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

Different parts of the nail express different keratins, showing unique patterns of differentiation.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

B-Raf and C-Raf are essential for maintaining melanocyte stem cells to prevent hair graying.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

The treatments stopped hair regrowth in mice.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

MEF2C is crucial for normal hair cycle progression.

Different forms of FGF5 either promote or inhibit hair growth.

The new skin-targeted COVID-19 vaccine creates strong immune responses and could improve vaccination methods.

PP2Acα is essential for proper hair and skin development.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Blocking CCR5 can prevent and improve hair loss in alopecia areata.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Sex steroids affect the MafB gene differently in male and female hamsters.

The DiLiCre mouse model is an effective tool for precise genome editing using light.