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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A man had an allergic skin reaction on his penis from a hair loss medication, which improved after stopping the medication.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Nemolizumab improved both severe atopic dermatitis and alopecia areata in one patient.

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

EETs can delay seizures by affecting GABA activity, offering potential new treatments for seizures.

Erlotinib can cause unexpected side effects like eyelash growth and scarring.

The cream effectively and safely reduces facial hair in women.

A 6-year-old girl had a rare allergic reaction to a hair regrowth treatment.

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

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Epristeride's metabolism involves key metabolites and proteins, affecting its use in doping tests.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Promising treatments for EBS include anti-inflammatory drugs, antibiotics, creams, mTOR inhibitors, and gene editing, but more trials are needed.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Upadacitinib effectively treats psoriasiform eczema and some related conditions.

A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

Chronic autoimmune urticaria can be managed with specific therapies and requires improved diagnosis and treatment methods.

Careful management of blood thinners is crucial for lupus patients with APS.

Arg1+ macrophages may play a role in Alopecia Areata, offering new treatment targets.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

A unique gene mutation was found in a family with monilethrix.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

Human hair keratin might be good for filtering out harmful substances from water.

Compounds from Eclipta prostrata L. plant have diabetes and obesity-fighting properties and reduce inflammation.

Zinc supplements and diet changes can effectively treat zinc deficiency and prevent complications.