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Platelet-Rich Plasma (PRP) is a low-risk treatment for Androgenic Alopecia (AGA) that generally improves hair count or density, but more research is needed for optimization.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Lower SHBG levels may increase the risk of PCOS.

PDGF-BB helps young melanocytes grow but stops mature ones from growing, and it makes melanocytes more specialized.

Targeting NETs may help reduce fibrosis in Crohn's disease.

Minoxidil foam 5% effectively treats hair loss in both frontal and vertex scalp regions.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

Humans can accurately guess age from faces, with women being slightly better at it, and age perception is linked to evolutionary factors.

Aromatase gene variation may increase female hair loss risk.

A blood pressure drug, diltiazem, may also help treat influenza.

Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

Scientists successfully purified a protein called Wnt3a, which is involved in processes like hair growth, but the overall yield was low, suggesting more work is needed to improve this.

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

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

Phospholipase A2 is necessary for the correct placement of PIN proteins in plant roots, affecting root growth.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

MALDI Imaging Mass Spectrometry is a useful method for studying skin conditions, but sample preparation is crucial for accurate results.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Skin cell clumping for hair growth is improved by a protein called fibronectin, which helps cells stick and move better.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Researchers created a lab model to study human hair growth, showing it can grow and self-regulate outside the body.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Eplerenone, a mineralocorticoid receptor antagonist, was found to promote hair growth in human hair follicles.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

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.