A5042361704- CRISPR and Genetic Engineering
- Cancer-related molecular mechanisms research
- Connective tissue disorders research
- Immune Cell Function and Interaction
- Pluripotent Stem Cells Research
- Immunotherapy and Immune Responses
- Neurological diseases and metabolism
- Metalloenzymes and iron-sulfur proteins
- Hearing, Cochlea, Tinnitus, Genetics
- T-cell and B-cell Immunology
- Telomeres, Telomerase, and Senescence
- Prenatal Screening and Diagnostics
- Circular RNAs in diseases
- Skin Protection and Aging
- MicroRNA in disease regulation
- Cellular transport and secretion
- Peptidase Inhibition and Analysis
- Microplastics and Plastic Pollution
- Cancer Genomics and Diagnostics
- Mycobacterium research and diagnosis
- Innovation and Socioeconomic Development
- Cancer-related gene regulation
- Tissue Engineering and Regenerative Medicine
- Cancer Immunotherapy and Biomarkers
- Virus-based gene therapy research
Texas A&M University
2023-2024
Shiraz University of Medical Sciences
2021-2024
Scientific research over the past decades has proven pivotal role of long non-coding RNAs (LncRNAs) in regulating gene expression. The immune responses are controlled through interaction pro-inflammatory (predominance T helper 17 cells (Th17)) and anti-inflammatory cytokines excretion Regulatory (Treg)). Recent studies have marked impact many diverse LncRNAs on Treg/Th17 imbalances. Moreover, some roots causes human diseases can be associated with alterations Th17/Treg ratio. In this review...
Aging causes numerous age-related diseases, leading the human species to death. Nevertheless, rejuvenating strategies based on cell epigenetic modifications are a possible approach counteract disease progression while getting old. Cell reprogramming of adult somatic cells toward pluripotency ought be promising tool for diseases. However, researchers do not have control over this process as lose their fate, and cause potential cancerous or unexpected phenotypes. Direct partial were introduced...
Researchers can now target specific DNA sequences and easily modify them thanks to recent developments in CRISPR technology, enabling genome manipulation with unmatched precision. Furthermore, cell reprogramming is one of the most fascinating fields which CRISPR-based techniques are being used. Nowadays, without using embryonic stem cells, scientists change type into another by inserting particular genetic alterations. This has significant implications for regenerative medicine since it...