| Year |
Citation |
Score |
| 2023 |
Marston S, Pinto JR. Suppression of lusitropy as a disease mechanism in cardiomyopathies. Frontiers in Cardiovascular Medicine. 9: 1080965. PMID 36698941 DOI: 10.3389/fcvm.2022.1080965 |
0.327 |
|
| 2022 |
Pavadai E, Rynkiewicz MJ, Yang Z, Gould IR, Marston SB, Lehman W. Modulation of cardiac thin filament structure by phosphorylated troponin-I analyzed by protein-protein docking and molecular dynamics simulation. Archives of Biochemistry and Biophysics. 725: 109282. PMID 35577070 DOI: 10.1016/j.abb.2022.109282 |
0.319 |
|
| 2022 |
Marston S. Force Measurements From Myofibril to Filament. Frontiers in Physiology. 12: 817036. PMID 35153821 DOI: 10.3389/fphys.2021.817036 |
0.356 |
|
| 2021 |
Marston SB. Richard Tregear, Co-founder of the Journal of Muscle Research and Cell Motility. Journal of Muscle Research and Cell Motility. PMID 33709246 DOI: 10.1007/s10974-021-09600-2 |
0.342 |
|
| 2020 |
Alsulami K, Marston S. Small Molecules acting on Myofilaments as Treatments for Heart and Skeletal Muscle Diseases. International Journal of Molecular Sciences. 21. PMID 33339418 DOI: 10.3390/ijms21249599 |
0.342 |
|
| 2020 |
Copeland O, Messer A, Jabbour A, Poggesi C, Prasad S, Marston S. Pressure Overload Is Associated With Low Levels of Troponin I and Myosin Binding Protein C Phosphorylation in the Hearts of Patients With Aortic Stenosis. Frontiers in Physiology. 11: 241. PMID 32265736 DOI: 10.3389/Fphys.2020.00241 |
0.365 |
|
| 2019 |
Ehler E, Marston SB. The European Muscle Conference 2019 Special Issue. Journal of Muscle Research and Cell Motility. PMID 31267353 DOI: 10.1007/s10974-019-09533-x |
0.412 |
|
| 2019 |
Marston S. Small molecule studies: the fourth wave of muscle research. Journal of Muscle Research and Cell Motility. PMID 31228047 DOI: 10.1007/S10974-019-09526-W |
0.433 |
|
| 2019 |
Marston S, Zamora JE. Troponin structure and function: a view of recent progress. Journal of Muscle Research and Cell Motility. PMID 31030382 DOI: 10.1007/S10974-019-09513-1 |
0.382 |
|
| 2018 |
Piroddi N, Witjas-Paalberends ER, Ferrara C, Ferrantini C, Vitale G, Scellini B, Wijnker PJM, Sequiera V, Dooijes D, Dos Remedios C, Schlossarek S, Leung MC, Messer A, Ward DG, Biggeri A, ... ... Marston SB, et al. The homozygous K280N troponin T mutation alters cross-bridge kinetics and energetics in human HCM. The Journal of General Physiology. PMID 30578328 DOI: 10.1085/jgp.201812160 |
0.307 |
|
| 2018 |
Marston S. The Molecular Mechanisms of Mutations in Actin and Myosin that Cause Inherited Myopathy. International Journal of Molecular Sciences. 19. PMID 29997361 DOI: 10.3390/Ijms19072020 |
0.467 |
|
| 2017 |
Rynkiewicz MJ, Prum T, Hollenberg S, Kiani FA, Fagnant PM, Marston SB, Trybus KM, Fischer S, Moore JR, Lehman W. Tropomyosin Must Interact Weakly with Actin to Effectively Regulate Thin Filament Function. Biophysical Journal. 113: 2444-2451. PMID 29211998 DOI: 10.1016/J.Bpj.2017.10.004 |
0.351 |
|
| 2017 |
Marston S. Obscurin variants and inherited cardiomyopathies. Biophysical Reviews. PMID 28510120 DOI: 10.1007/S12551-017-0264-8 |
0.301 |
|
| 2016 |
Marston SB. Why Is there a Limit to the Changes in Myofilament Ca(2+)-Sensitivity Associated with Myopathy Causing Mutations? Frontiers in Physiology. 7: 415. PMID 27725803 DOI: 10.3389/fphys.2016.00415 |
0.388 |
|
| 2016 |
Chan C, Fan J, Messer AE, Marston SB, Iwamoto H, Ochala J. Myopathy-inducing mutation H40Y in ACTA1 hampers actin filament structure and function. Biochimica Et Biophysica Acta. PMID 27112274 DOI: 10.1016/j.bbadis.2016.04.013 |
0.371 |
|
| 2016 |
Marston S, Papadaki M, Memo M, Messer A, Donkervoort S, Bonneman C, Nowak K, Ong R, McNamara E. Molecular Mechanism of Novel Deletions in TPM3 that cause a Hypercontractile Phenotype with Congenital Muscle Stiffness Biophysical Journal. 110: 14a-15a. DOI: 10.1016/J.Bpj.2015.11.136 |
0.473 |
|
| 2015 |
Marston S, Messer A, Papadaki M. (De-)sensitization vs. uncoupling: what drives cardiomyopathies in the thin filament? Reply. Cardiovascular Research. PMID 26464332 DOI: 10.1093/Cvr/Cvv233 |
0.393 |
|
| 2015 |
Wilkinson R, Song W, Smoktunowicz N, Marston S. A DILATED CARDIOMYOPATHY MUTATION BLUNTS ADRENERGIC RESPONSE AND INDUCES CONTRACTILE DYSFUNCTION UNDER CHRONIC ANGIOTENSIN II STRESS. American Journal of Physiology. Heart and Circulatory Physiology. ajpheart.00327.2015. PMID 26432839 DOI: 10.1152/Ajpheart.00327.2015 |
0.31 |
|
| 2015 |
Donkervoort S, Papadaki M, de Winter JM, Neu MB, Kirschner J, Bolduc V, Yang ML, Gibbons MA, Hu Y, Dastgir J, Leach ME, Rutkowski A, Foley AR, Krüger M, Wartchow EP, ... ... Marston SB, et al. TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype. Annals of Neurology. PMID 26418456 DOI: 10.1002/ana.24535 |
0.406 |
|
| 2015 |
Marston S, Montgiraud C, Munster AB, Copeland O, Choi O, Dos Remedios C, Messer AE, Ehler E, Knöll R. OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency. Plos One. 10: e0138568. PMID 26406308 DOI: 10.1371/Journal.Pone.0138568 |
0.357 |
|
| 2015 |
Yuen M, Cooper ST, Marston SB, Nowak KJ, McNamara E, Mokbel N, Ilkovski B, Ravenscroft G, Rendu J, de Winter JM, Klinge L, Beggs AH, North KN, Ottenheijm CA, Clarke NF. Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres. Human Molecular Genetics. PMID 26307083 DOI: 10.1093/Hmg/Ddv334 |
0.402 |
|
| 2015 |
Marston S. Important announcement: a rational nomenclature for tropomyosin variants. Journal of Muscle Research and Cell Motility. 36: 145. PMID 25361644 DOI: 10.1007/S10974-014-9393-X |
0.324 |
|
| 2015 |
Papadaki M, Vikhorev P, Marston S, Messer A. Epigallocatechin-3-Gallate Reverses the Defects in Modulation of Ca2+-Sensitivity by Troponin I Phosphorylation Caused by Hypertrophic and Dilated Cardiomyopathy Mutations in Cardiac Muscle Biophysical Journal. 108: 361a-362a. DOI: 10.1016/J.Bpj.2014.11.1983 |
0.378 |
|
| 2015 |
Marston S, Knoll R, dos Remedios C, Munster A, Copeland O, Montgiraud C. Obscurin Mutations Cause Haploinsufficiency and are Common in Patients with Familial Dilated Cardiomyopathy (FDCM) Biophysical Journal. 108: 292a. DOI: 10.1016/J.Bpj.2014.11.1593 |
0.307 |
|
| 2014 |
Marttila M, Lehtokari VL, Marston S, Nyman TA, Barnerias C, Beggs AH, Bertini E, Ceyhan-Birsoy O, Cintas P, Gerard M, Gilbert-Dussardier B, Hogue JS, Longman C, Eymard B, Frydman M, et al. Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies. Human Mutation. 35: 779-90. PMID 24692096 DOI: 10.1002/Humu.22554 |
0.355 |
|
| 2013 |
Marston S, Gautel M. Introducing a special edition of the Journal of Muscle Research and Cell Motility on tropomyosin: Form and function Journal of Muscle Research and Cell Motility. 34: 151-153. PMID 24101402 DOI: 10.1007/S10974-013-9361-X |
0.444 |
|
| 2013 |
Marston S, Memo M, Messer A, Papadaki M, Nowak K, Mcnamara E, Ong R, El-Mezgueldi M, Li X, Lehman W. Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients Human Molecular Genetics. 22: 4978-4987. PMID 23886664 DOI: 10.1093/Hmg/Ddt345 |
0.356 |
|
| 2013 |
Memo M, Marston S. Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain- or loss-of-function Journal of Muscle Research and Cell Motility. 34: 165-169. PMID 23719967 DOI: 10.1007/S10974-013-9344-Y |
0.418 |
|
| 2013 |
Song W, Vikhorev PG, Kashyap MN, Rowlands C, Ferenczi MA, Woledge RC, MacLeod K, Marston S, Curtin NA. Mechanical and energetic properties of papillary muscle from ACTC E99K transgenic mouse models of hypertrophic cardiomyopathy American Journal of Physiology - Heart and Circulatory Physiology. 304: H1513-H1524. PMID 23604709 DOI: 10.1152/Ajpheart.00951.2012 |
0.531 |
|
| 2013 |
Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari VL, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, ... ... Marston S, et al. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Brain : a Journal of Neurology. 136: 494-507. PMID 23378224 DOI: 10.1093/Brain/Aws348 |
0.404 |
|
| 2013 |
Al-Khayat HA, Kensler RW, Squire JM, Marston SB, Morris EP. Atomic model of the human cardiac muscle myosin filament. Proceedings of the National Academy of Sciences of the United States of America. 110: 318-23. PMID 23251030 DOI: 10.1073/pnas.1212708110 |
0.329 |
|
| 2013 |
Morris E, Kensler R, Marston S, Squire J, AL-Khayat H. Structure of the Human Cardiac Muscle Myosin Filament Microscopy and Microanalysis. 19: 78-79. DOI: 10.1017/S1431927613002389 |
0.359 |
|
| 2013 |
Chen L, Caorsi V, Toepfer C, Song W, Marston SB, Ferenczi MA. Using FRET to Characterize the Actomyosin Complex in Cardiac Muscle Biophysical Journal. 104: 16a. DOI: 10.1016/j.bpj.2012.11.122 |
0.368 |
|
| 2012 |
Li XE, Suphamungmee W, Janco M, Geeves MA, Marston SB, Fischer S, Lehman W. The flexibility of two tropomyosin mutants, D175N and E180G, that cause hypertrophic cardiomyopathy Biochemical and Biophysical Research Communications. 424: 493-496. PMID 22789852 DOI: 10.1016/J.Bbrc.2012.06.141 |
0.447 |
|
| 2012 |
Jain RK, Jayawant S, Squier W, Muntoni F, Sewry CA, Manzur A, Quinlivan R, Lillis S, Jungbluth H, Sparrow JC, Ravenscroft G, Nowak KJ, Memo M, Marston SB, Laing NG. Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation. Neurology. 78: 1100-3. PMID 22442437 DOI: 10.1212/WNL.0b013e31824e8ebe |
0.383 |
|
| 2012 |
Vydyanath A, Gurnett CA, Marston S, Luther PK. Axial distribution of myosin binding protein-C is unaffected by mutations in human cardiac and skeletal muscle Journal of Muscle Research and Cell Motility. 33: 61-74. PMID 22415774 DOI: 10.1007/s10974-012-9286-9 |
0.333 |
|
| 2012 |
Marttila M, Lemola E, Wallefeld W, Memo M, Donner K, Laing NG, Marston S, Grönholm M, Wallgren-Pettersson C. Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy. The Biochemical Journal. 442: 231-9. PMID 22084935 DOI: 10.1042/Bj20111030 |
0.548 |
|
| 2012 |
Marston S, Copeland O, Gehmlich K, Schlossarek S, Carrrier L. How do MYBPC3 mutations cause hypertrophic cardiomyopathy? Journal of Muscle Research and Cell Motility. 33: 75-80. PMID 22057632 DOI: 10.1007/S10974-011-9268-3 |
0.345 |
|
| 2012 |
Memo M, Clarke N, Laing N, Nowak K, Ravenscroft G, Sewry C, Jain R, Jayawant S, Lehtokari V, Marttila M, Wallgren-Pettersson C, Marston S. C.P.18 Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain or loss of function Neuromuscular Disorders. 22: 846. DOI: 10.1016/j.nmd.2012.06.146 |
0.389 |
|
| 2012 |
Ching Leung M, Messer AE, Copeland O, Marston SB. O-Glcnacylation in the Long Isoform of ZASP in Human Heart Muscle Biophysical Journal. 102: 143a. DOI: 10.1016/j.bpj.2011.11.787 |
0.302 |
|
| 2012 |
Memo M, Clarke NF, Laing NG, Nowak KJ, Ravenscroft G, Sewry C, Jain RK, Jaywant S, Lehtokari V, Marttila M, Wallgren-Petersen C, Marston S. Skeletal Muscle Myopathy Mutations at the Actin-Tropomyosin Interface that Cause Gain Or Loss of Function Biophysical Journal. 102: 231a. DOI: 10.1016/J.Bpj.2011.11.1266 |
0.442 |
|
| 2011 |
Bayliss C, Messer A, Dos Remedios C, Van der Velden J, Marston S. The HCM-Associated Cardiac Troponin T Mutation K273N in a Human Heart Sample Studied by in Vitro Motility Assay Biophysical Journal. 100: 115a. DOI: 10.1016/J.Bpj.2010.12.837 |
0.463 |
|
| 2010 |
Copeland O, Nowak KJ, Laing NG, Ravenscroft G, Messer AE, Bayliss CR, Marston SB. Investigation of changes in skeletal muscle α-actin expression in normal and pathological human and mouse hearts Journal of Muscle Research and Cell Motility. 31: 207-214. PMID 20706863 DOI: 10.1007/s10974-010-9224-7 |
0.42 |
|
| 2010 |
Song W, Dyer E, Stuckey D, Leung MC, Memo M, Mansfield C, Ferenczi M, Liu K, Redwood C, Nowak K, Harding S, Clarke K, Wells D, Marston S. Investigation of a transgenic mouse model of familial dilated cardiomyopathy. Journal of Molecular and Cellular Cardiology. 49: 380-9. PMID 20600154 DOI: 10.1016/J.Yjmcc.2010.05.009 |
0.361 |
|
| 2010 |
Marston SB, Messer AE, Gallon CE, Sancho-Sollis R, Walker JW. 020 Determination of troponin I phosphorylation sites in human heart muscle Heart. 96: e6-e6. DOI: 10.1136/hrt.2009.191064h |
0.349 |
|
| 2009 |
Messer AE, Gallon CE, McKenna WJ, Dos Remedios CG, Marston SB. The use of phosphate-affinity SDS-PAGE to measure the cardiac troponin I phosphorylation site distribution in human heart muscle. Proteomics. Clinical Applications. 3: 1371-82. PMID 21136957 DOI: 10.1002/prca.200900071 |
0.31 |
|
| 2009 |
Dyer EC, Jacques AM, Hoskins AC, Ward DG, Gallon CE, Messer AE, Kaski JP, Burch M, Kentish JC, Marston SB. Functional analysis of a unique troponin c mutation, gly159asp, that causes Familial dilated cardiomyopathy, studied in explanted heart muscle Circulation: Heart Failure. 2: 456-464. PMID 19808376 DOI: 10.1161/CIRCHEARTFAILURE.108.818237 |
0.329 |
|
| 2009 |
Feng JJ, Marston S. Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathies Neuromuscular Disorders. 19: 6-16. PMID 18976909 DOI: 10.1016/J.Nmd.2008.09.005 |
0.442 |
|
| 2009 |
Copeland O, Ravenscroft G, Nowak K, Laing N, Marston S. Quantitative Assay of Skeletal Muscle alpha-actin Expression In Normal and Pathological Human and Mouse Hearts Biophysical Journal. 96: 499a. DOI: 10.1016/J.Bpj.2008.12.2574 |
0.537 |
|
| 2009 |
Marston S, Copeland O, Jacques A, McKenna W, Tsang V, Livesey K, Carballo S, Redwood C, Watkins H. Direct Evidence In Man For Haploinsufficiency As The Mechanism Of Action Of Myosin-binding Protein C Mutations That Cause Hypertrophic Cardiomyopathy Biophysical Journal. 96: 371a. DOI: 10.1016/J.Bpj.2008.12.1998 |
0.41 |
|
| 2009 |
Messer AE, Gallon CE, McKenna WJ, Dos Remedios CG, Marston SB. The use of phosphate-affinity SDS-PAGE to measure the cardiac troponin I phosphorylation site distribution in human heart muscle Proteomics - Clinical Applications. 3: 1371-1382. DOI: 10.1002/prca.200900071 |
0.31 |
|
| 2008 |
Marston S, El-Mezgueldi M. Role of tropomyosin in the regulation of contraction in smooth muscle. Advances in Experimental Medicine and Biology. 644: 110-23. PMID 19209817 |
0.455 |
|
| 2008 |
Marston S. How does genotype define phenotype? Microphysiology of a tropomyosin mutation in situ shows the limitations of reductionism Journal of Physiology. 586: 2821. PMID 18556722 DOI: 10.1113/Jphysiol.2008.155606 |
0.5 |
|
| 2008 |
Jacques AM, Briceno N, Messer AE, Gallon CE, Jalilzadeh S, Garcia E, Kikonda-Kanda G, Goddard J, Harding SE, Watkins H, Esteban MT, Tsang VT, McKenna WJ, Marston SB. The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy Cardiovascular Research. 79: 481-491. PMID 18411228 DOI: 10.1093/Cvr/Cvn094 |
0.341 |
|
| 2008 |
Matsson H, Eason J, Bookwalter CS, Klar J, Gustavsson P, Sunnegårdh J, Enell H, Jonzon A, Vikkula M, Gutierrez I, Granados-Riveron J, Pope M, Bu'Lock F, Cox J, Robinson TE, ... ... Marston S, et al. Alpha-cardiac actin mutations produce atrial septal defects. Human Molecular Genetics. 17: 256-65. PMID 17947298 DOI: 10.1093/Hmg/Ddm302 |
0.325 |
|
| 2008 |
Jacques A, Copeland O, McKenna W, Tsang V, Marston S. MyBP-C phosphorylation in donor, failing and HOCM human heart muscle Journal of Molecular and Cellular Cardiology. 44: 730-731. DOI: 10.1016/J.Yjmcc.2008.02.047 |
0.441 |
|
| 2008 |
Marston S, El-Mezgueldi M. Role of tropomyosin in the regulation of contraction in smooth muscle Advances in Experimental Medicine and Biology. 644: 110-123. DOI: 10.1007/978-0-387-85766-4_9 |
0.425 |
|
| 2007 |
Clarke NF, Ilkovski B, Cooper S, Valova VA, Robinson PJ, Nonaka I, Feng JJ, Marston S, North K. The pathogenesis of ACTA1-related congenital fiber type disproportion. Annals of Neurology. 61: 552-61. PMID 17387733 DOI: 10.1002/Ana.21112 |
0.484 |
|
| 2007 |
Mirza M, Robinson P, Kremneva E, Copeland O, Nikolaeva O, Watkins H, Levitsky D, Redwood C, El-Mezgueldi M, Marston S. The effect of mutations in α-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments Journal of Biological Chemistry. 282: 13487-13497. PMID 17360712 DOI: 10.1074/Jbc.M701071200 |
0.32 |
|
| 2006 |
D'Amico A, Graziano C, Pacileo G, Petrini S, Nowak KJ, Boldrini R, Jacques A, Feng JJ, Porfirio B, Sewry CA, Santorelli FM, Limongelli G, Bertini E, Laing N, Marston SB. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation Neuromuscular Disorders. 16: 548-552. PMID 16945537 DOI: 10.1016/j.nmd.2006.07.005 |
0.363 |
|
| 2006 |
Alahyan M, Webb MR, Marston SB, El-Mezgueldi M. The mechanism of smooth muscle caldesmon-tropomyosin inhibition of the elementary steps of the actomyosin ATPase Journal of Biological Chemistry. 281: 19433-19448. PMID 16540476 DOI: 10.1074/jbc.M507602200 |
0.337 |
|
| 2006 |
Dyer E, Wells D, Redwood C, Marston S. Functional investigation of a transgenic mouse model of dilated cardiomyopathy with the Glu361Gly mutation in cardiac actin Journal of Molecular and Cellular Cardiology. 40: 941. DOI: 10.1016/J.Yjmcc.2006.03.072 |
0.331 |
|
| 2005 |
Mirza M, Marston S, Willott R, Ashley C, Mogensen J, McKenna W, Robinson P, Redwood C, Watkins H. Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype. The Journal of Biological Chemistry. 280: 28498-506. PMID 15923195 DOI: 10.1074/Jbc.M412281200 |
0.356 |
|
| 2004 |
Marston S, Mirza M, Abdulrazzak H, Sewry C. Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathy. Neuromuscular Disorders : Nmd. 14: 167-74. PMID 14733965 DOI: 10.1016/J.Nmd.2003.11.003 |
0.415 |
|
| 2003 |
Ansari S, El-Mezgueldi M, Marston S. Cooperative inhibition of actin filaments in the absence of tropomyosin. Journal of Muscle Research and Cell Motility. 24: 513-20. PMID 14870966 DOI: 10.1023/B:Jure.0000009812.74980.13 |
0.321 |
|
| 2003 |
Marston S. Random walks with thin filaments: application of in vitro motility assay to the study of actomyosin regulation. Journal of Muscle Research and Cell Motility. 24: 149-56. PMID 14609026 DOI: 10.1023/A:1026097313020 |
0.349 |
|
| 2002 |
Robinson P, Mirza M, Knott A, Abdulrazzak H, Willott R, Marston S, Watkins H, Redwood C. Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy. The Journal of Biological Chemistry. 277: 40710-6. PMID 12186860 DOI: 10.1074/Jbc.M203446200 |
0.32 |
|
| 2002 |
Marston SB, Ingwall JS, Glueck SB. Calcium, contractions, and tropomyosin Focus on "divergent abnormal muscle relaxation by hypertrophic cardiomyopathy and nemaline myopathy mutant tropomyosins". Physiological Genomics. 9: 57-8. PMID 12006671 DOI: 10.1152/physiolgenomics.00038.2002 |
0.406 |
|
| 2002 |
Knott A, Purcell I, Marston S. In vitro motility analysis of thin filaments from failing and non-failing human heart: troponin from failing human hearts induces slower filament sliding and higher Ca(2+) sensitivity. Journal of Molecular and Cellular Cardiology. 34: 469-82. PMID 11991735 DOI: 10.1006/Jmcc.2002.1528 |
0.308 |
|
| 2002 |
Burton D, Abdulrazzak H, Knott A, Elliott K, Redwood C, Watkins H, Marston S, Ashley C. Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility. The Biochemical Journal. 362: 443-51. PMID 11853553 DOI: 10.1042/0264-6021:3620443 |
0.433 |
|
| 2001 |
Borovikov YS, Avrova SV, Vikhoreva NN, Vikhorev PG, Ermakov VS, Copeland O, Marston SB. C-terminal actin-binding sites of smooth muscle caldesmon switch actin between conformational states. The International Journal of Biochemistry & Cell Biology. 33: 1151-9. PMID 11606251 DOI: 10.1016/S1357-2725(01)00091-7 |
0.343 |
|
| 2001 |
Marston SB, Hodgkinson JL. Cardiac and skeletal myopathies: can genotype explain phenotype? Journal of Muscle Research and Cell Motility. 22: 1-4. PMID 11563546 DOI: 10.1023/A:1010355716511 |
0.448 |
|
| 2000 |
Notarianni G, Gusev N, Lafitte D, Hill TJ, Cooper HS, Derrick PJ, Marston SB. A novel Ca2+ binding protein associated with caldesmon in Ca2+-regulated smooth muscle thin filaments: evidence for a structurally altered form of calmodulin. Journal of Muscle Research and Cell Motility. 21: 537-49. PMID 11206132 DOI: 10.1023/A:1026589704750 |
0.376 |
|
| 2000 |
Bing W, Knott A, Marston SB. A simple method for measuring the relative force exerted by myosin on actin filaments in the in vitro motility assay: evidence that tropomyosin and troponin increase force in single thin filaments. The Biochemical Journal. 350: 693-9. PMID 10970781 DOI: 10.1042/0264-6021:3500693 |
0.317 |
|
| 2000 |
Bing W, Knott A, Redwood C, Esposito G, Purcell I, Watkins H, Marston S. Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha -tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay. Journal of Molecular and Cellular Cardiology. 32: 1489-98. PMID 10900175 DOI: 10.1006/Jmcc.2000.1182 |
0.372 |
|
| 2000 |
Redwood C, Lohmann K, Bing W, Esposito GM, Elliott K, Abdulrazzak H, Knott A, Purcell I, Marston S, Watkins H. Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein. Circulation Research. 86: 1146-52. PMID 10850966 DOI: 10.1161/01.Res.86.11.1146 |
0.35 |
|
| 2000 |
Marston S, Purcell I, Knott A. Does a decrease in troponin I phosphorylation explain the altered functional properties of troponin in failing heart muscle? European Journal of Heart Failure. 2: 79-79. DOI: 10.1016/S1388-9842(00)80287-1 |
0.481 |
|
| 1998 |
Marston SB, Burton D, Copeland O, Fraser I, Gao Y, Hodgkinson J, Huber P, Levine B, El-Mezgueldi M, Notarianni G. Structural interactions between actin, tropomyosin, caldesmon and calcium binding protein and the regulation of smooth muscle thin filaments Acta Physiologica Scandinavica. 164: 401-414. PMID 9887964 |
0.377 |
|
| 1998 |
Bing W, Razzaq A, Sparrow J, Marston S. Tropomyosin and troponin regulation of wild type and E93K mutant actin filaments from Drosophila flight muscle. Charge reversal on actin changes actin-tropomyosin from on to off state Journal of Biological Chemistry. 273: 15016-15021. PMID 9614109 DOI: 10.1074/Jbc.273.24.15016 |
0.421 |
|
| 1997 |
Hodgkinson JL, Marston SB, Craig R, Vibert P, Lehman W. Three-dimensional image reconstruction of reconstituted smooth muscle thin filaments: Effects of caldesmon Biophysical Journal. 72: 2398-2404. PMID 9168017 DOI: 10.1016/S0006-3495(97)78885-4 |
0.368 |
|
| 1996 |
El-Mezgueldi M, Marston SB. The effects of smooth muscle calponin on the strong and weak myosin binding sites of F-actin Journal of Biological Chemistry. 271: 28161-28167. PMID 8910431 DOI: 10.1074/jbc.271.45.28161 |
0.33 |
|
| 1995 |
Marston S. Ca2+-dependent protein switches in actomyosin based contractile systems International Journal of Biochemistry and Cell Biology. 27: 97-108. PMID 7767791 DOI: 10.1016/1357-2725(94)00080-U |
0.342 |
|
| 1995 |
Fraser IDC, Marston SB. In vitro motility analysis of actin-tropomyosin regulation by troponin and calcium. The thin filament is switched as a single cooperative unit Journal of Biological Chemistry. 270: 7836-7841. PMID 7713874 DOI: 10.1074/jbc.270.14.7836 |
0.331 |
|
| 1995 |
Fraser IDC, Marston SB. In vitro motility analysis of smooth muscle caldesmon control of actin- tropomyosin filament movement Journal of Biological Chemistry. 270: 19688-19693. PMID 7649978 DOI: 10.1074/jbc.270.34.19688 |
0.368 |
|
| 1995 |
Hodgkinson JL, Newman TM, Marston SB, Severs NJ. The structure of the contractile apparatus in ultrarapidly frozen smooth muscle: Freeze-fracture, deep-etch, and freeze-substitution studies Journal of Structural Biology. 114: 93-104. PMID 7612400 DOI: 10.1006/jsbi.1995.1009 |
0.303 |
|
| 1994 |
Marston SB, Fraser IDC, Huber PAJ. Smooth muscle caldesmon controls the strong binding interaction between actin-tropomyosin and myosin Journal of Biological Chemistry. 269: 32104-32109. PMID 7798205 |
0.365 |
|
| 1994 |
Gusev NB, Pritchard K, Hodgkinson JL, Marston SB. Filamin and gelsolin influence Ca2+-sensitivity of smooth muscle thin filaments Journal of Muscle Research and Cell Motility. 15: 672-681. PMID 7706423 DOI: 10.1007/BF00121074 |
0.349 |
|
| 1993 |
Lehman W, Denault D, Marston S. The caldesmon content of vertebrate smooth muscle. Biochimica Et Biophysica Acta. 1203: 53-9. PMID 8218392 DOI: 10.1016/0167-4838(93)90035-P |
0.5 |
|
| 1992 |
Marston S, Pinter K, Bennett P. Caldesmon binds to smooth muscle myosin and myosin rod and crosslinks thick filaments to actin filaments. Journal of Muscle Research and Cell Motility. 13: 206-18. PMID 1534566 DOI: 10.1007/Bf01874158 |
0.485 |
|
| 1991 |
Marston S. Stoichiometry and stability of caldesmon in native thin filaments from sheep aorta smooth muscle. The Biochemical Journal. 272: 305-10. PMID 2268260 DOI: 10.1042/bj2720305 |
0.331 |
|
| 1991 |
Bennett PM, Marston SB. Calcium regulated thin filaments from molluscan catch muscles contain a caldesmon-like regulatory protein. Journal of Muscle Research and Cell Motility. 11: 302-12. PMID 2254439 DOI: 10.1007/BF01766668 |
0.474 |
|
| 1991 |
Pritchard K, Marston SB. Ca(2+)-dependent regulation of vascular smooth-muscle caldesmon by S.100 and related smooth-muscle proteins. The Biochemical Journal. 819-24. PMID 1831352 DOI: 10.1042/bj2770819 |
0.394 |
|
| 1990 |
Taggart MJ, Marston S. A study of the physiological function of the smooth muscle contractile protein caldesmon Journal of Molecular and Cellular Cardiology. 22: S22. DOI: 10.1016/0022-2828(90)91595-X |
0.677 |
|
| 1990 |
Nesterov VP, Peiper U, Hiller J, Krienke B, Schüttler K, Szymanski C, Bottinelli R, Cappelli V, Minelli R, Reggiani C, Schiaffino S, Carlhoff D, D'Haese J, Dabrowska R, Nowak E, ... ... Marston SB, ... ... Marston S, et al. Abstracts of the XVIII European Conference on Muscle and Motility Journal of Muscle Research & Cell Motility. 11: 56-78. DOI: 10.1007/Bf01833326 |
0.696 |
|
| 1989 |
Marston S, Pritchard K, Redwood C, Taggart M. Ca2+ regulation of the thin filaments: biochemical mechanism and physiological role. Biochemical Society Transactions. 16: 494-7. PMID 3208977 DOI: 10.1042/Bst0160494 |
0.673 |
|
| 1989 |
Marston S. Calcium ion-dependent regulation of uterine smooth muscle thin filaments by caldesmon. American Journal of Obstetrics and Gynecology. 160: 252-7. PMID 2912089 DOI: 10.1016/0002-9378(89)90131-2 |
0.381 |
|
| 1989 |
Marston SB. What is latch? New ideas about tonic contraction in smooth muscle. Journal of Muscle Research and Cell Motility. 10: 97-100. PMID 2668329 DOI: 10.1007/BF01739965 |
0.431 |
|
| 1989 |
Marston SB. A tight-binding interaction between smooth-muscle native thin filaments and heavy meromyosin in the presence of MgATP. The Biochemical Journal. 259: 303-6. PMID 2524187 DOI: 10.1042/bj2590303 |
0.426 |
|
| 1988 |
Taggart MJ, Marston SB. The effects of vascular smooth muscle caldesmon on force production by 'desensitised' skeletal muscle fibres. Febs Letters. 242: 171-4. PMID 3144465 DOI: 10.1016/0014-5793(88)81009-3 |
0.658 |
|
| 1988 |
Marston S. Aorta caldesmon inhibits actin activation of thiophosphorylated heavy meromyosin Mg2+-ATPase activity by slowing the rate of product release. Febs Letters. 238: 147-50. PMID 2971572 DOI: 10.1016/0014-5793(88)80245-X |
0.308 |
|
| 1988 |
Marston SB, Redwood CS, Lehman W. Reversal of caldesmon function by anti-caldesmon antibodies confirms its role in the calcium regulation of vascular smooth muscle thin filaments. Biochemical and Biophysical Research Communications. 155: 197-202. PMID 2970847 DOI: 10.1016/S0006-291X(88)81068-4 |
0.383 |
|
| 1988 |
TAGGART MJ, MARSTON SB. Caldesmon can relax ‘desensitized’ skeletal muscle fibres Biochemical Society Transactions. 16: 360-361. DOI: 10.1042/Bst0160360 |
0.66 |
|
| 1986 |
Marston SB, Smith CW. The thin filaments of smooth muscles. Journal of Muscle Research and Cell Motility. 6: 669-708. PMID 3937845 DOI: 10.1007/BF00712237 |
0.426 |
|
| 1985 |
Marston SB, Moody C, Smith C. Mechanisms of the regulation of myofibrillar function in vascular smooth muscle. Biochemical Society Transactions. 12: 945-8. PMID 6530043 DOI: 10.1042/bst0120945 |
0.376 |
|
| 1985 |
Marston SB, Smith CW. Purification and properties of Ca2+-regulated thin filaments and F-actin from sheep aorta smooth muscle. Journal of Muscle Research and Cell Motility. 5: 559-75. PMID 6150941 DOI: 10.1007/BF00713261 |
0.323 |
|
| 1985 |
Marston SB, Lehman W. Caldesmon is a Ca2+-regulatory component of native smooth-muscle thin filaments. The Biochemical Journal. 231: 517-22. PMID 2934055 DOI: 10.1042/Bj2310517 |
0.393 |
|
| 1985 |
Moody CJ, Marston SB, Smith CW. Bundling of actin filaments by aorta caldesmon is not related to its regulatory function. Febs Letters. 191: 107-12. PMID 2932345 DOI: 10.1016/0014-5793(85)81003-6 |
0.306 |
|
| 1985 |
MOODY C, SMITH C, MARSTON S. The mechanism of Ca2+-dependent thin filament regulation in vascular smooth muscle Journal of Molecular and Cellular Cardiology. 17: 11-11. DOI: 10.1016/S0022-2828(85)80176-0 |
0.376 |
|
| 1984 |
Marston SB, Tregear RT. Modification of the interactions of myosin with actin and 5'-adenylyl imidodiphosphate by substitution of ethylene glycol for water Biochemical Journal. 217: 169-177. PMID 6141791 |
0.653 |
|
| 1984 |
SMITH C, MARSTON S. A 120kDa regulatory protein from vascular smooth muscle thin filaments* Journal of Molecular and Cellular Cardiology. 16: 65-65. DOI: 10.1016/S0022-2828(84)80550-7 |
0.388 |
|
| 1984 |
MARSTON S, SMITH C, MOODY C. Regulation of the contractile protein of vascular smooth muscle involves the concerted interaction of at least six different proteins* Journal of Molecular and Cellular Cardiology. 16: 64-64. DOI: 10.1016/S0022-2828(84)80549-0 |
0.325 |
|
| 1983 |
Marston SB. The regulation of smooth muscle contractile proteins. Progress in Biophysics and Molecular Biology. 41: 1-41. PMID 6130572 DOI: 10.1016/0079-6107(83)90024-X |
0.416 |
|
| 1983 |
Marston S, Smith C. The contractile mechanism of vascular smooth muscle I: Isolation and characterisation of Ca2+ regulated thin filaments from sheep aorta☆ Journal of Molecular and Cellular Cardiology. 15: 17-17. DOI: 10.1016/0022-2828(83)90822-2 |
0.376 |
|
| 1982 |
Tregear RT, Clarke ML, Marston SB, Rodger CD, Bordas J, Koch M. A study of demembranated muscle fibers under equilibrium conditions. Society of General Physiologists Series. 37: 131-141. PMID 7146945 |
0.718 |
|
| 1982 |
Walters M, Marston SB. Phosphorylation of the calcium ion-regulated thin filaments from vascular smooth muscle. A new regulatory mechanism? The Biochemical Journal. 197: 127-39. PMID 6459087 DOI: 10.1042/bj1970127 |
0.32 |
|
| 1980 |
Marston SB, Taylor EW. Comparison of the myosin and actomyosin ATPase mechanisms of the four types of vertebrate muscles Journal of Molecular Biology. 139: 573-600. PMID 6447797 DOI: 10.1016/0022-2836(80)90050-9 |
0.623 |
|
| 1980 |
Marston SB, Trevett RM, Walters M. Calcium ion-regulated thin filaments from vascular smooth muscle. The Biochemical Journal. 185: 355-65. PMID 6446898 DOI: 10.1042/bj1850355 |
0.357 |
|
| 1980 |
MARSTON S, WALTERS M. Phosphorylation of thin filaments regulates vascular smooth muscle actomyosin ATPase activity Cell Biology International Reports. 4: 799. DOI: 10.1016/0309-1651(80)90152-6 |
0.389 |
|
| 1979 |
Marston SB, Tregear RT, Rodger CD, Clarke ML. Coupling between the enzymatic site of myosin and the mechanical output of muscle Journal of Molecular Biology. 128: 111-126. PMID 430572 DOI: 10.1016/0022-2836(79)90121-9 |
0.735 |
|
| 1979 |
Tregear RT, Marston SB. The crossbridge theory. Annual Review of Physiology. 41: 723-736. PMID 373607 |
0.487 |
|
| 1978 |
Marston SB, Taylor EW. Mechanism of myosin and actomyosin ATPase in chicken Gizzard smooth muscle Febs Letters. 86: 167-170. PMID 146612 DOI: 10.1016/0014-5793(78)80555-9 |
0.642 |
|
| 1977 |
Marston S. Contractile systems in non-muscle tissues Trends in Biochemical Sciences. 2: 240. DOI: 10.1016/0968-0004(77)90131-1 |
0.337 |
|
| 1976 |
Marston SB, Rodger CD, Tregear RT. Changes in muscle crossbridges when β,γ-imido-ATP binds to myosin Journal of Molecular Biology. 104: 263-276. PMID 957434 DOI: 10.1016/0022-2836(76)90012-7 |
0.646 |
|
| 1975 |
Marston S, Weber A. The dissociation constant of the actin-heavy meromyosin subfragment-1 complex. Biochemistry. 14: 3868-73. PMID 126077 DOI: 10.1021/Bi00688A021 |
0.627 |
|
| 1974 |
Marston S, Lehman W. ADP binding to relaxed scallop myofibrils. Nature. 252: 38-9. PMID 4279338 DOI: 10.1038/252038A0 |
0.379 |
|
| 1974 |
Marston SB, Tregear RT. Nucleotide binding to myosin in calcium activated muscle Bba - Bioenergetics. 333: 581-584. PMID 4277060 DOI: 10.1016/0005-2728(74)90143-1 |
0.66 |
|
| 1974 |
Marston S, Tregear RT. Calcium binding and the activation of fibrillar insect flight muscle Bba - Bioenergetics. 347: 311-318. PMID 4276206 DOI: 10.1016/0005-2728(74)90054-1 |
0.649 |
|
| 1973 |
Marston S. The nucleotide complexes of myosin in glycerol-extracted muscle fibres. Biochimica Et Biophysica Acta. 305: 397-412. PMID 4270181 DOI: 10.1016/0005-2728(73)90186-2 |
0.373 |
|
| 1972 |
Marston SB, Tregear RT. Evidence for a complex between myosin and ADP in relaxed muscle fibres. Nature: New Biology. 235: 23-24. PMID 4259810 |
0.68 |
|
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