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You searched for +publisher:"The Ohio State University" +contributor:("Pei, Dehua"). Showing records 1 – 22 of 22 total matches.

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The Ohio State University

1. Zhang, Yanyan. Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design.

Degree: PhD, Biochemistry, 2009, The Ohio State University

  Src homology-2 (SH2) domains are small modular domains that recognize phosphotyrosine (pY)-containing proteins and promote the formation of protein complexes, thus playing an essential… (more)

Subjects/Keywords: Biology; Biomedical Research; Biophysics; Chemistry; SH2 domain; binding specificity; binding kinetics; cyclic peptidyl inhibitor; structure; SHIP2 SH2; Grb2 SH2; X-ray; NMR; SHP2 NSH2

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APA (6th Edition):

Zhang, Y. (2009). Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1259766230

Chicago Manual of Style (16th Edition):

Zhang, Yanyan. “Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design.” 2009. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1259766230.

MLA Handbook (7th Edition):

Zhang, Yanyan. “Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design.” 2009. Web. 17 Jun 2019.

Vancouver:

Zhang Y. Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259766230.

Council of Science Editors:

Zhang Y. Investigation of SH2 Domains: Ligand Binding, Structure and Inhibitor Design. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259766230


The Ohio State University

2. Thakkar, Amit. Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries.

Degree: PhD, Chemistry, 2009, The Ohio State University

  Combinatorial chemistry provides a powerful method for the rapid identification of high affinity ligands of macromolecular targets. In this work, we recognize three principles… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Chemistry; Combinatorial Chemistry; cyclization efficiency; peptoids; PED/MS; sequencing; cyclic peptoids

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APA (6th Edition):

Thakkar, A. (2009). Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1259775104

Chicago Manual of Style (16th Edition):

Thakkar, Amit. “Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries.” 2009. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1259775104.

MLA Handbook (7th Edition):

Thakkar, Amit. “Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries.” 2009. Web. 17 Jun 2019.

Vancouver:

Thakkar A. Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259775104.

Council of Science Editors:

Thakkar A. Combinatorial Synthesis, Sequencing, and Biological Applications of Peptide and Peptidomimetic Libraries. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259775104


The Ohio State University

3. Joo, Sang Hoon. Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries.

Degree: PhD, Chemistry, 2007, The Ohio State University

 One-bead one-compound (OBOC) peptide libraries have been useful tools in the biomedical sciences. However, OBOC peptide libraries usually display the N-termini of peptides on the… (more)

Subjects/Keywords: Chemistry, Biochemistry; One-bead One-Compound (OBOC); partial Edman degradation; split-and-pool synthesis; cyclic peptides; Free C-terminal; peptide library; PDZ domain

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APA (6th Edition):

Joo, S. H. (2007). Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1195561420

Chicago Manual of Style (16th Edition):

Joo, Sang Hoon. “Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries.” 2007. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1195561420.

MLA Handbook (7th Edition):

Joo, Sang Hoon. “Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries.” 2007. Web. 17 Jun 2019.

Vancouver:

Joo SH. Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1195561420.

Council of Science Editors:

Joo SH. Synthesis and screening of support-bound combinatorial cyclic peptide and free C-terminal peptide libraries. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1195561420


The Ohio State University

4. McMullen, Justin G. In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores.

Degree: MS, Chemistry, 2009, The Ohio State University

 Quorum sensing (QS) is the process by which bacteria communicate with one another via small molecule or peptide signaling molecules called AutoInducers (AIs). Quorum sensing… (more)

Subjects/Keywords: Biochemistry; AutoInducer-2; Quorum Sensing; Fluorophore; bacterial cell-to-cell communication; Lux-S

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APA (6th Edition):

McMullen, J. G. (2009). In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1242672266

Chicago Manual of Style (16th Edition):

McMullen, Justin G. “In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores.” 2009. Masters Thesis, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1242672266.

MLA Handbook (7th Edition):

McMullen, Justin G. “In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores.” 2009. Web. 17 Jun 2019.

Vancouver:

McMullen JG. In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores. [Internet] [Masters thesis]. The Ohio State University; 2009. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1242672266.

Council of Science Editors:

McMullen JG. In vitro Detection of AutoInducer-2 by Small Molecule Fluorophores. [Masters Thesis]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1242672266


The Ohio State University

5. Selner, Nicholas. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.

Degree: PhD, Chemistry, 2013, The Ohio State University

 Many signaling pathways are mediated by protein tyrosine phosphorylation. Regulation of protein tyrosine phosphorylation is balanced between protein tyrosine kinases (PTKs) and protein tyrosine phosphatases… (more)

Subjects/Keywords: Chemistry; Biochemistry; Combinatorial library, catalytic activity, kinetics, phosphotyrosine, phosphatase, PTP, substrate specificity

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APA (6th Edition):

Selner, N. (2013). PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733

Chicago Manual of Style (16th Edition):

Selner, Nicholas. “PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.” 2013. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733.

MLA Handbook (7th Edition):

Selner, Nicholas. “PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES.” 2013. Web. 17 Jun 2019.

Vancouver:

Selner N. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733.

Council of Science Editors:

Selner N. PROFILING THE INTRINSIC SEQUENCE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1384269733


The Ohio State University

6. Luechapanichkul, Rinrada. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.

Degree: PhD, Chemistry, 2014, The Ohio State University

  Protein phosphorylation is a post-translational modification controlled by two counteracting enzyme families, protein kinases and phosphatases. Protein phosphatases have been demonstrated to regulate many… (more)

Subjects/Keywords: Chemistry; protein phosphatases, sequence specificity

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APA (6th Edition):

Luechapanichkul, R. (2014). Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380

Chicago Manual of Style (16th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

MLA Handbook (7th Edition):

Luechapanichkul, Rinrada. “Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases.” 2014. Web. 17 Jun 2019.

Vancouver:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380.

Council of Science Editors:

Luechapanichkul R. Determination of the Sequence Specificity and Protein Substrates of Protein Phosphatases. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1398868380


The Ohio State University

7. Liu, Tao. Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach.

Degree: PhD, Biochemistry Program, Ohio State, 2011, The Ohio State University

 Cyclic peptides are widely produced in nature and possess a broad range of biological activities. Their enhanced proteolytic stability in vivo and improved receptor binding… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Chemistry; Cyclic Peptides; Combinatorial Chemistry; One-Bead-One-Compound (OBOC) Library; Prolactin Recepotr; Pin1; HIV Capsid; Calcineurin; Cell Penetrating Peptide (CPP)

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APA (6th Edition):

Liu, T. (2011). Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1306865559

Chicago Manual of Style (16th Edition):

Liu, Tao. “Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1306865559.

MLA Handbook (7th Edition):

Liu, Tao. “Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach.” 2011. Web. 17 Jun 2019.

Vancouver:

Liu T. Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306865559.

Council of Science Editors:

Liu T. Development Of Cyclic Peptidyl Ligands Through A Combinatorial Library Approach. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306865559


The Ohio State University

8. Qian, Ziqing. Developments and Applications of Cyclic Cell Penetrating Peptides.

Degree: PhD, Chemistry, 2014, The Ohio State University

 Cell penetrating peptides (CPP) have been featured as a powerful delivery vector for the intracellular delivery of membrane-impermeable cargoes. This dissertation primarily focuses on the… (more)

Subjects/Keywords: Chemistry; Cell Penetrating Peptide; Drug delivery; cyclic peptide; cyclic cell penetrating peptide; protein delivery; endosomal escape; calcineurin; VIVIT

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APA (6th Edition):

Qian, Z. (2014). Developments and Applications of Cyclic Cell Penetrating Peptides. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891

Chicago Manual of Style (16th Edition):

Qian, Ziqing. “Developments and Applications of Cyclic Cell Penetrating Peptides.” 2014. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891.

MLA Handbook (7th Edition):

Qian, Ziqing. “Developments and Applications of Cyclic Cell Penetrating Peptides.” 2014. Web. 17 Jun 2019.

Vancouver:

Qian Z. Developments and Applications of Cyclic Cell Penetrating Peptides. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891.

Council of Science Editors:

Qian Z. Developments and Applications of Cyclic Cell Penetrating Peptides. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891


The Ohio State University

9. Tan, Pauline H. Sequence Specificity of Src Homology-2 Domains.

Degree: PhD, Chemistry, 2012, The Ohio State University

 Src-homology domains are small modular domains that recognize phosphotyrosine-containing proteins and couple activated protein kinases to intracellular signaling pathways. Since they often have overlapping functions,… (more)

Subjects/Keywords: Biochemistry; Chemistry; SH2 Domain; Binding Specificity; Src kinase; kinase; SHP2; SH2 mutant; protein-protein interaction; peptide library; protein binding

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APA (6th Edition):

Tan, P. H. (2012). Sequence Specificity of Src Homology-2 Domains. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526

Chicago Manual of Style (16th Edition):

Tan, Pauline H. “Sequence Specificity of Src Homology-2 Domains.” 2012. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526.

MLA Handbook (7th Edition):

Tan, Pauline H. “Sequence Specificity of Src Homology-2 Domains.” 2012. Web. 17 Jun 2019.

Vancouver:

Tan PH. Sequence Specificity of Src Homology-2 Domains. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526.

Council of Science Editors:

Tan PH. Sequence Specificity of Src Homology-2 Domains. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526


The Ohio State University

10. Chen, Xianwen. PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING.

Degree: PhD, Chemistry, 2011, The Ohio State University

 Protein tyrosine phosphatases (PTPs) hydrolyze phosphotyrosine (pY) back to tyrosine and inorganic phosphate, functioning in coordinate with protein tyrosine kinases (PTKs) to regulate a broad… (more)

Subjects/Keywords: Biochemistry; Protein tyrosine phosphatases; One-bead-one-compound peptide library; enzyme kinetics

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APA (6th Edition):

Chen, X. (2011). PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1315341322

Chicago Manual of Style (16th Edition):

Chen, Xianwen. “PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1315341322.

MLA Handbook (7th Edition):

Chen, Xianwen. “PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING.” 2011. Web. 17 Jun 2019.

Vancouver:

Chen X. PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1315341322.

Council of Science Editors:

Chen X. PROFILING THE SUBSTRATE SPECIFICITY OF PROTEIN TYROSINE PHOSPHATASES BY COMBINATORIAL LIBRARY SCREENING. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1315341322


The Ohio State University

11. Trinh, Thi Ba. Synthesis and Screening of Peptide Libraries for Biological Applications.

Degree: PhD, Chemistry, 2014, The Ohio State University

 Combinatorial chemistry is a powerful tool in medicinal chemistry as well as chemical biology. In this work, we have applied combinatorial chemistry toward the analysis… (more)

Subjects/Keywords: Chemistry; Combinatorial library, peptide cyclization, kinase profiling

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APA (6th Edition):

Trinh, T. B. (2014). Synthesis and Screening of Peptide Libraries for Biological Applications. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102

Chicago Manual of Style (16th Edition):

Trinh, Thi Ba. “Synthesis and Screening of Peptide Libraries for Biological Applications.” 2014. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102.

MLA Handbook (7th Edition):

Trinh, Thi Ba. “Synthesis and Screening of Peptide Libraries for Biological Applications.” 2014. Web. 17 Jun 2019.

Vancouver:

Trinh TB. Synthesis and Screening of Peptide Libraries for Biological Applications. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102.

Council of Science Editors:

Trinh TB. Synthesis and Screening of Peptide Libraries for Biological Applications. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405520102


The Ohio State University

12. You, Jia. Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry.

Degree: PhD, Chemistry, 2012, The Ohio State University

  In this dissertation, efforts were focused on the development of targeted proteomic assays to elucidate differences in protein profiles present in diseases and their… (more)

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APA (6th Edition):

You, J. (2012). Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1345493946

Chicago Manual of Style (16th Edition):

You, Jia. “Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry.” 2012. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1345493946.

MLA Handbook (7th Edition):

You, Jia. “Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry.” 2012. Web. 17 Jun 2019.

Vancouver:

You J. Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1345493946.

Council of Science Editors:

You J. Discovery and Quantitation of Protein Modifications using Targeted Mass Spectrometry. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1345493946


The Ohio State University

13. Kumar, Sandeep. Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus.

Degree: PhD, Chemistry, 2008, The Ohio State University

  This work describes the multi-faceted characterization of DNA polymerase X (Pol X) from African Swine Fever Virus (ASFV), the smallest known DNA polymerase belonging… (more)

Subjects/Keywords: Biochemistry; DNA polymerase; fidelity; lesion bypass; mismatch incorporation; order of substrate binding

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APA (6th Edition):

Kumar, S. (2008). Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1211380265

Chicago Manual of Style (16th Edition):

Kumar, Sandeep. “Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus.” 2008. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1211380265.

MLA Handbook (7th Edition):

Kumar, Sandeep. “Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus.” 2008. Web. 17 Jun 2019.

Vancouver:

Kumar S. Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1211380265.

Council of Science Editors:

Kumar S. Biochemical, Mechanistic, and Structural Characterization of DNA Polymerase X from African Swine Fever Virus. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1211380265


The Ohio State University

14. Tu, Shengjiang. Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2.

Degree: PhD, Chemistry, 2008, The Ohio State University

 In the post-genome era, the regulation of gene transcription is the central topic in biomedical research. In recent years, it is found that posttranslational modifications… (more)

Subjects/Keywords: Biochemistry; epigenetics; histone modifications; histone demethylases; NMR structure; RBP2; Rph1; Jhd2; Jhd1; Gis1; Ecm5

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APA (6th Edition):

Tu, S. (2008). Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1211487400

Chicago Manual of Style (16th Edition):

Tu, Shengjiang. “Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2.” 2008. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1211487400.

MLA Handbook (7th Edition):

Tu, Shengjiang. “Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2.” 2008. Web. 17 Jun 2019.

Vancouver:

Tu S. Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1211487400.

Council of Science Editors:

Tu S. Identification Of Histone Demthylases In Budding Yeast And DNA Binding Motifs Of Human Demethylase RBP2. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1211487400


The Ohio State University

15. Hard, Ryan Lawrence. Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains.

Degree: PhD, Biochemistry, 2013, The Ohio State University

 Src Homology 2 (SH2), Post-Synaptic Density-95/Discs Large/Zonula Occludens-1 (PDZ), Binder of Ubiquitin Zinc Finger (BUZ), and BRCA1 C-terminal (BRCT) domains are short peptide-binding modules that… (more)

Subjects/Keywords: Biochemistry; PDZ; BUZ; BRCT

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APA (6th Edition):

Hard, R. L. (2013). Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1377005582

Chicago Manual of Style (16th Edition):

Hard, Ryan Lawrence. “Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains.” 2013. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1377005582.

MLA Handbook (7th Edition):

Hard, Ryan Lawrence. “Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains.” 2013. Web. 17 Jun 2019.

Vancouver:

Hard RL. Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1377005582.

Council of Science Editors:

Hard RL. Sequence Specificity of BUZ, PDZ, SH2, and Tandem BRCT Domains. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1377005582

16. Kunys, Andrew Richard. Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library.

Degree: MS, Chemistry, 2013, The Ohio State University

 Src homology 2 Domains (SH2 domains) are modular protein binding domains which recognize a phosphotyrosine and the residues adjacent to the phosphotyrosine. Although they are… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Biology; Chemistry; SH2 domains, Protein-Protein Interactions, Combinatorial Chemistry, Cell Signalling, Tyrosine Phosphorylation, One-Bead-One-Compound, Partial Edman Degradation, Peptide

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kunys, A. R. (2013). Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1374185732

Chicago Manual of Style (16th Edition):

Kunys, Andrew Richard. “Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library.” 2013. Masters Thesis, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1374185732.

MLA Handbook (7th Edition):

Kunys, Andrew Richard. “Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library.” 2013. Web. 17 Jun 2019.

Vancouver:

Kunys AR. Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library. [Internet] [Masters thesis]. The Ohio State University; 2013. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1374185732.

Council of Science Editors:

Kunys AR. Binding Specificity of SH2 Domains Revealed by a Combinatorial Peptide Library. [Masters Thesis]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1374185732


The Ohio State University

17. Nguyen, Kiet T. Mechanism, function, and inhibition of peptide deformylase.

Degree: PhD, Ohio State Biochemistry Program, 2005, The Ohio State University

 Peptide deformylase (PDF) was originally thought as unique and essential only to the prokaryotes and apparently was absent from the eukaryotes. In this work, two… (more)

Subjects/Keywords: Chemistry, Biochemistry; Peptide deformylase; Human peptide deformylase; Plasmodium peptide deformylase; Peptide deformylase inhibitor; Deformylation

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APA (6th Edition):

Nguyen, K. T. (2005). Mechanism, function, and inhibition of peptide deformylase. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1110038706

Chicago Manual of Style (16th Edition):

Nguyen, Kiet T. “Mechanism, function, and inhibition of peptide deformylase.” 2005. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1110038706.

MLA Handbook (7th Edition):

Nguyen, Kiet T. “Mechanism, function, and inhibition of peptide deformylase.” 2005. Web. 17 Jun 2019.

Vancouver:

Nguyen KT. Mechanism, function, and inhibition of peptide deformylase. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1110038706.

Council of Science Editors:

Nguyen KT. Mechanism, function, and inhibition of peptide deformylase. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1110038706


The Ohio State University

18. Zhu, Jinge. Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS).

Degree: PhD, Ohio State Biochemistry Program, 2005, The Ohio State University

  <i>S</i>-Ribosylhomocysteinase (LuxS) catalyzes the cleavage of the thioether bond in <i>S</i>-ribosylhomocysteine to produce L-homocysteine and 4,5-dihydroxy-2,3-pentanedione, the precursor of type II bacterial quorum sensing… (more)

Subjects/Keywords: Chemistry, Biochemistry; LUXS; SRH; 1H; ¿¿¿¿M; 2-ketone; 2H-and

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APA (6th Edition):

Zhu, J. (2005). Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS). (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1115841808

Chicago Manual of Style (16th Edition):

Zhu, Jinge. “Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS).” 2005. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1115841808.

MLA Handbook (7th Edition):

Zhu, Jinge. “Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS).” 2005. Web. 17 Jun 2019.

Vancouver:

Zhu J. Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS). [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1115841808.

Council of Science Editors:

Zhu J. Mechanistic and inhibitory studies of S-ribosylhomocysteinase (LuxS). [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1115841808


The Ohio State University

19. Sweeney, Michael Cameron. Synthetic combinatorial peptide libraries and their application in decoding biological interactions.

Degree: PhD, Ohio State Biochemistry Program, 2005, The Ohio State University

 The synthesis of peptides was revolutionized by the adoption of solid-phase synthetic techniques. Subsequent improvement, evolution, and refinement of this chemical technique has allowed research… (more)

Subjects/Keywords: Chemistry, Biochemistry; SH2; SH2 domains; PEPTIDE; SHP-2; SHP-1

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APA (6th Edition):

Sweeney, M. C. (2005). Synthetic combinatorial peptide libraries and their application in decoding biological interactions. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1118952919

Chicago Manual of Style (16th Edition):

Sweeney, Michael Cameron. “Synthetic combinatorial peptide libraries and their application in decoding biological interactions.” 2005. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1118952919.

MLA Handbook (7th Edition):

Sweeney, Michael Cameron. “Synthetic combinatorial peptide libraries and their application in decoding biological interactions.” 2005. Web. 17 Jun 2019.

Vancouver:

Sweeney MC. Synthetic combinatorial peptide libraries and their application in decoding biological interactions. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1118952919.

Council of Science Editors:

Sweeney MC. Synthetic combinatorial peptide libraries and their application in decoding biological interactions. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1118952919


The Ohio State University

20. Wavreille, Anne-Sophie Marie. SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors.

Degree: PhD, Chemistry, 2006, The Ohio State University

 Protein-protein interactions form the molecular basis of a wide variety of cellular processes. A large fraction of these interactions are mediated by small modular domains,… (more)

Subjects/Keywords: Chemistry, Biochemistry; SH2 domain; Binding specificity; SHP-1; SHP-2; Tensin; peptide library; protein interaction; cell-permeable inhibitor

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wavreille, A. M. (2006). SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1164738844

Chicago Manual of Style (16th Edition):

Wavreille, Anne-Sophie Marie. “SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors.” 2006. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1164738844.

MLA Handbook (7th Edition):

Wavreille, Anne-Sophie Marie. “SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors.” 2006. Web. 17 Jun 2019.

Vancouver:

Wavreille AM. SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors. [Internet] [Doctoral dissertation]. The Ohio State University; 2006. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1164738844.

Council of Science Editors:

Wavreille AM. SRC homology 2 domain proteins binding specificity: from combinatorial chemistry to cell-permeable inhibitors. [Doctoral Dissertation]. The Ohio State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1164738844


The Ohio State University

21. Park, Junguk. Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism.

Degree: PhD, Chemistry, 2005, The Ohio State University

 Reversible phosphorylation of proteins on tyrosyl residues is one of the most important processes in various cellular signaling pathways. A proper level of phosphorylation is… (more)

Subjects/Keywords: Chemistry, Biochemistry; PTPs; Cinn-GEE; PTP1B; SH2; TBNS; SH2 domains; INHIBITOR

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Park, J. (2005). Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1133278132

Chicago Manual of Style (16th Edition):

Park, Junguk. “Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism.” 2005. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1133278132.

MLA Handbook (7th Edition):

Park, Junguk. “Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism.” 2005. Web. 17 Jun 2019.

Vancouver:

Park J. Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1133278132.

Council of Science Editors:

Park J. Development of neutral phosphotyrosine memetics as a protein tyrosine phosphatase inhibitor and studies on its inhibition mechanism. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1133278132


The Ohio State University

22. Wang, Peng. Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands.

Degree: PhD, Chemistry, 2003, The Ohio State University

 A method for the rapid identification of high-affinity ligands was used to study the specificity of the interaction between FHA2 domain of Rad53 and phosphotyrosyl… (more)

Subjects/Keywords: PEPTIDE LIBRARY; FHA2; SHP-1; bead

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wang, P. (2003). Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1039797438

Chicago Manual of Style (16th Edition):

Wang, Peng. “Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands.” 2003. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1039797438.

MLA Handbook (7th Edition):

Wang, Peng. “Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands.” 2003. Web. 17 Jun 2019.

Vancouver:

Wang P. Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands. [Internet] [Doctoral dissertation]. The Ohio State University; 2003. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039797438.

Council of Science Editors:

Wang P. Screening Combinatorial Peptide Library for Optimal Enzyme Substrates and High Affinity Protein Ligands. [Doctoral Dissertation]. The Ohio State University; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039797438

.