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Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

MCHR2 gene duplications may be linked to alopecia areata.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

TAK-279 effectively reduces psoriasis symptoms and is safe.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

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

Certain gene variations are linked to the thickness of cashmere goat hair.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Certain gene variations might be linked to severe acne in women but not in men.

MOF controls skin development by regulating genes for mitochondria and cilia.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A new test using NOS2 and CCL27 genes can better diagnose and treat psoriasis and eczema.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

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

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

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Samcyprone ointment is effective for treating common warts if a sensitization reaction occurs first.