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The N-K GM Series offers highly selective, eco-friendly antimicrobials free for everyone.

The new method can measure sleep-related hormones in hair effectively and could help track long-term sleep patterns.

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Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Figleaf gourd is more resistant to cinnamic acid stress than cucumber.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Hair restoration surgery is available in Bethesda.

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CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Semecarpus anacardium Linn. has multiple medicinal benefits, including anti-inflammatory and antioxidant effects.

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Armadillo Repeat Only proteins are essential for proper plant growth and response by regulating calcium channels.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

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The conclusion is that using light-sheet fluorescence microscopy with a special solution can effectively create detailed 3D images of human skin for dermatological research.

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The research found specific genes that are more active in balding cells, which could be causing hair loss.

Banana (Musa × paradisiaca) may help fight cervical cancer and skin cancer.

Probe detects finasteride with high selectivity and low detection limit.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

Blocking certain receptors in the lungs might help treat a specific type of asthma.

EISA uses enzymes to create precise nanostructures in cells, offering new ways to design adaptive materials and therapies.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

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