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

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

Atorvastatin reversed memory problems caused by cancer drug trastuzumab and improved its cancer-fighting abilities without causing hair loss.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Jagged-1 in skin Tregs is crucial for timely wound healing by recruiting specific immune cells.

ABCG2 protein marks stem-like skin cells in human epidermis.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Claudin-1 is crucial for maintaining skin barrier and preventing inflammation.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new gene mutation causes insulin resistance in a girl and her mother.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

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

TLR3 activation helps improve skin and hair follicle healing in mice.

Immunocompromised patients can develop skin and hair issues due to a virus.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

MCHR2 gene duplications may be linked to alopecia areata.

Understanding cellular interactions in VCA may lead to better treatments and reduce rejection.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.

Vitamin D receptor is crucial for starting hair growth after birth.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.