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A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A reliable method was developed to measure Tamsulosin and Finasteride in tablets accurately.

Combining gemcitabine with paclitaxel is more effective than with pemetrexed for advanced lung cancer.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

The method effectively measures drug impact on DHT levels in prostate treatments.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Dual wavelength LEDs may help reduce hair loss by lowering DHT levels.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

CyRL-QN15 peptide boosts hair growth in diabetic mice by activating specific cell pathways.

Specific gene variants affect wool traits in Chinese Tan sheep.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A girl had rickets due to a gene mutation affecting vitamin D response.

Fermented Liriope platyphylla helps hair grow in mice with hair loss.

New therapy helps treat hair loss.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Thermobalancing therapy is safe and effective for treating enlarged prostates.

FLCN helps control iron levels in cells.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

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