Muriel T. Davisson

Overview

Best Publications

• Retinal degeneration mutants in the mouse.

  B. Chang;N.L. Hawes;R.E. Hurd;M.T. Davisson

  1082
  Citations

• Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice

  Elizabeth M. Simpson;Carol C. Linder;Evelyn E. Sargent;Muriel T. Davisson

  847
  Citations

• Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

  Jeong Woong Lee;Kirk Beebe;Leslie A. Nangle;Jaeseon Jang

  718
  Citations

• Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.

  Simon W M John;Richard S. Smith;Olga V. Savinova;Norman L. Hawes

  639
  Citations

• Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

  B. Chang;N.L. Hawes;M.T. Pardue;M.T. Pardue;A.M. German

  474
  Citations

• Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta.

  Stewart D. Chipman;Hope O. Sweet;Daniel J. McBride;Muriel T. Davisson

  452
  Citations

• Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

  J.M. Newton;Orit Cohen-Barak;Nobuko Hagiwara;John M. Gardner

  448
  Citations

• Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage.

  E J Michaud;M J van Vugt;S J Bultman;H O Sweet

  390
  Citations

• Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

  Bo Chang;Richard S Smith;Norman L Hawes;Michael G Anderson

  321
  Citations

• Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions.

  Katheleen Gardiner;Andrew Fortna;Lawrence Bechtel;Muriel T Davisson

  301
  Citations

• VAC14 Nucleates a Protein Complex Essential for the Acute Interconversion of PI3P and PI(3,5)P2 in Yeast and Mouse

  Natsuko Jin;Clement Y Chow;Li Liu;Sergey N Zolov

  297
  Citations

• Report of the committee on comparative mapping

  P. L. Pearson;T. H. Roderick;M. T. Davisson;J. J. Garver

  296
  Citations

• A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

  Novrouz B. Akhmedov;Natik I. Piriev;Bo Chang;Ana Lia Rapoport

  295
  Citations

• Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)

  Ji Jing Pang;Bo Chang;Norman L. Hawes;Ronald E. Hurd

  284
  Citations

• The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.

  Bo Chang;John R. Heckenlively;Philippa R. Bayley;Nicholas C. Brecha

  238
  Citations

• Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

  H. O. Sweet;R. T. Bronson;K. R. Johnson;S. A. Cook

  222
  Citations

• Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome

  Carmen Martı́nez-Cué;Carmela Baamonde;Marian Lumbreras;Jesús Paz

  214
  Citations

• Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease).

  Roderick T. Bronson;Brian D. Lake;Susan Cook;Susanne Taylor

  211
  Citations

• The fatty liver dystrophy (fld) mutation: A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities

  C A Langner;E H Birkenmeier;O Ben-Zeev;M C Schotz

  205
  Citations

• Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn

  Laura G. Reinholdt;Yueming Ding;Griffith T. Gilbert;Anne Czechanski

  196
  Citations