Search

everythinglearnresearchcommunity

for

Search:↓

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Parkinson's disease is linked to skin disorders and skin cells help in studying the disease.

Genetic marker rs12558842 strongly linked to male hair loss.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

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

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

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

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Researchers found a new mutation causing total hair loss from birth.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Wait 3 months after COVID-19 before trying assisted reproduction and further research is needed on COVID-19's effects on male hormones and fertility.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.