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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

The ZmNF-YC1–ZmAPRG pathway in maize improves phosphorus efficiency and grain yield, suggesting it as a target for breeding better crops.

Food deprivation increases MST enzyme in the brain, possibly affecting energy balance.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

CCC1 is essential for ion balance and proper plant cell function.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Low androgen levels can still cause female pattern hair loss.

Researchers developed a method to create artificial hair follicles that may help with hair loss treatment and research.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Autophagy helps activate hair stem cells and hair growth by changing their energy use to glycolysis.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.

ROXY proteins help plants respond to nitrate shortage by affecting nutrient sensing and growth.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

PADI4 enzyme slows down cell growth in developing hair follicles.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

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

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Rushton's hyaline bodies form from hair keratin and blood substances.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Two new gene mutations cause a rare hair disorder.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Hexahydrobenzo[f]quinolines are effective at blocking the enzyme 5α-reductase.