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You searched for subject:(protein nucleic acid). Showing records 1 – 29 of 29 total matches.

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University of Minnesota

1. Solomon, William. Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2015, University of Minnesota

 Humans express the APOBEC3 family of proteins to defend against endogenous and exogenous DNA pathogens. APOBEC3 proteins display significant activity towards HIV-1 through incorporation into… (more)

Subjects/Keywords: APOBEC3G; HIV; NMR; protein-nucleic acid interactions

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

APA (6th Edition):

Solomon, W. (2015). Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/175337

Chicago Manual of Style (16th Edition):

Solomon, William. “Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination.” 2015. Doctoral Dissertation, University of Minnesota. Accessed April 01, 2020. http://hdl.handle.net/11299/175337.

MLA Handbook (7th Edition):

Solomon, William. “Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination.” 2015. Web. 01 Apr 2020.

Vancouver:

Solomon W. Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/11299/175337.

Council of Science Editors:

Solomon W. Structural and Mechanistic Insight into APOBEC3G DNA Binding and Deamination. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/175337


University of Colorado

2. Dickey, Thayne Henderson. Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  Telomere dysfunction has been implicated in several diseases including cancer and aging. The two main roles of telomeres are often defined as end-protection and… (more)

Subjects/Keywords: Plasticity; Pombe; Pot1; protein nucleic acid; shelterin; telomere; Biochemistry; Molecular Genetics

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APA (6th Edition):

Dickey, T. H. (2014). Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/111

Chicago Manual of Style (16th Edition):

Dickey, Thayne Henderson. “Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1.” 2014. Doctoral Dissertation, University of Colorado. Accessed April 01, 2020. https://scholar.colorado.edu/chem_gradetds/111.

MLA Handbook (7th Edition):

Dickey, Thayne Henderson. “Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1.” 2014. Web. 01 Apr 2020.

Vancouver:

Dickey TH. Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Apr 01]. Available from: https://scholar.colorado.edu/chem_gradetds/111.

Council of Science Editors:

Dickey TH. Structural Plasticity in the Recognition of ssDNA by the Telomeric Protein Pot1. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chem_gradetds/111


The Ohio State University

3. Ma, Xin. MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS.

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

 The development of analytical techniques for biological molecules provides analytical tools for biochemistry and structural biology, and the application of mass spectrometry (MS) in this… (more)

Subjects/Keywords: Chemistry; Biophysics; native mass spectrometry; ion mobility; surface induced dissociation; protein-protein; protein-nucleic acid; DNA; RNA

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APA (6th Edition):

Ma, X. (2014). MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1397773864

Chicago Manual of Style (16th Edition):

Ma, Xin. “MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS.” 2014. Doctoral Dissertation, The Ohio State University. Accessed April 01, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1397773864.

MLA Handbook (7th Edition):

Ma, Xin. “MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS.” 2014. Web. 01 Apr 2020.

Vancouver:

Ma X. MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Apr 01]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397773864.

Council of Science Editors:

Ma X. MASS SPECTROMETRY DISSOCIATION STUDIES OF PROTEIN-PROTEIN AND PROTEIN-NUCLEIC ACID COMPLEXES AND 13C FLUX OF AMINO ACIDS. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397773864


University of Colorado

4. McUmber, Aaron Christopher. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.

Degree: PhD, Chemical & Biochemical Engineering, 2015, University of Colorado

  Biopolymers, such as proteins and nucleic acids, are omnipresent in modern applications. The need to control interfacial molecular systems is becoming increasingly important in… (more)

Subjects/Keywords: Aggregation; Interface; Nucleic Acid; Protein; Single Molecule; TIRFM; Biochemical and Biomolecular Engineering

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APA (6th Edition):

McUmber, A. C. (2015). Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chbe_gradetds/88

Chicago Manual of Style (16th Edition):

McUmber, Aaron Christopher. “Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.” 2015. Doctoral Dissertation, University of Colorado. Accessed April 01, 2020. https://scholar.colorado.edu/chbe_gradetds/88.

MLA Handbook (7th Edition):

McUmber, Aaron Christopher. “Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics.” 2015. Web. 01 Apr 2020.

Vancouver:

McUmber AC. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. [Internet] [Doctoral dissertation]. University of Colorado; 2015. [cited 2020 Apr 01]. Available from: https://scholar.colorado.edu/chbe_gradetds/88.

Council of Science Editors:

McUmber AC. Understanding How Non-Covalent Interactions Affect Interfacial Biomolecular Dynamics. [Doctoral Dissertation]. University of Colorado; 2015. Available from: https://scholar.colorado.edu/chbe_gradetds/88


University of Illinois – Urbana-Champaign

5. Hwang, Helen. Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity.

Degree: MS, 0408, 2011, University of Illinois – Urbana-Champaign

 Single molecule FRET (F??rster Resonance Energy Transfer) has been recently widely used for monitoring the interactions between a protein and a nucleic acid. It typically… (more)

Subjects/Keywords: Single Molecule; Protein Induced Fluorescence Enhancement; DNA nucleic acid interactions; F??rster Resonance Energy Transfer

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APA (6th Edition):

Hwang, H. (2011). Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18496

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hwang, Helen. “Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed April 01, 2020. http://hdl.handle.net/2142/18496.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hwang, Helen. “Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity.” 2011. Web. 01 Apr 2020.

Vancouver:

Hwang H. Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/2142/18496.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hwang H. Characterization of protein induced fluorescence enhancement (PIFE): A label-free protein assay with short distance sensitivity. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18496

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Tennessee – Knoxville

6. Cheng, Cheng. Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections.

Degree: 2017, University of Tennessee – Knoxville

 A highly sensitive, specific, real time, and field-deployable surveillance tool is critical to the control of pathogens and infections, as well as ecological impact of… (more)

Subjects/Keywords: capacitive sensing; ACEK; point of care; virus; protein; nucleic acid; Biomedical; Electrical and Electronics; Electronic Devices and Semiconductor Manufacturing

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APA (6th Edition):

Cheng, C. (2017). Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/4450

Chicago Manual of Style (16th Edition):

Cheng, Cheng. “Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections.” 2017. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed April 01, 2020. https://trace.tennessee.edu/utk_graddiss/4450.

MLA Handbook (7th Edition):

Cheng, Cheng. “Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections.” 2017. Web. 01 Apr 2020.

Vancouver:

Cheng C. Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2017. [cited 2020 Apr 01]. Available from: https://trace.tennessee.edu/utk_graddiss/4450.

Council of Science Editors:

Cheng C. Development of a low cost biosensing platform for highly sensitive and specific on-site detection of pathogens and infections. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2017. Available from: https://trace.tennessee.edu/utk_graddiss/4450


University of Oregon

7. Prikryl, Jana, 1976-. Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression.

Degree: 2009, University of Oregon

 My dissertation research has centered on understanding how nuclear encoded proteins affect chloroplast gene expression in higher plants. I investigated the functions of three proteins… (more)

Subjects/Keywords: Nucleic acid binding protein; Chloroplast; Gene expression; Pentotricopeptide repats; Group II introns; Molecular biology; Plant biology; Biochemistry

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APA (6th Edition):

Prikryl, Jana, 1. (2009). Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/10614

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Prikryl, Jana, 1976-. “Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression.” 2009. Thesis, University of Oregon. Accessed April 01, 2020. http://hdl.handle.net/1794/10614.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Prikryl, Jana, 1976-. “Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression.” 2009. Web. 01 Apr 2020.

Vancouver:

Prikryl, Jana 1. Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression. [Internet] [Thesis]. University of Oregon; 2009. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/1794/10614.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Prikryl, Jana 1. Functions of organelle-specific nucleic acid binding protein families in chloroplast gene expression. [Thesis]. University of Oregon; 2009. Available from: http://hdl.handle.net/1794/10614

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Uniwersytet im. Adama Mickiewicza w Poznaniu

8. Izbiańska, Karolina. Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary .

Degree: 2018, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Celem badań było zweryfikowanie udziału nadtlenoazotynu (ONOO¯) oraz poznanie funkcjonalnych modyfikacji via ONOO¯ w odporności liści ziemniaka na Phytophthora infestans. Doświadczenia prowadzono na liściach ziemniaka… (more)

Subjects/Keywords: nadtlenoazotyn; peroxynitrite; nitrowanie białek; protein nitration; nitrowanie kwasów nukleinowych; nucleic acid nitration; Phytophthora infestans; odporność roślin; plant immunity

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APA (6th Edition):

Izbiańska, K. (2018). Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/24451

Chicago Manual of Style (16th Edition):

Izbiańska, Karolina. “Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary .” 2018. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed April 01, 2020. http://hdl.handle.net/10593/24451.

MLA Handbook (7th Edition):

Izbiańska, Karolina. “Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary .” 2018. Web. 01 Apr 2020.

Vancouver:

Izbiańska K. Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2018. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/10593/24451.

Council of Science Editors:

Izbiańska K. Funkcje nadtlenoazotynu w odporności liści ziemniaka (Solanum tuberosum L.) na Phytophthora infestans (Mont.) de Bary . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2018. Available from: http://hdl.handle.net/10593/24451


Indian Institute of Science

9. Sathyapriya, R. Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches.

Degree: 2007, Indian Institute of Science

 The flow of genetic information from genes to proteins is mediated through proteins which interact with the nucleic acids at several stages to successfully transmit… (more)

Subjects/Keywords: Protein-Nucleic Acid Interactions; Protein-RNA Interactions; Protein Structure Graphs; Protein Nucleotide Graphs (PNG); Protein-DNA Complexes; Protein-RNA Complexes; Aminoacyl-tRNA Synthetase; Glutaminyl-tRNA Synthetase (GlnRS); Proteins - Short Hydrogen Bonds; Protein Structure Networks; Protein-RNA Interaction; Structure Graphs; Protein-RNA Graphs; 70S Ribosome; Biochemical Genetics

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APA (6th Edition):

Sathyapriya, R. (2007). Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/624

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sathyapriya, R. “Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches.” 2007. Thesis, Indian Institute of Science. Accessed April 01, 2020. http://hdl.handle.net/2005/624.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sathyapriya, R. “Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches.” 2007. Web. 01 Apr 2020.

Vancouver:

Sathyapriya R. Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches. [Internet] [Thesis]. Indian Institute of Science; 2007. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/2005/624.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sathyapriya R. Exploring Protein-Nucleic Acid Interactions Using Graph And Network Approaches. [Thesis]. Indian Institute of Science; 2007. Available from: http://hdl.handle.net/2005/624

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

10. Ramesh, V. Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners.

Degree: 2009, Indian Institute of Science

 PTB (HnRNP I) is a multifunctional RNA binding protein which participates in a variety of RNA metabolic processes put together called as post transcriptional gene… (more)

Subjects/Keywords: Proteins; Polypyrimidine Tract Binding Protein (PTB); RNA Binding Protein; Plasmid DNA; Gene Regulation; Heterogeneous Nuclear Ribonucleoprotein(HnRNP); Messenger Ribo Nucleic Acid (mRNA); Biochemistry

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APA (6th Edition):

Ramesh, V. (2009). Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/659

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ramesh, V. “Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners.” 2009. Thesis, Indian Institute of Science. Accessed April 01, 2020. http://hdl.handle.net/2005/659.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ramesh, V. “Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners.” 2009. Web. 01 Apr 2020.

Vancouver:

Ramesh V. Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners. [Internet] [Thesis]. Indian Institute of Science; 2009. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/2005/659.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ramesh V. Studies On Polypyrimidine Tract Binding Protein : Identification Of Interacting Partners. [Thesis]. Indian Institute of Science; 2009. Available from: http://hdl.handle.net/2005/659

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

11. Chu, Chih-Chi. DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation.

Degree: PhD, Chemistry, 2017, University of Illinois – Urbana-Champaign

 Proteins and RNA are known to be enzymes in nature. These biopolymers have complex secondary and tertiary structures that can enable substrate binding and catalysis.… (more)

Subjects/Keywords: Nucleic acids; DNAzymes; Deoxyribozymes; Deoxyribonucleic acid (DNA) enzymes; Site-specific; Protein modification; Peptide modification; Peptide-nucleic acid conjugation; Lysine methylation; Recruiting; Histidine tag; TrisNTA; Modified nucleotides; Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC); Click chemistry

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APA (6th Edition):

Chu, C. (2017). DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99165

Chicago Manual of Style (16th Edition):

Chu, Chih-Chi. “DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed April 01, 2020. http://hdl.handle.net/2142/99165.

MLA Handbook (7th Edition):

Chu, Chih-Chi. “DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation.” 2017. Web. 01 Apr 2020.

Vancouver:

Chu C. DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/2142/99165.

Council of Science Editors:

Chu C. DNA enzymes for peptide-nucleic acid conjugation and for lysine methylation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99165

12. Sharma, Rajhans. Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids.

Degree: Docteur es, Biophysique et biologie structurale, 2018, Université de Strasbourg

La protéine de la nucléocapside (NC) possède un rôle important dans le cycle de viral du VIH-1 grâce à sa propriété chaperone des acides nucléiques… (more)

Subjects/Keywords: VIH-1; Nucléocapside protéine; Analogues nucléosidiques fluorescents; Thiéoguanosine; Primer binding site; SL3; Acides nucléiques dynamique; Fluorescence spectroscopie; Protéine-acides nucléiques interaction; HIV-1; Nucleocapsid protein; Fluorescent nucleobase analogues; Thieoguanosine; Primer binding site; SL3; Nucleic acid dynamics; Fluorescence spectroscopy; Protein-nucleic acids interaction; 579.2; 616.91

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APA (6th Edition):

Sharma, R. (2018). Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAJ014

Chicago Manual of Style (16th Edition):

Sharma, Rajhans. “Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed April 01, 2020. http://www.theses.fr/2018STRAJ014.

MLA Handbook (7th Edition):

Sharma, Rajhans. “Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids.” 2018. Web. 01 Apr 2020.

Vancouver:

Sharma R. Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2020 Apr 01]. Available from: http://www.theses.fr/2018STRAJ014.

Council of Science Editors:

Sharma R. Caractérisation et ciblage de la reconnaissance dynamique de Trp37-G lors de l’interaction de la protéine NCp7 de HIV-1 avec des acides nucléiques : Characterization and targeting the dynamic recognition of Trp37-G during the interaction of NCp7 protein of HIV-1 with nucleic acids. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAJ014


Queensland University of Technology

13. Ashton, Nicholas W. Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications.

Degree: 2016, Queensland University of Technology

 Human single-stranded DNA-binding protein 1 (hSSB1) is required for the timely repair of double-strand DNA breaks, as well as the stabilisation and restart of stalled… (more)

Subjects/Keywords: Human single-stranded DNA-binding protein 1; Nucleic acid-binding protein 2; OB-fold containing protein 2B; Sensor of single-stranded DNA complex subunit B; DNA-dependent protein kinase (DNA-PK); PPP-family protein phosphatases; Integrator complex subunit 3 (INTS3); hSSB1; NABP2; OBFC2B

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APA (6th Edition):

Ashton, N. W. (2016). Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/98660/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ashton, Nicholas W. “Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications.” 2016. Thesis, Queensland University of Technology. Accessed April 01, 2020. https://eprints.qut.edu.au/98660/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ashton, Nicholas W. “Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications.” 2016. Web. 01 Apr 2020.

Vancouver:

Ashton NW. Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications. [Internet] [Thesis]. Queensland University of Technology; 2016. [cited 2020 Apr 01]. Available from: https://eprints.qut.edu.au/98660/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ashton NW. Characterisation of human single-stranded DNA-binding protein 1 (hSSB1) regulation by post-translational modifications. [Thesis]. Queensland University of Technology; 2016. Available from: https://eprints.qut.edu.au/98660/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

14. Barthes, Nicolas. Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1.

Degree: Docteur es, Chimie, 2015, Nice

La méthylation de l'ADN est une des marques épigénétiques majeures qui intervient dans la régulation de processus physiologiques importants. Par ailleurs, elle a été reconnue… (more)

Subjects/Keywords: Méthylation de l'ADN; Interaction ADN/protéine; Sondes fluorescentes ratiométriques; 3-hydroxychromone; Nucléosides; DNA Methylation; Nucleic acid/protein interactions; Ratiometric fluorescent probe; 3-hydroxychromone; Nucleosides

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APA (6th Edition):

Barthes, N. (2015). Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2015NICE4124

Chicago Manual of Style (16th Edition):

Barthes, Nicolas. “Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1.” 2015. Doctoral Dissertation, Nice. Accessed April 01, 2020. http://www.theses.fr/2015NICE4124.

MLA Handbook (7th Edition):

Barthes, Nicolas. “Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1.” 2015. Web. 01 Apr 2020.

Vancouver:

Barthes N. Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1. [Internet] [Doctoral dissertation]. Nice; 2015. [cited 2020 Apr 01]. Available from: http://www.theses.fr/2015NICE4124.

Council of Science Editors:

Barthes N. Épigénétique et méthylation de l’ADN : développement d’outils pour la compréhension du mécanisme de méthylation de l’ADN impliquant UHRF1 : Epigenetics and DNA methylation : development of new tools to understand DNA methylation mechanism involving UHRF1. [Doctoral Dissertation]. Nice; 2015. Available from: http://www.theses.fr/2015NICE4124


University of Arizona

15. Porter, Jason Robert. SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF .

Degree: 2009, University of Arizona

 The interactions between protein-protein, protein-nucleic acid, and protein-small molecules are central to biological processes and are key for the design of new therapeutics. Rapid and… (more)

Subjects/Keywords: Bcl-2; High Throughput; In Vitro Translation; Protein-Nucleic Acid; Protein-Protein; Split-Protein Complementation

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APA (6th Edition):

Porter, J. R. (2009). SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/194359

Chicago Manual of Style (16th Edition):

Porter, Jason Robert. “SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF .” 2009. Doctoral Dissertation, University of Arizona. Accessed April 01, 2020. http://hdl.handle.net/10150/194359.

MLA Handbook (7th Edition):

Porter, Jason Robert. “SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF .” 2009. Web. 01 Apr 2020.

Vancouver:

Porter JR. SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF . [Internet] [Doctoral dissertation]. University of Arizona; 2009. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/10150/194359.

Council of Science Editors:

Porter JR. SPLIT-PROTEIN REASSEMBLY METHODS FOR THE DETECTION AND INTERROGATION OF BIOMOLECULAR INTERACTIONS AND MODULATORS THEREOF . [Doctoral Dissertation]. University of Arizona; 2009. Available from: http://hdl.handle.net/10150/194359

16. Cirillo, Davide. Prediction of protein and nucleic acid interactions.

Degree: Departament de Ciències Experimentals i de la Salut, 2016, Universitat Pompeu Fabra

 Mis estudios de doctorado han tenido como propósito principal el desarrollo de herramientas bioinformáticas para la evaluación de interacciones entre proteínas y ácidos nucleicos (ANs)… (more)

Subjects/Keywords: DNA-binding proteins; RNA-binding proteins; Neurodegenerative diseases; Protein-protein interacion networks; Interacciones entre proteínas y ácidos nucleicos; Proteínas que se unen a ADN; Proteínas que se unen a ARN; Enfermedades neurodegenerativas; Red de interacción proteína-proteína; Protein-nucleic acid interactions; 577

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APA (6th Edition):

Cirillo, D. (2016). Prediction of protein and nucleic acid interactions. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/403537

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cirillo, Davide. “Prediction of protein and nucleic acid interactions.” 2016. Thesis, Universitat Pompeu Fabra. Accessed April 01, 2020. http://hdl.handle.net/10803/403537.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cirillo, Davide. “Prediction of protein and nucleic acid interactions.” 2016. Web. 01 Apr 2020.

Vancouver:

Cirillo D. Prediction of protein and nucleic acid interactions. [Internet] [Thesis]. Universitat Pompeu Fabra; 2016. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/10803/403537.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cirillo D. Prediction of protein and nucleic acid interactions. [Thesis]. Universitat Pompeu Fabra; 2016. Available from: http://hdl.handle.net/10803/403537

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

17. C. Annoni. NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS.

Degree: 2014, Università degli Studi di Milano

 In the late 19th century, scientists microscopically observed the association of proteins with DNA strands. Since then, researchers have used a variety of in vitro… (more)

Subjects/Keywords: protein-nucleic acid interactions; biopolymers; DNA binding domain; molecular dymanics; homology models; ribonucleopeptide biosensors; DNA origami; molecular switchboard; AFM analyses; Settore CHIM/03 - Chimica Generale e Inorganica; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Annoni, C. (2014). NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/232405

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Annoni, C.. “NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS.” 2014. Thesis, Università degli Studi di Milano. Accessed April 01, 2020. http://hdl.handle.net/2434/232405.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Annoni, C.. “NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS.” 2014. Web. 01 Apr 2020.

Vancouver:

Annoni C. NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/2434/232405.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Annoni C. NEW DIMENSIONS INTO PROTEIN-NUCLEIC ACIDS INTERACTIONS. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/232405

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Freie Universität Berlin

18. Müller, Uwe. Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins.

Degree: 1999, Freie Universität Berlin

 Crystal Structure of ALAwt and ALAC70 The acceptor stem of tRNAAla from E. coli contains the main identity element for specific aminoacylation by it´s cognate… (more)

Subjects/Keywords: nucleic acid and protein structure; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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APA (6th Edition):

Müller, U. (1999). Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-5132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Müller, Uwe. “Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins.” 1999. Thesis, Freie Universität Berlin. Accessed April 01, 2020. http://dx.doi.org/10.17169/refubium-5132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Müller, Uwe. “Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins.” 1999. Web. 01 Apr 2020.

Vancouver:

Müller U. Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins. [Internet] [Thesis]. Freie Universität Berlin; 1999. [cited 2020 Apr 01]. Available from: http://dx.doi.org/10.17169/refubium-5132.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Müller U. Macromolecular Crystallography at Atomic Resolution: Synthetic Nucleic acid fragments and bacterial Cold-shock proteins. [Thesis]. Freie Universität Berlin; 1999. Available from: http://dx.doi.org/10.17169/refubium-5132

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

19. Gao, Yang. Top-Down Interrogation And Characterization Of Biological Macromolecules.

Degree: PhD, Chemistry, 2013, Purdue University

  Analytical mass spectrometry has been widely applied in the field of biomolecule identification and characterization. It provides fast, accurate and robust information relevant to… (more)

Subjects/Keywords: collision-induced dissociation; electron transfer dissociation; mass spectrometry; nucleic acid; protein; top-down; Analytical Chemistry

…Page 1.1 Summary of methods used to dissociate nucleic acid ions. See abbreviations for… …Page 1.1 Nucleic acid fragment ion nomenclature proposed (a) by Cerny et al.17… …chapter summarizes literature describing the gas phase fragmentation of nucleic acid ions under… …dissociation of nucleic acid ions is determined by ion type, charge state, the energy deposition… …fragment ion series were observed for the backbone cleavages of nucleic acid ions upon FAB-MS… 

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

APA (6th Edition):

Gao, Y. (2013). Top-Down Interrogation And Characterization Of Biological Macromolecules. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/117

Chicago Manual of Style (16th Edition):

Gao, Yang. “Top-Down Interrogation And Characterization Of Biological Macromolecules.” 2013. Doctoral Dissertation, Purdue University. Accessed April 01, 2020. https://docs.lib.purdue.edu/open_access_dissertations/117.

MLA Handbook (7th Edition):

Gao, Yang. “Top-Down Interrogation And Characterization Of Biological Macromolecules.” 2013. Web. 01 Apr 2020.

Vancouver:

Gao Y. Top-Down Interrogation And Characterization Of Biological Macromolecules. [Internet] [Doctoral dissertation]. Purdue University; 2013. [cited 2020 Apr 01]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/117.

Council of Science Editors:

Gao Y. Top-Down Interrogation And Characterization Of Biological Macromolecules. [Doctoral Dissertation]. Purdue University; 2013. Available from: https://docs.lib.purdue.edu/open_access_dissertations/117


University of Windsor

20. Tu, Yu. The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618.

Degree: MS, Biological Sciences, 1970, University of Windsor

Subjects/Keywords: 1618; A; ACID; AMO; CELL; GROWTH; NUCLEIC; PEA; PLANTS; PROTEIN; RELATION; RETARDANT; SYNTHESIS; TALL; TREATED; WALL

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APA (6th Edition):

Tu, Y. (1970). The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618. (Masters Thesis). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/6628

Chicago Manual of Style (16th Edition):

Tu, Yu. “The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618.” 1970. Masters Thesis, University of Windsor. Accessed April 01, 2020. https://scholar.uwindsor.ca/etd/6628.

MLA Handbook (7th Edition):

Tu, Yu. “The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618.” 1970. Web. 01 Apr 2020.

Vancouver:

Tu Y. The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618. [Internet] [Masters thesis]. University of Windsor; 1970. [cited 2020 Apr 01]. Available from: https://scholar.uwindsor.ca/etd/6628.

Council of Science Editors:

Tu Y. The relation between cell wall protein and nucleic acid synthesis in tall pea plants treated with a growth retardant AMO-1618. [Masters Thesis]. University of Windsor; 1970. Available from: https://scholar.uwindsor.ca/etd/6628

21. Webb, Robin. THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE.

Degree: 2013, University of Kentucky

 The ZNF9 gene on chromosome 3 encodes the cellular nucleic acid binding protein (CNBP), a ubiquitously expressed, 177 amino acid (≈19.5kDa) protein that is highly… (more)

Subjects/Keywords: Alzheimer’s disease; Cellular Nucleic Acid Binding Protein; Translational Regulation; Down syndrome; RNA binding protein; Molecular and Cellular Neuroscience; Molecular Biology

…Significance CNBP Introduction and Discovery The cellular nucleic acid binding protein (CNBP… …accumulating evidence has identified the cellular nucleic acid binding protein (CNBP) as a… …dissimilar in nature, a protein kinase (DMPK) and a nucleic acid binding protein (… …x28;DMPK) and a nucleic acid binding protein (CNBP). Although the genes… …years, accumulating evidence has identified the cellular nucleic acid binding protein (… 

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APA (6th Edition):

Webb, R. (2013). THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/biochem_etds/7

Chicago Manual of Style (16th Edition):

Webb, Robin. “THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE.” 2013. Doctoral Dissertation, University of Kentucky. Accessed April 01, 2020. https://uknowledge.uky.edu/biochem_etds/7.

MLA Handbook (7th Edition):

Webb, Robin. “THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE.” 2013. Web. 01 Apr 2020.

Vancouver:

Webb R. THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE. [Internet] [Doctoral dissertation]. University of Kentucky; 2013. [cited 2020 Apr 01]. Available from: https://uknowledge.uky.edu/biochem_etds/7.

Council of Science Editors:

Webb R. THE CELLULAR NUCLEIC ACID BINDING PROTEIN IN AGING AND DISEASE. [Doctoral Dissertation]. University of Kentucky; 2013. Available from: https://uknowledge.uky.edu/biochem_etds/7

22. Reza, Faisal. Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes .

Degree: 2010, Duke University

  Interactions between nucleic acid substrates and the proteins and enzymes that bind and catalyze them are ubiquitous and essential for reading, writing, replicating, repairing,… (more)

Subjects/Keywords: Engineering, Biomedical; Computer Science; Biology, Bioinformatics; binding protein; computational biology; molecular engineering; nucleic acid; protein design; synthetic biology

…139 5.3. Modeling flexibility in nucleic acid binding protein redesign........... 140 5.4… …nucleic acid binding protein (e.g. DBP or RBP) NDB Nucleic Acid Database NHEJ non… …52 3. Single-conformation engineering of nucleic acid binding proteins ............. 53 3.1… …85 viii 4. Multiple-conformation engineering of nucleic acid binding proteins… …183 A.5. Nucleic acid templates… 

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APA (6th Edition):

Reza, F. (2010). Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/2278

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Reza, Faisal. “Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes .” 2010. Thesis, Duke University. Accessed April 01, 2020. http://hdl.handle.net/10161/2278.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Reza, Faisal. “Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes .” 2010. Web. 01 Apr 2020.

Vancouver:

Reza F. Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes . [Internet] [Thesis]. Duke University; 2010. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/10161/2278.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Reza F. Computational Molecular Engineering Nucleic Acid Binding Proteins and Enzymes . [Thesis]. Duke University; 2010. Available from: http://hdl.handle.net/10161/2278

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. McAninch, Damian S. Neuronal GQ Structures in Neurodegeneration.

Degree: PhD, Chemistry and Biochemistry, 2017, Duquesne University

  This study investigates protein nucleic acid interactions between various proteins and G quadruplex (GQ) forming messenger RNAs (mRNAs) in human neurological disorders. GQ structures… (more)

Subjects/Keywords: ALS/FTD; Hepatitis C Virus; Fragile X Syndrom; Protein; Nucleic Acid; Biophysical Characterization; Neurodegeneration; Biochemistry; Biophysics; Structural Biology

…Peptide nucleic acid PSD-95 Postsynaptic density protein 95 RGG Arginine-glycine-glycine… …2006), allowing for monitoring of protein-nucleic acid interactions. Increments of FUS… …protein-nucleic acid interactions and health of the neuronal cell. 15 Chapter 2: (G4C2… …90 Figure 32. Nucleic acid and PNA structures… …28 CHAPTER 3: Fragile X Mental Retardation Protein Recognizes a GQ Structure in Survival… 

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APA (6th Edition):

McAninch, D. S. (2017). Neuronal GQ Structures in Neurodegeneration. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/241

Chicago Manual of Style (16th Edition):

McAninch, Damian S. “Neuronal GQ Structures in Neurodegeneration.” 2017. Doctoral Dissertation, Duquesne University. Accessed April 01, 2020. https://dsc.duq.edu/etd/241.

MLA Handbook (7th Edition):

McAninch, Damian S. “Neuronal GQ Structures in Neurodegeneration.” 2017. Web. 01 Apr 2020.

Vancouver:

McAninch DS. Neuronal GQ Structures in Neurodegeneration. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2020 Apr 01]. Available from: https://dsc.duq.edu/etd/241.

Council of Science Editors:

McAninch DS. Neuronal GQ Structures in Neurodegeneration. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/241


Freie Universität Berlin

24. Max, Klaas E. A. Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen.

Degree: 2007, Freie Universität Berlin

 Die bakteriellen Kälteschockproteine (cold shock proteins - CSP) sind ein wesentlicher Bestandteil der bakteriellen Kälteschockantwort. Diese kleinen, 65-70 Aminosäuren umfassenden Proteine binden einzelsträngige Nukleinsäuren mit… (more)

Subjects/Keywords: OB fold; cold shock proteins; nucleic-acid binding; domain swap; protein stability; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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APA (6th Edition):

Max, K. E. A. (2007). Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6312

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Max, Klaas E A. “Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen.” 2007. Thesis, Freie Universität Berlin. Accessed April 01, 2020. http://dx.doi.org/10.17169/refubium-6312.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Max, Klaas E A. “Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen.” 2007. Web. 01 Apr 2020.

Vancouver:

Max KEA. Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen. [Internet] [Thesis]. Freie Universität Berlin; 2007. [cited 2020 Apr 01]. Available from: http://dx.doi.org/10.17169/refubium-6312.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Max KEA. Nukleinsäurebindung, die Architektur eines Domänentauschs und Mechanismen, die zu ihrer Stabilisierung beitragen. [Thesis]. Freie Universität Berlin; 2007. Available from: http://dx.doi.org/10.17169/refubium-6312

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Folly da Silva Constantino, Laura. An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets.

Degree: MS, Pharmaceutical Sciences and Experimental Therapeutics, 2017, University of Iowa

  Docking is a computer simulation method used to predict the preferred orientation of two interacting chemical species that has been successfully applied to numerous… (more)

Subjects/Keywords: allostery; docking; non-traditional targets; protein-nucleic acid interactions; ROC curves; structure based drug design and discovery; Pharmacy and Pharmaceutical Sciences

…ligands that stabilize forms of the nucleic acid unbound to the protein that are unsuitable for… …variety of inhibitors has been discovered, they do not target many proteinnucleic acid… …1 1.1.1 MODULATORS OF PROTEINNUCLEIC ACIDS INTERACTIONS ....................... 2 1.1.2… …subcellular transport, nucleic acid binding, signal transduction, transcription, translation, and… …Wilson & Simeonov, 2010). 1.1.1 MODULATORS OF PROTEINNUCLEIC ACIDS INTERACTIONS Protein… 

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APA (6th Edition):

Folly da Silva Constantino, L. (2017). An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets. (Masters Thesis). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5754

Chicago Manual of Style (16th Edition):

Folly da Silva Constantino, Laura. “An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets.” 2017. Masters Thesis, University of Iowa. Accessed April 01, 2020. https://ir.uiowa.edu/etd/5754.

MLA Handbook (7th Edition):

Folly da Silva Constantino, Laura. “An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets.” 2017. Web. 01 Apr 2020.

Vancouver:

Folly da Silva Constantino L. An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets. [Internet] [Masters thesis]. University of Iowa; 2017. [cited 2020 Apr 01]. Available from: https://ir.uiowa.edu/etd/5754.

Council of Science Editors:

Folly da Silva Constantino L. An effective layered workflow of virtual screening for identification of active ligands of challenging protein targets. [Masters Thesis]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5754


Royal Holloway, University of London

26. Alnasir, Jamie. The analysis of high-throughput biological datasets utilising distributed computing.

Degree: PhD, 2018, Royal Holloway, University of London

 This thesis explores the analysis of high-throughput biological datasets using distributed computing, particularly sequencing data produced by high-throughput technologies, which is increasing at an unprecedented… (more)

Subjects/Keywords: High-Throughput sequencing; Next-generation Sequencing; NGS; Transcriptomics; Genomics; MapReduce; Hadoop; Spark; Bioinformatics; Computational Biology; Batch-scheduled Computing; Cluster Computing; DNA-Sequencing; RNA-Sequencing; Nanopore-Sequencing; Metadata; Sequence Read Archive; High Performance Computing; Protein Databank; PDB; Nucleic Acid Sequencing; Bias; Workflows; Pipelines; HDFS; LSF; Openlava; Distributed Computing; IVT; In-vitro transcription; Drosophila melanogaster; Homo sapiens; PCR; Illumina; YARN; Apache; molecular docking; torsional angles; dihedral angles; Random Hexamer priming; GC content; mRNA selection; Read distribution; Vina; Structural Alignment; Sequence alignment; Sequencing workflows; sequence-specific bias

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APA (6th Edition):

Alnasir, J. (2018). The analysis of high-throughput biological datasets utilising distributed computing. (Doctoral Dissertation). Royal Holloway, University of London. Retrieved from https://pure.royalholloway.ac.uk/portal/en/publications/the-analysis-of-highthroughput-biological-datasets-utilising-distributed-computing(c523fb19-39cf-43ab-9284-7a58d4d646fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792808

Chicago Manual of Style (16th Edition):

Alnasir, Jamie. “The analysis of high-throughput biological datasets utilising distributed computing.” 2018. Doctoral Dissertation, Royal Holloway, University of London. Accessed April 01, 2020. https://pure.royalholloway.ac.uk/portal/en/publications/the-analysis-of-highthroughput-biological-datasets-utilising-distributed-computing(c523fb19-39cf-43ab-9284-7a58d4d646fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792808.

MLA Handbook (7th Edition):

Alnasir, Jamie. “The analysis of high-throughput biological datasets utilising distributed computing.” 2018. Web. 01 Apr 2020.

Vancouver:

Alnasir J. The analysis of high-throughput biological datasets utilising distributed computing. [Internet] [Doctoral dissertation]. Royal Holloway, University of London; 2018. [cited 2020 Apr 01]. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/the-analysis-of-highthroughput-biological-datasets-utilising-distributed-computing(c523fb19-39cf-43ab-9284-7a58d4d646fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792808.

Council of Science Editors:

Alnasir J. The analysis of high-throughput biological datasets utilising distributed computing. [Doctoral Dissertation]. Royal Holloway, University of London; 2018. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/the-analysis-of-highthroughput-biological-datasets-utilising-distributed-computing(c523fb19-39cf-43ab-9284-7a58d4d646fa).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792808


ETH Zürich

27. Hellwig, Robert. Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene.

Degree: 1999, ETH Zürich

Subjects/Keywords: GAMMA-AMINOBUTTERSÄURE-REZEPTOREN (NEUROLOGIE); KOMPLEMENTÄRE DESOXYRIBONUKLEINSÄUREN; GENANALYSE (GENETISCHE TECHNIKEN); PROTEINKOMPLEXE; GAMMA-AMINOBUTYRIC ACID RECEPTORS (NEUROLOGY); COMPLEMENTARY DEOXYRIBONUCLEIC ACIDS (NUCLEIC ACIDS); GENE ANALYSIS (GENETIC TECHNIQUES); PROTEIN COMPLEXES; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Hellwig, R. (1999). Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/144005

Chicago Manual of Style (16th Edition):

Hellwig, Robert. “Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene.” 1999. Doctoral Dissertation, ETH Zürich. Accessed April 01, 2020. http://hdl.handle.net/20.500.11850/144005.

MLA Handbook (7th Edition):

Hellwig, Robert. “Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene.” 1999. Web. 01 Apr 2020.

Vancouver:

Hellwig R. Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene. [Internet] [Doctoral dissertation]. ETH Zürich; 1999. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/20.500.11850/144005.

Council of Science Editors:

Hellwig R. Identification of a candidate cDNA for BSF1, a protein recognising a DNA element in the GABAA receptor {delta} subunit gene. [Doctoral Dissertation]. ETH Zürich; 1999. Available from: http://hdl.handle.net/20.500.11850/144005


Georgia Tech

28. Agrawal, Amit. Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells.

Degree: PhD, Biomedical Engineering, 2006, Georgia Tech

 Semiconductor quantum dots (QDs) have emerged as a new class of fluorescent probes and labeling agents for biological samples. QDs are bright, highly photostable and… (more)

Subjects/Keywords: Immunoassay; Single molecule detection; Live cell imaging; Quantum dots; Fluorescence; Motor protein; Viral trafficking; Dynein; Microtubule; Spectroscopy; Respiratory syncytial virus; Spectrin; Nucleic acid; Nanotechnology; Intracellular delivery; Color colocalization; Proteins; Magneto optical; Enrichment; Nanoparticles; Molecular probes; Quantum dots; Fluorescent probes; Cells

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

APA (6th Edition):

Agrawal, A. (2006). Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/19798

Chicago Manual of Style (16th Edition):

Agrawal, Amit. “Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells.” 2006. Doctoral Dissertation, Georgia Tech. Accessed April 01, 2020. http://hdl.handle.net/1853/19798.

MLA Handbook (7th Edition):

Agrawal, Amit. “Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells.” 2006. Web. 01 Apr 2020.

Vancouver:

Agrawal A. Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2006. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/1853/19798.

Council of Science Editors:

Agrawal A. Nanoparticle Probes for Ultrasensitive Biological Detection and Motor Protein Tracking inside Living Cells. [Doctoral Dissertation]. Georgia Tech; 2006. Available from: http://hdl.handle.net/1853/19798


Oklahoma State University

29. Sun, Tzeli Julia. Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability.

Degree: Biochemistry, 1987, Oklahoma State University

Subjects/Keywords: gossypium hirsutum; xanthomonas campestris pv. malvacearum; 2,7-dihydroxycadalene; lacinilene c; sesquiterpenoid phytoalexins; photosensitizer; dna cleavage; active oxygen; deoxyribonuclease I; malate dehydrogenase; cauliflower mosaic virus; brassica rapa; photoactivation; dna-protein cross-linking; infectivity; cyshis box; nucleic acid binding domain; phytoalexin; antiviral

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APA (6th Edition):

Sun, T. J. (1987). Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/14410

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sun, Tzeli Julia. “Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability.” 1987. Thesis, Oklahoma State University. Accessed April 01, 2020. http://hdl.handle.net/11244/14410.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sun, Tzeli Julia. “Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability.” 1987. Web. 01 Apr 2020.

Vancouver:

Sun TJ. Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability. [Internet] [Thesis]. Oklahoma State University; 1987. [cited 2020 Apr 01]. Available from: http://hdl.handle.net/11244/14410.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sun TJ. Photoactivated DNA cleavage, enzyme inactivation, bacterial inhibition, and viral inactivation by the cotton phytoalexin 2,7-dihydroxycadalene, isolation of phytoalexin-resistant mutants of the cotton pathogen Xanthomonas campestris pv. malvacearum, and characterization of the pathogen's mutability. [Thesis]. Oklahoma State University; 1987. Available from: http://hdl.handle.net/11244/14410

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.