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Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Researchers found a new mite species causing severe hair loss and skin problems in yellow-bellied marmots.

Defects in certain proteins cause major heart abnormalities during early development.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

A man's skin condition, pemphigus vulgaris, came back after he was treated with interleukin 2 for cancer.

Cell adhesion molecules are important in the development of certain skin diseases.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

PCOS is linked to chronic low-grade inflammation, but the role of certain infections is unclear.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Lambs' skin showed similar but more severe responses to a second orf virus infection, involving immune cells and new skin formation.

The Apc gene is crucial for normal skin and thymus development.

Specific keratin gene mutations can cause monilethrix.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Recognizing macro-TSH is crucial to avoid unnecessary treatments.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

A 9-year-old girl developed type 1 diabetes and alopecia after being treated for a rare kidney disease.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.