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PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

CDP is crucial for lung and hair follicle cell development.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Certain IL-18 gene variations may increase the risk of alopecia areata.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Certain gene variations are linked to the thickness of cashmere goat hair.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

SGK3 is essential for proper hair growth and health.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

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

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Minoxidil can reduce functions related to androgen receptors.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.