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Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Chitin nanofibrils can improve skin health and help deliver active ingredients into the skin.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

Certain biomarkers can help distinguish between irritant and allergic contact dermatitis.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Porcine and human pilosebaceous units are very similar.

Higher CSF 5-HIAA levels may predict better response to serotonin re-uptake inhibitors in trichotillomania.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

The author now believes tricholemmal carcinoma is a rare type of infundibular squamous cell carcinoma and more research is needed on these tumors.

A family had a rare fungal infection called white piedra, identified as Trichosporon inkin.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Paneth cells and intestinal stem cells work together metabolically for stem cell function and regeneration.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Oclacitinib effectively treated a skin condition in dogs that didn't respond to other immunosuppressants.

CGRP may help protect hair follicles from immune system attacks, potentially slowing hair loss.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

AVT is highly conserved and may have antimicrobial properties.

Tinea capitis is a fungal infection of the scalp that mainly affects children and can cause symptoms from mild itching to severe inflammation.

Endothelin-1 helps amelanotic melanocytes stick and move better on certain proteins.

Tinea capitis can rarely cause urticarial skin reactions in children.