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The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

The research helps in creating genetically modified animals to study hair growth.

Unique genes in hair follicle cells help tissue regeneration.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

CXCR2 in skin cells promotes tumor growth.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Most mouse hair keratin genes are on chromosomes 11 and 15.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

RCDP NCs are promising anti-aging cosmetic ingredients that improve skin health by reducing oxidative stress and enhancing cell function.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A CCS patient with severe complications was successfully treated using combined therapies.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Certain hormone levels can help diagnose P450 oxidoreductase deficiency.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Ribonucleotide excision repair is crucial to prevent skin cancer.