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A specific gene mutation causes varying hair loss severity in a Pakistani family.

Dapagliflozin helps protect heart cells under stress by improving mitochondrial function and reducing cell damage.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

A rare ovarian tumor was successfully treated with surgery and chemotherapy.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

PCS rats show significant inner ear damage and zinc deficiency, similar to liver cirrhosis patients.

New ultrasound criteria for diagnosing PCOS in North African patients were successfully established.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

The procedure involving seminal vesiculoscopy, TURED, and balloon dilation effectively treated a man's hematospermia and improved his dysorgasmia.

DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Mite infestations severely harm the health of endangered Amargosa voles.

New treatments using stem cells and special materials show promise for severe eye surface disease.

Women with PCOS have a higher risk of diabetes and heart problems, especially when they get older.

Cats can have hypersomatotropism without diabetes, suggesting current diagnosis methods may miss cases.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Desmoglein 3 is important for keeping hair follicle stem cells inactive and maintaining their special properties.

Increasing TSPO in the brain reduces anxiety and depression.

BST2 protein and certain T cells increase in early alopecia areata.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Non-canonical Wnt signaling helps intestinal stem cells move to injury sites for tissue repair.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Oxytocin from hair cells helps hair growth and stem cell increase.

Mini pulse corticosteroid therapy with oral dexamethasone is effective and has fewer side effects for treating extensive alopecia areata.

Calcium channels are vital for normal skin function and their dysfunction can lead to skin issues.