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Chromosomal differences affect how muscle cells respond to testosterone.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

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

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

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

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.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

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

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

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

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

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.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

Alopecia in captive rhesus macaques is affected by season, sex, age, housing, and stress, with complex links between stress hormones and hair loss.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Different monkey species in a lab showed varying levels of hair loss due to factors like type, sex, age, season, and living conditions.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Most youth with gender dysphoria received hormones, had minor complications, and showed a decrease in suicide attempts after treatment.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A 10-year-old boy had the earliest reported case of hair that became progressively kinkier but eventually returned to normal on its own.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

Aromatase gene variation may increase female hair loss risk.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.