P. Shepard

发表

Conserved RNA secondary structures promote alternative splicing.

Peter J. Shepard, P. Shepard, K. J. Hertel, 2008, RNA.

Comparison of base-line and chemical-induced transcriptomic responses in HepaRG and RPTEC/TERT1 cells using TempO-Seq

Paul Jennings, Alice Limonciel, Bob van de Water, 2018, Archives of Toxicology.

Complex and dynamic landscape of RNA polyadenylation revealed by PAS-Seq.

Peter J. Shepard, P. Shepard, K. J. Hertel, 2011, RNA.

The SR protein family

Peter J. Shepard, P. Shepard, K. J. Hertel, 2009, Genome Biology.

Development of a Zebrafish S1500+ Sentinel Gene Set for High-Throughput Transcriptomics

Peter J. Shepard, P. Shepard, Ruchir R. Shah, 2019, Zebrafish.

Aberrant DNA Methylation in Human iPSCs Associates with MYC-Binding Motifs in a Clone-Specific Manner Independent of Genetics.

Peter J. Shepard, K. Frazer, K. Diffenderfer, 2017, Cell stem cell.

Competing Upstream 5′ Splice Sites Enhance the Rate of Proximal Splicing

Peter J. Shepard, P. Shepard, William F. Mueller, 2010, Molecular and Cellular Biology.

sites enhance the rate of proximal splicing.

Peter J. Shepard, P. Shepard, W. Müller, 2010 .

Conserved RNA secondary structures promote alternative splicing data

P. Shepard, K. Hertel, 2022 .

Consanguinity and rare mutations outside of MCCC genes underlie nonspecific phenotypes of MCCD

Peter J. Shepard, K. Frazer, M. Baumgartner, 2014, Genetics in Medicine.

A trichostatin A expression signature identified by TempO-Seq targeted whole transcriptome profiling

Joanne M Yeakley, Peter J. Shepard, P. Shepard, 2017, PloS one.

Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development

Christopher M. DeBoever, Christian L. Barrett, Emanuela M. Ghia, 2015, Blood Cancer Journal.

Transcriptome Sequencing Reveals Potential Mechanism of Cryptic 3’ Splice Site Selection in SF3B1-mutated Cancers

Dennis Carson, Christopher M. DeBoever, Kristen Jepsen, 2015, PLoS Comput. Biol..

Comparison of base-line and chemical-induced transcriptomic responses in HepaRG and RPTEC/TERT1 cells using TempO-Seq

P. Shepard, M. Vinken, B. Seligmann, 2018, Archives of Toxicology.

Extraction-free whole transcriptome gene expression analysis of FFPE sections and histology-directed subareas of tissue

Peter J. Shepard, P. Shepard, B. Seligmann, 2018, bioRxiv.

Efficient internal exon recognition depends on near equal contributions from the 3′ and 5′ splice sites

Anke Busch, Klemens J. Hertel, Peter J. Shepard, 2011, Nucleic acids research.

The tubby family proteins

Peter J. Shepard, P. Shepard, P. Jackson, 2011, Genome Biology.

Use of a chemically modified antisense oligonucleotide library to identify and validate Eg5 (kinesin-like 1) as a target for antineoplastic drug development.

Peter J. Shepard, P. Shepard, R. Glazer, 2006, Cancer research.

Genetic ancestry of participants in the National Children’s Study

Peter J. Shepard, K. Frazer, P. Shepard, 2014, Genome Biology.

A chemical–biological similarity-based grouping of complex substances as a prototype approach for evaluating chemical alternatives† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6gc01147k Click here for additional data file.

Fred A. Wright, Ivan Rusyn, David M. Reif, 2016, Green chemistry : an international journal and green chemistry resource : GC.

Genetic ancestry of participants in the National Children’s Study

K. Frazer, P. Shepard, Erin N. Smith, 2014, Genome Biology.