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Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Genetic discoveries are leading to new treatments for alopecia areata.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

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

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

Hair loss gene found on chromosome 3q26.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Low and ultralow doses of flutamide can cause liver damage in young women with high androgen levels, regardless of dose or birth control use, with higher risk for those with higher BMI and liver enzyme levels before treatment.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

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

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Hormones affect prostate health and disease, with certain hormone imbalances linked to prostate cancer and benign prostatic hyperplasia.

HOXC13 is essential for hair and nail development by regulating Foxn1.

No genetic link between prostaglandins and hair loss found.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Six new hair loss factors in men not linked to female hair loss.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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