BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 33612456)

  • 21. Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece.
    Avgeris S; Fostira F; Vagena A; Ninios Y; Delimitsou A; Vodicka R; Vrtel R; Youroukos S; Stravopodis DJ; Vlassi M; Astrinidis A; Yannoukakos D; Voutsinas GE
    Sci Rep; 2017 Dec; 7(1):16697. PubMed ID: 29196670
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetically engineered human cortical spheroid models of tuberous sclerosis.
    Blair JD; Hockemeyer D; Bateup HS
    Nat Med; 2018 Oct; 24(10):1568-1578. PubMed ID: 30127391
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes.
    Lin S; Zeng JB; Zhao GX; Yang ZZ; Huang HP; Lin MT; Wu ZY; Wang N; Chen WJ; Fang L
    Seizure; 2019 Oct; 71():322-327. PubMed ID: 31525612
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical and genetic study patients with tuberous sclerosis complex].
    Rubilar C; López F; Troncoso M; Barrios A; Herrera L
    Rev Chil Pediatr; 2017 Feb; 88(1):41-49. PubMed ID: 28288225
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Monoallelic germline TSC1 mutations are permissive for T lymphocyte development and homeostasis in tuberous sclerosis complex individuals.
    Pilipow K; Basso V; Migone N; Mondino A
    PLoS One; 2014; 9(3):e91952. PubMed ID: 24633152
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Antenatal screening and diagnosis of tuberous sclerosis complex by fetal echocardiography and targeted genomic sequencing.
    Gu X; Han L; Chen J; Wang J; Hao X; Zhang Y; Zhang J; Ge S; He Y
    Medicine (Baltimore); 2018 Apr; 97(15):e0112. PubMed ID: 29642139
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Revisiting Brain Tuberous Sclerosis Complex in Rat and Human: Shared Molecular and Cellular Pathology Leads to Distinct Neurophysiological and Behavioral Phenotypes.
    Kútna V; O'Leary VB; Newman E; Hoschl C; Ovsepian SV
    Neurotherapeutics; 2021 Apr; 18(2):845-858. PubMed ID: 33398801
    [TBL] [Abstract][Full Text] [Related]  

  • 29. TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling.
    Martin P; Wagh V; Reis SA; Erdin S; Beauchamp RL; Shaikh G; Talkowski M; Thiele E; Sheridan SD; Haggarty SJ; Ramesh V
    Mol Autism; 2020; 11(1):2. PubMed ID: 31921404
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tuberous sclerosis: a review of the past, present, and future.
    Uysal SP; Şahin M
    Turk J Med Sci; 2020 Nov; 50(SI-2):1665-1676. PubMed ID: 32222129
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex.
    Kashii H; Kasai S; Sato A; Hagino Y; Nishito Y; Kobayashi T; Hino O; Mizuguchi M; Ikeda K
    Hum Genomics; 2023 Feb; 17(1):4. PubMed ID: 36732866
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fetal cardiac tumor: echocardiography, clinical outcome and genetic analysis in 53 cases.
    Chen J; Wang J; Sun H; Gu X; Hao X; Fu Y; Zhang Y; Liu X; Zhang H; Han L; He Y
    Ultrasound Obstet Gynecol; 2019 Jul; 54(1):103-109. PubMed ID: 29877000
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel 23-base-pair duplication mutation in TSC1 exon 15 in an infant presenting with cardiac rhabdomyomas.
    Smith M; Sperling D
    Am J Med Genet; 1999 Jun; 84(4):346-9. PubMed ID: 10340649
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular genetic, cardiac and neurodevelopmental findings in cases of prenatally diagnosed rhabdomyoma associated with tuberous sclerosis complex.
    Lee KA; Won HS; Shim JY; Lee PR; Kim A
    Ultrasound Obstet Gynecol; 2013 Mar; 41(3):306-11. PubMed ID: 22791573
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Establishment of human induced pluripotent stem cell lines, KMUGMCi006, from a patient with Tuberous sclerosis complex (TSC) bearing mosaic nonsense mutations in the Tuberous sclerosis complex 2 (TSC2) gene.
    Ura H; Togi S; Ozaki M; Hatanaka H; Niida Y
    Stem Cell Res; 2023 Aug; 70():103129. PubMed ID: 37271041
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation landscape of TSC1/TSC2 in Chinese patients with tuberous sclerosis complex.
    Meng Y; Yu C; Chen M; Yu X; Sun M; Yan H; Zhao W; Yu S
    J Hum Genet; 2021 Mar; 66(3):227-236. PubMed ID: 32917966
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mourning Dr. Alfred G. Knudson: the two-hit hypothesis, tumor suppressor genes, and the tuberous sclerosis complex.
    Hino O; Kobayashi T
    Cancer Sci; 2017 Jan; 108(1):5-11. PubMed ID: 27862655
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Deficient TSC1/TSC2-complex suppression of SOX9-osteopontin-AKT signalling cascade constrains tumour growth in tuberous sclerosis complex.
    Jin F; Jiang K; Ji S; Wang L; Ni Z; Huang F; Li C; Chen R; Zhang H; Hu Z; Zha X
    Hum Mol Genet; 2017 Jan; 26(2):407-419. PubMed ID: 28013293
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Rhabdomyomas and tuberous sclerosis complex: our experience in 33 cases.
    Sciacca P; Giacchi V; Mattia C; Greco F; Smilari P; Betta P; Distefano G
    BMC Cardiovasc Disord; 2014 May; 14():66. PubMed ID: 24884933
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cardiac rhabdomyomas in tuberous sclerosis complex show apoptosis regulation and mTOR pathway abnormalities.
    Kotulska K; Larysz-Brysz M; Grajkowska W; Jóźwiak J; Włodarski P; Sahin M; Lewin-Kowalik J; Domańska-Pakieła D; Jóźwiak S
    Pediatr Dev Pathol; 2009; 12(2):89-95. PubMed ID: 17990907
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.