| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1987PNAS...84.8623K |
| P356 | DOI | 10.1073/PNAS.84.23.8623 |
| P932 | PMC publication ID | 299598 |
| P698 | PubMed publication ID | 2825199 |
| P5875 | ResearchGate publication ID | 20331444 |
| P2093 | author name string | T Mukai | |
| H Kishi | |||
| H Fujii | |||
| S Miwa | |||
| K Hori | |||
| A Hirono | |||
| P2860 | cites work | Complete amino acid sequence for human aldolase B derived from cDNA and genomic clones | Q24596462 |
| Human aldolase isozyme gene: the structure of multispecies aldolase B mRNAs | Q24626248 | ||
| A simple and very efficient method for generating cDNA libraries | Q27860461 | ||
| Red cell aldolase deficiency and hemolytic anemia: a new syndrome | Q28245598 | ||
| Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a japanese family | Q28281724 | ||
| Dideoxy sequencing method using denatured plasmid templates | Q29620525 | ||
| Molecular gene mapping of human aldolase A (ALDOA) gene to chromosome 16. | Q34184131 | ||
| Nucleotide sequence of a cDNA clone for human aldolase: a messenger RNA in the liver | Q34192291 | ||
| EVOLUTION OF ALDOLASE | Q34541205 | ||
| Structure and expression of mouse aldolase genes. Brain-specific aldolase C amino acid sequence is closely related to aldolase A. | Q36424915 | ||
| Diagnosis of genetic disease using recombinant DNA. | Q39502026 | ||
| Structure and expression of human and rat aldolase isozyme genes: multiple mRNA species of aldolase A produced from a single gene | Q39659151 | ||
| 15 Fructose-diphosphate aldolase, pyruvate kinase, and pyridine nucleotide-linked activities after electrophoresis | Q40318279 | ||
| Purification and characterization of aldolase from human erythrocytes | Q44056657 | ||
| Tissue-specific expression of rat aldolase A mRNAs. Three molecular species differing only in the 5'-terminal sequences. | Q44115008 | ||
| Rat aldolase A messenger RNA: the nucleotide sequence and multiple mRNA species with different 5'-terminal regions | Q44170902 | ||
| Expression of three mRNA species from a single rat aldolase A gene, differing in their 5' non-coding regions | Q48361539 | ||
| Characterization of the chicken aldolase B gene. | Q48379747 | ||
| Structure and genomic organization of the rat aldolase B gene | Q48382103 | ||
| The complete nucleotide sequence for rabbit muscle aldolase A messenger RNA. | Q48393071 | ||
| Amino acid sequence of an invertebrate FBP aldolase (from Drosophila melanogaster). | Q52466151 | ||
| International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis. | Q53447530 | ||
| [The enzymatic defect of benign fructosuria.] | Q79614894 | ||
| P433 | issue | 23 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Aldolase A deficiency | Q4713937 |
| P304 | page(s) | 8623-7 | |
| P577 | publication date | 1987-12-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation | |
| P478 | volume | 84 |
| Q34504736 | A thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia |
| Q33368998 | Accumulation of citrullinated proteins by up-regulated peptidylarginine deiminase 2 in brains of scrapie-infected mice: a possible role in pathogenesis |
| Q38380755 | Acute rhabdomyolysis and inflammation |
| Q41001236 | Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes |
| Q28539070 | Fructose-bisphosphate aldolase a is a potential metastasis-associated marker of lung squamous cell carcinoma and promotes lung cell tumorigenesis and migration |
| Q24299725 | Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr) |
| Q35198508 | Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene |
| Q24307537 | Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function |
| Q24653674 | Human liver type pyruvate kinase: complete amino acid sequence and the expression in mammalian cells |
| Q34480525 | Identification of minor proteins of human colostrum and mature milk by two-dimensional electrophoresis |
| Q40957048 | Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes |
| Q35764142 | Oxidative proteome alterations during skeletal muscle ageing |
| Q40087921 | Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins. |
| Q33643522 | Proteomic identification of nitrated brain proteins in early Alzheimer's disease inferior parietal lobule |
| Q57348273 | Rapamycin inhibits aldolase A expression during human lymphocyte activation |
| Q30394816 | Roles of 3-nitrotyrosine- and 4-hydroxynonenal-modified brain proteins in the progression and pathogenesis of Alzheimer's disease |
| Q30328103 | SNPs, protein structure, and disease. |
| Q27650507 | Structure of a rabbit muscle fructose-1,6-bisphosphate aldolase A dimer variant |
| Q48034083 | Studies with type I aldolase to understand fructose intolerance and combat parasitic disease |
| Q36278816 | Subunit interface mutants of rabbit muscle aldolase form active dimers |
| Q67588359 | The relationship between homozygosity level and animal physiology: iron content of plasma and whole blood as well as total iron binding capacity by transferrin (TIBC) in rats of various inbreeding coefficient |
| Q44237412 | The temperature dependence of activity and structure for the most prevalent mutant aldolase B associated with hereditary fructose intolerance |
| Q44689324 | Thermodynamic analysis of the dissociation of the aldolase tetramer substituted at one or both of the subunit interfaces |
| Q53414303 | Two homozygous cases of erythrocyte pyruvate kinase (PK) deficiency in Japan: PK sendai and PK shinshu |
| Q41614673 | Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes. |
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