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The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A mutation in mice causes hair loss and immune problems.

A genetic hair protein variant is more common in Japanese people and is inherited.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A new genetic mutation was found causing hair and eye issues in a boy.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

New mutations in the hairless gene may cause hair loss and affect bone development.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Ets2 gene is crucial for placental development in mice.

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

Ablative fractional laser treatment nearly matches the gene reduction effects of topical vismodegib in skin cancer.

Copper supplements during pregnancy improve survival and development in mutant mice.

Somatic BHD mutations are rare in Japanese renal tumors.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

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

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

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

Mice with extra sheep genes had hair that fell out and regrew in cycles.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.