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 *

166 related articles for article (PubMed ID: 19181091)

  • 1. Nebulin--a giant chameleon.
    Pelin K; Wallgren-Pettersson C
    Adv Exp Med Biol; 2008; 642():28-39. PubMed ID: 19181091
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy.
    Lehtokari VL; Pelin K; Herczegfalvi A; Karcagi V; Pouget J; Franques J; Pellissier JF; Figarella-Branger D; von der Hagen M; Huebner A; Schoser B; Lochmüller H; Wallgren-Pettersson C
    Neuromuscul Disord; 2011 Aug; 21(8):556-62. PubMed ID: 21724397
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.
    Pelin K; Hilpelä P; Donner K; Sewry C; Akkari PA; Wilton SD; Wattanasirichaigoon D; Bang ML; Centner T; Hanefeld F; Odent S; Fardeau M; Urtizberea JA; Muntoni F; Dubowitz V; Beggs AH; Laing NG; Labeit S; de la Chapelle A; Wallgren-Pettersson C
    Proc Natl Acad Sci U S A; 1999 Mar; 96(5):2305-10. PubMed ID: 10051637
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Nebulin expression in patients with nemaline myopathy.
    Gurgel-Giannetti J; Reed U; Bang ML; Pelin K; Donner K; Marie SK; Carvalho M; Fireman MA; Zanoteli E; Oliveira AS; Zatz M; Wallgren-Pettersson C; Labeit S; Vainzof M
    Neuromuscul Disord; 2001 Mar; 11(2):154-62. PubMed ID: 11257471
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy.
    Ottenheijm CA; Buck D; de Winter JM; Ferrara C; Piroddi N; Tesi C; Jasper JR; Malik FI; Meng H; Stienen GJ; Beggs AH; Labeit S; Poggesi C; Lawlor MW; Granzier H
    Brain; 2013 Jun; 136(Pt 6):1718-31. PubMed ID: 23715096
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormalities in the expression of nebulin in chromosome-2 linked nemaline myopathy.
    Sewry CA; Brown SC; Pelin K; Jungbluth H; Wallgren-Pettersson C; Labeit S; Manzur A; Muntoni F
    Neuromuscul Disord; 2001 Mar; 11(2):146-53. PubMed ID: 11257470
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nemaline myopathy type 2 (NEM2): two novel mutations in the nebulin (NEB) gene.
    Gajda A; Horváth E; Hortobágyi T; Gergev G; Szabó H; Farkas K; Nagy N; Széll M; Sztriha L
    J Child Neurol; 2015 Apr; 30(5):627-30. PubMed ID: 24056153
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutations.
    de Winter JM; Buck D; Hidalgo C; Jasper JR; Malik FI; Clarke NF; Stienen GJ; Lawlor MW; Beggs AH; Ottenheijm CA; Granzier H
    J Med Genet; 2013 Jun; 50(6):383-92. PubMed ID: 23572184
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy.
    Sztal TE; McKaige EA; Williams C; Oorschot V; Ramm G; Bryson-Richardson RJ
    Acta Neuropathol Commun; 2018 May; 6(1):40. PubMed ID: 29848386
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nebulin regulates thin filament length, contractility, and Z-disk structure in vivo.
    Witt CC; Burkart C; Labeit D; McNabb M; Wu Y; Granzier H; Labeit S
    EMBO J; 2006 Aug; 25(16):3843-55. PubMed ID: 16902413
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy.
    Li F; Buck D; De Winter J; Kolb J; Meng H; Birch C; Slater R; Escobar YN; Smith JE; Yang L; Konhilas J; Lawlor MW; Ottenheijm C; Granzier HL
    Hum Mol Genet; 2015 Sep; 24(18):5219-33. PubMed ID: 26123491
    [TBL] [Abstract][Full Text] [Related]  

  • 12. NEB-related core-rod myopathy with distinct clinical and pathological features.
    Park YE; Shin JH; Kang B; Lee CH; Kim DS
    Muscle Nerve; 2016 Mar; 53(3):479-84. PubMed ID: 26562614
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The nebulin SH3 domain is dispensable for normal skeletal muscle structure but is required for effective active load bearing in mouse.
    Yamamoto DL; Vitiello C; Zhang J; Gokhin DS; Castaldi A; Coulis G; Piaser F; Filomena MC; Eggenhuizen PJ; Kunderfranco P; Camerini S; Takano K; Endo T; Crescenzi M; Luther PK; Lieber RL; Chen J; Bang ML
    J Cell Sci; 2013 Dec; 126(Pt 23):5477-89. PubMed ID: 24046450
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism.
    Lindqvist J; Ma W; Li F; Hernandez Y; Kolb J; Kiss B; Tonino P; van der Pijl R; Karimi E; Gong H; Strom J; Hourani Z; Smith JE; Ottenheijm C; Irving T; Granzier H
    Nat Commun; 2020 Jun; 11(1):2699. PubMed ID: 32483185
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expressing a Z-disk nebulin fragment in nebulin-deficient mouse muscle: effects on muscle structure and function.
    Li F; Kolb J; Crudele J; Tonino P; Hourani Z; Smith JE; Chamberlain JS; Granzier H
    Skelet Muscle; 2020 Jan; 10(1):2. PubMed ID: 31992366
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the nebulin gene can cause severe congenital nemaline myopathy.
    Wallgren-Pettersson C; Donner K; Sewry C; Bijlsma E; Lammens M; Bushby K; Giovannucci Uzielli ML; Lapi E; Odent S; Akcoren Z; Topaloğlu H; Pelin K
    Neuromuscul Disord; 2002 Oct; 12(7-8):674-9. PubMed ID: 12207937
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neb: a zebrafish model of nemaline myopathy due to nebulin mutation.
    Telfer WR; Nelson DD; Waugh T; Brooks SV; Dowling JJ
    Dis Model Mech; 2012 May; 5(3):389-96. PubMed ID: 22159874
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene.
    Kiiski KJ; Lehtokari VL; Vihola AK; Laitila JM; Huovinen S; Sagath LJ; Evilä AE; Paetau AE; Sewry CA; Hackman PB; Pelin KB; Wallgren-Pettersson C; Udd B
    Neuromuscul Disord; 2019 Feb; 29(2):97-107. PubMed ID: 30679003
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A childhood-onset nemaline myopathy caused by novel heterozygote variants in the nebulin gene with literature review.
    Wen Q; Chang X; Guo J
    Acta Neurol Belg; 2020 Dec; 120(6):1351-1360. PubMed ID: 31696431
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nemaline myopathies: a current view.
    Sewry CA; Laitila JM; Wallgren-Pettersson C
    J Muscle Res Cell Motil; 2019 Jun; 40(2):111-126. PubMed ID: 31228046
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.