Search research articles
Contact Us
Filters
Showing results (31-40 of 63) with videos related to
Page
of 7
Sort By:
Nature
|
February 4, 2021
Author Correction: Transcript expression-aware annotation improves rare variant interpretation
Beryl B Cummings, Konrad J Karczewski, Jack A Kosmicki, et al.
Nature Communications
|
August 18, 2016
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq)
Julien Lagarde, Barbara Uszczynska-Ratajczak, Javier Santoyo-Lopez, et al.
Journal of Proteome Research
|
November 8, 2024
The 2024 Report on the Human Proteome from the HUPO Human Proteome Project
Gilbert S Omenn, Sandra Orchard, Lydie Lane, et al.
Molecular Cell
|
February 22, 2023
Evolutionary origins and interactomes of human, young microproteins and small peptides translated from short open reading frames
Clara-L Sandmann, Jana F Schulz, Jorge Ruiz-Orera, et al.
Journal of Proteome Research
|
January 6, 2026
The 2025 Report on the Human Proteome from the HUPO Human Proteome Project
Eric W Deutsch, Cecilia Lindskog, Bogdan Budnik, et al.
Haematologica
|
July 25, 2020
Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas
Luigi Grassi, Osagie G Izuogu, Natasha A N Jorge, et al.
Acta Neuropathologica
|
May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
Katri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
Plos One
|
January 13, 2012
Evidence for transcript networks composed of chimeric RNAs in human cells
Sarah Djebali, Julien Lagarde, Philipp Kapranov, et al.
NPJ Genomic Medicine
|
December 10, 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>
Charles A Steward, Jolien Roovers, Marie-Marthe Suner, et al.
Nucleic Acids Research
|
November 11, 2017
Consensus coding sequence (CCDS) database: a standardized set of human and mouse protein-coding regions supported by expert curation
Shashikant Pujar, Nuala A O'Leary, Catherine M Farrell, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Nature
|
February 4, 2021
Author Correction: Transcript expression-aware annotation improves rare variant interpretation
Beryl B Cummings, Konrad J Karczewski, Jack A Kosmicki, et al.
Nature Communications
|
August 18, 2016
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq)
Julien Lagarde, Barbara Uszczynska-Ratajczak, Javier Santoyo-Lopez, et al.
Journal of Proteome Research
|
November 8, 2024
The 2024 Report on the Human Proteome from the HUPO Human Proteome Project
Gilbert S Omenn, Sandra Orchard, Lydie Lane, et al.
Molecular Cell
|
February 22, 2023
Evolutionary origins and interactomes of human, young microproteins and small peptides translated from short open reading frames
Clara-L Sandmann, Jana F Schulz, Jorge Ruiz-Orera, et al.
Journal of Proteome Research
|
January 6, 2026
The 2025 Report on the Human Proteome from the HUPO Human Proteome Project
Eric W Deutsch, Cecilia Lindskog, Bogdan Budnik, et al.
Haematologica
|
July 25, 2020
Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas
Luigi Grassi, Osagie G Izuogu, Natasha A N Jorge, et al.
Acta Neuropathologica
|
May 13, 2022
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility
Katri Silvennoinen, Kinga Gawel, Despina Tsortouktzidis, et al.
Plos One
|
January 13, 2012
Evidence for transcript networks composed of chimeric RNAs in human cells
Sarah Djebali, Julien Lagarde, Philipp Kapranov, et al.
NPJ Genomic Medicine
|
December 10, 2019
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in <i>SCN1A</i>
Charles A Steward, Jolien Roovers, Marie-Marthe Suner, et al.
Nucleic Acids Research
|
November 11, 2017
Consensus coding sequence (CCDS) database: a standardized set of human and mouse protein-coding regions supported by expert curation
Shashikant Pujar, Nuala A O'Leary, Catherine M Farrell, et al.
Page
of 7