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Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

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

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

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

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

A specific gene mutation causes congenital hair loss.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A gene called BMAL1 plays a role in controlling hair growth.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Gene linked to common hair loss found, may lead to new treatments.

AP-2α and AP-2β are crucial for healthy skin and hair.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

New genes linked to male pattern baldness were found on chromosome 20p11.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

A mutation in mice causes hair loss and immune problems.