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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.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

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.

The document explains how to identify different hair problems using a microscope.

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.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

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

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.