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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Insulin resistance and high male hormone levels are major causes of Polycystic Ovary Syndrome.

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

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Bone marrow stem cells and their medium help hair regrowth.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

Some women with PCOS have rare genetic variants linked to the condition.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

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

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Hair follicles are key to treating vitiligo and alopecia areata, but challenges exist.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

The conclusion is that accurately identifying the cause of high androgen levels in women with PCOS is crucial and requires specific tests.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

A new 3D culture system helps grow and study mouse skin stem cells for a long time.

Hordenine may help hair grow by activating a specific cell growth pathway.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

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

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

The CORIN gene variant causes the golden color in Siberian cats.