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

CITED2 mutations potentially cause idiopathic premature ovarian failure.

Translational research : the journal of laboratory and clinical medicine - 1 Nov 2012

Fonseca Dora Janeth, Ojeda Diego, Lakhal Besma, Braham Rim, Eggers Stefanie, Turbitt Erin, White Stefan, Grover Sonia, Warne Garry, Zacharin Margaret, Nevin Lam Alexandra, Landolsi Hanène, Elghezal Hatem, Saâd Ali, Restrepo Carlos Martín, Fellous Marc, Sinclair Andrew, Koopman Peter, Laissue Paul

Abstract excerpt

Anomalies in gonadal development in a mouse knockout model of Cited2 have been recently described. In Cited2(-/-) female gonads, an ectopic cell migration was observed and the female program of sex determination was transiently delayed. We hypothesize that, in humans, this temporary inhibition of...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Primary Ovarian Insufficiency

Share to Repressor Proteins

Share to Trans-Activators

Source

Identifiers

PMID: 22709740
DOI: 10.1016/j.trsl.2012.05.006

Genes

CITED2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22709740-2026-09-04.2. 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

CITED2 mutations potentially cause idiopathic premature ovarian failure.PMID 22709740Read ↗

Novel WEE2 gene variants identified in patients with fertilization failure and female infertilitySemantic proximity Read ↗

Rare variants in FANCA induce premature ovarian insufficiencySemantic proximity Read ↗

Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity?Semantic proximity Read ↗

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.Semantic proximity Read ↗

[Homozygous Variant of FANCM of the Fanconi Anemia Pathway Causes Premature Ovarian Insufficiency: Investigation of the Pathogenic Mechanism].Semantic proximity Read ↗

Genetic Etiologic Analysis in 74 Chinese Han Women with Idiopathic Premature Ovarian Insufficiency by Combined Molecular Genetic TestingSemantic proximity Read ↗

Heterozygous FMN2 Missense Variant Found in A Family Case of Premature Ovarian InsufficiencySemantic proximity Read ↗

Homozygous variants in SYCP2L cause premature ovarian insufficiency.Semantic proximity Read ↗

Identification of novel mutations in FOXL2 associated with premature ovarian failure.Semantic proximity Read ↗

Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort.Semantic proximity Read ↗

Effects of a mutation in the transmembrane and coiled-coil domains 2 gene on ovarian function and reproductive aging.Semantic proximity Read ↗

A Novel Homozygous Missense Mutation of WEE2 Causes Female Infertility Characterized by Fertilization FailureSemantic proximity Read ↗

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