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hsa_circ_0001079 may help diagnose and treat hair loss.

Different small areas within hair follicles send specific signals that control what type of cells stem cells become.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Using existing drugs for new purposes could be a cost-effective way to treat chest pain and non-clogged heart arteries, with some drugs for lung blood pressure showing promise but needing more testing.

Combining dermoscopy and calcium fluorescent white staining improves diagnosis and treatment of hair fungal infections.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

A pet ferret had a serious infection from Mycobacterium xenopi, which can spread to humans.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The main prostate diseases in dogs are benign growth, infections, and cancer, with various treatments ranging from drugs to surgery, but cancer treatments have limited success.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Type 1 Diabetes prevents hair growth by causing cell death in hair follicles.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

The document concludes that there have been significant advances in the treatment and diagnosis of various skin conditions.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

The yeast found in a sea lion's skin lesion was almost identical to that on healthy skin, suggesting environmental factors may affect fungal growth and the cause of the lesion is unclear.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

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

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.