink M, Janssen I, Janssen HA, van den Berg E, Fisher SE, Craig I, Geurts van Kessel A. Weterman MA, et al. Cytogenet Cell Genet. 1996;75(1):2-6. doi: 10.1159/000134444. Cytogenet Cell Genet. 1996. PMID: 8995477

3

Long-range organization of reiterated sequences, including the SSX1 cDNA at the OATL1 cluster in Xp11.23.

Chand A, Clark J, Cooper CS, Craig IW. Chand A, et al. Among authors: craig iw. Genomics. 1995 Dec 10;30(3):545-52. doi: 10.1006/geno.1995.1275. Genomics. 1995. PMID: 8825641

4

Localisation of the gene for human aromatic L-amino acid decarboxylase (DDC) to chromosome 7p13-->p11 by in situ hybridisation.

Craig SP, Thai AL, Weber M, Craig IW. Craig SP, et al. Among authors: craig iw. Cytogenet Cell Genet. 1992;61(2):114-6. doi: 10.1159/000133384. Cytogenet Cell Genet. 1992. PMID: 1395716

5

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis).

Fisher SE, Black GC, Lloyd SE, Hatchwell E, Wrong O, Thakker RV, Craig IW. Fisher SE, et al. Among authors: craig iw. Hum Mol Genet. 1994 Nov;3(11):2053-9. Hum Mol Genet. 1994. PMID: 7874126

6

High-resolution comparative mapping of the proximal region of the mouse X chromosome.

Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y. Blair HJ, et al. Among authors: craig iw. Genomics. 1995 Jul 20;28(2):305-10. doi: 10.1006/geno.1995.1146. Genomics. 1995. PMID: 8530041

7

Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.

Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW. Fisher SE, et al. Among authors: craig iw. Genomics. 1995 Sep 20;29(2):496-502. doi: 10.1006/geno.1995.9976. Genomics. 1995. PMID: 8666400

8

Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.

Boyd Y, Cockburn D, Holt S, Munro E, Van Ommen GJ, Gillard B, Affara N, Ferguson-Smith M, Craig I. Boyd Y, et al. Cytogenet Cell Genet. 1988;48(1):28-34. doi: 10.1159/000132581. Cytogenet Cell Genet. 1988. PMID: 3180845

9

Localization of human tryptophan hydroxylase (TPH) to chromosome 11p15.3----p14 by in situ hybridization.

Craig SP, Boularand S, Darmon MC, Mallet J, Craig IW. Craig SP, et al. Among authors: craig iw. Cytogenet Cell Genet. 1991;56(3-4):157-9. doi: 10.1159/000133075. Cytogenet Cell Genet. 1991. PMID: 2055111

10

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

Lloyd SE, Gunther W, Pearce SH, Thomson A, Bianchi ML, Bosio M, Craig IW, Fisher SE, Scheinman SJ, Wrong O, Jentsch TJ, Thakker RV. Lloyd SE, et al. Among authors: craig iw. Hum Mol Genet. 1997 Aug;6(8):1233-9. doi: 10.1093/hmg/6.8.1233. Hum Mol Genet. 1997. PMID: 9259268

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