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The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Hoxc13 gene is essential for hair, nail, and papilla development.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

MPA increases cancer spread by boosting Eph A2 activity.

Severe CCCA may be biologically and clinically different from milder forms.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

The same gene mutation can cause different symptoms in family members.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Lack of functional CYLD in mice leads to early aging and cancer.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

TBX3 gene affects horse coat color, with higher expression in darker areas.

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

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Id2 gene helps keep hair follicle stem cells inactive.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

The E2 protein affects gene activity in hair follicles of mice.