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DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

New treatments targeting specific genes show promise for treating keratin disorders.

Mutations in the Whn gene affect hair keratin gene expression differently.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Excess vitamin A causes lasting gland changes in mouse hair follicles.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A specific gene mutation causes sparse, brittle hair in a family.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Hirosaki hairless rats have sparse, twisted hair due to missing hair keratin genes.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Mutations in keratin genes cause skin, hair, and nail disorders, with future treatments possible.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

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

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.