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.
295 related articles for article (PubMed ID: 22186027)
1. LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle. Dialynas G; Flannery KM; Zirbel LN; Nagy PL; Mathews KD; Moore SA; Wallrath LL Hum Mol Genet; 2012 Apr; 21(7):1544-56. PubMed ID: 22186027 [TBL] [Abstract][Full Text] [Related]
2. In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies. Hinz BE; Walker SG; Xiong A; Gogal RA; Schnieders MJ; Wallrath LL Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681887 [TBL] [Abstract][Full Text] [Related]
3. Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway. Dialynas G; Shrestha OK; Ponce JM; Zwerger M; Thiemann DA; Young GH; Moore SA; Yu L; Lammerding J; Wallrath LL PLoS Genet; 2015 May; 11(5):e1005231. PubMed ID: 25996830 [TBL] [Abstract][Full Text] [Related]
4. Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases. Walker SG; Langland CJ; Viles J; Hecker LA; Wallrath LL Cells; 2023 Apr; 12(8):. PubMed ID: 37190051 [TBL] [Abstract][Full Text] [Related]
5. Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signaling. Chandran S; Suggs JA; Wang BJ; Han A; Bhide S; Cryderman DE; Moore SA; Bernstein SI; Wallrath LL; Melkani GC Hum Mol Genet; 2019 Feb; 28(3):351-371. PubMed ID: 30239736 [TBL] [Abstract][Full Text] [Related]
6. Laminopathies: what can humans learn from fruit flies. Pałka M; Tomczak A; Grabowska K; Machowska M; Piekarowicz K; Rzepecka D; Rzepecki R Cell Mol Biol Lett; 2018; 23():32. PubMed ID: 30002683 [TBL] [Abstract][Full Text] [Related]
7. A comparative study of Drosophila and human A-type lamins. Schulze SR; Curio-Penny B; Speese S; Dialynas G; Cryderman DE; McDonough CW; Nalbant D; Petersen M; Budnik V; Geyer PK; Wallrath LL PLoS One; 2009 Oct; 4(10):e7564. PubMed ID: 19855837 [TBL] [Abstract][Full Text] [Related]
8. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration. Bakay M; Wang Z; Melcon G; Schiltz L; Xuan J; Zhao P; Sartorelli V; Seo J; Pegoraro E; Angelini C; Shneiderman B; Escolar D; Chen YW; Winokur ST; Pachman LM; Fan C; Mandler R; Nevo Y; Gordon E; Zhu Y; Dong Y; Wang Y; Hoffman EP Brain; 2006 Apr; 129(Pt 4):996-1013. PubMed ID: 16478798 [TBL] [Abstract][Full Text] [Related]
9. Lamin A/C Assembly Defects in Bertrand AT; Brull A; Azibani F; Benarroch L; Chikhaoui K; Stewart CL; Medalia O; Ben Yaou R; Bonne G Cells; 2020 Mar; 9(4):. PubMed ID: 32244403 [No Abstract] [Full Text] [Related]
11. Characterization of lamin mutation phenotypes in Drosophila and comparison to human laminopathies. Muñoz-Alarcón A; Pavlovic M; Wismar J; Schmitt B; Eriksson M; Kylsten P; Dushay MS PLoS One; 2007 Jun; 2(6):e532. PubMed ID: 17565385 [TBL] [Abstract][Full Text] [Related]
12. Loss of Drosophila A-type lamin C initially causes tendon abnormality including disintegration of cytoskeleton and nuclear lamina in muscular defects. Uchino R; Nonaka YK; Horigome T; Sugiyama S; Furukawa K Dev Biol; 2013 Jan; 373(1):216-27. PubMed ID: 22982669 [TBL] [Abstract][Full Text] [Related]
13. The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in mice. Pilat U; Dechat T; Bertrand AT; Woisetschläger N; Gotic I; Spilka R; Biadasiewicz K; Bonne G; Foisner R J Cell Sci; 2013 Apr; 126(Pt 8):1753-62. PubMed ID: 23444379 [TBL] [Abstract][Full Text] [Related]
14. Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy. Brown CA; Lanning RW; McKinney KQ; Salvino AR; Cherniske E; Crowe CA; Darras BT; Gominak S; Greenberg CR; Grosmann C; Heydemann P; Mendell JR; Pober BR; Sasaki T; Shapiro F; Simpson DA; Suchowersky O; Spence JE Am J Med Genet; 2001 Sep; 102(4):359-67. PubMed ID: 11503164 [TBL] [Abstract][Full Text] [Related]
15. Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling. Zwerger M; Jaalouk DE; Lombardi ML; Isermann P; Mauermann M; Dialynas G; Herrmann H; Wallrath LL; Lammerding J Hum Mol Genet; 2013 Jun; 22(12):2335-49. PubMed ID: 23427149 [TBL] [Abstract][Full Text] [Related]
16. A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus. Barateau A; Vadrot N; Vicart P; Ferreiro A; Mayer M; Héron D; Vigouroux C; Buendia B PLoS One; 2017; 12(1):e0169189. PubMed ID: 28125586 [TBL] [Abstract][Full Text] [Related]
17. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation. Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843 [TBL] [Abstract][Full Text] [Related]
18. Laminopathies; Mutations on single gene and various human genetic diseases. Kang SM; Yoon MH; Park BJ BMB Rep; 2018 Jul; 51(7):327-337. PubMed ID: 29764566 [TBL] [Abstract][Full Text] [Related]
19. Molecular genetic analysis of the nested Drosophila melanogaster lamin C gene. Schulze SR; Curio-Penny B; Li Y; Imani RA; Rydberg L; Geyer PK; Wallrath LL Genetics; 2005 Sep; 171(1):185-96. PubMed ID: 15965247 [TBL] [Abstract][Full Text] [Related]
20. The role of Drosophila Lamin C in muscle function and gene expression. Dialynas G; Speese S; Budnik V; Geyer PK; Wallrath LL Development; 2010 Sep; 137(18):3067-77. PubMed ID: 20702563 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]