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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Plant sterols have health benefits like lowering cholesterol, but more research is needed to understand their effects and improve their extraction and sustainability.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Both genetics and lifestyle factors contribute to male pattern baldness.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Toothpaste containing α-tocopherol acetate, l-menthol, and stevioside can promote hair growth in mice.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

Cyclosporine A may help treat hair loss by blocking a protein that inhibits hair growth.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Androgens are important for normal ovarian function and estrogen production, but may not be the main cause of follicle death.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Human hair contains diverse proteins, including keratins and histones, which could help assess hair health and aging.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Researchers developed a new method to identify animal hair in textiles, which is effective for various fibers and more reliable than previous methods.

Prolactin may affect hair growth differently based on gender and scalp area.

The document concludes that there are various treatments for different types of alopecia, but more research is needed for evidence-based treatments.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Wait 3 months after COVID-19 before trying assisted reproduction and further research is needed on COVID-19's effects on male hormones and fertility.