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Cyclosporin A, a drug, reduces TGF-β2 expression in skin cells, potentially causing excessive hair growth through a process involving the calcineurin/NFAT pathway.

The PP2A-B55α protein is essential for brain and skin development in embryos.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Increasing calcium sensing receptor speeds up skin and hair development in mice.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Topical IKKα inhibitors may help prevent CCS tumours.

Keratins are crucial for cell structure, growth, and disease risk.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

XEDAR triggers a specific signaling pathway in cells.

Rat hair follicle stem cells have functional oxytocin receptors, useful for studying neuropsychiatric disorders.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

New genetic variants linked to inherited ichthyoses were identified, offering insights for potential gene therapy.

New genetic mutations linked to rare skin disorders were found in three newborns.

Cathepsin E is crucial for normal skin cell differentiation and development.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Human skin cells can be turned into heart cells.

A girl had rickets due to a gene mutation affecting vitamin D response.

Various medications and vaccines can cause serious side effects.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

Pro-IGF-II improves muscle repair in old mice.

E13 fetal mouse fibroblast vesicles may help reduce scarring.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.