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Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Hex gene plays a crucial role in starting feather development in chick embryos.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

ECM1-modified stem cells can effectively treat liver cirrhosis.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

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

Premature canities is linked to low vitamin D and B12, family history, and higher MHR.

Farudodstat may effectively treat alopecia areata without harmful side effects.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Hair follicle cells help maintain and support stem cells and blood cell formation.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Compound 4 is a promising treatment for hair loss with low toxicity.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

A new gene mutation is linked to monilethrix in the studied family.

Two siblings have a rare hair condition caused by a new genetic variant.

PADI4 enzyme slows down cell growth in developing hair follicles.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.