90 related articles for article (PubMed ID: 10321732)
1. JTB: a novel membrane protein gene at 1q21 rearranged in a jumping translocation.
Hatakeyama S; Osawa M; Omine M; Ishikawa F
Oncogene; 1999 Mar; 18(12):2085-90. PubMed ID: 10321732
[TBL] [Abstract][Full Text] [Related]
2. The structure of the extracellular domain of the jumping translocation breakpoint protein reveals a variation of the midkine fold.
Rousseau F; Pan B; Fairbrother WJ; Bazan JF; Lingel A
J Mol Biol; 2012 Jan; 415(1):22-8. PubMed ID: 22079049
[TBL] [Abstract][Full Text] [Related]
3. Characterization of Jumping translocation breakpoint (JTB) gene product isolated as a TGF-beta1-inducible clone involved in regulation of mitochondrial function, cell growth and cell death.
Kanome T; Itoh N; Ishikawa F; Mori K; Kim-Kaneyama JR; Nose K; Shibanuma M
Oncogene; 2007 Sep; 26(41):5991-6001. PubMed ID: 17369841
[TBL] [Abstract][Full Text] [Related]
4. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.
Odero MD; Vizmanos JL; Román JP; Lahortiga I; Panizo C; Calasanz MJ; Zeleznik-Le NJ; Rowley JD; Novo FJ
Genes Chromosomes Cancer; 2002 Sep; 35(1):11-9. PubMed ID: 12203785
[TBL] [Abstract][Full Text] [Related]
5. A novel chromosomal translocation t(1;14)(q25;q32) in pre-B acute lymphoblastic leukemia involves the LIM homeodomain protein gene, Lhx4.
Kawamata N; Sakajiri S; Sugimoto KJ; Isobe Y; Kobayashi H; Oshimi K
Oncogene; 2002 Jul; 21(32):4983-91. PubMed ID: 12118377
[TBL] [Abstract][Full Text] [Related]
6. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
7. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
Jamieson RV; Farrar N; Stewart K; Perveen R; Mihelec M; Carette M; Grigg JR; McAvoy JW; Lovicu FJ; Tam PP; Scambler P; Lloyd IC; Donnai D; Black GC
Hum Mutat; 2007 Oct; 28(10):968-77. PubMed ID: 17492639
[TBL] [Abstract][Full Text] [Related]
8. Shortened telomeres involved in a case with a jumping translocation at 1q21.
Hatakeyama S; Fujita K; Mori H; Omine M; Ishikawa F
Blood; 1998 Mar; 91(5):1514-9. PubMed ID: 9473214
[TBL] [Abstract][Full Text] [Related]
9. Physical mapping of a functional cluster of epidermal differentiation genes on chromosome 1q21.
Volz A; Korge BP; Compton JG; Ziegler A; Steinert PM; Mischke D
Genomics; 1993 Oct; 18(1):92-9. PubMed ID: 8276421
[TBL] [Abstract][Full Text] [Related]
10. A t(11;15) fuses MLL to two different genes, AF15q14 and a novel gene MPFYVE on chromosome 15.
Chinwalla V; Chien A; Odero M; Neilly MB; Zeleznik-Le NJ; Rowley JD
Oncogene; 2003 Mar; 22(9):1400-10. PubMed ID: 12618766
[TBL] [Abstract][Full Text] [Related]
11. Acute myeloid leukemia possessing jumping translocation is related to highly elevated levels of EAT/mcl-1, a Bcl-2 related gene with anti-apoptotic functions.
Okita H; Umezawa A; Fukuma M; Ando T; Urano F; Sano M; Nakata Y; Mori T; Hata J
Leuk Res; 2000 Jan; 24(1):73-7. PubMed ID: 10634649
[TBL] [Abstract][Full Text] [Related]
12. Genomic structure, chromosomal localization and expression profile of a novel melanoma differentiation associated (mda-7) gene with cancer specific growth suppressing and apoptosis inducing properties.
Huang EY; Madireddi MT; Gopalkrishnan RV; Leszczyniecka M; Su Z; Lebedeva IV; Kang D; Jiang H; Lin JJ; Alexandre D; Chen Y; Vozhilla N; Mei MX; Christiansen KA; Sivo F; Goldstein NI; Mhashilkar AB; Chada S; Huberman E; Pestka S; Fisher PB
Oncogene; 2001 Oct; 20(48):7051-63. PubMed ID: 11704829
[TBL] [Abstract][Full Text] [Related]
13. Identification of the TCL1/MTCP1-like 1 (TML1) gene from the region next to the TCL1 locus.
Sugimoto J; Hatakeyama T; Narducci MG; Russo G; Isobe M
Cancer Res; 1999 May; 59(10):2313-7. PubMed ID: 10344735
[TBL] [Abstract][Full Text] [Related]
14. Jumping translocations in hematological malignancies: a cytogenetic study of five cases.
Manola KN; Georgakakos VN; Stavropoulou C; Spyridonidis A; Angelopoulou MK; Vlachadami I; Katsigiannis A; Roussou P; Pantelias GE; Sambani C
Cancer Genet Cytogenet; 2008 Dec; 187(2):85-94. PubMed ID: 19027489
[TBL] [Abstract][Full Text] [Related]
15. Investigating the Function of Human Jumping Translocation Breakpoint Protein (hJTB) and Its Interacting Partners through In-Solution Proteomics of MCF7 Cells.
Jayathirtha M; Whitham D; Alwine S; Donnelly M; Neagu AN; Darie CC
Molecules; 2022 Nov; 27(23):. PubMed ID: 36500393
[TBL] [Abstract][Full Text] [Related]
16. Jumping translocations in myelodysplastic syndromes.
Yeung CCS; Deeg HJ; Pritchard C; Wu D; Fang M
Cancer Genet; 2016 Sep; 209(9):395-402. PubMed ID: 27751357
[TBL] [Abstract][Full Text] [Related]
17. UQCRH gene encoding mitochondrial Hinge protein is interrupted by a translocation in a soft-tissue sarcoma and epigenetically inactivated in some cancer cell lines.
Modena P; Testi MA; Facchinetti F; Mezzanzanica D; Radice MT; Pilotti S; Sozzi G
Oncogene; 2003 Jul; 22(29):4586-93. PubMed ID: 12881716
[TBL] [Abstract][Full Text] [Related]
18. A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia.
Mikhail FM; Coignet L; Hatem N; Mourad ZI; Farawela HM; El Kaffash DM; Farahat N; Nucifora G
Genes Chromosomes Cancer; 2004 Feb; 39(2):110-8. PubMed ID: 14695990
[TBL] [Abstract][Full Text] [Related]
19. Nonrandom fusion of L-plastin(LCP1) and LAZ3(BCL6) genes by t(3;13)(q27;q14) chromosome translocation in two cases of B-cell non-Hodgkin lymphoma.
Galiègue-Zouitina S; Quief S; Hildebrand MP; Denis C; Detourmignies L; Laï JL; Kerckaert JP
Genes Chromosomes Cancer; 1999 Oct; 26(2):97-105. PubMed ID: 10469447
[TBL] [Abstract][Full Text] [Related]
20. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome.
Maestrini E; Monaco AP; McGrath JA; Ishida-Yamamoto A; Camisa C; Hovnanian A; Weeks DE; Lathrop M; Uitto J; Christiano AM
Nat Genet; 1996 May; 13(1):70-7. PubMed ID: 8673107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]