检索结果 - Gary Steel

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  1. 1
    Engaging adolescent participants in academic research: the use of photo-elicitation interviews to evaluate school-based outdoor education programmes

    Engaging adolescent participants in academic research: the use of photo-elicitation interviews to evaluate school-based outdoor education programmes 由 Erin F. Smith, Bob Gidlow, Gary Steel

    出版 2012
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  2. 2
    Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina

    Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retina 由 Tao Wang, Gary Steel, Ann H. Milam, David Valle

    出版 2000
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  3. 3
    Validation of the New Zealand Physical Activity Questionnaire (NZPAQ-LF) and the International Physical Activity Questionnaire (IPAQ-LF) with accelerometry

    Validation of the New Zealand Physical Activity Questionnaire (NZPAQ-LF) and the International Physical Activity Questionnaire (IPAQ-LF) with accelerometry 由 Ryan Boon, Michael J. Hamlin, Gary Steel, Jenny J. Ross

    出版 2008
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  4. 4
    Identification of a Fourth Half ABC Transporter in the Human Peroxisomal Membrane

    Identification of a Fourth Half ABC Transporter in the Human Peroxisomal Membrane 由 Noam Shani, Gerardo Jiménez‐Sánchez, Gary Steel, Michael Dean, David Valle

    出版 1997
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  5. 5
    Homozygous deletion in MYL9 expands the molecular basis of megacystis–microcolon–intestinal hypoperistalsis syndrome

    Homozygous deletion in MYL9 expands the molecular basis of megacystis–microcolon–intestinal hypoperistalsis syndrome 由 Carolina Moreno, Nara Sobreira, Elizabeth Pugh, Peng Zhāng, Gary Steel, Fábio Torres, Denise P. Cavalcanti

    出版 2018
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  6. 6
    Functional Consequences of PRODH Missense Mutations

    Functional Consequences of PRODH Missense Mutations 由 Hans‐Ulrich Bender, Shlomo Almashanu, Gary Steel, Chien-an A. Hu, Wei‐Wen Lin, Alecia Willis, Ann E. Pulver, David Valle

    出版 2005
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  7. 7
    Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene.

    Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene. 由 Grant A. Mitchell, James E. Looney, Lawrence C. Brody, Gary Steel, Maureen K. Suchanek, John F. Engelhardt, H.F. Willard, David Valle

    出版 1988
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  8. 8
    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. 由 Grant A. Mitchell, Damian Labuda, G Fontaine, Jean Marie Saudubray, Jean‐Paul Bonnefont, Stanislas Lyonnet, Lawrence C. Brody, Gary Steel, Cassandra Obie, David Valle

    出版 1991
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  9. 9
    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

    Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences. 由 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

    出版 1992
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  10. 10
    An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.

    An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina. 由 Grant A. Mitchell, Lawrence C. Brody, James E. Looney, Gary Steel, Maureen K. Suchanek, Carol E. Dowling, V Der Kaloustian, Muriel I. Kaiser‐Kupfer, David Valle

    出版 1988
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  11. 11
    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. 由 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

    出版 1989
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  12. 12
    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 由 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

    出版 2002
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  13. 13
    Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios

    Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios 由 M. Daniele Fallin, Virginia K. Lasseter, Dimitrios Avramopoulos, Kristin K. Nicodemus, Paula Wolyniec, John A. McGrath, Gary Steel, Gerald Nestadt, Kung‐Yee Liang, Richard L. Huganir, David Valle, Ann E. Pulver

    出版 2005
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  14. 14
    Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia

    Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia 由 Pei-Lung Chen, Dimitrios Avramopoulos, Virginia K. Lasseter, John A. McGrath, M. Daniele Fallin, Kung‐Yee Liang, Gerald Nestadt, Ningping Feng, Gary Steel, Andrew S. Cutting, Paula Wolyniec, Ann E. Pulver, David Valle

    出版 2009
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