Page last updated: 2024-08-17

nad and Methemoglobinemia

nad has been researched along with Methemoglobinemia in 49 studies

Research

Studies (49)

Timeframe	Studies, this research(%)	All Research%
pre-1990	37 (75.51)	18.7374
1990's	3 (6.12)	18.2507
2000's	5 (10.20)	29.6817
2010's	2 (4.08)	24.3611
2020's	2 (4.08)	2.80

Authors

Authors	Studies
Ahmad, W; Basit, S; Khurshid, B; Mahmood, A; Samad, A; Shah, AA; Syed, F; Ullah, A; Ur Rehman, H	1
Inanami, O; Otsuka-Yamasaki, Y; Sato, R; Shino, H; Yamasaki, M	1
Spyker, DA; Yip, L	1
Koul, PA; Lingam, B; Lorenzo, FR; Nussenzveig, R; Phillips, JD; Prchal, JT; Schrier, SL	1
Gibson, Q	1
SCOTT, EM	2
KLEIHAUER, E	1
BEHLEN, CH; CAWEIN, M; COHN, JE; LAPPAT, EJ	1
BERTOLINI, AM	1
JAFFE, ER; NEURMANN, G	1
FISCHER, D; HARTLEYB, H; HEIDT, P; LAUSECKER, C; LOHR, GW	1
Barber, MJ; Bewley, MC; Davis, CA; Marohnic, CC; Taormina, D	1
Barber, MJ; Crowley, LJ; Davis, CA; Hughes, J; Lappin, TR; McMahon, C; McMullin, MF; Percy, MJ; Quinn, RJ; Savage, G; Smith, O	1
Jaffé, ER	2
Gould, SA; Moss, GS; Rice, CL; Rosen, AL; Sehgal, HL; Sehgal, LR	1
Chen, JY; Libnoch, JA; Matteson, KJ; Taketa, F	1
Kahn, A; Kaplan, JC; Leroux, A; Vieira, LM	1
Agnes, F; Baglioni, T; Paltrinieri, S; Sartorelli, P	1
Cheung, KL; de Rijk, T; Dekker, J; Eppink, MH; Law, LK; Li, AM; Remacha, AF; Roos, D; van Berkel, WJ; van Zwieten, R	1
Barber, MJ; Bewley, MC; Marohnic, CC	1
Hultquist, DE; Sannes, LJ	1
Froslie, A	1
Hibbard, BZ; Koenig, HM; Lightsey, AL; Nelson, DP; Seaward, DA	1
Borgese, N; Hall, MK; Hegesh, E; Moore, MR; Moreno, H; Prchal, JT	1
Asakura, T; Kanazawa, Y; Minakami, S; Nakao, K; Yoshikawa, H	1
Bartos, HR; Desforges, JF	1
Angelopoulos, B; Eleftheriadou, A; Karalis, D; Tsoukantas, A	1
Gärtner, C	1
Jaffé, ER; Neumann, G	1
Izumi, N; Kumagai, T; Yokota, K	1
Hultquist, DE; Passon, PG	1
Barthelmai, W; Vetrella, M	1
Rogers, LE	1
Marković, O; Mijatović, B; Stanulović, M	1
Hsieh, HS; Jaffe, ER	1
Davies, HE; Lay, H	1
DiPillo, F; Paress, PS; Rizek, R; Ross, JM; Schwartz, JM	1
Gotlieb, A; Hegesh, E; Nordan, UZ	1
Derviz, GV; Il'inskaia, II; Lavrova, OP; Tokarev, IuN	1
Faber, K; Heni, F; Schmidt, K	1
Beutler, E; Kaplan, JC	1
Konopka, K	1
Bloom, GE; Zarkowsky, HS	1
Waller, HD	1
Kaplan, JC; Leroux, A	1
Astedt, B; Barthelmai, W; Neuvians, D; Vetrella, M	1
Hirayama, K; Ishizawa, S; Kuma, F; Nakajima, H	1

Reviews

4 review(s) available for nad and Methemoglobinemia

Article	Year
THE BIOLOGICAL ROLE OF ENZYME CHANGES IN THE AGING OF THE ORGANISM. Gerontologia, 1964, Volume: 69 Topics: Acid Phosphatase; Aging; Alkaline Phosphatase; Enzymes; Erythrocytes; Geriatrics; Metabolism; Methemoglobinemia; NAD; Nucleotides; Pyrophosphatases; Research	1964
Methaemoglobinaemia. Clinics in haematology, 1981, Volume: 10, Issue:1 Topics: Ascorbic Acid; Cytochrome-B(5) Reductase; Erythrocytes; Glutathione; Hemoglobins; Humans; Intellectual Disability; Methemoglobin; Methemoglobinemia; Metmyoglobin; NAD; NADP; Oxidation-Reduction	1981
DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia. Seminars in hematology, 1971, Volume: 8, Issue:4 Topics: Cyanosis; Electrophoresis; Erythrocytes; Genetic Variation; Hemoglobins; Humans; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; NAD; Oxidation-Reduction; Oxidoreductases	1971
[Enzymatic defects of red cells]. Postepy biochemii, 1968, Volume: 14, Issue:1 Topics: Adenosine Triphosphate; Anemia, Hemolytic, Congenital Nonspherocytic; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Hematologic Diseases; Humans; Methemoglobinemia; NAD; NADP	1968

Other Studies

45 other study(ies) available for nad and Methemoglobinemia

Article	Year
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in Medicina (Kaunas, Lithuania), 2023, Feb-16, Volume: 59, Issue:2 Topics: Cyanosis; Cytochrome-B(5) Reductase; Humans; Methemoglobinemia; Molecular Dynamics Simulation; Mutation; NAD	2023
Characterization of a novel nicotinamide adenine dinucleotide-cytochrome b5 reductase mutation associated with canine hereditary methemoglobinemia. The Journal of veterinary medical science, 2021, Mar-05, Volume: 83, Issue:2 Topics: Animals; Cat Diseases; Cats; Cytochrome-B(5) Reductase; Cytochromes b5; Dog Diseases; Dogs; Methemoglobinemia; Mutation; NAD	2021
NADH-methemoglobin reductase activity: adult versus child. Clinical toxicology (Philadelphia, Pa.), 2018, Volume: 56, Issue:9 Topics: Adult; Age Factors; Cytochrome-B(5) Reductase; Erythrocytes; Female; Hemoglobins; Humans; Infant; Methemoglobin; Methemoglobinemia; NAD	2018
Molecular basis of two novel mutations found in type I methemoglobinemia. Blood cells, molecules & diseases, 2011, Apr-15, Volume: 46, Issue:4 Topics: Binding Sites; Cytochrome-B(5) Reductase; Enzyme Stability; Flavin-Adenine Dinucleotide; Greece; Humans; India; Kinetics; Methemoglobinemia; Mexico; Mutation; NAD; Phenotype; Thermodynamics	2011
Introduction: congenital methemoglobinemia revisited. Blood, 2002, Nov-15, Volume: 100, Issue:10 Topics: Electron Transport Complex IV; History, 20th Century; Humans; Methemoglobin; Methemoglobinemia; NAD; Northern Ireland; Oxidation-Reduction	2002
Purification of diphosphopyridine nucleotide diaphorase from methemoglobinemic erythrocytes. Biochemical and biophysical research communications, 1962, Sep-25, Volume: 9 Topics: Dihydrolipoamide Dehydrogenase; Erythrocytes; Methemoglobinemia; NAD; Oxidoreductases	1962
[ON SOME NEW METHODS IN THE DIAGNOSIS OF HEMATOLOGICAL DISEASES]. Annales Nestle. [Deutsche Aufl.], 1963, Volume: 20 Topics: Anemia; Anemia, Hemolytic; Clinical Enzyme Tests; Clinical Laboratory Techniques; Fetal Hemoglobin; Hemoglobins; Hemoglobins, Abnormal; Humans; Methemoglobinemia; NAD; NADP; Thalassemia	1963
HEREDITARY DIAPHORASE DEFICIENCY AND METHEMOGLOBINEMIA. Archives of internal medicine, 1964, Volume: 113 Topics: Blood Protein Electrophoresis; Cyanosis; Cytochrome-B(5) Reductase; Deficiency Diseases; Dihydrolipoamide Dehydrogenase; Erythrocytes; Genetics, Medical; Glucosephosphate Dehydrogenase; Glutathione; Hemoglobinometry; Humans; Methemoglobinemia; Methylene Blue; NAD; Spectrophotometry	1964
A COMPARISION OF THE EFFECT OF MENADIONE, METHYLENE BLUE AND ASCORBIC ACID ON THE REDUCTION OF METHEMOGLOBIN IN VIVO. Nature, 1964, May-09, Volume: 202 Topics: Ascorbic Acid; Dihydrolipoamide Dehydrogenase; Drug Therapy; Erythrocytes; Humans; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; Methylene Blue; NAD; Sulfites; Vitamin K; Vitamin K 3	1964
[A NEW CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA LINKED WITH A DIAPHORASE I DEFICIENCY]. Archives francaises de pediatrie, 1964, Volume: 21 Topics: Ascorbic Acid; Cytochrome-B(5) Reductase; Dihydrolipoamide Dehydrogenase; Drug Therapy; Genetics, Medical; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Methemoglobinemia; Methylene Blue; NAD; NADP	1964
The structure of the S127P mutant of cytochrome b5 reductase that causes methemoglobinemia shows the AMP moiety of the flavin occupying the substrate binding site. Biochemistry, 2003, Nov-18, Volume: 42, Issue:45 Topics: Adenosine Monophosphate; Amino Acid Substitution; Animals; Binding Sites; Crystallography, X-Ray; Cytochrome-B(5) Reductase; Flavin-Adenine Dinucleotide; Humans; Kinetics; Methemoglobinemia; Mutagenesis, Site-Directed; NAD; Proline; Protein Conformation; Rats; Recombinant Proteins; Serine; Spectrophotometry, Ultraviolet; Substrate Specificity	2003
Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase. British journal of haematology, 2005, Volume: 129, Issue:6 Topics: Adolescent; Crystallography, X-Ray; Cytochrome-B(5) Reductase; Female; Genes, Recessive; Haplotypes; Humans; Infant, Newborn; Male; Methemoglobinemia; Mutagenesis, Site-Directed; Mutation; NAD; Polymerase Chain Reaction; Thermodynamics	2005
Control of methemoglobin formation in stroma-free hemoglobin solutions. The Journal of surgical research, 1981, Volume: 31, Issue:1 Topics: Animals; Blood Substitutes; Exchange Transfusion, Whole Blood; Hemoglobins; Male; Methemoglobin; Methemoglobinemia; NAD; NADP; Papio; Time Factors	1981
Methemoglobin reduction in red cells: effect of a high oxygen affinity hemoglobin. Blood, 1980, Volume: 55, Issue:1 Topics: Dihydrolipoamide Dehydrogenase; Female; Hemoglobin A; Hemoglobins; Humans; Male; Methemoglobin; Methemoglobinemia; Mutation; NAD; Oxidation-Reduction; Oxygen; Primaquine; Time Factors	1980
Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II. Blood, 1995, Apr-15, Volume: 85, Issue:8 Topics: Amino Acid Sequence; Base Sequence; Binding Sites; Codon; Cytochrome Reductases; Cytochrome-B(5) Reductase; DNA Mutational Analysis; DNA, Complementary; Exons; Flavin-Adenine Dinucleotide; Genes; Genes, Recessive; Humans; Introns; Methemoglobinemia; Molecular Sequence Data; Mutation; NAD; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Protein Conformation; Sequence Deletion	1995
Role of inosine in prevention of methaemoglobinaemia in the pig: in vitro studies. Zentralblatt fur Veterinarmedizin. Reihe A, 1996, Volume: 43, Issue:8 Topics: Animals; Cattle; Erythrocytes; Glucose; Humans; In Vitro Techniques; Incidence; Inosine; Methemoglobin; Methemoglobinemia; NAD; Swine; Swine Diseases	1996
Seven new mutations in the nicotinamide adenine dinucleotide reduced-cytochrome b(5) reductase gene leading to methemoglobinemia type I. Blood, 2001, Feb-15, Volume: 97, Issue:4 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Binding Sites; Child; Consanguinity; Cytochrome Reductases; Cytochrome-B(5) Reductase; DNA, Complementary; Exons; Female; Flavin-Adenine Dinucleotide; Genotype; Humans; Male; Methemoglobinemia; Models, Molecular; Molecular Sequence Data; NAD; Pedigree; Point Mutation; Protein Conformation; Sequence Alignment; Sequence Homology, Amino Acid	2001
The structure and biochemistry of NADH-dependent cytochrome b5 reductase are now consistent. Biochemistry, 2001, Nov-13, Volume: 40, Issue:45 Topics: Amino Acid Sequence; Animals; Crystallization; Crystallography, X-Ray; Cytochrome Reductases; Cytochrome-B(5) Reductase; Humans; Lysine; Methemoglobinemia; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; NAD; Protein Conformation; Rats; Sequence Homology, Amino Acid; Swine	2001
Effects of hemolysate concentration, ionic strength and cytochrome b5 concentration on the rate of methemoglobin reduction in hemolysates of human erythrocytes. Biochimica et biophysica acta, 1978, Dec-18, Volume: 544, Issue:3 Topics: Cytochrome-B(5) Reductase; Cytochromes; Erythrocytes; Hemolysis; Kinetics; Methemoglobin; Methemoglobinemia; NAD; NADH, NADPH Oxidoreductases; NADP; Osmolar Concentration; Oxidation-Reduction	1978
Methaemoglobin reduction and NADH-dependent methaemoglobin reductase activity following DNBP-and nitrite induced methaemoglobinemia in sheep. Acta pharmacologica et toxicologica, 1976, Volume: 38, Issue:1 Topics: Animals; Cytochrome-B(5) Reductase; Dinitrophenols; Hemoglobins; Methemoglobinemia; NAD; NADH, NADPH Oxidoreductases; Nitrites; Sheep; Time Factors	1976
Severe methemoglobinemia in an infant with glucose-6-phosphate dehydrogenase deficiency. The Journal of pediatrics, 1978, Volume: 93, Issue:5 Topics: Cytochrome-B(5) Reductase; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Humans; Infant; Male; Methemoglobinemia; NAD; Oxidation-Reduction	1978
Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families. The American journal of medicine, 1990, Volume: 89, Issue:4 Topics: Adolescent; Adult; Cytochrome-B(5) Reductase; Erythrocytes; Female; Humans; Methemoglobin; Methemoglobinemia; Mutation; NAD; Sulfhemoglobin	1990
Effect of phosphate on the activity of NADH-diaphorase from erythrocytes of hereditary methemoglobinemia. Clinica chimica acta; international journal of clinical chemistry, 1965, Volume: 12, Issue:1 Topics: Erythrocytes; Humans; In Vitro Techniques; Methemoglobinemia; NAD; Oxidoreductases; Phosphates; Spectrophotometry	1965
Erythrocyte DPNH dependent diaphorase levels in infants. Pediatrics, 1966, Volume: 37, Issue:6 Topics: Dihydrolipoamide Dehydrogenase; Erythrocytes; Humans; Infant, Newborn; Methemoglobin; Methemoglobinemia; NAD; Spectrophotometry	1966
Hereditary methemoglobinemia due to DPNH-methemoglobin reductase deficiency: report of a family. Acta haematologica, 1967, Volume: 37, Issue:5 Topics: Adult; Blood Protein Electrophoresis; Child, Preschool; Cyanosis; Dihydrolipoamide Dehydrogenase; Erythrocytes; Female; Genotype; Hemoglobinometry; Humans; Male; Methemoglobinemia; NAD; Oxidoreductases; Pedigree; Spectrum Analysis; Transaminases	1967
[Diminished activity of DPN dependent methemoglobinreductase in erythrocytes of newborn infants as cause of decreased methemoglobin reduction]. Zeitschrift fur Kinderheilkunde, 1966, Volume: 96, Issue:2 Topics: Adult; Erythrocytes; Flavin-Adenine Dinucleotide; Humans; Infant, Newborn; Methemoglobinemia; NAD; Oxidoreductases	1966
A comparison of two methods of determining DPNH-methemoglobin reductase. Clinica chimica acta; international journal of clinical chemistry, 1969, Volume: 23, Issue:3 Topics: Dihydrolipoamide Dehydrogenase; Female; Ferrocyanides; Heterozygote; Homozygote; Humans; Indophenol; Male; Methemoglobin; Methemoglobinemia; NAD; Oxidoreductases; Pedigree	1969
Is it bad to be blue? The New England journal of medicine, 1969, Oct-23, Volume: 281, Issue:17 Topics: Electrophoresis; Erythrocytes; Hemolysis; Humans; Male; Methemoglobin; Methemoglobinemia; NAD; Oxidoreductases; Primaquine	1969
Hereditary methemoglobinemia, toxic methemoglobinemia and the reduction of methemoglobin. Annals of the New York Academy of Sciences, 1968, Jul-31, Volume: 151, Issue:2 Topics: Erythrocytes; Glucose; Glutathione; Hemoglobins; Heterozygote; Homozygote; Humans; Lactates; Methemoglobin; Methemoglobinemia; NAD; Niacinamide; Nicotinic Acids; Nitrites; Nucleotides; Oxidation-Reduction; Postural Balance; Pyridines; Pyruvates; Ribose; Time Factors	1968
[Case of methemoglobulinemia due to phenacetin]. Nihon Shonika Gakkai zasshi. Acta paediatrica Japonica, 1970, Mar-01, Volume: 74, Issue:3 Topics: Humans; Infant, Newborn; Male; Methemoglobinemia; NAD; Oxidoreductases; Phenacetin; Spectrophotometry	1970
Catalysis of methaemoglobin reduction by erythrocyte cytochrome B5 and cytochrome B5 reductase. Nature: New biology, 1971, Feb-24, Volume: 229, Issue:8 Topics: Catalysis; Cytochromes; Erythrocytes; Humans; Methemoglobin; Methemoglobinemia; NAD; Oxidoreductases	1971
[Erythrocyte enzymes in human fetuses]. Monatsschrift fur Kinderheilkunde, 1971, Volume: 119, Issue:7 Topics: Adenine Nucleotides; Adenosine Triphosphatases; Enzymes; Erythrocytes; Fetus; Fructose-Bisphosphate Aldolase; Gestational Age; Glucose-6-Phosphate Isomerase; Glucosephosphate Dehydrogenase; Glutathione; Glutathione Reductase; Glyceraldehyde-3-Phosphate Dehydrogenases; Hexokinase; Humans; Infant, Newborn; L-Lactate Dehydrogenase; Methemoglobin; Methemoglobinemia; NAD; Oxidoreductases; Peroxidases; Phosphofructokinase-1; Phosphoglucomutase; Phosphogluconate Dehydrogenase; Phosphoglycerate Kinase; Phosphopyruvate Hydratase; Phosphotransferases; Pyruvate Kinase	1971
Rapid method for detection of erythrocyte NADH-methemoglobin reductase deficiency. American journal of clinical pathology, 1972, Volume: 57, Issue:2 Topics: Adolescent; Adult; Child; Child, Preschool; Erythrocytes; Humans; Indicators and Reagents; Infant; Infant, Newborn; Iron; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; Methods; NAD; Oxidoreductases	1972
[Congenital methemoglobinemia caused by the NADH-diaphorase deficiency]. Medicinski pregled, 1971, Volume: 24, Issue:9 Topics: Adolescent; Child; Dihydrolipoamide Dehydrogenase; Female; Homozygote; Humans; Male; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; NAD; Oxidoreductases	1971
A case of hereditary methaemoglobinaemia. Australian paediatric journal, 1971, Volume: 7, Issue:4 Topics: Cyanosis; Dihydrolipoamide Dehydrogenase; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Metabolism, Inborn Errors; Methemoglobinemia; NAD	1971
Unstable variant of NADH methemoglobin reductase in Puerto Ricans with hereditary methemoglobinemia. The Journal of clinical investigation, 1972, Volume: 51, Issue:6 Topics: Adolescent; Adult; Aspartate Aminotransferases; Dihydrolipoamide Dehydrogenase; Edetic Acid; Electrophoresis, Starch Gel; Erythrocyte Aging; Erythrocytes; Ethnicity; Female; Glucosephosphate Dehydrogenase; Glutathione Reductase; Humans; Isoenzymes; Kinetics; Methemoglobinemia; Middle Aged; Molecular Weight; NAD; Oxidoreductases; Puerto Rico; Spectrophotometry	1972
An enzyme variation in a case of congenital methemoglobinemia. Israel journal of medical sciences, 1973, Volume: 9, Issue:7 Topics: Ascorbic Acid; Dihydrolipoamide Dehydrogenase; Electrophoresis, Polyacrylamide Gel; Erythrocytes; Female; Hemoglobins; Humans; Infant; Methemoglobinemia; Methylene Blue; NAD; Oxidation-Reduction; Pedigree	1973
[Enzymatic methemoglobinemia]. Problemy gematologii i perelivaniia krovi, 1973, Volume: 18, Issue:11 Topics: Female; Humans; Male; Methemoglobinemia; NAD	1973
[Enterogenons methemoglobinemia caused by heterozygotic deficiency of erythrocytic NADH-methemoglobin reductase]. Blut, 1974, Volume: 29, Issue:1 Topics: Ascorbic Acid; Cyanosis; Dihydrolipoamide Dehydrogenase; Erythrocytes; Female; Heterozygote; Humans; Intestines; Kinetics; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; Middle Aged; NAD; Neomycin	1974
Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes. Nature, 1968, Jan-20, Volume: 217, Issue:5125 Topics: Dihydrolipoamide Dehydrogenase; Electrophoresis; Erythrocytes; Gels; Genotype; Glutathione Reductase; Humans; Leukocytes; Methemoglobinemia; Molecular Biology; NAD; NADP; Polymorphism, Genetic; Starch	1968
Heterogeneity of the enzymatic defect in congenital methemoglobinemia. The New England journal of medicine, 1969, Oct-23, Volume: 281, Issue:17 Topics: Electrophoresis; Female; Gels; Humans; Methemoglobin; Methemoglobinemia; NAD; NADP; Oxidoreductases; Starch	1969
Inherited methemoglobinemia (enzyme deficiencies). Humangenetik, 1970, Volume: 9, Issue:3 Topics: Erythrocytes; Humans; Metabolism, Inborn Errors; Methemoglobin; Methemoglobinemia; NAD; NADP	1970
[Diaphorasic NADPH and NADH systems in human blood cells]. Bulletin de la Societe de chimie biologique, 1970, Volume: 52, Issue:11 Topics: Blood Cells; Blood Platelets; Dihydrolipoamide Dehydrogenase; Electrophoresis; Erythrocytes; Leukocytes; Methemoglobinemia; NAD; NADP; Oxidoreductases	1970
Activity of NADH- and NADPH-dependent methemoglobin reductases in erythrocytes from fetal to adult age. A parallel assessment. Klinische Wochenschrift, 1971, Sep-01, Volume: 49, Issue:17 Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Erythrocytes; Female; Fetus; Gestational Age; Humans; Infant; Infant, Newborn; Infant, Premature; Intellectual Disability; Methemoglobin; Methemoglobinemia; NAD; NADP; Oxidoreductases; Pregnancy	1971
Studies on methemoglobin reductase. I. Comparative studies of diaphorases from normal and methemoglobinemic erythrocytes. The Journal of biological chemistry, 1972, Jan-25, Volume: 247, Issue:2 Topics: Chromatography, Gel; Chromatography, Ion Exchange; Dihydrolipoamide Dehydrogenase; Electrophoresis; Enzyme Activation; Erythrocytes; Homozygote; Hot Temperature; Humans; Indophenol; Japan; Kinetics; Mathematics; Methemoglobin; Methemoglobinemia; NAD; NADP; Phenols; Phosphates; Protein Denaturation	1972