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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

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

MC4R gene variants not linked to female hair loss.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Mutation in hairless gene may increase hair loss risk.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Certain gene variations increase the risk of alopecia areata in Koreans.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

The Shh gene controls cell growth and death in cashmere goat hair follicles, affecting hair growth.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

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.

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.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

A gene-based model predicts lung adenocarcinoma outcomes and helps guide treatment decisions.

A specific gene variation in goats is linked to better growth traits.

A specific gene variant may increase the risk of developing Alopecia Areata.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

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