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Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Corin speeds up wound healing by helping skin cells move and grow.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A new mutation in mice causes crooked whiskers and messy hair.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

KRT72 gene helps form hair.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

Acid inside cells speeds up aging and turns on aging signs in mice.

Neutrophils are key in causing chronic itch in atopic dermatitis, and blocking CXCR3 could reduce this itch.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

ING5 is crucial for stem cell maintenance and preventing certain cancers.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Cronkhite-Canada syndrome can sometimes show unusual colonic adenomatous polyps.

Activated protein C helps protect mice from radiation damage.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Activating CB1 can reduce keratin levels, potentially helping manage psoriasis and aid wound healing.

Increasing XIAP and DDRGK1 can help prevent hearing loss from loud noise.

CAP1 helps Arabidopsis plants grow better under ammonium stress.