T. Parks

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A second proteinase encoded by a plant potyvirus genome.

J. Carrington, W. Dougherty, S. M. Cary, 1989, The EMBO journal.

Composite plants for a composite plant: an efficient protocol for root studies in the sunflower using composite plants approach

T. Parks, Y. Yordanov, 2020, Plant Cell, Tissue and Organ Culture (PCTOC).

Composite plants for a composite plant: an efficient protocol for root studies in the sunflower using composite plants approach

T. Parks, Y. Yordanov, 2019, bioRxiv.

RNA-mediated virus resistance in transgenic plants: exploitation of a cellular pathway possibly involved in RNA degradation.

H. A. Smith, W. Dougherty, T. Parks, 1994, Molecular plant-microbe interactions : MPMI.

Characterization of the catalytic residues of the tobacco etch virus 49-kDa proteinase.

R. Fletterick, J. Bazan, W. Dougherty, 1989, Virology.

Plant Defense Responses of Host Plants with Determinate Nodules Induced by EPS-Defective e x o B Mutants of Bradyrhizobium j a

H. A. Smith, W., T. Parks, 2011 .

Application of TEV Protease in Protein Production.

S. A. Johnston, S. Johnston, W. Dougherty, 1998, Methods in molecular medicine.

Molecular genetic analyses of the soybean mosaic virus NIa proteinase.

H. A. Smith, S. Ghabrial, W. Dougherty, 1990, The Journal of general virology.

Expression and purification of a recombinant tobacco etch virus NIa proteinase: biochemical analyses of the full-length and a naturally occurring truncated proteinase form.

W. Dougherty, T. Parks, D. Arp, 1995, Virology.

Vectors for cell-free expression and mutagenesis of protein-coding sequences.

J. Carrington, W. Dougherty, S. M. Cary, 1987, Nucleic acids research.

An Efficient Protocol for Root Studies in the Common Sunflower Using Composite Plants

T. Parks, 2018 .

Identification of an aspartate transfer RNA gene in maize mitochondrial DNA

W. Dougherty, T. Parks, C. S. Levings, 2004, Current Genetics.

Identification of two methionine transfer RNA genes in the maize mitochondrial genome.

W. Dougherty, T. Parks, C. S. Levings, 1984, Plant physiology.

Feed-back regulation of gibberellin biosynthesis and gene expression in Pisum sativum L.

P. Hedden, T. Lange, W. Dougherty, 2004, Planta.

Transgenic plant virus resistance mediated by untranslatable sense RNAs: expression, regulation, and fate of nonessential RNAs.

H. A. Smith, W. Dougherty, T. Parks, 1994, The Plant cell.

Biochemical analysis of the capsid protein gene and capsid protein of tobacco etch virus: N-terminal amino acids are located on the virion's surface.

R. Johnston, W. Dougherty, T. Parks, 1985, Virology.

Expression of the potyvirus genome: the role of proteolytic processing.

H. A. Smith, W. Dougherty, T. Parks, 1990 .

Molecular genetic and biochemical evidence for the involvement of the heptapeptide cleavage sequence in determining the reaction profile at two tobacco etch virus cleavage sites in cell-free assays.

W. Dougherty, T. Parks, 1989, Virology.

Molecular genetic analysis of a plant virus polyprotein cleavage site: a model.

W. Dougherty, S. M. Cary, T. Parks, 1989, Virology.

Transgenes and gene suppression: telling us something new?

W. Dougherty, T. Parks, W G Dougherty, 1995, Current opinion in cell biology.

Cleavage profiles of tobacco etch virus (TEV)-derived substrates mediated by precursor and processed forms of the TEV NIa proteinase.

H. A. Smith, W. Dougherty, T. Parks, 1992, The Journal of general virology.

Biochemical and mutational analysis of a plant virus polyprotein cleavage site.

J. Carrington, W. Dougherty, S. M. Cary, 1988, The EMBO journal.

Translation Start Sequences Affect the Efficiency of Silencing of Agrobacterium tumefaciens T-DNA Oncogenes1

Josh T. Cuperus, C. Whistler, T. Parks, 2003, Plant Physiology.

Post-translational processing of the tobacco etch virus 49-kDa small nuclear inclusion polyprotein: identification of an internal cleavage site and delimitation of VPg and proteinase domains.

W. Dougherty, T. Parks, 1991, Virology.

Release of proteins and peptides from fusion proteins using a recombinant plant virus proteinase.

S. A. Johnston, S. Johnston, W. Dougherty, 1994, Analytical biochemistry.

Substrate recognition by the NIa proteinase of two potyviruses involves multiple domains: characterization using genetically engineered hybrid proteinase molecules.

W. Dougherty, T. Parks, 1991, Virology.

Autocatalytic activity of the tobacco etch virus NIa proteinase in viral and foreign protein sequences.

M. Bevan, W. Dougherty, T. Parks, 1992, The Journal of general virology.

Genetic and biochemical dissection of transgenic RNA-mediated virus resistance.

W. Dougherty, T. Parks, W G Dougherty, 1996, The Plant cell.

Isolation of the genomic clone for pathogenesis-related protein 1a from Nicotiana tabacum cv. Xanthi-nc

J. Ryals, T. Parks, J. Metraux, 1988, Plant Molecular Biology.

Nucleotide sequence at the 3' terminus of pepper mottle virus genomic RNA: evidence for an alternative mode of potyvirus capsid protein gene organization.

R. Johnston, W. Dougherty, T. Parks, 1985, Virology.