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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

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

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

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

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

A specific gene mutation causes severe skin and nail issues and hair loss.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

ALRN-6924 may prevent hair loss caused by chemotherapy.