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Spheroid culture in agarose dishes improves survival and nerve cell growth in thawed human fat-derived stem cells.

New Australian advertising rules improved stem cell marketing practices but further regulation is needed for consumer safety.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Androgenetic alopecia is less common in Chilean Mapuche than Caucasians, but more common than Asians, with racial differences in prevalence and types.

People with alopecia areata often have lower iron levels than healthy people.

Patients in Australia underwent costly, unproven stem cell treatments due to weak regulations and aggressive marketing.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

The MLPH gene is not linked to seasonal hair loss in Rhodesian Ridgeback dogs.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Lipase H is important for hair follicle function and shaping hair fibers.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Hair analysis can track haloperidol dosage history.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

The skin of both rat strains showed similar lectin binding patterns.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Certain types of alopecia areata are linked to allergies, autoimmune diseases, and family history.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The study found certain scalp biopsy features can help tell apart alopecia areata from pattern hair loss even when typical immune cells are not seen.

People with rheumatoid arthritis have a higher risk of developing alopecia areata.