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

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

Overexpression of HDGF in melanocytes does not cause cancer.

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

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

Using both TGA and DTDG in hair straightening reduces hair damage compared to using TGA alone.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

2-iminothiorane hydrochloride improves hair waving permanence without damage.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

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

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

LHX2, with other markers, can identify hair placodes in rats.

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

Dihydrotestosterone specifically binds to hamster sebaceous glands, with a higher affinity than testosterone.

TGF-β2 plays a key role in human hair growth and development.

Activating ALDH2 can boost hair growth.