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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Cantú syndrome may be linked to pituitary adenomas.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

Men with CCCA often face delayed diagnosis and severe hair loss, highlighting the need for earlier recognition and treatment.

Certain gene variants are linked to severe acne, especially in males.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

A new perming method is less damaging to hair and works as well as traditional methods.

Scientists made glow-in-the-dark dots from human hair that can detect iron, prevent counterfeiting, and reveal fingerprints.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Hair cortisol concentration partly reflects HPA axis regulation but doesn't capture all its complexities.

High chromogranin A levels are linked to obesity and inflammation in polycystic ovary syndrome.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

The gene Prss53 affects hair shape and bone development in rabbits.

A mouse gene mutation increases the risk of skin cancer.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Hox genes control hair follicle stem cell regeneration in different body regions.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

The B2C promoter works in sheep cells but not in mouse embryos.