Search

everythinglearnresearchcommunity

for

Search:↓

Certain bacteria and fungi are linked to healthy scalps and dandruff, suggesting that the scalp's microbial balance affects its health.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The document concludes that mouse models are helpful but have limitations for skin wound healing research, and suggests using larger animals and genetically modified mice for better human application.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Different types of stem cells with unique roles exist in blood, skin, and intestines, and this variety is important for tissue repair.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Mutations in certain receptors can cause diseases and offer new treatment options.

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

Mycorrhizal fungi and shading improve tea plant growth and nutrient uptake by changing hormone levels and gene expression.

Researchers developed a method to identify and analyze cyclosporin compounds and their structures effectively.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Syphilis is becoming more common and remains a major health problem due to challenges in prevention and treatment.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

People with atopic dermatitis have different skin bacteria, and targeting these bacteria might help treat the condition.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Gut health affects skin diseases, and probiotics might help.