Capn3

Calcium Mechanisms in LimbGirdle Muscular Dystrophy with CAPN3 Mutations

Representative CAPN3 isoforms generated by alternative splicing of

Calcium Mechanisms in LimbGirdle Muscular Dystrophy with CAPN3 Mutations

A Model for Capn3 activation Capn3 is mainly present in a

Threedimensional structure model of CAPN3 protein A Whole and local

Recurrent CAPN3 pAsp753Asn Variant Supports a Potential Dominant

CAPN3 pathogenic mutations K254E and R489W do not affect proteolytic

Capn3 is activated through autolysis in the active site which involves

Model of BTZ effect on CAPN3deficient muscle fibers CAPN3

Capn3 ectopic expression leads to cell rounding and nuclear

Capn3 deficiency induces a mitochondrial metabolism deficiency in

Calciumdependence of CAPN3 and CAPN1 autolysis and redistribution of

Calcium Mechanisms in LimbGirdle Muscular Dystrophy with CAPN3 Mutations

Model of BTZ effect on CAPN3deficient muscle fibers CAPN3

Muscle MRI muscle biopsy CAPN3 immunoblot and RTPCR in patients

Capn3 colocalizes with its substrates in vivo at the Z disk M line

DNA sequencing of CAPN3 gene and multiple sequence alignment A

Integrative variants haplotypes and diplotypes of the CAPN3 and FRMD5

Representative CAPN3 isoforms generated by alternative splicing of

CAPN3 in mechanically skinned rat EDL fibres autolyses in solutions

Functional recovery of CAPN3 expression A Left western blot from

Mutations in the CAPN3 gene in the patient of family 4 Pedigree of

Overview of CAPN3 substrates and tested peptides Download Table

Unraveling Novel Pathogenic CAPN3 Variants in LimbGirdle Muscular

Nonphysiological high Na with zero K results in CAPN3

CAPN3 deficiency in human myotubes reduces SERCA protein levels and

Bothcatenin and Mcadherin are substrates for CAPN3 proteaseCatenin

CAPN3 gene expression in rat gastrocnemius muscle after sciatic nerve

Table 1 from Mutations of CAPN3 in Korean Patients with LimbGirdle

Verification of putative CAPN3 targets ABD Skeletal muscle

Unraveling Novel Pathogenic CAPN3 Variants in LimbGirdle Muscular

Endogenous expression of Capn3 during myogenic differentiation of C2C12

Interaction of CAPN3 with SERCA1 SERCA2 and sAnk1 in human skeletal

Recurrent CAPN3 pAsp753Asn Variant Supports a Potential Dominant

CAPN3 gene expression in rat gastrocnemius muscle after sciatic nerve

Overview of CAPN3 substrates and tested peptides Download Table

Unraveling Novel Pathogenic CAPN3 Variants in LimbGirdle Muscular

Capn3 colocalizes with its substrates in vivo at the Z disk M line

Molecular characterization of the CAPN3 c1992 2TG variant A

Verification of putative CAPN3 targets ABD Skeletal muscle

Missense mutation of c635 T C in CAPN3 impairs muscle injury repair

Recurrent CAPN3 pAsp753Asn Variant Supports a Potential Dominant

The C2L domain of CAPN3 binds to calmodulin A schematic of monomeric

a Multiple sequence alignment of CAPN3 protein in different species

Transcriptional analysis of Capn3 expression level after ectopic up or

CAPN3 gene expression in rat gastrocnemius muscle after sciatic nerve

Recurrent CAPN3 pAsp753Asn Variant Supports a Potential Dominant

Functional recovery of CAPN3 expression A Left western blot from

Calmodulin specifically promotes CAPN3 autolysis A Western blot

Transcriptional analysis of Capn3 expression level after ectopic up or

Variants in CAPN3 Causing Autosomal Dominant LimbGirdle Muscular

International Journal of Molecular Medicine

CAPN3 A muscle specific calpain with an important role in the

Figure 1 from The N and Cterminal autolytic fragments of CAPN3p94

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Nonproteolytic functions of calpain3 in sarcoplasmic reticulum in

Cas9induced single cut enables highly efficient and templatefree

In situ detection of activation of CAPN3 a responsible gene product

Def determines the nucleolar localisation of Capn3 A Download

Def directly interacts with CAPN3 and they form a complex in the

Developing fluorescence sensor probe to capture activated muscle

Capn3deficient and Capn3sufficient immortalized primary muscle cells

Developing fluorescence sensor probe to capture activated muscle

Capn3deficient and Capn3sufficient immortalized primary muscle cells

In situ detection of activation of CAPN3 a responsible gene product

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Identification and functional characterization of a novel heterozygous

Calapin3 Hua

Restriction of Calpain3 Expression to the Skeletal Muscle Prevents

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Restriction of Calpain3 Expression to the Skeletal Muscle Prevents

Age muscle and gender specific characterization of muscle

Calpain 3 deficiency affects SERCA expression and function in the

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Figure 1 from The N and Cterminal autolytic fragments of CAPN3p94

International Journal of Molecular Medicine

In situ detection of activation of CAPN3 a responsible gene product

Musclespecific calpain3 is phosphorylated in its unique insertion

Na treatment of human skeletal muscle samples causes autolysis and

In situ detection of activation of CAPN3 a responsible gene product

Calpain 3 deficiency affects SERCA expression and function in the

In situ detection of activation of CAPN3 a responsible gene product

CAPN3 A muscle specific calpain with an important role in the

Restriction of Calpain3 Expression to the Skeletal Muscle Prevents

Mitochondrial dysfunction and consequences in calpain3deficient

Oligomerdependent and oligomerindependent pathogenesis of muscular

Restriction of Calpain3 Expression to the Skeletal Muscle Prevents

Novel Biomarkers for Limb Girdle Muscular Dystrophy LGMD

PDF A musclespecific calpain CAPN3 forms a homotrimer

The effect of Calpain inhibitors ALLN and Calpeptin on the level of

施回课题组在《EMBO Journal》发文揭示蛋白酶CAPN3介导的染色质重塑新机制

EMBO JournalCAPN3

BOSTER Biological Technology coltd 19932026

Restriction of Calpain3 Expression to the Skeletal Muscle Prevents

Oligomerdependent and oligomerindependent pathogenesis of muscular

Fig S3 Structurebased amino acid sequence alignment of calpains

CAPN3 A muscle specific calpain with an important role in the

In situ detection of activation of CAPN3 a responsible gene product

Protein BousounisGen677S12

CAPN autolysis in different ionic conditions in skeletal muscle human

Systemic delivery of AAVrh74tMCKhCAPN3 rescues the phenotype in a

The N and Cterminal autolytic fragments of CAPN3p94calpain3

In situ detection of activation of CAPN3 a responsible gene product

Calpain3 Is Not a Sodium Dependent Protease and Simply Requires

Loss of Calpain 3 dysregulates storeoperated calcium entry and its

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Gene expression profiling of Capn3deficient vs Capn3sufficient

Calpain 3 Expression Pattern during Gastrocnemius Muscle Atrophy and

In situ detection of activation of CAPN3 a responsible gene product

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Disruption of sAnk1 expression and localisation in CAPN3deficient

Calpain 3 Expression Pattern during Gastrocnemius Muscle Atrophy and

Gene expression profiling of Capn3deficient vs Capn3sufficient

Calpain3 Is Not a Sodium Dependent Protease and Simply Requires

The N and Cterminal autolytic fragments of CAPN3p94calpain3

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by

Tridimensional model of calpain3 protein showing the functional

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