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5. 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]
6. 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]
7. 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]
8. 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]
9. Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function. Sztal TE; Zhao M; Williams C; Oorschot V; Parslow AC; Giousoh A; Yuen M; Hall TE; Costin A; Ramm G; Bird PI; Busch-Nentwich EM; Stemple DL; Currie PD; Cooper ST; Laing NG; Nowak KJ; Bryson-Richardson RJ Acta Neuropathol; 2015 Sep; 130(3):389-406. PubMed ID: 25931053 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb. Laitila JM; McNamara EL; Wingate CD; Goullee H; Ross JA; Taylor RL; van der Pijl R; Griffiths LM; Harries R; Ravenscroft G; Clayton JS; Sewry C; Lawlor MW; Ottenheijm CAC; Bakker AJ; Ochala J; Laing NG; Wallgren-Pettersson C; Pelin K; Nowak KJ Acta Neuropathol Commun; 2020 Feb; 8(1):18. PubMed ID: 32066503 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
20. 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] [Next] [New Search]