Her scientific interests lie mostly in Cell biology, Neuroscience, CDKL5, Rett syndrome and Genetics. Her research investigates the connection between Cell biology and topics such as Endocrinology that intersect with problems in Aristaless related homeobox. Her Neuroscience research is multidisciplinary, incorporating elements of Cellular differentiation and Transplantation.
Her study looks at the intersection of Cellular differentiation and topics like Dopamine with Progenitor cell and Anatomy. Her biological study spans a wide range of topics, including P19 cell and Neuroepithelial cell. Her CDKL5 research is multidisciplinary, relying on both Neurodevelopmental disorder, FOXG1 and Atypical Rett syndrome.
Her primary areas of study are Cell biology, Cellular differentiation, Neuroscience, Genetics and Stem cell. Her study in Cell biology is interdisciplinary in nature, drawing from both Embryonic stem cell, Reprogramming, Gene and Induced pluripotent stem cell. As a member of one scientific family, Vania Broccoli mostly works in the field of Cellular differentiation, focusing on Cell fate determination and, on occasion, Endocrinology and Internal medicine.
Her studies examine the connections between Stem cell and genetics, as well as such issues in Neurosphere, with regards to Multipotent Stem Cell and Neuroepithelial cell. Her Forebrain research focuses on subjects like GABAergic, which are linked to Anatomy and Interneuron. Vania Broccoli has researched Progenitor cell in several fields, including Cancer research and Transplantation.
Vania Broccoli mostly deals with Cell biology, Neuroscience, Genetic enhancement, Dendritic spine and Transcription factor. Vania Broccoli interconnects Embryonic stem cell, Gene, Somatic cell and Haploinsufficiency in the investigation of issues within Cell biology. Her studies deal with areas such as Genome editing and CRISPR as well as Neuroscience.
The study incorporates disciplines such as Cancer research, Mutant and Gene expression in addition to Genetic enhancement. Her Cancer research research integrates issues from Transgene, Neurodevelopmental disorder, MECP2, Gene duplication and Rett syndrome. Her Reprogramming study incorporates themes from Progenitor cell, Metachromatic leukodystrophy, Immunology and Transplantation.
Vania Broccoli mainly focuses on Cell biology, Epigenetics, Gene, Haploinsufficiency and Genetic enhancement. Vania Broccoli integrates Cell biology with Sodium channel in her study. Her study looks at the relationship between Epigenetics and topics such as Neural development, which overlap with Neural stem cell.
Her studies in Neural stem cell integrate themes in fields like Cancer research, Progenitor cell, Reprogramming, Immunology and Metachromatic leukodystrophy. Her work in the fields of Gene, such as Gene expression, KMT2A, MECOM and Brain morphogenesis, overlaps with other areas such as Atypical chronic myeloid leukemia. Her research integrates issues of Interneuron, Gene dosage, Regulation of gene expression, Gene product and Parvalbumin in her study of Haploinsufficiency.
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Neurons derived from reprogrammed fibroblasts functionally integrate into the fetal brain and improve symptoms of rats with Parkinson's disease
Marius Wernig;Jian Ping Zhao;Jan Pruszak;Eva Hedlund.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Direct generation of functional dopaminergic neurons from mouse and human fibroblasts
Massimiliano Caiazzo;Maria Teresa Dell’Anno;Elena Dvoretskova;Dejan Lazarevic;Dejan Lazarevic.
Mapping Wnt/β-catenin signaling during mouse development and in colorectal tumors
Silvia Maretto;Michelangelo Cordenonsi;Sirio Dupont;Paola Braghetta.
Proceedings of the National Academy of Sciences of the United States of America (2003)
The meso-angioblast: A multipotent, self-renewing cell that originates from the dorsal aorta and differentiates into most mesodermal tissues
Maria G. Minasi;Mara Riminucci;Luciana De Angelis;Ugo Borello.
FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome
Francesca Ariani;Giuseppe Hayek;Dalila Rondinella;Rosangela Artuso.
American Journal of Human Genetics (2008)
Tbr2 Directs Conversion of Radial Glia into Basal Precursors and Guides Neuronal Amplification by Indirect Neurogenesis in the Developing Neocortex
Alessandro Sessa;Chai an Mao;Anna Katerina Hadjantonakis;William H. Klein.
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
Francesca Mari;Sara Azimonti;Ilaria Bertani;Fabrizio Bolognese.
Human Molecular Genetics (2005)
The caudal limit of Otx2 expression positions the isthmic organizer
Vania Broccoli;Edoardo Boncinelli;Wolfgang Wurst.
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport
Fatima Ferreirinha;Angelo Quattrini;Marinella Pirozzi;Valentina Valsecchi.
Journal of Clinical Investigation (2004)
Site-specific integration and tailoring of cassette design for sustainable gene transfer.
Angelo Lombardo;Daniela Cesana;Pietro Genovese;Bruno Di Stefano.
Nature Methods (2011)
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