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 *

128 related articles for article (PubMed ID: 34138518)

  • 1. Human myelin protein P2: from crystallography to time-lapse membrane imaging and neuropathy-associated variants.
    Uusitalo M; Klenow MB; Laulumaa S; Blakeley MP; Simonsen AC; Ruskamo S; Kursula P
    FEBS J; 2021 Dec; 288(23):6716-6735. PubMed ID: 34138518
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2.
    Ruskamo S; Nieminen T; Kristiansen CK; Vatne GH; Baumann A; Hallin EI; Raasakka A; Joensuu P; Bergmann U; Vattulainen I; Kursula P
    Sci Rep; 2017 Jul; 7(1):6510. PubMed ID: 28747762
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Structure and dynamics of a human myelin protein P2 portal region mutant indicate opening of the β barrel in fatty acid binding proteins.
    Laulumaa S; Nieminen T; Raasakka A; Krokengen OC; Safaryan A; Hallin EI; Brysbaert G; Lensink MF; Ruskamo S; Vattulainen I; Kursula P
    BMC Struct Biol; 2018 Jun; 18(1):8. PubMed ID: 29940944
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cryo-EM, X-ray diffraction, and atomistic simulations reveal determinants for the formation of a supramolecular myelin-like proteolipid lattice.
    Ruskamo S; Krokengen OC; Kowal J; Nieminen T; Lehtimäki M; Raasakka A; Dandey VP; Vattulainen I; Stahlberg H; Kursula P
    J Biol Chem; 2020 Jun; 295(26):8692-8705. PubMed ID: 32265298
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dynamics of the Peripheral Membrane Protein P2 from Human Myelin Measured by Neutron Scattering--A Comparison between Wild-Type Protein and a Hinge Mutant.
    Laulumaa S; Nieminen T; Lehtimäki M; Aggarwal S; Simons M; Koza MM; Vattulainen I; Kursula P; Natali F
    PLoS One; 2015; 10(6):e0128954. PubMed ID: 26068118
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PMP2/FABP8 induces PI(4,5)P
    Abe M; Makino A; Murate M; Hullin-Matsuda F; Yanagawa M; Sako Y; Kobayashi T
    Cell Rep; 2021 Nov; 37(6):109935. PubMed ID: 34758297
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
    Motley WW; Palaima P; Yum SW; Gonzalez MA; Tao F; Wanschitz JV; Strickland AV; Löscher WN; De Vriendt E; Koppi S; Medne L; Janecke AR; Jordanova A; Zuchner S; Scherer SS
    Brain; 2016 Jun; 139(Pt 6):1649-56. PubMed ID: 27009151
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis.
    Punetha J; Mackay-Loder L; Harel T; Coban-Akdemir Z; Jhangiani SN; Gibbs RA; Lee I; Terespolsky D; Lupski JR; Posey JE
    Mol Genet Metab; 2018 Nov; 125(3):302-304. PubMed ID: 30249361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
    Hong YB; Joo J; Hyun YS; Kwak G; Choi YR; Yeo HK; Jwa DH; Kim EJ; Mo WM; Nam SH; Kim SM; Yoo JH; Koo H; Park HT; Chung KW; Choi BO
    PLoS Genet; 2016 Feb; 12(2):e1005829. PubMed ID: 26828946
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Production, crystallization and neutron diffraction of fully deuterated human myelin peripheral membrane protein P2.
    Laulumaa S; Blakeley MP; Raasakka A; Moulin M; Härtlein M; Kursula P
    Acta Crystallogr F Struct Biol Commun; 2015 Nov; 71(Pt 11):1391-5. PubMed ID: 26527266
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early onset demyelinating Charcot-Marie-Tooth disease caused by a novel in-frame isoleucine deletion in peripheral myelin protein 2.
    Geroldi A; Prada V; Veneri F; Trevisan L; Origone P; Grandis M; Schenone A; Gemelli C; Lanteri P; Fossa P; Mandich P; Bellone E
    J Peripher Nerv Syst; 2020 Jun; 25(2):102-106. PubMed ID: 32277537
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Peripheral myelin protein 2 - a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy.
    Palaima P; Chamova T; Jander S; Mitev V; Van Broeckhoven C; Tournev I; Peeters K; Jordanova A
    Orphanet J Rare Dis; 2019 Aug; 14(1):197. PubMed ID: 31412900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Quasielastic Neutron Scattering Investigation on the Molecular Self-Dynamics of Human Myelin Protein P2.
    Laulumaa S; Koza MM; Seydel T; Kursula P; Natali F
    J Phys Chem B; 2019 Oct; 123(39):8178-8185. PubMed ID: 31483648
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for
    Zhao X; Jiang MM; Yan YZ; Liu L; Xie YZ; Li XB; Hu ZM; Zi XH; Xia K; Tang BS; Zhang RX
    Chin Med J (Engl); 2018 Jan; 131(2):151-155. PubMed ID: 29336362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Atomic resolution view into the structure-function relationships of the human myelin peripheral membrane protein P2.
    Ruskamo S; Yadav RP; Sharma S; Lehtimäki M; Laulumaa S; Aggarwal S; Simons M; Bürck J; Ulrich AS; Juffer AH; Kursula I; Kursula P
    Acta Crystallogr D Biol Crystallogr; 2014 Jan; 70(Pt 1):165-76. PubMed ID: 24419389
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural and functional characterization of human peripheral nervous system myelin protein P2.
    Majava V; Polverini E; Mazzini A; Nanekar R; Knoll W; Peters J; Natali F; Baumgärtel P; Kursula I; Kursula P
    PLoS One; 2010 Apr; 5(4):e10300. PubMed ID: 20421974
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effects of Lid Domain Structural Changes on the Interactions between Peripheral Myelin Protein 2 and a Lipid Bilayer.
    Chen J; Tieleman DP; Liang Q
    J Phys Chem Lett; 2022 Feb; 13(4):991-996. PubMed ID: 35060724
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unraveling the etiology of myelin disorders: the P2 case in Charcot-Marie-Tooth disease.
    Pusterla J; Montich GG; Oliveira RG
    FEBS J; 2021 Dec; 288(23):6677-6679. PubMed ID: 34327848
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Production and crystallization of a panel of structure-based mutants of the human myelin peripheral membrane protein P2.
    Lehtimäki M; Laulumaa S; Ruskamo S; Kursula P
    Acta Crystallogr Sect F Struct Biol Cryst Commun; 2012 Nov; 68(Pt 11):1359-62. PubMed ID: 23143249
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.