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Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Human hair contains a substance that shows blood group A activity.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Different keratin types have unique amino acid patterns that are evolutionarily conserved.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Two new gene mutations cause a rare hair disorder.

Hair straightening products with glyoxylic acid can cause skin irritation and kidney damage.

Human hair protein modifications could potentially indicate heart disease risk.

Glyoxylic acid is a safer alternative to formaldehyde for hair straightening and effectively changes hair structure.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Glyoxylic acid straighteners cause more protein loss but have similar hair strength effects as traditional alkaline straighteners.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

A specific gene variant may increase the risk of developing Alopecia Areata.

Aleglitazar and its major metabolite are safe enough to proceed to Phase 3 clinical trials.

Amino acid levels in milk increase with protein and align with key growth stages in Macropus eugenii.

Thioglycolate compounds in brow lamination can cause skin irritation and other health issues.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

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

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Keratin in people with androgenetic alopecia shows specific changes that could help develop new treatments.

A man had two rare autoimmune diseases that might be connected.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.