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C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

Type II porcine hair keratin supports cell growth but hinders cell differentiation.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

New LPP subtype affects vellus hairs, mimics AGA, and needs biopsy for diagnosis.

Eflornithine improved symptoms in Bachmann–Bupp Syndrome patients.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Different sPLA2 enzymes have unique roles in phospholipid metabolism and biological processes.

New genetic variants linked to albinism were found in Pakistani families.

Most patients with cutaneous lupus erythematosus in Bangladesh are young women, with chronic forms and photosensitivity being common.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

Bisphenol-A (BPA) increases connections between brain cells and boosts their activity, but it blocks the effects of a male hormone on brain cell plasticity.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Basal cell carcinomas need extra mutations to grow from small to large tumors.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Rushton's hyaline bodies form from hair keratin and blood substances.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Different PCOS subgroups have similar metabolic features, but those without menstrual problems have milder issues.

A new gene mutation linked to a skin condition was found in a Spanish family.

LPA 4 helps control blood and lymph vessel development in zebrafish.