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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Rizatriptan benzoate-loaded dissolving microneedles are effective and convenient for treating acute migraines.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

NF-κB activity is crucial for keeping hair in the growth phase.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

Valproic acid and crocin together boost cell growth and may help treat nerve injuries.

The HR protein's role as a repressor is essential for controlling hair growth.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

PDRN from salmon may slow skin aging by improving skin quality and reducing inflammation.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Long-term use of Risperidone may be linked to a serious skin condition in bipolar patients, affecting their overall well-being.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.