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Merremia peltata leaf extract, particularly the bufotalinin compound, shows potential for treating hair loss.

PCE-DP brightens skin and promotes hair growth by enhancing cell growth and reducing melanin uptake.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

p63 controls Satb1 to help skin develop properly.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

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

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Immunotherapy with pembrolizumab significantly reduced cancer in a young woman with adrenocortical carcinoma.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Certain blood miRNAs are linked to severe alopecia areata and could lead to new treatments.

Four antibodies were developed to help study hair follicle cell differentiation.

The bar-cartridge type implanter is the best for implanting dermal papilla cells efficiently and at controlled depths.

A new easy-to-use biosensor was made to detect androgen receptor mRNA, which could help diagnose related conditions quickly.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Different levels of microRNAs in different parts of the scalp can cause male pattern baldness.

MK-5108 is safe and shows potential against tumors, especially alone.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

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A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.