Search

everythinglearnresearchcommunity

for

Search:↓

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Fatty acid transport protein 4 is essential for skin and hair development.

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

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Patients with Alopecia areata have fewer specific immune cells that normally regulate the immune system, which may contribute to the condition.

Safflower has been used in traditional medicine for centuries and shows promise in treating heart, brain, and inflammatory conditions, but more research is needed to ensure its safety.

Hair amino acid levels can indicate metabolic disorders.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

The guidelines suggest lifestyle changes, diet adjustments, and personalized medication to manage dyslipidemia and reduce heart disease risk.

Auxin and ethylene hormones both work together and against each other to control plant growth.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

PCOS is a complex disorder in women that can lead to various health risks and requires personalized treatment.