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The document concludes that while significant progress has been made in understanding skin biology and stem cells, more research is needed to fully understand their interactions with their environment.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

Scientists made the first metal-based compounds from a nonsteroidal antiandrogen drug, which showed potential in fighting both hormone-dependent and independent prostate cancer cells.

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

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

Hair color loss can indicate the effectiveness of a drug targeting the KIT protein in mice and humans.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

Platelet-Rich Plasma (PRP) increases the number of new hair follicles and speeds up hair formation.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

EGFR-TKIs can cause significant skin, nail, and organ side effects.

Wnt, Eda, and Shh pathways are crucial for different stages of sweat gland development in mice.

TGFβ's manipulation of inflammation and immune cells affects cancer spread, suggesting new treatment strategies and biomarkers.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

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

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Certain skin conditions may indicate or increase the risk of Parkinson's disease.

Premature graying of hair may suggest health issues and currently lacks effective treatments.