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The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

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

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Researchers found a gene mutation responsible for a rare hair loss condition.

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.

MPZL3 protein affects hair growth cycles and could help manage hair loss.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Blocking certain immune signals can reduce skin damage from radiation therapy.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A specific gene change is linked to severe hair loss.

Variation in the TCHH gene affects wool curliness in sheep.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

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

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

A genetic variant linked to hair thinning in Japanese women was found.