Isabelle Callebaut mainly focuses on Genetics, Cell biology, Biochemistry, Sequence analysis and Molecular biology. Her studies in Genetics integrate themes in fields like Molecular model, Melatonin and Computational biology. Her Cell biology research includes elements of Exocytosis and Tudor domain.
Her Biochemistry study deals with Biophysics intersecting with Mutation, Intracellular, Transporter and Binding protein. Her Sequence analysis course of study focuses on Eukaryotic DNA replication and DNA methylation, Transcriptional regulation and Homology. Her Molecular biology research includes themes of LIG4 syndrome, Replication protein A, DCLRE1C Gene, DCLRE1C and Complementary DNA.
The scientist’s investigation covers issues in Genetics, Cell biology, Molecular biology, Biochemistry and Gene. Genetics is represented through her Sequence analysis, Mutation, Missense mutation, DNA repair and DNA research. Her Mutation research incorporates elements of Cancer research and Cystic fibrosis transmembrane conductance regulator.
Isabelle Callebaut is interested in GTPase, which is a field of Cell biology. Her Molecular biology study combines topics in areas such as Epitope, Bovine leukemia virus, Binding domain and Complementary DNA. Biochemistry is closely attributed to Biophysics in her study.
Her main research concerns Mutation, Cell biology, Immunology, Cystic fibrosis and Cystic fibrosis transmembrane conductance regulator. Her Mutation research is within the category of Genetics. Genetics connects with themes related to Molecular biology in her study.
Her Cell biology research is multidisciplinary, relying on both Biochemistry, Major facilitator superfamily, Telomere, Transcription and DNA replication. Her work in Immunology addresses subjects such as Germline, which are connected to disciplines such as Common variable immunodeficiency. Her Cystic fibrosis transmembrane conductance regulator research is multidisciplinary, incorporating perspectives in Biophysics, Mutant, Function and ATP-binding cassette transporter.
Her primary areas of investigation include Immunology, Mutation, Cancer research, Exome sequencing and Cystic fibrosis transmembrane conductance regulator. Her work in the fields of Immunology, such as Myeloid, B cell and Common variable immunodeficiency, overlaps with other areas such as Mechanism. Her biological study spans a wide range of topics, including Molecular biology, Gene knockdown, Microcephaly and DNA repair.
Her Cancer research study combines topics from a wide range of disciplines, such as Congenital Neutropenia, Exocrine pancreatic insufficiency, Shwachman–Diamond syndrome, Unfolded protein response and Membrane protein. Her study in Exome sequencing is interdisciplinary in nature, drawing from both Fanconi anemia, Rheumatoid arthritis, Genetic predisposition and Pathology. Her Cystic fibrosis transmembrane conductance regulator research focuses on ATP-binding cassette transporter and how it connects with Drug discovery, Computational biology, In silico, Function and Cystic fibrosis.
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Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency
Despina Moshous;Isabelle Callebaut;Régina de Chasseval;Barbara Corneo.
Cell (2001)
Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
Jérôme Feldmann;Isabelle Callebaut;Graça Raposo;Stéphanie Certain.
Cell (2003)
Conserved catalytic machinery and the prediction of a common fold for several families of glycosyl hydrolases
Bernard Henrissat;Isabelle Callebaut;Sylvie Fabrega;Pierre Lehn.
Proceedings of the National Academy of Sciences of the United States of America (1995)
From BRCA1 to RAP1: a widespread BRCT module closely associated with DNA repair
Isabelle Callebaut;Jean-Paul Mornon.
FEBS Letters (1997)
Mutation in bone morphogenetic protein receptor-IB is associated with increased ovulation rate in Booroola Mérino ewes
Philippe Mulsant;Frédéric Lecerf;Stéphane Fabre;Laurent Schibler.
Proceedings of the National Academy of Sciences of the United States of America (2001)
Cloning and characterization of MN, a human tumor-associated protein with a domain homologous to carbonic anhydrase and a putative helix - Loop - helix DNA binding segment
J. Pastorek;S. Pastorekova;I. Callebaut;Jp. Mornon.
Oncogene (1994)
Deciphering protein sequence information through hydrophobic cluster analysis (HCA): current status and perspectives.
I. Callebaut;G. Labesse;P. Durand;A. Poupon.
Cellular and Molecular Life Sciences (1997)
Domain-specific Interactions of Human HP1-type Chromodomain Proteins and Inner Nuclear Membrane Protein LBR
Qian Ye;Isabelle Callebaut;Arash Pezhman;Jean-Claude Courvalin.
Journal of Biological Chemistry (1997)
MAN1, an Inner Nuclear Membrane Protein That Shares the LEM Domain with Lamina-associated Polypeptide 2 and Emerin
Feng Lin;Deborah L. Blake;Isabelle Callebaut;Ilona S. Skerjanc.
Journal of Biological Chemistry (2000)
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations
Nadia Jeremiah;Bénédicte Neven;Matteo Gentili;Isabelle Callebaut.
Journal of Clinical Investigation (2014)
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