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The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

A male with aromatase deficiency improved bone health with estradiol treatment.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

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

The 3D scaffold helped maintain hair cell traits and could improve hair loss treatments.

Hair can regrow in large wounds through a process similar to how hair forms in embryos, and understanding this could lead to new treatments for hair loss or scarring.

Mice with CBS deficiency are healthier on a low-methionine diet.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Caucasian and Asian women with PCOS generally show similar symptoms, except Asian women have less chest hair.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

VDR regulation varies by tissue and is crucial for its biological functions.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Scientists have created a method to deliver specific cells that can regenerate hair follicles, potentially offering a new treatment for hair loss.

A gene mutation in mice causes permanent hair loss and skin issues.

Women with PCOS in Sicily show different levels of metabolic problems depending on their PCOS type, with obesity and abnormal lipid profiles being common.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

ADM scaffolds help skin heal by promoting a healing-type immune response.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

Measuring the distance from the anus to the clitoris may moderately help diagnose polycystic ovary syndrome, especially in certain cases.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Scientists can grow human hair follicle stem cells in a lab without changing their nature, which could help treat hair loss.

Certain drugs change freshwater snail shells to a "banana" shape.