Rezultati pretrage - Jeffery M. Vance

Detaljiziraj rezultate
  1. 1
    Hereditary motor and sensory neuropathies.

    Hereditary motor and sensory neuropathies. od Jeffery M. Vance

    Izdano 1991
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  2. 2
    Nitric oxide synthase genes and their interactions with environmental factors in Parkinson’s disease

    Nitric oxide synthase genes and their interactions with environmental factors in Parkinson’s disease od Dana B. Hancock, Eden R. Martin, Jeffery M. Vance, William K. Scott

    Izdano 2008
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  3. 3
    No Gene Is an Island: The Flip-Flop Phenomenon

    No Gene Is an Island: The Flip-Flop Phenomenon od Ping‐I Lin, Jeffery M. Vance, Margaret A. Pericak‐Vance, Eden R. Martin

    Izdano 2007
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  4. 4
    SRRM2, a Potential Blood Biomarker Revealing High Alternative Splicing in Parkinson's Disease

    SRRM2, a Potential Blood Biomarker Revealing High Alternative Splicing in Parkinson's Disease od Lina A. Shehadeh, Kristine M. Yu, Liyong Wang, Alexandra Guevara, Carlos Singer, Jeffery M. Vance, Spyridon Papapetropoulos

    Izdano 2010
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  5. 5
    The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress

    The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress od Yoshiharu Kawaguchi, Jeffrey J. Kovacs, Adam C. McLaurin, Jeffery M. Vance, Akihiro Ito, Tso-Pang Yao

    Izdano 2003
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  6. 6
    Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease

    Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease od Sofia A. Oliveira, Yi‐Ju Li, Maher Noureddine, Stephan Züchner, Xuejun Qin, Margaret A. Pericak‐Vance, Jeffery M. Vance

    Izdano 2005
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  7. 7
    The transcription factor orthodenticle homeobox 2 influences axonal projections and vulnerability of midbrain dopaminergic neurons

    The transcription factor orthodenticle homeobox 2 influences axonal projections and vulnerability of midbrain dopaminergic neurons od Chee Yeun Chung, Pawel Licznerski, Kambiz N. Alavian, Antonio Simeone, Zhicheng Lin, Eden R. Martin, Jeffery M. Vance, Ole Isacson

    Izdano 2010
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  8. 8
    Vitamin D Receptor Gene as a Candidate Gene for Parkinson Disease

    Vitamin D Receptor Gene as a Candidate Gene for Parkinson Disease od Megan W. Butler, Amber Burt, Todd L. Edwards, Stephan Züchner, William K. Scott, Eden R. Martin, Jeffery M. Vance, Liyong Wang

    Izdano 2011
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  9. 9
    SNPselector: a web tool for selecting SNPs for genetic association studies

    SNPselector: a web tool for selecting SNPs for genetic association studies od Hong Xu, Simon G. Gregory, Elizabeth R. Hauser, Judith E. Stenger, Margaret A. Pericak‐Vance, Jeffery M. Vance, Stephan Züchner, Michael A. Hauser

    Izdano 2005
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  10. 10
    Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

    Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31 od Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha Nance, P. C. Gaskell, Jeffery M. Vance, Allison E. Ashley‐Koch, Margaret A. Pericak‐Vance

    Izdano 2006
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  11. 11
    Variation in the miRNA-433 Binding Site of FGF20 Confers Risk for Parkinson Disease by Overexpression of α-Synuclein

    Variation in the miRNA-433 Binding Site of FGF20 Confers Risk for Parkinson Disease by Overexpression of α-Synuclein od Gaofeng Wang, Joelle M. van der Walt, Gregory M. Mayhew, Yi‐Ju Li, Stephan Züchner, William K. Scott, Eden R. Martin, Jeffery M. Vance

    Izdano 2008
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  12. 12
    The mtDNA Mutation Spectrum of the Progeroid Polg Mutator Mouse Includes Abundant Control Region Multimers

    The mtDNA Mutation Spectrum of the Progeroid Polg Mutator Mouse Includes Abundant Control Region Multimers od Siôn L. Williams, Jia Huang, Yvonne J. K. Edwards, Rick H. Ulloa, Lloye M. Dillon, Tomas A. Prolla, Jeffery M. Vance, Carlos T. Moraes, Stephan Züchner

    Izdano 2010
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  13. 13
    GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

    GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis od John P. Hussman, Ashley Beecham, Michael A. Schmidt, Eden R. Martin, Jacob L. McCauley, Jeffery M. Vance, Jonathan L. Haines, Margaret A. Pericak‐Vance

    Izdano 2016
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  14. 14
    Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer disease.

    Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer disease. od Warren J. Strittmatter, Ann M. Saunders, Michel Goedert, Karl H. Weisgraber, Li Dong, Ross Jakes, Daoyuan Huang, Jeffery M. Vance, D. E. Schmechel, Allen D. Roses

    Izdano 1994
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  15. 15
    Derivation of autism spectrum disorder-specific induced pluripotent stem cells from peripheral blood mononuclear cells

    Derivation of autism spectrum disorder-specific induced pluripotent stem cells from peripheral blood mononuclear cells od Brooke A. DeRosa, Jessica M. Van Baaren, Gaurav Dubey, Joycelyn M. Lee, Michael L. Cuccaro, Jeffery M. Vance, Margaret A. Pericak‐Vance, Derek M. Dykxhoorn

    Izdano 2012
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  16. 16
    Gene Expression Profiles in Parkinson Disease Prefrontal Cortex Implicate FOXO1 and Genes under Its Transcriptional Regulation

    Gene Expression Profiles in Parkinson Disease Prefrontal Cortex Implicate FOXO1 and Genes under Its Transcriptional Regulation od Alexandra Dumitriu, Jeanne C. Latourelle, Tiffany C. Hadzi, Nathan Pankratz, Dan Garza, John P. Miller, Jeffery M. Vance, Tatiana Foroud, Thomas G. Beach, Richard H. Myers

    Izdano 2012
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  17. 17
    myotilin Mutation Found in Second Pedigree with LGMD1A

    myotilin Mutation Found in Second Pedigree with LGMD1A od Michael A. Hauser, Cecı́lia Conde, Valeria Kowaljow, Guillermo Zeppa, Ana Lía Taratuto, Udana Torian, Jeffery M. Vance, Margaret A. Pericak‐Vance, Marcy C. Speer, Alberto L. Rosa

    Izdano 2002
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  18. 18
    Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family

    Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family od Gladys Montenegro, Eric Powell, Jiaqiang Huang, Fiorella Speziani, Yvonne J. K. Edwards, Gary W. Beecham, William Hulme, Carly E. Siskind, Jeffery M. Vance, Michael E. Shy, Stephan Züchner

    Izdano 2011
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  19. 19
    Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease

    Whole exome sequencing of rare variants in <i>EIF4G1</i> and <i>VPS35</i> in Parkinson disease od Karen Nuytemans, Güney Bademci, Vanessa Inchausti, Amy Dressen, Daniel D. Kinnamon, Arpit Mehta, Liyong Wang, Stephan Züchner, Gary W. Beecham, Eden R. Martin, William K. Scott, Jeffery M. Vance

    Izdano 2013
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  20. 20
    Vitamin D from different sources is inversely associated with Parkinson disease

    Vitamin D from different sources is inversely associated with Parkinson disease od Liyong Wang, Marian L. Evatt, Lizmarie Maldonado, William Perry, James Ritchie, Gary W. Beecham, Eden R. Martin, Jonathan L. Haines, Margaret A. Pericak‐Vance, Jeffery M. Vance, William K. Scott

    Izdano 2014
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