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The conclusion is that certain chemicals from Bacillus subtilis help improve plant root growth through a hormone-related process.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

The Wnt/β-catenin pathway helps tissue regeneration but can also cause fibrosis, and drugs that inhibit this pathway may aid in healing skin and heart tissues.

Fibromodulin treatment helps reduce scarring and improves wound healing by making it more like fetal healing.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

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 Plcd1 and Plcd3 together cause severe hair loss in mice.

Growth factors are crucial for hair development and could help treat hair diseases.

EGF controls hair growth by regulating hair follicles' growth phases.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Bacillus subtilis strain WM13-24 helps plant root growth through volatile compounds.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

RXRα is crucial for proper immune response and links diet to immune function.

Janus kinase inhibitors are promising drugs for treating autoimmune and inflammatory diseases.

Sorafenib often causes mucositis, hand-foot syndrome, rash, alopecia, diarrhea, and fatigue.

The document concludes that the skin's immune system is complex, involving interactions with hair follicles, nerves, and microbes, and can protect or cause disease, offering targets for new treatments.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Calcipotriol's effectiveness for treating alopecia areata is unclear and needs more research.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

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

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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

A specific genetic deletion in goats affects cashmere yield and thickness.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.