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You searched for subject:(site directed mutagenesis). Showing records 1 – 30 of 169 total matches.

[1] [2] [3] [4] [5] [6]

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NSYSU

1. Wu, Chun-Yi. Interaction between KLIP1 and SUMO-1.

Degree: Master, Biological Sciences, 2011, NSYSU

 Nuclear protein KLIP1 cooperates with myeloid leukemia factor 1 (MLF1) to inhibit the programmed cell death resulting in tumor formation. It also inhibits the activity… (more)

Subjects/Keywords: KLIP1; SUMO-1; site-directed mutagenesis

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APA (6th Edition):

Wu, C. (2011). Interaction between KLIP1 and SUMO-1. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014

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):

Wu, Chun-Yi. “Interaction between KLIP1 and SUMO-1.” 2011. Thesis, NSYSU. Accessed December 04, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014.

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

MLA Handbook (7th Edition):

Wu, Chun-Yi. “Interaction between KLIP1 and SUMO-1.” 2011. Web. 04 Dec 2020.

Vancouver:

Wu C. Interaction between KLIP1 and SUMO-1. [Internet] [Thesis]. NSYSU; 2011. [cited 2020 Dec 04]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014.

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

Council of Science Editors:

Wu C. Interaction between KLIP1 and SUMO-1. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0905111-105014

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


Stellenbosch University

2. De Villiers, Jacques Izak. Mutagenesis studies of a glycoside hydrolase family 2 enzyme.

Degree: MSc, Genetics, 2015, Stellenbosch University

ENGLISH ABSTRACT: Galactooligosaccharides are produced by the transglycosylation activity of β-galactosidases (β-gal, EC 3.2.1.23) when utilising lactose as a substrate. They have emerged as important… (more)

Subjects/Keywords: Beta-galactosidase; Site directed-mutagenesis; Exopolymer; UCTD

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APA (6th Edition):

De Villiers, J. I. (2015). Mutagenesis studies of a glycoside hydrolase family 2 enzyme. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/98110

Chicago Manual of Style (16th Edition):

De Villiers, Jacques Izak. “Mutagenesis studies of a glycoside hydrolase family 2 enzyme.” 2015. Masters Thesis, Stellenbosch University. Accessed December 04, 2020. http://hdl.handle.net/10019.1/98110.

MLA Handbook (7th Edition):

De Villiers, Jacques Izak. “Mutagenesis studies of a glycoside hydrolase family 2 enzyme.” 2015. Web. 04 Dec 2020.

Vancouver:

De Villiers JI. Mutagenesis studies of a glycoside hydrolase family 2 enzyme. [Internet] [Masters thesis]. Stellenbosch University; 2015. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10019.1/98110.

Council of Science Editors:

De Villiers JI. Mutagenesis studies of a glycoside hydrolase family 2 enzyme. [Masters Thesis]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/98110


Florida International University

3. Wang, Zheng. Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants.

Degree: Chemistry, 2011, Florida International University

  Mechanistically and structurally chloroperoxidase (CPO) occupies a unique niche among heme containing enzymes. Chloroperoxidase catalyzes a broad range of reactions, such as oxidation of… (more)

Subjects/Keywords: chloroperoxidase. enantioselectivity; site-directed mutagenesis; epoxidation; F103A

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APA (6th Edition):

Wang, Z. (2011). Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants. (Thesis). Florida International University. Retrieved from https://digitalcommons.fiu.edu/etd/414 ; 10.25148/etd.FI11050313 ; FI11050313

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):

Wang, Zheng. “Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants.” 2011. Thesis, Florida International University. Accessed December 04, 2020. https://digitalcommons.fiu.edu/etd/414 ; 10.25148/etd.FI11050313 ; FI11050313.

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

MLA Handbook (7th Edition):

Wang, Zheng. “Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants.” 2011. Web. 04 Dec 2020.

Vancouver:

Wang Z. Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants. [Internet] [Thesis]. Florida International University; 2011. [cited 2020 Dec 04]. Available from: https://digitalcommons.fiu.edu/etd/414 ; 10.25148/etd.FI11050313 ; FI11050313.

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

Council of Science Editors:

Wang Z. Characterization of Recombinant Chloroperoxidase, and F103A and C29H/C79H/C87H Mutants. [Thesis]. Florida International University; 2011. Available from: https://digitalcommons.fiu.edu/etd/414 ; 10.25148/etd.FI11050313 ; FI11050313

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


NSYSU

4. Lin, Cheng-Lin. Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis.

Degree: Master, Biological Sciences, 2000, NSYSU

 The genetic defects that results in TAL1 oncogene activation are commonly seen in leukemic cells of the patient with T-cell Acute Lymphoblastic Leukemia ( T-ALL… (more)

Subjects/Keywords: TAL1 oncoprotein; site-directed mutagenesis

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APA (6th Edition):

Lin, C. (2000). Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0711100-144111

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):

Lin, Cheng-Lin. “Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis.” 2000. Thesis, NSYSU. Accessed December 04, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0711100-144111.

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

MLA Handbook (7th Edition):

Lin, Cheng-Lin. “Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis.” 2000. Web. 04 Dec 2020.

Vancouver:

Lin C. Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis. [Internet] [Thesis]. NSYSU; 2000. [cited 2020 Dec 04]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0711100-144111.

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

Council of Science Editors:

Lin C. Studying of the DNA binding of Tal1 oncoprotein by Site-Directed Mutagenesis. [Thesis]. NSYSU; 2000. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0711100-144111

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


University of Saskatchewan

5. Chen, Jian An. Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase.

Degree: 2011, University of Saskatchewan

 Lactococcus lactis, prolidase (Llaprol) hydrolyzes Xaa-Pro dipeptides. Since Xaa-Pro is known as bitter peptides, Llaprol is potentially applicable to reduce bitterness of fermented foods. Llaprol… (more)

Subjects/Keywords: Site-directed mutagenesis; Allosteric subsite; X-ray diffraction

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APA (6th Edition):

Chen, J. A. (2011). Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-02252011-095142

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):

Chen, Jian An. “Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase.” 2011. Thesis, University of Saskatchewan. Accessed December 04, 2020. http://hdl.handle.net/10388/etd-02252011-095142.

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

MLA Handbook (7th Edition):

Chen, Jian An. “Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase.” 2011. Web. 04 Dec 2020.

Vancouver:

Chen JA. Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10388/etd-02252011-095142.

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

Council of Science Editors:

Chen JA. Structure-function relationship study of a loop structure in allosteric behaviour and substrate inhibition of Lactococcus lactis prolidase. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/etd-02252011-095142

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


Universidade Nova

6. Alves, Márcia Maria da Silva. hCES2: studies on the role of glycosylation in activity.

Degree: 2013, Universidade Nova

Dissertação para obtenção do Grau de Mestre em Genética Molecular e Biomedicina

Human carboxylesterase 2 (hCES2) is becoming more relevant due to its role in… (more)

Subjects/Keywords: Carboxylesterase; Glycosylation; Deglycosylation; PNGase F; Tunicamycin; Site directed mutagenesis

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APA (6th Edition):

Alves, M. M. d. S. (2013). hCES2: studies on the role of glycosylation in activity. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10896

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):

Alves, Márcia Maria da Silva. “hCES2: studies on the role of glycosylation in activity.” 2013. Thesis, Universidade Nova. Accessed December 04, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10896.

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

MLA Handbook (7th Edition):

Alves, Márcia Maria da Silva. “hCES2: studies on the role of glycosylation in activity.” 2013. Web. 04 Dec 2020.

Vancouver:

Alves MMdS. hCES2: studies on the role of glycosylation in activity. [Internet] [Thesis]. Universidade Nova; 2013. [cited 2020 Dec 04]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10896.

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

Council of Science Editors:

Alves MMdS. hCES2: studies on the role of glycosylation in activity. [Thesis]. Universidade Nova; 2013. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10896

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


University of Ontario Institute of Technology

7. Salgado, Luis Fernando. Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus.

Degree: 2015, University of Ontario Institute of Technology

 In nature, polysaccharides, such as cellulose, are important biopolymers involved in numerous biological functions including prevention of cellular desiccation, energy storage, osmoregulation, and cell wall… (more)

Subjects/Keywords: Gluconacetobacter xylinus; Bacterial cellulose; Cellulose synthase; Pellicin; Site-directed mutagenesis

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APA (6th Edition):

Salgado, L. F. (2015). Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus. (Thesis). University of Ontario Institute of Technology. Retrieved from http://hdl.handle.net/10155/551

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):

Salgado, Luis Fernando. “Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus.” 2015. Thesis, University of Ontario Institute of Technology. Accessed December 04, 2020. http://hdl.handle.net/10155/551.

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

MLA Handbook (7th Edition):

Salgado, Luis Fernando. “Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus.” 2015. Web. 04 Dec 2020.

Vancouver:

Salgado LF. Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus. [Internet] [Thesis]. University of Ontario Institute of Technology; 2015. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10155/551.

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

Council of Science Editors:

Salgado LF. Genetic analysis of cellulose crystallization in Gluconacetobacter xylinus. [Thesis]. University of Ontario Institute of Technology; 2015. Available from: http://hdl.handle.net/10155/551

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


East Tennessee State University

8. Khaja, Sara. Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase.

Degree: MS, Biology, 2014, East Tennessee State University

  Flavonoids are plant secondary metabolites that have significant biochemical and physiological roles. Biosynthesis of these compounds involves several modifications, most predominantly glucosylation, which is… (more)

Subjects/Keywords: glucosyltransferase; flavonoids; Citrus; site-directed mutagenesis; Biochemistry; Biology; Plant Biology

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APA (6th Edition):

Khaja, S. (2014). Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase. (Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2453

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):

Khaja, Sara. “Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase.” 2014. Thesis, East Tennessee State University. Accessed December 04, 2020. https://dc.etsu.edu/etd/2453.

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

MLA Handbook (7th Edition):

Khaja, Sara. “Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase.” 2014. Web. 04 Dec 2020.

Vancouver:

Khaja S. Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase. [Internet] [Thesis]. East Tennessee State University; 2014. [cited 2020 Dec 04]. Available from: https://dc.etsu.edu/etd/2453.

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

Council of Science Editors:

Khaja S. Site-Directed Mutagenesis in Citrus paradisi Flavonol-Specific 3-O-Glucosyltransferase. [Thesis]. East Tennessee State University; 2014. Available from: https://dc.etsu.edu/etd/2453

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


University of Georgia

9. Kelley, Laura-Lee Clancy. Co-crystallization recombinant mouse antibody fragment library biotechnology.

Degree: 2014, University of Georgia

 Co-crystallization recombinant antibody fragments (crFabs) are antibody fragments derived from a parent antibody fragment that can be used to assemble a 3- dimensional matrix (crystal).… (more)

Subjects/Keywords: Antibody fragment library; Multi-site directed mutagenesis; Biotechnology; Crystallization

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APA (6th Edition):

Kelley, L. C. (2014). Co-crystallization recombinant mouse antibody fragment library biotechnology. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/20818

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):

Kelley, Laura-Lee Clancy. “Co-crystallization recombinant mouse antibody fragment library biotechnology.” 2014. Thesis, University of Georgia. Accessed December 04, 2020. http://hdl.handle.net/10724/20818.

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

MLA Handbook (7th Edition):

Kelley, Laura-Lee Clancy. “Co-crystallization recombinant mouse antibody fragment library biotechnology.” 2014. Web. 04 Dec 2020.

Vancouver:

Kelley LC. Co-crystallization recombinant mouse antibody fragment library biotechnology. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10724/20818.

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

Council of Science Editors:

Kelley LC. Co-crystallization recombinant mouse antibody fragment library biotechnology. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/20818

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


University of Pretoria

10. Van Wyk, Stefan George. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis .

Degree: 2011, University of Pretoria

 Novel conserved amino acid variations of papaya cystatin (PC) were investigated by amino acid substitutions using oryzacystatin-I (OCI) as a model plant cystatin for comparison.… (more)

Subjects/Keywords: Oryzacystatin; Papaya cystatin; Site-directed mutagenesis; Cysteine protease inhibitor; Inhibitor engineering; UCTD

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APA (6th Edition):

Van Wyk, S. G. (2011). Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-09192011-174830/

Chicago Manual of Style (16th Edition):

Van Wyk, Stefan George. “Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis .” 2011. Masters Thesis, University of Pretoria. Accessed December 04, 2020. http://upetd.up.ac.za/thesis/available/etd-09192011-174830/.

MLA Handbook (7th Edition):

Van Wyk, Stefan George. “Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis .” 2011. Web. 04 Dec 2020.

Vancouver:

Van Wyk SG. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis . [Internet] [Masters thesis]. University of Pretoria; 2011. [cited 2020 Dec 04]. Available from: http://upetd.up.ac.za/thesis/available/etd-09192011-174830/.

Council of Science Editors:

Van Wyk SG. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis . [Masters Thesis]. University of Pretoria; 2011. Available from: http://upetd.up.ac.za/thesis/available/etd-09192011-174830/


University of Texas Southwestern Medical Center

11. Sherbet, Daniel P. Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2.

Degree: 2006, University of Texas Southwestern Medical Center

 The 17beta -hydroxysteroid dehydrogenases (17beta -HSDs) types 1 and 2 interconvert the weak and potent estrogens estrone and 17beta -estradiol. In intact cells, each enzyme… (more)

Subjects/Keywords: Hydroxysteroid Dehydrogenases; Mutagenesis, Site-Directed; Chimeras

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APA (6th Edition):

Sherbet, D. P. (2006). Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/608

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):

Sherbet, Daniel P. “Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2.” 2006. Thesis, University of Texas Southwestern Medical Center. Accessed December 04, 2020. http://hdl.handle.net/2152.5/608.

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

MLA Handbook (7th Edition):

Sherbet, Daniel P. “Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2.” 2006. Web. 04 Dec 2020.

Vancouver:

Sherbet DP. Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2006. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2152.5/608.

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

Council of Science Editors:

Sherbet DP. Structural and Physiologic Determinants of Estrone/Estradiol Metabolism Catalyzed by Human 17beta -Hydroxysteroid Dehydrogenases Types 1 and 2. [Thesis]. University of Texas Southwestern Medical Center; 2006. Available from: http://hdl.handle.net/2152.5/608

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


University of Pretoria

12. Van Wyk, Stefan George. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis.

Degree: Plant Science, 2011, University of Pretoria

 Novel conserved amino acid variations of papaya cystatin (PC) were investigated by amino acid substitutions using oryzacystatin-I (OCI) as a model plant cystatin for comparison.… (more)

Subjects/Keywords: Oryzacystatin; Papaya cystatin; Site-directed mutagenesis; Cysteine protease inhibitor; Inhibitor engineering; UCTD

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

APA (6th Edition):

Van Wyk, S. G. (2011). Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/28047

Chicago Manual of Style (16th Edition):

Van Wyk, Stefan George. “Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis.” 2011. Masters Thesis, University of Pretoria. Accessed December 04, 2020. http://hdl.handle.net/2263/28047.

MLA Handbook (7th Edition):

Van Wyk, Stefan George. “Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis.” 2011. Web. 04 Dec 2020.

Vancouver:

Van Wyk SG. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis. [Internet] [Masters thesis]. University of Pretoria; 2011. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/2263/28047.

Council of Science Editors:

Van Wyk SG. Improving the inhibitory potency of papaya cystatin, using site-directed mutagenesis. [Masters Thesis]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/28047

13. André, Éric. Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin.

Degree: Docteur es, Chimie, 2017, Université Paris-Saclay (ComUE)

La neuroglobine humaine (Ngb) est une globine découverte en 2000 dont la fonction principale demeure encore inconnue. Par comparaison avec l’hémoglobine (Hb) et la myoglobine… (more)

Subjects/Keywords: Neuroglobine; Mutagénèse dirigée; Cinétique de réaction; Neuroglobin; Site-directed mutagenesis; Ligang binding kinetics

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APA (6th Edition):

André, E. (2017). Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS145

Chicago Manual of Style (16th Edition):

André, Éric. “Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 04, 2020. http://www.theses.fr/2017SACLS145.

MLA Handbook (7th Edition):

André, Éric. “Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin.” 2017. Web. 04 Dec 2020.

Vancouver:

André E. Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2017SACLS145.

Council of Science Editors:

André E. Étude de l’influence de modifications structurales sur la neuroglobine humaine : Study of the influence of structural modifications on the human neuroglobin. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS145

14. Alberti, Jean-Christophe. Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive.

Degree: Docteur es, Aspects moleculaires et cellulaires de la biologie, 2013, Corte

Les lipoxygénases (LOX, EC 1.13.11.12) sont des dioxygénases à fer non héminique très répandues. Chez les végétaux, ces enzymes sont à l’origine d’une voie métabolique… (more)

Subjects/Keywords: Lipoxygénase; Olive; Mutagénèse dirigée; Oxydation; Galactolipides; Lipoxygenase; Olive; Site-directed mutagenesis; Oxidation; Galactolipids; 572.8

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

APA (6th Edition):

Alberti, J. (2013). Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive. (Doctoral Dissertation). Corte. Retrieved from http://www.theses.fr/2013CORT0009

Chicago Manual of Style (16th Edition):

Alberti, Jean-Christophe. “Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive.” 2013. Doctoral Dissertation, Corte. Accessed December 04, 2020. http://www.theses.fr/2013CORT0009.

MLA Handbook (7th Edition):

Alberti, Jean-Christophe. “Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive.” 2013. Web. 04 Dec 2020.

Vancouver:

Alberti J. Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive. [Internet] [Doctoral dissertation]. Corte; 2013. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2013CORT0009.

Council of Science Editors:

Alberti J. Etude du mécanisme catalytique de la lipoxygenase 1 d’olive : Study of the catalytic mechanism of lipoxygenase 1 Olive. [Doctoral Dissertation]. Corte; 2013. Available from: http://www.theses.fr/2013CORT0009


University of Manchester

15. Hamdan, Mohd Fadhli Bin. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.

Degree: 2018, University of Manchester

 The first aim of this thesis was to exploit homologous recombination between two 1.4kb imperfect rbcL direct repeats (2.4% base divergence) to generate novel plastid… (more)

Subjects/Keywords: Plant biotechnology; Recombination; Rubisco modification; Site-directed mutagenesis; Dendra2; Photoconvertible fluorescent protein

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APA (6th Edition):

Hamdan, M. F. B. (2018). Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313836

Chicago Manual of Style (16th Edition):

Hamdan, Mohd Fadhli Bin. “Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.” 2018. Doctoral Dissertation, University of Manchester. Accessed December 04, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313836.

MLA Handbook (7th Edition):

Hamdan, Mohd Fadhli Bin. “Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.” 2018. Web. 04 Dec 2020.

Vancouver:

Hamdan MFB. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Dec 04]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313836.

Council of Science Editors:

Hamdan MFB. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313836

16. Meaden, Christopher W. Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1.

Degree: MS(M.S.), Molecular & Cellular Biology, 2010, U of Massachusetts : Masters

 Pac1/LIS1, an essential tip tracking protein of the WD40 super family, is required to target cytoplasmic dynein to the plus ends of astral microtubules in… (more)

Subjects/Keywords: Saccharomyces cerevisiae; dynein; LIS1; site directed mutagenesis; lissencephaly; mitosis; Life Sciences; Medicine and Health Sciences

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APA (6th Edition):

Meaden, C. W. (2010). Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/452

Chicago Manual of Style (16th Edition):

Meaden, Christopher W. “Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1.” 2010. Masters Thesis, U of Massachusetts : Masters. Accessed December 04, 2020. http://scholarworks.umass.edu/theses/452.

MLA Handbook (7th Edition):

Meaden, Christopher W. “Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1.” 2010. Web. 04 Dec 2020.

Vancouver:

Meaden CW. Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2010. [cited 2020 Dec 04]. Available from: http://scholarworks.umass.edu/theses/452.

Council of Science Editors:

Meaden CW. Identification of Dynein Binding Sites in Budding Yeast Pac1/LIS1. [Masters Thesis]. U of Massachusetts : Masters; 2010. Available from: http://scholarworks.umass.edu/theses/452


University of Western Ontario

17. Al Massri, Shahed. Characterizing the Cofactor Specificity of NQO2.

Degree: 2017, University of Western Ontario

 Quinone Reductase 2 (NQO2) is a part of an enzyme family implicated in detoxification of the cell. This enzyme differs from its highly similar sister… (more)

Subjects/Keywords: NQO1; NQO2; quinone oxidoreductase; enzyme kinetics; site-directed mutagenesis; cofactor specificity; Biochemistry

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

APA (6th Edition):

Al Massri, S. (2017). Characterizing the Cofactor Specificity of NQO2. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4586

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):

Al Massri, Shahed. “Characterizing the Cofactor Specificity of NQO2.” 2017. Thesis, University of Western Ontario. Accessed December 04, 2020. https://ir.lib.uwo.ca/etd/4586.

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

MLA Handbook (7th Edition):

Al Massri, Shahed. “Characterizing the Cofactor Specificity of NQO2.” 2017. Web. 04 Dec 2020.

Vancouver:

Al Massri S. Characterizing the Cofactor Specificity of NQO2. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2020 Dec 04]. Available from: https://ir.lib.uwo.ca/etd/4586.

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

Council of Science Editors:

Al Massri S. Characterizing the Cofactor Specificity of NQO2. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4586

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


University of Toronto

18. Hajighasemi, Mahbod. Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases.

Degree: PhD, 2017, University of Toronto

Several types of biodegradable polyesters with different physical properties have emerged to replace traditional petroleum-based polymers, including polylactic acid (PLA). However, the lack of a… (more)

Subjects/Keywords: biochemical characterization; biodegradable plastic; enzyme discovery; polyesterase; protein structure; site-directed mutagenesis; 0487

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

APA (6th Edition):

Hajighasemi, M. (2017). Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/93587

Chicago Manual of Style (16th Edition):

Hajighasemi, Mahbod. “Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases.” 2017. Doctoral Dissertation, University of Toronto. Accessed December 04, 2020. http://hdl.handle.net/1807/93587.

MLA Handbook (7th Edition):

Hajighasemi, Mahbod. “Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases.” 2017. Web. 04 Dec 2020.

Vancouver:

Hajighasemi M. Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1807/93587.

Council of Science Editors:

Hajighasemi M. Enzymatic Depolymerization of Synthetic Polyesters by Microbial Carboxylesterases. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/93587


University of Toronto

19. Dungan, Sarah. The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition.

Degree: PhD, 2018, University of Toronto

 Cetaceans (whales and dolphins) are fully aquatic mammals that have captured the imagination of biologists due to their iconic evolutionary transformation from terrestrial ancestors. Nevertheless,… (more)

Subjects/Keywords: adaptive evolution; codon models; protein evolution; site-directed mutagenesis; visual ecology; visual pigments; 0412

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APA (6th Edition):

Dungan, S. (2018). The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89712

Chicago Manual of Style (16th Edition):

Dungan, Sarah. “The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition.” 2018. Doctoral Dissertation, University of Toronto. Accessed December 04, 2020. http://hdl.handle.net/1807/89712.

MLA Handbook (7th Edition):

Dungan, Sarah. “The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition.” 2018. Web. 04 Dec 2020.

Vancouver:

Dungan S. The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/1807/89712.

Council of Science Editors:

Dungan S. The Molecular Evolution of Cetacean Dim-Light Vision: In Vitro Studies of Rhodopsin Over a Macroevolutionary Transition. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89712

20. Impellizzeri, Agata Antonina Rita. Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation.

Degree: 2012, Università degli Studi di Catania

 Serotonin (5-hydroxytryptamine, 5-HT) is a key neurotransmitter implicated in neuropsychiatric disturbance such as depression, anxiety and psychosis. Recent studies on knockout animals and using selective… (more)

Subjects/Keywords: Area 05 - Scienze biologiche; 5-HT7(a) serotonin receptor, site-directed mutagenesis, binding, activation

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APA (6th Edition):

Impellizzeri, A. A. R. (2012). Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/1169

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):

Impellizzeri, Agata Antonina Rita. “Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation.” 2012. Thesis, Università degli Studi di Catania. Accessed December 04, 2020. http://hdl.handle.net/10761/1169.

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

MLA Handbook (7th Edition):

Impellizzeri, Agata Antonina Rita. “Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation.” 2012. Web. 04 Dec 2020.

Vancouver:

Impellizzeri AAR. Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation. [Internet] [Thesis]. Università degli Studi di Catania; 2012. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10761/1169.

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

Council of Science Editors:

Impellizzeri AAR. Site-directed mutagenesis and molecular modeling studies of h5-HT7(a) receptor reveal important residues for binding and activation. [Thesis]. Università degli Studi di Catania; 2012. Available from: http://hdl.handle.net/10761/1169

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


Louisiana State University

21. Fontenot, Elena Batista. The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters.

Degree: PhD, 2014, Louisiana State University

 Phosphorus is an essential nutrient taken up by plants in the form of phosphate and is a component of key molecules, such as ATP, DNA,… (more)

Subjects/Keywords: transport; site-directed mutagenesis; phosphate; oligomerization; uptake; high-affinity phosphate transporters; arsenate; Arabidopsis thaliana

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APA (6th Edition):

Fontenot, E. B. (2014). The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-11122014-211555 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1256

Chicago Manual of Style (16th Edition):

Fontenot, Elena Batista. “The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters.” 2014. Doctoral Dissertation, Louisiana State University. Accessed December 04, 2020. etd-11122014-211555 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1256.

MLA Handbook (7th Edition):

Fontenot, Elena Batista. “The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters.” 2014. Web. 04 Dec 2020.

Vancouver:

Fontenot EB. The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters. [Internet] [Doctoral dissertation]. Louisiana State University; 2014. [cited 2020 Dec 04]. Available from: etd-11122014-211555 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1256.

Council of Science Editors:

Fontenot EB. The Effect of Modifying the Higher-Order Structure of Plant High-Affinity Phosphate Transporters. [Doctoral Dissertation]. Louisiana State University; 2014. Available from: etd-11122014-211555 ; https://digitalcommons.lsu.edu/gradschool_dissertations/1256


University of Manchester

22. Hamdan, Mohd Fadhli. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.

Degree: PhD, 2019, University of Manchester

 The first aim of this thesis was to exploit homologous recombination between two 1.4kb imperfect rbcL direct repeats (2.4% base divergence) to generate novel plastid… (more)

Subjects/Keywords: Photoconvertible fluorescent protein; Site-directed mutagenesis; Dendra2; Recombination; Plant biotechnology; Rubisco modification

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APA (6th Edition):

Hamdan, M. F. (2019). Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-plastid-recombination-and-fluorescent-protein-expression-in-transplastomic-plants(c433c5ed-6d25-42ad-af13-f2959c07bcc4).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.804092

Chicago Manual of Style (16th Edition):

Hamdan, Mohd Fadhli. “Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.” 2019. Doctoral Dissertation, University of Manchester. Accessed December 04, 2020. https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-plastid-recombination-and-fluorescent-protein-expression-in-transplastomic-plants(c433c5ed-6d25-42ad-af13-f2959c07bcc4).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.804092.

MLA Handbook (7th Edition):

Hamdan, Mohd Fadhli. “Analysis of plastid recombination and fluorescent protein expression in transplastomic plants.” 2019. Web. 04 Dec 2020.

Vancouver:

Hamdan MF. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Dec 04]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-plastid-recombination-and-fluorescent-protein-expression-in-transplastomic-plants(c433c5ed-6d25-42ad-af13-f2959c07bcc4).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.804092.

Council of Science Editors:

Hamdan MF. Analysis of plastid recombination and fluorescent protein expression in transplastomic plants. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/analysis-of-plastid-recombination-and-fluorescent-protein-expression-in-transplastomic-plants(c433c5ed-6d25-42ad-af13-f2959c07bcc4).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.804092


Bowling Green State University

23. Cholewa, Kelly M. Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein.

Degree: MS, Biological Sciences, 2016, Bowling Green State University

 The TonB energy transduction complex (TonB, ExbB, and ExbD) couples the proton motive force (PMF) to acquire and transport iron in gram-negative bacteria. ExbD is… (more)

Subjects/Keywords: Biology; Microbiology; Molecular Biology; ExbD; TonB System; Site-Directed Mutagenesis; E coli

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APA (6th Edition):

Cholewa, K. M. (2016). Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein. (Masters Thesis). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1479398493813069

Chicago Manual of Style (16th Edition):

Cholewa, Kelly M. “Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein.” 2016. Masters Thesis, Bowling Green State University. Accessed December 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1479398493813069.

MLA Handbook (7th Edition):

Cholewa, Kelly M. “Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein.” 2016. Web. 04 Dec 2020.

Vancouver:

Cholewa KM. Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein. [Internet] [Masters thesis]. Bowling Green State University; 2016. [cited 2020 Dec 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1479398493813069.

Council of Science Editors:

Cholewa KM. Identification of Potential TonB-Interactive Sites in the Periplasmic Domain of the ExbD Protein. [Masters Thesis]. Bowling Green State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1479398493813069


University of Kentucky

24. Mei, Xiaonan. HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE.

Degree: 2012, University of Kentucky

 A mutation (CTG to TTG) of FeSOD gene was found in Escherichia coli. Since they both encode leucine, it is a silent mutation. Site-­‐directed mutagenesis(more)

Subjects/Keywords: Iron-­‐containing superoxide dismutase; Metalloenzyme; Metal incorporation; Silent mutation; Site-­‐directed mutagenesis; EPR; Chemistry

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APA (6th Edition):

Mei, X. (2012). HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE. (Masters Thesis). University of Kentucky. Retrieved from https://uknowledge.uky.edu/chemistry_etds/9

Chicago Manual of Style (16th Edition):

Mei, Xiaonan. “HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE.” 2012. Masters Thesis, University of Kentucky. Accessed December 04, 2020. https://uknowledge.uky.edu/chemistry_etds/9.

MLA Handbook (7th Edition):

Mei, Xiaonan. “HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE.” 2012. Web. 04 Dec 2020.

Vancouver:

Mei X. HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE. [Internet] [Masters thesis]. University of Kentucky; 2012. [cited 2020 Dec 04]. Available from: https://uknowledge.uky.edu/chemistry_etds/9.

Council of Science Editors:

Mei X. HOW A SILENT MUTATION SUPPRESSES THE ACTIVITY AND IRON INCORPORATION IN SUPEROXIDE DISMUTASE. [Masters Thesis]. University of Kentucky; 2012. Available from: https://uknowledge.uky.edu/chemistry_etds/9


Virginia Tech

25. Shrestha, Manisha. Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa.

Degree: PhD, Biological Sciences, 2018, Virginia Tech

 Pseudomonas aeruginosa is a ubiquitous opportunistic pathogen that is a substantial threat, particularly in hospital settings, causing severe infections in immunocompromised patients that may lead… (more)

Subjects/Keywords: transcription activator; type three secretion system; pseudomonas aeruginosa; Crystal structure; site-directed mutagenesis

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APA (6th Edition):

Shrestha, M. (2018). Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/95966

Chicago Manual of Style (16th Edition):

Shrestha, Manisha. “Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa.” 2018. Doctoral Dissertation, Virginia Tech. Accessed December 04, 2020. http://hdl.handle.net/10919/95966.

MLA Handbook (7th Edition):

Shrestha, Manisha. “Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa.” 2018. Web. 04 Dec 2020.

Vancouver:

Shrestha M. Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2020 Dec 04]. Available from: http://hdl.handle.net/10919/95966.

Council of Science Editors:

Shrestha M. Mechanistic Studies of the Roles of the Transcriptional Activator ExsA and Anti-activator Protein ExsD in the Regulation of the Type Three Secretion System in Pseudomonas aeruginosa. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/95966


NSYSU

26. Lin, Li-cheng. Site-directed mutagenesis of TSG101 function domain.

Degree: Master, Biological Sciences, 2005, NSYSU

 TSG101 is a tumor susceptibility gene exhibits multiple biological function, including the regulation of cell progression, intracellular protein sorting and membrane trafficking, and transcription activity… (more)

Subjects/Keywords: TSG101; PTAP; sumoylation; site-directed mutagenesis; ub

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APA (6th Edition):

Lin, L. (2005). Site-directed mutagenesis of TSG101 function domain. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0218105-170416

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):

Lin, Li-cheng. “Site-directed mutagenesis of TSG101 function domain.” 2005. Thesis, NSYSU. Accessed December 04, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0218105-170416.

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

MLA Handbook (7th Edition):

Lin, Li-cheng. “Site-directed mutagenesis of TSG101 function domain.” 2005. Web. 04 Dec 2020.

Vancouver:

Lin L. Site-directed mutagenesis of TSG101 function domain. [Internet] [Thesis]. NSYSU; 2005. [cited 2020 Dec 04]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0218105-170416.

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

Council of Science Editors:

Lin L. Site-directed mutagenesis of TSG101 function domain. [Thesis]. NSYSU; 2005. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0218105-170416

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

27. Wang, Zhongya. AAV based site-specific integration in vivo.

Degree: MS, 2007, Oregon Health Sciences University

Subjects/Keywords: Adenoviruses, Human; Gene Therapy; Mutagenesis, Site-Directed

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APA (6th Edition):

Wang, Z. (2007). AAV based site-specific integration in vivo. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M42N508G ; http://digitalcommons.ohsu.edu/etd/843

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):

Wang, Zhongya. “AAV based site-specific integration in vivo.” 2007. Thesis, Oregon Health Sciences University. Accessed December 04, 2020. doi:10.6083/M42N508G ; http://digitalcommons.ohsu.edu/etd/843.

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

MLA Handbook (7th Edition):

Wang, Zhongya. “AAV based site-specific integration in vivo.” 2007. Web. 04 Dec 2020.

Vancouver:

Wang Z. AAV based site-specific integration in vivo. [Internet] [Thesis]. Oregon Health Sciences University; 2007. [cited 2020 Dec 04]. Available from: doi:10.6083/M42N508G ; http://digitalcommons.ohsu.edu/etd/843.

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

Council of Science Editors:

Wang Z. AAV based site-specific integration in vivo. [Thesis]. Oregon Health Sciences University; 2007. Available from: doi:10.6083/M42N508G ; http://digitalcommons.ohsu.edu/etd/843

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

28. Lan, Hongxiang. Structure and function of dopamine receptors : ligand binding and arrestin binding.

Degree: PhD, 2006, Oregon Health Sciences University

Subjects/Keywords: Receptors, Dopamine; Ligands; Arrestin; Mutagenesis, Site-Directed

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APA (6th Edition):

Lan, H. (2006). Structure and function of dopamine receptors : ligand binding and arrestin binding. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4GB2297 ; http://digitalcommons.ohsu.edu/etd/2891

Chicago Manual of Style (16th Edition):

Lan, Hongxiang. “Structure and function of dopamine receptors : ligand binding and arrestin binding.” 2006. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 04, 2020. doi:10.6083/M4GB2297 ; http://digitalcommons.ohsu.edu/etd/2891.

MLA Handbook (7th Edition):

Lan, Hongxiang. “Structure and function of dopamine receptors : ligand binding and arrestin binding.” 2006. Web. 04 Dec 2020.

Vancouver:

Lan H. Structure and function of dopamine receptors : ligand binding and arrestin binding. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2006. [cited 2020 Dec 04]. Available from: doi:10.6083/M4GB2297 ; http://digitalcommons.ohsu.edu/etd/2891.

Council of Science Editors:

Lan H. Structure and function of dopamine receptors : ligand binding and arrestin binding. [Doctoral Dissertation]. Oregon Health Sciences University; 2006. Available from: doi:10.6083/M4GB2297 ; http://digitalcommons.ohsu.edu/etd/2891

29. Cox, Barbara Alden. Characterization of dopamine D2 and D3 receptors.

Degree: PhD, 1993, Oregon Health Sciences University

Subjects/Keywords: Receptors, Dopamine D2; Receptors, Dopamine; Ligands; Mutagenesis, Site-Directed

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APA (6th Edition):

Cox, B. A. (1993). Characterization of dopamine D2 and D3 receptors. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4RR1WC9 ; http://digitalcommons.ohsu.edu/etd/1720

Chicago Manual of Style (16th Edition):

Cox, Barbara Alden. “Characterization of dopamine D2 and D3 receptors.” 1993. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 04, 2020. doi:10.6083/M4RR1WC9 ; http://digitalcommons.ohsu.edu/etd/1720.

MLA Handbook (7th Edition):

Cox, Barbara Alden. “Characterization of dopamine D2 and D3 receptors.” 1993. Web. 04 Dec 2020.

Vancouver:

Cox BA. Characterization of dopamine D2 and D3 receptors. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1993. [cited 2020 Dec 04]. Available from: doi:10.6083/M4RR1WC9 ; http://digitalcommons.ohsu.edu/etd/1720.

Council of Science Editors:

Cox BA. Characterization of dopamine D2 and D3 receptors. [Doctoral Dissertation]. Oregon Health Sciences University; 1993. Available from: doi:10.6083/M4RR1WC9 ; http://digitalcommons.ohsu.edu/etd/1720

30. Barou, Emilie. De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses.

Degree: Docteur es, Chimie, 2014, Université de Bourgogne

La détection de molécules odorantes représente un enjeu important dans divers domaines tels que l’industrie alimentaire, le diagnostic médical et la sécurité du territoire, par… (more)

Subjects/Keywords: OBP; Électrochimie; Biocapteurs; Mutagenèse dirigée; Voltammétrie à vagues carrées; OBP; Electrochemistry; Biosensors; Site-directed mutagenesis; Square-wave voltammetry; 541.37

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

APA (6th Edition):

Barou, E. (2014). De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2014DIJOS045

Chicago Manual of Style (16th Edition):

Barou, Emilie. “De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses.” 2014. Doctoral Dissertation, Université de Bourgogne. Accessed December 04, 2020. http://www.theses.fr/2014DIJOS045.

MLA Handbook (7th Edition):

Barou, Emilie. “De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses.” 2014. Web. 04 Dec 2020.

Vancouver:

Barou E. De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2014. [cited 2020 Dec 04]. Available from: http://www.theses.fr/2014DIJOS045.

Council of Science Editors:

Barou E. De l'ingénierie de protéines de liaison aux odorants à la détection électrochimique de molécules volatiles : vers la conception de biocapteurs et nez électroniques : From odorant-binding protein engineering to electrochemical detection of volatile molecules : towards design of biosensors and electronic noses. [Doctoral Dissertation]. Université de Bourgogne; 2014. Available from: http://www.theses.fr/2014DIJOS045

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