Search

everythinglearnresearchcommunity

for

Search:↓

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Improving artificial vascular grafts requires better materials and surface designs to reduce blood clotting and support blood vessel cell growth.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Genetically-altered adult stem cells can help in wound healing and are becoming crucial in regenerative medicine and drug design.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Certain gene variations are not a major cause of male infertility in Nigerian men.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

The most effective treatments for hair loss are minoxidil, finasteride, PRP, and hair transplants, with steroids and immunosuppressants for autoimmune types.

Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Brain hormones significantly affect hair color and could potentially be used to prevent or reverse grey hair.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Hair analysis can show nutritional status and environmental exposure, with phosphorus being very stable in hair and differences found based on gender and conditions like depression and autism.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

The hair-growth formula with L-cystine helps protect and grow hair cells.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Melatonin may benefit skin health and could be a promising treatment in dermatology.

The PDGF/PDGFR pathway is a potential drug target with mixed success in treating various diseases, including some cancers and fibrosis.

Melatonin helps regulate hair growth and protects the hair follicle from stress.

Olive oil compounds may help prevent cancer in animals, but human results are mixed.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Researchers identified specific genes that are important for mouse skin cell development and healing.

Researchers found a gene mutation responsible for a rare hair loss condition.