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The combination therapy significantly improved Riehl’s melanosis in patients without serious side effects.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

HPV8 E6 gene causes growth of certain skin stem cells.

Nevus comedonicus is a rare skin condition causing dark bumps, treatable with retinoic acid or surgery.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

Xenobiotic-free progenitor cells improve wound healing and blood vessel formation.

Higher fluences in 808-nm diode laser treatments are more effective for axillary hair removal.

Hemidesmosomes and Notch signaling help skin cells mature by moving them to the outer layer.

Microneedles improve drug delivery, patient compliance, and have potential in cancer treatment and skin care.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A unique gene mutation was found in a family with monilethrix.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

A 12-year-old girl's hair loss was linked to a rare genetic condition called ALX4-related frontonasal dysplasia.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Xiaoaiping reduces chemotherapy side effects and improves quality of life for breast cancer patients.

The N gene affects the protein makeup of mouse hair.

Krox20 (Egr2) is important for the function of epithelial stem cells.