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260 related items for PubMed ID: 2558334
1. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids. Finver SN, Martiniere C, Kagan J, Cavenee W, Croce CM. Oncogene Res; 1989; 5(2):143-8. PubMed ID: 2558334 [Abstract] [Full Text] [Related]
2. The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus. Boehm T, Lavenir I, Forster A, Wadey RB, Cowell JK, Harbott J, Lampert F, Waters J, Sherrington P, Couillin P. Oncogene; 1988 Dec; 3(6):691-5. PubMed ID: 2577871 [Abstract] [Full Text] [Related]
3. Translocations and rearrangements in T-cell acute leukemias with the t(11;14) (p13;q11) chromosomal translocations. Harvey RC, Martinerie C, Sun LH, Williams D, Showe LC. Oncogene; 1989 Mar; 4(3):341-9. PubMed ID: 2523031 [Abstract] [Full Text] [Related]
4. A study of chromosome 11p13 translocations involving TCR beta and TCR delta in human T cell leukaemia. Garcia IS, Kaneko Y, Gonzalez-Sarmiento R, Campbell K, White L, Boehm T, Rabbitts TH. Oncogene; 1991 Apr; 6(4):577-82. PubMed ID: 1827667 [Abstract] [Full Text] [Related]
5. Molecular cloning of the translocation breakpoint in T-ALL 11;14 (p13;q11): genomic map of TCR alpha and delta region on chromosome 14q11 and long-range map of region 11p13. Royer-Pokora B, Fleischer B, Ragg S, Loos U, Williams D. Hum Genet; 1989 Jun; 82(3):264-70. PubMed ID: 2543621 [Abstract] [Full Text] [Related]
6. [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 Jun; 57(5):389-422. PubMed ID: 8571670 [Abstract] [Full Text] [Related]
7. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Kaneko Y, Homma C, Maseki N, Sakurai M, Hata J. Cancer Res; 1991 Nov 01; 51(21):5937-42. PubMed ID: 1657374 [Abstract] [Full Text] [Related]
8. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO. Nature; 1991 Nov 01; 321(6073):882-7. PubMed ID: 3014343 [Abstract] [Full Text] [Related]
9. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. Genomics; 1989 Nov 01; 5(4):880-93. PubMed ID: 2574149 [Abstract] [Full Text] [Related]
10. A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Davis LM, Zabel B, Senger G, Lüdecke HJ, Metzroth B, Call K, Housman D, Claussen U, Horsthemke B, Shows TB. Genomics; 1991 Jul 01; 10(3):588-92. PubMed ID: 1653761 [Abstract] [Full Text] [Related]
11. Rearrangements in the human T-cell-receptor alpha-chain locus in patients with adult T-cell leukemia carrying translocations involving chromosome 14q11. Isobe M, Sadamori N, Russo G, Shimizu S, Yamamori S, Itoyama T, Yamada Y, Ikeda S, Ichimaru M, Kagan J. Cancer Res; 1990 Oct 01; 50(19):6171-5. PubMed ID: 2169336 [Abstract] [Full Text] [Related]
12. TTG-2, a new gene encoding a cysteine-rich protein with the LIM motif, is overexpressed in acute T-cell leukaemia with the t(11;14)(p13;q11). Royer-Pokora B, Loos U, Ludwig WD. Oncogene; 1991 Oct 01; 6(10):1887-93. PubMed ID: 1923511 [Abstract] [Full Text] [Related]
13. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci. Davis LM, Stallard R, Thomas GH, Couillin P, Junien C, Nowak NJ, Shows TB. Science; 1988 Aug 12; 241(4867):840-2. PubMed ID: 2841760 [Abstract] [Full Text] [Related]
14. Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor. Lewis WH, Yeger H, Bonetta L, Chan HS, Kang J, Junien C, Cowell J, Jones C, Dafoe LA. Genomics; 1988 Jul 12; 3(1):25-31. PubMed ID: 2851538 [Abstract] [Full Text] [Related]
15. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Rose EA, Glaser T, Jones C, Smith CL, Lewis WH, Call KM, Minden M, Champagne E, Bonetta L, Yeger H. Cell; 1990 Feb 09; 60(3):495-508. PubMed ID: 2154334 [Abstract] [Full Text] [Related]
16. The chromosome translocation (11;14)(p13;q11) associated with T-cell acute lymphocytic leukemia: an 11p13 breakpoint cluster region. Yoffe G, Schneider N, Van Dyk L, Yang CY, Siciliano M, Buchanan G, Capra JD, Baer R. Blood; 1989 Jul 09; 74(1):374-9. PubMed ID: 2526665 [Abstract] [Full Text] [Related]
17. Molecular and cellular biology of Wilms' tumour. Maitland NJ, Brown KW, Poirier V, Shaw AP, Williams J. Anticancer Res; 1989 Jul 09; 9(5):1417-26. PubMed ID: 2556071 [Abstract] [Full Text] [Related]
18. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK. Nature; 1988 Nov 24; 336(6197):374-6. PubMed ID: 2848199 [Abstract] [Full Text] [Related]
20. The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11. Cowell JK, Wadey RB, Buckle BB, Pritchard J. Hum Genet; 1989 May 24; 82(2):123-6. PubMed ID: 2542153 [Abstract] [Full Text] [Related] Page: [Next] [New Search]