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Dandruff scalps have unstable microbes, more Malassezia, less Cutibacterium, and targeting Lactobacillus may help.

The HPV type 11 region activates hair-specific gene expression in mice.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

FOXN1 gene variants cause low T cells and immune issues from birth.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

A rare gene variant causes hair and nail issues in a family.

Certain gene variations increase the risk of alopecia areata in Koreans.

A specific gene variant may increase the risk of developing Alopecia Areata.

Camellia japonica extract may improve scalp health and promote hair growth.

The MLPH gene is not linked to seasonal hair loss in Rhodesian Ridgeback dogs.

The SOSTDC1 gene is crucial for determining sheep wool type.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

The gene Prss53 affects hair shape and bone development in rabbits.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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