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Sebaceous glands are often preserved and PPARy expression is constant in some cases of Central Centrifugal Cicatricial Alopecia.

A new tool accurately identifies human cornea cell states and key factors.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

A young woman with severe symptoms of CPAN improved with intensive treatment but needed a leg amputation.

The CuCS/Cur wound dressing helps regenerate nerves and heal deep skin burns by rebuilding hair follicles.

Basal cell carcinomas need extra mutations to grow from small to large tumors.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

MPA increases cancer spread by boosting Eph A2 activity.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Dynlt3 is important for melanosome transport and skin coloration.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

Laminin-511 is essential for proper melanocyte movement and development in mice.

WNT signaling is crucial for starting mammary gland development.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

A scale was made to measure hair loss severity in African American women.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.