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

Certain gene variations might be linked to severe acne in women but not in men.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

A new gene causes hairlessness and skin cysts in rats.

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

ESR2 gene linked to female-pattern hair loss.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The WIF1 gene is crucial for hair growth in Angora rabbits.