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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

The oral supplement improved hair loss in patients with telogen effluvium.

Newborns with the common rash Erythema Toxicum have many active mast cells in their skin, but these cells don't produce the LL-37 peptide.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

ECCL should be considered in patients with specific skin and eye lesions.

A man developed skin lesions as a side effect of a gamma secretase inhibitor used for treating a tumor.

Tislelizumab can cause cutaneous lupus erythematosus.

Certain gene variations might be linked to severe acne in women but not in men.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

The treatment showed significant hair regrowth in alopecia areata patients without side effects.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Quercitrin may help treat Alzheimer's by boosting brain cell signaling without causing tumors.

SQSTM1 is linked to increased risk of alopecia areata.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.