Search

everythinglearnresearchcommunity

for

Search:↓

Scientists found a gene in mice that causes early hearing loss.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

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.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Skin stem cells maintain and repair the outer layer of skin, with some types being essential for healing wounds.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Research on epidermal stem cells has advanced significantly, showing promise for improved clinical therapies.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

Excessive hair growth in women often has no known cause and is not linked to race or other hormonal symptoms.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

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

Skin fat plays a key role in immune defense and healing beyond just storing energy.

These skin conditions in African men need combined medical treatments and lifestyle changes.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Hair follicles offer promising targets for delivering drugs to treat hair and skin conditions.

Human enzymes can detoxify harmful substances but might also increase their cancer risk.