Mould S - Search Results

1

Structural abnormalities of chromosome 7q in chronic lymphoproliferative disorders.

Oscier DG, Gardiner A, Mould S. Oscier DG, et al. Among authors: mould s. Cancer Genet Cytogenet. 1996 Nov;92(1):24-7. doi: 10.1016/s0165-4608(96)00025-8. Cancer Genet Cytogenet. 1996. PMID: 8956866

2

Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations.

Corcoran MM, Mould SJ, Orchard JA, Ibbotson RE, Chapman RM, Boright AP, Platt C, Tsui LC, Scherer SW, Oscier DG. Corcoran MM, et al. Among authors: mould sj. Oncogene. 1999 Nov 4;18(46):6271-7. doi: 10.1038/sj.onc.1203033. Oncogene. 1999. PMID: 10597225

3

Chromosome abnormalities in hairy cell leukaemia variant.

Brito-Babapulle V, Matutes E, Oscier D, Mould S, Catovsky D. Brito-Babapulle V, et al. Among authors: mould s. Genes Chromosomes Cancer. 1994 Jul;10(3):197-202. doi: 10.1002/gcc.2870100308. Genes Chromosomes Cancer. 1994. PMID: 7522043

4

Cytogenetic studies in splenic lymphoma with villous lymphocytes.

Oscier DG, Matutes E, Gardiner A, Glide S, Mould S, Brito-Babapulle V, Ellis J, Catovsky D. Oscier DG, et al. Among authors: mould s. Br J Haematol. 1993 Nov;85(3):487-91. doi: 10.1111/j.1365-2141.1993.tb03337.x. Br J Haematol. 1993. PMID: 8136270

5

Trisomy 12 and structural abnormalities of 13q14 occurring in the same clone in chronic lymphocytic leukaemia.

Mould S, Gardiner A, Corcoran M, Oscier DG. Mould S, et al. Br J Haematol. 1996 Feb;92(2):389-92. doi: 10.1046/j.1365-2141.1996.d01-1492.x. Br J Haematol. 1996. PMID: 8603005

6

Karyotypic evolution in a granulocytic sarcoma developing in a myeloproliferative disorder with a novel (3;4) translocation.

Myint H, Chacko J, Mould S, Ross F, Oscier DG. Myint H, et al. Among authors: mould s. Br J Haematol. 1995 Jun;90(2):462-4. doi: 10.1111/j.1365-2141.1995.tb05176.x. Br J Haematol. 1995. PMID: 7794773

7

Use of a retinoblastoma gene probe to investigate clonality in Richter's syndrome.

Kruger A, Sadullah S, Chapman R, Hodges E, Mould S, Hamblin TJ, Oscier DG. Kruger A, et al. Among authors: mould s. Leukemia. 1993 Nov;7(11):1891-5. Leukemia. 1993. PMID: 8231258 Review.

8

Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia.

Johnson EJ, Scherer SW, Osborne L, Tsui LC, Oscier D, Mould S, Cotter FE. Johnson EJ, et al. Among authors: mould s. Blood. 1996 May 1;87(9):3579-86. Blood. 1996. PMID: 8611680 Free article.

9

Identification of four new translocations involving FGFR1 in myeloid disorders.

Sohal J, Chase A, Mould S, Corcoran M, Oscier D, Iqbal S, Parker S, Welborn J, Harris RI, Martinelli G, Montefusco V, Sinclair P, Wilkins BS, van den Berg H, Vanstraelen D, Goldman JM, Cross NC. Sohal J, et al. Among authors: mould s. Genes Chromosomes Cancer. 2001 Oct;32(2):155-63. doi: 10.1002/gcc.1177. Genes Chromosomes Cancer. 2001. PMID: 11550283

10

A new minimal deleted region at 11q22.3 reveals the importance of interpretation of diminished FISH signals and the choice of probe for ATM deletion screening in chronic lymphocytic leukemia.

Gardiner A, Parker H, Glide S, Mould S, Robinson H, Tracy I, Stankovic T, Oscier D, Strefford J. Gardiner A, et al. Among authors: mould s. Leuk Res. 2012 Mar;36(3):307-10. doi: 10.1016/j.leukres.2011.08.002. Epub 2011 Sep 28. Leuk Res. 2012. PMID: 21955805

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