208 related articles for article (PubMed ID: 30379605)
1. 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]
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. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Prolonged myosin binding increases muscle stiffness in Drosophila models of Freeman-Sheldon syndrome.
Bell KM; Huang A; Kronert WA; Bernstein SI; Swank DM
Biophys J; 2021 Mar; 120(5):844-854. PubMed ID: 33524372
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle.
Racca AW; Beck AE; McMillin MJ; Korte FS; Bamshad MJ; Regnier M
Hum Mol Genet; 2015 Jun; 24(12):3348-58. PubMed ID: 25740846
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. 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]
15. The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects.
Walklate J; Vera C; Bloemink MJ; Geeves MA; Leinwand L
J Biol Chem; 2016 May; 291(19):10318-31. PubMed ID: 26945064
[TBL] [Abstract][Full Text] [Related]
16. Alterations in flightin phosphorylation in Drosophila flight muscles are associated with myofibrillar defects engendered by actin and myosin heavy-chain mutant alleles.
Vigoreaux JO
Biochem Genet; 1994 Aug; 32(7-8):301-14. PubMed ID: 7826316
[TBL] [Abstract][Full Text] [Related]
17. Kinetic analysis of Drosophila muscle myosin isoforms suggests a novel mode of mechanochemical coupling.
Miller BM; Nyitrai M; Bernstein SI; Geeves MA
J Biol Chem; 2003 Dec; 278(50):50293-300. PubMed ID: 14506231
[TBL] [Abstract][Full Text] [Related]
18. Alternative relay and converter domains tune native muscle myosin isoform function in Drosophila.
Kronert WA; Melkani GC; Melkani A; Bernstein SI
J Mol Biol; 2012 Mar; 416(4):543-57. PubMed ID: 22226837
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genetic dissection of Drosophila myofibril formation: effects of actin and myosin heavy chain null alleles.
Beall CJ; Sepanski MA; Fyrberg EA
Genes Dev; 1989 Feb; 3(2):131-40. PubMed ID: 2714648
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
