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Acne patients' skin, both with and without lesions, shows a strong immune response and higher antimicrobial activity.

Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Dermal EZH2 controls skin cell development and hair growth in mice.

FCO2 laser is a better treatment for alopecia areata than intralesional steroids.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

PCFCL may have unrecognized subtypes and needs more research.

Specific cross-linkages help make hair proteins stable and strong.

Erlotinib causes skin inflammation through IL-1, which can be reduced by anakinra.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

Cubosomes enhance antimicrobial peptide stability and effectiveness.

Laminin-511 may contribute to psoriasis by affecting skin cell growth and survival.

Certain immune cells in atopic dermatitis skin could be targeted for treatment.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Anti-IL-1 treatments might help with certain types of hair loss in people with high inflammation.

Fluphenazine and iloprost can induce hair growth.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

Defects in certain proteins cause major heart abnormalities during early development.

A man had two rare autoimmune diseases that might be connected.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

Stem cells in the cornea show unexpected flexibility and have important implications for medicine.

The new protocol using Cellutome™ and RCM safely assesses wound healing in detail.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

The conclusion is that the cornea has two types of stem cells, with Lrig1+ cells being key for renewal in aging corneas, independent of CD44.

The PROCLIPI study found markers that help predict outcomes in skin lymphoma patients.