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Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Two L-PRP treatments improve hair density in mild to moderate alopecia.

New hair loss subtype found, mimics common baldness.

Certain gene changes and hormone levels are linked to female hair loss.

A gene mutation in Lama3 is linked to a common type of hair loss.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

Platelet-rich plasma (PRP) is an effective treatment for lichen planopilaris.

Linear lichen planopilaris can affect the trunk, not just the face.

Researchers found two new genetic variants linked to Alzheimer's disease.

Androgenetic alopecia is more common in Chinese Han than in Chinese Yi in Liangshan.

A specific gene change is linked to severe hair loss.

DNA analysis can help tailor alopecia treatment.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

Nonionic liposomes are the best for delivering genes to skin cells.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Specific RNA patterns are linked to alopecia areata.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Male pattern baldness is largely genetic, linked to the androgen receptor gene, and may relate to certain health issues.

PC-associated alopecia has unique microscopic features.

FFA has higher long-term remission rates than LPP.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.