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MLO proteins help regulate calcium and ROS levels, promoting root hair growth in Arabidopsis.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

Growth hormone therapy can improve growth in Netherton syndrome patients with growth hormone deficiency.

Combining microneedling with drugs and stem cells shows promise for improving hair growth in androgenetic alopecia.

Lactobacillus plantarum-fermented plant extracts promote hair growth and thickness.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Injectable platelet-rich fibrin with microneedling is safe and effective for male hair loss but less supported than other treatments.

Some HIV treatments can harm mitochondria, potentially causing side effects like lactic acidosis and nerve damage.

The N-K GM Series offers highly selective, eco-friendly medicines targeting harmful microbes, free for personal use.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

Newborn screening for biotinidase deficiency is effective in preventing severe complications.

Special astroglia cells improved stroke recovery in rats, a hair growth drug reduced cancer spread, and tiny magnesium structures were more easily shaped.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

A man in his 30s had patchy hair loss on his leg due to primary follicular mucinosis.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

Biomimetic nanovesicles can speed up diabetic wound healing by regulating immune cell behavior and metabolism.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Thallium poisoning can cause worsening nerve damage and vision loss without typical symptoms.

Two sisters had a rare hair condition without other usual symptoms.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

Adult spiny mice recover better from heart attacks than common lab mice.

Hair follicle stem cells can become motor neurons and reduce muscle loss after nerve injury.

Copper injections improved symptoms and prevented brain damage in brindled mice.

4D scaffolds made with melt electrowriting can change shape for use in medicine.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.