Callen DF - Search Results

1

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. Among authors: callen df. Nat Genet. 1998 Apr;18(4):319-24. doi: 10.1038/ng0498-319. Nat Genet. 1998. PMID: 9537412

2

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7.

Settasatian C, Whitmore SA, Crawford J, Bilton RL, Cleton-Jansen AM, Sutherland GR, Callen DF. Settasatian C, et al. Among authors: callen df. Hum Genet. 1999 Jul-Aug;105(1-2):139-44. doi: 10.1007/s004399900087. Hum Genet. 1999. PMID: 10480368

3

C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain.

Bhalla K, Eyre HJ, Whitmore SA, Sutherland GR, Callen DF. Bhalla K, et al. Among authors: callen df. J Hum Genet. 1999;44(6):383-7. doi: 10.1007/s100380050183. J Hum Genet. 1999. PMID: 10570909

4

Refined physical mapping of chromosome 16-specific low-abundance repetitive DNA sequences.

Stallings RL, Whitmore SA, Doggett NA, Callen DF. Stallings RL, et al. Among authors: callen df. Cytogenet Cell Genet. 1993;63(2):97-101. doi: 10.1159/000133509. Cytogenet Cell Genet. 1993. PMID: 8467715

5

Positional cloning of the Fanconi anaemia group A gene.

Fanconi anaemia/Breast cancer consortium. Fanconi anaemia/Breast cancer consortium. Nat Genet. 1996 Nov;14(3):324-8. doi: 10.1038/ng1196-324. Nat Genet. 1996. PMID: 8896564

6

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.

Callen DF, Baker E, Lane S, Nancarrow J, Thompson A, Whitmore SA, MacLennan DH, Berger R, Cherif D, Järvelä I, et al. Callen DF, et al. Am J Hum Genet. 1991 Dec;49(6):1372-7. Am J Hum Genet. 1991. PMID: 1746562 Free PMC article.

7

Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16.

Whitmore SA, Apostolou S, Lane S, Nancarrow JK, Phillips HA, Richards RI, Sutherland GR, Callen DF. Whitmore SA, et al. Among authors: callen df. Genomics. 1994 Mar 15;20(2):169-75. doi: 10.1006/geno.1994.1150. Genomics. 1994. PMID: 8020963

8

Chromosomal assignment of the human SA gene to 16p13.11 and demonstration of its expression in the kidney.

Samani NJ, Whitmore SA, Kaiser MA, Harris J, See CG, Callen DF, Lodwick D. Samani NJ, et al. Among authors: callen df. Biochem Biophys Res Commun. 1994 Mar 15;199(2):862-8. doi: 10.1006/bbrc.1994.1308. Biochem Biophys Res Commun. 1994. PMID: 8135833

9

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.

Kozman HM, Gedeon AK, Whitmore S, Suthers GK, Callen DF, Sutherland GR, Mulley JC. Kozman HM, et al. Among authors: callen df. Genomics. 1991 Nov;11(3):756-9. doi: 10.1016/0888-7543(91)90085-s. Genomics. 1991. PMID: 1685482

10

Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3.

Savino M, d'Apolito M, Centra M, van Beerendonk HM, Cleton-Jansen AM, Whitmore SA, Crawford J, Callen DF, Zelante L, Savoia A. Savino M, et al. Among authors: callen df. Genomics. 1999 Oct 15;61(2):219-26. doi: 10.1006/geno.1999.5958. Genomics. 1999. PMID: 10534407

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