Resultats de la cerca - Muriel T. Davisson

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  1. 1
    Quantitative PCR genotyping assay for the Ts65Dn mouse model of Down syndrome

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

    Publicat 2003
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  2. 2
    Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6brd1

    Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6brd1 per Alberto C. S. Costa, Melissa R. Stasko, Cecilia Schmidt, Muriel T. Davisson

    Publicat 2009
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  3. 3
    Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcripts.

    Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcripts. per Scott J. Bultman, Mitchell Klebig, Edward J. Michaud, Hope O. Sweet, Muriel T. Davisson, Richard P. Woychik

    Publicat 1994
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  4. 4
    A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers

    A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers per Ron Korstanje, Christina R. Caputo, Rosalinda Doty, Susan A. Cook, Roderick T. Bronson, Muriel T. Davisson, Jeffrey H. Miner

    Publicat 2014
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  5. 5
    Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

    Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype per Jorge Luis Valdés González, Christopher J. Russo, Dan Goldowitz, Hope O. Sweet, Muriel T. Davisson, Christopher A. Walsh

    Publicat 1997
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  6. 6
    Comparative map for mice and humans

    Comparative map for mice and humans per Joseph H. Nadeau, Muriel T. Davisson, Donald P. Doolittle, Patricia Grant, A.L. Hillyard, Michael Kosowsky, Thomas H. Roderick

    Publicat 1992
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  7. 7
    Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage.

    Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage. per Edward J. Michaud, Martine J. van Vugt, Scott J. Bultman, Hope O. Sweet, Muriel T. Davisson, Richard P. Woychik

    Publicat 1994
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  8. 8
    The fatty liver dystrophy (fld) mutation

    The fatty liver dystrophy (fld) mutation per Cord Langner, E H Birkenmeier, Osnat Ben-Zeev, Michael C. Schotz, Hope O. Sweet, Muriel T. Davisson, Jeffrey I. Gordon

    Publicat 1989
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  9. 9
    Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

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

    Publicat 2001
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  10. 10
    Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease

    Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease per Gregory B. Potter, Marta B. Santos, Muriel T. Davisson, David H. Rowitch, Dan L. Marks, Ernesto R. Bongarzone, Magdalena A. Petryniak

    Publicat 2013
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  11. 11
    Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin

    Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin per Dan Goldowitz, Richard C. Cushing, Eric D. Laywell, Gabriella D’Arcangelo, Michael Sheldon, Hope O. Sweet, Muriel T. Davisson, Dennis A. Steindler, Tom Curran

    Publicat 1997
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  12. 12
    Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn

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

    Publicat 2011
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  13. 13
    Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.

    Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency. per E H Birkenmeier, Muriel T. Davisson, Wesley G. Beamer, R E Ganschow, Carole Vogler, Babette Gwynn, Kimberly A. Lyford, Lois M. Maltais, C.J. Wawrzyniak

    Publicat 1989
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  14. 14
    Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta.

    Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. per Stewart D. Chipman, H O Sweet, David J. McBride, Muriel T. Davisson, S. C. Marks, Alan R. Shuldiner, Richard Wenstrup, David W. Rowe, Jay R. Shapiro

    Publicat 1993
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  15. 15
    A standardized nomenclature for endogenous mouse mammary tumor viruses

    A standardized nomenclature for endogenous mouse mammary tumor viruses per Christine A. Kozak, Godefridus J. Peters, Robert J. Pauley, V L Morris, Rob Michalides, Jaquelin P. Dudley, M Green, Muriel T. Davisson, Om Prakash, Akhil B. Vaidya

    Publicat 1987
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  16. 16
    Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

    Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice per Michael G. Anderson, Richard S. Smith, Olga V. Savinova, Norman L. Hawes, Bo Chang, Adriana Zabaleta, Robert Y Wilpan, John R. Heckenlively, Muriel T. Davisson, Simon W. M. John

    Publicat 2001
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  17. 17
    ZFP191 is required by oligodendrocytes for CNS myelination

    ZFP191 is required by oligodendrocytes for CNS myelination per Shen Yi B. Howng, Robin L. Avila, Ben Emery, Μαρία Τράκα, Wensheng Lin, Trent A. Watkins, Susan A. Cook, Roderick T. Bronson, Muriel T. Davisson, Ben A. Barres, Brian Popko

    Publicat 2010
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  18. 18
    VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse

    VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse per Natsuko Jin, Clement Y. Chow, Li Liu, Sergey N. Zolov, Roderick Bronson, Muriel T. Davisson, Jason L. Petersen, Yanling Zhang, Sujin Park, Jason E. Duex, Dan Goldowitz, Miriam H. Meisler, Lois S. Weisman

    Publicat 2008
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  19. 19
    A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the <i>rd7</i> mouse

    A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the <i>rd7</i> mouse per N. B. Akhmedov, Natik Piri, Bo Chang, Ana Lia Rapoport, Norman L. Hawes, Patsy M. Nishina, Steven Nusinowitz, John R. Heckenlively, Thomas H. Roderick, Christine A. Kozak, Michael Danciger, Muriel T. Davisson, Debora B. Farber

    Publicat 2000
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  20. 20
    Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome

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

    Publicat 2008
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