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Melatonin improved mental health and metabolism in women with PCOS.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Researchers found a genetic region that influences the number of coat layers in dogs.

Women with hirsutism have different levels of omentin-1, which may be linked to the condition and its genetic aspects.

New models predict male pattern baldness better than old ones but still need improvement.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Certain genes may influence hair loss differently in men and women.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

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

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

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

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

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

A genetic variant linked to hair thinning in Japanese women was found.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

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

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

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

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

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A mother's diet at conception can cause lasting genetic changes in her child.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.