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Journal Abstract Search

118 related items for PubMed ID: 12185600

  • 1. WAVE3, an actin-polymerization gene, is truncated and inactivated as a result of a constitutional t(1;13)(q21;q12) chromosome translocation in a patient with ganglioneuroblastoma.
    Sossey-Alaoui K, Su G, Malaj E, Roe B, Cowell JK.
    Oncogene; 2002 Aug 29; 21(38):5967-74. PubMed ID: 12185600
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  • 2. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG.
    Verh K Acad Geneeskd Belg; 1995 Aug 29; 57(5):389-422. PubMed ID: 8571670
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  • 4. Constructing a physical map around a constitutional t(1;13)(q22;q12) breakpoint in a patient with a ganglioneuroblastoma.
    Michalski AJ, Cowell JK.
    Prog Clin Biol Res; 1994 Aug 29; 385():79-85. PubMed ID: 7972239
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  • 6. Genomic organization and expression profile of the human and mouse WAVE gene family.
    Sossey-Alaoui K, Head K, Nowak N, Cowell JK.
    Mamm Genome; 2003 May 29; 14(5):314-22. PubMed ID: 12856283
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  • 9. Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome.
    Hearn T, Renforth GL, Spalluto C, Hanley NA, Piper K, Brickwood S, White C, Connolly V, Taylor JF, Russell-Eggitt I, Bonneau D, Walker M, Wilson DI.
    Nat Genet; 2002 May 29; 31(1):79-83. PubMed ID: 11941370
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  • 13. NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma.
    Roberts T, Chernova O, Cowell JK.
    Hum Mol Genet; 1998 Jul 29; 7(7):1169-78. PubMed ID: 9618176
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  • 14. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May 29; 31(5):431-43. PubMed ID: 15478601
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  • 16. 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 17; 22(29):4586-93. PubMed ID: 12881716
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  • 17. 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 01; 13(9):983-90. PubMed ID: 15016767
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  • 18. A new member of the proprotein convertase gene family (LPC) is located at a chromosome translocation breakpoint in lymphomas.
    Meerabux J, Yaspo ML, Roebroek AJ, Van de Ven WJ, Lister TA, Young BD.
    Cancer Res; 1996 Feb 01; 56(3):448-51. PubMed ID: 8564950
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  • 19. Differential regulation of cortactin and N-WASP-mediated actin polymerization by missing in metastasis (MIM) protein.
    Lin J, Liu J, Wang Y, Zhu J, Zhou K, Smith N, Zhan X.
    Oncogene; 2005 Mar 17; 24(12):2059-66. PubMed ID: 15688017
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  • 20. Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2.
    Arai E, Ikeuchi T, Karasawa S, Tamura A, Yamamoto K, Kida M, Ichimura K, Yuasa Y, Tonomura A.
    Am J Med Genet; 1992 Sep 15; 44(2):163-7. PubMed ID: 1456285
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