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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

FER and TOR signaling help root hair growth in low temperature and low nitrate conditions.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A genetic variant in goats is linked to cashmere growth.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

CCL5 is important for the hair growth potential of human dermal papilla cells.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

A new mouse mutation causes skin and hair defects due to a gene change.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Human hair follicles have a scent receptor that can influence hair growth.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Targeting ornithine decarboxylase can help prevent skin cancer.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A missing mK6irs1 gene causes hair loss in mice.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

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

A mutation in the KRT25 gene causes woolly hair and hair loss.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

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

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

A new gene mutation linked to a skin condition was found in a Spanish family.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.