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AR gene not major factor in female hair loss; different from male hair loss.

The document concludes that accurate diagnosis and personalized treatment are important for skin problems in women with PCOS.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Forensic DNA phenotyping is becoming useful for predicting physical traits in criminal investigations but is limited by ethical concerns and incomplete genetic understanding.

cp-asiAR may effectively treat hair loss by targeting androgen receptors.

Gene regulation could revolutionize hair color by altering pigmentation from within.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

ODC transgenic mice can model human hair loss with skin lesions.

Newborns with ichthyosis need specific care based on their skin type.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Anovulatory PCOS patients are younger with longer cycles and higher blood pressure and hormone levels.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Baldness, especially at the front, may lower the risk of testicular cancer by 31%, but its link to prostate cancer is unclear.

PCOS is a hormonal disorder causing symptoms like excess hair, acne, irregular periods, and fertility issues.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

Women with Polycystic Ovary Syndrome (PCOS) have a lower health-related quality of life, especially those with an anovulatory phenotype, and may need specific interventions to improve it.

Women with Polycystic Ovary Syndrome (PCOS) have a lower health-related quality of life, especially those with an anovulatory phenotype, and need specific interventions to improve it.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Certain existing drugs, like glycopyrronium and botulinum toxin type A, may help treat excessive sweating.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

HOXC13 is essential for hair and nail development by regulating Foxn1.

PCOS is a hormonal disorder causing symptoms like irregular periods and acne, and increases the risk of diabetes and heart disease.

Melanoma patients can learn to check their skin, early balding in men may indicate similar risks as PCOS in women, certain criteria can help predict skin cancer behavior, small skin cancer may not need extra therapy after surgery, and sterile gloves don't reduce infection in minor surgeries.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.