Search

everythinglearnresearchcommunity

for

Search:↓

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

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

Researchers found 15 new genetic links to skin traits in Japanese women.

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

Researchers found two new genetic variants linked to Alzheimer's disease.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

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

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

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

A specific genetic deletion in goats affects cashmere yield and thickness.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

No significant link between male pattern baldness and COVID-19 severity was found.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

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

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.