95 related articles for article (PubMed ID: 10773672)
1. Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases.
Guenet L; Henry C; Toutain B; Dubourg C; Le Gall JY; David V; Le Treut A
Cytogenet Cell Genet; 2000; 88(1-2):82-6. PubMed ID: 10773672
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene.
Dubourg C; Toutain B; Hélias C; Henry C; Lessard M; Le Gall JY; Le Treut A; Guenet L
Cancer Genet Cytogenet; 2002 Apr; 134(1):33-7. PubMed ID: 11996793
[TBL] [Abstract][Full Text] [Related]
3. Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping.
Hansen LL; Jakobsen CG; Justesen J
Cytogenet Cell Genet; 1999; 87(3-4):256-7. PubMed ID: 10702684
[No Abstract] [Full Text] [Related]
4. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases.
Le Beau MM; Espinosa R; Neuman WL; Stock W; Roulston D; Larson RA; Keinanen M; Westbrook CA
Proc Natl Acad Sci U S A; 1993 Jun; 90(12):5484-8. PubMed ID: 8516290
[TBL] [Abstract][Full Text] [Related]
5. Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q).
Lai F; Godley LA; Joslin J; Fernald AA; Liu J; Espinosa R; Zhao N; Pamintuan L; Till BG; Larson RA; Qian Z; Le Beau MM
Genomics; 2001 Jan; 71(2):235-45. PubMed ID: 11161817
[TBL] [Abstract][Full Text] [Related]
6. Human release factor eRF1: structural organisation of the unique functional gene on chromosome 5 and of the three processed pseudogenes.
Guenet L; Toutain B; Guilleret I; Chauvel B; Deaven LL; Longmire JL; Le Gall JY; David V; Le Treut A
FEBS Lett; 1999 Jul; 454(1-2):131-6. PubMed ID: 10413110
[TBL] [Abstract][Full Text] [Related]
7. Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map.
Zhao N; Stoffel A; Wang PW; Eisenbart JD; Espinosa R; Larson RA; Le Beau MM
Proc Natl Acad Sci U S A; 1997 Jun; 94(13):6948-53. PubMed ID: 9192672
[TBL] [Abstract][Full Text] [Related]
8. Deletions of chromosome 5 in malignant myeloid disorders.
Le Beau MM
Cancer Surv; 1992; 15():143-59. PubMed ID: 1451109
[TBL] [Abstract][Full Text] [Related]
9. Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.
Gao Q; Horwitz M; Roulston D; Hagos F; Zhao N; Freireich EJ; Golomb HM; Olopade OI
Genes Chromosomes Cancer; 2000 Jun; 28(2):164-72. PubMed ID: 10825001
[TBL] [Abstract][Full Text] [Related]
10. Assignment of TTC4 to human chromosome band 1p31.3 and a pseudogene TTC4P to 7p14-->p13 by in situ hybridization.
Hey Y; Brintnell B; James LA; Varley JM
Cytogenet Cell Genet; 2000; 88(3-4):272-4. PubMed ID: 10828607
[No Abstract] [Full Text] [Related]
11. Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation.
Liu TX; Becker MW; Jelinek J; Wu WS; Deng M; Mikhalkevich N; Hsu K; Bloomfield CD; Stone RM; DeAngelo DJ; Galinsky IA; Issa JP; Clarke MF; Look AT
Nat Med; 2007 Jan; 13(1):78-83. PubMed ID: 17159988
[TBL] [Abstract][Full Text] [Related]
12. Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map.
Wang PW; Eisenbart JD; Espinosa R; Davis EM; Larson RA; Le Beau MM
Genomics; 2000 Jul; 67(1):28-39. PubMed ID: 10945467
[TBL] [Abstract][Full Text] [Related]
13. cDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins.
Lai F; Godley LA; Fernald AA; Orelli BJ; Pamintuan L; Zhao N; Le Beau MM
Genomics; 2000 Nov; 70(1):123-30. PubMed ID: 11087669
[TBL] [Abstract][Full Text] [Related]
14. The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours.
Morris CM; Haataja L; McDonald M; Gough S; Markie D; Groffen J; Heisterkamp N
Cytogenet Cell Genet; 2000; 89(1-2):18-23. PubMed ID: 10894930
[TBL] [Abstract][Full Text] [Related]
15. Characterization of the human laminin beta2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS).
Durkin ME; Jäger AC; Khurana TS; Nielsen FC; Albrechtsen R; Wewer UM
Cytogenet Cell Genet; 1999; 84(3-4):173-8. PubMed ID: 10393422
[TBL] [Abstract][Full Text] [Related]
16. Mapping of the human Voltage-Dependent Anion Channel isoforms 1 and 2 reconsidered.
Messina A; Oliva M; Rosato C; Huizing M; Ruitenbeek W; van den Heuvel LP; Forte M; Rocchi M; De Pinto V
Biochem Biophys Res Commun; 1999 Feb; 255(3):707-10. PubMed ID: 10049775
[TBL] [Abstract][Full Text] [Related]
17. Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.
de Bruijn DR; Kater-Baats E; Eleveld M; Merkx G; Geurts Van Kessel A
Cytogenet Cell Genet; 2001; 92(3-4):310-9. PubMed ID: 11435705
[TBL] [Abstract][Full Text] [Related]
18. Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes.
Johnson CV; Cool DE; Glaccum MB; Green N; Fischer EH; Bruskin A; Hill DE; Lawrence JB
Genomics; 1993 Jun; 16(3):619-29. PubMed ID: 8325634
[TBL] [Abstract][Full Text] [Related]
19. Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines.
MacGrogan D; Alvarez S; DeBlasio T; Jhanwar SC; Nimer SD
Oncogene; 2001 Jul; 20(31):4150-60. PubMed ID: 11464281
[TBL] [Abstract][Full Text] [Related]
20. A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequences.
Horrigan SK; Bartoloni L; Speer MC; Fulton N; Kravarusic J; Ramesar R; Vance JM; Yamaoka LH; Westbrook CA
Genomics; 1999 Apr; 57(1):24-35. PubMed ID: 10191080
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]