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Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

FLCN helps control iron levels in cells.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

BAF200 is essential for proper heart and coronary artery formation.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

A gene mutation causes monilethrix in a Chinese family.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

CD2 might be a new treatment target for patchy alopecia areata.

The gene HDC is important for the development of hair follicles in newborn mice.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.