Zobrazeno 1 - 10
of 38
pro vyhledávání: '"RNA-binding proteins (RBP)"'
Autor:
Wandi S. Zhu, Adam J. Litterman, Harshaan S. Sekhon, Robin Kageyama, Maya M. Arce, Kimberly E. Taylor, Wenxue Zhao, Lindsey A. Criswell, Noah Zaitlen, David J. Erle, K. Mark Ansel
Publikováno v:
Genome Biology, Vol 24, Iss 1, Pp 1-30 (2023)
Abstract GCLiPP is a global RNA interactome capture method that detects RNA-binding protein (RBP) occupancy transcriptome-wide. GCLiPP maps RBP-occupied sites at a higher resolution than phase separation-based techniques. GCLiPP sequence tags corresp
Externí odkaz:
https://doaj.org/article/d9d0f867d61c4eb2b44c5c8f804f28be
Autor:
Nicolas Curdy, Olivia Lanvin, Sarah Cadot, Camille Laurent, Jean-Jacques Fournié, Don-Marc Franchini
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2021)
Immune cell activation triggers transcriptional and translational programs eliciting cellular processes, such as differentiation or proliferation, essential for an efficient immune response. These dynamic processes require an intricate orchestration
Externí odkaz:
https://doaj.org/article/6eed090c3d4943ee9d0f3e5e29acd06a
Akademický článek
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Autor:
César Augusto Ramírez, Julián Camilo Casas, María Isabel Ospina, José María Requena, Concepción J. Puerta
Publikováno v:
Universitas Scientiarum, Vol 23, Iss 2, Pp 267-290 (2018)
In trypanosomatids, gene expression is mainly regulated at posttranscriptional level, through mechanisms based on the interaction between RNA Binding Proteins [RBPs] and motifs present in the untranslated regions [UTRs] of them RNAs, which altogether
Externí odkaz:
https://doaj.org/article/e6d6af8dd14d483abb6939d774822164
Autor:
Subha Saha, Krushna Chandra Murmu, Mayukh Biswas, Sohini Chakraborty, Jhinuk Basu, Swati Madhulika, Srinivasa Prasad Kolapalli, Santosh Chauhan, Amitava Sengupta, Punit Prasad
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Acute myeloid leukemia (AML) is a common and aggressive hematological malignancy. Acquisition of heterogeneous genetic aberrations and epigenetic dysregulation lead to the transformation of hematopoietic stem cells (HSC) into leukemic stem cells (LSC
Externí odkaz:
https://doaj.org/article/30803bc55e61450d97dcef14d86a8355
Autor:
Curdy, Nicolas, Lanvin, Olivia, Cadot, Sarah, Laurent, Camille, Fournié, Jean-Jacques, Franchini, Don-Marc
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, 2021, 8, ⟨10.3389/fcell.2020.611185⟩
Frontiers in Cell and Developmental Biology, Frontiers media, 2021, 8, ⟨10.3389/fcell.2020.611185⟩
Frontiers in Cell and Developmental Biology, 2021, 8, ⟨10.3389/fcell.2020.611185⟩
Frontiers in Cell and Developmental Biology, Frontiers media, 2021, 8, ⟨10.3389/fcell.2020.611185⟩
International audience; Immune cell activation triggers transcriptional and translational programs eliciting cellular processes, such as differentiation or proliferation, essential for an efficient immune response. These dynamic processes require an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::dbb0d1e55f0bc38f07b57db31b4880a6
https://hal.science/hal-03365427
https://hal.science/hal-03365427
Autor:
Katja Lohmann, Sokhna Haissatou Diaw
Publikováno v:
Brain
A TAF1 mutation that lowers levels of the transcript causes X-linked dystonia parkinsonism. Hernández et al. show reduced levels of TAF1, and of the RNA-binding protein SREK1 which targets TAF1, also in Huntington’s disease. SREK1 overexpression r
Autor:
Manuel Sánchez-Martín, Belén Pintado, José J. Lucas, Maria Jose Perez-Alvarez, Ramón García-Escudero, Verónica Domínguez, Ivó H. Hernández, María Santos-Galindo, Jorge Rubén Cabrera
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The Author(s) (2020).
Huntington’s disease and X-linked dystonia parkinsonism are two monogenic basal ganglia model diseases. Huntington’s disease is caused by a polyglutamine-encoding CAG repeat expansion in the Huntingtin (HTT) gene leadin
Huntington’s disease and X-linked dystonia parkinsonism are two monogenic basal ganglia model diseases. Huntington’s disease is caused by a polyglutamine-encoding CAG repeat expansion in the Huntingtin (HTT) gene leadin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c9d15d5e10c30c8d231053363eaed7
http://hdl.handle.net/10261/229569
http://hdl.handle.net/10261/229569
Autor:
Julián Camilo Casas, Elizabeth Ruiz, Concepción J. Puerta, César A. Ramírez, María Isabel Ospina, Jose M. Requena
Publikováno v:
Universitas Scientiarum, Vol 23, Iss 2, Pp 267-290 (2018)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
In trypanosomatids,geneexpressionismainlyregulated at posttranscriptional level,throughmechanisms based on the interaction between RNA Binding Proteins [RBPs] and motifs present in the untranslated regions [UTRs] of Them RNAs,whichaltogetherformribon
Autor:
Sohini Chakraborty, Krushna Chandra Murmu, Punit Prasad, Santosh Chauhan, Subha Saha, Mayukh Biswas, Jhinuk Basu, Srinivasa Prasad Kolapalli, Amitava Sengupta, Swati Madhulika
Publikováno v:
Frontiers in Oncology
Frontiers in Oncology, Vol 9 (2019)
Frontiers in Oncology, Vol 9 (2019)
Acute myeloid leukemia (AML) is a common and aggressive hematological malignancy. Acquisition of heterogeneous genetic aberrations and epigenetic dysregulation lead to the transformation of hematopoietic stem cells (HSC) into leukemic stem cells (LSC