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 *

159 related articles for article (PubMed ID: 14629778)

  • 1. An over-expression system for characterizing Ppt1 function in Drosophila.
    Korey CA; MacDonald ME
    BMC Neurosci; 2003 Nov; 4():30. PubMed ID: 14629778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Palmitoyl-protein thioesterase 1 deficiency in Drosophila melanogaster causes accumulation of abnormal storage material and reduced life span.
    Hickey AJ; Chotkowski HL; Singh N; Ault JG; Korey CA; MacDonald ME; Glaser RL
    Genetics; 2006 Apr; 172(4):2379-90. PubMed ID: 16452138
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of Drosophila palmitoyl-protein thioesterase 1.
    Glaser RL; Hickey AJ; Chotkowski HL; Chu-LaGraff Q
    Gene; 2003 Jul; 312():271-9. PubMed ID: 12909364
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1)--distinct characteristics in neurons.
    Lyly A; von Schantz C; Salonen T; Kopra O; Saarela J; Jauhiainen M; Kyttälä A; Jalanko A
    BMC Cell Biol; 2007 Jun; 8():22. PubMed ID: 17565660
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Altered glutamate receptor function in the cerebellum of the Ppt1-/- mouse, a murine model of infantile neuronal ceroid lipofuscinosis.
    Finn R; Kovács AD; Pearce DA
    J Neurosci Res; 2012 Feb; 90(2):367-75. PubMed ID: 21971706
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Batten disease Palmitoyl Protein Thioesterase 1 gene regulates neural specification and axon connectivity during Drosophila embryonic development.
    Chu-LaGraff Q; Blanchette C; O'Hern P; Denefrio C
    PLoS One; 2010 Dec; 5(12):e14402. PubMed ID: 21203506
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cln1-mutations suppress Rab7-RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosis.
    Sarkar C; Sadhukhan T; Bagh MB; Appu AP; Chandra G; Mondal A; Saha A; Mukherjee AB
    J Inherit Metab Dis; 2020 Sep; 43(5):1082-1101. PubMed ID: 32279353
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CNS-directed AAV2-mediated gene therapy ameliorates functional deficits in a murine model of infantile neuronal ceroid lipofuscinosis.
    Griffey MA; Wozniak D; Wong M; Bible E; Johnson K; Rothman SM; Wentz AE; Cooper JD; Sands MS
    Mol Ther; 2006 Mar; 13(3):538-47. PubMed ID: 16364693
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ppt1-deficiency dysregulates lysosomal Ca
    Mondal A; Appu AP; Sadhukhan T; Bagh MB; Previde RM; Sadhukhan S; Stojilkovic S; Liu A; Mukherjee AB
    J Inherit Metab Dis; 2022 May; 45(3):635-656. PubMed ID: 35150145
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund.
    Sanders DN; Farias FH; Johnson GS; Chiang V; Cook JR; O'Brien DP; Hofmann SL; Lu JY; Katz ML
    Mol Genet Metab; 2010 Aug; 100(4):349-56. PubMed ID: 20494602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis.
    Lange J; Haslett LJ; Lloyd-Evans E; Pocock JM; Sands MS; Williams BP; Cooper JD
    Acta Neuropathol Commun; 2018 Aug; 6(1):74. PubMed ID: 30089511
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuronal ceroid lipofuscinosis with DNAJC5/CSPα mutation has PPT1 pathology and exhibit aberrant protein palmitoylation.
    Henderson MX; Wirak GS; Zhang YQ; Dai F; Ginsberg SD; Dolzhanskaya N; Staropoli JF; Nijssen PC; Lam TT; Roth AF; Davis NG; Dawson G; Velinov M; Chandra SS
    Acta Neuropathol; 2016 Apr; 131(4):621-37. PubMed ID: 26659577
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of palmitoyl-protein thioesterase in cell death: implications for infantile neuronal ceroid lipofuscinosis.
    Cho S; Dawson PE; Dawson G
    Eur J Paediatr Neurol; 2001; 5 Suppl A():53-5. PubMed ID: 11589008
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease.
    Segal-Salto M; Hansson K; Sapir T; Kaplan A; Levy T; Schweizer M; Frotscher M; James P; Reiner O
    Hum Mol Genet; 2017 May; 26(9):1678. PubMed ID: 28334871
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL.
    Zhang Z; Lee YC; Kim SJ; Choi MS; Tsai PC; Xu Y; Xiao YJ; Zhang P; Heffer A; Mukherjee AB
    Hum Mol Genet; 2006 Jan; 15(2):337-46. PubMed ID: 16368712
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.
    Kim SJ; Zhang Z; Lee YC; Mukherjee AB
    Hum Mol Genet; 2006 May; 15(10):1580-6. PubMed ID: 16571600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stop codon read-through with PTC124 induces palmitoyl-protein thioesterase-1 activity, reduces thioester load and suppresses apoptosis in cultured cells from INCL patients.
    Sarkar C; Zhang Z; Mukherjee AB
    Mol Genet Metab; 2011 Nov; 104(3):338-45. PubMed ID: 21704547
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Intrathecal enzyme replacement therapy improves motor function and survival in a preclinical mouse model of infantile neuronal ceroid lipofuscinosis.
    Lu JY; Nelvagal HR; Wang L; Birnbaum SG; Cooper JD; Hofmann SL
    Mol Genet Metab; 2015; 116(1-2):98-105. PubMed ID: 25982063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Computational and structural investigation of Palmitoyl-Protein Thioesterase 1 (PPT1) protein causing Neuronal Ceroid Lipofuscinoses (NCL).
    Thirumal Kumar D; Shaikh N; Udhaya Kumar S; George Priya Doss C
    Adv Protein Chem Struct Biol; 2022; 132():89-109. PubMed ID: 36088080
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disorders.
    Chandra G; Bagh MB; Peng S; Saha A; Sarkar C; Moralle M; Zhang Z; Mukherjee AB
    Hum Mol Genet; 2015 Oct; 24(19):5416-32. PubMed ID: 26160911
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.