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Topic Review
MicroRNAs in Dystrophinopathy
Dystrophinopathies are a group of X-linked inheritance disorders characterized by loss of limbs, loss of respiratory and cardiac muscle strength, and destruction of nerve tissue. There are two main forms of dystrophinopathy: Duchenne muscular dystrophy (DMD), which develops in early childhood and presents with severe symptoms, and Becker muscular dystrophy (BMD), which develops late as a milder form.
  • 397
  • 28 Jul 2022
Topic Review
Involvement of Immune Cells in CC Immunosuppressive TIME
Cervical cancer (CC) is a major health problem in women of childbearing age. The immune response plays a crucial role in detecting and preventing the development of CC. However, factors such as age, prior or repeated human papillomavirus (HPV) infection, changes in the microbiota of the reproductive tract, and lifestyle choices can lead to immune dysregulation and increase the risk of CC. One of the critical components of the TIME is tumor-infiltrating lymphocytes (TILs), which are altered in CC and can contribute to tumor growth. 
  • 398
  • 04 Jul 2023
Topic Review
PTP1B
The tyrosine phosphatase 1B (PTP1B) acts as a key negative regulator of insulin receptor, and a plethora of studies confirmed that uncontrolled activity of this enzyme is one of the main causes that lead to IR (insulin resistance). According to this hypothesis, it has been demonstrated that the overexpression of PTP1B promotes IR in liver, muscle, adipose tissue, pancreas, and brain.
  • 396
  • 29 Sep 2021
Topic Review
Effect of H. sabdariffa Extract on Obesity
H. sabdariffa derived bioactive compounds are potent in the treatment of obesity with an evident reduction in body weight, inhibition of lipid accumulation and suppression of adipogenesis through the PPARγ pathway and other transcriptional factors. 
  • 396
  • 30 Nov 2021
Topic Review
Alpha Thalassemia Abnormal Morphogenesis
Alpha Thalassemia-Abnormal Morphogensis is a group of blood disorders that affect the way the body makes hemoglobin. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. It's made up of alpha globin and beta globin. Normally each person has four genes for alpha globin, Alpha thalassemia happens when one or more of the genes that control the making of alpha globin is absent or defective. It can cause anemia ranging from mild to severe. Also causing Genital abnormalities and terminal transverse limb defectiveness which is why it is called abnormal morphogenesis. This is most commonly found in people of African, Middle Eastern, Chinese, Southeast Asian and occasionally, Mediterranean descent.
  • 396
  • 29 Sep 2022
Topic Review
Galectin-3 Targeting Drugs in Various Diseases
Galectin-3 (Gal3) is one of the most studied members of the galectin family that mediate various biological processes such as growth regulation, immune function, cancer metastasis, and apoptosis. Since Gal3 is pro-inflammatory, it is involved in many diseases that are associated with chronic inflammation such as cancer, organ fibrosis, and type 2 diabetes.
  • 396
  • 12 May 2023
Topic Review
Cellular Differentiation
Across embryonic development to late adulthood, highly regulated cellular differentiation is imperative for proper development and growth, as well as for the maintenance of specialized tissues throughout life. In general, this crucial cellular process underlies organogenesis and tissue regeneration, and its dysregulation or pathological dysfunction may accelerate aging and/or the onset of disease. Furthermore, the effects of cannabinoids on cellular differentiation are seen across a broad variety of tissues, including many peripheral tissues such as muscle, bone, and blood.
  • 397
  • 04 Jul 2023
Topic Review
Alternate Causes for Pathogenesis of Exfoliation Glaucoma
Exfoliation glaucoma (XFG) is the most recognizable form of secondary open-angle glaucoma associated with a high risk of blindness. This disease is characterized by white flaky granular deposits in the anterior chamber that leads to the elevation of intraocular pressure (IOP) and subsequent glaucomatous optic nerve damage. Conventionally, XFG is known to respond poorly to medical therapy, and surgical intervention is the only management option in most cases.
  • 395
  • 11 Mar 2022
Topic Review
Intertumoural and Intratumoural Heterogeneity in Melanoma
Tumour heterogeneity is a phenomenon where the cancer cells evolve diversely over the course of the disease. As a result of the evolution, the cancer cells can be found to be genetically, epigenetically and/or phenotypically different in order to survive in the human body. The tumour microenvironment also plays a crucial role during the evolution.
  • 395
  • 01 Jul 2022
Topic Review
NRF2 and Key Transcriptional Targets
Melanocytes are dendritic, pigment-producing cells located in the skin and are responsible for its protection against the deleterious effects of solar ultraviolet radiation (UVR), which include DNA damage and elevated reactive oxygen species (ROS). They do so by synthesizing photoprotective melanin pigments and distributing them to adjacent skin cells (e.g., keratinocytes). However, melanocytes encounter a large burden of oxidative stress during this process, due to both exogenous and endogenous sources.To protect themselves, they utilize numerous antioxidant systems to reduce the amount of reactive oxygen and nitrogen species present in the cell and this activity then contributes towards the prevention of cancer formation. However, after the formation of melanoma these same antioxidant systems are often coopted by the cancer in order to promote its uncontrolled growth and metastasis.
  • 394
  • 06 Apr 2022
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