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Mitochondrial transport protein
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Ebook "Cell biology of the axon" focus on endogenous cytoskeletal systems that structurally organize the axon, confer tensile strength, and mediate intracellular transport and growth cone motility. Specifically, Shea et al. address issues of how organizational dynamics of neurofilaments are regulated, including mechanisms of transport, and how dysregulation of transport can contribute to motor neuron disease.
369p
tracanhphuonghoa1007
22-04-2024
5
1
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In ebook "Mitochondria: The dynamic organelle" the term mitochondrion is derived from Latin, with mitos meaning thread and chondrion meaning granules. Indeed, under the light microscope, mitochondria often appear as rods or granules within the cytoplasm. For decades after initial visualization of mitochondria by light microscopy, mitochondrial function remained clouded.
359p
cotieubac1004
15-03-2024
4
0
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Part 2 book "Marks' basic medical biochemistry - A clinical approach" includes content: Basic concepts in the regulation of fuel metabolism by insulin; glucagon, and other hormones, cellular bioenergetics - adenosine triphosphate and O2; digestion, absorption, and transport of carbohydrates; generation of adenosine triphosphate from glucose, fructose, and galactose - glycolysis; tricarboxylic acid cycle; oxidative phosphorylation and mitochondrial function; oxygen toxicity and free radical injury; formation and degradation of glycogen.... and other contents.
366p
oursky07
24-10-2023
4
3
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Mitochondrial DNA (mtDNA) codes for products necessary for electron transport and mitochondrial gene translation. mtDNA mutations can lead to human disease and influence organismal fitness.
15p
vihagrid
30-01-2023
4
3
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The cytokinin production and transport from root to leaves is hindered under water stress causing leaf senescence due to the synthesis of hydrolytic enzymes. A part of stress effect may be linked to the regulation of osmotic solutes and maintenance of turgidity for stomatal conductance, photosynthesis and protein synthesis accompanied with reduced peroxidation of chloroplast and mitochondrial membranes in pearl millet under kinetin and cycocel treatments.
9p
angicungduoc8
07-11-2020
12
2
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Many cancer cells exhibit reduced mitochondrial respiration as part of metabolic reprogramming to support tumor growth. Mitochondrial localization of several protein tyrosine kinases is linked to this characteristic metabolic shift in solid tumors, but remains largely unknown in blood cancer.
14p
viamsterdam
18-09-2020
17
1
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We recently reported, using immunoscreening of a T7 complementary DNA (cDNA) library of breast cancer (BC) proteins with sera from patients with BC, the presence of autoantibodies targeting several mitochondrial DNA (mtDNA)-encoded subunits of the electron transport chain (ETC) in complexes I, IV, and V.
12p
vikuala271
13-06-2020
11
1
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Recently we showed that de novo expression of a turtle riboflavin-binding protein (RfBP) in transgenic Arabidopsis increased H2O2 concentrations inside leaf cells, enhanced the expression of floral regulatory gene FD and floral meristem identity gene AP1 at the shoot apex, and induced early flowering.
16p
viminato2711
22-05-2020
12
2
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In filamentous fungi, transport of organic acids across the mitochondrial membrane is facilitated by active transport via shuttle proteins. These transporters may transfer different organic acids across the membrane while taking others the opposite direction.
8p
vihamax2711
21-04-2020
18
2
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Mitochondrial dysfunction has been previously identified in neurodegenerative diseases such as Alzheimer disease, Huntington disease, and Parkinson disease.
21p
nutifooddau
27-01-2019
22
2
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To gain better insight into the insulin secretory activity of fetalbcells in response to glucose, the expression of glucose transporter 2 (GLUT-2), glucokinase and mitochondrial glycerol phosphate dehydrogenase (mGDH) were studied. Expression ofGLUT-2mRNA and protein in pancreatic islets and liver was signi®cantly lower in fetal and suckling rats than in adult rats.
9p
research12
29-04-2013
44
2
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Mitochondrial fatty acid oxidation deficiencies are due to genetic defects in enzymes of fatty acidb-oxidation and transport proteins.Genetic defects have been identified in most of the genes where nearly all types of sequence vari-ations (mutation types) have beenassociatedwithdisease.In this paper, we will discuss the effects of the various types of sequence variations encountered and review current know-ledge regarding the genotype–phenotype relationship, espe-cially in patients with acyl-CoA dehydrogenase deficiencies where sufficient material exists for a meaningful discussion....
13p
dell39
03-04-2013
47
2
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Alr1p is an integral plasma membrane protein essential for uptake of Mg2+ into yeast cells. Homologs of Alr1p are restricted to fungi and some protozoa. Alr1-type proteins are distant relatives of the mitochondrial and bacterial Mg 2+ -transport proteins, Mrs2p and CorA, respectively, with which they have two adjacent TM domains and a short Mg 2+ signature motif in common.
14p
inspiron33
25-03-2013
46
3
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The mitochondrial carriers are a family of transport proteins that shuttle metabolites, nucleotides and cofactors across the inner mitochondrial mem-brane. The genome ofDrosophila melanogasterencodes at least 46 mem-bers of this family. Only five of these have been characterized, whereas the transport functions of the remainder cannot be assessed with certainty.
10p
mobifone23
18-01-2013
33
2
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