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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new type of nerve cell involved in itch perception was discovered.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Vitamin D and calcium are essential for effective wound healing.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

miR-140-5p in certain cell vesicles helps hair growth by boosting cell proliferation.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

VEGF and its receptor might cause hair loss.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Targeting Vδ1+T-cells may help treat alopecia areata.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Somatic BHD mutations are rare in Japanese renal tumors.

EP 2 receptor is essential for heart repair by helping macrophages work properly.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

PP2Acα is essential for proper hair and skin development.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.