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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Some breast cancer treatments cause hair loss similar to male pattern baldness, which can be improved with minoxidil.

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

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Blocking mTORC1 reduces skin tumor growth in mice.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

Mice with human skin protein K8 had more skin problems and cancer.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A genetic variant in the KRT25 gene causes tightly curled hair.

Blocking DPP4 can potentially speed up hair growth and regeneration, especially after injury or in cases of hair loss.

Circ 0020938 slows down hair growth in cashmere goats.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The Foxn1 gene is essential for normal nail and hair development.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Dynlt3 is important for melanosome transport and skin coloration.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

RIPK1 inhibitors might help prevent alopecia areata.

Disrupting Bcl-xL in mice reduces skin cancer risk.

Iron deficiency in mothers causes hair loss in their baby mice.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.