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Key genes linked to immune response are upregulated in hair follicles and skin tissues in chronic discoid lupus erythematosus.

Laminin-511 is essential for proper melanocyte movement and development in mice.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Aconiti Lateralis Preparata Radix helps mouse stem cells grow and turn into bone cells faster than usual methods.

Hair and nails contain stable RNA, useful for personalized medicine and screening.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

CXCL12 protein slows down hair growth through its receptor CXCR4. Blocking this can potentially increase hair growth.

Mrp3 may aid in wound healing and hair growth.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

PX-12 may help treat psoriasis by blocking inflammation and cell death.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The microneedle patch effectively promotes hair regrowth by delivering miR-218.

Low-dose naltrexone helps reduce symptoms and slow down lichen planopilaris without side effects.

Finasteride helps female-pattern hair loss.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

A comprehensive human skin cell atlas was created to better understand skin biology and disease.

The package offers tools for exploring potential miRNA changes in female hair loss.

The new treatment using nanoparticles with ISX9 can effectively regrow hair without major side effects.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

ΔNp63α helps control a protein that stops cancer cells from spreading.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Researchers found a non-functional sheep keratin gene due to mutations.