Topic Review
Effects of Vitamin D on Satellite Cells
Vitamin D is a micronutrient that plays a role in the homeostasis of various body organs, including skeletal muscle. Skeletal muscle growth and regeneration are critically affected by satellite cells, skeletal muscle stem cells. The discovery of vitamin D receptors on satellite cells supports the role of vitamin D in regulating satellite cell function. In vivo studies have shown the effect of vitamin D on skeletal muscle growth in early life, muscle homeostasis in aging, and skeletal muscle regeneration in conditions of muscle injury or chronic disease.
  • 614
  • 10 Nov 2022
Topic Review
Cyclic Adenosine Monophosphate
Cyclic adenosine monophosphate (cAMP, cyclic AMP, or 3',5'-cyclic adenosine monophosphate) is a second messenger important in many biological processes. cAMP is a derivative of adenosine triphosphate (ATP) and used for intracellular signal transduction in many different organisms, conveying the cAMP-dependent pathway.
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  • 10 Nov 2022
Topic Review
List of R1a Frequency by Population
Haplogroup R1a is one of the major classifications (called clades) of Y-chromosome types found in human male lines. It is widespread all across Eurasia. Many sample studies therefore carry information on the incidence of R1a and/or its subclassifications, in particular the dominant branching line represented by the haplogroups R1a1 and R1a1a. The table below collates information from a number of such sample studies, with incidence frequencies in sample data reported as percentages, along with the associated sample sizes.
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  • 09 Nov 2022
Topic Review
TAL Effector
TAL (transcription activator-like) effectors (often referred to as TALEs, but not to be confused with the three amino acid loop extension homeobox class of proteins) are proteins secreted by Xanthomonas bacteria via their type III secretion system when they infect various plant species. These proteins can bind promoter sequences in the host plant and activate the expression of plant genes that aid bacterial infection. They recognize plant DNA sequences through a central repeat domain consisting of a variable number of ~34 amino acid repeats. There appears to be a one-to-one correspondence between the identity of two critical amino acids in each repeat and each DNA base in the target sequence. These proteins are interesting to researchers both for their role in disease of important crop species and the relative ease of retargeting them to bind new DNA sequences. Similar proteins can be found in the pathogenic bacterium Ralstonia solanacearum and Burkholderia rhizoxinica., as well as yet unidentified marine microorganisms. The term TALE-likes is used to refer to the putative protein family encompassing the TALEs and these related proteins.
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  • 08 Nov 2022
Topic Review
Crosstalk
Biological crosstalk refers to instances in which one or more components of one signal transduction pathway affects another. This can be achieved through a number of ways with the most common form being crosstalk between proteins of signaling cascades. In these signal transduction pathways, there are often shared components that can interact with either pathway. A more complex instance of crosstalk can be observed with transmembrane crosstalk between the extracellular matrix (ECM) and the cytoskeleton.
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  • 08 Nov 2022
Topic Review
Dlx Genes in Skeletal Development and Maintenance
Skeletal shape and mechanical properties define, to a large extent, vertebrate morphology and physical capacities. During development, skeletal morphogenesis results from dynamic communications between chondrocytes, osteoblasts, osteoclasts and other cellular components of the skeleton. Later in life, skeletal integrity depends from the regulatory cascades that assure the equilibrium between bone formation and resorption. Finally, during aging, skeletal catabolism prevails over anabolism resulting in progressive skeletal degradation. These cellular processes depend on the transcriptional cascades that control cell division and differentiation in each cell type. Most Distal-less (Dlx) homeobox transcription factors are directly involved in determining the proliferation and differentiation of chondrocytes and osteoblasts and, indirectly, of osteoclasts. The role of these genes in the maintenance of bone integrity has been only partially studied. Dlx genes appear to be involved in several bone pathologies including, for example, osteoporosis. Indeed, at least five large-scale GWAS studies aimed to detect loci associated to human bone mineral density (BMD) have identified a known DLX5/6 regulatory region within chromosome 7q21.3 in proximity of SEM1/FLJ42280/DSS1 coding sequences, suggesting that DLX5/6 expression is critical in determining healthy BMD. 
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  • 08 Nov 2022
Topic Review
Enzymatical Processes
Enzymatical processes topic wants to enhance the central role of enzymes, the real workers from whose silent and tireless work depends the well-being of all cells in fact, intra-cellular reactions that take place in the cells are facilitated and therefore accelerated by enzymes.
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  • 08 Nov 2022
Topic Review
Virus Information Table
Viruses are extremely diverse in nature. Even their method of storing genetic information differs tremendously, from double-stranded DNA to negative sense RNA, as denoted in the Baltimore Classification System. Other features, such as entry and release details, or capsid structure may be important in classifying and understanding viruses.
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  • 08 Nov 2022
Topic Review
Metabolic Regulation of Mitochondrial Protein Biogenesis in neurons
Neurons critically depend on mitochondria for ATP production and Ca2+ buffering. They are highly compartmentalized cells and therefore a finely tuned mitochondrial network constantly adapting to the local requirements is necessary. For neuronal maintenance, old or damaged mitochondria need to be degraded, while the functional mitochondrial pool needs to be replenished with freshly synthesized components. Mitochondrial biogenesis is known to be primarily regulated via the PGC-1α-NRF1/2-TFAM pathway at the transcriptional level. However, while transcriptional regulation of mitochondrial genes can change the global mitochondrial content in neurons, it does not explain how a morphologically complex cell like a neuron adapts to local differences in mitochondrial demand. 
  • 489
  • 07 Nov 2022
Topic Review
Factor V Leiden
Factor V Leiden (rs6025 or F5 p.R506Q) is a variant (mutated form) of human factor V (one of several substances that helps blood clot), which causes an increase in blood clotting (hypercoagulability). Due to this mutation, protein C, an anticoagulant protein that normally inhibits the pro-clotting activity of factor V, is not able to bind normally to factor V, leading to a hypercoagulable state, i.e., an increased tendency for the patient to form abnormal and potentially harmful blood clots. Factor V Leiden is the most common hereditary hypercoagulability (prone to clotting) disorder amongst ethnic Europeans. It is named after the Dutch city of Leiden, where it was first identified in 1994 by Rogier Maria Bertina under the direction of (and in the laboratory of) Pieter Hendrick Reitsma. Despite the increased risk of venous thromboembolisms, people with one copy of this gene have not been found to have shorter lives than the general population.
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