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A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

A specific gene mutation causes a severe skin disorder in a family.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

The HCR gene contributes to psoriasis risk.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

p63 controls Satb1 to help skin develop properly.

Spermidine is essential for plant growth and adaptation to stress.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

The FOS gene helps hair growth in Tan sheep.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

Sex-determining genes may affect male baldness.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

WNT10A gene mutations cause short anagen hair syndrome.

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