These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

305 related articles for article (PubMed ID: 16624901)

  • 1. A defect in protein farnesylation suppresses a loss of Schizosaccharomyces pombe tsc2+, a homolog of the human gene predisposing to tuberous sclerosis complex.
    Nakase Y; Fukuda K; Chikashige Y; Tsutsumi C; Morita D; Kawamoto S; Ohnuki M; Hiraoka Y; Matsumoto T
    Genetics; 2006 Jun; 173(2):569-78. PubMed ID: 16624901
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pas1, a G1 cyclin, regulates amino acid uptake and rescues a delay in G1 arrest in Tsc1 and Tsc2 mutants in Schizosaccharomyces pombe.
    van Slegtenhorst M; Mustafa A; Henske EP
    Hum Mol Genet; 2005 Oct; 14(19):2851-8. PubMed ID: 16115814
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tsc1+ and tsc2+ regulate arginine uptake and metabolism in Schizosaccharomyces pombe.
    van Slegtenhorst M; Carr E; Stoyanova R; Kruger WD; Henske EP
    J Biol Chem; 2004 Mar; 279(13):12706-13. PubMed ID: 14718525
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Birt-Hogg-Dube and tuberous sclerosis complex homologs have opposing roles in amino acid homeostasis in Schizosaccharomyces pombe.
    van Slegtenhorst M; Khabibullin D; Hartman TR; Nicolas E; Kruger WD; Henske EP
    J Biol Chem; 2007 Aug; 282(34):24583-90. PubMed ID: 17556368
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical and functional characterizations of small GTPase Rheb and TSC2 GAP activity.
    Li Y; Inoki K; Guan KL
    Mol Cell Biol; 2004 Sep; 24(18):7965-75. PubMed ID: 15340059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Crystal structure of the yeast TSC1 core domain and implications for tuberous sclerosis pathological mutations.
    Sun W; Zhu YJ; Wang Z; Zhong Q; Gao F; Lou J; Gong W; Xu W
    Nat Commun; 2013; 4():2135. PubMed ID: 23857276
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The RHEB-mTOR axis regulates expression of
    Nakase Y; Matsumoto T
    J Cell Sci; 2018 Nov; 131(22):. PubMed ID: 30301783
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex.
    Zeng LH; Rensing NR; Zhang B; Gutmann DH; Gambello MJ; Wong M
    Hum Mol Genet; 2011 Feb; 20(3):445-54. PubMed ID: 21062901
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Biallelic TSC gene inactivation in tuberous sclerosis complex.
    Crino PB; Aronica E; Baltuch G; Nathanson KL
    Neurology; 2010 May; 74(21):1716-23. PubMed ID: 20498439
    [TBL] [Abstract][Full Text] [Related]  

  • 10.
    He J; Zhou W; Shi J; Lin J; Zhang B; Sun Z
    Genet Test Mol Biomarkers; 2020 Jan; 24(1):1-5. PubMed ID: 31855466
    [No Abstract]   [Full Text] [Related]  

  • 11. Structure of the Tuberous Sclerosis Complex 2 (TSC2) N Terminus Provides Insight into Complex Assembly and Tuberous Sclerosis Pathogenesis.
    Zech R; Kiontke S; Mueller U; Oeckinghaus A; Kümmel D
    J Biol Chem; 2016 Sep; 291(38):20008-20. PubMed ID: 27493206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The TSC1 and TSC2 tumor suppressors are required for proper ER stress response and protect cells from ER stress-induced apoptosis.
    Kang YJ; Lu MK; Guan KL
    Cell Death Differ; 2011 Jan; 18(1):133-44. PubMed ID: 20616807
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comprehensive genetic and phenotype analysis of 95 individuals with mosaic tuberous sclerosis complex.
    Klonowska K; Giannikou K; Grevelink JM; Boeszoermenyi B; Thorner AR; Herbert ZT; Afrin A; Treichel AM; Hamieh L; Kotulska K; Jozwiak S; Moss J; Darling TN; Kwiatkowski DJ
    Am J Hum Genet; 2023 Jun; 110(6):979-988. PubMed ID: 37141891
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Role of the Tsc1-Tsc2 complex in signaling and transport across the cell membrane in the fission yeast Schizosaccharomyces pombe.
    Matsumoto S; Bandyopadhyay A; Kwiatkowski DJ; Maitra U; Matsumoto T
    Genetics; 2002 Jul; 161(3):1053-63. PubMed ID: 12136010
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosis.
    Jones AC; Daniells CE; Snell RG; Tachataki M; Idziaszczyk SA; Krawczak M; Sampson JR; Cheadle JP
    Hum Mol Genet; 1997 Nov; 6(12):2155-61. PubMed ID: 9328481
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reported.
    Niida Y; Wakisaka A; Tsuji T; Yamada H; Kuroda M; Mitani Y; Okumura A; Yokoi A
    J Hum Genet; 2013 Apr; 58(4):216-25. PubMed ID: 23389244
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of novel single amino acid changes that result in hyperactivation of the unique GTPase, Rheb, in fission yeast.
    Urano J; Comiso MJ; Guo L; Aspuria PJ; Deniskin R; Tabancay AP; Kato-Stankiewicz J; Tamanoi F
    Mol Microbiol; 2005 Nov; 58(4):1074-86. PubMed ID: 16262791
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 16.