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The technique effectively improved upper eyelid symmetry in patients with mild and moderate blepharoptosis.

Cell division orientation varies by body site and is linked to epidermal thickness and cell density.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

A new training model using an orange helps surgeons practice parietal whorl hair transplants effectively.

OCT can effectively examine and reveal details about human hair and scalp conditions.

The outer root sheath in hair follicles changes during growth, with different keratinization processes in its layers.

Hair follicles form hard α-keratin filaments in four steps, showing structural differences.

HB24 helps convert IBA to IAA, promoting root hair growth.

The research found a link between certain molecular features and the biological activity of BC3, which can help identify or create new active compounds.

Benzo[c]quinolizin-3-ones are effective nonsteroidal inhibitors of human steroid 5α-reductase 1.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A rare ovarian tumor caused high testosterone and excess hair in a woman, which was resolved after tumor removal.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

ARHGEF3 is essential for proper hair follicle development in mice.

3D virtual planning can help in precise skull reconstruction for advanced skin cancer, but patient-specific factors must be considered.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Women with idiopathic hirsutism and PCOS have higher RBP4 levels, and PCOS is linked to greater insulin resistance; weight management may help both conditions.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

A 6-group geometric classification of human scalp hair is more reliable and objective for testing than an 8-group system.

Ovarian stromal hyperplasia can cause high testosterone in postmenopausal women and is treated by removing the ovaries.

Calcium hydroxide in an ayurvedic product caused hair breakage.

Keratin proteins are crucial for hair growth and structure.

Idiopathic hypoparathyroidism is rare and can be managed with dihydrotachysterol.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.