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Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Human hair follicle stem cells show signs of low oxygen levels, which may be important for hair growth and preventing baldness.

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

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.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Mice with CBS deficiency are healthier on a low-methionine diet.

Hair loss risk is influenced by multiple genes.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

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

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

GPR39 is linked to certain cells in the sebaceous gland and helps with skin healing.

Alopecia areata involves specific T-cells, unlike androgenetic alopecia.

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

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

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

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

ACTH may be an effective first-line treatment for acute calcium pyrophosphate crystal arthritis.

AHCC reduces hair loss and liver injury caused by chemotherapy in rodents.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

Researchers developed a way to study human body clocks using hair tissue, which works similarly in both healthy and dementia patients.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Finasteride reduces melanin production, possibly treating hyperpigmentation and melanoma, but needs more safety research.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Hair growth is influenced by hormones and goes through different phases; androgens can both promote and inhibit hair growth depending on the body area.