Ngā hua rapu - Cassandra Obie

  • E whakaatu ana i te 1 - 7 hua o te 7
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  1. 1
    The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency

    The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency mā Matthias R. Baumgartner, Shlomo Almashanu, Terttu Suormala, Cassandra Obie, Robert N. Cole, Seymour Packman, E. R. Baumgartner, David Valle

    I whakaputaina 2001
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation.

    Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. mā Grant A. Mitchell, Damian Labuda, G Fontaine, Jean Marie Saudubray, Jean‐Paul Bonnefont, Stanislas Lyonnet, Lawrence C. Brody, Gary Steel, Cassandra Obie, David Valle

    I whakaputaina 1991
    Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Expression of PEX11β Mediates Peroxisome Proliferation in the Absence of Extracellular Stimuli

    Expression of PEX11β Mediates Peroxisome Proliferation in the Absence of Extracellular Stimuli mā Michael Schrader, Bernadette E. Reuber, James C. Morrell, Gerardo Jiménez‐Sánchez, Cassandra Obie, Tina A. Stroh, David Valle, Trina A. Schroer, Stephen J. Gould

    I whakaputaina 1998
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. mā Larry Brody, Grant A. Mitchell, Cassandra Obie, Jacques L. Michaud, Gary Steel, G Fontaine, M.F. Robert, Ilkka Sipilä, Muriel I. Kaiser‐Kupfer, David Valle

    I whakaputaina 1992
    Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

    At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns. mā Grant A. Mitchell, Lawrence C. Brody, Ilkka Sipilä, James E. Looney, C Wong, John F. Engelhardt, Achyut S. Patel, Gary Steel, Cassandra Obie, Muriel I. Kaiser‐Kupfer

    I whakaputaina 1989
    Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Mutation analysis ofPEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype

    Mutation analysis ofPEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype mā Nancy Braverman, Li Chen, Paul Lin, Cassandra Obie, Gary Steel, Pamela K. Douglas, Pranesh Chakraborty, Joe T.R. Clarke, Avihu Boneh, Ann B. Moser, Hugo W. Moser, David Valle

    I whakaputaina 2002
    Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome

    Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome mā Nancy Braverman, Paul Lin, Fabian F. Moebius, Cassandra Obie, Ann B. Moser, Hartmut Glossmann, William R. Wilcox, David L. Rimoin, Moyra Smith, Lisa E. Kratz, Richard I. Kelley, David Valle

    I whakaputaina 1999
    Whiwhi kuputuhi katoa
    Artigo
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