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

Mutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.

American journal of respiratory cell and molecular biology - 1 Mar 2009

Fernandez-Gonzalez Angeles, Kourembanas Stella, Wyatt Todd A, Mitsialis S Alex

Abstract excerpt

Primary ciliary dyskinesia (PCD) is a genetically and phenotypically heterogeneous disorder, characterized by progressive development of bronchiectasis, inflammation, and features characteristic of chronic obstructive pulmonary disease. We report here that a murine mutation of the evolutionarily...

Read the complete abstract on PubMed

Topics

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

Share to Adenylate Kinase
Share to Cilia
Share to Frameshift Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kartagener Syndrome

Share to Ovalbumin

Share to Respiratory Mucosa

Share to Tissue Distribution

Share to Transgenes

Source

Open in PubMed Open full text

Identifiers

PMID: 18776131
DOI: 10.1165/rcmb.2008-0102OC
PMCID: PMC2645528

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18776131-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.PMID 18776131Read ↗

Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesiaSemantic proximity Read ↗

Novel centriolar defects underlie a primary ciliary dyskinesia phenotype in an adenylate kinase 7 deficient ciliated epitheliumSemantic proximity Read ↗

Centriolar defects underlie a primary ciliary dyskinesia phenotype in an adenylate kinase 7 deficient ciliated epithelium.Semantic proximity Read ↗

New adenylate kinase 7 (AK7) mutation in primary ciliary dyskinesia.Semantic proximity Read ↗

Restoring Ciliary Function: Gene Therapeutics for Primary Ciliary DyskinesiaSemantic proximity Read ↗

Chronic airway disease in primary ciliary dyskinesia-spiced with geno-phenotype associations.Semantic proximity Read ↗

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice.Semantic proximity Read ↗

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalusSemantic proximity Read ↗

A human ciliopathy reveals essential functions for NEK10 in airway mucociliary clearance.Semantic proximity Read ↗

Airway ciliary microenvironment responses in mice with primary ciliary dyskinesia and central pair apparatus defects.Semantic proximity Read ↗

Semi-Lethal Primary Ciliary Dyskinesia in Rats Lacking the Nme7 Gene.Semantic proximity Read ↗

Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD.Semantic proximity Read ↗

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