Member of the European Molecular Biology Organization (EMBO)
Maria Carmo-Fonseca mainly investigates Molecular biology, Cell biology, RNA splicing, snRNP and RNA. Her research in Molecular biology intersects with topics in Gene expression, Ribonucleoprotein, Nucleolus, Transcription factories and Transcription. Her studies in Cell biology integrate themes in fields like Heterogeneous ribonucleoprotein particle, Nuclear protein and Biochemistry.
Her RNA splicing study is concerned with the field of Genetics as a whole. Her biological study spans a wide range of topics, including Splicing Factor U2AF and Coilin. Her work carried out in the field of RNA brings together such families of science as Chromatin, Binding domain, Membrane and Messenger RNA.
Maria Carmo-Fonseca spends much of her time researching Cell biology, RNA splicing, Molecular biology, Genetics and RNA. She usually deals with Cell biology and limits it to topics linked to Spliceosome and Precursor mRNA. The RNA splicing study combines topics in areas such as Alternative splicing and Intron.
As a part of the same scientific study, Maria Carmo-Fonseca usually deals with the Molecular biology, concentrating on Nucleolus and frequently concerns with Small nucleolar RNA. Her research investigates the connection between RNA and topics such as Transcription that intersect with issues in Gene expression. Her study in Cell nucleus is interdisciplinary in nature, drawing from both Cajal body and Nuclear pore.
Her primary areas of investigation include Cell biology, Induced pluripotent stem cell, RNA splicing, RNA and Transcription. Her Cell biology study integrates concerns from other disciplines, such as Respiratory chain, Cell type and Smaug. RNA splicing is a subfield of Gene that Maria Carmo-Fonseca tackles.
The RNA study combines topics in areas such as Messenger RNA, Computational biology and Intron. The concepts of her Transcription study are interwoven with issues in Molecular biology and Genome instability. Her Spliceosome study integrates concerns from other disciplines, such as Cytoplasm, Exon junction complex, snRNP, MRNA transport and Small nuclear ribonucleoprotein.
Maria Carmo-Fonseca focuses on Cell biology, RNA splicing, Stem cell, Induced pluripotent stem cell and Exon. Her work on Cell biology is being expanded to include thematically relevant topics such as Nonsense-mediated decay. Maria Carmo-Fonseca interconnects Polyadenylation and Intron in the investigation of issues within RNA splicing.
Her Exon study introduces a deeper knowledge of Genetics. Her work on Chromatin and Transcription as part of general Gene study is frequently linked to RNA polymerase II, bridging the gap between disciplines. Maria Carmo-Fonseca performs multidisciplinary studies into RNA polymerase II and Molecular biology in her work.
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.
Retinoic acid regulates aberrant nuclear localization of PML-RARα in acute promyelocytic leukemia cells
Karsten Weis;Sophie Rambaud;Catherine Lavau;Joop Jansen.
Cell (1994)
To be or not to be in the nucleolus
Maria Carmo-Fonseca;Luís Mendes-Soares;Isabel Campos.
Nature Cell Biology (2000)
Molecular mechanisms involved in cisplatin cytotoxicity.
P. Jordan;M. Carmo-Fonseca.
Cellular and Molecular Life Sciences (2000)
Transcription-dependent colocalization of the U1, U2, U4/U6, and U5 snRNPs in coiled bodies
M Carmo-Fonseca;R Pepperkok;MT Carvalho;AI Lamond.
Journal of Cell Biology (1992)
Mammalian NET-Seq Reveals Genome-wide Nascent Transcription Coupled to RNA Processing
Takayuki Nojima;Tomás Gomes;Ana Rita Fialho Grosso;Hiroshi Kimura.
Cell (2015)
The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates.
A. Bachi;I. C. Braun;J. P. Rodrigues;N. Panté.
RNA (2000)
The small nucleolar RNP protein NOP1 (fibrillarin) is required for pre-rRNA processing in yeast.
D. Tollervey;H. Lehtonen;M. Carmo-Fonseca;E. C. Hurt.
The EMBO Journal (1991)
Targeting of adenovirus E1A and E4-ORF3 proteins to nuclear matrix-associated PML bodies.
T Carvalho;J S Seeler;K Ohman;P Jordan.
Journal of Cell Biology (1995)
Dbp5, a DEAD-box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p.
Christel Schmitt;Cayetano von Kobbe;Angela Bachi;Nelly Panté.
The EMBO Journal (1999)
Deep intronic mutations and human disease.
Rita Vaz-Drago;Noélia Custódio;Maria Carmo-Fonseca.
Human Genetics (2017)
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