Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration von Longo-Guess, Chantal M, Sundberg, John P, Davisson, Muriel T, Schimmel, Paul, Ackerman, Susan L, Lee, Jeong Woong, Beebe, Kirk, Jang, Jaeseon, Nangle, Leslie A, Cook, Susan A

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Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn von Reinholdt, Laura G, Ding, Yueming, Gilbert, Griffith T, Czechanski, Anne, Solzak, Jeffrey P, Roper, Randall J, Johnson, Mark T, Donahue, Leah Rae, Lutz, Cathleen, Davisson, Muriel T

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Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene von Chang, B., Hawes, N.L., Pardue, M.T., German, A.M., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Rengarajan, K., Boyd, A.P., Sidney, S.S., Phillips, M.J., Stewart, R.E., Chaudhury, R., Nickerson, J.M., Heckenlively, J.R., Boatright, J.H.

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Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4 von Newton, J.M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.

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Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome von Voronov, Sergey V, Frere, Samuel G, Giovedi, Silvia, Pollina, Elizabeth A, Borel, Christelle, Zhang, Hong, Schmidt, Cecilia, Akeson, Ellen C, Wenk, Markus R, Cimasoni, Laurent, Arancio, Ottavio, Davisson, Muriel T, Antonarakis, Stylianos E, Gardiner, Katheleen, De Camilli, Pietro, Di Paolo, Gilbert

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Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice von Simpson, Elizabeth M, Linder, Carol C, Sargent, Evelyn E, Davisson, Muriel T, Mobraaten, Larry E, Sharp, John J

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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions von Gardiner, Katheleen, Fortna, Andrew, Bechtel, Lawrence, Davisson, Muriel T

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IoT-Based Wearable and Smart Health Device Solutions for Capnography: Analysis and Perspectives von Morais, Davisson F. T, Fernandes, Gilberto, Lima, Gildário D, Rodrigues, Joel J. P. C

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Retinal degeneration mutants in the mouse von Chang, B., Hawes, N.L., Hurd, R.E., Davisson, M.T., Nusinowitz, S., Heckenlively, J.R.

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Loss of Correlations among Proteins in Brains of the Ts65Dn Mouse Model of Down Syndrome von Ahmed, Md. Mahiuddin, Sturgeon, Xiaolu, Ellison, Misoo, Davisson, Muriel T, Gardiner, Katheleen J

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Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome von Martı́nez-Cué, Carmen, Baamonde, Carmela, Lumbreras, Marian, Paz, Jesús, Davisson, Muriel T, Schmidt, Cecilia, Dierssen, Mara, Flórez, Jesús

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Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice von John, Simon W M, Chang, Bo, Smith, Richard S, Hawes, Norman L, Anderson, Michael G, Zabaleta, Adriana, Savinova, Olga, Roderick, Thomas H, Heckenlively, John R, Davisson, Muriel T

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Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse von Lindfors, Charlotte, Nilsson, Ida A. K, Garcia-Roves, Pablo M, Zuberi, Aamir R, Karimi, Mohsen, Donahue, Leah Rae, Roopenian, Derry C, Mulder, Jan, Uhlén, Mathias, Ekström, Tomas J, Davisson, Muriel T, Hökfelt, Tomas G. M, Schalling, Martin, Johansen, Jeanette E

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A mouse model for Down syndrome exhibits learning and behaviour deficits von Reeves, Roger H, Irving, Nicholas G, Moran, Timothy H, Wohn, Anny, Kitt, Cheryl, Sisodia, Sangram S, Schmidt, Cecilia, Bronson, Roderick T, Davisson, Muriel T

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Motor dysfunction in a mouse model for Down syndrome von Costa, Alberto C.S, Walsh, Kathryn, Davisson, Muriel T

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Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse von Simon-Chazottes, Dominique, Tutois, Sylvie, Kuehn, Michael, Evans, Martin, Bourgade, Franck, Cook, Sue, Davisson, Muriel T., Guénet, Jean-Louis

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Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome von Liu, Dong P, Schmidt, Cecilia, Billings, Timothy, Davisson, Muriel T

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Behavioral, cognitive and biochemical responses to different environmental conditions in male Ts65Dn mice, a model of Down syndrome von Martínez-Cué, Carmen, Rueda, Noemí, García, Eva, Davisson, Muriel T., Schmidt, Cecilia, Flórez, Jesús

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A spontaneous mutation in contactin 1 in the mouse von Davisson, Muriel T, Bronson, Roderick T, Tadenev, Abigail L D, Motley, William W, Krishnaswamy, Arjun, Seburn, Kevin L, Burgess, Robert W

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A-to-I pre-mRNA editing of the serotonin 2C receptor: Comparisons among inbred mouse strains von Du, Yunzhi, Davisson, Muriel T., Kafadar, Karen, Gardiner, Katheleen

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