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About
James M Ervasti
Author PubWeight™ 46.81
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia.
Nature
2012
2.52
2
Gamma-actin is required for cytoskeletal maintenance but not development.
Proc Natl Acad Sci U S A
2009
1.74
3
Cytoplasmic gamma-actin contributes to a compensatory remodeling response in dystrophin-deficient muscle.
Proc Natl Acad Sci U S A
2006
1.68
4
Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation.
Biochem J
2005
1.56
5
β-Actin specifically controls cell growth, migration, and the G-actin pool.
Mol Biol Cell
2011
1.46
6
Utrophin binds laterally along actin filaments and can couple costameric actin with sarcolemma when overexpressed in dystrophin-deficient muscle.
Mol Biol Cell
2002
1.44
7
Cytoplasmic gamma-actin is not required for skeletal muscle development but its absence leads to a progressive myopathy.
Dev Cell
2006
1.43
8
Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.
J Biol Chem
2010
1.43
9
The actin gene family: function follows isoform.
Cytoskeleton (Hoboken)
2010
1.39
10
Dystrophin is a microtubule-associated protein.
J Cell Biol
2009
1.38
11
Dystrophin and utrophin bind actin through distinct modes of contact.
J Biol Chem
2006
1.36
12
Functional substitution by TAT-utrophin in dystrophin-deficient mice.
PLoS Med
2009
1.30
13
β-actin and γ-actin are each dispensable for auditory hair cell development but required for Stereocilia maintenance.
PLoS Genet
2010
1.30
14
Contributions of the LG modules and furin processing to laminin-2 functions.
J Biol Chem
2002
1.28
15
Crystal structure and cell surface anchorage sites of laminin alpha1LG4-5.
J Biol Chem
2007
1.27
16
Molecular dissection of the alpha-dystroglycan- and integrin-binding sites within the globular domain of human laminin-10.
J Biol Chem
2003
1.26
17
An ex vivo gene therapy approach to treat muscular dystrophy using inducible pluripotent stem cells.
Nat Commun
2013
1.17
18
The utrophin actin-binding domain binds F-actin in two different modes: implications for the spectrin superfamily of proteins.
J Cell Biol
2002
1.12
19
Delayed embryonic development and impaired cell growth and survival in Actg1 null mice.
Cytoskeleton (Hoboken)
2010
1.11
20
Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophy.
Hum Mol Genet
2002
1.10
21
Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic instability and protein aggregation.
Proc Natl Acad Sci U S A
2010
1.04
22
Identification of spectrin-like repeats required for high affinity utrophin-actin interaction.
J Biol Chem
2005
1.01
23
Axonal regeneration and neuronal function are preserved in motor neurons lacking ß-actin in vivo.
PLoS One
2011
1.01
24
Internal deletion compromises the stability of dystrophin.
Hum Mol Genet
2011
1.00
25
Context-dependent functional substitution of alpha-skeletal actin by gamma-cytoplasmic actin.
FASEB J
2009
0.99
26
β-Actin and fascin-2 cooperate to maintain stereocilia length.
J Neurosci
2013
0.99
27
Microtubule binding distinguishes dystrophin from utrophin.
Proc Natl Acad Sci U S A
2014
0.98
28
Dystrophin and utrophin have distinct effects on the structural dynamics of actin.
Proc Natl Acad Sci U S A
2009
0.98
29
Core 1 glycans on alpha-dystroglycan mediate laminin-induced acetylcholine receptor clustering but not laminin binding.
J Biol Chem
2003
0.91
30
Skeletal muscle-specific ablation of gamma(cyto)-actin does not exacerbate the mdx phenotype.
PLoS One
2008
0.90
31
Restricted morphological and behavioral abnormalities following ablation of β-actin in the brain.
PLoS One
2012
0.90
32
TAT-μUtrophin mitigates the pathophysiology of dystrophin and utrophin double-knockout mice.
J Appl Physiol (1985)
2011
0.87
33
Brain alpha-dystroglycan displays unique glycoepitopes and preferential binding to laminin-10/11.
FEBS Lett
2006
0.86
34
Actin isoforms in neuronal development and function.
Int Rev Cell Mol Biol
2013
0.85
35
The carboxy-terminal third of dystrophin enhances actin binding activity.
J Mol Biol
2011
0.85
36
Quadriceps myopathy caused by skeletal muscle-specific ablation of β(cyto)-actin.
J Cell Sci
2011
0.85
37
Cytoplasmic gamma-actin expression in diverse animal models of muscular dystrophy.
Neuromuscul Disord
2007
0.85
38
Destabilization of the dystrophin-glycoprotein complex without functional deficits in alpha-dystrobrevin null muscle.
PLoS One
2008
0.84
39
Impacts of dystrophin and utrophin domains on actin structural dynamics: implications for therapeutic design.
J Mol Biol
2012
0.84
40
Transgenic overexpression of γ-cytoplasmic actin protects against eccentric contraction-induced force loss in mdx mice.
Skelet Muscle
2011
0.82
41
Structural and functional properties of the actin gene family.
Crit Rev Eukaryot Gene Expr
2011
0.80