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

Mutational analysis of BFSP1, CRYBB1, GALK1, and GJA8 in captive-bred vervet monkeys (Chlorocebus aethiops).

Journal of medical primatology - 1 Apr 2020

Ngqaneka Thobile, Khoza Sanele, Magwebu Zandisiwe E, Chauke Chesa G

Abstract excerpt

BACKGROUND: Congenital cataract has been reported in a colony of captive-bred vervet monkeys (Chlorocebus aethiops). METHODS: Molecular tools such as genotyping and gene expression were used to identify mutations associated with congenital cataract in this vervet colony. Beaded filament structural protein 1 (BFSP1), beta-crystallin B1 (CRYBB1), galactokinase1 (GALK1), and gap junction alpha-8 protein (GJA8) were...

Read the complete abstract on PubMed

Topics

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

Share to Cataract
Share to Chlorocebus aethiops
Share to Eye Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Monkey Diseases

Share to Mutation

Source

Identifiers

PMID: 31975409
DOI: 10.1111/jmp.12455

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutational analysis of BFSP1, CRYBB1, GALK1, and GJA8 in captive-bred vervet monkeys (Chlorocebus aethiops).PMID 31975409Read ↗

Variants of BEST1 and CRYBB2 cause a complex ocular phenotype comprising microphthalmia, microcornea, cataract, and vitelliform macular dystrophy: case report.Semantic proximity Read ↗

Molecular and structural analysis of genetic variations in congenital cataract.Semantic proximity Read ↗

Mutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2.Semantic proximity Read ↗

Autosomal recessive juvenile onset cataract associated with mutation in BFSP1.Semantic proximity Read ↗

Crystallin gene mutations in Indian families with inherited pediatric cataract.Semantic proximity Read ↗

A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.Semantic proximity Read ↗

FYCO1 Frameshift Deletion in Wirehaired Pointing Griffon Dogs with Juvenile Cataract.Semantic proximity Read ↗

A novel beaded filament structural protein 1 (BFSP1) gene mutation associated with autosomal dominant congenital cataract in a Chinese family.Semantic proximity Read ↗

Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts.Semantic proximity Read ↗

Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract.Semantic proximity Read ↗

A novel p.G112E mutation in BFSP2 associated with autosomal dominant pulverulent cataract with sutural opacities.Semantic proximity Read ↗

CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle.Semantic proximity Read ↗

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