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

Heterogeneous expression of hydrocephalic phenotype in the hyh mice carrying a point mutation in alpha-SNAP.

Neurobiology of disease - 1 Jul 2006

Bátiz Luis Federico, Páez Patricia, Jiménez Antonio J, Rodríguez Sara, Wagner Carolina, Pérez-Fígares José Manuel, Rodríguez Esteban Martín

Abstract excerpt

The hyh mouse carrying a point mutation in the gene encoding for soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein alpha (alpha-SNAP) develops inherited hydrocephalus. The investigation was designed to study: (i) the clinical evolution of hyh mice; (ii) factors other than the alp...

Read the complete abstract on PubMed

Topics

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

Share to Hydrocephalus
Share to Immunohistochemistry
Share to Maternal Age

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mice, Mutant Strains

Share to Microscopy, Electron, Scanning

Share to Parity

Share to Point Mutation

Share to Sex Factors

Source

Identifiers

PMID: 16697210
DOI: 10.1016/j.nbd.2006.02.009

Genes

NSF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16697210-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Heterogeneous expression of hydrocephalic phenotype in the hyh mice carrying a point mutation in alpha-SNAP.PMID 16697210Read ↗

The gene for soluble N-ethylmaleimide sensitive factor attachment protein alpha is mutated in hydrocephaly with hop gait (hyh) mice.Semantic proximity Read ↗

A simple PCR-based genotyping method for M105I mutation of alpha-SNAP enhances the study of early pathological changes in hyh phenotype.Semantic proximity Read ↗

Hydrocephalus in the H-Tx rat: a monogenic disease?Semantic proximity Read ↗

The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fate.Semantic proximity Read ↗

Spontaneous congenital hydrocephalus in the mutant mouse hyh. Changes in the ventricular system and the subcommissural organ.Semantic proximity Read ↗

Chromosomal linkage associated with disease severity in the hydrocephalic H-Tx rat.Semantic proximity Read ↗

Analysis of cerebellum proteomics in the hydrocephalic H-Tx rat.Semantic proximity Read ↗

Hemorrhagic hydrocephalus (hhy): a novel mutation on mouse chromosome 12.Semantic proximity Read ↗

Multigenic factors associated with a hydrocephalus-like phenotype found in inter-subspecific consomic mouse strains.Semantic proximity Read ↗

Experimental models of congenital hydrocephalus and comparable clinical problems in the fetal and neonatal periods.Semantic proximity Read ↗

Neurons lacking huntingtin differentially colonize brain and survive in chimeric mice.Semantic proximity Read ↗

Aquaporin-4 Mediates Permanent Brain Alterations in a Mouse Model of Hypoxia-Aged Hydrocephalus.Semantic proximity Read ↗

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