241 related articles for article (PubMed ID: 14991915)
1. Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome.
Trembath DG; Semina EV; Jones DH; Patil SR; Qian Q; Amendt BA; Russo AF; Murray JC
Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):82-91. PubMed ID: 14991915
[TBL] [Abstract][Full Text] [Related]
2. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
Matsumoto N; David DE; Johnson EW; Konecki D; Burmester JK; Ledbetter DH; Weber JL
Eur J Hum Genet; 2000 Nov; 8(11):875-83. PubMed ID: 11093278
[TBL] [Abstract][Full Text] [Related]
3. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
4. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
5. Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes).
Kehrer-Sawatzki H; Sandig C; Chuzhanova N; Goidts V; Szamalek JM; Tänzer S; Müller S; Platzer M; Cooper DN; Hameister H
Hum Mutat; 2005 Jan; 25(1):45-55. PubMed ID: 15580561
[TBL] [Abstract][Full Text] [Related]
6. Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement.
Rodríguez-Perales S; Meléndez B; Gribble SM; Valle L; Carter NP; Santamaría I; Conde L; Urioste M; Benítez J; Cigudosa JC
Hum Mol Genet; 2004 May; 13(9):983-90. PubMed ID: 15016767
[TBL] [Abstract][Full Text] [Related]
7. Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
Lynch RA; Piper M; Bankier A; Bhugra B; Surti U; Liu J; Buckler A; Dear PH; Menon AG
Genomics; 1998 Aug; 52(1):17-26. PubMed ID: 9740667
[TBL] [Abstract][Full Text] [Related]
8. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
Tosi S; Ballabio E; Teigler-Schlegel A; Boultwood J; Bruch J; Harbott J
Genes Chromosomes Cancer; 2005 Nov; 44(3):225-32. PubMed ID: 16028218
[TBL] [Abstract][Full Text] [Related]
9. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
[TBL] [Abstract][Full Text] [Related]
10. Identification of a recurrent t(4;6) chromosomal translocation in prostate cancer.
Lane TM; Strefford JC; Yáñez-Muñoz RJ; Purkis P; Forsythe E; Nia T; Hines J; Lu YJ; Oliver RT
J Urol; 2007 May; 177(5):1907-12. PubMed ID: 17437846
[TBL] [Abstract][Full Text] [Related]
11. Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.
Popovici C; Basset C; Bertucci F; Orsetti B; Adélaide J; Mozziconacci MJ; Conte N; Murati A; Ginestier C; Charafe-Jauffret E; Ethier SP; Lafage-Pochitaloff M; Theillet C; Birnbaum D; Chaffanet M
Genes Chromosomes Cancer; 2002 Nov; 35(3):204-18. PubMed ID: 12353263
[TBL] [Abstract][Full Text] [Related]
12. Paint-assisted microdissection-FISH: Rapid and simple mapping of translocation breakpoints in the embryonal rhabdomyosarcoma cell line RD.
Roberts I; Foster N; Nacheva E; Coleman N
Cytometry A; 2004 Apr; 58(2):177-84. PubMed ID: 15057971
[TBL] [Abstract][Full Text] [Related]
13. Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene.
Flomen RH; Vatcheva R; Gorman PA; Baptista PR; Groet J; Barisić I; Ligutic I; Nizetić D
Genomics; 1998 Feb; 47(3):409-13. PubMed ID: 9480756
[TBL] [Abstract][Full Text] [Related]
14. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
Mignon-Ravix C; Depetris D; Luciani JJ; Cuoco C; Krajewska-Walasek M; Missirian C; Collignon P; Delobel B; Croquette MF; Moncla A; Kroisel PM; Mattei MG
Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
[TBL] [Abstract][Full Text] [Related]
15. Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.
van Asseldonk M; Schepens M; de Bruijn D; Janssen B; Merkx G; Geurts van Kessel A
Genomics; 2000 May; 66(1):35-42. PubMed ID: 10843802
[TBL] [Abstract][Full Text] [Related]
16. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
17. Breakpoint within the nucleolus organizer region resulting in a reciprocal translocation t (4;14)(q21;p12).
Grabowski M; Fauth C; Wirtz A; Speicher MR
Am J Med Genet; 2000 Jun; 92(4):264-8. PubMed ID: 10842293
[TBL] [Abstract][Full Text] [Related]
18. Translocation t(X;11)(q13;q23) in B-cell chronic lymphocytic leukemia disrupts two novel genes.
Kalla C; Nentwich H; Schlotter M; Mertens D; Wildenberger K; Döhner H; Stilgenbauer S; Lichter P
Genes Chromosomes Cancer; 2005 Feb; 42(2):128-43. PubMed ID: 15543602
[TBL] [Abstract][Full Text] [Related]
19. Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.
Schleiermacher G; Bourdeaut F; Combaret V; Picrron G; Raynal V; Aurias A; Ribeiro A; Janoueix-Lerosey I; Delattre O
Oncogene; 2005 May; 24(20):3377-84. PubMed ID: 15735707
[TBL] [Abstract][Full Text] [Related]
20. Molecular cytogenetic analysis of the breakpoint region at 6q21-22 in T-cell lymphoma/leukemia cell lines.
Tagawa H; Miura I; Suzuki R; Suzuki H; Hosokawa Y; Seto M
Genes Chromosomes Cancer; 2002 Jun; 34(2):175-85. PubMed ID: 11979551
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
