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

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

TMPRSS2 affects COVID-19 severity and treatment options.

A new anti-baldness patch effectively treats hair loss by blocking enzymes linked to the condition.

Kojyl cinnamate ester derivatives can promote hair growth by increasing adiponectin production in fat tissues.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

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

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

ABCG2 protein marks stem-like skin cells in human epidermis.

The TPAP method effectively categorizes androgenetic alopecia patients with high accuracy, but needs real-world validation.

Combining PRP with Procapil is more effective for hair loss treatment than PRP alone.

Two new compounds can block androgen receptor activity in different ways and may lead to new treatments for androgen-related diseases.

4-aminopyridine helps skin wounds heal faster and better.

Encapsulating ascorbyl palmitate in curcumin-grafted particles improves its stability and skin penetration.

Platycladi Cacumen may help treat hair loss by affecting certain biological pathways.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A hepatitis B patient lost hair in patches after starting and stopping a treatment with pegylated interferon alpha2a.

KRTAP28-1 gene can help breed sheep with finer wool.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

Upadacitinib improves life quality for Alopecia Areata patients without worsening skin issues.