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Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

IVL-DrugFluidic® can mass-produce high-quality, long-acting injectable drug microspheres, improving patient compliance and reducing side effects.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Long non-coding RNAs play a key role in yak hair growth cycles.

Lipedematous alopecia involves a thickened scalp and hair loss, with limited effective treatments available.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

Monoclonal antibodies LT-1, LT-2, and LT-7 help diagnose certain blood cancers.

The fuzzy gene is crucial for controlling hair growth cycles.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Certain genes control the color of human hair by affecting pigment production.

New mutations in the DSG4 gene cause a rare hair condition.

The technique effectively shows how human skin and hair cells form into ball-like structures.

Aging changes the red part of lips, affecting life quality and sparking cosmetic interest.

Dermal lymphatic vessels help hair growth by affecting hair cycle phases.

The conclusion is that certain scalp tissue changes are characteristic of lichen planopilaris, with mucinous perifollicular fibroplasia being a new feature for diagnosis.

A sphingolipid from human placenta may help treat vitiligo by activating melanocyte stem cells.

The protein's size was reduced, but more work is needed to confirm its function.

Lrig1 and Lgr6 stem cells help maintain hair follicles and influence skin cancer development.

A mutation in the human hairless gene causes alopecia universalis.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

TGFβ signaling prevents sebaceous gland cells from producing fats.