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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Upadacitinib may effectively treat both alopecia universalis and Crohn's disease.

A specific gene change in APCDD1 increases the risk of hair loss.

Cytotoxic T cells cause hair loss in chronic alopecia areata.

ILC1-like cells can cause alopecia areata by themselves.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

All Indian dromedary camel breeds have the same KRTAP7 gene affecting hair quality.

Acitretin improved monilethrix symptoms temporarily, but they returned after stopping treatment.

Aconiti Ciliare Tuber extract may help hair grow by activating a specific cell signaling pathway.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

K31 can identify clear secretory cells in human sweat glands.

The new cocrystal KET-PABA is a more effective and safe anti-inflammatory treatment for skin conditions in mice.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Zinc supplements effectively treat acrodermatitis enteropathica.

Reduced plakoglobin and steroid abuse increase the risk of heart rhythm issues.

β1 integrin may indicate and influence the severity of hair loss in androgenetic alopecia.

Human liver cells stick to hair protein materials mainly through the liver's asialoglycoprotein receptor.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

Acitretin can cause eyebrow and eyelash hair loss.

Activated protein C helps protect mice from long-term radiation damage.

Patients with acanthosis nigricans often have insulin resistance and signs of increased male hormones, but treatment targeting these male hormones is generally ineffective.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

The ABHRS has outlined its goals for the next year.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.