Her primary areas of investigation include Cell biology, Neurotrophin, Signal transduction, Mitochondrion and Neurotrophic factors. Her work deals with themes such as Internal medicine, Trk receptor and Programmed cell death, which intersect with Cell biology. In her research on the topic of Internal medicine, Endocrinology, Cellular differentiation and Neural crest is strongly related with SH-SY5Y.
Her Programmed cell death study is concerned with the field of Apoptosis as a whole. In her research, Neuroscience is intimately related to Brain-derived neurotrophic factor, which falls under the overarching field of Neurotrophin. Her biological study spans a wide range of topics, including Unfolded protein response, Endoplasmic reticulum, Downregulation and upregulation and Nerve growth factor.
Her main research concerns Cell biology, Apoptosis, Programmed cell death, Molecular biology and Neuroscience. Her studies deal with areas such as Neurotrophic factors, Trk receptor, Neurotrophin and Neurite as well as Cell biology. As a part of the same scientific study, Joan X. Comella usually deals with the Neurotrophin, concentrating on Brain-derived neurotrophic factor and frequently concerns with Protein kinase B and SH-SY5Y.
Her research investigates the connection with Apoptosis and areas like Downregulation and upregulation which intersect with concerns in Heat shock protein, Caspase 12, XBP1, Unfolded protein response and Endoplasmic reticulum. The various areas that Joan X. Comella examines in her Programmed cell death study include Cell, Cancer research, Flip and Mitochondrion. Her Neuroscience study combines topics in areas such as Neuroinflammation and Intracellular.
Joan X. Comella mainly focuses on Cell biology, Apoptosis, Neuroscience, Cancer research and Dendritic spine. The Cell biology study combines topics in areas such as Inhibitor of apoptosis, XIAP, Neurite, Receptor and Gene isoform. Her Apoptosis research incorporates elements of Immunology and Receptor antagonist.
Her studies in Neuroscience integrate themes in fields like Neuroinflammation, Knockout mouse, Neurodegeneration and Guanylate kinase. Her research in Cancer research focuses on subjects like Downregulation and upregulation, which are connected to Kinase and Cellular differentiation. Her Dendritic spine research integrates issues from Neurogenesis and Biophysics.
Her primary areas of study are Synaptogenesis, Neurogenesis, Dendritic spine, Neuroscience and Cell biology. Joan X. Comella has included themes like Dentate gyrus, Hippocampal formation, Reelin, DAB1 and Intracellular in her Synaptogenesis study. She combines topics linked to Biophysics with her work on Neurogenesis.
She connects Dendritic spine with Focused ion beam in her study. Her Cell biology study incorporates themes from Cancer research, Transcription factor and Downregulation and upregulation. The study incorporates disciplines such as Tumor Virus, Cancer, Molecular oncology and MAPK/ERK pathway in addition to Cancer research.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Sequential Treatment of SH‐SY5Y Cells with Retinoic Acid and Brain‐Derived Neurotrophic Factor Gives Rise to Fully Differentiated, Neurotrophic Factor‐Dependent, Human Neuron‐Like Cells
Mario Encinas;Montse Iglesias;Yuhui Liu;Hongyin Wang.
Journal of Neurochemistry (2002)
Extracellular-regulated kinases and phosphatidylinositol 3-kinase are involved in brain-derived neurotrophic factor-mediated survival and neuritogenesis of the neuroblastoma cell line SH-SY5Y.
M. Encinas;M. Iglesias;N. Llecha;J. X. Comella.
Journal of Neurochemistry (2002)
Receptors of the glial cell line-derived neurotrophic factor family of neurotrophic factors signal cell survival through the phosphatidylinositol 3-kinase pathway in spinal cord motoneurons.
Rosa M. Soler;Xavier Dolcet;Mario Encinas;Joaquim Egea.
The Journal of Neuroscience (1999)
Oxidative stress and proinflammatory cytokines contribute to demyelination and axonal damage in a cerebellar culture model of neuroinflammation.
Alessandra di Penta;Beatriz Moreno;Stephanie Reix;Begoña Fernandez-Diez.
PLOS ONE (2013)
c-Src is required for glial cell line-derived neurotrophic factor (GDNF) family ligand-mediated neuronal survival via a phosphatidylinositol-3 kinase (PI-3K)-dependent pathway.
Mario Encinas;Malú G. Tansey;Brian A. Tsui-Pierchala;Joan X. Comella.
The Journal of Neuroscience (2001)
A TrkB/EphrinA Interaction Controls Retinal Axon Branching and Synaptogenesis
Katharine J. M. Marler;Elena Becker-Barroso;Albert Martínez;Marta Llovera.
The Journal of Neuroscience (2008)
Induction of ER stress in response to oxygen-glucose deprivation of cortical cultures involves the activation of the PERK and IRE-1 pathways and of caspase-12
Nahuai Badiola;Nahuai Badiola;Clara Penas;Clara Penas;Alfredo Miñano-Molina;Alfredo Miñano-Molina;Bruna Barneda-Zahonero;Bruna Barneda-Zahonero.
Cell Death and Disease (2011)
Activation of phosphatidylinositol 3-kinase, but not extracellular-regulated kinases, is necessary to mediate brain-derived neurotrophic factor-induced motoneuron survival.
Xavier Dolcet;Joaquim Egea;Rosa M. Soler;Dionisio Martin‐Zanca.
Journal of Neurochemistry (2002)
Terminal sprouting in mouse neuromuscular junctions poisoned with botulinum type a toxin: Morphological and electrophysiological features
D. Angaut-Petit;J. Molgó;J.X. Comella;L. Faille.
Neuroscience (1990)
Reactive Oxygen Species and p38 Mitogen-Activated Protein Kinase Activate Bax to Induce Mitochondrial Cytochrome c Release and Apoptosis in Response to Malonate
M. Gomez-Lazaro;M. F. Galindo;R. M. Melero-Fernandez de Mera;F. J. Fernandez-Gómez.
Molecular Pharmacology (2007)
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