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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Changing disulfide bonds in human hair affects its melting behavior and thermal stability.

Tenascin is present in normal skin and certain skin tumors but not in sebaceous glands or their tumors.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

The KRTAP22-2 gene in sheep does not significantly affect wool traits.

Keratins are important for skin cell health and their problems can cause diseases.

Hair structural proteins are synthesized sequentially in specific cells, offering a new way to study hair proteins and defects.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Researchers isolated and identified structural components of human hair follicles, providing a model for studying hair formation.

PKM2 is a promising target for heart repair and regeneration.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Formononetin may help protect the brain and treat neurological diseases.

Human hair proteins have similar cysteine and glycine levels to skin proteins.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Targeting NETs may help reduce fibrosis in Crohn's disease.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Sphingosine 1-phosphate helps control mechanical pain.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

FOXN1 duplication can cause excessive hair growth.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

A new gene mutation causes a rare type of hair loss.