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Activins and follistatins, part of the TGFβ family, are crucial for hair follicle development and skin health, affecting growth, repair, and the hair cycle.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

Follistatin helps hair growth and cycling, while activin prevents it.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Targeting colon cancer stem cells might lead to better treatment results.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Pannexin 3 is important for bone formation and the development of bone cells.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

PRP treatment increased hair density, especially in men and younger patients with AGA.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Effective PCOS treatments require targeting specific signaling pathways.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The research identified key proteins and genes that may influence wool bending in goats.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Higher sebum levels are linked to more severe male baldness.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Minoxidil improved hair growth in a child with a rare genetic disorder.