BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 16114042)

  • 21. Tuberous sclerosis complex: everything old is new again.
    Ess KC
    J Neurodev Disord; 2009 Jun; 1(2):141-9. PubMed ID: 21547713
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multifocal drug-resistant epilepsy in a patient with a newly discovered mutation in tuberous sclerosis complex 1 gene treated by deep brain stimulation in the anterior thalamic nucleus.
    Sobstyl M; Jezierski P; Konopko M; Stapińska-Syniec A
    Epilepsy Behav Rep; 2024; 25():100637. PubMed ID: 38152567
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study.
    Grau J; Zöllner JP; Schubert-Bast S; Kurlemann G; Hertzberg C; Wiemer-Kruel A; Bast T; Bertsche A; Bettendorf U; Fiedler B; Hahn A; Hartmann H; Hornemann F; Immisch I; Jacobs J; Kieslich M; Klein KM; Klotz KA; Kluger G; Knuf M; Mayer T; Marquard K; Meyer S; Muhle H; Müller-Schlüter K; Noda AH; Ruf S; Sauter M; Schlump JU; Syrbe S; Thiels C; Trollmann R; Wilken B; Willems LM; Rosenow F; Strzelczyk A
    Orphanet J Rare Dis; 2021 Jun; 16(1):282. PubMed ID: 34154622
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Human
    Wundrach D; Martinetti LE; Stafford AM; Bilinovich SM; Angara K; Prokop JW; Crandall SR; Vogt D
    Front Mol Neurosci; 2020; 13():573409. PubMed ID: 33071758
    [TBL] [Abstract][Full Text] [Related]  

  • 25.
    Riley VA; Shankar V; Holmberg JC; Sokolov AM; Neckles VN; Williams K; Lyman R; Mackay TFC; Feliciano DM
    iScience; 2023 Dec; 26(12):108442. PubMed ID: 38107199
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literature.
    Milon V; Malinge MC; Blanluet M; Tessarech M; Battault C; Prestwich S; Vary B; Gueracher P; Legoff L; Barth M; Houdayer C; Guichet A; Rousseau A; Bonneau D; Procaccio V; Bris C; Colin E
    Eur J Hum Genet; 2024 May; ():. PubMed ID: 38806662
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit.
    Brown JA; Faley SL; Judge M; Ward P; Ihrie RA; Carson R; Armstrong L; Sahin M; Wikswo JP; Ess KC; Neely MD
    bioRxiv; 2023 Dec; ():. PubMed ID: 38168450
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Case report: Response to everolimus in a patient with platinum resistant, high grade serous ovarian carcinoma with biallelic
    Peterson M; Kolin DL; Konstantinopoulos PA
    Front Oncol; 2024; 14():1357980. PubMed ID: 38601768
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Spectrum of germline and somatic mitochondrial DNA variants in Tuberous Sclerosis Complex.
    Giannikou K; Martin KR; Abdel-Azim AG; Pamir KJ; Hougard TR; Bagwe S; Tang Y; MacKeigan JP; Kwiatkowski DJ; Henske EP; Lam HC
    Front Genet; 2022; 13():917993. PubMed ID: 36793390
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tuberous sclerosis complex - The importance of genetic testing.
    Borges JP; Grenha Pereira J; Rainha Campos A; Santos F
    Pediatr Int; 2023 Jan; 65(1):e15444. PubMed ID: 36527179
    [No Abstract]   [Full Text] [Related]  

  • 31. Prevalence of Liver Steatosis in Tuberous Sclerosis Complex Patients: A Retrospective Cross-Sectional Study.
    De Bock T; Brussaard C; François S; François K; Seynaeve L; Jansen A; Wissing KM; Janssens P
    J Clin Med; 2024 May; 13(10):. PubMed ID: 38792433
    [No Abstract]   [Full Text] [Related]  

  • 32. Recurrent Tuberous Sclerosis Complex​​​​​/Mammalian Target of Rapamycin Mutations Define Primary Renal Hemangioblastoma as a Unique Entity Distinct From Its Central Nervous System Counterpart.
    Wang XT; Fang R; He HY; Zhang W; Li Q; Sun SA; Wang X; Zhang RS; Teng XD; Zhou XJ; Xia QY; Zhao M; Rao Q
    Am J Surg Pathol; 2024 Mar; ():. PubMed ID: 38501656
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Early development of the Tsc1 Purkinje cell specific mouse knockouts.
    Sługocka A; Przybyła MA; Barski JJ
    Acta Neurobiol Exp (Wars); 2023 Dec; 83(4):404-413. PubMed ID: 38224281
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Improved detection of synthetic lethal interactions in
    Housden BE; Li Z; Kelley C; Wang Y; Hu Y; Valvezan AJ; Manning BD; Perrimon N
    Proc Natl Acad Sci U S A; 2017 Dec; 114(50):E10755-E10762. PubMed ID: 29183982
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chance Bias Arising from TSC2 Mutation Imbalance in the PREVeNT Trial.
    Samanta D
    Ann Neurol; 2024 Feb; 95(2):413-414. PubMed ID: 38081751
    [No Abstract]   [Full Text] [Related]  

  • 36. Reply to "Chance Bias Arising from TSC2 Mutation Imbalance in the PREVeNT Trial".
    Bebin EM
    Ann Neurol; 2024 Feb; 95(2):414. PubMed ID: 38081750
    [No Abstract]   [Full Text] [Related]  

  • 37. 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]  

  • 38. Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex.
    Hoogeveen-Westerveld M; Wentink M; van den Heuvel D; Mozaffari M; Ekong R; Povey S; den Dunnen JT; Metcalfe K; Vallee S; Krueger S; Bergoffen J; Shashi V; Elmslie F; Kwiatkowski D; Sampson J; Vidales C; Dzarir J; Garcia-Planells J; Dies K; Maat-Kievit A; van den Ouweland A; Halley D; Nellist M
    Hum Mutat; 2011 Apr; 32(4):424-35. PubMed ID: 21309039
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular and clinical analyses of 84 patients with tuberous sclerosis complex.
    Hung CC; Su YN; Chien SC; Liou HH; Chen CC; Chen PC; Hsieh CJ; Chen CP; Lee WT; Lin WL; Lee CN
    BMC Med Genet; 2006 Sep; 7():72. PubMed ID: 16981987
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Carrier testing for severe childhood recessive diseases by next-generation sequencing.
    Bell CJ; Dinwiddie DL; Miller NA; Hateley SL; Ganusova EE; Mudge J; Langley RJ; Zhang L; Lee CC; Schilkey FD; Sheth V; Woodward JE; Peckham HE; Schroth GP; Kim RW; Kingsmore SF
    Sci Transl Med; 2011 Jan; 3(65):65ra4. PubMed ID: 21228398
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.