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

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Whale genes show changes that help them live in water, like less hair and better flippers.

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

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

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

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

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.

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

FGF5 gene mutations cause long hair in domestic cats.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Genetic discoveries are leading to new treatments for alopecia areata.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Melatonin helps improve Cashmere goat hair quality by promoting hair follicle growth through a specific cell signaling pathway.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Blocking IL-12/IL-23 does not help with hair loss in alopecia areata for mice or humans.