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Combining fractional CO₂ laser with type III collagen improves acne scar treatment.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

LLPS is crucial for RALF signaling, aiding plant growth and stress resilience.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Three genes linked to the development of trichilemmal cysts were found.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

CK15 is not a reliable marker for stem cells in damaged hair follicles from patients with CCCA.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Dock5 is important for skin healing and could help treat diabetic wounds.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

ECCL should be considered in patients with specific skin and eye lesions.

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

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

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

CRET therapy affects inflammation in skin cells by changing cytokine levels and activating certain proteins.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.