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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

Long-lived proteins may predict age-related diseases.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Chemical lumbar sympathectomy is an effective and safe treatment for idiopathic livedo reticularis.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

p2y5, now called LPA6, is a receptor important for human hair growth.

Lichen planus is a skin condition that can resolve on its own, is linked to hepatitis C, and increases the risk of skin cancer.

BLMP-1 is important for regular molting and gene expression cycles in worms.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

Mutations in the SNRPE gene cause hereditary hair loss.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Controlling Tslp can improve health in AEC syndrome patients.

Tph cells are linked to the severity of systemic lupus erythematosus.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A 12-year-old boy's rare skin condition improved with topical treatments and may resolve by puberty.

Platelet-rich plasma may successfully treat lichen planopillaris, as shown by one patient's symptom regression.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Trps1 is essential for proper hair follicle development.

LRIG1 is linked to better survival in Merkel cell carcinoma.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.