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 *

134 related articles for article (PubMed ID: 38514365)

  • 1. Amphiphysin-2 (BIN1) functions and defects in cardiac and skeletal muscle.
    Giraud Q; Laporte J
    Trends Mol Med; 2024 Jun; 30(6):579-591. PubMed ID: 38514365
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies.
    Toussaint A; Cowling BS; Hnia K; Mohr M; Oldfors A; Schwab Y; Yis U; Maisonobe T; Stojkovic T; Wallgren-Pettersson C; Laugel V; Echaniz-Laguna A; Mandel JL; Nishino I; Laporte J
    Acta Neuropathol; 2011 Feb; 121(2):253-66. PubMed ID: 20927630
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutant BIN1-Dynamin 2 complexes dysregulate membrane remodeling in the pathogenesis of centronuclear myopathy.
    Fujise K; Okubo M; Abe T; Yamada H; Nishino I; Noguchi S; Takei K; Takeda T
    J Biol Chem; 2021; 296():100077. PubMed ID: 33187981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy.
    Böhm J; Vasli N; Maurer M; Cowling BS; Shelton GD; Kress W; Toussaint A; Prokic I; Schara U; Anderson TJ; Weis J; Tiret L; Laporte J
    PLoS Genet; 2013 Jun; 9(6):e1003430. PubMed ID: 23754947
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mice with muscle-specific deletion of Bin1 recapitulate centronuclear myopathy and acute downregulation of dynamin 2 improves their phenotypes.
    Silva-Rojas R; Nattarayan V; Jaque-Fernandez F; Gomez-Oca R; Menuet A; Reiss D; Goret M; Messaddeq N; Lionello VM; Kretz C; Cowling BS; Jacquemond V; Laporte J
    Mol Ther; 2022 Feb; 30(2):868-880. PubMed ID: 34371181
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cells Control BIN1-Mediated Membrane Tubulation by Altering the Membrane Charge.
    Gowrisankaran S; Wang Z; Morgan DG; Milosevic I; Mim C
    J Mol Biol; 2020 Feb; 432(4):1235-1250. PubMed ID: 31857086
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Centronuclear Myopathy Caused by Defective Membrane Remodelling of Dynamin 2 and BIN1 Variants.
    Fujise K; Noguchi S; Takeda T
    Int J Mol Sci; 2022 Jun; 23(11):. PubMed ID: 35682949
    [TBL] [Abstract][Full Text] [Related]  

  • 8. N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy.
    Falcone S; Roman W; Hnia K; Gache V; Didier N; Lainé J; Auradé F; Marty I; Nishino I; Charlet-Berguerand N; Romero NB; Marazzi G; Sassoon D; Laporte J; Gomes ER
    EMBO Mol Med; 2014 Nov; 6(11):1455-75. PubMed ID: 25262827
    [TBL] [Abstract][Full Text] [Related]  

  • 9. BIN1 regulates dynamic t-tubule membrane.
    Fu Y; Hong T
    Biochim Biophys Acta; 2016 Jul; 1863(7 Pt B):1839-47. PubMed ID: 26578114
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation.
    Cowling BS; Prokic I; Tasfaout H; Rabai A; Humbert F; Rinaldi B; Nicot AS; Kretz C; Friant S; Roux A; Laporte J
    J Clin Invest; 2017 Dec; 127(12):4477-4487. PubMed ID: 29130937
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Differential physiological roles for BIN1 isoforms in skeletal muscle development, function and regeneration.
    Prokic I; Cowling BS; Kutchukian C; Kretz C; Tasfaout H; Gache V; Hergueux J; Wendling O; Ferry A; Toussaint A; Gavriilidis C; Nattarayan V; Koch C; Lainé J; Combe R; Tiret L; Jacquemond V; Pilot-Storck F; Laporte J
    Dis Model Mech; 2020 Nov; 13(11):. PubMed ID: 32994313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MTM1 overexpression prevents and reverts BIN1-related centronuclear myopathy.
    Giraud Q; Spiegelhalter C; Messaddeq N; Laporte J
    Brain; 2023 Oct; 146(10):4158-4173. PubMed ID: 37490306
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2.
    Hohendahl A; Roux A; Galli V
    J Struct Biol; 2016 Oct; 196(1):37-47. PubMed ID: 27343996
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.
    Böhm J; Biancalana V; Malfatti E; Dondaine N; Koch C; Vasli N; Kress W; Strittmatter M; Taratuto AL; Gonorazky H; Laforêt P; Maisonobe T; Olivé M; Gonzalez-Mera L; Fardeau M; Carrière N; Clavelou P; Eymard B; Bitoun M; Rendu J; Fauré J; Weis J; Mandel JL; Romero NB; Laporte J
    Brain; 2014 Dec; 137(Pt 12):3160-70. PubMed ID: 25260562
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amphiphysin 2 modulation rescues myotubular myopathy and prevents focal adhesion defects in mice.
    Lionello VM; Nicot AS; Sartori M; Kretz C; Kessler P; Buono S; Djerroud S; Messaddeq N; Koebel P; Prokic I; Hérault Y; Romero NB; Laporte J; Cowling BS
    Sci Transl Med; 2019 Mar; 11(484):. PubMed ID: 30894500
    [TBL] [Abstract][Full Text] [Related]  

  • 16. BIN1 localizes the L-type calcium channel to cardiac T-tubules.
    Hong TT; Smyth JW; Gao D; Chu KY; Vogan JM; Fong TS; Jensen BC; Colecraft HM; Shaw RM
    PLoS Biol; 2010 Feb; 8(2):e1000312. PubMed ID: 20169111
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutations in amphiphysin 2 (BIN1) cause autosomal recessive centronuclear myopathy].
    Toussaint A; Nicot AS; Mandel JL; Laporte J
    Med Sci (Paris); 2007 Dec; 23(12):1080-2. PubMed ID: 18154705
    [No Abstract]   [Full Text] [Related]  

  • 18. Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation.
    Böhm J; Yiş U; Ortaç R; Cakmakçı H; Kurul SH; Dirik E; Laporte J
    Orphanet J Rare Dis; 2010 Dec; 5():35. PubMed ID: 21129173
    [TBL] [Abstract][Full Text] [Related]  

  • 19. BIN1 modulation in vivo rescues dynamin-related myopathy.
    Lionello VM; Kretz C; Edelweiss E; Crucifix C; Gómez-Oca R; Messaddeq N; Buono S; Koebel P; Massana Muñoz X; Diedhiou N; Cowling BS; Bitoun M; Laporte J
    Proc Natl Acad Sci U S A; 2022 Mar; 119(9):. PubMed ID: 35217605
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Uncovering the BIN1-SH3 interactome underpinning centronuclear myopathy.
    Zambo B; Edelweiss E; Morlet B; Negroni L; Pajkos M; Dosztanyi Z; Ostergaard S; Trave G; Laporte J; Gogl G
    Elife; 2024 Jul; 13():. PubMed ID: 38995680
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.