BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 16835931)

  • 1. Extensive acrochordons and pancreatic islet-cell tumors in tuberous sclerosis associated with TSC2 mutations.
    Merritt JL; Davis DM; Pittelkow MR; Babovic-Vuksanovic D
    Am J Med Genet A; 2006 Aug; 140(15):1669-72. PubMed ID: 16835931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Malignant pancreatic endocrine tumor in a child with tuberous sclerosis.
    Francalanci P; Diomedi-Camassei F; Purificato C; Santorelli FM; Giannotti A; Dominici C; Inserra A; Boldrini R
    Am J Surg Pathol; 2003 Oct; 27(10):1386-9. PubMed ID: 14508401
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Imaging features of tuberous sclerosis complex with autosomal-dominant polycystic kidney disease: a contiguous gene syndrome.
    Back SJ; Andronikou S; Kilborn T; Kaplan BS; Darge K
    Pediatr Radiol; 2015 Mar; 45(3):386-95. PubMed ID: 25355409
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The analysis of mutations and exon deletions at TSC2 gene in angiomyolipomas associated with tuberous sclerosis complex.
    Yang HM; Choi HJ; Hong DP; Joo SY; Lee NE; Song JY; Choi YL; Lee J; Choi D; Kim B; Park HJ; Park JB; Kim SJ
    Exp Mol Pathol; 2014 Dec; 97(3):440-4. PubMed ID: 25281918
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Well-differentiated pancreatic neuroendocrine carcinoma in tuberous sclerosis--case report and review of the literature.
    Arva NC; Pappas JG; Bhatla T; Raetz EA; Macari M; Ginsburg HB; Hajdu CH
    Am J Surg Pathol; 2012 Jan; 36(1):149-53. PubMed ID: 22173120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel TSC1 and TSC2 gene mutations in Chinese patients with tuberous sclerosis complex.
    Yu T; He Y; Li N; Zhou Y; Wang Z; Fu Q; Wang J; Wang J
    Clin Neurol Neurosurg; 2017 Mar; 154():104-108. PubMed ID: 28178598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pancreatic neuroendocrine tumors in patients with tuberous sclerosis complex.
    Larson AM; Hedgire SS; Deshpande V; Stemmer-Rachamimov AO; Harisinghani MG; Ferrone CR; Shah U; Thiele EA
    Clin Genet; 2012 Dec; 82(6):558-63. PubMed ID: 22035404
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood.
    Verhoef S; van Diemen-Steenvoorde R; Akkersdijk WL; Bax NM; Ariyurek Y; Hermans CJ; van Nieuwenhuizen O; Nikkels PG; Lindhout D; Halley DJ; Lips K; van den Ouweland AM
    Eur J Pediatr; 1999 Apr; 158(4):284-7. PubMed ID: 10206124
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenesis of multifocal micronodular pneumocyte hyperplasia and lymphangioleiomyomatosis in tuberous sclerosis and association with tuberous sclerosis genes TSC1 and TSC2.
    Maruyama H; Ohbayashi C; Hino O; Tsutsumi M; Konishi Y
    Pathol Int; 2001 Aug; 51(8):585-94. PubMed ID: 11564212
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TSC2 c.1864C>T variant associated with mild cases of tuberous sclerosis complex.
    Farach LS; Gibson WT; Sparagana SP; Nellist M; Stumpel CT; Hietala M; Friedman E; Pearson DA; Creighton SP; Wagemans A; Segel R; Ben-Shalom E; Au KS; Northrup H
    Am J Med Genet A; 2017 Mar; 173(3):771-775. PubMed ID: 28211972
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Glioblastoma multiforme in a child with tuberous sclerosis complex.
    Vignoli A; Lesma E; Alfano RM; Peron A; Scornavacca GF; Massimino M; Schiavello E; Ancona S; Cerati M; Bulfamante G; Gorio A; Canevini MP
    Am J Med Genet A; 2015 Oct; 167A(10):2388-93. PubMed ID: 25946256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of 65 tuberous sclerosis complex (TSC) patients by TSC2 DGGE, TSC1/TSC2 MLPA, and TSC1 long-range PCR sequencing, and report of 28 novel mutations.
    Rendtorff ND; Bjerregaard B; Frödin M; Kjaergaard S; Hove H; Skovby F; Brøndum-Nielsen K; Schwartz M;
    Hum Mutat; 2005 Oct; 26(4):374-83. PubMed ID: 16114042
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tuberous sclerosis complex mutations in patients with pancreatic neuroendocrine tumors. Observations on phenotypic and treatment-related associations.
    Navale P; Chatterjee D; Itani M; Trikalinos NA
    Virchows Arch; 2023 Aug; 483(2):167-175. PubMed ID: 37354253
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of hypomelanotic macules is associated with constitutive activated mTORC1 in tuberous sclerosis complex.
    Møller LB; Schönewolf-Greulich B; Rosengren T; Larsen LJ; Ostergaard JR; Sommerlund M; Ostenfeldt C; Stausbøl-Grøn B; Linnet KM; Gregersen PA; Jensen UB
    Mol Genet Metab; 2017 Apr; 120(4):384-391. PubMed ID: 28336152
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome.
    Papadopoulou A; Dinopoulos A; Koutsodontis G; Pons R; Vorgia P; Koute V; Vratimos A; Zafeiriou D
    Eur J Paediatr Neurol; 2018 May; 22(3):419-426. PubMed ID: 29500070
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas.
    Henske EP; Neumann HP; Scheithauer BW; Herbst EW; Short MP; Kwiatkowski DJ
    Genes Chromosomes Cancer; 1995 Aug; 13(4):295-8. PubMed ID: 7547639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Novel mutation in TSC2 gene in pediatric patient with clinical diagnosis of tuberous sclerosis].
    Caicedo-Herrera G; Candelo E; Pachajoa H
    Arch Argent Pediatr; 2017 Oct; 115(5):e287-e290. PubMed ID: 28895704
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.