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Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

Keratin 14 may be an autoantigen in autoimmune skin diseases.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Sulfasalazine can cause severe allergic reactions leading to long-term autoimmune issues like hair loss and skin discoloration.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

Two new gene mutations cause a rare hair disorder.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Trichothiodystrophy causes unusual hair and developmental issues.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

A severe medication reaction required long treatment and led to hair loss and thyroid issues.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Finger length ratios might predict risk for skin condition in males.

Aging reduces stem cell activation, leading to hair loss in mice lacking a specific enzyme.

Type 1 diabetes may cause certain autoimmune diseases in Europeans.

Polyamines help repair DNA breaks and may influence cancer development.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

PDRN is effective and safe for healing wounds and skin issues.

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