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Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

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

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

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

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Hairless protein can block vitamin D activation in skin cells.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Most mouse hair keratin genes are on chromosomes 11 and 15.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

HPV-150 and HPV-151 are rare skin viruses linked to warts and some skin cancers.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Researchers found a gene mutation responsible for a rare hair loss condition.

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

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

VR1 signaling can inhibit hair growth by affecting cell processes and increasing hair growth inhibitors.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Family members have similar hair protein patterns, which could be useful for genetic studies.

The HCR gene contributes to psoriasis risk.

HPV type 56 can hide in hair follicles even without visible warts.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.