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The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Genetically-altered adult stem cells can help in wound healing and are becoming crucial in regenerative medicine and drug design.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

People with PCOS have higher levels of PAI-1, which may increase their risk of heart disease and fertility issues.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Stopping S100A3 activity slows down hair growth in mice.

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

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

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

HO-1 helps skin health and healing but can worsen melanoma; it's a potential treatment target for skin diseases.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Men with Frontal fibrosing alopecia typically lose hair on the front scalp and sometimes on sideburns and upper lip, with treatments showing varied success.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

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