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You searched for subject:( Biosynthesis). Showing records 1 – 30 of 1311 total matches.

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Texas A&M University

1. Dey, Sanghamitra. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.

Degree: 2009, Texas A&M University

 Mycobacterium tuberculosis (Mtb) utilizes different metabolic pathways for its survival during infection. Enzymes of these pathways are often targets for antibiotic development. Genetic studies indicate… (more)

Subjects/Keywords: serine biosynthesis; biotin biosynthesis

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APA (6th Edition):

Dey, S. (2009). Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2882

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):

Dey, Sanghamitra. “Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.” 2009. Thesis, Texas A&M University. Accessed July 14, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2882.

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

MLA Handbook (7th Edition):

Dey, Sanghamitra. “Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.” 2009. Web. 14 Jul 2020.

Vancouver:

Dey S. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2882.

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

Council of Science Editors:

Dey S. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2882

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


University of Utah

2. Schwarz, Elisabeth Lisawaty. Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;.

Degree: MS;, Pathology;, 2006, University of Utah

 Lysyl hydroxylase is an ascorbate dependent enzyme responsible for the posttranslation hydroxylation of lysyl residues on procollagen molecules. Several isoforms of Lysyl hydroxylase, encoded by… (more)

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Schwarz, E. L. (2006). Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1212/rec/788

Chicago Manual of Style (16th Edition):

Schwarz, Elisabeth Lisawaty. “Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;.” 2006. Masters Thesis, University of Utah. Accessed July 14, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1212/rec/788.

MLA Handbook (7th Edition):

Schwarz, Elisabeth Lisawaty. “Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;.” 2006. Web. 14 Jul 2020.

Vancouver:

Schwarz EL. Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;. [Internet] [Masters thesis]. University of Utah; 2006. [cited 2020 Jul 14]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1212/rec/788.

Council of Science Editors:

Schwarz EL. Measurement of lysyl hydroxylase in fibroblasts by tandem mass spectrometry;. [Masters Thesis]. University of Utah; 2006. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1212/rec/788


University of Georgia

3. Hobson, David Richard. Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases.

Degree: MS, Biochemistry and Molecular Biology, 2010, University of Georgia

 Current gene annotation methods based on sequence similarity have greatly expanded the ability to search growing databases of genomic information. This system of identification falls… (more)

Subjects/Keywords: Heme biosynthesis

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APA (6th Edition):

Hobson, D. R. (2010). Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/hobson_david_r_201008_ms

Chicago Manual of Style (16th Edition):

Hobson, David Richard. “Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases.” 2010. Masters Thesis, University of Georgia. Accessed July 14, 2020. http://purl.galileo.usg.edu/uga_etd/hobson_david_r_201008_ms.

MLA Handbook (7th Edition):

Hobson, David Richard. “Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases.” 2010. Web. 14 Jul 2020.

Vancouver:

Hobson DR. Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases. [Internet] [Masters thesis]. University of Georgia; 2010. [cited 2020 Jul 14]. Available from: http://purl.galileo.usg.edu/uga_etd/hobson_david_r_201008_ms.

Council of Science Editors:

Hobson DR. Acinetobacter ADP1 as a system for in vivo identification of bacterial coproporphyrinogen III oxidases. [Masters Thesis]. University of Georgia; 2010. Available from: http://purl.galileo.usg.edu/uga_etd/hobson_david_r_201008_ms


University of Georgia

4. Thurmond, Stephanie. Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1.

Degree: MS, Genetics, 2014, University of Georgia

 As part of a large-scale regulatory investigation, cysteine biosynthesis was examined in a soil bacterium, Acinetobacter baylyi ADP1. This pathway involves the reductive assimilation of… (more)

Subjects/Keywords: Cysteine biosynthesis

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APA (6th Edition):

Thurmond, S. (2014). Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/thurmond_stephanie_201408_ms

Chicago Manual of Style (16th Edition):

Thurmond, Stephanie. “Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1.” 2014. Masters Thesis, University of Georgia. Accessed July 14, 2020. http://purl.galileo.usg.edu/uga_etd/thurmond_stephanie_201408_ms.

MLA Handbook (7th Edition):

Thurmond, Stephanie. “Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1.” 2014. Web. 14 Jul 2020.

Vancouver:

Thurmond S. Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1. [Internet] [Masters thesis]. University of Georgia; 2014. [cited 2020 Jul 14]. Available from: http://purl.galileo.usg.edu/uga_etd/thurmond_stephanie_201408_ms.

Council of Science Editors:

Thurmond S. Regulation of cysteine biosynthesis in Acinetobacter baylyi ADP1. [Masters Thesis]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/thurmond_stephanie_201408_ms


Macquarie University

5. Farmer, Phyllis Renee. In-planta studies of magnesium chelatase.

Degree: 2013, Macquarie University

"June 30, 2012"

Bibliography: pages 207-235.

1. Introduction  – 2. Cloning of Zea mays magnesium chelatase subunits  – 3. Phenotypic analysis of magnesium chelatase subunit… (more)

Subjects/Keywords: Tetrapyrroles  – Biosynthesis

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APA (6th Edition):

Farmer, P. R. (2013). In-planta studies of magnesium chelatase. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/264330

Chicago Manual of Style (16th Edition):

Farmer, Phyllis Renee. “In-planta studies of magnesium chelatase.” 2013. Doctoral Dissertation, Macquarie University. Accessed July 14, 2020. http://hdl.handle.net/1959.14/264330.

MLA Handbook (7th Edition):

Farmer, Phyllis Renee. “In-planta studies of magnesium chelatase.” 2013. Web. 14 Jul 2020.

Vancouver:

Farmer PR. In-planta studies of magnesium chelatase. [Internet] [Doctoral dissertation]. Macquarie University; 2013. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1959.14/264330.

Council of Science Editors:

Farmer PR. In-planta studies of magnesium chelatase. [Doctoral Dissertation]. Macquarie University; 2013. Available from: http://hdl.handle.net/1959.14/264330


McGill University

6. Dong, Dao Cong. Syntheses and reactivities of cage compounds.

Degree: PhD, Department of Chemistry., 1979, McGill University

Subjects/Keywords: Biosynthesis.

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APA (6th Edition):

Dong, D. C. (1979). Syntheses and reactivities of cage compounds. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile72707.pdf

Chicago Manual of Style (16th Edition):

Dong, Dao Cong. “Syntheses and reactivities of cage compounds.” 1979. Doctoral Dissertation, McGill University. Accessed July 14, 2020. http://digitool.library.mcgill.ca/thesisfile72707.pdf.

MLA Handbook (7th Edition):

Dong, Dao Cong. “Syntheses and reactivities of cage compounds.” 1979. Web. 14 Jul 2020.

Vancouver:

Dong DC. Syntheses and reactivities of cage compounds. [Internet] [Doctoral dissertation]. McGill University; 1979. [cited 2020 Jul 14]. Available from: http://digitool.library.mcgill.ca/thesisfile72707.pdf.

Council of Science Editors:

Dong DC. Syntheses and reactivities of cage compounds. [Doctoral Dissertation]. McGill University; 1979. Available from: http://digitool.library.mcgill.ca/thesisfile72707.pdf


Oregon State University

7. Ju, Shyh-chen. Biosynthesis of acivicin and 4-hydroxyacivicin.

Degree: PhD, Chemistry, 1988, Oregon State University

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Ju, S. (1988). Biosynthesis of acivicin and 4-hydroxyacivicin. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/37377

Chicago Manual of Style (16th Edition):

Ju, Shyh-chen. “Biosynthesis of acivicin and 4-hydroxyacivicin.” 1988. Doctoral Dissertation, Oregon State University. Accessed July 14, 2020. http://hdl.handle.net/1957/37377.

MLA Handbook (7th Edition):

Ju, Shyh-chen. “Biosynthesis of acivicin and 4-hydroxyacivicin.” 1988. Web. 14 Jul 2020.

Vancouver:

Ju S. Biosynthesis of acivicin and 4-hydroxyacivicin. [Internet] [Doctoral dissertation]. Oregon State University; 1988. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1957/37377.

Council of Science Editors:

Ju S. Biosynthesis of acivicin and 4-hydroxyacivicin. [Doctoral Dissertation]. Oregon State University; 1988. Available from: http://hdl.handle.net/1957/37377


Oregon State University

8. Hartz, Judith Ann. Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis.

Degree: MS, Biochemistry and Biophysics, 1967, Oregon State University

 Preliminary work on a crude in vitro system for glutamic-γ-semialdehyde synthesis in Escherichia coli has been described. The cell extract synthesis of GSA is inhibited… (more)

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Hartz, J. A. (1967). Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/47381

Chicago Manual of Style (16th Edition):

Hartz, Judith Ann. “Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis.” 1967. Masters Thesis, Oregon State University. Accessed July 14, 2020. http://hdl.handle.net/1957/47381.

MLA Handbook (7th Edition):

Hartz, Judith Ann. “Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis.” 1967. Web. 14 Jul 2020.

Vancouver:

Hartz JA. Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis. [Internet] [Masters thesis]. Oregon State University; 1967. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1957/47381.

Council of Science Editors:

Hartz JA. Synthesis of Glutamic-γ-semialdehyde in Escherichia coli : isolation of a low molecular weight compound required for in vitro synthesis: Isolation of a low molecular weight compound required for in vitro synthesis. [Masters Thesis]. Oregon State University; 1967. Available from: http://hdl.handle.net/1957/47381


Oregon State University

9. Adams, Gerald Springer. Isoprenoids of bovine aorta : isolation, purification, and biosynthesis.

Degree: PhD, Biochemistry and Biophysics, 1970, Oregon State University

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Adams, G. S. (1970). Isoprenoids of bovine aorta : isolation, purification, and biosynthesis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/45514

Chicago Manual of Style (16th Edition):

Adams, Gerald Springer. “Isoprenoids of bovine aorta : isolation, purification, and biosynthesis.” 1970. Doctoral Dissertation, Oregon State University. Accessed July 14, 2020. http://hdl.handle.net/1957/45514.

MLA Handbook (7th Edition):

Adams, Gerald Springer. “Isoprenoids of bovine aorta : isolation, purification, and biosynthesis.” 1970. Web. 14 Jul 2020.

Vancouver:

Adams GS. Isoprenoids of bovine aorta : isolation, purification, and biosynthesis. [Internet] [Doctoral dissertation]. Oregon State University; 1970. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1957/45514.

Council of Science Editors:

Adams GS. Isoprenoids of bovine aorta : isolation, purification, and biosynthesis. [Doctoral Dissertation]. Oregon State University; 1970. Available from: http://hdl.handle.net/1957/45514


University of Cambridge

10. Potter, Helen Katherine. Investigating intermediates in 6-methylsalicylic acid biosynthesis.

Degree: PhD, 2011, University of Cambridge

 6-Methylsalicylic acid (6-MSA) is one of the oldest known polyketides. It is synthesised in vivo by the polyketide synthase 6-methylsalicylic acid synthase (6-MSAS), a multifunctional… (more)

Subjects/Keywords: Biosynthesis; Polyketide

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APA (6th Edition):

Potter, H. K. (2011). Investigating intermediates in 6-methylsalicylic acid biosynthesis. (Doctoral Dissertation). University of Cambridge. Retrieved from http://www.dspace.cam.ac.uk/handle/1810/239407https://www.repository.cam.ac.uk/bitstream/1810/239407/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/239407/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/239407/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/239407/8/HPotter_final%20thesis%20for%20printing.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/9/HPotter_final%20thesis%20for%20printing.pdf.jpg

Chicago Manual of Style (16th Edition):

Potter, Helen Katherine. “Investigating intermediates in 6-methylsalicylic acid biosynthesis.” 2011. Doctoral Dissertation, University of Cambridge. Accessed July 14, 2020. http://www.dspace.cam.ac.uk/handle/1810/239407https://www.repository.cam.ac.uk/bitstream/1810/239407/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/239407/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/239407/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/239407/8/HPotter_final%20thesis%20for%20printing.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/9/HPotter_final%20thesis%20for%20printing.pdf.jpg.

MLA Handbook (7th Edition):

Potter, Helen Katherine. “Investigating intermediates in 6-methylsalicylic acid biosynthesis.” 2011. Web. 14 Jul 2020.

Vancouver:

Potter HK. Investigating intermediates in 6-methylsalicylic acid biosynthesis. [Internet] [Doctoral dissertation]. University of Cambridge; 2011. [cited 2020 Jul 14]. Available from: http://www.dspace.cam.ac.uk/handle/1810/239407https://www.repository.cam.ac.uk/bitstream/1810/239407/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/239407/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/239407/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/239407/8/HPotter_final%20thesis%20for%20printing.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/9/HPotter_final%20thesis%20for%20printing.pdf.jpg.

Council of Science Editors:

Potter HK. Investigating intermediates in 6-methylsalicylic acid biosynthesis. [Doctoral Dissertation]. University of Cambridge; 2011. Available from: http://www.dspace.cam.ac.uk/handle/1810/239407https://www.repository.cam.ac.uk/bitstream/1810/239407/2/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/3/license_url ; https://www.repository.cam.ac.uk/bitstream/1810/239407/4/license_text ; https://www.repository.cam.ac.uk/bitstream/1810/239407/5/license_rdf ; https://www.repository.cam.ac.uk/bitstream/1810/239407/8/HPotter_final%20thesis%20for%20printing.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/239407/9/HPotter_final%20thesis%20for%20printing.pdf.jpg


Cornell University

11. Zhu, Xuling. Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 .

Degree: 2011, Cornell University

 Diphthamide, the target of diphtheria toxin, is a unique posttranslational modification on eukaryotic and archaeal translation elongation factor 2 (EF2). The proposed biosynthesis of diphthamide… (more)

Subjects/Keywords: Diphthamide Biosynthesis

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APA (6th Edition):

Zhu, X. (2011). Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33651

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):

Zhu, Xuling. “Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 .” 2011. Thesis, Cornell University. Accessed July 14, 2020. http://hdl.handle.net/1813/33651.

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

MLA Handbook (7th Edition):

Zhu, Xuling. “Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 .” 2011. Web. 14 Jul 2020.

Vancouver:

Zhu X. Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1813/33651.

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

Council of Science Editors:

Zhu X. Diphthamide Biosynthesis: Characterization And Mechanistic Studies Of An Unconventional Radical Sam Enzyme Phdph2 . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33651

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


Michigan State University

12. Jia, Xiaofei. Delineation of aspects of kanosamine biosynthesis.

Degree: MS, Department of Chemistry, 2004, Michigan State University

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Jia, X. (2004). Delineation of aspects of kanosamine biosynthesis. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:33608

Chicago Manual of Style (16th Edition):

Jia, Xiaofei. “Delineation of aspects of kanosamine biosynthesis.” 2004. Masters Thesis, Michigan State University. Accessed July 14, 2020. http://etd.lib.msu.edu/islandora/object/etd:33608.

MLA Handbook (7th Edition):

Jia, Xiaofei. “Delineation of aspects of kanosamine biosynthesis.” 2004. Web. 14 Jul 2020.

Vancouver:

Jia X. Delineation of aspects of kanosamine biosynthesis. [Internet] [Masters thesis]. Michigan State University; 2004. [cited 2020 Jul 14]. Available from: http://etd.lib.msu.edu/islandora/object/etd:33608.

Council of Science Editors:

Jia X. Delineation of aspects of kanosamine biosynthesis. [Masters Thesis]. Michigan State University; 2004. Available from: http://etd.lib.msu.edu/islandora/object/etd:33608


Michigan State University

13. Reimann, Jessica Elizabeth. A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one.

Degree: PhD, Department of Chemistry, 1963, Michigan State University

Subjects/Keywords: Biosynthesis

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APA (6th Edition):

Reimann, J. E. (1963). A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35053

Chicago Manual of Style (16th Edition):

Reimann, Jessica Elizabeth. “A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one.” 1963. Doctoral Dissertation, Michigan State University. Accessed July 14, 2020. http://etd.lib.msu.edu/islandora/object/etd:35053.

MLA Handbook (7th Edition):

Reimann, Jessica Elizabeth. “A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one.” 1963. Web. 14 Jul 2020.

Vancouver:

Reimann JE. A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one. [Internet] [Doctoral dissertation]. Michigan State University; 1963. [cited 2020 Jul 14]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35053.

Council of Science Editors:

Reimann JE. A study on the biosynthesis of 2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one. [Doctoral Dissertation]. Michigan State University; 1963. Available from: http://etd.lib.msu.edu/islandora/object/etd:35053


Georgia Tech

14. Ichikawa, Hiroyuki. Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase.

Degree: PhD, Chemistry and Biochemistry, 2019, Georgia Tech

BIOSYNTHESIS OF THE THIOPEPTINS AND IDENTIFICATION OF AN F420H2-DEPENDENT DEHYDROPIPERIDINE REDUCTASE Hiro Ichikawa 230 pages Directed by Dr. Wendy L. Kelly Thiopeptins are highly decorated… (more)

Subjects/Keywords: Biosynthesis thiopeptide

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APA (6th Edition):

Ichikawa, H. (2019). Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62709

Chicago Manual of Style (16th Edition):

Ichikawa, Hiroyuki. “Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase.” 2019. Doctoral Dissertation, Georgia Tech. Accessed July 14, 2020. http://hdl.handle.net/1853/62709.

MLA Handbook (7th Edition):

Ichikawa, Hiroyuki. “Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase.” 2019. Web. 14 Jul 2020.

Vancouver:

Ichikawa H. Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/1853/62709.

Council of Science Editors:

Ichikawa H. Biosynthesis of the Thiopetins and Identification of an F420H2-Dependent Dehydropiperidine Reductase. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62709


Montana State University

15. Duffus, Benjamin Richard. Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG.

Degree: College of Letters & Science, 2014, Montana State University

 Iron-sulfur (Fe-S) clusters are ubiquitous in biology, and serve as catalysts in a vast array of chemical transformations that comprise central metabolic reactions and small… (more)

Subjects/Keywords: Adenosylmethionine.; Biosynthesis.; Hydrogenase.

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APA (6th Edition):

Duffus, B. R. (2014). Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9129

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):

Duffus, Benjamin Richard. “Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG.” 2014. Thesis, Montana State University. Accessed July 14, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9129.

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

MLA Handbook (7th Edition):

Duffus, Benjamin Richard. “Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG.” 2014. Web. 14 Jul 2020.

Vancouver:

Duffus BR. Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG. [Internet] [Thesis]. Montana State University; 2014. [cited 2020 Jul 14]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9129.

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

Council of Science Editors:

Duffus BR. Mechanism of diatomic ligand biosynthesis by radical s-adenosylmethionine [FeFe]-hydrogenase maturase HydG. [Thesis]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9129

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


University of Manchester

16. Chinnan Velmurugan, Karthikeyan. Halogenases for biosynthesis and biocatalysis.

Degree: 2014, University of Manchester

 Halogenation is an important chemical and biological process in the production of industrially important halogenated compounds. The presence of the halogen enhances the desirable properties… (more)

Subjects/Keywords: halogenation; biocatalysis; biosynthesis

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APA (6th Edition):

Chinnan Velmurugan, K. (2014). Halogenases for biosynthesis and biocatalysis. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:217896

Chicago Manual of Style (16th Edition):

Chinnan Velmurugan, Karthikeyan. “Halogenases for biosynthesis and biocatalysis.” 2014. Doctoral Dissertation, University of Manchester. Accessed July 14, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:217896.

MLA Handbook (7th Edition):

Chinnan Velmurugan, Karthikeyan. “Halogenases for biosynthesis and biocatalysis.” 2014. Web. 14 Jul 2020.

Vancouver:

Chinnan Velmurugan K. Halogenases for biosynthesis and biocatalysis. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Jul 14]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:217896.

Council of Science Editors:

Chinnan Velmurugan K. Halogenases for biosynthesis and biocatalysis. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:217896


Boston College

17. Guo, Wenyue. A study of structure and function of two enzymes in pyrimidine biosynthesis.

Degree: PhD, Chemistry, 2012, Boston College

 Nucleotides, the building blocks for nucleic acids, are essential for cell growth and replication. In E. coli the enzyme responsible for the regulation of pyrimidine… (more)

Subjects/Keywords: pyrimidine nucleotide biosynthesis

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APA (6th Edition):

Guo, W. (2012). A study of structure and function of two enzymes in pyrimidine biosynthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101896

Chicago Manual of Style (16th Edition):

Guo, Wenyue. “A study of structure and function of two enzymes in pyrimidine biosynthesis.” 2012. Doctoral Dissertation, Boston College. Accessed July 14, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101896.

MLA Handbook (7th Edition):

Guo, Wenyue. “A study of structure and function of two enzymes in pyrimidine biosynthesis.” 2012. Web. 14 Jul 2020.

Vancouver:

Guo W. A study of structure and function of two enzymes in pyrimidine biosynthesis. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2020 Jul 14]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101896.

Council of Science Editors:

Guo W. A study of structure and function of two enzymes in pyrimidine biosynthesis. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101896


University of Texas – Austin

18. Lin, Chia-I. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.

Degree: PhD, Chemistry, 2019, University of Texas – Austin

 The dissertation describes biosynthetic studies of lincomycin A, a thiosugarcontaining natural product. Lincomycin A was isolated from Streptomyces lincolnensis and has been used clinically as… (more)

Subjects/Keywords: Biosynthesis; Lincomycin; Thiosugar

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APA (6th Edition):

Lin, C. (2019). Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2237

Chicago Manual of Style (16th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed July 14, 2020. http://dx.doi.org/10.26153/tsw/2237.

MLA Handbook (7th Edition):

Lin, Chia-I. “Biosynthetic studies of lincomycin A, a thiosugar-containing natural product.” 2019. Web. 14 Jul 2020.

Vancouver:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Jul 14]. Available from: http://dx.doi.org/10.26153/tsw/2237.

Council of Science Editors:

Lin C. Biosynthetic studies of lincomycin A, a thiosugar-containing natural product. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2237


Purdue University

19. Sullivan, Kelly L. A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE.

Degree: PhD, Biochemistry, 2015, Purdue University

 Purines are the basic building block for essential biomolecules such as DNA, RNA, NADH, CoA, and several essential vitamin cofactors. Most organisms have the ability… (more)

Subjects/Keywords: PurE; Purine biosynthesis

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APA (6th Edition):

Sullivan, K. L. (2015). A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1190

Chicago Manual of Style (16th Edition):

Sullivan, Kelly L. “A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE.” 2015. Doctoral Dissertation, Purdue University. Accessed July 14, 2020. https://docs.lib.purdue.edu/open_access_dissertations/1190.

MLA Handbook (7th Edition):

Sullivan, Kelly L. “A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE.” 2015. Web. 14 Jul 2020.

Vancouver:

Sullivan KL. A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2020 Jul 14]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1190.

Council of Science Editors:

Sullivan KL. A Comparison of Functionally Divergent Forms of the Purine Biosynthesis Enzyme PurE. [Doctoral Dissertation]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1190


Hong Kong University of Science and Technology

20. Keung, Po Yee. Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027.

Degree: 2011, Hong Kong University of Science and Technology

 A hot-dog fold thioesterase is found in all known biosynthetic gene clusters of enediyne natural products. Previous studies have suggested that it is a type… (more)

Subjects/Keywords: Enediynes ; Biosynthesis ; Esterases

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APA (6th Edition):

Keung, P. Y. (2011). Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7383 ; https://doi.org/10.14711/thesis-b1155626 ; http://repository.ust.hk/ir/bitstream/1783.1-7383/1/th_redirect.html

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):

Keung, Po Yee. “Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed July 14, 2020. http://repository.ust.hk/ir/Record/1783.1-7383 ; https://doi.org/10.14711/thesis-b1155626 ; http://repository.ust.hk/ir/bitstream/1783.1-7383/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Keung, Po Yee. “Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027.” 2011. Web. 14 Jul 2020.

Vancouver:

Keung PY. Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Jul 14]. Available from: http://repository.ust.hk/ir/Record/1783.1-7383 ; https://doi.org/10.14711/thesis-b1155626 ; http://repository.ust.hk/ir/bitstream/1783.1-7383/1/th_redirect.html.

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

Council of Science Editors:

Keung PY. Characterization of the type II hot-dog thioesterase in biosynthesis of the nine-membered enediyne C-1027. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7383 ; https://doi.org/10.14711/thesis-b1155626 ; http://repository.ust.hk/ir/bitstream/1783.1-7383/1/th_redirect.html

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


University of Illinois – Urbana-Champaign

21. Melby, Joel Oliver. On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Thiazole/oxazole-modified microcins (TOMMs) comprise a family of ribosomally synthesized and post-translationally modified peptides (RiPPs) that all contain thiazole and oxazole heterocycles derived from cysteine, serine,… (more)

Subjects/Keywords: Natural Products; Biosynthesis

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APA (6th Edition):

Melby, J. O. (2015). On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/87954

Chicago Manual of Style (16th Edition):

Melby, Joel Oliver. “On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 14, 2020. http://hdl.handle.net/2142/87954.

MLA Handbook (7th Edition):

Melby, Joel Oliver. “On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides.” 2015. Web. 14 Jul 2020.

Vancouver:

Melby JO. On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/2142/87954.

Council of Science Editors:

Melby JO. On the biosynthesis and discovery of ribosomally synthesized and post-translationally modified peptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/87954


University of Cambridge

22. Potter, Helen Katherine. Investigating intermediates in 6-methylsalicylic acid biosynthesis.

Degree: PhD, 2011, University of Cambridge

 6-Methylsalicylic acid (6-MSA) is one of the oldest known polyketides. It is synthesised in vivo by the polyketide synthase 6-methylsalicylic acid synthase (6-MSAS), a multifunctional… (more)

Subjects/Keywords: 547.6; Biosynthesis; Polyketide

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APA (6th Edition):

Potter, H. K. (2011). Investigating intermediates in 6-methylsalicylic acid biosynthesis. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/239407 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541927

Chicago Manual of Style (16th Edition):

Potter, Helen Katherine. “Investigating intermediates in 6-methylsalicylic acid biosynthesis.” 2011. Doctoral Dissertation, University of Cambridge. Accessed July 14, 2020. https://www.repository.cam.ac.uk/handle/1810/239407 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541927.

MLA Handbook (7th Edition):

Potter, Helen Katherine. “Investigating intermediates in 6-methylsalicylic acid biosynthesis.” 2011. Web. 14 Jul 2020.

Vancouver:

Potter HK. Investigating intermediates in 6-methylsalicylic acid biosynthesis. [Internet] [Doctoral dissertation]. University of Cambridge; 2011. [cited 2020 Jul 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/239407 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541927.

Council of Science Editors:

Potter HK. Investigating intermediates in 6-methylsalicylic acid biosynthesis. [Doctoral Dissertation]. University of Cambridge; 2011. Available from: https://www.repository.cam.ac.uk/handle/1810/239407 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541927


Indian Institute of Science

23. Sapa, Hima Rani. Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants.

Degree: 2013, Indian Institute of Science

 Lipids are stored in a cell for providing energy. The main advantages of storing lipids over carbohydrates like glycogen is that, lipids yield more energy… (more)

Subjects/Keywords: Proteins; Diacylglycerol Acyltransferases; Triacylglycerol Biosynthesis; Storage Lipids; Yeast - Triacylglycerol Biosynthesis; Plants - Triacylglycerol Biosynthesis; Cutin Biosynthesis; Rhodotorula Glutinis - Storage Lipid Formation; Fatty Acids - Biosynthesis; Arabidopsis thaliana - Cutin Biosynthesis; Biochemistry

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APA (6th Edition):

Sapa, H. R. (2013). Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3399 ; http://etd.iisc.ernet.in/abstracts/4265/G25862-Abs.pdf

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):

Sapa, Hima Rani. “Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants.” 2013. Thesis, Indian Institute of Science. Accessed July 14, 2020. http://etd.iisc.ernet.in/2005/3399 ; http://etd.iisc.ernet.in/abstracts/4265/G25862-Abs.pdf.

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

MLA Handbook (7th Edition):

Sapa, Hima Rani. “Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants.” 2013. Web. 14 Jul 2020.

Vancouver:

Sapa HR. Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants. [Internet] [Thesis]. Indian Institute of Science; 2013. [cited 2020 Jul 14]. Available from: http://etd.iisc.ernet.in/2005/3399 ; http://etd.iisc.ernet.in/abstracts/4265/G25862-Abs.pdf.

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

Council of Science Editors:

Sapa HR. Implications of Soluble Diacylglycerol Acyltransferases in Triacylglycerol Biosynthesis in Yeast and Plants. [Thesis]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ernet.in/2005/3399 ; http://etd.iisc.ernet.in/abstracts/4265/G25862-Abs.pdf

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


University of Utah

24. Peabody, David Scott. Synthesis and binding properties of hybrid immunoglobulin light chain dimers.

Degree: PhD, Biochemistry;, 1981, University of Utah

 Bence-Jones proteins are dimers of identical immunoglobulin light chains held together by noncovalent interactions and a single interchain disulfide bond. They are structurally and functionally… (more)

Subjects/Keywords: Biosynthesis; Biochemistry

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APA (6th Edition):

Peabody, D. S. (1981). Synthesis and binding properties of hybrid immunoglobulin light chain dimers. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/497/rec/1124

Chicago Manual of Style (16th Edition):

Peabody, David Scott. “Synthesis and binding properties of hybrid immunoglobulin light chain dimers.” 1981. Doctoral Dissertation, University of Utah. Accessed July 14, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/497/rec/1124.

MLA Handbook (7th Edition):

Peabody, David Scott. “Synthesis and binding properties of hybrid immunoglobulin light chain dimers.” 1981. Web. 14 Jul 2020.

Vancouver:

Peabody DS. Synthesis and binding properties of hybrid immunoglobulin light chain dimers. [Internet] [Doctoral dissertation]. University of Utah; 1981. [cited 2020 Jul 14]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/497/rec/1124.

Council of Science Editors:

Peabody DS. Synthesis and binding properties of hybrid immunoglobulin light chain dimers. [Doctoral Dissertation]. University of Utah; 1981. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/497/rec/1124


University of Utah

25. Winters, Suzanne. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1987, University of Utah

 Poly(ethylene oxide) has some unique solubility and hydrogen-bonding characteristics which have been used to explain its apparent inertness with regard to blood protein absorption and… (more)

Subjects/Keywords: Pharmacokinetics; Biosynthesis

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APA (6th Edition):

Winters, S. (1987). Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646

Chicago Manual of Style (16th Edition):

Winters, Suzanne. “Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.” 1987. Doctoral Dissertation, University of Utah. Accessed July 14, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646.

MLA Handbook (7th Edition):

Winters, Suzanne. “Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;.” 1987. Web. 14 Jul 2020.

Vancouver:

Winters S. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. [Internet] [Doctoral dissertation]. University of Utah; 1987. [cited 2020 Jul 14]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646.

Council of Science Editors:

Winters S. Immobilized heparin via a long chain poly(ethylene oxide) spacer for protein and platelet compatibility;. [Doctoral Dissertation]. University of Utah; 1987. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/523/rec/646


University of Georgia

26. Yuan, Shenghua. Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.).

Degree: PhD, Forest Resources, 2006, University of Georgia

 This dissertation describes investigations into the gene structure and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase in loblolly pine (Pinus taeda L.). A cDNA clone, PtACO1, and… (more)

Subjects/Keywords: Ethylene biosynthesis

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APA (6th Edition):

Yuan, S. (2006). Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.). (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/yuan_shenghua_200605_phd

Chicago Manual of Style (16th Edition):

Yuan, Shenghua. “Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.).” 2006. Doctoral Dissertation, University of Georgia. Accessed July 14, 2020. http://purl.galileo.usg.edu/uga_etd/yuan_shenghua_200605_phd.

MLA Handbook (7th Edition):

Yuan, Shenghua. “Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.).” 2006. Web. 14 Jul 2020.

Vancouver:

Yuan S. Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.). [Internet] [Doctoral dissertation]. University of Georgia; 2006. [cited 2020 Jul 14]. Available from: http://purl.galileo.usg.edu/uga_etd/yuan_shenghua_200605_phd.

Council of Science Editors:

Yuan S. Promoters and regulation of 1-aminocyclopropane-1-carboxylate (ACC) oxidase genes from loblolly pine (Pinus taeda L.). [Doctoral Dissertation]. University of Georgia; 2006. Available from: http://purl.galileo.usg.edu/uga_etd/yuan_shenghua_200605_phd

27. Celis Luna, Arianna I. A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC).

Degree: College of Letters & Science, 2018, Montana State University

 Heme b is one of nature's most ancient and versatile co-factors and is essential for aerobic life. As such, heme b is synthesized by almost… (more)

Subjects/Keywords: Heme.; Biosynthesis.; Bacteria.; Lyases.; Catalysts.

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APA (6th Edition):

Celis Luna, A. I. (2018). A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC). (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/14685

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):

Celis Luna, Arianna I. “A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC).” 2018. Thesis, Montana State University. Accessed July 14, 2020. https://scholarworks.montana.edu/xmlui/handle/1/14685.

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

MLA Handbook (7th Edition):

Celis Luna, Arianna I. “A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC).” 2018. Web. 14 Jul 2020.

Vancouver:

Celis Luna AI. A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC). [Internet] [Thesis]. Montana State University; 2018. [cited 2020 Jul 14]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14685.

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

Council of Science Editors:

Celis Luna AI. A molecular, structural, and cellular multiple-level study aimed at understanding the unique reaction catalyzed by the last enzyme in the heme-biosynthesis pathway of gram-positive bacteria, coproheme decarboxylase (CHDC). [Thesis]. Montana State University; 2018. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14685

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


Montana State University

28. Partovi, Sarah Eve. The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2.

Degree: College of Letters & Science, 2018, Montana State University

 The metabolically versatile bacterium Xanthobacter autotrophicus Py2 has been the focus of many studies within the field of bioenergy sciences, as it contains two unique… (more)

Subjects/Keywords: Enzymes.; Biosynthesis.; Bacteria.; Carbon dioxide.

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APA (6th Edition):

Partovi, S. E. (2018). The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/14189

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):

Partovi, Sarah Eve. “The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2.” 2018. Thesis, Montana State University. Accessed July 14, 2020. https://scholarworks.montana.edu/xmlui/handle/1/14189.

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

MLA Handbook (7th Edition):

Partovi, Sarah Eve. “The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2.” 2018. Web. 14 Jul 2020.

Vancouver:

Partovi SE. The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2. [Internet] [Thesis]. Montana State University; 2018. [cited 2020 Jul 14]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14189.

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

Council of Science Editors:

Partovi SE. The coenzyme M biosynthetic pathway in proteobacterium Xanthobacter autotrophicus Py2. [Thesis]. Montana State University; 2018. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14189

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


University of Utah

29. Martin, Robert Packard. Biochemical conversion of progesterone to orchic androgens;.

Degree: PhD, Biochemistry;, 1956, University of Utah

 1. A new system of chromatography has been described which allows resolution of the less polar steroids“ such as cholesterol and congeners. It is a… (more)

Subjects/Keywords: Physiology; Biosynthesis

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

APA (6th Edition):

Martin, R. P. (1956). Biochemical conversion of progesterone to orchic androgens;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/365/rec/98

Chicago Manual of Style (16th Edition):

Martin, Robert Packard. “Biochemical conversion of progesterone to orchic androgens;.” 1956. Doctoral Dissertation, University of Utah. Accessed July 14, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/365/rec/98.

MLA Handbook (7th Edition):

Martin, Robert Packard. “Biochemical conversion of progesterone to orchic androgens;.” 1956. Web. 14 Jul 2020.

Vancouver:

Martin RP. Biochemical conversion of progesterone to orchic androgens;. [Internet] [Doctoral dissertation]. University of Utah; 1956. [cited 2020 Jul 14]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/365/rec/98.

Council of Science Editors:

Martin RP. Biochemical conversion of progesterone to orchic androgens;. [Doctoral Dissertation]. University of Utah; 1956. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/365/rec/98


University of Pretoria

30. Du Plessis, David Johannes Francois. Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population.

Degree: Microbiology and Plant Pathology, 2009, University of Pretoria

 Pseudomonas aeruginosa, a ubiquitous environmental bacterium and an opportunistic human pathogen, forms biofilms through a series of interactions between the cells and adherence to surfaces.… (more)

Subjects/Keywords: Rhamnolipid biosynthesis; Pseudomonas aeruginosa; UCTD

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

APA (6th Edition):

Du Plessis, D. J. (2009). Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/27353

Chicago Manual of Style (16th Edition):

Du Plessis, David Johannes. “Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population.” 2009. Masters Thesis, University of Pretoria. Accessed July 14, 2020. http://hdl.handle.net/2263/27353.

MLA Handbook (7th Edition):

Du Plessis, David Johannes. “Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population.” 2009. Web. 14 Jul 2020.

Vancouver:

Du Plessis DJ. Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population. [Internet] [Masters thesis]. University of Pretoria; 2009. [cited 2020 Jul 14]. Available from: http://hdl.handle.net/2263/27353.

Council of Science Editors:

Du Plessis DJ. Regulation of rhamnolipid biosynthesis in the Pseudomonas aeruginosa PAOI biofilm population. [Masters Thesis]. University of Pretoria; 2009. Available from: http://hdl.handle.net/2263/27353

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