Richard E. Tashian

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

William S. Sly, David Hewett‐Emmett, Michael P. Whyte et al. · Proceedings of the National Academy of Sciences · 1983 · 618 citations · Full text

Electrolyte Disorder, Carbonic Anhydrase Ii, Pathology +16

Functional Diversity, Conservation, and Convergence in the Evolution of the α-, β-, and γ-Carbonic Anhydrase Gene Families

David Hewett‐Emmett, Richard E. Tashian · Molecular Phylogenetics and Evolution · 1996 · 606 citations

Biology, Biosynthesis, Phylogenetics +15

Carbonic Anhydrase II Deficiency in 12 Families with the Autosomal Recessive Syndrome of Osteopetrosis with Renal Tubular Acidosis and Cerebral Calcification

William S. Sly, Michael P. Whyte, Vasantha Sundaram et al. · New England Journal of Medicine · 1985 · 324 citations

Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genes

John Czelusniak, Morris Goodman, David Hewett‐Emmett et al. · Nature · 1982 · 187 citations · Full text

Phylogenetics, Mammalian Haemoglobin Genes, Natural Sciences +12

N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.

Susan E. Lewis, Robert P. Erickson, Lois B. Barnett et al. · Proceedings of the National Academy of Sciences · 1988 · 158 citations · Full text

Mouse Car-2 Locus, Genetics, Renal Pathology +17