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The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Antibiotics can reduce acne but may lead to resistant bacteria, and understanding the skin's bacteria is important for treatment.

MicroRNA-302 helps improve the conversion of body cells into stem cells by blocking NR2F2.

Estrogens help reduce skin aging, and SERMs might offer similar benefits without the risks of hormone therapy.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

The document explains how the male reproductive system works, its role in making testosterone, and how conditions like obesity can disrupt it, leading to low testosterone and fertility issues.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

AR polyglycine repeat doesn't cause baldness.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

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

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

A gene called HDAC9 might be a new factor in male-pattern baldness.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Short-term testosterone therapy in women seems safe with few mild side effects, but long-term effects need more research.

Exosomes can improve skin health and offer new treatments for skin repair and rejuvenation.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.