BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 12127149)

  • 1. Aggresome formation in neuropathy models based on peripheral myelin protein 22 mutations.
    Ryan MC; Shooter EM; Notterpek L
    Neurobiol Dis; 2002 Jul; 10(2):109-18. PubMed ID: 12127149
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Emerging role for autophagy in the removal of aggresomes in Schwann cells.
    Fortun J; Dunn WA; Joy S; Li J; Notterpek L
    J Neurosci; 2003 Nov; 23(33):10672-80. PubMed ID: 14627652
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model.
    Fortun J; Li J; Go J; Fenstermaker A; Fletcher BS; Notterpek L
    J Neurochem; 2005 Mar; 92(6):1531-41. PubMed ID: 15748170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alterations in degradative pathways and protein aggregation in a neuropathy model based on PMP22 overexpression.
    Fortun J; Go JC; Li J; Amici SA; Dunn WA; Notterpek L
    Neurobiol Dis; 2006 Apr; 22(1):153-64. PubMed ID: 16326107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inducible HSP70 is critical in preventing the aggregation and enhancing the processing of PMP22.
    Chittoor-Vinod VG; Lee S; Judge SM; Notterpek L
    ASN Neuro; 2015; 7(1):. PubMed ID: 25694550
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction.
    Tobler AR; Notterpek L; Naef R; Taylor V; Suter U; Shooter EM
    J Neurosci; 1999 Mar; 19(6):2027-36. PubMed ID: 10066256
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular alterations resulting from frameshift mutations in peripheral myelin protein 22: implications for neuropathy severity.
    Johnson JS; Roux KJ; Fletcher BS; Fortun J; Notterpek L
    J Neurosci Res; 2005 Dec; 82(6):743-52. PubMed ID: 16273544
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biochemical characterization of protein quality control mechanisms during disease progression in the C22 mouse model of CMT1A.
    Chittoor VG; Sooyeon L; Rangaraju S; Nicks JR; Schmidt JT; Madorsky I; Narvaez DC; Notterpek L
    ASN Neuro; 2013 Dec; 5(5):e00128. PubMed ID: 24175617
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones.
    Fortun J; Verrier JD; Go JC; Madorsky I; Dunn WA; Notterpek L
    Neurobiol Dis; 2007 Feb; 25(2):252-65. PubMed ID: 17174099
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Colocalization Analysis of Peripheral Myelin Protein-22 and Lamin-B1 in the Schwann Cell Nuclei of Wt and TrJ Mice.
    Di Tomaso MV; Vázquez Alberdi L; Olsson D; Cancela S; Fernández A; Rosillo JC; Reyes Ábalos AL; Álvarez Zabaleta M; Calero M; Kun A
    Biomolecules; 2022 Mar; 12(3):. PubMed ID: 35327648
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases.
    Shames I; Fraser A; Colby J; Orfali W; Snipes GJ
    J Neuropathol Exp Neurol; 2003 Jul; 62(7):751-64. PubMed ID: 12901701
    [TBL] [Abstract][Full Text] [Related]  

  • 12. UCH-L1 aggresome formation in response to proteasome impairment indicates a role in inclusion formation in Parkinson's disease.
    Ardley HC; Scott GB; Rose SA; Tan NG; Robinson PA
    J Neurochem; 2004 Jul; 90(2):379-91. PubMed ID: 15228595
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells.
    Colby J; Nicholson R; Dickson KM; Orfali W; Naef R; Suter U; Snipes GJ
    Neurobiol Dis; 2000 Dec; 7(6 Pt B):561-73. PubMed ID: 11114256
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.
    D'Urso D; Prior R; Greiner-Petter R; Gabreëls-Festen AA; Müller HW
    J Neurosci; 1998 Jan; 18(2):731-40. PubMed ID: 9425015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of early postnatal peripheral nerve abnormalities in Trembler-J and PMP22 transgenic mice.
    Robertson AM; Huxley C; King RH; Thomas PK
    J Anat; 1999 Oct; 195 ( Pt 3)(Pt 3):331-9. PubMed ID: 10580849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Peripheral myelin protein 22 modulates store-operated calcium channel activity, providing insights into Charcot-Marie-Tooth disease etiology.
    Vanoye CG; Sakakura M; Follis RM; Trevisan AJ; Narayan M; Li J; Sanders CR; Carter BD
    J Biol Chem; 2019 Aug; 294(32):12054-12065. PubMed ID: 31213528
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The alpha-chemokine CXCL14 is up-regulated in the sciatic nerve of a mouse model of Charcot-Marie-Tooth disease type 1A and alters myelin gene expression in cultured Schwann cells.
    Barbaria EM; Kohl B; Buhren BA; Hasenpusch-Theil K; Kruse F; Küry P; Martini R; Müller HW
    Neurobiol Dis; 2009 Mar; 33(3):448-58. PubMed ID: 19111616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A.
    Sancho S; Young P; Suter U
    Brain; 2001 Nov; 124(Pt 11):2177-87. PubMed ID: 11673320
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy.
    Notterpek L; Shooter EM; Snipes GJ
    J Neurosci; 1997 Jun; 17(11):4190-200. PubMed ID: 9151736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation.
    Waelter S; Boeddrich A; Lurz R; Scherzinger E; Lueder G; Lehrach H; Wanker EE
    Mol Biol Cell; 2001 May; 12(5):1393-407. PubMed ID: 11359930
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.