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hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

Using CD123 to detect certain immune cells helps diagnose a type of hair loss condition.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Hair follicle stem cell exosomes help nerve regeneration.

Neuregulin3 affects cell development in the skin and mammary glands.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

CTHRC1 helps hair grow back, and plantar dermis mixture boosts it.

High doses of nandrolone decanoate disrupt ovarian hormones and receptors in rats, with recovery only at lower doses and longer recovery times.

miR-214-3p helps nerve repair and recovery.

Neurons from hair follicles can help repair damaged nerves.

The document concludes that central centrifugal cicatricial alopecia (CCCA) should be considered in African American men with vertex hair loss and scalp symptoms, and that prompt diagnosis and treatment can slow disease progression.

Early diagnosis with trichoscopy can improve management and quality of life for CCCA patients.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Black women with CCCA are more likely to have uterine fibroids.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Most patients with Central Centrifugal Cicatricial Alopecia at the reviewed institution were middle-aged Black women, often with no symptoms, and commonly treated with topical medications.

3D models from confocal microscopy improve melanoma detection on sun-damaged skin.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

A new genetic mutation was found causing hair and eye issues in a boy.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Calcium signaling in skin cells is crucial for communication and regeneration.

Hair follicle stem cell exosomes help nerve regeneration.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.