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The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Some early COVID-19 mutations in patients predicted future common virus mutations.

ETS2 drives cancer progression in squamous cell carcinoma and is linked to poor patient outcomes.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Certain RNA molecules are important for the development of wool follicles in sheep.

Researchers created a new mouse model for studying scleroderma.

Scientists discovered two versions of a new human hair keratin gene.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A gene mutation in mice causes severe skin disorder similar to a human condition.

STIM1 is essential for sweat secretion.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Certain immune cells help hair growth by regulating iron in the skin.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

Removing the VDR gene in skin cells reduces their growth and affects hair-related genes.

Involucrin helps strengthen the inner parts of human hair.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Reducing IGF-1 can help rejuvenate hair follicles and prevent hair graying and loss.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Vitamin D receptor helps control hair growth genes in skin cells.

Mrp3 may aid in wound healing and hair growth.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

WIF1 helps keep skin stem cells inactive to prevent excessive cell growth.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.