Search

everythinglearnresearchcommunity

for

Search:↓

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

A woman's male-like symptoms and high testosterone were due to ovarian hilus-cell hyperplasia, which improved after surgery.

An 80-year-old woman's severe hair loss was caused by a hormone-secreting ovarian tumor.

The treatment temporarily improved symptoms of hyperandrogenism in adolescents.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Organoid technology is advancing and entering commercial use, with applications in disease modeling, drug development, and personalized medicine.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

A baby girl had two brain-related growths removed and is developing normally.

A woman's masculine features were caused by a rare ovarian tumor that produced male hormones.

A woman's male-like physical changes were caused by two rare ovarian conditions.

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

A 15-year-old female labrador had a large ovarian tumor removed.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

The document highlights recent findings and treatments in urology, including prostate cancer diagnostics, urinary incontinence, and new therapies.

Lower dosages of 2-(difluoromethyl)-dl-ornithine might reduce side effects, supporting further research.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Markers help differentiate between apocrine and eccrine sweat glands to identify sweat gland tumors.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Cepharanthine may help hair growth by increasing IGF-I in scalp cells.

The conclusion is that a new test was created to find substances that affect specific ion channels, and it works well for drug discovery.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

A rare ovarian cancer with a good outlook was found in a woman with unusual hair growth and abdominal symptoms.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

BAY 43-9006 helps control kidney cancer growth but doesn't significantly increase overall survival.

Surgery is the main treatment for liver hydatidosis, but has risks; albendazole is the most effective drug but can have side effects.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.