「GLYCOGEN」の共起表現一覧(1語右で並び替え)
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| Iodine solution will also react with | glycogen, although the color produced is browner and m |
| It is a precursor of | glycogen and can be converted into UDP-galactose and U |
| They store | glycogen and neutralize toxins.These are yellowish in |
| ing which store and transport substances like | glycogen and other nitrogenous wastes. |
| en und seine Beziehungen zur Zuckerkrankheit ( | Glycogen and its Relationship to Diabetes), 1905 |
| gestion inhibits glycogenolysis (breakdown of | glycogen) and gluconeogenesis, resulting in severe hyp |
| Their enlargement is due to | glycogen and lipid accumulation in the cytoplasm allow |
| ade through a muscle biopsy that shows excess | glycogen and then further tests that will show the lev |
| Muscle cell | glycogen appears to function as an immediate reserve s |
| Small amounts of | glycogen are found in the kidneys, and even smaller am |
| fatigue, and predominately uses intracellular | glycogen as a substrate. |
| nder nitrogen-limiting conditions synthesizes | glycogen as an internal reserve material. |
| em has a strong negative regulatory effect on | glycogen biosynthesis, glyconeogenesis and glycogen ca |
| ng a genetic screen for factors that regulate | glycogen biosynthesis. |
| glucose 1-phosphate instead of glucose during | glycogen breakdown is that the very polar phosphorylat |
| An example of this is | glycogen breakdown by glycogen phosphorylase, which ca |
| concluded that the patient had a disorder of | glycogen breakdown that specifically affected skeletal |
| During hypoglycemia, the | glycogen can be converted back to G6P and then convert |
| Much research has been done on | glycogen degradation through studying the structure an |
| ts the phosphofructokinase enzyme, leading to | glycogen depletion and hepatic shift. |
| ubule function in the pinworm adults, causing | glycogen depletion, thereby effectively starving the p |
| The uterus also stores | glycogen during pregnancy to nourish the embryo. |
| ut not on galactose, glucose, maltose, starch | glycogen, ethanol, methanol, formamide, formate, malat |
| Thus, it allows glucose to be converted into | glycogen, fatty acids, and cholesterol even when hexok |
| ge is in the liver and muscles in the form of | glycogen for most multicellular animals, and in intrac |
| ose-glycogen glucosyltransferase phosphatase, | glycogen glucosyltransferase phosphatase, glycogen syn |
| likely the site at which the enzyme binds to | glycogen granules before initiating cleavage of termin |
| Examples of inclusions are | glycogen granules in the liver and muscle cells, lipid |
| phosphorylase in the cell exists as bound to | glycogen granules rather than free floating. |
| ons in the utilization of stored energy, like | glycogen in animals, as well as in the breakdown of ce |
| he plant starches amylose and amylopectin and | glycogen in animal cells. |
| volved in the biosynthesis and degradation of | glycogen in the body. |
| sed on the interconversion of lactic acid and | glycogen in muscle, recapitulating the work of Otto Me |
| uce hepatic glycogenolysis (transformation of | glycogen into glucose) and to reduce the absorption of |
| on demand, readily do break down their stored | glycogen into glucose and send it through the blood st |
| acetate, a substance that blocks breakdown of | glycogen into glucose and prevents the formation of la |
| enzymes that convert | glycogen into glucose |
| Glycogenolysis - the breakdown of | glycogen into glucose, which provides a glucose supply |
| omers connected via beta-glycosidic linkages; | glycogen is a branched form, where the glucose monomer |
| Glycogen is a molecule the body uses to store carbohyd | |
| Glycogen is also a suitable storage substance due to i | |
| and exocrine), it also has effects on hepatic | glycogen levels and gastrointestinal secretions. |
| In this case, due to the low | glycogen levels in the ketogenic diet, competitive ath |
| rable to hydrolysis (like in the breakdown of | glycogen or starch, as in the example above) because g |
| y tissues (which then either accumulate it as | glycogen or use it for energy production); the consequ |
| glucose 6-phosphate may also be converted to | glycogen or starch for storage. |
| te) may be converted to G1P for conversion to | glycogen, or it is alternatively converted by glycolys |
| clude PR-enzyme, phosphorylase a phosphatase, | glycogen phosphorylase phosphatase, protein phosphatas |
| glycogen phosphorylase | |
| Glycogen phosphorylase isoenzyme BB (abbreviation: GPB | |
| Glycogen phosphorylase is activated by phosphorylation | |
| Epinephrine not only activates | glycogen phosphorylase but also inhibits glycogen synt |
| Mutations in the muscle isoform of | glycogen phosphorylase (PYGM) are associated with McAr |
| The final, perhaps most curious site on the | glycogen phosphorylase protein is the so-called glycog |
| s the direct product of the reaction in which | glycogen phosphorylase cleaves off a molecule of gluco |
| Other enzymes related to | glycogen phosphorylase are abbreviated as GPLL (liver) |
| Glycogen phosphorylase is regulated by both allosteric | |
| PLP is also found on | glycogen phosphorylase in the liver, where it is used |
| hers, is shared with related enzymes, such as | glycogen phosphorylase and other glycosyltransferases |
| Phosphorylase is also a common name used for | glycogen phosphorylase in honor of Earl W. Sutherland |
| orylase is a form of phosphorylase similar to | glycogen phosphorylase, except that it acts upon starc |
| Returning to | glycogen phosphorylase, the less active form (b) can i |
| phorylase is the muscle isoform of the enzyme | glycogen phosphorylase. |
| of glucose-1-phosphate from a glucan such as | glycogen, starch or maltodextrin. |
| syndrome, tyrosinemia (Type I), galactosemia, | glycogen storage diseases, and fructose intolerance. |
| n the PFKM gene results in Tarui's disease, a | glycogen storage disease where the ability of certain |
| Glycogen storage disease type V - muscle glycogen | |
| Glycogen storage disease type XI is a form of glycogen | |
| Glycogen storage disease type 0 is characterized by a | |
| Unlike most other | glycogen storage diseases, it directly affects glycoly |
| Glycogen storage disease (GSD, also glycogenosis and d | |
| nts with type 2 diabetes normally exhibit low | glycogen storage levels, and this indicates that insul |
| Errors in this gene cause | glycogen storage disease type II (Pompe disease). |
| GeneReviews/NCBI/NIH/UW entry on | Glycogen Storage Disease Type III |
| A deficiency is associated with | Glycogen storage disease type V, also known as "McArdl |
| Phosphofructokinase deficiency, also known as | Glycogen storage disease type VII or Tarui's disease, |
| gene are associated with a particular type of | glycogen storage disease called Fanconi-Bickel syndrom |
| agnosed with a severe neuromuscular disorder, | Glycogen storage disease type II, also called Pompe di |
| Defects in this gene are the cause of | glycogen storage disease II, also known as Pompe disea |
| 00 000 births (1 in 43,000) have some form of | glycogen storage disease. |
| However, the amount of | glycogen stored in the body-especially within the musc |
| Only the | glycogen stored in the liver can be made accessible to |
| a) to refill depleted | glycogen stores |
| Since the | glycogen stores in their liver and muscles are deplete |
| ats more carbs than is needed to refill their | glycogen stores. |
| Glycogen structure segment. | |
| It can then return to the greater | glycogen structure via glycogen synthase. |
| se-2 mRNA, and lead to the phosphorylation of | glycogen synthase kinase-3. |
| it is phosphorylated on the amino terminus by | glycogen synthase kinase (GSK 3β), which contributes t |
| Glycogen synthase kinase 3 (GSK-3) is a serine/threoni | |
| n protein kinase PK40erk, cdk5/p20, CDK5/p23, | glycogen synthase kinase-3beta, GSK, protein tau kinas |
| glycogen synthase | |
| Glycogen synthase kinase is an enzyme. | |
| Phosphorylation of | glycogen synthase decreases its activity. |
| Glycogen synthase kinase 3 (GSK-3) could be inhibited | |
| Although | glycogen synthase deficiency does not result in storag |
| Glycogen synthase kinase-3 (GSK-3) is a proline-direct | |
| In its asymmetric form, | glycogen synthase is found as a dimer, whose monomers |
| The crystal structure of | glycogen synthase from Agrobacterium tumefaciens, howe |
| Glycogen synthase kinase 3 beta, also known as GSK3B, | |
| is phosphorylation of the Ser-571 residue by | glycogen synthase kinase 3 (GSK3) in response to low s |
| In addition to | glycogen synthase, GSK-3 has many other substrates. |
| nd, much less is known about the structure of | glycogen synthase, the key regulatory enzyme of glycog |
| deactivated, and prevented from deactivating | glycogen synthase. |
| Glycogen synthesis is also stimulated by the insulin r | |
| glucose metabolism in the liver by inhibiting | glycogen synthesis, stimulating glycogenolysis and enc |
| In this roundabout manner, insulin increases | glycogen synthesis. |
| quired to pass glucose into the blood, so the | glycogen they store is destined for internal use and i |
| se, which is essential for the degradation of | glycogen to glucose in lysosomes. |
| This causes excess amounts of an abnormal | glycogen to be deposited in the liver, muscles and, in |
| This prevents proper release of glucose from | glycogen, uses up free phosphate, and causes a rise in |
| Its counterpart in animals is | glycogen, which has the same composition and structure |
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