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Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

Trps1 is essential for proper hair follicle development.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Key proteins and pathways regulate yak hair growth, with lipid metabolism aiding adaptation to high altitudes.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Epimorphin helps start hair growth in mice.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

ZPK helps skin cells mature and may affect skin health.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

PADs are crucial for healthy skin and hair, and their imbalance can cause skin and hair disorders.

The protein hairless is important for hair regrowth because it stops the protein wise from blocking the hair cycle.

A mix of Polygonatum sibiricum and Nelumbinis semen may ease menopause symptoms with fewer side effects.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

CUX1 boosts sheep hair cell growth and affects curl patterns.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

S100A6 is important for cell functions and can help diagnose and treat diseases.

Key proteins affecting cashmere fiber quality were identified for better breeding.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Neuropeptides affect skin inflammation, repair, and hair growth, with potential for therapy.

Keratin hydrogel improves nerve regeneration and motor recovery.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Vitamin B3 may help prevent hair loss and promote hair growth by protecting scalp cells from stress and reducing hair growth-blocking proteins.