Search

everythinglearnresearchcommunity

for

Search:↓

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Cellular senescence has both cancer-blocking and cancer-promoting effects, and targeting senescent cells may improve health and lifespan.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

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.

Female Pattern Hair Loss affects women's self-esteem and needs more research for better treatment.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

New research is helping develop better treatments for alopecia areata.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Women with PCOS are more likely to have impaired glucose tolerance and type 2 diabetes, especially if they are Asian or obese.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

People with alopecia areata have more Th17 cells and fewer Treg cells, which may be key to the condition's development.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

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

Special immune cells called Regulatory T cells help control skin inflammation and repair in various skin diseases.

Certain microRNAs are linked to various skin diseases and could be used to diagnose and treat these conditions.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Fine wool sheep have more genes for wool quality, while coarse wool sheep have more for skin and muscle traits.

The document concludes that diagnosing and treating hair loss is complex and requires understanding its psychological effects and underlying causes, while also calling for more research and new treatments.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

Redheaded people may have evolved to efficiently make vitamin D in areas with less sunlight.

New treatments targeting T-cell pathways are needed for better alopecia areata management.

Minoxidil, a common alopecia medication, might cause eye changes due to its properties and lack of tissue selectivity.