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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.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

Msx2 deficiency in mice leads to bone growth and organ development problems.

VEGF and microvessel density are closely linked and peak during specific hair growth phases in cashmere goats.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

CAP7.1 is generally safe at 200 mg/m²/day, but can cause fatigue, nausea, hair loss, fever, and blood-related issues.

Glucosylceramides are essential for healthy skin and proper wound healing.

Eruptive vellus hair cysts likely originate from the infrainfundibulum and sebaceous duct.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

The nano-carrier makes etoposide safer and more effective against lung cancer.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

The cornea develops independently of the lens, following its own default pathway.

Camellia japonica extract may improve scalp health and promote hair growth.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Artemis phosphorylation at Ser516 may help regulate skin and hair structures.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Low IRES/Cap translation is linked to higher stem cell potential.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

The method using ionic liquid improves observation of cell structures with less damage.

17β-estradiol may help hair growth by increasing cannabinoid receptor type 1.