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The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

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

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Hormones and genes affect hair growth and male baldness.

Antiandrogen therapy helps treat genetic hair loss.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

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

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

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

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

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

Chicken feather growth involves specific genes and shares similarities with hair development.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Mutations in specific llama genes may affect fiber quality for textiles.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

FGF13 gene changes cause excessive hair growth in a rare condition.

The document explains the genetic causes and characteristics of inherited hair disorders.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Baldness and shaved heads change how traits are seen but don't really affect leader preferences.