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ZPK helps skin cells mature and may affect skin health.

New compounds may help treat heart disease by activating specific potassium channels.

Basonuclin is crucial for hair follicle development and cycling in mice.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

CCCA can affect both genders and all ages, and it has a genetic component.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

Cinchonine Nanostructured Lipid Carriers serum safely and effectively stimulates hair growth and increases the number and size of hair follicles.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

MCHR2 gene duplications may be linked to alopecia areata.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

Kallmann syndrome can cause eye issues and other health problems, requiring various treatments.

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

Neurokinin B levels are higher in the placentas of women with PCOS who have female babies.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

Erythrocyte-anchored nanoparticles improved Cepharanthine delivery and effectiveness for treating acute lung injury.

Touch dome keratinocytes in adult skin have traits of different skin cell types.

Ki-67 levels do not predict treatment response in triple-negative breast cancer.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

The study identified diverse cell types and gene expressions in ovarian steroid cell tumors, improving understanding of this rare tumor.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.