Wainscoat JS - Search Results

1

Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Kostrzewa M, Jaju RJ, Müller U, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Genomics. 2000 May 15;66(1):26-34. doi: 10.1006/geno.2000.6193. Genomics. 2000. PMID: 10843801

2

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Gama S, Kearney L, Tosi S, Kasprzyk A, Cheng JF, Jaju RJ, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Blood. 2002 Jun 15;99(12):4638-41. doi: 10.1182/blood.v99.12.4638. Blood. 2002. PMID: 12036901 Free article.

3

The 5q-syndrome.

Boultwood J, Lewis S, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Blood. 1994 Nov 15;84(10):3253-60. Blood. 1994. PMID: 7949083 Free article. Review. No abstract available.

4

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.

Boultwood J, Fidler C, Lewis S, Kelly S, Sheridan H, Littlewood TJ, Buckle VJ, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Genomics. 1994 Feb;19(3):425-32. doi: 10.1006/geno.1994.1090. Genomics. 1994. PMID: 8188284

5

Novel genes mapping to the critical region of the 5q- syndrome.

Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Genomics. 1997 Oct 1;45(1):88-96. doi: 10.1006/geno.1997.4899. Genomics. 1997. PMID: 9339364 Free article.

6

Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.

Jaju RJ, Boultwood J, Oliver FJ, Kostrzewa M, Fidler C, Parker N, McPherson JD, Morris SW, Müller U, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: wainscoat js. Genes Chromosomes Cancer. 1998 Jul;22(3):251-6. doi: 10.1002/(sici)1098-2264(199807)22:3<251::aid-gcc11>3.0.co;2-r. Genes Chromosomes Cancer. 1998. PMID: 9624537

7

The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.

Fidler C, Wainscoat JS, Boultwood J. Fidler C, et al. Among authors: wainscoat js. Genomics. 1999 Feb 15;56(1):134-6. doi: 10.1006/geno.1998.5687. Genomics. 1999. PMID: 10036195 No abstract available.

8

Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.

Boultwood J, Strickson AJ, Jabs EW, Cheng JF, Fidler C, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Hum Genet. 2000 Jan;106(1):127-9. doi: 10.1007/s004399900215. Hum Genet. 2000. PMID: 10982193

9

Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome.

Jaju RJ, Jones M, Boultwood J, Kelly S, Mason DY, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: wainscoat js. Genes Chromosomes Cancer. 2000 Nov;29(3):276-80. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1035>3.0.co;2-l. Genes Chromosomes Cancer. 2000. PMID: 10992302

10

Clonality in the myelodysplastic syndromes.

Boultwood J, Wainscoat JS. Boultwood J, et al. Among authors: wainscoat js. Int J Hematol. 2001 Jun;73(4):411-415. doi: 10.1007/BF02994002. Int J Hematol. 2001. PMID: 11503954 Review.

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