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Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Inhibiting 5α-reductase can help reduce prostate cancer risk and improve treatment.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Fatty acid transport protein 4 is essential for skin and hair development.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The EDAR gene greatly affects hair thickness in Asian populations.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

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

A new gene, JMJD1C, may affect testosterone levels in men.

Muscles and nerves that cause goosebumps also help control hair growth.

New treatments for male hypogonadism are effective and should be personalized.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

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

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Scientists found a gene in mice that causes early hearing loss.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Products should be called 'sperm-safe' only after thorough, well-designed tests.