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A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Keratin 17 is crucial for early hair strength and cell survival.

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

Boron/nitrogen-doped carbon nano-onions improve targeted breast cancer treatment by enhancing drug delivery and reducing side effects.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

New microneedle method improves hair regrowth treatment delivery.

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Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

A new treatment effectively kills antibiotic-resistant bacteria and helps wounds heal faster by boosting the immune response.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

The InCISE score is a promising tool for assessing wound healing in head and neck surgery but needs more research for broader use.

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

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

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

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Hinokitiol in cationic vesicles promotes hair growth better due to higher skin retention.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.