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Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

The authors agree that standardizing how PRP methods are reported could help compare results, but note that the link between PRP's contents and hair growth is unclear, and recommend avoiding split-scalp designs in future trials.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

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

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

A new microneedle patch significantly improves melanoma treatment by using a special material to activate cancer-fighting drugs and disrupt cancer cells.

PAON shows skin patterns due to genetic mosaicism.

Neuroactive steroids affect cocaine's rewarding effects through the ς₁ receptor.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

Compounds from Pterocarpus indicus may help treat benign prostatic hyperplasia by stopping cell growth.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Lysophospholipids can act as anti-inflammatory agents through specific receptors, but more research is needed.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

RoPod helps study plant root cell changes and autophagy with minimal stress.

PKM2 is a promising target for heart repair and regeneration.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Trichorrhexis nodosa is mainly caused by hair trauma, not a metabolic defect.

ATP increases melanin production in skin after UV exposure, with the P2X7 receptor being crucial for this process.