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Gary Steel

Showing results (1-10 of 11) with videos related to

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Amino Acids|June 6, 2008
PRODH variants and risk for schizophreniaAlecia Willis, Hans Uli Bender, Gary Steel, et al.
American Journal of Human Genetics|April 29, 2005
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesisSabine Weller, Ivelisse Cajigas, James Morrell, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndromeCarolina Araujo Moreno, Nara Sobreira, Elizabeth Pugh, et al.
American Journal of Medical Genetics. Part A|October 29, 2014
An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: further definition of the phenotypic heterogeneity of LBR-bone dysplasiasNara Sobreira, Peggy Modaff, Gary Steel, et al.
American Journal of Human Genetics|January 22, 2005
Functional consequences of PRODH missense mutationsHans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Molecular and Cellular Biochemistry|July 29, 2006
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosisChien-an A Hu, Steven P Donald, Jian Yu, et al.
Molecular Neuropsychiatry|September 9, 2016
Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic DisordersLindsay N Hayes, Alexey Shevelkin, Mariela Zeledon, et al.
Human Mutation|September 27, 2002
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotypeNancy Braverman, Li Chen, Paul Lin, et al.
American Journal of Human Genetics|December 29, 2005
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent triosM Daniele Fallin, Virginia K Lasseter, Dimitrios Avramopoulos, et al.
American Journal of Human Genetics|January 3, 2009
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaPei-Lung Chen, Dimitrios Avramopoulos, Virginia K Lasseter, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Amino Acids|June 6, 2008
PRODH variants and risk for schizophreniaAlecia Willis, Hans Uli Bender, Gary Steel, et al.
American Journal of Human Genetics|April 29, 2005
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesisSabine Weller, Ivelisse Cajigas, James Morrell, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndromeCarolina Araujo Moreno, Nara Sobreira, Elizabeth Pugh, et al.
American Journal of Medical Genetics. Part A|October 29, 2014
An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: further definition of the phenotypic heterogeneity of LBR-bone dysplasiasNara Sobreira, Peggy Modaff, Gary Steel, et al.
American Journal of Human Genetics|January 22, 2005
Functional consequences of PRODH missense mutationsHans-Ulrich Bender, Shlomo Almashanu, Gary Steel, et al.
Molecular and Cellular Biochemistry|July 29, 2006
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosisChien-an A Hu, Steven P Donald, Jian Yu, et al.
Molecular Neuropsychiatry|September 9, 2016
Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic DisordersLindsay N Hayes, Alexey Shevelkin, Mariela Zeledon, et al.
Human Mutation|September 27, 2002
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotypeNancy Braverman, Li Chen, Paul Lin, et al.
American Journal of Human Genetics|December 29, 2005
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent triosM Daniele Fallin, Virginia K Lasseter, Dimitrios Avramopoulos, et al.
American Journal of Human Genetics|January 3, 2009
Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaPei-Lung Chen, Dimitrios Avramopoulos, Virginia K Lasseter, et al.
Pageof 2