Functional Diversity, Conservation, and Convergence in the Evolution of the α-, β-, and γ-Carbonic Anhydrase Gene Families von Hewett-Emmett, David, Tashian, Richard E.

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Molecular Basis of Human Carbonic Anhydrase II Deficiency von Roth, Donna E., Venta, Patrick J., Tashian, Richard E., Sly, William S.

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N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome von Lewis, Susan E., Erickson, Robert P., Barnett, Lois B., Venta, Patrick J., Tashian, Richard E.

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The carbonic anhydrases: Widening perspectives on their evolution, expression and function von Tashian, Richard E.

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Carbonic Anhydrase II Deficiency Identified as the Primary Defect in the Autosomal Recessive Syndrome of Osteopetrosis with Renal Tubular Acidosis and Cerebral Calcification von Sly, William S., Hewett-Emmett, David, Whyte, Michael P., Yu, Ya-Shiou L., Tashian, Richard E.

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Carbonic anhydrase II deficiency : single-base deletion in Exon 7 is the predominant mutation in Caribbean hispanic patients von HU, P. Y, ERNST, A. R, SLY, W. S, VENTA, P. J, SKAGGS, L. A, TASHIAN, R. E

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Mice carrying a CAR-2 null allele lack carbonic anhydrase II immunohistochemically and show vascular calcification von Spicer, SS, Lewis, SE, Tashian, RE, Schulte, BA

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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... von VENTA, R. J, WELTY, R. J, JOHNSON, T. M, SLY, W. S, TASHIAN, R. E

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Carbonic Anhydrase II Deficiency in 12 Families with the Autosomal Recessive Syndrome of Osteopetrosis with Renal Tubular Acidosis and Cerebral Calcification von Sly, William S, Whyte, Michael P, Sundaram, Vasantha, Tashian, Richard E, Hewett-Emmett, David, Guibaud, Pierre, Vainsel, Marc, Baluarte, H. Jorge, Gruskin, Alan, Al-Mosawi, M, Sakati, Nadia, Ohlsson, Arne

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Membrane-associated carbonic anhydrase activity in the kidney of CA II- deficient mice von Ridderstrale, Y, Wistrand, PJ, Tashian, RE

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Characterization of the human gene for a newly discovered carbonic anhydrase, CA VII, and its localization to chromosome 16 von Montgomery, Jeffry C., Venta, Patrick J., Eddy, Roger L., Fukushima, Yao-Shan, Shows, Thomas B., Tashian, Richard E.

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Localization of the mitochondrial carbonic anhydrase V gene, Car5, on mouse chromosome 8 von Lakkis, M M, Venta, P J, Tashian, R E

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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 Scan... von Nils C. H. Bergenhem, Venta, Patrick J., Hopkins, Penelope J., Kim, Hyung J., Tashian, Richard E.

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Molecular analysis of G+C-rich upstream sequences regulating transcription of the human carbonic anhydrase II gene von SHAPIRO, L. H, VENTA, P. J, TASHIAN, R. E

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Oligodendrocytes express a normal phenotype in carbonic anhydrase II-deficient mice von Ghandour, M. S., Skoff, R. P., Venta, P. J., Tashian, R. E.

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Immunocytochemical demonstration of carbonic anhydrase in human epithelial cells von Spicer, SS, Sens, MA, Tashian, RE

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Structure and exon to protein domain relationships of the mouse carbonic anhydrase II gene von Venta, P J, Montgomery, J C, Hewett-Emmett, D, Wiebauer, K, Tashian, R E

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PCR detection of a BstNI RSP in exon 6 of the human carbonic anydrase II locus, CA2 von VENTA, P. J, TASHIAN, R. E. T

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The Catalytic Properties of Murine Carbonic Anhydrase VII von Earnhardt, J. Nicole, Qian, Minzhang, Tu, Chingkuang, Lakkis, Maha M, Bergenhem, Nils C. H, Laipis, Philip J, Tashian, Richard E, Silverman, David N

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Unexpected expression of carbonic anhydrase I and selenium-binding protein as the only major non-heme proteins in erythrocytes of the subterranean mole rat ( Spalax ehrenbergi) von Yang, Hong, Nevo, Eviatar, Tashian, Richard E

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