215 related articles for article (PubMed ID: 27107639)
1. 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]
2. 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]
3. 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]
4. Mutations in Drosophila myosin rod cause defects in myofibril assembly.
Salvi SS; Kumar RP; Ramachandra NB; Sparrow JC; Nongthomba U
J Mol Biol; 2012 May; 419(1-2):22-40. PubMed ID: 22370558
[TBL] [Abstract][Full Text] [Related]
5. Myosin transducer mutations differentially affect motor function, myofibril structure, and the performance of skeletal and cardiac muscles.
Cammarato A; Dambacher CM; Knowles AF; Kronert WA; Bodmer R; Ocorr K; Bernstein SI
Mol Biol Cell; 2008 Feb; 19(2):553-62. PubMed ID: 18045988
[TBL] [Abstract][Full Text] [Related]
6. Reductions in ATPase activity, actin sliding velocity, and myofibril stability yield muscle dysfunction in Drosophila models of myosin-based Freeman-Sheldon syndrome.
Rao DS; Kronert WA; Guo Y; Hsu KH; Sarsoza F; Bernstein SI
Mol Biol Cell; 2019 Jan; 30(1):30-41. PubMed ID: 30379605
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Hypertrophic cardiomyopathy R403Q mutation in rabbit β-myosin reduces contractile function at the molecular and myofibrillar levels.
Lowey S; Bretton V; Joel PB; Trybus KM; Gulick J; Robbins J; Kalganov A; Cornachione AS; Rassier DE
Proc Natl Acad Sci U S A; 2018 Oct; 115(44):11238-11243. PubMed ID: 30322937
[TBL] [Abstract][Full Text] [Related]
9. The R369 Myosin Residue within Loop 4 Is Critical for Actin Binding and Muscle Function in
Trujillo AS; Hsu KH; Viswanathan MC; Cammarato A; Bernstein SI
Int J Mol Sci; 2022 Feb; 23(5):. PubMed ID: 35269675
[TBL] [Abstract][Full Text] [Related]
10. Alternative S2 hinge regions of the myosin rod differentially affect muscle function, myofibril dimensions and myosin tail length.
Suggs JA; Cammarato A; Kronert WA; Nikkhoy M; Dambacher CM; Megighian A; Bernstein SI
J Mol Biol; 2007 Apr; 367(5):1312-29. PubMed ID: 17316684
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The R249Q hypertrophic cardiomyopathy myosin mutation decreases contractility in Drosophila by impeding force production.
Bell KM; Kronert WA; Huang A; Bernstein SI; Swank DM
J Physiol; 2019 May; 597(9):2403-2420. PubMed ID: 30950055
[TBL] [Abstract][Full Text] [Related]
13. Aging-affiliated post-translational modifications of skeletal muscle myosin affect biochemical properties, myofibril structure, muscle function, and proteostasis.
Neal CL; Kronert WA; Camillo JRT; Suggs JA; Huxford T; Bernstein SI
Aging Cell; 2024 Jun; 23(6):e14134. PubMed ID: 38506610
[TBL] [Abstract][Full Text] [Related]
14. Mapping interactions between myosin relay and converter domains that power muscle function.
Kronert WA; Melkani GC; Melkani A; Bernstein SI
J Biol Chem; 2014 May; 289(18):12779-90. PubMed ID: 24627474
[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. Assembly of thick filaments and myofibrils occurs in the absence of the myosin head.
Cripps RM; Suggs JA; Bernstein SI
EMBO J; 1999 Apr; 18(7):1793-804. PubMed ID: 10202143
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The UNC-45 chaperone is critical for establishing myosin-based myofibrillar organization and cardiac contractility in the Drosophila heart model.
Melkani GC; Bodmer R; Ocorr K; Bernstein SI
PLoS One; 2011; 6(7):e22579. PubMed ID: 21799905
[TBL] [Abstract][Full Text] [Related]
19. Molecular and ultrastructural defects in a Drosophila myosin heavy chain mutant: differential effects on muscle function produced by similar thick filament abnormalities.
O'Donnell PT; Bernstein SI
J Cell Biol; 1988 Dec; 107(6 Pt 2):2601-12. PubMed ID: 2462566
[TBL] [Abstract][Full Text] [Related]
20. Alternative relay domains of Drosophila melanogaster myosin differentially affect ATPase activity, in vitro motility, myofibril structure and muscle function.
Kronert WA; Dambacher CM; Knowles AF; Swank DM; Bernstein SI
J Mol Biol; 2008 Jun; 379(3):443-56. PubMed ID: 18462751
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
