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A child was initially wrongly diagnosed with a fungal scalp infection but actually had a non-scarring hair loss condition called Temporal Triangular Alopecia.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A rare EGFR mutation in newborns leads to severe health issues and early death.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

BSSP may help skin tumors grow and could be a marker or target for skin cancer treatment.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Early sunburn treatment with certain inhibitors may reduce skin cancer risk.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

The p53 protein helps control hair follicle shrinking by promoting cell death in mice.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

SOX4 is crucial for the development of melanoma.

Smart nano-PROTACs improve cancer treatment by targeting proteins more precisely and reducing side effects.

Birth control pills change the activity of certain inflammation and blood clotting genes in women with PCOS.

Certain plasma proteins and genes are linked to obstructive sleep apnea, suggesting potential new treatments.

Chronic T. gondii infection may harm male fertility.

Inhibiting ODC can prevent UV-induced skin cancer.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

TMPRSS2 affects COVID-19 severity and treatment options.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

Trps1 plays a key role in hair follicle development and cycling.

Increasing COX-2 in mouse skin causes bigger sebaceous glands and thinner hair, but stopping COX-2 can reverse hair thinning.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.