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The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Type II spiral ganglion neurites avoid high concentrations of laminin and fibronectin.

Calcium signals and SHH guide the direction of feather growth in chicken skin.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Merkel cells likely attract sensory nerve fibers.

Careful light microscopy is crucial for detecting mild cases of pili annulati, which weakens hair and varies widely in expression.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Ion channels play a key role in ovarian cancer growth and treatment resistance.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A new genetic mutation was found causing hair and eye issues in a boy.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

A gene mutation causes monilethrix in a Chinese family.

Blocking CXCR4 may help treat hidradenitis suppurativa.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

A new DSG4 gene mutation causes hair defects in a young girl.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

Deleting part of a gene in mice causes wavy hair and high pup loss.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Endothelin-1 helps amelanotic melanocytes stick and move better on certain proteins.

Phospholipase Cδ1 is crucial for normal skin and hair development.

Zinc made mice's coarse hair turn into fine hair without affecting skin structure.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

Exosomes are crucial for protecting sensory hair cells in the inner ear.

TRPV3 is important for skin health and could be a target for treating skin diseases.

Targeting the TRPV4 channel may help treat intestinal diseases.