glutamate dehydrogenase遺伝子異常
WordNet
- (genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism (同)genetic mutation, chromosomal_mutation
- a change or alteration in form or qualities
- (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
- a salt or ester of glutamic acid
- informal term for information; "give me the gen on your new line of computers"
PrepTutorEJDIC
- 変化,俸転 / (生物の)突然変異;その変種
- 遺伝子
UpToDate Contents
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English Journal
- Improvement of the ammonia assimilation for enhancing L-arginine production of Corynebacterium crenatum.
- Guo J1, Man Z1, Rao Z2,3, Xu M1, Yang T1, Zhang X1, Xu Z4.
- Journal of industrial microbiology & biotechnology.J Ind Microbiol Biotechnol.2017 Mar;44(3):443-451. doi: 10.1007/s10295-017-1900-9. Epub 2017 Jan 25.
- PMID 28120129
- Amino Acid Catabolism in Staphylococcus aureus and the Function of Carbon Catabolite Repression.
- Halsey CR1, Lei S2, Wax JK1, Lehman MK1, Nuxoll AS3, Steinke L4, Sadykov M1, Powers R5, Fey PD6.
- mBio.MBio.2017 Feb 14;8(1). pii: e01434-16. doi: 10.1128/mBio.01434-16.
- PMID 28196956
- A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase.
- Barrosse-Antle M1, Su C2, Chen P3, Boodhansingh KE3, Smith TJ4, Stanley CA1,3, De León DD1,3, Li C1,3.
- Pediatric diabetes.Pediatr Diabetes.2017 Feb 6. doi: 10.1111/pedi.12507. [Epub ahead of print]
- PMID 28165182
Japanese Journal
- Mutational analysis of <i>ABCC8</i>, <i>KCNJ11</i>, <i>GLUD1</i>, <i>HNF4A</i> and <i>GCK</i> genes in 30 Chinese patients with congenital hyperinsulinism
- Unregulated elevation of glutamate dehydrogenase activity induces glutamate-stimulated insulin secretion : identification and characterization of a GLUT1 gene mutation and insulin secretion studies with MIN6 cells overexpressing the mutant glutamate dehydrogenase
- A Japanese Case of Congenital Hyperinsulinism with Hyperammonemia Due to a Mutation in Glutamate Dehydrogenase (GLUD1) Gene
Related Links
- Consumer-friendly information about human genetics from the U.S. National Library of Medicine. ... From NCBI Gene: This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes ...
- This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in ...
★リンクテーブル★
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- 英
- glutamate dehydrogenase gene mutation
- 関
- グルタミン酸脱水素酵素
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グルタミン酸、グルタメート、グルタメイト、(化合物)グルタミン酸塩
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グルタミン酸脱水素酵素、グルタミン酸デヒドロゲナーゼ、GDH、GLDH
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脱水素酵素 デヒドロゲナーゼ
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脱水素酵素 デヒドロゲナーゼ