Genetics, Gene, Molecular biology, Cell biology and Ataxia are his primary areas of study. His Genetics research focuses on Inbred strain, Provirus, Genome, Quantitative trait locus and Candidate gene. His research in the fields of Genetic marker, Gene expression profiling, Model organism and Mouse mammary tumor virus overlaps with other disciplines such as Expression quantitative trait loci.
His biological study spans a wide range of topics, including Tumor necrosis factor alpha, Fas ligand, Cytokine, Ectodomain and c-jun. The various areas that Wayne N. Frankel examines in his Cell biology study include Phenotype, Biochemistry and Free radical scavenger. His Ataxia study incorporates themes from Cerebellum, Protein subunit, Cav2.1, Mutant and Epilepsy.
His scientific interests lie mostly in Genetics, Gene, Epilepsy, Molecular biology and Mutant. His Genetics study is mostly concerned with Gene mapping, Allele, Phenotype, Mutation and Genome. His studies deal with areas such as Computational biology, DNA and Mus spretus as well as Genome.
His studies in Epilepsy integrate themes in fields like Quantitative trait locus, Genetic model and Internal medicine, Hippocampus. The Molecular biology study which covers Provirus that intersects with Insertion and Murine leukemia virus. His biological study spans a wide range of topics, including Ataxia, Cell biology and Missense mutation.
The scientist’s investigation covers issues in Epilepsy, Neuroscience, Cell biology, Excitatory postsynaptic potential and Genetics. His research in Epilepsy intersects with topics in Phenotype, In vivo, Speech recognition and Bioinformatics. His Cell biology research incorporates themes from Dentate gyrus, Intracellular vesicle and Endocytic cycle.
His work on Genetics deals in particular with Inbred strain, Strain, Allele, Pleiotropy and Loss function. His research investigates the link between Allele and topics such as GRIA4 that cross with problems in Gene. His Heterozygote advantage research is multidisciplinary, incorporating perspectives in Endocrinology and Internal medicine.
Wayne N. Frankel spends much of his time researching Epilepsy, Neuroscience, Genetics, In vivo and Mutation. His Epilepsy research incorporates elements of Precision medicine and Bioinformatics. His study looks at the relationship between Neuroscience and fields such as Phenotype, as well as how they intersect with chemical problems.
Wayne N. Frankel works on Genetics which deals in particular with Inbred strain. His work deals with themes such as Ranolazine, Pharmacology and Drug, which intersect with In vivo. His Mutation study combines topics in areas such as Molecular biology, Transferrin, Vesicle scission and Mutant.
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Initial sequencing and comparative analysis of the mouse genome.
Robert H. Waterston;Kerstin Lindblad-Toh;Ewan Birney;Jane Rogers.
The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity
L. de Lecea;T. S. Kilduff;C. Peyron;X.-B. Gao.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies.
Jacqueline N. Crawley;John K. Belknap;Allan Collins;John C. Crabbe.
TRANCE Is a Novel Ligand of the Tumor Necrosis Factor Receptor Family That Activates c-Jun N-terminal Kinase in T Cells*
Brian R. Wong;Jaerang Rho;Joseph Arron;Elizabeth Robinson.
Journal of Biological Chemistry (1997)
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
Colin F Fletcher;Cathleen M Lutz;T.Norene O'Sullivan;John D Shaughnessy.
The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
Verity A. Letts;Ricardo Felix;Gloria H. Biddlecome;Jyothi Arikkath.
Nature Genetics (1998)
Maps from two interspecific backcross DNA panels available as a community genetic mapping resource
L. B. Rowe;J. H. Nadeau;R. Turner;W. N. Frankel.
Mammalian Genome (1994)
The harlequin mouse mutation downregulates apoptosis-inducing factor
Jeffrey A. Klein;Chantal M. Longo-Guess;Marlies P. Rossmann;Kevin L. Seburn.
Disruption of the nuclear hormone receptor RORα in staggerer mice
Bruce A. Hamilton;Wayne N. Frankel;Anne W. Kerrebrock;Trevor L. Hawkins.
An enzymatic cascade of Rab5 effectors regulates phosphoinositide turnover in the endocytic pathway
Hye-Won Shin;Mitsuko Hayashi;Savvas Christoforidis;Sandra Lacas-Gervais.
Journal of Cell Biology (2005)
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