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Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Red fluorescence in AGA scalps is linked to different microbes.

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

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

Vitamin D receptor is crucial for bone health and mineral metabolism.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Alopecia areata involves immune response and gene changes affecting hair loss.

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

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Vitamin E affects liver metabolism, enhancing stress resistance, reducing blood clotting, and altering hormone processing.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

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

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

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