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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.

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

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.

Finasteride increases hair density in female androgenetic alopecia, but individual results may vary.

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.

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.

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.

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

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.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Early diagnosis and aggressive treatment are crucial for better outcomes in lymphomatoid granulomatosis.

No link found between new male baldness genes and female hair loss.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.