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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

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.

Zebrafish are useful for studying and developing treatments for human skin diseases.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

Human skin xenografting could improve our understanding of skin development, renewal, and healing.

Creating specific biological indicators is important for early detection and treatment of PCOS.

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

Different hair follicles in the skin are innervated by unique combinations of mechanosensory neurons, crucial for touch sensation.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Certain immune cells in the skin release a protein that stops hair growth by keeping hair stem cells inactive.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Notch signaling disruptions can cause various skin diseases.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

Atopic dermatitis increases the risk of some autoimmune diseases.

Innate immunity genes in hair follicle stem cells might have new roles beyond traditional immune functions.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

New research shows that skin diversity is influenced by different types of dermal fibroblasts and their development, especially involving the Wnt/β-catenin pathway.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Genomic research can help improve the quality and production of natural fibers in animals.