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

Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome.

The Journal of steroid biochemistry and molecular biology - 1 Apr 1997

Bevan C L, Hughes I A, Patterson M N

Abstract excerpt

Androgen insensitivity syndrome (AIS) is a disorder of male sexual differentiation caused by mutations in the androgen receptor (AR) gene. The partial form (PAIS), associated with varying degrees of receptor dysfunction, presents with a range of undervirilization phenotypes. The complete form (CAIS) is characterized by normal female external appearance at birth. In these cases the receptor is often absent or...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to HeLa Cells
Share to Kinetics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Molecular Sequence Data

Share to Mutation

Share to Recombinant Fusion Proteins

Share to Sequence Alignment

Share to Transcriptional Activation

Source

Identifiers

PMID: 9328206
DOI: 10.1016/s0960-0760(97)00001-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome.PMID 9328206Read ↗

Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome.Semantic proximity Read ↗

Characterization of mutant androgen receptors causing partial androgen insensitivity syndrome.Semantic proximity Read ↗

Molecular defects of the androgen receptor.Semantic proximity Read ↗

Androgen receptor abnormalities.Semantic proximity Read ↗

Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome.Semantic proximity Read ↗

Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity.Semantic proximity Read ↗

Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.Semantic proximity Read ↗

Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.Semantic proximity Read ↗

Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.Semantic proximity Read ↗

In-vitro characterization of androgen receptor mutations associated with complete androgen insensitivity syndrome reveals distinct functional deficits.Semantic proximity Read ↗

Comparison of the molecular consequences of different mutations at residue 754 and 690 of the androgen receptor (AR) and androgen insensitivity syndrome (AIS) phenotype.Semantic proximity Read ↗

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome.Semantic proximity Read ↗

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