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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Nanogels with hydrophobic modifications improve oral drug delivery for intestinal disease treatment.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A rare skin tumor with extra hair growth was found and safely removed from a 27-year-old woman.

Monilethrix is linked to a gene cluster on chromosome 12.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

A specific gene mutation causes sparse, brittle hair in a family.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

A specific gene mutation causes a severe skin disorder in a family.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

The cell membrane complex in mammalian hair has three distinct types with different structures and chemical properties.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A new amino acid derivative, ATS, improves hair texture and moisture, making it easier to straighten curly hair.

Curved human hair has different structures on each side, which might cause its shape and is similar to wool.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

Modified wheat protein in shampoo repairs and smooths damaged hair effectively.

Keratin-associated proteins are crucial for hair strength and structure.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Capitate trichomes have more endoplasmic reticulum and vacuoles, while peltate trichomes have more plastids and larger subcuticular spaces.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Sinus hair follicles in mammals have different nerve fiber types with species-specific patterns, especially in cats.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

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

A special diet can fix hair problems in argininosuccinase deficiency.