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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

CXCR2 in skin cells promotes tumor growth.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

SLVs help maintain muscle stretch sensitivity and could aid in treating hypertension and muscle spasticity.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

PCOS involves genetic and immune factors, especially T cells, affecting its development.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

A new tool accurately identifies human cornea cell states and key factors.

Weak cell junctions disrupt hair follicle stem cell rest.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Trichohyalin is a versatile protein involved in hair and skin structure.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

Blocking CXCR4 may help treat hidradenitis suppurativa.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

Wnt7a helps corneal cells grow and stick together, aiding in repair.

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

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

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

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Defective protein folding due to a mutation is key in ANE syndrome.

The new model helps understand and develop treatments for genetic skin disorders like AEC.