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R E TASHIAN

Showing results (41-50 of 64) with videos related to

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Molecular Reproduction and Development|October 1, 1990
Ectopic expression of chloramphenicol acetyltransferase (CAT) in the cerebellum in mice transgenic for a carbonic anhydrase II promoter-CAT construct that is without apparent phenotypic effectR P Erickson, A Bevilacqua, P J Venta, et al.
The Journal of Biological Chemistry|October 5, 1985
Structure and exon to protein domain relationships of the mouse carbonic anhydrase II geneP J Venta, J C Montgomery, D Hewett-Emmett, et al.
Biochemical Genetics|June 1, 1979
Chemical characterization of a new Japanese variant of carbonic anhydrase I, CA INagasaki 1 (76 arg leads to gln)K Goriki, R E Tashian, S K Stroup, et al.
Cytogenetics and Cell Genetics|January 1, 1987
The gene for human carbonic anhydrase II (CA2) is located at chromosome 8q22H Nakai, M G Byers, P J Venta, et al.
Biochemical Genetics|June 1, 1981
Amino acid substitution and chemical characterization of a Japanese variant of carbonic anhydrase I: CA I Hiroshima-1 (86 Asp replaced by Gly)T Kageoka, D Hewett-Emmett, S K Stroup, et al.
Biochemical Genetics|August 1, 1982
Cross-reactions among carbonic anhydrases I, II, and III studied by binding tests and with monoclonal antibodiesR P Erickson, G Kay, D Hewett-Emmett, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the gene for human carbonic anhydrase VIII(CA8) to chromosome 8q11-->q12N C Bergenhem, S S Sait, R L Eddy, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translationN C Bergenhem, P J Venta, P J Hopkins, et al.
Life Sciences|July 23, 1998
Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal tubular cellsL W Lai, R P Erickson, P J Venta, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, D Hewett-Emmett, M P Whyte, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Molecular Reproduction and Development|October 1, 1990
Ectopic expression of chloramphenicol acetyltransferase (CAT) in the cerebellum in mice transgenic for a carbonic anhydrase II promoter-CAT construct that is without apparent phenotypic effectR P Erickson, A Bevilacqua, P J Venta, et al.
The Journal of Biological Chemistry|October 5, 1985
Structure and exon to protein domain relationships of the mouse carbonic anhydrase II geneP J Venta, J C Montgomery, D Hewett-Emmett, et al.
Biochemical Genetics|June 1, 1979
Chemical characterization of a new Japanese variant of carbonic anhydrase I, CA INagasaki 1 (76 arg leads to gln)K Goriki, R E Tashian, S K Stroup, et al.
Cytogenetics and Cell Genetics|January 1, 1987
The gene for human carbonic anhydrase II (CA2) is located at chromosome 8q22H Nakai, M G Byers, P J Venta, et al.
Biochemical Genetics|June 1, 1981
Amino acid substitution and chemical characterization of a Japanese variant of carbonic anhydrase I: CA I Hiroshima-1 (86 Asp replaced by Gly)T Kageoka, D Hewett-Emmett, S K Stroup, et al.
Biochemical Genetics|August 1, 1982
Cross-reactions among carbonic anhydrases I, II, and III studied by binding tests and with monoclonal antibodiesR P Erickson, G Kay, D Hewett-Emmett, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the gene for human carbonic anhydrase VIII(CA8) to chromosome 8q11-->q12N C Bergenhem, S S Sait, R L Eddy, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translationN C Bergenhem, P J Venta, P J Hopkins, et al.
Life Sciences|July 23, 1998
Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal tubular cellsL W Lai, R P Erickson, P J Venta, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificationW S Sly, D Hewett-Emmett, M P Whyte, et al.
Pageof 7