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R E TASHIAN

Showing results (51-60 of 64) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndromeS E Lewis, R P Erickson, L B Barnett, et al.
Gene|January 23, 1995
Characterization of the gene encoding carbonic anhydrase I from the pigtail macaqueP J Hopkins, N C Bergenhem, P J Venta, et al.
Annals of the New York Academy of Sciences|January 1, 1984
The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular rolesR E Tashian, D Hewett-Emmett, S J Dodgson, et al.
Gene|November 1, 1983
The nucleotide sequence and derived amino acid sequence of cDNA coding for mouse carbonic anhydrase IIP J Curtis, E Withers, D Demuth, et al.
American Journal of Human Genetics|November 1, 1991
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II geneP J Venta, R J Welty, T M Johnson, et al.
The American Journal of Anatomy|January 1, 1990
Comparative distribution of carbonic anhydrase isozymes III and II in rodent tissuesS S Spicer, Z H Ge, R E Tashian, et al.
FEBS Letters|January 9, 1984
Novel inhibition of carbonic anhydrase isozymes I, II and III by carbamoyl phosphateN D Carter, W R Chegwidden, D Hewett-Emmett, et al.
Nature|July 15, 1982
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genesJ Czelusniak, M Goodman, D Hewett-Emmett, et al.
Genomics|December 1, 1991
Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16J C Montgomery, P J Venta, R L Eddy, et al.
American Journal of Human Genetics|April 1, 1994
Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patientsP Y Hu, A R Ernst, W S Sly, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndromeS E Lewis, R P Erickson, L B Barnett, et al.
Gene|January 23, 1995
Characterization of the gene encoding carbonic anhydrase I from the pigtail macaqueP J Hopkins, N C Bergenhem, P J Venta, et al.
Annals of the New York Academy of Sciences|January 1, 1984
The value of inherited deficiencies of human carbonic anhydrase isozymes in understanding their cellular rolesR E Tashian, D Hewett-Emmett, S J Dodgson, et al.
Gene|November 1, 1983
The nucleotide sequence and derived amino acid sequence of cDNA coding for mouse carbonic anhydrase IIP J Curtis, E Withers, D Demuth, et al.
American Journal of Human Genetics|November 1, 1991
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II geneP J Venta, R J Welty, T M Johnson, et al.
The American Journal of Anatomy|January 1, 1990
Comparative distribution of carbonic anhydrase isozymes III and II in rodent tissuesS S Spicer, Z H Ge, R E Tashian, et al.
FEBS Letters|January 9, 1984
Novel inhibition of carbonic anhydrase isozymes I, II and III by carbamoyl phosphateN D Carter, W R Chegwidden, D Hewett-Emmett, et al.
Nature|July 15, 1982
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genesJ Czelusniak, M Goodman, D Hewett-Emmett, et al.
Genomics|December 1, 1991
Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16J C Montgomery, P J Venta, R L Eddy, et al.
American Journal of Human Genetics|April 1, 1994
Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patientsP Y Hu, A R Ernst, W S Sly, et al.
Pageof 7