Ngā hua rapu - 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 mā Dong P. Liu, Cecilia Schmidt, Timothy Billings, Muriel T. Davisson

    I whakaputaina 2003
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Alberto C. S. Costa, Melissa R. Stasko, Cecilia Schmidt, Muriel T. Davisson

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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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. mā Scott J. Bultman, Mitchell Klebig, Edward J. Michaud, Hope O. Sweet, Muriel T. Davisson, Richard P. Woychik

    I whakaputaina 1994
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Ron Korstanje, Christina R. Caputo, Rosalinda Doty, Susan A. Cook, Roderick T. Bronson, Muriel T. Davisson, Jeffrey H. Miner

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Jorge Luis Valdés González, Christopher J. Russo, Dan Goldowitz, Hope O. Sweet, Muriel T. Davisson, Christopher A. Walsh

    I whakaputaina 1997
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Comparative map for mice and humans

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

    I whakaputaina 1992
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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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. mā Edward J. Michaud, Martine J. van Vugt, Scott J. Bultman, Hope O. Sweet, Muriel T. Davisson, Richard P. Woychik

    I whakaputaina 1994
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    The fatty liver dystrophy (fld) mutation

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

    I whakaputaina 1989
    Whiwhi kuputuhi katoa
    Artigo
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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 mā J.M. Newton, Orit Cohen‐Barak, Nobuko Hagiwara, John M. Gardner, Muriel T. Davisson, Richard A. King, Murray H. Brilliant

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā Gregory B. Potter, Marta B. Santos, Muriel T. Davisson, David H. Rowitch, Dan L. Marks, Ernesto R. Bongarzone, Magdalena A. Petryniak

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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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 mā Dan Goldowitz, Richard C. Cushing, Eric D. Laywell, Gabriella D’Arcangelo, Michael Sheldon, Hope O. Sweet, Muriel T. Davisson, Dennis A. Steindler, Tom Curran

    I whakaputaina 1997
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2011
    Whiwhi kuputuhi katoa
    Artigo
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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. mā 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

    I whakaputaina 1989
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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. mā 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

    I whakaputaina 1993
    Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    A standardized nomenclature for endogenous mouse mammary tumor viruses

    A standardized nomenclature for endogenous mouse mammary tumor viruses mā 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

    I whakaputaina 1987
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  17. 17
    ZFP191 is required by oligodendrocytes for CNS myelination

    ZFP191 is required by oligodendrocytes for CNS myelination mā 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

    I whakaputaina 2010
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2000
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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