BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 16314844)

  • 21. Rines/RNF180, a novel RING finger gene-encoded product, is a membrane-bound ubiquitin ligase.
    Ogawa M; Mizugishi K; Ishiguro A; Koyabu Y; Imai Y; Takahashi R; Mikoshiba K; Aruga J
    Genes Cells; 2008 Apr; 13(4):397-409. PubMed ID: 18363970
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
    Crider-Miller SJ; Reid LH; Higgins MJ; Nowak NJ; Shows TB; Futreal PA; Weissman BE
    Genomics; 1997 Dec; 46(3):355-63. PubMed ID: 9441738
    [TBL] [Abstract][Full Text] [Related]  

  • 23. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.
    Steenman MJ; Zijlstra N; Kruitbosch DL; Wiesmeijer C; Larizza L; Voûte PA; Westerveld A; Mannens MM
    Cytogenet Cell Genet; 2000; 88(3-4):289-95. PubMed ID: 10828613
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autoantigen Ro52 is an E3 ubiquitin ligase.
    Wada K; Kamitani T
    Biochem Biophys Res Commun; 2006 Jan; 339(1):415-21. PubMed ID: 16297862
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
    Tsuchida Y; Yokomori K; Choi SH
    Nihon Rinsho; 1995 Nov; 53(11):2742-8. PubMed ID: 8538037
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The overlap between Sotos and Beckwith-Wiedemann syndromes.
    Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB
    J Pediatr; 2010 Jun; 156(6):1035-1036. PubMed ID: 20394943
    [No Abstract]   [Full Text] [Related]  

  • 28. Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma.
    Matsumoto T; Kinoshita E; Maeda H; Niikawa N; Kurosaki N; Harada N; Yun K; Sawai T; Aoki S; Kondoh T
    Jpn J Hum Genet; 1994 Jun; 39(2):225-34. PubMed ID: 8086640
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genomic imprinting and Wilms' tumor.
    Moulton T; Chung WY; Yuan L; Hensle T; Waber P; Nisen P; Tycko B
    Med Pediatr Oncol; 1996 Nov; 27(5):476-83. PubMed ID: 8827077
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor.
    Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Lausch E; Reutzel D; Fees S; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B
    Nat Genet; 2005 Aug; 37(8):785-6; author reply 786-7. PubMed ID: 16049499
    [No Abstract]   [Full Text] [Related]  

  • 31. UbcH6 interacts with and ubiquitinates the SCA1 gene product ataxin-1.
    Hong S; Lee S; Cho SG; Kang S
    Biochem Biophys Res Commun; 2008 Jun; 371(2):256-60. PubMed ID: 18439907
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.
    Montagna M; Menin C; Chieco-Bianchi L; D'Andrea E
    J Cancer Res Clin Oncol; 1994; 120(12):732-6. PubMed ID: 7798299
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Wilms' tumors and malformation complexes].
    Hata J; Fukuzawa R; Takata A; Kikuchi H
    Nihon Rinsho; 2000 Jul; 58(7):1419-25. PubMed ID: 10921316
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autoregulation of an E2 enzyme by ubiquitin-chain assembly on its catalytic residue.
    Ravid T; Hochstrasser M
    Nat Cell Biol; 2007 Apr; 9(4):422-7. PubMed ID: 17310239
    [TBL] [Abstract][Full Text] [Related]  

  • 35. UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene.
    Wake NC; Ricketts CJ; Morris MR; Prigmore E; Gribble SM; Skytte AB; Brown M; Clarke N; Banks RE; Hodgson S; Turnell AS; Maher ER; Woodward ER
    Hum Mutat; 2013 Dec; 34(12):1650-61. PubMed ID: 24000165
    [TBL] [Abstract][Full Text] [Related]  

  • 36. TEB4 is a C4HC3 RING finger-containing ubiquitin ligase of the endoplasmic reticulum.
    Hassink G; Kikkert M; van Voorden S; Lee SJ; Spaapen R; van Laar T; Coleman CS; Bartee E; Früh K; Chau V; Wiertz E
    Biochem J; 2005 Jun; 388(Pt 2):647-55. PubMed ID: 15673284
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour.
    Ogawa O; Eccles MR; Szeto J; McNoe LA; Yun K; Maw MA; Smith PJ; Reeve AE
    Nature; 1993 Apr; 362(6422):749-51. PubMed ID: 8097018
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The degradation of promyelocytic leukemia and Sp100 proteins by herpes simplex virus 1 is mediated by the ubiquitin-conjugating enzyme UbcH5a.
    Gu H; Roizman B
    Proc Natl Acad Sci U S A; 2003 Jul; 100(15):8963-8. PubMed ID: 12855769
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new gun in town: the U box is a ubiquitin ligase domain.
    Patterson C
    Sci STKE; 2002 Jan; 2002(116):pe4. PubMed ID: 11805346
    [TBL] [Abstract][Full Text] [Related]  

  • 40. p57K1P2 is expressed in Wilms' tumor with LOH of 11p15.5.
    Overall ML; Spencer J; Bakker M; Dziadek M; Smith PJ
    Genes Chromosomes Cancer; 1996 Sep; 17(1):56-9. PubMed ID: 8889507
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.