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

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

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.

Aromatase gene variation may increase female hair loss risk.

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

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.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

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.

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

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

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

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.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

A special microbe helps plants absorb rock phosphate by growing on their root hairs.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

The cause of atypical Cushing's syndrome in dogs, possibly linked to sex hormones, is not yet proven.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Longer CAG repeats in gene linked to more severe hair loss in females.