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Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

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

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Different markers are found in stem cells of the scalp's hair follicle bulge and the surrounding skin.

Scientists found out the structure of a human enzyme linked to prostate cancer and hair loss, which could help in designing drugs.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

pCLCA2 protein may help maintain skin structure and function.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

Diabetic neuropathy in mice is linked to poor mitochondria function and lower brain hormone production.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

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

Cholesterol-related compounds can stop hair growth and cause inflammation in a type of scarring hair loss.

Scientists found genes linked to the growth of high-quality brush hair in Chinese Haimen goats.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Hyaluronic acid injections improve skin thickness and quality, protecting against aging in rats.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

TGF-β signaling is crucial for stem cell maintenance, differentiation, and has implications for cancer treatment.

JAK inhibitors show promise for treating skin and hair disorders but need more research on long-term safety and effectiveness.

Thai rice bran extracts, especially from Tubtim Chumphae rice, can significantly reduce the activity of hair loss genes, with x-tocopherol showing potential as an anti-hair loss product.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.