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Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Future hair cosmetics will be safer and more effective.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Different genes are linked to various types of hair loss.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

Caffeine may help hair growth in hereditary hair loss.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Woolly hair is a rare genetic condition with no effective treatments.

A gene mutation causes woolly hair in a Syrian patient.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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

The document explains how to identify different hair problems using a microscope.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.