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RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

pCLCA2 protein may help maintain skin structure and function.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

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

Eyelid cells share signaling components but differ in pathway activity.

Targeting regulatory T cells may help treat age-related diseases.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

The Celsr1 gene is crucial for normal hair patterning in mice.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

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

BLMP-1 is important for regular molting and gene expression cycles in worms.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Grasp protein helps maintain skin health after UVB exposure.

miR-370-3p slows sheep hair cell growth by blocking SMAD4.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

Meis2 is essential for touch sensation and nerve function in mice.

AP-1 controls tumor cell type by affecting key signaling pathways.

The research found changes in gene expression related to cell death in mouse skin that help understand hair follicle development and skin health.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

miR-124 helps mouse hair follicle stem cells become nerve cells by blocking Ptbp1 and Sox9.