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The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Hair loss gene found on chromosome 3q26.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A new gene mutation causes a rare type of hair loss.

Centipedegrass extract may promote hair growth by activating certain cell pathways.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Researchers found a gene mutation responsible for a rare hair loss condition.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

A genetic variant in goats is linked to cashmere growth.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

CGF treatment effectively and safely improves hair loss in androgenic alopecia patients.

SCUBE3 is a potential target for cancer and alopecia treatment but is challenging to target due to its varied roles.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A specific gene mutation causes long hair in Angora rabbits.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.