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

The effect of AMPD1 genotype on blood flow response to sprint exercise.

European journal of applied physiology - 1 May 2008

Norman Barbara, Nygren Anders T, Nowak Jacek, Sabina Richard L

Abstract excerpt

Inherited deficiency of skeletal muscle myoadenylate deaminase (mAMPD) is a genetic disorder characterized primarily by a 34C>T transition in exon 2 of the AMPD1 gene. mAMPD deficient individuals exhibit alterations in ATP catabolic flow, resulting in greater adenosine accumulation during high intensity exercise that may possibly enhance exercise-induced hyperaemia. This study tested the hypothesis that...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine
Share to AMP Deaminase
Share to Blood Flow Velocity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Exercise

Share to Femoral Artery

Share to Muscle Contraction

Share to Regional Blood Flow

Share to Running

Source

Identifiers

PMID: 18224333
DOI: 10.1007/s00421-008-0683-0

Genes

AMPD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The effect of AMPD1 genotype on blood flow response to sprint exercise.PMID 18224333Read ↗

AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects.Semantic proximity Read ↗

AMPD1 gene polymorphism and the vasodilatory response to ischemia.Semantic proximity Read ↗

AMPD1 genotypes and exercise capacity in McArdle patients.Semantic proximity Read ↗

Effects of AMPD1 common mutation on the metabolic-chronotropic relationship: Insights from patients with myoadenylate deaminase deficiency.Semantic proximity Read ↗

Regulation of skeletal muscle ATP catabolism by AMPD1 genotype during sprint exercise in asymptomatic subjects.Semantic proximity Read ↗

Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study.Semantic proximity Read ↗

Genetic and other determinants of AMP deaminase activity in healthy adult skeletal muscle.Semantic proximity Read ↗

Augmented hyperemia and reduced tissue injury in response to ischemia in subjects with the 34C > T variant of the AMPD1 geneSemantic proximity Read ↗

Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?Semantic proximity Read ↗

Frequency of the C34T mutation of the AMPD1 gene in world-class endurance athletes: does this mutation impair performance?Semantic proximity Read ↗

AMPD1 C34T Polymorphism (rs17602729) Is Not Associated with Post-Exercise Changes of Body Weight, Body Composition, and Biochemical Parameters in Caucasian Females.Semantic proximity Read ↗

Decreased cardiac activity of AMP deaminase in subjects with the AMPD1 mutation--a potential mechanism of protection in heart failure.Semantic proximity Read ↗

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