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The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

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

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Keratin mutations cause skin diseases and could lead to new treatments.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The document concludes that while finding animal models for the skin disease Hidradenitis suppurativa is challenging, certain mouse mutations may provide useful insights for research and drug testing.

Hair loss in men treated best with early medication or transplant, new treatments researched.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Cantú syndrome may be linked to pituitary adenomas.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.