Genetics, Doublecortin, Lissencephaly, Microtubule and Gene are her primary areas of study. Her study connects Molecular biology and Genetics. In her study, Human brain and Neuron is strongly linked to Cell biology, which falls under the umbrella field of Doublecortin.
Her research in Lissencephaly tackles topics such as Cytoskeleton which are related to areas like Neuroblast differentiation, Corticogenesis, Soma and Transfection. Her Microtubule research incorporates themes from TUBG1, Germline, Microcephaly and Cortical dysplasia. Her research investigates the connection between Microtubule-associated protein and topics such as Neuroscience that intersect with issues in OMIM : Online Mendelian Inheritance in Man.
Her scientific interests lie mostly in Genetics, Neuroscience, Doublecortin, Gene and Cell biology. Her is doing research in Missense mutation, Contig, Gene mapping, X chromosome and Exon, both of which are found in Genetics. Her Doublecortin research is multidisciplinary, incorporating perspectives in Microtubule-associated protein, Knockout mouse, Lissencephaly and Anatomy.
Her research in Lissencephaly focuses on subjects like Phenotype, which are connected to Wild type. When carried out as part of a general Gene research project, her work on Homology and Gene expression is frequently linked to work in PHEX and NKG2, therefore connecting diverse disciplines of study. In the field of Cell biology, her study on Microtubule and Neural stem cell overlaps with subjects such as PAX6.
Her main research concerns Cell biology, Cerebral cortex, Microtubule, Neuroscience and Progenitor cell. Her Cell biology study combines topics in areas such as Golgi apparatus and Mutant. Her Cerebral cortex research integrates issues from Heterozygote advantage, Corticogenesis, Corpus callosum and Heterotopia.
A large part of her Microtubule studies is devoted to Tubulin. Her work carried out in the field of Neuroscience brings together such families of science as Regulation of gene expression, Clinical phenotype and Disease. Her research on Progenitor cell also deals with topics like
Her primary scientific interests are in Progenitor cell, Cell cycle, Cell biology, Cerebral cortex and Microtubule end. Her Progenitor cell study frequently draws connections to other fields, such as Cell growth. Many of her research projects under Cell biology are closely connected to PAX6 with PAX6, tying the diverse disciplines of science together.
Her Cerebral cortex study improves the overall literature in Neuroscience. Microtubule end is connected with Neurogenesis, Pachygyria, Microcephaly, Ciliogenesis and Interneuron migration in her study.
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.
The DNA sequence of human chromosome 21
M. Hattori;A. Fujiyama;T. D. Taylor;H. Watanabe.
The DNA sequence of the human X chromosome
Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer.
Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons.
Fiona Francis;Annette Koulakoff;Dominique Boucher;Philippe Chafey.
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
Johanna Aaltonen;Petra Björses;Jaakko Perheentupa;Nina Horelli–Kuitunen.
Nature Genetics (1997)
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
F. Francis;S. Hennig;B. Korn;R. Reinhardt.
Nature Genetics (1995)
Mutations in TUBG1 , DYNC1H1 , KIF5C and KIF2A cause malformations of cortical development and microcephaly
Karine Poirier;Nicolas Lebrun;Nicolas Lebrun;Loic Broix;Loic Broix;Guoling Tian.
Nature Genetics (2013)
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.
Jane E. Hewitt;Jane E. Hewitt;Robert Lyle;Lorraine N. Clark;Elizabeth M. Valleley.
Human Molecular Genetics (1994)
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
Thierry Bienvenu;Karine Poirier;Gaelle Friocourt;Nadia Bahi.
Human Molecular Genetics (2002)
Genetics and pathophysiology of mental retardation.
Jamel Chelly;Malik Khelfaoui;Fiona Francis;Beldjord Chérif.
European Journal of Human Genetics (2006)
Doublecortin, a Stabilizer of Microtubules
David Horesh;Tamar Sapir;Fiona Francis;Sharon Grayer Wolf.
Human Molecular Genetics (1999)
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