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Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Gray hair can potentially be reversed, leading to new treatments.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

No clear link between specific gene and hair loss in Mexican brothers.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

The document does not determine if adults with aphallia are fertile.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

The document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Alopecia areata treatment should be personalized, using topical or systemic therapies based on severity, with promising options like JAK inhibitors needing more research.

The treatment was ineffective in humans.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

A group has developed therapies that show promise for treating cancer and various other conditions.

A specific genetic deletion in goats affects cashmere yield and thickness.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Wild African goats have genetic adaptations for surviving harsh desert conditions.