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Human Genetics
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August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomas
Kamil J Cygan, Rachel Soemedi, Christy L Rhine, et al.
Genome Biology
|
March 3, 2019
MMSplice: modular modeling improves the predictions of genetic variant effects on splicing
Jun Cheng, Thi Yen Duong Nguyen, Kamil J Cygan, et al.
Plos Genetics
|
March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutations
Christy L Rhine, Kamil J Cygan, Rachel Soemedi, et al.
Nucleic Acids Research
|
September 22, 2017
Widespread intra-dependencies in the removal of introns from human transcripts
Seong Won Kim, Allison J Taggart, Claire Heintzelman, et al.
Genome Research
|
November 15, 2015
RNA structure replaces the need for U2AF2 in splicing
Chien-Ling Lin, Allison J Taggart, Kian Huat Lim, et al.
Human Mutation
|
July 13, 2019
Future directions for high-throughput splicing assays in precision medicine
Christy L Rhine, Christopher Neil, David T Glidden, et al.
Nature Genetics
|
April 19, 2017
Pathogenic variants that alter protein code often disrupt splicing
Rachel Soemedi, Kamil J Cygan, Christy L Rhine, et al.
Methods (San Diego, Calif.)
|
June 10, 2017
The effects of structure on pre-mRNA processing and stability
Rachel Soemedi, Kamil J Cygan, Christy L Rhine, et al.
Genome Medicine
|
September 10, 2021
Non-cancer-related pathogenic germline variants and expression consequences in ten-thousand cancer genomes
Zishan Wang, Xiao Fan, Yufeng Shen, et al.
Molecular Medicine (Cambridge, Mass.)
|
August 24, 2018
Changes in the process of alternative RNA splicing results in soluble B and T lymphocyte attenuator with biological and clinical implications in critical illness
Sean F Monaghan, Debasree Banerjee, Chun-Shiang Chung, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Human Genetics
|
August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomas
Kamil J Cygan, Rachel Soemedi, Christy L Rhine, et al.
Genome Biology
|
March 3, 2019
MMSplice: modular modeling improves the predictions of genetic variant effects on splicing
Jun Cheng, Thi Yen Duong Nguyen, Kamil J Cygan, et al.
Plos Genetics
|
March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutations
Christy L Rhine, Kamil J Cygan, Rachel Soemedi, et al.
Nucleic Acids Research
|
September 22, 2017
Widespread intra-dependencies in the removal of introns from human transcripts
Seong Won Kim, Allison J Taggart, Claire Heintzelman, et al.
Genome Research
|
November 15, 2015
RNA structure replaces the need for U2AF2 in splicing
Chien-Ling Lin, Allison J Taggart, Kian Huat Lim, et al.
Human Mutation
|
July 13, 2019
Future directions for high-throughput splicing assays in precision medicine
Christy L Rhine, Christopher Neil, David T Glidden, et al.
Nature Genetics
|
April 19, 2017
Pathogenic variants that alter protein code often disrupt splicing
Rachel Soemedi, Kamil J Cygan, Christy L Rhine, et al.
Methods (San Diego, Calif.)
|
June 10, 2017
The effects of structure on pre-mRNA processing and stability
Rachel Soemedi, Kamil J Cygan, Christy L Rhine, et al.
Genome Medicine
|
September 10, 2021
Non-cancer-related pathogenic germline variants and expression consequences in ten-thousand cancer genomes
Zishan Wang, Xiao Fan, Yufeng Shen, et al.
Molecular Medicine (Cambridge, Mass.)
|
August 24, 2018
Changes in the process of alternative RNA splicing results in soluble B and T lymphocyte attenuator with biological and clinical implications in critical illness
Sean F Monaghan, Debasree Banerjee, Chun-Shiang Chung, et al.
Page
of 3