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CSRP3 encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. Zusätzlich bieten wir Ihnen CSRP3 Antikörper (81) und CSRP3 Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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MLP contributes to the maintenance of cardiomyocyte cytoarchitecture by a mechanism involving its self-association and actin filament cross-linking.
study reports the discovery of an alternative splice variant of muscle lim protein encoded by the CSRP3 gene, designated as MLP-b, showing distinct expression in neuromuscular disease and direct roles in actin dynamics and muscle differentiation
KLF5 (zeige KLF5 ELISA Kits) reverses hhLIM function from anti-proliferation to pro-proliferation through its interaction with hhLIM on the cyclin E (zeige CCNE1 ELISA Kits) promoter.
CSRP3 is involved in cardiac mechanosensory processes, is localized to the sarcomeric Z-disc and human mutations cause cardiomyopathy(DCM)and heart failure.
CSRP3, MUSTN1 (zeige MUSTN1 ELISA Kits), SIX1 (zeige SIX1 ELISA Kits), and FBXO32 (zeige FBXO32 ELISA Kits) expression changes in response to lengthening and shortening contractions in human muscle
A myocardial actin-binding protein that increases actin cytoskeleton stability by promoting bundling of actin filaments.
These findings suggest that hhLIM is a typical LIM (zeige PDLIM5 ELISA Kits) family member with powerful transcription activation.
Study used linkage analysis and identified a CSRP3 missense mutation in a large German family affected by hypertrophic cardiomyopathy.
CSRP3 mutation was found involved in hypertrophic cardiomyopathy.
The structure of both LIM (zeige PDLIM5 ELISA Kits) domains of human MLP (zeige MUC2 ELISA Kits) by nuclear magnetic resonance spectroscopy.
Cardiac overexpression of muscle LIM protein (zeige CSRP2 ELISA Kits) does not modulate the heart's response to various forms of pathological stress.
Loss of MLP (zeige MARCKSL1 ELISA Kits) leads to dilated cardiomyopathy and hearts of surviving MLP (zeige MARCKSL1 ELISA Kits) knockout mice show transient changes of intracellular calcium handling.
Reduced MLP-calcineurin signaling predisposes to adverse remodeling after myocardial infarct.
This detailed physiological characterization during a phase of rapid anatomical remodeling suggests that systolic function in the MLP (zeige MARCKSL1 ELISA Kits)(-/-) mice may temporarily improve as a result of alterations in chamber compliance, which are mediated by dilatation.
Mice with knockout of muscle-LIM protein (zeige CSRP2 ELISA Kits) exhibit prolongation of atrial and ventricular conduction and an increased ventricular vulnerability.
MLP (zeige MARCKSL1 ELISA Kits) binds directly to CFL2 (zeige CFL2 ELISA Kits) in human cardiac and skeletal muscles.
data support the high potential of the CSRP3 as a marker gene for the improvement of growth performance and carcass traits in selection programs
CSRP3 coding gene from porcine muscle was isolated and characterized and Phylogenic analyses demonstrated that CSRP3 diverged first and is distinguished from two other members, CSRP1 (zeige CSRP1 ELISA Kits) and CSRP2 (zeige CSRP2 ELISA Kits).
is only expressed in the differentiated heart during early development and is expressed in a subset of other striated (zeige NSDHL ELISA Kits) muscles during later stages
This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene.
LIM domain only 4
, cardiac LIM domain protein
, cysteine and glycine-rich protein 3
, muscle LIM protein
, LIM domain protein, cardiac
, cardiac LIM protein
, cysteine-rich protein 3
, cysteine- and glycine-rich protein 3
, Cysteine and glycine-rich protein 3
, Muscle LIM protein
, cysteine and glycine-rich protein 3 (cardiac LIM protein)