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Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

The study aims to create a model to predict health attributes using diverse health data from Japanese adults.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

Dutasteride effectively treats benign prostatic hyperplasia and may reduce prostate cancer risk.

Genetic variations contribute to over 10% of recurrent early pregnancy loss cases.

Gonadal biopsy is the best method to diagnose gonadal dysgenesis.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

FGF13 gene changes cause excessive hair growth in a rare condition.

Chromosomal differences affect how muscle cells respond to testosterone.

Human dermal fibroblasts help microvascular endothelial cells grow, but not vice versa.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Childhood growth hormone deficiency can be accurately diagnosed using gene expression data and random forest analysis.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

A new method shows promise for regenerating hair follicles to treat hair loss.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Cell processes depend on time-of-day and protein complex flexibility for skin health.

Black holes with primary Proca hair can have unique shadows with inner rings, affecting how we observe them.