211 related articles for article (PubMed ID: 22496423)
1. Expression of the inclusion body myopathy 3 mutation in Drosophila depresses myosin function and stability and recapitulates muscle inclusions and weakness.
Wang Y; Melkani GC; Suggs JA; Melkani A; Kronert WA; Cammarato A; Bernstein SI
Mol Biol Cell; 2012 Jun; 23(11):2057-65. PubMed ID: 22496423
[TBL] [Abstract][Full Text] [Related]
2. A
Suggs JA; Melkani GC; Glasheen BM; Detor MM; Melkani A; Marsan NP; Swank DM; Bernstein SI
Dis Model Mech; 2017 Jun; 10(6):761-771. PubMed ID: 28258125
[TBL] [Abstract][Full Text] [Related]
3. Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age.
Tajsharghi H; Thornell LE; Darin N; Martinsson T; Kyllerman M; Wahlström J; Oldfors A
Neurology; 2002 Mar; 58(5):780-6. PubMed ID: 11889243
[TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.
Darin N; Kyllerman M; Wahlström J; Martinsson T; Oldfors A
Ann Neurol; 1998 Aug; 44(2):242-8. PubMed ID: 9708547
[TBL] [Abstract][Full Text] [Related]
5. Hereditary inclusion-body myopathies.
Broccolini A; Mirabella M
Biochim Biophys Acta; 2015 Apr; 1852(4):644-50. PubMed ID: 25149037
[TBL] [Abstract][Full Text] [Related]
6. Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy.
Li S; Zhang P; Freibaum BD; Kim NC; Kolaitis RM; Molliex A; Kanagaraj AP; Yabe I; Tanino M; Tanaka S; Sasaki H; Ross ED; Taylor JP; Kim HJ
Hum Mol Genet; 2016 Mar; 25(5):936-50. PubMed ID: 26744327
[TBL] [Abstract][Full Text] [Related]
7. Drosophila myosin mutants model the disparate severity of type 1 and type 2B distal arthrogryposis and indicate an enhanced actin affinity mechanism.
Guo Y; Kronert WA; Hsu KH; Huang A; Sarsoza F; Bell KM; Suggs JA; Swank DM; Bernstein SI
Skelet Muscle; 2020 Aug; 10(1):24. PubMed ID: 32799913
[TBL] [Abstract][Full Text] [Related]
8. Myosin storage myopathy mutations yield defective myosin filament assembly in vitro and disrupted myofibrillar structure and function in vivo.
Viswanathan MC; Tham RC; Kronert WA; Sarsoza F; Trujillo AS; Cammarato A; Bernstein SI
Hum Mol Genet; 2017 Dec; 26(24):4799-4813. PubMed ID: 28973424
[TBL] [Abstract][Full Text] [Related]
9. A Failure to Communicate: MYOSIN RESIDUES INVOLVED IN HYPERTROPHIC CARDIOMYOPATHY AFFECT INTER-DOMAIN INTERACTION.
Kronert WA; Melkani GC; Melkani A; Bernstein SI
J Biol Chem; 2015 Dec; 290(49):29270-80. PubMed ID: 26446785
[TBL] [Abstract][Full Text] [Related]
10. Mutating the converter-relay interface of Drosophila myosin perturbs ATPase activity, actin motility, myofibril stability and flight ability.
Kronert WA; Melkani GC; Melkani A; Bernstein SI
J Mol Biol; 2010 May; 398(5):625-32. PubMed ID: 20362584
[TBL] [Abstract][Full Text] [Related]
11. Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy.
Findlay AR; Harms MB; Pestronk A; Weihl CC
Neuromuscul Disord; 2018 Aug; 28(8):675-679. PubMed ID: 29934118
[TBL] [Abstract][Full Text] [Related]
12.
Dahl-Halvarsson M; Olive M; Pokrzywa M; Ejeskär K; Palmer RH; Uv AE; Tajsharghi H
Proc Natl Acad Sci U S A; 2018 Jul; 115(28):E6566-E6575. PubMed ID: 29946036
[TBL] [Abstract][Full Text] [Related]
13. A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in Drosophila.
Achal M; Trujillo AS; Melkani GC; Farman GP; Ocorr K; Viswanathan MC; Kaushik G; Newhard CS; Glasheen BM; Melkani A; Suggs JA; Moore JR; Swank DM; Bodmer R; Cammarato A; Bernstein SI
J Mol Biol; 2016 Jun; 428(11):2446-2461. PubMed ID: 27107639
[TBL] [Abstract][Full Text] [Related]
14. Myosin heavy chain mutations that cause Freeman-Sheldon syndrome lead to muscle structural and functional defects in Drosophila.
Das S; Kumar P; Verma A; Maiti TK; Mathew SJ
Dev Biol; 2019 May; 449(2):90-98. PubMed ID: 30826400
[TBL] [Abstract][Full Text] [Related]
15. Myosin dilated cardiomyopathy mutation S532P disrupts actomyosin interactions, leading to altered muscle kinetics, reduced locomotion, and cardiac dilation in
Trujillo AS; Hsu KH; Puthawala J; Viswanathan MC; Loya A; Irving TC; Cammarato A; Swank DM; Bernstein SI
Mol Biol Cell; 2021 Aug; 32(18):1690-1706. PubMed ID: 34081531
[TBL] [Abstract][Full Text] [Related]
16. Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotype.
Madigan NN; Polzin MJ; Cui G; Liewluck T; Alsharabati MH; Klein CJ; Windebank AJ; Mer G; Milone M
Acta Neuropathol Commun; 2021 Apr; 9(1):79. PubMed ID: 33926564
[TBL] [Abstract][Full Text] [Related]
17. A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness.
Willis T; Hedberg-Oldfors C; Alhaswani Z; Kulshrestha R; Sewry C; Oldfors A
J Neurol; 2016 Jul; 263(7):1427-33. PubMed ID: 27177998
[TBL] [Abstract][Full Text] [Related]
18. The molecular mechanisms of a high Ca
Avrova SV; Karpicheva OE; Simonyan AO; Sirenko VV; Redwood CS; Borovikov YS
Biochem Biophys Res Commun; 2019 Jul; 515(2):372-377. PubMed ID: 31155291
[TBL] [Abstract][Full Text] [Related]
19. A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies.
D'Amico A; Fattori F; Bellacchio E; Catteruccia M; Servidei S; Bertini E
Neuromuscul Disord; 2013 May; 23(5):437-40. PubMed ID: 23489661
[TBL] [Abstract][Full Text] [Related]
20. An alternative domain near the nucleotide-binding site of Drosophila muscle myosin affects ATPase kinetics.
Miller BM; Zhang S; Suggs JA; Swank DM; Littlefield KP; Knowles AF; Bernstein SI
J Mol Biol; 2005 Oct; 353(1):14-25. PubMed ID: 16154586
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
