BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 21567926)

  • 1. Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex.
    Spreafico F; Notarangelo LD; Schumacher RF; Savoldi G; Gamba B; Terenziani M; Collini P; Fasoli S; Giordano L; Luisa B; Porta F; Massimino M; Radice P; Perotti D
    Am J Med Genet A; 2011 Jun; 155A(6):1419-24. PubMed ID: 21567926
    [TBL] [Abstract][Full Text] [Related]  

  • 2. WT1, WTX and CTNNB1 mutation analysis in 43 patients with sporadic Wilms' tumor.
    Cardoso LC; De Souza KR; De O Reis AH; Andrade RC; Britto AC; De Lima MA; Dos Santos AC; De Faria PS; Ferman S; Seuánez HN; Vargas FR
    Oncol Rep; 2013 Jan; 29(1):315-20. PubMed ID: 23117548
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs.
    Dabora SL; Jozwiak S; Franz DN; Roberts PS; Nieto A; Chung J; Choy YS; Reeve MP; Thiele E; Egelhoff JC; Kasprzyk-Obara J; Domanska-Pakiela D; Kwiatkowski DJ
    Am J Hum Genet; 2001 Jan; 68(1):64-80. PubMed ID: 11112665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.
    Au KS; Williams AT; Roach ES; Batchelor L; Sparagana SP; Delgado MR; Wheless JW; Baumgartner JE; Roa BB; Wilson CM; Smith-Knuppel TK; Cheung MY; Whittemore VH; King TM; Northrup H
    Genet Med; 2007 Feb; 9(2):88-100. PubMed ID: 17304050
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children.
    Haruta M; Arai Y; Watanabe N; Fujiwara Y; Honda S; Ohshima J; Kasai F; Nakadate H; Horie H; Okita H; Hata J; Fukuzawa M; Kaneko Y
    Cancer Sci; 2012 Jun; 103(6):1129-35. PubMed ID: 22409817
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney disease.
    Longa L; Brusco A; Carbonara C; Polidoro S; Scolari F; Valzorio B; Riegler P; Tardanico R; Migone N
    Contrib Nephrol; 1997; 122():91-5. PubMed ID: 9399046
    [No Abstract]   [Full Text] [Related]  

  • 7. Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene.
    Sampson JR; Maheshwar MM; Aspinwall R; Thompson P; Cheadle JP; Ravine D; Roy S; Haan E; Bernstein J; Harris PC
    Am J Hum Genet; 1997 Oct; 61(4):843-51. PubMed ID: 9382094
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.
    Jones AC; Shyamsundar MM; Thomas MW; Maynard J; Idziaszczyk S; Tomkins S; Sampson JR; Cheadle JP
    Am J Hum Genet; 1999 May; 64(5):1305-15. PubMed ID: 10205261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosis.
    Maheshwar MM; Cheadle JP; Jones AC; Myring J; Fryer AE; Harris PC; Sampson JR
    Hum Mol Genet; 1997 Oct; 6(11):1991-6. PubMed ID: 9302281
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex.
    Vrtel R; Verhoef S; Bouman K; Maheshwar MM; Nellist M; van Essen AJ; Bakker PL; Hermans CJ; Bink-Boelkens MT; van Elburg RM; Hoff M; Lindhout D; Sampson J; Halley DJ; van den Ouweland AM
    J Med Genet; 1996 Jan; 33(1):47-51. PubMed ID: 8825048
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patients.
    Au KS; Rodriguez JA; Finch JL; Volcik KA; Roach ES; Delgado MR; Rodriguez E; Northrup H
    Am J Hum Genet; 1998 Feb; 62(2):286-94. PubMed ID: 9463313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Gene diagnosis for a child with tuberous sclerosis].
    Zhang Y; Ding H; Yin A; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):770-3. PubMed ID: 25449086
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and analysis of mutations in WTX and WT1 genes in peripheral blood and tumor tissue of children with Wilms' tumor.
    Wang H; Shen Y; Sun N; Jiang YP; Li ML; Sun L
    Chin Med J (Engl); 2012 May; 125(10):1733-9. PubMed ID: 22800892
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis Complex.
    Fox J; Ben-Shachar S; Uliel S; Svirsky R; Saitsu H; Matsumoto N; Fattal-Valevski A
    Am J Med Genet A; 2017 Mar; 173(3):744-748. PubMed ID: 28127866
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A shower of second hit events as the cause of multifocal renal cell carcinoma in tuberous sclerosis complex.
    Tyburczy ME; Jozwiak S; Malinowska IA; Chekaluk Y; Pugh TJ; Wu CL; Nussbaum RL; Seepo S; Dzik T; Kotulska K; Kwiatkowski DJ
    Hum Mol Genet; 2015 Apr; 24(7):1836-42. PubMed ID: 25432535
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complete inactivation of the TSC2 gene leads to formation of hamartomas.
    Au KS; Hebert AA; Roach ES; Northrup H
    Am J Hum Genet; 1999 Dec; 65(6):1790-5. PubMed ID: 10577937
    [No Abstract]   [Full Text] [Related]  

  • 17. Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions.
    Niida Y; Stemmer-Rachamimov AO; Logrip M; Tapon D; Perez R; Kwiatkowski DJ; Sims K; MacCollin M; Louis DN; Ramesh V
    Am J Hum Genet; 2001 Sep; 69(3):493-503. PubMed ID: 11468687
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.
    Verhoef S; Vrtel R; Bakker L; Stolte-Dijkstra I; Nellist M; Begeer JH; Zaremba J; Jozwiak S; Tempelaars AM; Lindhout D; Halley DJ; van den Ouweland AM
    Hum Mutat; 1998; Suppl 1():S85-7. PubMed ID: 9452050
    [No Abstract]   [Full Text] [Related]  

  • 19. Two novel TSC2 mutations in Chinese patients with tuberous sclerosis complex and a literature review of 20 patients reported in China.
    Zhao XY; Yang S; Zhou HL; Zhu YG; Wei L; Du WH; Ren YQ; Liang YH; Hou YX; Chen JJ; Zhang XJ
    Br J Dermatol; 2006 Nov; 155(5):1070-3. PubMed ID: 17034546
    [No Abstract]   [Full Text] [Related]  

  • 20. [Analysis of TSC gene mutations in five patients with tuberous sclerosis complex].
    Liu L; Zhang Z; Mu Y; Xiong F; Yang H; Yang P; Liu Y; Chen X; Sui W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):164-168. PubMed ID: 28397210
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.