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Miscanthus sinensis flower extract may help promote hair growth and prevent hair loss.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

PDRN, derived from salmon sperm, shows promise in healing wounds, reducing inflammation, and regenerating tissues, but more research is needed to understand its mechanisms and improve its use.

Eyebrow follicles are best for accurate genetic testing after stem cell transplants.

DNA methylation changes are linked to skin diseases with inflammation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Editing the FGF5 gene in sheep increases fine wool growth.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Circ 0020938 slows down hair growth in cashmere goats.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

The peptide GPIGS helps hair cells grow and speeds up hair regrowth in mice.

Targeting the TNFRSF1B gene may help treat hair loss.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

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

A new microneedle patch helps repair spinal cord injuries by reducing scarring and promoting nerve growth.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

TP0427736 may help treat hair loss by blocking a specific protein and promoting hair growth.

Two siblings have a rare hair condition caused by a new genetic variant.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Mice hair follicles take in the amino acid cystine.