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Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Nilotinib can cause generalized keratosis pilaris.

Treatments improved hair surface and scale structure but didn't increase certain bonds in the hair cortex.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Two new types of eyelid cysts were identified, each with different treatment challenges.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

Minoxidil boosts hair growth by undergoing a process in hair follicles and certain skin cells, and by increasing the production of compounds essential for hair growth and maintenance.

PEI diffuses into hair at a constant rate, and urea speeds up this process.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Urea helps hair dye penetrate better and last longer.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

New wig coating technique makes them more durable, UV resistant, and less static.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

The KRTAP21-2 gene affects wool length and quality in sheep.

Minoxidil may help treat hair loss by reducing the activity of a specific enzyme linked to baldness.

The extract reduced sebum production and promoted hair growth.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

Hair fibers may have a unique, non-protein sheath not previously identified.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.