134 related articles for article (PubMed ID: 6430166)
1. The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular roles.
Tashian RE; Hewett-Emmett D; Dodgson SJ; Forster RE; Sly WS
Ann N Y Acad Sci; 1984; 429():262-75. PubMed ID: 6430166
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Carbonic anhydrase isozymes IV and II in urinary membranes from carbonic anhydrase II-deficient patients.
Sato S; Zhu XL; Sly WS
Proc Natl Acad Sci U S A; 1990 Aug; 87(16):6073-6. PubMed ID: 2117271
[TBL] [Abstract][Full Text] [Related]
4. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
Sly WS; Hewett-Emmett D; Whyte MP; Yu YS; Tashian RE
Proc Natl Acad Sci U S A; 1983 May; 80(9):2752-6. PubMed ID: 6405388
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Carbonic anhydrase II deficiency: diagnosis and carrier detection using differential enzyme inhibition and inactivation.
Sundaram V; Rumbolo P; Grubb J; Strisciuglio P; Sly WS
Am J Hum Genet; 1986 Feb; 38(2):125-36. PubMed ID: 3080873
[TBL] [Abstract][Full Text] [Related]
7. Evaluation of carbonic anhydrase isozymes in disorders involving osteopetrosis and/or renal tubular acidosis.
Sly WS; Sato S; Zhu XL
Clin Biochem; 1991 Aug; 24(4):311-8. PubMed ID: 1959222
[TBL] [Abstract][Full Text] [Related]
8. Expression of carbonic anhydrase IV in carbonic anhydrase II-deficient mice.
Brion LP; Cammer W; Satlin LM; Suarez C; Zavilowitz BJ; Schuster VL
Am J Physiol; 1997 Aug; 273(2 Pt 2):F234-45. PubMed ID: 9277584
[TBL] [Abstract][Full Text] [Related]
9. Red cells genetically deficient in carbonic anhydrase II have elevated levels of a carbonic anhydrase indistinguishable from muscle CA III.
Carter ND; Heath R; Welty RJ; Hewett-Emmett D; Jeffery S; Shiels A; Tashian RE
Ann N Y Acad Sci; 1984; 429():284-6. PubMed ID: 6430168
[No Abstract] [Full Text] [Related]
10. Positive renal response to intravenous acetazolamide in patients with carbonic anhydrase II deficiency.
Sly WS; Whyte MP; Krupin T; Sundaram V
Pediatr Res; 1985 Oct; 19(10):1033-6. PubMed ID: 3932950
[TBL] [Abstract][Full Text] [Related]
11. Cerebral calcification, osteopetrosis and renal tubular acidosis: is it carbonic anhydrase-II deficiency?
Sh Ali AA; Al-Mashta SA
Saudi J Kidney Dis Transpl; 2013 May; 24(3):561-5. PubMed ID: 23640632
[TBL] [Abstract][Full Text] [Related]
12. Metabolic acidosis stimulates carbonic anhydrase activity in rabbit proximal tubule and medullary collecting duct.
Brion LP; Zavilowitz BJ; Suarez C; Schwartz GJ
Am J Physiol; 1994 Feb; 266(2 Pt 2):F185-95. PubMed ID: 8141319
[TBL] [Abstract][Full Text] [Related]
13. Carbonic anhydrase II deficiency in three unrelated Japanese patients.
Aramaki S; Yoshida I; Yoshino M; Kondo M; Sato Y; Noda K; Jo R; Okue A; Sai N; Yamashita F
J Inherit Metab Dis; 1993; 16(6):982-90. PubMed ID: 8127074
[TBL] [Abstract][Full Text] [Related]
14. [Carbonic anhydrase II deficiency: osteopetrosis, renal tubular acidosis and intracranial calcifications. Review of the literature and 3 cases].
Cochat P; Loras-Duclaux I; Guibaud P
Pediatrie; 1987; 42(2):121-8. PubMed ID: 3112731
[TBL] [Abstract][Full Text] [Related]
15. Biochemical genetics of carbonic anhydrase.
Tashian RE; Carter ND
Adv Hum Genet; 1976; 7():1-56. PubMed ID: 827930
[No Abstract] [Full Text] [Related]
16. Carbonic anhydrase.
Maren TH
N Engl J Med; 1985 Jul; 313(3):179-81. PubMed ID: 3925338
[No Abstract] [Full Text] [Related]
17. Red blood cell carbonic anhydrase activity in children with distal renal tubular acidosis.
Kaplan BS; Mills M; Hechtman P; Leblanc D
Pediatr Res; 1977 Oct; 11(10 Pt 1):1039-42. PubMed ID: 409983
[TBL] [Abstract][Full Text] [Related]
18. Cytoplasmic carbonic anhydrase isozymes in rainbow trout Oncorhynchus mykiss: comparative physiology and molecular evolution.
Esbaugh AJ; Perry SF; Bayaa M; Georgalis T; Nickerson J; Tufts BL; Gilmour KM
J Exp Biol; 2005 May; 208(Pt 10):1951-61. PubMed ID: 15879075
[TBL] [Abstract][Full Text] [Related]
19. Case report 668. Carbonic anhydrase II deficiency syndrome (osteopetrosis associated with renal tubular acidosis and cerebral calcification).
Schwartz GJ; Brion LP; Corey HE; Dorfman HD
Skeletal Radiol; 1991; 20(6):447-52. PubMed ID: 1925679
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
