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PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

pCLCA2 protein may help maintain skin structure and function.

Defective nuclear transport may cause gene expression changes in Progeria.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

MESTSV is a rare tumor that is mostly benign but needs long-term monitoring due to potential recurrence.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Noggin promotes skin tumors by activating certain cell signaling pathways.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

Vitamin D receptor helps prevent skin tumors.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Vitamin D receptor helps prevent skin tumors.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Activating certain hair follicle cells could prevent hair loss from cancer treatments.

UV-enhanced trichoscopy helps diagnose hair shaft disorders like pili annulati.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Pueraria thunbergiana extract may help prevent hair from turning gray.

Prolactin affects hair growth cycles and can cause early hair follicle regression.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Nested PCR can reliably identify fungal infections when traditional methods fail.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.