127 related articles for article (PubMed ID: 16845657)
1. High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
Wieland I; Muschke P; Volleth M; Röpke A; Pelz AF; Stumm M; Wieacker P
Genes Chromosomes Cancer; 2006 Oct; 45(10):945-9. PubMed ID: 16845657
[TBL] [Abstract][Full Text] [Related]
2. Renal cell carcinoma and a constitutional t(11;22)(q23;q11.2): case report and review of the potential link between the constitutional t(11;22) and cancer.
Doyen J; Carpentier X; Haudebourg J; Hoch B; Karmous-Benailly H; Ambrosetti D; Fabas T; Amiel J; Lambert JC; Pedeutour F
Cancer Genet; 2012 Nov; 205(11):603-7. PubMed ID: 23117075
[TBL] [Abstract][Full Text] [Related]
3. Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.
Lindblom A; Sandelin K; Iselius L; Dumanski J; White I; Nordenskjöld M; Larsson C
Am J Hum Genet; 1994 May; 54(5):871-6. PubMed ID: 8178827
[TBL] [Abstract][Full Text] [Related]
4. Molecular cloning of a constitutional t(7;22) translocation associated with risk of hematological malignancy.
Hill AS; MacCallum PK; Young BD; Lillington DM
Genes Chromosomes Cancer; 2003 Nov; 38(3):260-4. PubMed ID: 14506701
[TBL] [Abstract][Full Text] [Related]
5. A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.
Jobanputra V; Chung WK; Hacker AM; Emanuel BS; Warburton D
Prenat Diagn; 2005 Aug; 25(8):683-6. PubMed ID: 16049998
[TBL] [Abstract][Full Text] [Related]
6. Balanced t(11;15)(q23;q15) in a TP53+/+ breast cancer patient from a Li-Fraumeni syndrome family.
Sherif ZA; Danielsen M
Cancer Genet Cytogenet; 2006 Jul; 168(1):50-8. PubMed ID: 16772121
[TBL] [Abstract][Full Text] [Related]
7. Specific subtelomere loss on chromosome der(11)t(3;11)(q23;q23)x2 in anaplastic thyroid cancer cell line OCUT-1.
Kammori M; Onoda N; Nakamura K; Izumiyama N; Ogisawa K; Kurabayashi R; Ogawa T; Kaminishi M; Poon SS; Takubo K
Int J Mol Med; 2006 Jul; 18(1):9-16. PubMed ID: 16786150
[TBL] [Abstract][Full Text] [Related]
8. Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males.
Kurahashi H; Emanuel BS
Nat Genet; 2001 Oct; 29(2):139-40. PubMed ID: 11586296
[TBL] [Abstract][Full Text] [Related]
9. Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study.
Schoemaker MJ; Jones ME; Higgins CD; Wright AF; ; Swerdlow AJ
Int J Cancer; 2019 Sep; 145(6):1493-1498. PubMed ID: 30496607
[TBL] [Abstract][Full Text] [Related]
10. Incidence of the main genetic markers in glioblastoma multiforme is independent of tumor topology.
Necesalová E; Vranová V; Kuglík P; Cejpek P; Jarosová M; Pesáková M; Relichová J; Veselská R
Neoplasma; 2007; 54(3):212-8. PubMed ID: 17447852
[TBL] [Abstract][Full Text] [Related]
11. Cryptic deletion of EGR1 in association with a novel balanced t(5;22)(q31;q11.2) in a patient with myelodysplastic syndrome.
Hoffman MW; Janney S; Batanian JR
Cancer Genet Cytogenet; 2009 Jun; 191(2):106-8. PubMed ID: 19446747
[TBL] [Abstract][Full Text] [Related]
12. Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
Bonne A; Vreede L; Kuiper RP; Bodmer D; Jansen C; Eleveld M; van Erp F; Arkesteijn G; Hoogerbrugge N; van Ravenswaaij C; Schoenmakers EF; Geurts van Kessel A
Cancer Genet Cytogenet; 2007 Nov; 179(1):11-8. PubMed ID: 17981209
[TBL] [Abstract][Full Text] [Related]
13. The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombination.
Hill AS; Foot NJ; Chaplin TL; Young BD
Hum Mol Genet; 2000 Jun; 9(10):1525-32. PubMed ID: 10888603
[TBL] [Abstract][Full Text] [Related]
14. Cryptic insertion into 11q23 of MLLT10 not involved in t(1;15;11;10)(p36;q11;q23;q24) in infant acute biphenotypic leukemia.
Matsuda K; Tanaka M; Araki S; Yanagisawa R; Yamauchi K; Koike K
Cancer Genet Cytogenet; 2009 Apr; 190(2):113-20. PubMed ID: 19380030
[TBL] [Abstract][Full Text] [Related]
15. Partial trisomy (11;22) syndrome with manifestations of Goldenhar sequence due to maternal balanced t(11;22).
Balci S; Engiz O; Yilmaz Z; Baltaci V
Genet Couns; 2006; 17(3):281-9. PubMed ID: 17100195
[TBL] [Abstract][Full Text] [Related]
16. Fluorescence in situ hybridization dissection of a chronic myeloid leukemia case bearing the apparently balanced translocations (9;22)(q34;q11.2) and (11;11)(p15;q13).
Malvestiti F; Colombo D; Perego D; Rodeschini O; Finelli P; Larizza L; Giardino D
Cancer Genet Cytogenet; 2009 Jan; 188(1):42-7. PubMed ID: 19061779
[TBL] [Abstract][Full Text] [Related]
17. DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) translocation.
Rajaram V; Knezevich S; Bove KE; Perry A; Pfeifer JD
Genes Chromosomes Cancer; 2007 May; 46(5):508-13. PubMed ID: 17311249
[TBL] [Abstract][Full Text] [Related]
18. Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).
Takeuchi M; Katayama Y; Okamura A; Yamamoto K; Shimoyama M; Matsui T
Cancer Genet Cytogenet; 2007 Nov; 179(1):85-7. PubMed ID: 17981222
[No Abstract] [Full Text] [Related]
19. Translocation (10;11)(p12;q23) in childhood acute myeloid leukemia: incidence and complex mechanism.
Stasevich I; Utskevich R; Kustanovich A; Litvinko N; Savitskaya T; Chernyavskaya S; Saharova O; Aleinikova O
Cancer Genet Cytogenet; 2006 Sep; 169(2):114-20. PubMed ID: 16938568
[TBL] [Abstract][Full Text] [Related]
20. Increased radiosensitivity as an indicator of genes conferring breast cancer susceptibility.
Varga D; Vogel W; Bender A; Surowy H; Maier C; Kreienberg R; Deissler H; Sauer G
Strahlenther Onkol; 2007 Dec; 183(12):655-60. PubMed ID: 18040608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]