288 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]
10. Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Owens DJ; Messéant J; Moog S; Viggars M; Ferry A; Mamchaoui K; Lacène E; Roméro N; Brull A; Bonne G; Butler-Browne G; Coirault C
Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33396724
[TBL] [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]
