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Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

Mutations in the KRT85 gene cause hair and nail problems.

Blocking a specific protein signal can make hair grow on mouse nipples.

Long-term minoxidil use can cause pseudoacromegaly, but stopping it improves symptoms.

Aging alone rarely causes significant hair loss; hormones are a bigger factor.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Wnt/ß-catenin signaling is crucial for regulating skin stem cells and hair growth, with the right levels and timing needed for proper function.

Dental erosion is common in adolescents and is linked to diet and higher socioeconomic status.

Platelet-rich plasma treatment for non-scarring hair loss shows mixed results and needs more research.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

NFIC helps human dental stem cells grow and become tooth-like cells.

Light microscopy is useful for diagnosing different hair disorders.

Tigason improved hair growth in a boy with monilethrix without side effects.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Higher fluoride levels may delay puberty in boys.

Whale genes show changes that help them live in water, like less hair and better flippers.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

Researchers found a new mutation causing total hair loss from birth.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Nanotechnology improves cosmetics' effectiveness and safety.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Grouping certain skin cells together activates a growth pathway that helps create new hair follicles.

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

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Substances from dental stem cells might help treat hair loss.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.