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A new DSG4 gene mutation causes hair defects in a young girl.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

BTNL2 helps protect hair follicles from immune attacks.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Specific gene variants affect wool traits in Chinese Tan sheep.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

The scraggly mutation causes hair loss and skin defects in mice.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

CDP is crucial for lung and hair follicle cell development.

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

The agouti gene may help understand and treat obesity.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

Specific genes influence hair and cashmere growth in Laiwu black goats.

A genetic variant in the KRT25 gene causes tightly curled hair.

New genes and pathways are important for testosterone production and male sexual development.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Immune cells boost stem cell activity in hairy moles, causing more hair growth.