Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 179

Similar articles for PubMed (Select 7847806)

1.

Rearrangement of chromosome band 11q13 in HeLa cells.

Jesudasan RA, Slovak ML, Sen S, Srivatsan ES.

Anticancer Res. 1994 Sep-Oct;14(5A):1727-33.

PMID:
7847806
2.

Behavioral characterization of a white-throated sparrow homozygous for the ZAL2(m) chromosomal rearrangement.

Horton BM, Hu Y, Martin CL, Bunke BP, Matthews BS, Moore IT, Thomas JW, Maney DL.

Behav Genet. 2013 Jan;43(1):60-70. doi: 10.1007/s10519-012-9574-6. Epub 2012 Dec 21.

3.

Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone.

Trombetta D, Macchia G, Mandahl N, Nord KH, Mertens F.

Cancer Genet. 2012 Jul-Aug;205(7-8):410-3. doi: 10.1016/j.cancergen.2012.05.002.

PMID:
22868002
4.
5.

Molecular cytogenetic characterization of alien introgressions with gene Fhb3 for resistance to Fusarium head blight disease of wheat.

Qi LL, Pumphrey MO, Friebe B, Chen PD, Gill BS.

Theor Appl Genet. 2008 Nov;117(7):1155-66. doi: 10.1007/s00122-008-0853-9. Epub 2008 Aug 20.

PMID:
18712343
6.

Relationship between FRA11F and 11q13 gene amplification in oral cancer.

Reshmi SC, Huang X, Schoppy DW, Black RC, Saunders WS, Smith DI, Gollin SM.

Genes Chromosomes Cancer. 2007 Feb;46(2):143-54.

PMID:
17099871
7.

Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).

Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.

In Vivo. 2006 Jul-Aug;20(4):473-8.

8.

The coincidence of chromosome 15 aberrations and beta2-microglobulin gene mutations is causative for the total loss of human leukocyte antigen class I expression in melanoma.

Paschen A, Arens N, Sucker A, Greulich-Bode KM, Fonsatti E, Gloghini A, Striegel S, Schwinn N, Carbone A, Hildenbrand R, Cerwenka A, Maio M, Schadendorf D.

Clin Cancer Res. 2006 Jun 1;12(11 Pt 1):3297-305.

9.

[Minute chromosome rearrangement detected by human telomeric band painting probes].

Qian WP, Tan YM, Tan YQ, Song D, Xu XQ, Li LY, Lu GX.

Yi Chuan. 2006 May;28(5):518-20. Chinese.

PMID:
16735227
10.

Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas.

Jones TD, Eble JN, Wang M, MacLennan GT, Delahunt B, Brunelli M, Martignoni G, Lopez-Beltran A, Bonsib SM, Ulbright TM, Zhang S, Nigro K, Cheng L.

Clin Cancer Res. 2005 Oct 15;11(20):7226-33.

11.

A 700-kb physical and transcription map of the cervical cancer tumor suppressor gene locus on chromosome 11q13.

Zainabadi K, Benyamini P, Chakrabarti R, Veena MS, Chandrasekharappa SC, Gatti RA, Srivatsan ES.

Genomics. 2005 Jun;85(6):704-14. Epub 2005 Apr 9.

PMID:
15885497
12.

A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.

Tirado CA, Lager J, Rosoff PM, Golembiski-Ruiz V, Gong JZ, Goodman BK.

Cancer Genet Cytogenet. 2004 Oct 1;154(1):57-9.

PMID:
15381373
13.

Homozygous deletions within the 11q13 cervical cancer tumor-suppressor locus in radiation-induced, neoplastically transformed human hybrid cells.

Mendonca MS, Farrington DL, Mayhugh BM, Qin Y, Temples T, Comerford K, Chakrabarti R, Zainabadi K, Redpath JL, Stanbridge EJ, Srivatsan ES.

Genes Chromosomes Cancer. 2004 Apr;39(4):277-87.

PMID:
14978789
14.

Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.

Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.

Chin Med J (Engl). 2003 Sep;116(9):1298-303.

PMID:
14527352
15.

Genomic imbalances in CML blast crisis: 8q24.12-q24.13 segment identified as a common region of over-representation.

Gribble SM, Reid AG, Roberts I, Grace C, Green AR, Nacheva EP.

Genes Chromosomes Cancer. 2003 Aug;37(4):346-58.

PMID:
12800146
16.

A mortality gene(s) for the human adenocarcinoma line HeLa maps to a 130-kb region of human chromosome 4q22-q23.

Bryce SD, Morrison V, Craig NJ, Forsyth NR, Fitzsimmons SA, Ireland H, Cuthbert AP, Newbold RF, Parkinson EK.

Neoplasia. 2002 Nov-Dec;4(6):544-50.

18.

Molecular-cytogenetic analysis of fragmentation of chromosome 17 in the breast cancer cell line EFM-19.

Rogalla P, Helbig R, Drieschner N, Flohr AM, Krohn M, Bullerdiek J.

Anticancer Res. 2002 Jul-Aug;22(4):1987-92.

PMID:
12174875
19.

Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.

Srivatsan ES, Chakrabarti R, Zainabadi K, Pack SD, Benyamini P, Mendonca MS, Yang PK, Kang K, Motamedi D, Sawicki MP, Zhuang Z, Jesudasan RA, Bengtsson U, Sun C, Roe BA, Stanbridge EJ, Wilczynski SP, Redpath JL.

Oncogene. 2002 Aug 15;21(36):5631-42.

20.

Somatic DNA alterations in endometriosis: high frequency of chromosome 17 and p53 loss in late-stage endometriosis.

Bischoff FZ, Heard M, Simpson JL.

J Reprod Immunol. 2002 May-Jun;55(1-2):49-64.

PMID:
12062821
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk