Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Structure and function of Ca2+ pump and diseases caused by its gene mutations].

Seikagaku. The Journal of Japanese Biochemical Society - 1 Sept 2003

Suzuki Hiroshi

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Biological Transport
Share to Calcium
Share to Calcium-Transporting ATPases
Share to Darier Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Isoenzymes

Share to Protein Conformation

Share to Protein Structure, Tertiary

Share to Sarcoplasmic Reticulum

Source

Identifiers

PMID: 14577351

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Structure and function of Ca2+ pump and diseases caused by its gene mutations].PMID 14577351Read ↗

[Cellular calcium ion signalling--from basic research to benefits for patients].Semantic proximity Read ↗

Role of Ca2+ in healthy and pathologic cardiac function: from normal excitation-contraction coupling to mutations that cause inherited arrhythmia.Semantic proximity Read ↗

[Intracellular calcium: physiology and physiopathology].Semantic proximity Read ↗

When calcium goes wrong: genetic alterations of a ubiquitous signaling route.Semantic proximity Read ↗

A Ca(2+)-sensing receptor: from physiology to inherited disorders of calcium homeostasis.Semantic proximity Read ↗

[Mechanism of ca(2+) pump as revealed by mutations, development of stable analogs of phosphorylated intermediates, and their structural analyses].Semantic proximity Read ↗

Disease causing mutations of calcium channels.Semantic proximity Read ↗

Arrhythmia-associated cardiac Ca²(+) cycling proteins and gene mutations.Semantic proximity Read ↗

Structure/function analysis of the Ca2+ binding and translocation domain of SERCA1 and the role in Brody disease of the ATP2A1 gene encoding SERCA1.Semantic proximity Read ↗

Calcium channelopathies.Semantic proximity Read ↗

[Calcium channel mutations and disorders of synaptic transmission].Semantic proximity Read ↗

[Diseases caused by disorders of membrane transport: an overview].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.