Still I - Search Results

1

Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization.

Chernova O, Still I, Kalaycio M, Hoeltge G, Cowell JK. Chernova O, et al. Among authors: still i. Genes Chromosomes Cancer. 1998 Feb;21(2):160-5. doi: 10.1002/(sici)1098-2264(199802)21:2<160::aid-gcc12>3.0.co;2-v. Genes Chromosomes Cancer. 1998. PMID: 9491328

2

Fine structure physical mapping of a 1.9 Mb region of chromosome 13q12.

Still IH, Roberts T, Cowell JK. Still IH, et al. Ann Hum Genet. 1997 Jan;61(Pt 1):15-24. doi: 10.1046/j.1469-1809.1997.6110015.x. Ann Hum Genet. 1997. PMID: 9066924

3

Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting.

Still IH, Vince P, Cowell JK. Still IH, et al. Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10373-8. doi: 10.1073/pnas.94.19.10373. Proc Natl Acad Sci U S A. 1997. PMID: 9294218 Free PMC article.

4

Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11.

Still IH, Chernova O, Hurd D, Stone RM, Cowell JK. Still IH, et al. Blood. 1997 Oct 15;90(8):3136-41. Blood. 1997. PMID: 9376595 Free article.

5

The third member of the transforming acidic coiled coil-containing gene family, TACC3, maps in 4p16, close to translocation breakpoints in multiple myeloma, and is upregulated in various cancer cell lines.

Still IH, Vince P, Cowell JK. Still IH, et al. Genomics. 1999 Jun 1;58(2):165-70. doi: 10.1006/geno.1999.5829. Genomics. 1999. PMID: 10366448

6

Incorporation of 35 novel gene transcripts into the physical and genetic map of human chromosome 13.

Still IH, Roberts T, Bia B, Hawthorn L, Auffray C, Cowell J. Still IH, et al. Genomics. 1996 Apr 15;33(2):159-66. doi: 10.1006/geno.1996.0179. Genomics. 1996. PMID: 8660963

7

The Brn-3a transcription factor gene (POU4F1) maps close to the locus for the variant late infantile form of neuronal ceroid-lipofuscinosis.

Still IH, Cowell J. Still IH, et al. Cytogenet Cell Genet. 1996;74(3):225-6. doi: 10.1159/000134422. Cytogenet Cell Genet. 1996. PMID: 8941380

8

Identification of a novel gene (ADPRTL1) encoding a potential Poly(ADP-ribosyl)transferase protein.

Still IH, Vince P, Cowell JK. Still IH, et al. Genomics. 1999 Dec 15;62(3):533-6. doi: 10.1006/geno.1999.6024. Genomics. 1999. PMID: 10644454

9

The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13.

Still IH, Cowell JK. Still IH, et al. Blood. 1998 Aug 15;92(4):1456-8. Blood. 1998. PMID: 9694738 Free article. No abstract available.

10

Cloning of TACC1, an embryonically expressed, potentially transforming coiled coil containing gene, from the 8p11 breast cancer amplicon.

Still IH, Hamilton M, Vince P, Wolfman A, Cowell JK. Still IH, et al. Oncogene. 1999 Jul 8;18(27):4032-8. doi: 10.1038/sj.onc.1202801. Oncogene. 1999. PMID: 10435627

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