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PBM therapy improves mitochondrial function and promotes tissue regeneration in dental pulp stem cells.

Finasteride helps female-pattern hair loss.

Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Silencing certain circadian clock genes increases skin pigmentation.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Detecting early breast arterial calcifications can help assess cardiovascular disease risk.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

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The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

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

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

The ABHRS held a test in Capri, Italy.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A new therapy for a skin blistering condition has not been developed yet.

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

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.

MYB83 limits root hair growth and helps plants tolerate nutrient deficiencies.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

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