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IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

New genetic mutations causing hair loss were found in a Chinese family.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Papain from papaya may help treat cardiovascular diseases by breaking down fibrin.

Markers CRABP1, Nestin, and Ephrin B2 are present in skin cancer environments and may influence their development.

Claudin-1 is crucial for maintaining skin barrier and preventing inflammation.

The study found a unique vein pattern around the aorta and two arteries in the right kidney.

HAPLN1 can promote hair growth and may help treat hair loss.

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

Understanding cellular interactions in VCA may lead to better treatments and reduce rejection.

The protein ARA70/ELE1 is involved in male pattern baldness, and lower levels of its short form may lead to hair thinning.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Activin B improves wound healing and hair growth by helping stem cells move using certain cell signals.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Blocking LFA-1 prevents hair loss in mice.

The new assay can help develop products for hair re-growth.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

The enzyme PA-PLA1α is important for proper hair follicle development.

Interleukin‐1 α reduces androgen receptor levels and increases certain cytokines in human scalp cells.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.