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

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

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

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.

Epigenetic changes are crucial for stem cell behavior in skin wound healing and their disruption may lead to cancer.

New genes linked to male pattern baldness were found on chromosome 20p11.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Tofacitinib is safe and effective for severe alopecia areata, but hair loss may return 2 months after stopping treatment.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

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

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

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

New genes found linked to balding, may help develop future treatments.

The document concludes that computational methods using networks and various data can improve the process of finding new uses for existing drugs.

The document concludes that understanding hair follicle cell cycles is crucial for hair growth and alopecia research, and recommends specific techniques and future research directions.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Placental growth factor may help treat hair loss.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

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

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

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

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.

Understanding hair biology is key to developing better treatments for hair and scalp issues.