Bernard Massie focuses on Molecular biology, Cell culture, Cell biology, Gene expression and Programmed cell death. His biological study spans a wide range of topics, including Complementary DNA, Gene, Viral vector and Reporter gene. The Cell culture study combines topics in areas such as Biochemistry, Recombinant DNA and Microbiology.
His Gene expression research incorporates elements of Adenoviridae and Expression cassette. His research on Programmed cell death focuses in particular on Caspase 3. His research in Caspase 3 focuses on subjects like Caspase, which are connected to Chaperone, Signal transduction, Peptide binding and Cytochrome c.
Bernard Massie mainly investigates Molecular biology, Cell culture, Recombinant DNA, Virology and Genetic enhancement. The various areas that he examines in his Molecular biology study include Expression cassette, Gene expression, Gene, Green fluorescent protein and Viral vector. While the research belongs to areas of Cell culture, he spends his time largely on the problem of Cell biology, intersecting his research to questions surrounding Programmed cell death and Heat shock protein.
In his work, Internal ribosome entry site is strongly intertwined with Chinese hamster ovary cell, which is a subfield of Recombinant DNA. His Virology research is multidisciplinary, relying on both Apoptosis, Ribonucleotide reductase, Immune system and Fusion protein. When carried out as part of a general Genetic enhancement research project, his work on Adenoviridae is frequently linked to work in Functional genomics, therefore connecting diverse disciplines of study.
Molecular biology, Recombinant DNA, Virology, Genetic enhancement and Gene expression are his primary areas of study. His Molecular biology study integrates concerns from other disciplines, such as Fas receptor, Caspase, FADD, Caspase 8 and Death domain. His work in Recombinant DNA tackles topics such as Chinese hamster ovary cell which are related to areas like Fragment crystallizable region, Transduction, Internal ribosome entry site, Multiplicity of infection and Transfection.
His work carried out in the field of Virology brings together such families of science as Myocyte, Gene, Transgene and Fusion protein. His work deals with themes such as Receptor, Stromal cell, Metastasis and Viral vector, which intersect with Genetic enhancement. His Repressor study in the realm of Gene expression interacts with subjects such as Population.
Bernard Massie spends much of his time researching Molecular biology, Recombinant DNA, Gene expression, Chinese hamster ovary cell and Multiplicity of infection. Bernard Massie combines subjects such as Fas receptor, Caspase, FADD, Caspase 8 and Death domain with his study of Molecular biology. His research in Recombinant DNA intersects with topics in Neutralizing antibody, Immune system, Virology, Porcine reproductive and respiratory syndrome virus and Viremia.
His Gene expression research is multidisciplinary, incorporating elements of Inducer, Expression vector and Escherichia coli. His study with Chinese hamster ovary cell involves better knowledge in Cell culture. His research in Multiplicity of infection intersects with topics in Fragment crystallizable region, Internal ribosome entry site, Transduction and Green fluorescent protein.
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Role of the human heat shock protein hsp70 in protection against stress-induced apoptosis.
Dick D. Mosser;Antoine W. Caron;Lucie Bourget;Claude Denis-Larose.
Molecular and Cellular Biology (1997)
The chaperone function of hsp70 is required for protection against stress-induced apoptosis.
Dick D. Mosser;Antoine W. Caron;Lucie Bourget;Anatoli B. Meriin.
Molecular and Cellular Biology (2000)
The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants.
Johnny Huard;H. Lochmüller;G. Acsadi;A. Jani.
Gene Therapy (1995)
Induction of apoptosis in nutrient‐deprived cultures of hybridoma and myeloma cells
Sylvain Mercille;Bernard Massie.
Biotechnology and Bioengineering (1994)
Intracellular synthesis, processing, and transport of proteins encoded by ORFs 5 to 7 of porcine reproductive and respiratory syndrome virus.
Helmi Mardassi;Bernard Massie;Serge Dea.
Virology (1996)
A differential efficiency of adenovirus-mediated in vivo gene transfer into skeletal muscle cells of different maturity
Gyula Acsadi;Agnes Jani;Bernard Massie;Maude Simoneau.
Human Molecular Genetics (1994)
The DNA-binding activity of the human heat shock transcription factor is regulated in vivo by hsp70.
D D Mosser;J Duchaine;B Massie.
Molecular and Cellular Biology (1993)
Emergence of Early Region 1-Containing Replication-Competent Adenovirus in Stocks of Replication-Defective Adenovirus Recombinants (ΔE1 + ΔE3) During Multiple Passages in 293 Cells
H. Lochmuller;A. Jani;Johnny Huard;S. Prescott.
Human Gene Therapy (1994)
Gene Transfer into Skeletal Muscles by Isogenic Myoblasts
Johnny Huard;Gyula Acsadi;Agnes Jani;Bernard Massie.
Human Gene Therapy (1994)
Hsp72-mediated suppression of c-Jun N-terminal kinase is implicated in development of tolerance to caspase-independent cell death.
Vladimir L. Gabai;Julia A. Yaglom;Vladimir Volloch;Anatoli B. Meriin.
Molecular and Cellular Biology (2000)
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