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Anke Busch

Showing results (41-50 of 47) with videos related to

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Nucleic Acids Research|January 18, 2023
Depletion of the RNA-binding protein PURA triggers changes in posttranscriptional gene regulation and loss of P-bodiesLena Molitor, Melina Klostermann, Sabrina Bacher, et al.
Nature Communications|September 22, 2022
High-throughput mutagenesis identifies mutations and RNA-binding proteins controlling CD19 splicing and CART-19 therapy resistanceMariela Cortés-López, Laura Schulz, Mihaela Enculescu, et al.
Journal of Medical Genetics|January 17, 2014
A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndromeTaraneh Esmailpour, Hamidreza Riazifar, Linan Liu, et al.
Nucleic Acids Research|May 23, 2018
Freiburg RNA tools: a central online resource for RNA-focused research and teachingMartin Raden, Syed M Ali, Omer S Alkhnbashi, et al.
The EMBO Journal|January 11, 2021
Ythdf is a N6-methyladenosine reader that modulates Fmr1 target mRNA selection and restricts axonal growth in DrosophilaLina Worpenberg, Chiara Paolantoni, Sara Longhi, et al.
Molecular Cell|July 28, 2023
FUBP1 is a general splicing factor facilitating 3' splice site recognition and splicing of long intronsStefanie Ebersberger, Clara Hipp, Miriam M Mulorz, et al.
Plos Genetics|March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndromeMariella Simon, Elodie M Richard, Xinjian Wang, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Nucleic Acids Research|January 18, 2023
Depletion of the RNA-binding protein PURA triggers changes in posttranscriptional gene regulation and loss of P-bodiesLena Molitor, Melina Klostermann, Sabrina Bacher, et al.
Nature Communications|September 22, 2022
High-throughput mutagenesis identifies mutations and RNA-binding proteins controlling CD19 splicing and CART-19 therapy resistanceMariela Cortés-López, Laura Schulz, Mihaela Enculescu, et al.
Journal of Medical Genetics|January 17, 2014
A splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndromeTaraneh Esmailpour, Hamidreza Riazifar, Linan Liu, et al.
Nucleic Acids Research|May 23, 2018
Freiburg RNA tools: a central online resource for RNA-focused research and teachingMartin Raden, Syed M Ali, Omer S Alkhnbashi, et al.
The EMBO Journal|January 11, 2021
Ythdf is a N6-methyladenosine reader that modulates Fmr1 target mRNA selection and restricts axonal growth in DrosophilaLina Worpenberg, Chiara Paolantoni, Sara Longhi, et al.
Molecular Cell|July 28, 2023
FUBP1 is a general splicing factor facilitating 3' splice site recognition and splicing of long intronsStefanie Ebersberger, Clara Hipp, Miriam M Mulorz, et al.
Plos Genetics|March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndromeMariella Simon, Elodie M Richard, Xinjian Wang, et al.
Pageof 5