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The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Alopecia areata is an incurable autoimmune condition causing hair loss, with research aiming for better treatments.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Topical minoxidil is the best-supported treatment for female hair loss, but personalized plans are needed.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

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

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Bimatoprost is safe and effective for improving eyebrow hair.

The study suggests that a new protease inhibitor can make hair harder to pull out, potentially reducing hair loss.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Trichoscopy helps diagnose and monitor alopecia areata by looking at a combination of specific hair and scalp features.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

Yellow dots and short vellus hairs are the most common signs of Alopecia Areata (AA), and trichoscopy can help diagnose AA and track treatment progress.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Bimatoprost is promising for treating some types of hair loss but needs more testing for androgenetic alopecia.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.