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American Journal of Human Genetics
|
December 19, 2012
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex
Sandra M Pasternack, Melanie Refke, Elham Paknia, et al.
Molecular Cell
|
November 30, 2021
MYCN recruits the nuclear exosome complex to RNA polymerase II to prevent transcription-replication conflicts
Dimitrios Papadopoulos, Daniel Solvie, Apoorva Baluapuri, et al.
Plos One
|
August 11, 2012
Binding of the heterogeneous ribonucleoprotein K (hnRNP K) to the Epstein-Barr virus nuclear antigen 2 (EBNA2) enhances viral LMP2A expression
Henrik Gross, Christine Hennard, Ilias Masouris, et al.
Molecular Cell
|
February 5, 2020
The Alazami Syndrome-Associated Protein LARP7 Guides U6 Small Nuclear RNA Modification and Contributes to Splicing Robustness
Daniele Hasler, Rajyalakshmi Meduri, Maciej Bąk, et al.
Nature Methods
|
August 4, 2015
ProteoPlex: stability optimization of macromolecular complexes by sparse-matrix screening of chemical space
Ashwin Chari, David Haselbach, Jan-Martin Kirves, et al.
Nature
|
May 4, 2022
Selective inhibition of miRNA processing by a herpesvirus-encoded miRNA
Thomas Hennig, Archana B Prusty, Benedikt B Kaufer, et al.
Nature Microbiology
|
December 22, 2020
The SARS-CoV-2 RNA-protein interactome in infected human cells
Nora Schmidt, Caleb A Lareau, Hasmik Keshishian, et al.
EMBO Molecular Medicine
|
November 28, 2015
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes
Beata Stepniak, Anne Kästner, Giulia Poggi, et al.
Molecular Cell
|
February 5, 2020
LARP7-Mediated U6 snRNA Modification Ensures Splicing Fidelity and Spermatogenesis in Mice
Xin Wang, Zhi-Tong Li, Yue Yan, et al.
Nature Neuroscience
|
August 6, 2013
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
Georg Stoll, Olli P H Pietiläinen, Bastian Linder, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 101) with videos related to
Sort By:
Page
of 11
American Journal of Human Genetics
|
December 19, 2012
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex
Sandra M Pasternack, Melanie Refke, Elham Paknia, et al.
Molecular Cell
|
November 30, 2021
MYCN recruits the nuclear exosome complex to RNA polymerase II to prevent transcription-replication conflicts
Dimitrios Papadopoulos, Daniel Solvie, Apoorva Baluapuri, et al.
Plos One
|
August 11, 2012
Binding of the heterogeneous ribonucleoprotein K (hnRNP K) to the Epstein-Barr virus nuclear antigen 2 (EBNA2) enhances viral LMP2A expression
Henrik Gross, Christine Hennard, Ilias Masouris, et al.
Molecular Cell
|
February 5, 2020
The Alazami Syndrome-Associated Protein LARP7 Guides U6 Small Nuclear RNA Modification and Contributes to Splicing Robustness
Daniele Hasler, Rajyalakshmi Meduri, Maciej Bąk, et al.
Nature Methods
|
August 4, 2015
ProteoPlex: stability optimization of macromolecular complexes by sparse-matrix screening of chemical space
Ashwin Chari, David Haselbach, Jan-Martin Kirves, et al.
Nature
|
May 4, 2022
Selective inhibition of miRNA processing by a herpesvirus-encoded miRNA
Thomas Hennig, Archana B Prusty, Benedikt B Kaufer, et al.
Nature Microbiology
|
December 22, 2020
The SARS-CoV-2 RNA-protein interactome in infected human cells
Nora Schmidt, Caleb A Lareau, Hasmik Keshishian, et al.
EMBO Molecular Medicine
|
November 28, 2015
Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes
Beata Stepniak, Anne Kästner, Giulia Poggi, et al.
Molecular Cell
|
February 5, 2020
LARP7-Mediated U6 snRNA Modification Ensures Splicing Fidelity and Spermatogenesis in Mice
Xin Wang, Zhi-Tong Li, Yue Yan, et al.
Nature Neuroscience
|
August 6, 2013
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
Georg Stoll, Olli P H Pietiläinen, Bastian Linder, et al.
Page
of 11