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CP-690,550 significantly reduced itching in patients with moderate-to-severe plaque psoriasis.

Wool fiber curliness is linked to the presence of certain proteins and K38.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Keratinocyte growth factor significantly alters skin and tissue development.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

BECD helps straighten wavy hair by reducing undulation.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

Cepharanthine analogues, especially tetrandrine, show potential for treating COVID-19.

Endocrine-disrupting chemicals cause irreversible harm to children's development, increasing disease risk.

KIT's role in skin cells is not entirely independent, as other cells can influence its function.

Ectodermal dysplasia syndromes are caused by disruptions in key signaling pathways affecting tooth and hair development.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Different bovine tissues show varying types of cytokeratins.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Epristeride's metabolism in zebrafish helps improve doping detection methods.

CK15 is not a reliable marker for stem cells in damaged hair follicles from patients with CCCA.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Potassium cyanide treatment changes hair's disulfide bonds, making it more elastic.

Potassium changes lead root hair growth, with calcium and other factors regulating the process.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Charge-conversion chemistry improves hair-rebonding by enhancing penetration and strength.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Keratosis pilaris is common in young females, and dermoscopy helps diagnose it accurately.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

CD200 is not a reliable marker for identifying stem cells in all skin types.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.