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Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

The anti-viral drug Elvitegravir may protect brain cells from damage related to neurodegenerative diseases.

A severe virus outbreak in yaks on the Qinghai-Tibet Plateau caused high death rates and requires targeted control measures.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

Melanocytic matricoma can look like skin cancer but is usually harmless; surgery and follow-up are advised.

Pododermatitis in farmed mink is likely caused by an unknown infectious agent with secondary bacterial infection.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Basal cell carcinoma may originate from vellus hair cysts.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

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

Skin changes help detect graft-versus-host reaction early after bone marrow transplants.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Newborns with the common rash Erythema Toxicum have many active mast cells in their skin, but these cells don't produce the LL-37 peptide.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

Alpha-melanocyte-stimulating hormone helps manage skin inflammation and protect against UV damage.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Mast cell and nerve fiber interactions in mouse skin change with the hair cycle.

The antibody created from BCC tissues reacts similarly to both BCC and hair follicles, suggesting BCC may come from hair follicle cells.