His primary areas of investigation include Cell biology, Endoplasmic reticulum, Golgi apparatus, Biochemistry and Secretory pathway. His study in Cell biology is interdisciplinary in nature, drawing from both Vesicle and Vesicular transport protein. William E. Balch has researched Endoplasmic reticulum in several fields, including GTP-binding protein regulators, Vesicular stomatitis virus, Membrane transport and Transmembrane protein.
His Golgi apparatus study combines topics from a wide range of disciplines, such as Transport protein, GTPase, G protein and Cytosol. His work on Chaperone and Protein folding as part of general Biochemistry study is frequently connected to Methanobacterium thermoautotrophicum, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Secretory pathway study incorporates themes from Cathepsin D, LY294002, Mutant, Wortmannin and Vacuole.
His main research concerns Cell biology, Endoplasmic reticulum, Golgi apparatus, Biochemistry and Secretory pathway. His research in Cell biology focuses on subjects like Vesicle, which are connected to Budding. The study incorporates disciplines such as Transport protein, Vesicular stomatitis virus, Vesicular transport protein and Protein folding in addition to Endoplasmic reticulum.
His Golgi apparatus research is multidisciplinary, incorporating elements of Cell-free system, G protein and Cytosol. William E. Balch works mostly in the field of Biochemistry, limiting it down to concerns involving Amyloid disease and, occasionally, Amyloidosis. William E. Balch combines subjects such as Cellular compartment and Secretory protein with his study of Secretory pathway.
The scientist’s investigation covers issues in Cell biology, Proteostasis, Computational biology, Protein folding and NPC1. His study in Cell biology focuses on Chaperone in particular. The various areas that William E. Balch examines in his Proteostasis study include Proteome, Bioinformatics, Alpha 1-antitrypsin deficiency, Function and Protein structure.
His Computational biology research is multidisciplinary, incorporating perspectives in Precision medicine, Epigenetics, Genetic variation and Disease. He has included themes like Signal transduction and Heat shock in his Protein folding study. His Endosome research also works with subjects such as
His scientific interests lie mostly in Cell biology, Lung, Proteostasis, NPC1 and Cystic fibrosis transmembrane conductance regulator. His biological study spans a wide range of topics, including Proteome and Proteomics. His Lung research includes elements of Transcriptome, Immunology and Pathology.
His Proteostasis research focuses on subjects like Computational biology, which are linked to Phenotype, Natural selection, Whole genome sequencing, Genomics and Phenomics. His NPC1 study integrates concerns from other disciplines, such as Vorinostat, Maladaptation and Niemann–Pick disease, type C. His Niemann–Pick disease, type C study is concerned with the larger field of Biochemistry.
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Methanogens: reevaluation of a unique biological group.
W E Balch;G E Fox;L J Magrum;C R Woese.
Microbiological Research (1979)
Adapting proteostasis for disease intervention.
William E. Balch;Richard I. Morimoto;Andrew Dillin;Jeffery W. Kelly.
Science (2008)
The Phylogeny of Prokaryotes
GE Fox;E Stackebrandt;RB Hespell;J Gibson.
Science (1980)
Biological and Chemical Approaches to Diseases of Proteostasis Deficiency
Evan T. Powers;Richard I. Morimoto;Andrew Dillin;Jeffery W. Kelly.
Annual Review of Biochemistry (2009)
Functional amyloid--from bacteria to humans.
Douglas M. Fowler;Atanas V. Koulov;William E. Balch;Jeffery W. Kelly.
Trends in Biochemical Sciences (2007)
Functional amyloid formation within mammalian tissue
Douglas M Fowler;Atanas V Koulov;Christelle Alory-Jost;Michael S Marks.
PLOS Biology (2005)
Reconstitution of the transport of protein between successive compartments of the golgi measured by the coupled incorporation of N-acetylglucosamine
William E. Balch;William G. Dunphy;William A. Braell;James E. Rothman.
Cell (1984)
A Di-Acidic Signal Required for Selective Export from the Endoplasmic Reticulum
Noriyuki Nishimura;William E. Balch.
Science (1997)
Hsp90 Cochaperone Aha1 Downregulation Rescues Misfolding of CFTR in Cystic Fibrosis
Xiaodong Wang;John Venable;Paul LaPointe;Darren M. Hutt.
Cell (2006)
Rab1 Recruitment of p115 into a cis-SNARE Complex: Programming Budding COPII Vesicles for Fusion
Bernard B. Allan;Bryan D. Moyer;William E. Balch.
Science (2000)
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