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Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Two peptides, RMYYY and VMYMI, may be effective anti-inflammatory drugs.

MPZL3 protein is important for controlling hair growth cycles.

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

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Frequent hairdryer use may worsen hair fragility in people with Pili Annulati.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

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

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Rac1 is crucial for normal hair structure and pigmentation.

The package offers tools for exploring potential miRNA changes in female hair loss.

Follistatin helps hair growth and cycling, while activin prevents it.

A hormone affects hair growth, certain molecules may prevent skin damage, a skin disease is linked to immune cells, glycerol helps skin hydration, and psoriasis treatment trials need improvement.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

SFRP2 and PTGDS may be key factors in female hair loss.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Hair follicle stem cells are a practical and ethical option for nerve repair in regenerative medicine.

Excessive sun protection might contribute to frontal fibrosing alopecia.

Elevated luteinizing hormone contributes to female-pattern hair loss, and blocking certain channels may help prevent it.