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A new DSG4 gene mutation causes hair defects in a young girl.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

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

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

AKN might be a skin marker for metabolic syndrome.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

ILC1-like cells may contribute to hair loss in alopecia areata.

Diphencyprone treatment increases CD8 lymphocytes in the scalp, which is associated with hair regrowth in alopecia areata patients.

ABCG2 protein marks stem-like skin cells in human epidermis.

A genetic marker linked to a type of hair loss was found in most patients studied.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.