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ATIR101 improves survival in stem cell transplant patients; Australian stem cell treatment decisions are influenced by regulation changes.

Fetal-maternal stem cells in a mother's hair can help with tissue repair and regeneration long after childbirth.

Skin problems are common after stem cell transplants, and early treatment by dermatologists can improve patient outcomes.

Skin changes like hair loss, white patches, and nail changes are common in children after bone marrow transplants, often linked to chronic rejection.

Cancer treatments can cause skin-related side effects that may affect patient quality of life and require changes in treatment.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Found new possible treatments for hair loss.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

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

The Rotterdam Study aims to understand various diseases in older adults.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Certain inhibitors slow down plant growth by causing early cell specialization without changing the cell development pattern.

Restoring hair bulb immune privilege is crucial for managing alopecia areata.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Genetic marker rs12558842 strongly linked to male hair loss.

Dihydrotestosterone causes p27 protein breakdown in ovarian and breast cancer cells by binding with SKP2.

Heparin and protamine are promising in tissue repair and organ regeneration, including skin and hair.

Hairless gene not strongly linked to baldness.

ACTH may be an effective first-line treatment for acute calcium pyrophosphate crystal arthritis.

Mutation in hairless gene may increase hair loss risk.

Certain gene variations increase the risk of alopecia areata in Koreans.

Androgens can both increase body hair and cause scalp hair loss.