Cylindrical Crystallization of Ca

Jun Nakamura, Genichi Tajima, Makiko Suwa, Chikara Sato

Abstract readReview

In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it

0cells of the map it votes in

0citing papers in PubMed

–field-weighted citation impact

1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Jun NakamuraJun Nakamura Institute, Moniwa-dai 2-3-21, Taihaku-ku, Sendai-shi, Miyagi 982-0252, Japan.

Genichi TajimaInstitute for Excellence in Higher Education, Tohoku University, 41 Kawauchi, Aoba-ku, Sendai-shi, Miyagi 980-8576, Japan.

Makiko SuwaBiological Science Course, Graduate School of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuou-ku, Sagamihara-shi, Kanagawa 252-5258, Japan.

Chikara SatoBiological Science Course, Graduate School of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuou-ku, Sagamihara-shi, Kanagawa 252-5258, Japan.

Funding

Japan Society for the Promotion of Science KAKENHI 16K12630, 19K10091, 19H04209

6 · The paper itself

Abstract

How do ryanodine receptors (RyRs) open simultaneously to trigger the contraction of whole myofibrils within a large skeletal muscle cell? One possible answer is the uniformity of mechanosensitive RyRs, which is mechanically forced by the neighboring environment, including proteins. Here, we review papers addressing this proposed "mechanical sarcoplasmic reticulum (SR) paradigm". Crystals of the molecular complexes comprising RyR and L-type voltage-gated Ca

Indexed as

Calcium-Transporting ATPasesSarcoplasmic ReticulumAnimalsCalciumCrystallizationHumansMuscle, SkeletalRabbitsRyanodine Receptor Calcium Release ChannelCalciumCalcium-Transporting ATPasesRyanodine Receptor Calcium Release Channelcalcium traffickingexcitation-contraction couplingmuscle contractionorganelleprotein crystallizationryanodine receptorskeletal muscle

Identifiers

PMID42196294

DOI10.3390/ijms27104314

PMCPMC13207445

What OpenQuestion holds

Textmetadata

LicenceCC BY

Read underepoch 390

Registered trials

None linked

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.