Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations increase the risk of alopecia areata in Koreans.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

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.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

The document concludes that Cutaneous Lupus Erythematosus has different forms, is influenced by genetic and environmental factors, and can be treated with various medications, but more targeted therapies are needed.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Alopecia areata involves immune response and gene changes affecting hair loss.

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

The Itpr3 gene causes a specific hair pattern in mice.

ESR2 gene linked to female-pattern hair loss.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Most people with systemic lupus erythematosus have skin problems, and skin symptoms are often the first sign of the disease.

The EDAR gene greatly affects hair thickness in Asian populations.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

The document concludes that rapid identification, isolation, and strict infection control are crucial to manage SARS outbreaks.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

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

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A gene variation is linked to hair thickness in Asians.

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