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University: University of California – Berkeley

You searched for subject:( Biochemistry). Showing records 1 – 30 of 189 total matches.

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University of California – Berkeley

1. Dietrich, Jeffrey Allen. Transcription Factor-Based Small-Molecule Screens and Selections.

Degree: Bioengineering, 2011, University of California – Berkeley

 Directed evolution of E. coli for improved small-molecule production requires a combination of rational design and high-throughput screening technologies. Rational design-based directed evolution schemes use… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Dietrich, J. A. (2011). Transcription Factor-Based Small-Molecule Screens and Selections. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7j6805gf

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):

Dietrich, Jeffrey Allen. “Transcription Factor-Based Small-Molecule Screens and Selections.” 2011. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/7j6805gf.

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

MLA Handbook (7th Edition):

Dietrich, Jeffrey Allen. “Transcription Factor-Based Small-Molecule Screens and Selections.” 2011. Web. 18 Oct 2019.

Vancouver:

Dietrich JA. Transcription Factor-Based Small-Molecule Screens and Selections. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/7j6805gf.

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

Council of Science Editors:

Dietrich JA. Transcription Factor-Based Small-Molecule Screens and Selections. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/7j6805gf

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


University of California – Berkeley

2. Wong, Roger Hoi Fung. Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c.

Degree: Comparative Biochemistry, 2010, University of California – Berkeley

 Transcription of genes encoding enzymes involved in fatty acid and triacylglycerol synthesis, including fatty acid synthase and mitochondrial glycerol-3-phosphate acyltransferase, is coordinately induced in lipogenic… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Wong, R. H. F. (2010). Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3zc4j28d

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):

Wong, Roger Hoi Fung. “Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/3zc4j28d.

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

MLA Handbook (7th Edition):

Wong, Roger Hoi Fung. “Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c.” 2010. Web. 18 Oct 2019.

Vancouver:

Wong RHF. Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/3zc4j28d.

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

Council of Science Editors:

Wong RHF. Regulation of lipogenic gene transcription during fasting and feeding/insulin: Role of USF, SREBP-1c, and BAF60c. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/3zc4j28d

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


University of California – Berkeley

3. Hejab, Nisreen M A. Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies.

Degree: Comparative Biochemistry, 2016, University of California – Berkeley

 Microtubules (MTs) are essential components of the eukaryotic cytoskeleton. They form by the polymerization of tubulin into cylindrical polymers composed of protofilaments. MTs are involved… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Hejab, N. M. A. (2016). Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7zb0x85p

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):

Hejab, Nisreen M A. “Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/7zb0x85p.

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

MLA Handbook (7th Edition):

Hejab, Nisreen M A. “Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies.” 2016. Web. 18 Oct 2019.

Vancouver:

Hejab NMA. Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/7zb0x85p.

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

Council of Science Editors:

Hejab NMA. Characterization of Tau and Anticancer Drug Interactions with Microtubules via Cryo-Electron Microscopy Studies. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/7zb0x85p

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


University of California – Berkeley

4. Fernhoff, Nathaniel Bernard. On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology.

Degree: Molecular & Cell Biology, 2010, University of California – Berkeley

 Nitric oxide (NO) is an important physiological mediator of vasodilation, platelet aggregation, and neurotransmission. An NO signal regulates these processes by signal transduction through the… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Fernhoff, N. B. (2010). On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2cq0g1wq

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):

Fernhoff, Nathaniel Bernard. “On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/2cq0g1wq.

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

MLA Handbook (7th Edition):

Fernhoff, Nathaniel Bernard. “On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology.” 2010. Web. 18 Oct 2019.

Vancouver:

Fernhoff NB. On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/2cq0g1wq.

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

Council of Science Editors:

Fernhoff NB. On the Molecular Mechanisms of Functional and Dysfunction NO Signaling in Mammalian Physiology. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/2cq0g1wq

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


University of California – Berkeley

5. Dunkle, Jack A. Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics.

Degree: Molecular & Cell Biology, 2010, University of California – Berkeley

 Protein synthesis takes place in four stages: initiation, elongation, termination and recycling. Elongation consists of delivery of a charged tRNA to the ribosome, peptide bond… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Dunkle, J. A. (2010). Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/49m7m9bs

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):

Dunkle, Jack A. “Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/49m7m9bs.

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

MLA Handbook (7th Edition):

Dunkle, Jack A. “Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics.” 2010. Web. 18 Oct 2019.

Vancouver:

Dunkle JA. Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/49m7m9bs.

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

Council of Science Editors:

Dunkle JA. Structural Studies of the Elongation Cycle of Protein Synthesis and Its Inhibition by Antibiotics. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/49m7m9bs

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


University of California – Berkeley

6. Shen, Sam. In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes.

Degree: Chemistry, 2010, University of California – Berkeley

 In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytesThe function of adipocytes was initially thought to be fat storage, thermal insulation,… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Shen, S. (2010). In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8br113n1

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):

Shen, Sam. “In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/8br113n1.

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

MLA Handbook (7th Edition):

Shen, Sam. “In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes.” 2010. Web. 18 Oct 2019.

Vancouver:

Shen S. In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/8br113n1.

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

Council of Science Editors:

Shen S. In search of a physiological role for amine oxidase,copper containing-3 (AOC3) in adipocytes. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/8br113n1

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


University of California – Berkeley

7. Olszewski, Michal M. Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway.

Degree: Molecular & Cell Biology, 2018, University of California – Berkeley

 The ubiquitin proteasome system (UPS) controls essential cellular processes such as cell cycle progression, cellular signaling, stress responses and maintenance of protein folding homeostasis via… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Olszewski, M. M. (2018). Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1h25d3p8

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):

Olszewski, Michal M. “Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway.” 2018. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/1h25d3p8.

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

MLA Handbook (7th Edition):

Olszewski, Michal M. “Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway.” 2018. Web. 18 Oct 2019.

Vancouver:

Olszewski MM. Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway. [Internet] [Thesis]. University of California – Berkeley; 2018. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/1h25d3p8.

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

Council of Science Editors:

Olszewski MM. Role of Cdc48 unfoldase in the ubiquitin-proteasome proteolytic pathway. [Thesis]. University of California – Berkeley; 2018. Available from: http://www.escholarship.org/uc/item/1h25d3p8

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


University of California – Berkeley

8. Liu, Joyce. Biosynthesis and Heterologous Expression of Medicinally Active Natural Products.

Degree: Bioengineering, 2016, University of California – Berkeley

 Natural products have long been appreciated for their potent biological activities, and their unique scaffolds and pharmacophores have served as inspiration for many pharmaceuticals. As… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Liu, J. (2016). Biosynthesis and Heterologous Expression of Medicinally Active Natural Products. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5qt4j4tc

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):

Liu, Joyce. “Biosynthesis and Heterologous Expression of Medicinally Active Natural Products.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/5qt4j4tc.

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

MLA Handbook (7th Edition):

Liu, Joyce. “Biosynthesis and Heterologous Expression of Medicinally Active Natural Products.” 2016. Web. 18 Oct 2019.

Vancouver:

Liu J. Biosynthesis and Heterologous Expression of Medicinally Active Natural Products. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/5qt4j4tc.

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

Council of Science Editors:

Liu J. Biosynthesis and Heterologous Expression of Medicinally Active Natural Products. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/5qt4j4tc

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


University of California – Berkeley

9. Lawson, Michael Robert. Mechanistic Studies of the Rho Helicase.

Degree: Molecular & Cell Biology, 2016, University of California – Berkeley

 All cellular organisms rely on transcriptional regulatory mechanisms to control the levels and timing of gene expression. Bacterial transcription is in part regulated by Rho,… (more)

Subjects/Keywords: Biochemistry

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

APA (6th Edition):

Lawson, M. R. (2016). Mechanistic Studies of the Rho Helicase. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9m20v9bb

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):

Lawson, Michael Robert. “Mechanistic Studies of the Rho Helicase.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/9m20v9bb.

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

MLA Handbook (7th Edition):

Lawson, Michael Robert. “Mechanistic Studies of the Rho Helicase.” 2016. Web. 18 Oct 2019.

Vancouver:

Lawson MR. Mechanistic Studies of the Rho Helicase. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/9m20v9bb.

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

Council of Science Editors:

Lawson MR. Mechanistic Studies of the Rho Helicase. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/9m20v9bb

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


University of California – Berkeley

10. Ad, Omer. Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase.

Degree: Chemistry, 2017, University of California – Berkeley

 Macrolide natural products have been a rich source of medicinally relevant molecules. Macrolides are assembled by large protein complexes known as polyketide synthases (PKSs) via… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Ad, O. (2017). Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7fq3w7m3

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):

Ad, Omer. “Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase.” 2017. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/7fq3w7m3.

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

MLA Handbook (7th Edition):

Ad, Omer. “Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase.” 2017. Web. 18 Oct 2019.

Vancouver:

Ad O. Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/7fq3w7m3.

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

Council of Science Editors:

Ad O. Engineered production of fluorinated polyketides inspired by mechanistic studies of a polyketide synthase. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/7fq3w7m3

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


University of California – Berkeley

11. Agarwal, Paresh. Chemical Methods to Modify Proteins and Glycans.

Degree: Chemistry, 2015, University of California – Berkeley

 The ability to chemically modify biomolecules has facilitated our ability to detect, manipulate, and study them both in vitro and in vivo, as well as… (more)

Subjects/Keywords: Chemistry; Biochemistry

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

APA (6th Edition):

Agarwal, P. (2015). Chemical Methods to Modify Proteins and Glycans. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/16x9d1ss

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):

Agarwal, Paresh. “Chemical Methods to Modify Proteins and Glycans.” 2015. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/16x9d1ss.

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

MLA Handbook (7th Edition):

Agarwal, Paresh. “Chemical Methods to Modify Proteins and Glycans.” 2015. Web. 18 Oct 2019.

Vancouver:

Agarwal P. Chemical Methods to Modify Proteins and Glycans. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/16x9d1ss.

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

Council of Science Editors:

Agarwal P. Chemical Methods to Modify Proteins and Glycans. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/16x9d1ss

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


University of California – Berkeley

12. Hatzios, Stavroula. Investigations of Metabolic Pathways in Mycobacterium tuberculosis.

Degree: Chemistry, 2010, University of California – Berkeley

 Mycobacterium tuberculosis (Mtb), the bacterium that causes tuberculosis in humans, infects roughly two billion people worldwide. However, less than one percent of infected individuals are… (more)

Subjects/Keywords: Chemistry; Biochemistry

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APA (6th Edition):

Hatzios, S. (2010). Investigations of Metabolic Pathways in Mycobacterium tuberculosis. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9jn7277b

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):

Hatzios, Stavroula. “Investigations of Metabolic Pathways in Mycobacterium tuberculosis.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/9jn7277b.

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

MLA Handbook (7th Edition):

Hatzios, Stavroula. “Investigations of Metabolic Pathways in Mycobacterium tuberculosis.” 2010. Web. 18 Oct 2019.

Vancouver:

Hatzios S. Investigations of Metabolic Pathways in Mycobacterium tuberculosis. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/9jn7277b.

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

Council of Science Editors:

Hatzios S. Investigations of Metabolic Pathways in Mycobacterium tuberculosis. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/9jn7277b

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


University of California – Berkeley

13. Bond-Watts, Brooks Bennett. Construction and characterization of an n-butanol synthetic pathway in Escherichia coli.

Degree: Chemistry, 2013, University of California – Berkeley

 A diverse array of molecular functions has evolved in biological systems. The ability to reorganize and utilize these remarkable capabilities in order to design pathways… (more)

Subjects/Keywords: Chemistry; Biochemistry

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APA (6th Edition):

Bond-Watts, B. B. (2013). Construction and characterization of an n-butanol synthetic pathway in Escherichia coli. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6rg5z7qm

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):

Bond-Watts, Brooks Bennett. “Construction and characterization of an n-butanol synthetic pathway in Escherichia coli.” 2013. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/6rg5z7qm.

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

MLA Handbook (7th Edition):

Bond-Watts, Brooks Bennett. “Construction and characterization of an n-butanol synthetic pathway in Escherichia coli.” 2013. Web. 18 Oct 2019.

Vancouver:

Bond-Watts BB. Construction and characterization of an n-butanol synthetic pathway in Escherichia coli. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/6rg5z7qm.

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

Council of Science Editors:

Bond-Watts BB. Construction and characterization of an n-butanol synthetic pathway in Escherichia coli. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6rg5z7qm

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

14. Haurwitz, Rachel Elizabeth. The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs.

Degree: Molecular & Cell Biology, 2012, University of California – Berkeley

 Many prokaryotes contain clustered regularly interspaced short palindromic repeats (CRISPRs) that together with CRISPR-associated (cas) genes confer resistance to invasive genetic elements. Central to this… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Haurwitz, R. E. (2012). The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0rh5940p

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):

Haurwitz, Rachel Elizabeth. “The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs.” 2012. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/0rh5940p.

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

MLA Handbook (7th Edition):

Haurwitz, Rachel Elizabeth. “The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs.” 2012. Web. 18 Oct 2019.

Vancouver:

Haurwitz RE. The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/0rh5940p.

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

Council of Science Editors:

Haurwitz RE. The CRISPR endoribonuclease Csy4 utilizes unusual sequence- and structure-specific mechanisms to recognize and process crRNAs. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/0rh5940p

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


University of California – Berkeley

15. Patel, Kieren Jay. Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts.

Degree: Molecular & Cell Biology, 2011, University of California – Berkeley

 Cytoplasmic Linker Associated Proteins (CLASPs) comprise a class of microtubule (MT) plus end-binding proteins (+Tips) that contribute to the dynamics and organization of MTs during… (more)

Subjects/Keywords: Molecular biology; Biochemistry

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APA (6th Edition):

Patel, K. J. (2011). Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7s38c9s3

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):

Patel, Kieren Jay. “Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts.” 2011. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/7s38c9s3.

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

MLA Handbook (7th Edition):

Patel, Kieren Jay. “Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts.” 2011. Web. 18 Oct 2019.

Vancouver:

Patel KJ. Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/7s38c9s3.

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

Council of Science Editors:

Patel KJ. Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/7s38c9s3

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

16. Craney, Allison Christine. Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The Anaphase Promoting Complex (APC/C) is a multi-subunit ubiquitin ligase that is essential for cell cycle progression. Ube2S and Ube2C are dedicated APC/C E2-conjuating enzymes… (more)

Subjects/Keywords: Cellular biology; Biochemistry

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APA (6th Edition):

Craney, A. C. (2015). Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9rm2b4h1

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):

Craney, Allison Christine. “Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation.” 2015. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/9rm2b4h1.

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

MLA Handbook (7th Edition):

Craney, Allison Christine. “Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation.” 2015. Web. 18 Oct 2019.

Vancouver:

Craney AC. Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/9rm2b4h1.

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

Council of Science Editors:

Craney AC. Dual mechanism for APC/C activation by integrated ubiquitylation and dephosphorylation. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/9rm2b4h1

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


University of California – Berkeley

17. Dedeo, Michel Toussaint. Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus.

Degree: Chemistry, 2012, University of California – Berkeley

 The utility of a previously developed TMV-based light harvesting system has been dramatically expanded through the introduction of reactive handles for the site-specific modification of… (more)

Subjects/Keywords: Nanotechnology; Chemistry; Biochemistry

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APA (6th Edition):

Dedeo, M. T. (2012). Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4fz7j4vf

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):

Dedeo, Michel Toussaint. “Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus.” 2012. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/4fz7j4vf.

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

MLA Handbook (7th Edition):

Dedeo, Michel Toussaint. “Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus.” 2012. Web. 18 Oct 2019.

Vancouver:

Dedeo MT. Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/4fz7j4vf.

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

Council of Science Editors:

Dedeo MT. Development of Scaffolds for Light Harvesting and Photocatalysis from the Coat Protein of Tobacco Mosaic Virus. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/4fz7j4vf

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


University of California – Berkeley

18. Noland, Cameron Ladd. Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference.

Degree: Molecular & Cell Biology, 2012, University of California – Berkeley

 RNA interference (RNAi) pathways are critical eukaryotic post-transcriptional gene regulatory systems that control the expression of at least one third of all human coding genes.… (more)

Subjects/Keywords: Biochemistry; Molecular biology

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APA (6th Edition):

Noland, C. L. (2012). Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6dm4z1j9

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):

Noland, Cameron Ladd. “Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference.” 2012. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/6dm4z1j9.

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

MLA Handbook (7th Edition):

Noland, Cameron Ladd. “Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference.” 2012. Web. 18 Oct 2019.

Vancouver:

Noland CL. Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/6dm4z1j9.

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

Council of Science Editors:

Noland CL. Mechanistic Studies of Human RISC Loading Complex Function in RNA Interference. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/6dm4z1j9

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


University of California – Berkeley

19. Weaver, Lane Justin. Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli.

Degree: Bioengineering, 2013, University of California – Berkeley

 Owing to economic, political, and environmental concerns, the nature of finite natural resources will increasingly necessitate a transition to renewable resources over the next century.… (more)

Subjects/Keywords: Biomedical engineering; Biochemistry; metabolic engineering

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APA (6th Edition):

Weaver, L. J. (2013). Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1ss913cv

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):

Weaver, Lane Justin. “Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli.” 2013. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/1ss913cv.

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

MLA Handbook (7th Edition):

Weaver, Lane Justin. “Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli.” 2013. Web. 18 Oct 2019.

Vancouver:

Weaver LJ. Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/1ss913cv.

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

Council of Science Editors:

Weaver LJ. Towards predictive metabolic engineering: kinetic modeling and experimental analysis of a heterologous mevalonate pathway in E. coli. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/1ss913cv

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


University of California – Berkeley

20. Zhang, Elisa Tiannuo. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The regulation of eukaryotic gene expression is critical for proper cell homeostasis and development and relies largely on appropriate initiation of transcription. Transcriptional regulators, such… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Structural biology

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APA (6th Edition):

Zhang, E. T. (2015). Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/08k0g39d

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):

Zhang, Elisa Tiannuo. “Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.” 2015. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/08k0g39d.

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

MLA Handbook (7th Edition):

Zhang, Elisa Tiannuo. “Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.” 2015. Web. 18 Oct 2019.

Vancouver:

Zhang ET. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/08k0g39d.

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

Council of Science Editors:

Zhang ET. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/08k0g39d

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


University of California – Berkeley

21. Worden, Evan Josiah. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.

Degree: Molecular & Cell Biology, 2016, University of California – Berkeley

 The 26S proteasome is responsible for selective protein degradation in eukaryotic cells. Polyubiquitin chains mark proteins for degradation by the proteasome, but before degradation can… (more)

Subjects/Keywords: Biochemistry; deubiquitinase; proteasome; ubiquitin

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APA (6th Edition):

Worden, E. J. (2016). Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2138s3gn

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):

Worden, Evan Josiah. “Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/2138s3gn.

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

MLA Handbook (7th Edition):

Worden, Evan Josiah. “Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11.” 2016. Web. 18 Oct 2019.

Vancouver:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/2138s3gn.

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

Council of Science Editors:

Worden EJ. Structural and Functional Characterization of the Proteasomal Deubiquitinase Rpn11. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/2138s3gn

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


University of California – Berkeley

22. Kelly, Aileen Marie. Mechanisms Regulating Ubiquitin Chain Formation during Mitosis.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The small protein ubiquitin is a post-translational modification that is essential for regulating many cellular processes in eukaryotes. In a series of enzymatic steps, ubiquitin… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Cellular biology

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APA (6th Edition):

Kelly, A. M. (2015). Mechanisms Regulating Ubiquitin Chain Formation during Mitosis. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/56q8f7fp

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):

Kelly, Aileen Marie. “Mechanisms Regulating Ubiquitin Chain Formation during Mitosis.” 2015. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/56q8f7fp.

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

MLA Handbook (7th Edition):

Kelly, Aileen Marie. “Mechanisms Regulating Ubiquitin Chain Formation during Mitosis.” 2015. Web. 18 Oct 2019.

Vancouver:

Kelly AM. Mechanisms Regulating Ubiquitin Chain Formation during Mitosis. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/56q8f7fp.

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

Council of Science Editors:

Kelly AM. Mechanisms Regulating Ubiquitin Chain Formation during Mitosis. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/56q8f7fp

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


University of California – Berkeley

23. Davis, Zoe Hartman. Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes.

Degree: Infectious Diseases & Immunity, 2015, University of California – Berkeley

 Mapping host-pathogen interactions has proven instrumental for understanding how viruses manipulate host machinery and how numerous cellular processes are regulated. DNA viruses such as herpesviruses… (more)

Subjects/Keywords: Virology; Biochemistry; Molecular biology

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APA (6th Edition):

Davis, Z. H. (2015). Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9gd8f4ch

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):

Davis, Zoe Hartman. “Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes.” 2015. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/9gd8f4ch.

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

MLA Handbook (7th Edition):

Davis, Zoe Hartman. “Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes.” 2015. Web. 18 Oct 2019.

Vancouver:

Davis ZH. Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/9gd8f4ch.

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

Council of Science Editors:

Davis ZH. Global mapping of herpesvirus-host protein complexes reveals a novel transcription strategy for late genes. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/9gd8f4ch

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


University of California – Berkeley

24. Leskoske, Kristin. Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae.

Degree: Molecular & Cell Biology, 2017, University of California – Berkeley

 Target of Rapamycin (TOR) Complex 2 (TORC2) is a conserved multi-subunit protein kinase associated with the plasma membrane that is an essential regulator of growth.… (more)

Subjects/Keywords: Cellular biology; Biochemistry; Molecular biology

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APA (6th Edition):

Leskoske, K. (2017). Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6ns2z6bb

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):

Leskoske, Kristin. “Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae.” 2017. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/6ns2z6bb.

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

MLA Handbook (7th Edition):

Leskoske, Kristin. “Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae.” 2017. Web. 18 Oct 2019.

Vancouver:

Leskoske K. Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/6ns2z6bb.

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

Council of Science Editors:

Leskoske K. Modulation of TOR Complex 2 signaling and maintenance of plasma membrane homeostasis in Saccharomyces cerevisiae. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/6ns2z6bb

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


University of California – Berkeley

25. Horner, Geoffrey Ashworth. Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations.

Degree: Molecular & Cell Biology, 2010, University of California – Berkeley

 This thesis includes work from three major projects. In the first chapter I describe work on the structural heterogeneity of the folding intermediate of RNase… (more)

Subjects/Keywords: Biophysics, General; Chemistry, Biochemistry

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APA (6th Edition):

Horner, G. A. (2010). Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3cw7f4mn

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):

Horner, Geoffrey Ashworth. “Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/3cw7f4mn.

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

MLA Handbook (7th Edition):

Horner, Geoffrey Ashworth. “Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations.” 2010. Web. 18 Oct 2019.

Vancouver:

Horner GA. Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/3cw7f4mn.

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

Council of Science Editors:

Horner GA. Investigating Protein Folding and Function by Manipulating Rare and Partially-Folded Conformations. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/3cw7f4mn

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


University of California – Berkeley

26. RoseFigura, Jordan M. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.

Degree: Chemistry, 2010, University of California – Berkeley

 PQQ is an exogenous, tricyclic, quino-cofactor for a number of bacterial dehydrogenase reaction. It has also been proposed to play a role as a bacterial… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Oxygen activation; PQQ

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APA (6th Edition):

RoseFigura, J. M. (2010). Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4jh004zw

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):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/4jh004zw.

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

MLA Handbook (7th Edition):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Web. 18 Oct 2019.

Vancouver:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/4jh004zw.

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

Council of Science Editors:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/4jh004zw

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


University of California – Berkeley

27. Jin, Lingyan. Study of Ubiquitinating Enzymes Essential for Cell Proliferation.

Degree: Molecular & Cell Biology, 2012, University of California – Berkeley

 Ubiquitination is a form of post-translational modification of proteins, in which the 76-residue ubiquitin polypeptide is conjugated to the lysine residues of either the substrate… (more)

Subjects/Keywords: Molecular biology; Cellular biology; Biochemistry

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APA (6th Edition):

Jin, L. (2012). Study of Ubiquitinating Enzymes Essential for Cell Proliferation. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6q6470w2

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):

Jin, Lingyan. “Study of Ubiquitinating Enzymes Essential for Cell Proliferation.” 2012. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/6q6470w2.

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

MLA Handbook (7th Edition):

Jin, Lingyan. “Study of Ubiquitinating Enzymes Essential for Cell Proliferation.” 2012. Web. 18 Oct 2019.

Vancouver:

Jin L. Study of Ubiquitinating Enzymes Essential for Cell Proliferation. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/6q6470w2.

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

Council of Science Editors:

Jin L. Study of Ubiquitinating Enzymes Essential for Cell Proliferation. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/6q6470w2

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


University of California – Berkeley

28. Ho, Jaclyn J. Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming.

Degree: Molecular & Cell Biology, 2016, University of California – Berkeley

 Embryonic stem cells (ESCs), like all tissues, largely rely on precise transcriptional and epigenetic regulation for proper cell specification and differentiation. General transcription factors, transcriptional… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Cellular biology

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APA (6th Edition):

Ho, J. J. (2016). Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0p0198jq

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):

Ho, Jaclyn J. “Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/0p0198jq.

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

MLA Handbook (7th Edition):

Ho, Jaclyn J. “Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming.” 2016. Web. 18 Oct 2019.

Vancouver:

Ho JJ. Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/0p0198jq.

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

Council of Science Editors:

Ho JJ. Transcriptional and Epigenetic Regulation of Embryonic Stem Cell Pluripotency and Reprogramming. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/0p0198jq

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


University of California – Berkeley

29. Hesser, Charles. N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection.

Degree: Molecular & Cell Biology, 2018, University of California – Berkeley

 More than 100 types of RNA modifications are known to exist, regulating key aspects of cellular biology and metabolism. First discovered to be present on… (more)

Subjects/Keywords: Biochemistry; Virology; KSHV; m6A; methyladenosine

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

APA (6th Edition):

Hesser, C. (2018). N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/96p1m241

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):

Hesser, Charles. “N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection.” 2018. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/96p1m241.

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

MLA Handbook (7th Edition):

Hesser, Charles. “N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection.” 2018. Web. 18 Oct 2019.

Vancouver:

Hesser C. N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection. [Internet] [Thesis]. University of California – Berkeley; 2018. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/96p1m241.

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

Council of Science Editors:

Hesser C. N6-methyladenosine modification and the YTHDF2 reader protein play cell type specific roles in lytic viral gene expression during Kaposi’s sarcoma-associated herpesvirus infection. [Thesis]. University of California – Berkeley; 2018. Available from: http://www.escholarship.org/uc/item/96p1m241

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


University of California – Berkeley

30. Nunez, James Karlo. Mechanism of CRISPR–Cas Immunological Memory.

Degree: Molecular & Cell Biology, 2016, University of California – Berkeley

 Immunological memory, defined as the ability for cells to rapidly respond to previously encountered pathogens, has long been thought to be present solely in eukaryotes.… (more)

Subjects/Keywords: Biochemistry; Biology; Biophysics; Biochemistry; CRISPR; X-ray crystallography

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

APA (6th Edition):

Nunez, J. K. (2016). Mechanism of CRISPR–Cas Immunological Memory. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/26n3b6f5

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):

Nunez, James Karlo. “Mechanism of CRISPR–Cas Immunological Memory.” 2016. Thesis, University of California – Berkeley. Accessed October 18, 2019. http://www.escholarship.org/uc/item/26n3b6f5.

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

MLA Handbook (7th Edition):

Nunez, James Karlo. “Mechanism of CRISPR–Cas Immunological Memory.” 2016. Web. 18 Oct 2019.

Vancouver:

Nunez JK. Mechanism of CRISPR–Cas Immunological Memory. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/26n3b6f5.

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

Council of Science Editors:

Nunez JK. Mechanism of CRISPR–Cas Immunological Memory. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/26n3b6f5

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

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