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ALRN-6924 may prevent hair loss caused by chemotherapy.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Ptprq has multiple forms that change during inner ear development.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

The type 3 IP3 receptor is important for controlling hair loss and growth.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

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

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Targeting immune pathways like JAK/STAT may help treat frontal fibrosing alopecia.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Certain peptides can prevent hair loss in young rats caused by a cancer drug.

HB24 helps convert IBA to IAA, promoting root hair growth.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Mutations in the hairless protein gene cause hair loss.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

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

Kidney cancer cells without folliculin are more sensitive to radiation due to increased self-eating cell death.

AgK114 protein helps in hamster skin injury recovery.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

A peptide from hair follicle stem cells can boost hair growth.