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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

New genetic mutations causing hair loss were found in a Chinese family.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Atoh1 expression can create new Merkel cells in the skin.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

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

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

MCHR2 gene duplications may be linked to alopecia areata.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Longer CAG repeats in gene linked to more severe hair loss in females.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

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

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.