Search

everythinglearnresearchcommunity

for

Search:↓

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

The hair-growth formula with L-cystine helps protect and grow hair cells.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

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

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Targeting lipid metabolism can help treat advanced, resistant cancers.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Selenium in proteins helps prevent over-oxidation and supports chemical reversibility.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Biotinidase deficiency can be easily diagnosed and treated with biotin to prevent serious harm.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Polygoni Cuspidati Rhizoma et Radix contains compounds that inhibit certain enzymes.

A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

An over-the-counter vitamin/mineral supplement improved hair loss and blood sugar control in a woman with non-classic 11-hydroxylase deficiency.

Mustard gas exposure causes hair loss, but treating with N-acetylcysteine can prevent it.

Copper therapy improved health and enzyme activity in mice with copper deficiency.

Valproic acid treatment increases a specific acid in urine by blocking an enzyme, possibly causing skin rash and hair loss.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.