| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF01534650 |
| P953 | full work available at URL | http://link.springer.com/article/10.1007/BF01534650/fulltext.html |
| http://link.springer.com/content/pdf/10.1007/BF01534650 | ||
| http://link.springer.com/content/pdf/10.1007/BF01534650.pdf | ||
| P698 | PubMed publication ID | 3399966 |
| P2093 | author name string | H. F. Willard | |
| B. H. Robinson | |||
| G. Otulakowski | |||
| P2860 | cites work | Fast-twitch and slow-twitch/cardiac Ca2+ ATPase genes map to human chromosomes 16 and 12 | Q28281289 |
| Inhibition of glycine oxidation by pyruvate, alpha-ketoglutarate, and branched-chain alpha-keto acids in rat liver mitochondria: presence of interaction between the glycine cleavage system and alpha-keto acid dehydrogenase complexes | Q28304026 | ||
| Isolation and characterization of a major tandem repeat family from the human X chromosome | Q35673611 | ||
| Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency | Q42255121 | ||
| Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy | Q48248667 | ||
| Nucleotide sequence of the lipoamide dehydrogenase gene of Escherichia coli K12 | Q48395805 | ||
| The pyruvate dehydrogenase complex of Escherichia coli K12. Nucleotide sequence encoding the dihydrolipoamide acetyltransferase component | Q48397719 | ||
| The Pyruvate Dehydrogenase Complex of Escherichia coli K12. Nucleotide Sequence Encoding the Pyruvate Dehydrogenase Component | Q48398168 | ||
| A Defect in Branched-Chain Amino Acid Metabolism in a Patient with Congenital Lactic Acidosis due to Dihydrolipoyl Dehydrogenase Deficiency | Q67320811 | ||
| Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders | Q69805341 | ||
| Assignment of human gamma crystallin multigene family to chromosome 2 | Q70098891 | ||
| A decrease in glycine cleavage activity in the liver of a patient with dihydrolipoyl dehydrogenase deficiency | Q70333116 | ||
| Cloning and sequence analysis of the pyruvate and 2-oxoglutarate dehydrogenase complex genes of Escherichia coli | Q70354174 | ||
| Pyruvate dehydrogenase subcomplex with lipoamide dehydrogenase deficiency in a patient with lactic acidosis and branched chain ketoaciduria | Q70488925 | ||
| A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids | Q70937066 | ||
| Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency | Q71853077 | ||
| Rat liver mitochondria contain two immunologically distinct dihydrolipoamide dehydrogenases | Q93539238 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| genetics | Q7162 | ||
| P304 | page(s) | 411-414 | |
| P577 | publication date | 1988-07-01 | |
| P1433 | published in | Somatic Cell and Molecular Genetics | Q7559232 |
| P1476 | title | Gene for lipoamide dehydrogenase maps to human chromosome 7 | |
| P478 | volume | 14 |
| Q30795128 | Characterization of the transcriptional regulatory region of the human dihydrolipoamide dehydrogenase gene |
| Q42656697 | Formation of reactive oxygen species by human and bacterial pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes reconstituted from recombinant components |
| Q28119036 | Identification of two missense mutations in a dihydrolipoamide dehydrogenase-deficient patient |
| Q40683934 | Maple syrup urine disease 1954 to 1993. |
| Q24679357 | Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1 |
| Q73731348 | Specificity determinants for the pyruvate dehydrogenase component reaction mapped with mutated and prosthetic group modified lipoyl domains |
| Q34018938 | Three genes for enzymes of the pyruvate dehydrogenase complex map to human chromosomes 3, 7, and X. |
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