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Rat hair follicle stem cells have functional oxytocin receptors, useful for studying neuropsychiatric disorders.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Humic acids enhance plant growth by improving root development and photobiology.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Scientists made all eight versions of a compound called cyoctol, but found it's not an anti-androgen and it fully breaks down in the skin.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Lipase H is important for hair follicle function and shaping hair fibers.

Human hair keratins were cataloged, showing their roles in hair differentiation stages.

OXI1 kinase is essential for plant defense and root hair growth in Arabidopsis.

The enzyme is crucial for skin cell development and can be activated without proteolytic activation.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Calanthoside may help hair growth by boosting cell proliferation.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

A CCS patient with severe complications was successfully treated using combined therapies.

Biotin supplements significantly improved a young girl's uncombable hair.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

Foreskin keratinocytes and SVK14 cells express certain cytochrome P450 enzymes, unlike hair follicle keratinocytes.

A specific gene mutation causes woolly hair and hair loss.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.