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J Cygan

Showing results (11-20 of 24) with videos related to

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Human Genetics|August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomasKamil 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 splicingJun Cheng, Thi Yen Duong Nguyen, Kamil J Cygan, et al.
Plos Genetics|March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutationsChristy 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 transcriptsSeong Won Kim, Allison J Taggart, Claire Heintzelman, et al.
Genome Research|November 15, 2015
RNA structure replaces the need for U2AF2 in splicingChien-Ling Lin, Allison J Taggart, Kian Huat Lim, et al.
Human Mutation|July 13, 2019
Future directions for high-throughput splicing assays in precision medicineChristy L Rhine, Christopher Neil, David T Glidden, et al.
Nature Genetics|April 19, 2017
Pathogenic variants that alter protein code often disrupt splicingRachel 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 stabilityRachel 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 genomesZishan 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 illnessSean F Monaghan, Debasree Banerjee, Chun-Shiang Chung, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Human Genetics|August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomasKamil 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 splicingJun Cheng, Thi Yen Duong Nguyen, Kamil J Cygan, et al.
Plos Genetics|March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutationsChristy 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 transcriptsSeong Won Kim, Allison J Taggart, Claire Heintzelman, et al.
Genome Research|November 15, 2015
RNA structure replaces the need for U2AF2 in splicingChien-Ling Lin, Allison J Taggart, Kian Huat Lim, et al.
Human Mutation|July 13, 2019
Future directions for high-throughput splicing assays in precision medicineChristy L Rhine, Christopher Neil, David T Glidden, et al.
Nature Genetics|April 19, 2017
Pathogenic variants that alter protein code often disrupt splicingRachel 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 stabilityRachel 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 genomesZishan 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 illnessSean F Monaghan, Debasree Banerjee, Chun-Shiang Chung, et al.
Pageof 3