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Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Recognizing trichofolliculomas is important to avoid unnecessary surgery.

Researchers developed a method to create artificial hair follicles that may help with hair loss treatment and research.

Rac1 is crucial for normal hair structure and pigmentation.

A 47-year-old man was diagnosed with a specific type of hair loss and advised to use certain medications and avoid hair transplants.

Nevus psiloliparus lacks mature hair follicles but keeps other skin structures intact.

Overexpressing follistatin in mice delays wound healing and reduces scar size.

Apoptotic cells may trigger cell death in hair follicles during their regression cycle.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Overactive Wnt5a disrupts hair follicle orientation in mice.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Wnt and SHH pathways help form hair follicles by coordinating cell processes.

Certain gene variations may increase the risk and severity of alopecia areata.

Activating β-catenin can turn skin cells into hair follicles.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A man in his 30s had patchy hair loss on his leg due to primary follicular mucinosis.

ODC transgenic mice can model human hair loss with skin lesions.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

A woman's male-like physical changes were caused by two rare ovarian conditions.

A genetic variant in goats is linked to cashmere growth.

The p53 protein helps control hair follicle shrinking by promoting cell death in mice.