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The fuzzy gene is crucial for controlling hair growth cycles.

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

A new compound that could treat various androgen-related conditions was created and analyzed.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Keratin 15 helps keep skin cells in a young, undifferentiated state.

Phosphatidylinositol 4-kinases are crucial for root growth, defense, and immunity in Arabidopsis thaliana.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

The correction does not change the study's main findings.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

HDAC1 is crucial for skin development and preventing tumors.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Hairless protein can block vitamin D activation in skin cells.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

IL-15 helps maintain hair growth and protects the immune status of hair follicles.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

A specific gene mutation causes congenital hair loss.

LIPH mutations cause woolly hair in some Chinese people.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.