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Phaeodactylum tricornutum extract helps hair follicle cells grow by activating the ERK1/2 pathway.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Valproic acid treatment increases a specific acid in urine by blocking an enzyme, possibly causing skin rash and hair loss.

The more lipophilic the progesterone derivative, the better it binds to androgen receptors and has antiandrogenic effects.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

MLPH helps hair grow by activating IGF-1 signaling in hair cells.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

Thymosin β4 helps with healing, inflammation, and organ protection.

The exact molecular mechanisms of sebaceous gland function are still unclear.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Oleoylethanolamide (OEA) safely boosts fat production in skin cells and may help treat dry skin and reduce inflammation.

Lysophospholipids can act as anti-inflammatory agents through specific receptors, but more research is needed.

YAP and TAZ proteins control skin cell growth and repair.

Mutations in the LIPH gene cause woolly hair in a child.

YAP1 helps fat cell formation by influencing the Hippo pathway.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

Phospholipase Cδ1 is crucial for normal skin and hair development.

Blocking cholesterol production may help control hair loss in Primary Cicatricial Alopecia by affecting key regulators.

Enzymatic phosphorylation of hair keratin improves the effectiveness of hair products with cationic ingredients.

Sebum from sebocytes is important for skin health and linked to conditions like acne and hair loss.