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FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Endothelial TLR2 is crucial for timely wound healing, but HFSC TLR2 is not needed.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

A genetic variant in the KRT25 gene causes tightly curled hair.

TRPV1 helps regulate hair growth cycles.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Isolated rheumatic tricuspid valve disease is very rare.

TEDAR is crucial for skin cell differentiation and barrier formation.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

Trichohyalin makes hair follicles stronger.

Some cancer treatments can cause abnormal fine hair growth.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

The skin of both rat strains showed similar lectin binding patterns.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

TRPV1 is involved in pain, various body functions, and diseases, but targeting it for treatment is challenging.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

Targeting the HEDGEHOG-GLI1 pathway could help treat keloids.