Results 31 to 40 of about 2,650 (160)

Characterization of the Goose CAPN3 Gene and its Expression Pattern in Muscle Tissues of Sichuan White Geese at Different Growth Stages

open access: yesThe Journal of Poultry Science, 2018
Calpain 3 (CAPN3), also known as p94, is associated with multiple production traits in domestic animals. However, the molecular characteristics of the CAPN3 gene and its expression profile in goose tissues have not been reported.
Hengyong Xu   +8 more
doaj   +1 more source

CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review)

open access: yesInternational Journal of Molecular Medicine, 2021
Calpains are a family of Ca2+‑dependent cysteine proteases that participate in various cellular processes. Calpain 3 (CAPN3) is a classical calpain with unique N‑terminus and insertion sequence 1 and 2 domains that confer characteristics such as rapid autolysis, Ca2+‑independent activation and Na+ activation of the protease.
Chen, Lin   +5 more
openaire   +3 more sources

A case of pseudodominant inheritance of limb-girdle muscular dystrophy caused by mutations in the CAPN3 gene

open access: yesАнналы клинической и экспериментальной неврологии, 2021
Introduction. Limb-girdle muscular dystrophy (LGMD) includes more than 30 forms caused by mutations in genes located on autosomes. The most common form is calpain-3-related LGMD, with autosomal recessive inheritance pattern (OMIM 253600).
Inna V. Sharkova   +4 more
doaj   +1 more source

An eccentric calpain, CAPN3/p94/calpain-3

open access: yesBiochimie, 2016
Calpains are Ca(2+)-regulated proteolytic enzymes that are involved in a variety of biological phenomena. Calpains process substrates by limited proteolysis to modulate various protein functions in the cell, and are thus called "modulator proteases." CAPN3, previously called p94 or calpain-3, has unique features that are not found in any of the other ...
Ono, Yasuko   +4 more
openaire   +2 more sources

PLEIAD/SIMC1/C5orf25, a Novel Autolysis Regulator for a Skeletal-Muscle-Specific Calpain, CAPN3, Scaffolds a CAPN3 Substrate, CTBP1

open access: yesJournal of Molecular Biology, 2013
CAPN3/p94/calpain-3 is a skeletal-muscle-specific member of the calpain protease family. Multiple muscle cell functions have been reported for CAPN3, and mutations in this protease cause limb-girdle muscular dystrophy type 2A. Little is known about the molecular mechanisms that allow CAPN3 to be so multifunctional. One hypothesis is that the very rapid
Ono, Yasuko   +7 more
openaire   +2 more sources

Treg cells retain stable lineage commitment during pregnancy in mice after late gestation inflammatory challenge. [PDF]

open access: yesImmunol Cell Biol
In this study, we used Foxp3‐fatemapping mice to examine the cell lineage stability of Treg cells in pregnancy. Ex‐Foxp3 cells were identified in gestational tissues. However, Treg cells retained lineage stability with no increased ex‐Foxp3 generation, regardless of inflammatory challenges that induce preterm birth.
Foyle KL   +6 more
europepmc   +2 more sources

CRISPR/Cas9 Genome Editing in LGMD2A/R1 Patient-Derived Induced Pluripotent Stem and Skeletal Muscle Progenitor Cells

open access: yesStem Cells International, 2023
Large numbers of Calpain 3 (CAPN3) mutations cause recessive forms of limb-girdle muscular dystrophy (LGMD2A/LGMDR1) with selective atrophy of the proximal limb muscles.
Lampros Mavrommatis   +9 more
doaj   +1 more source

Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations

open access: yesYonsei Medical Journal, 2016
This study was designed to investigate the characteristics of Korean patients with calpainopathy.Thirteen patients from ten unrelated families were diagnosed with calpainopathy via direct or targeted sequencing of the CAPN3 gene. Clinical, mutational, and pathological spectra were then analyzed.Nine different mutations, including four novel mutations ...
Park, Hyung Jun   +10 more
openaire   +3 more sources

Impaired regeneration in calpain-3 null muscle is associated with perturbations in mTORC1 signaling and defective mitochondrial biogenesis

open access: yesSkeletal Muscle, 2017
Background Previous studies in patients with limb-girdle muscular dystrophy type 2A (LGMD2A) have suggested that calpain-3 (CAPN3) mutations result in aberrant regeneration in muscle.
Mehmet E. Yalvac   +9 more
doaj   +1 more source

A New Insight into the Role of Calpains in Post-mortem Meat Tenderization in Domestic Animals: A review [PDF]

open access: yesAsian-Australasian Journal of Animal Sciences, 2013
Tenderness is the most important meat quality trait, which is determined by intracellular environment and extracellular matrix. Particularly, specific protein degradation and protein modification can disrupt the architecture and integrity of muscle cells
Ting Lian, Linjie Wang, Yiping Liu
doaj   +1 more source

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