125 related articles for article (PubMed ID: 6815658)
1. Effect of metabolic acidosis on hydrogen ion excretion in a pigtail macaque with erythrocyte carbonic anhydrase I deficiency.
Ferrell RE; Osborne WR; Tashian RE
Proc Soc Exp Biol Med; 1981 Nov; 168(2):155-8. PubMed ID: 6815658
[No Abstract] [Full Text] [Related]
2. Genetic variation in the carbonic anhydrase isozymes of macaque monkeys. II. Inheritance of red cell carbonic anhydrase levels in different carbonic anhydrase I genotypes of the pig-tailed macaque, Macaca nemestrina.
DeSimone J; Magid E; Tashian RE
Biochem Genet; 1973 Feb; 8(2):165-74. PubMed ID: 4632296
[No Abstract] [Full Text] [Related]
3. Isoenzymes of erythrocytic carbonic anhydrase in acidaemic newborn infants [proceedings].
Moynihan JB
Biochem Soc Trans; 1980 Feb; 8(1):86-7. PubMed ID: 6768617
[No Abstract] [Full Text] [Related]
4. Erythrocyte carbonic anhydrase I: inherited deficiency in humans.
Kendall AG; Tashian RE
Science; 1977 Jul; 197(4302):471-2. PubMed ID: 406674
[TBL] [Abstract][Full Text] [Related]
5. Carbonic anhydrase isoenzyme B in erythrocytes of subjects with chronic acidosis.
Mondrup M; Anker N
Clin Chim Acta; 1979 Mar; 92(3):361-6. PubMed ID: 108037
[TBL] [Abstract][Full Text] [Related]
6. Transfusion of carbonic anhydrase-replete erythrocytes fails to correct the acidification defect in the syndrome of osteopetrosis, renal tubular acidosis, and cerebral calcification (carbonic anhydrase-II deficiency).
Whyte MP; Hamm LL; Sly WS
J Bone Miner Res; 1988 Aug; 3(4):385-8. PubMed ID: 3146897
[TBL] [Abstract][Full Text] [Related]
7. Genetic variation in the carbonic anhydrase isozymes of macaque monkeys. IV. Degradation by heat and proteolysis of normal and variant carbonic anhydrase isozymes of Macaca nemestrina.
Osborne WR; Tashian RE
Arch Biochem Biophys; 1984 Apr; 230(1):222-6. PubMed ID: 6424570
[TBL] [Abstract][Full Text] [Related]
8. Comparison of carbonic anhydrase in neonatal and maternal red blood cells with different levels of acidosis in newborn calves.
Szenci O; Gálfi P; Lajcsák A
Zentralbl Veterinarmed A; 1984 Jul; 31(6):437-40. PubMed ID: 6435343
[No Abstract] [Full Text] [Related]
9. Carbonic anhydrase isoenzyme B in erythrocytes of anemic and non-anemic uremic subjects.
Anker N; Mondrup M
Clin Chim Acta; 1977 Sep; 79(2):341-7. PubMed ID: 408056
[TBL] [Abstract][Full Text] [Related]
10. The amino acid substitution and some chemical properties of a variant human erythrocyte carbonic anhydrase: carbonic anhydrase Id-Michigan.
Shows TB
Biochem Genet; 1967 Sep; 1(2):171-95. PubMed ID: 4975354
[No Abstract] [Full Text] [Related]
11. The purification and properties of carbonic anhydrases from guinea-pig erythrocytes and mucosae of the gastrointestinal tract.
Carter MJ; Parsons DS
Biochem J; 1970 Dec; 120(4):797-808. PubMed ID: 4992954
[TBL] [Abstract][Full Text] [Related]
12. Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.
Kondo T; Taniguchi N; Taniguchi K; Matsuda I; Murao M
J Clin Invest; 1978 Sep; 62(3):610-7. PubMed ID: 99456
[TBL] [Abstract][Full Text] [Related]
13. Carbonic anhydrase isoenzymes in the erythrocytes of new-born premature and full-term infants.
Mondrup M; Anker N
Clin Chim Acta; 1975 Jun; 61(2):127-33. PubMed ID: 805677
[TBL] [Abstract][Full Text] [Related]
14. Isoenzymes of carbonic anhydrase I from primate red blood cells.
Headings VE; Tashian RE
Biochim Biophys Acta; 1971 Apr; 236(1):353-9. PubMed ID: 4996028
[No Abstract] [Full Text] [Related]
15. Quantitative genetic variation in carbonic anhydrase isozymes from tissues of the pig-tailed macaque, Macaca nemestrina.
Headings VE; Tashian RE
Biochem Genet; 1971 Aug; 5(4):333-45. PubMed ID: 4999527
[No Abstract] [Full Text] [Related]
16. Siblings with renal tubular acidosis and nerve deafness. The first family in Japan.
Anai T; Yamamoto J; Matsuda I; Taniguchi N; Kondo T; Nagai B
Hum Genet; 1984; 66(2-3):282-5. PubMed ID: 6425198
[TBL] [Abstract][Full Text] [Related]
17. Multiple molecular forms of carbonic anhydrase in erythrocytes.
Edsall JT
Ann N Y Acad Sci; 1968 Jun; 151(1):41-63. PubMed ID: 4975695
[No Abstract] [Full Text] [Related]
18. Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
Sly WS; Whyte MP; Sundaram V; Tashian RE; Hewett-Emmett D; Guibaud P; Vainsel M; Baluarte HJ; Gruskin A; Al-Mosawi M
N Engl J Med; 1985 Jul; 313(3):139-45. PubMed ID: 3925334
[TBL] [Abstract][Full Text] [Related]
19. Genetic variation and evolution in the red cell carbonic anhydrase isozymes of macaque monkeys.
Tashian RE; Goodman M; Headings VE; Ward RH; DeSimone J
Biochem Genet; 1971 Apr; 5(2):183-200. PubMed ID: 4998128
[No Abstract] [Full Text] [Related]
20. Inhibition by cupric ions of 18O exchange catalyzed by human carbonic anhydrase II. Relation to the interaction between carbonic anhydrase and hemoglobin.
Tu C; Wynns GC; Silverman DN
J Biol Chem; 1981 Sep; 256(18):9466-70. PubMed ID: 6793570
[No Abstract] [Full Text] [Related]
[Next] [New Search]