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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Keratins are crucial for cell structure, growth, and disease risk.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

The article concludes that proper antifungal treatment is essential for treating scalp fungal infections in children, and trichoscopy is useful for diagnosis and monitoring.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Steroids are the best treatment for Alopecia Areata with few side effects.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Short daily photoperiods improve cashmere production in Inner Mongolia white cashmere goats.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Light microscopy is useful for diagnosing different hair disorders.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Vimentin and transthyretin proteins are linked to black coat color in sheep.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

A new gene variant causes glucocorticoid resistance in a mother and son.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

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.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.