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miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Some natural compounds may help overcome drug resistance in certain cancers, but more research is needed.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

The SOSTDC1 gene is crucial for determining sheep wool type.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

Different substances that activate or block the androgen receptor can affect male development and treat conditions like prostate cancer.

Taking 5α-reductase inhibitors with prednisolone can worsen its negative effects on metabolism.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The document concludes that understanding hair follicle cell cycles is crucial for hair growth and alopecia research, and recommends specific techniques and future research directions.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Diet changes can protect against harmful environmental effects on fetal development.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Understanding and manipulating epigenetic changes can potentially lead to human organ regeneration therapies, but more research is needed to improve these methods and minimize risks.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

No clear link between androgen receptor variation and hair loss, but more research needed.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

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