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Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

PCOS is a common hormonal disorder in women that can affect skin, fertility, and metabolism, and treatment is tailored to individual needs.

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.

Effective treatments for premature hair graying still require significant research.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Sustained-release sodium valproate is effective in treating epilepsy, with some side effects influenced by genetics.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

There's no significant genetic link between male pattern baldness and COVID-19.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

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

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Hormones and genes affect hair growth and male baldness.

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.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Mutant mice help researchers understand hair growth and related genetic factors.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.