2012 - Fellow of the American Association for the Advancement of Science (AAAS)
In his works, Jeffery M. Vance undertakes multidisciplinary study on Radiography and Nuclear medicine. Jeffery M. Vance integrates Nuclear medicine and Medical physics in his research. Jeffery M. Vance incorporates Medical physics and Radiology in his research. He combines Radiology and Radiography in his studies. He combines Chromosome and Locus (genetics) in his research. He merges Locus (genetics) with Genetics in his study. His work often combines Genetics and Chromosome studies. In his works, Jeffery M. Vance performs multidisciplinary study on Genetic linkage and Gene mapping. He merges Gene mapping with Genetic linkage in his study.
In his research on the topic of Damper, Stiffness is strongly related with Structural engineering. His work on Stiffness is being expanded to include thematically relevant topics such as Structural engineering. Jeffery M. Vance combines Quantum mechanics and Mechanics in his research. Jeffery M. Vance undertakes interdisciplinary study in the fields of Mechanics and Quantum mechanics through his works. He performs integrative study on Internal medicine and Surgery in his works. He combines Surgery and Internal medicine in his research. Jeffery M. Vance merges Genetics with Genetic linkage in his research. Jeffery M. Vance incorporates Genetic linkage and Gene mapping in his studies. Jeffery M. Vance incorporates Gene mapping and Chromosome in his research.
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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner;Stephan Züchner;Irina V Mersiyanova;Maria Muglia;Nisrine Bissar-Tadmouri;Nisrine Bissar-Tadmouri.
Nature Genetics (2004)
The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress
Yoshiharu Kawaguchi;Jeffrey J. Kovacs;Adam McLaurin;Jeffery M. Vance.
Cell (2003)
A Mutation in the TRPC6 Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
Michelle P. Winn;Peter J. Conlon;Kelvin L. Lynn;Merry Kay Farrington.
Science (2005)
PGC-1α, A Potential Therapeutic Target for Early Intervention in Parkinson’s Disease
Bin Zheng;Zhixiang Liao;Joseph J. Locascio;Kristen A. Lesniak.
Science Translational Medicine (2010)
Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy
Satoru Noguchi;Elizabeth M. McNally;Kamel Ben Othmane;Yasuko Hagiwara.
Science (1995)
Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V
Anthony Antonellis;Anthony Antonellis;Rachel E. Ellsworth;Nyamkhishig Sambuughin;Imke Puls.
American Journal of Human Genetics (2003)
Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease
Joelle M. van der Walt;Kristin K. Nicodemus;Eden R. Martin;William K. Scott.
American Journal of Human Genetics (2003)
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.
James R. Burke;Jan J. Enghild;Margaret E. Martin;Yuh Shan Jou.
Nature Medicine (1996)
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.
Christina M. Lill;Johannes T. Roehr;Johannes T. Roehr;Matthew B. McQueen;Fotini K. Kavvoura;Fotini K. Kavvoura;Fotini K. Kavvoura.
PLOS Genetics (2012)
Molecular markers of early Parkinson's disease based on gene expression in blood
Clemens R. Scherzer;Clemens R. Scherzer;Aron C. Eklund;Lee J. Morse;Zhixiang Liao.
Proceedings of the National Academy of Sciences of the United States of America (2007)
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