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Molecular Cell
|
February 4, 2010
The role of ABCE1 in eukaryotic posttermination ribosomal recycling
Andrey V Pisarev, Maxim A Skabkin, Vera P Pisareva, et al.
Molecular Cell
|
June 10, 2008
Distinct eRF3 requirements suggest alternate eRF1 conformations mediate peptide release during eukaryotic translation termination
Hua Fan-Minogue, Ming Du, Andrey V Pisarev, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Genes & Development
|
May 7, 2009
Structural insights into eRF3 and stop codon recognition by eRF1
Zhihong Cheng, Kazuki Saito, Andrey V Pisarev, et al.
The Journal of Clinical Investigation
|
August 12, 2025
Platelet-specific SLFN14 deletion causes macrothrombocytopenia and platelet dysfunction through dysregulated megakaryocyte and platelet gene expression
Rachel J Stapley, Xenia Sawkulycz, Gabriel Hm Da Mota Araujo, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Molecular Cell
|
February 4, 2010
The role of ABCE1 in eukaryotic posttermination ribosomal recycling
Andrey V Pisarev, Maxim A Skabkin, Vera P Pisareva, et al.
Molecular Cell
|
June 10, 2008
Distinct eRF3 requirements suggest alternate eRF1 conformations mediate peptide release during eukaryotic translation termination
Hua Fan-Minogue, Ming Du, Andrey V Pisarev, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Genes & Development
|
May 7, 2009
Structural insights into eRF3 and stop codon recognition by eRF1
Zhihong Cheng, Kazuki Saito, Andrey V Pisarev, et al.
The Journal of Clinical Investigation
|
August 12, 2025
Platelet-specific SLFN14 deletion causes macrothrombocytopenia and platelet dysfunction through dysregulated megakaryocyte and platelet gene expression
Rachel J Stapley, Xenia Sawkulycz, Gabriel Hm Da Mota Araujo, et al.
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of 3