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Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Allopregnanolone changes gene expression in glioblastoma cells.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

These gene variations are not linked to alopecia areata in Egyptians.

Suppressing ODC activity reduces tumor growth in hair follicles.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

Normal skin results from interactions between EGF and the Tabby mutation.

New mouse models help study melanocytic cells for melanoma research.

Gonadal hormones significantly affect the severity of alopecia areata in mice.

Fos protein is crucial for cell transition to cornification in keratinized tissues.

Targeting androgen receptor signaling may improve acute myeloid leukemia treatment.

Genetic marker rs12558842 strongly linked to male hair loss.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

Akt2 protein is essential for normal cell division in early mouse embryos.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Polyethylene alanine caused hair loss in young lab animals but not in adults, with hair regrowth occurring within 20 days.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Certain tyrosine kinases may regulate hair growth and could help develop hair loss treatments.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Akt2 and SGK3 are both important for normal hair growth and development.

The mTOR pathway proteins are altered in the hair follicles of patients with Lichen Planopilaris and Frontal Fibrosing Alopecia.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

High levels of ERK activity are key for tissue regeneration in spiny mice, and activating ERK can potentially redirect scar-forming healing towards regenerative healing in mammals.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

The lncRNA LOXL1-AS1 may help diagnose and treat androgenic alopecia.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.