Massimiliano Memo - Concepedia

Author

Massimiliano Memo

Imperial College London

Also Known As

Massimiliano Memo, Memo, Massimiliano

Publications

485

Citations

H-Index

Concepts

All Affiliations

Imperial College London The University of Western Australia Harry Perkins Institute of Medical Research University of Helsinki The University of Sydney

About

Massimiliano Memo is an author at Imperial College London specializing in medicine, molecular physiology, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	330
2	Cellular Physiology	4	4	242
3	Health Sciences	3	3	134
4	Cell Biology	3	3	232
5	Natural Sciences	1	1	127

Massimiliano Memo

Publications

480

Citations

H-Index

Page 1

	Year	Citations
β Integrin Tyrosine Phosphorylation Is a Conserved Mechanism for Regulating Talin-induced Integrin Activation Nicholas J. Anthis, Jacob R. Haling, Camilla L. Oxley, Journal of Biological Chemistry Cell AdhesionTalin-induced Integrin ActivationMolecular BiologyConserved MechanismIntegrin Adhesiveness	2009	127
Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients Steven B. Marston, Massimiliano Memo, Andrew E. Messer, Human Molecular Genetics	2013	82
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca2+ sensitivity Massimiliano Memo, Man Ching Leung, Douglas G. Ward, Cardiovascular Research	2013	68
Investigation of a transgenic mouse model of familial dilated cardiomyopathy Weihua Song, Emma Dyer, Daniel J. Stuckey, Journal of Molecular and Cellular Cardiology Cardiac MuscleCardiomyopathyHeart FailureTransgenic Mouse ModelsGenetics	2010	59
K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity Nancy Mokbel, Biljana Ilkovski, Michaela Kreissl, Brain Myofibre Calcium SensitivityGeneticsPathologyMolecular BiologyCytoskeleton	2013	53
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in <i>TPM2</i>-related nemaline and cap myopathy M. Marttila, Elina Lemola, William Wallefeld, Biochemical Journal Muscle FunctionPathologyCytoskeletonMechanotransductionCap Myopathy	2011	52
Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain- or loss-of-function Massimiliano Memo, Steven B. Marston Journal of Muscle Research and Cell Motility MechanobiologyMuscle FunctionSkeletal MuscleMedicinePhysiology	2013	29
Mutations in thin Filament Proteins that Cause Familial Dilated Cardiomyopathy Uncouple Troponin I Phosphorylation from Changes in Myofibrillar Ca2+-Sensitivity Massimiliano Memo, Andrew E. Messer, Man Ching Leung, Biophysical Journal Cardiac MuscleCardiomyopathySignal TransductionMolecular PhysiologyMyofibrillar Ca2+-sensitivity	2012	10

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