Search

everythinglearnresearchcommunity

for

Search:↓

Hepatitis B virus alters steroid hormones in male mice, reducing dihydrotestosterone to inhibit viral replication.

Hidradenitis suppurativa may mainly affect vellus hair follicles, not terminal ones.

DHEA may play a complex role in PCOS, affecting hormones, metabolism, and symptoms.

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

DHT inhibition may increase spinal bone growth in ankylosing spondylitis.

Spironolactone reduces the enzyme activity that converts testosterone to DHT, helping treat excessive hair growth in women.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A woman's severe insulin resistance improved with treatment, but she still had high testosterone levels due to ovarian issues.

Early biotin treatment can reverse symptoms of congenital biotinidase deficiency.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Leydig cell tumors can cause hormone issues in postmenopausal women even if imaging looks normal.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

The vitamin D receptor can affect gene activity even without its usual hormone in hair and skin.

DHEA acts like a male hormone on rat skin glands and doesn't turn into female hormones there.

DHEA treatment helps grow pubic hair and boosts mood in girls with adrenal issues.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

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

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Targeting impaired Nrf2 signaling might help treat hidradenitis suppurativa early on.

Vitamin D receptor is crucial for starting hair growth after birth.

Venous catheterization may help diagnose the cause of female hyperandrogenism when imaging is unclear.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

Lack of cystatin M/E causes thin hair and dry skin.

Inhaled steroids in children may cause excessive hair growth and not always go away after stopping the medication.