ArticleJournal of muscle research and cell motility1993
Postnatal development of rabbit fast-twitch skeletal muscle: accumulation, isoform transition and fibre distribution of calsequestrin.
Article in Journal of muscle research and cell motility, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
21 citing papers in PubMed, 40 citations in OpenAlex.
- Article
- Single-cell RNAseq provides insight into altered immune cell populations in human fracture nonunions.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023Article
- Constitutive assembly of Ca2+ entry units in soleus muscle from calsequestrin knockout mice.The Journal of general physiology · 2022Article
- Ablation of Calsequestrin-1, CaFrontiers in physiology · 2022Review
- Calsequestrin, a key protein in striated muscle health and disease.Journal of muscle research and cell motility · 2021Review
- Calcium entry units (CEUs): perspectives in skeletal muscle function and disease.Journal of muscle research and cell motility · 2021Article
- Calsequestrin: a well-known but curious protein in skeletal muscle.Experimental & molecular medicine · 2020Review
- Gene Expression Profiling in Slow-Type Calf Soleus Muscle of 30 Days Space-Flown Mice.PloS one · 2017Article
- Characterization of fast-twitch and slow-twitch skeletal muscles of calsequestrin 2 (CASQ2)-knock out mice: unexpected adaptive changes of fast-twitch muscles only.Journal of muscle research and cell motility · 2016Article
- Oxidative stress, mitochondrial damage, and cores in muscle from calsequestrin-1 knockout mice.Skeletal muscle · 2015Article
- Lessons from calsequestrin-1 ablation in vivo: much more than a Ca(2+) buffer after all.Journal of muscle research and cell motility · 2011Article
- Differential effect of calsequestrin ablation on structure and function of fast and slow skeletal muscle fibers.Journal of biomedicine & biotechnology · 2011Article
- Massive alterations of sarcoplasmic reticulum free calcium in skeletal muscle fibers lacking calsequestrin revealed by a genetically encoded probe.Proceedings of the National Academy of Sciences of the United States of America · 2010Article
- Deconstructing calsequestrin. Complex buffering in the calcium store of skeletal muscle.The Journal of physiology · 2009Review
- Anesthetic- and heat-induced sudden death in calsequestrin-1-knockout mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009Article
- A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.The American journal of pathology · 2009Article
- Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin-1.The Journal of physiology · 2007Article
- Post-natal developmental expression of alphaKAP splice variants in rabbit fast-twitch and slow-twitch skeletal muscle.Journal of muscle research and cell motility · 2004Article
- Interaction of triadin with histidine-rich Ca(2+)-binding protein at the triadic junction in skeletal muscle fibers.Journal of muscle research and cell motility · 1999Article
- Differential response of the membrane systems involved in excitation-contraction coupling to early and later postnatal denervation in rat skeletal muscle.Journal of muscle research and cell motility · 1999Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
The time-course of disappearance of slow-cardiac calsequestrin (CS) and that of appearance of the skeletal CS isoform were investigated in developing fast-twitch skeletal muscle of the rabbit between postnatal days 1 and 60, along with changes in density of the ryanodine receptor (RyR)/Ca2+ release channel. Western blot data on skeletal muscle membranes, purification of two CS isoforms by phenyl-Sepharose chromatography, and their immunolocalization in muscle fibres, all show that both CS isoforms are coexpressed in neonatal muscles. Our results, at the protein level, indicate that the turning off of synthesis of cardiac CS and its total disappearance from fast-twitch fibres take place at critical periods between two and four weeks postnatally, i.e. past changes in the respective mRNA. In contrast, the accumulation in muscle membranes of both the RyR and the skeletal CS isoform proceeds steadily up to one month, to reach adult values at about two months of age. These findings seem to argue that myogenic factors, in addition to the morphogenetic influence on the sarcoplasmic reticulum from the neural input to the muscle, may be involved in the developmental transition of CS isoforms in mammalian fast-twitch muscle fibres.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.