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Dept: Cell Biology

You searched for subject:(Cellular Biology). Showing records 1 – 30 of 47 total matches.

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University of California – San Francisco

1. Pincus, David. Homeostasis in the Unfolded Protein Response.

Degree: Cell Biology, 2012, University of California – San Francisco

 The endoplasmic reticulum (ER) is the compartment in eukaryotic cells in which secreted and membrane-spanning proteins are folded, modified and assembled. These proteins are the… (more)

Subjects/Keywords: Cellular biology

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

APA (6th Edition):

Pincus, D. (2012). Homeostasis in the Unfolded Protein Response. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0mh706n8

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):

Pincus, David. “Homeostasis in the Unfolded Protein Response.” 2012. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/0mh706n8.

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

MLA Handbook (7th Edition):

Pincus, David. “Homeostasis in the Unfolded Protein Response.” 2012. Web. 17 Aug 2019.

Vancouver:

Pincus D. Homeostasis in the Unfolded Protein Response. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/0mh706n8.

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

Council of Science Editors:

Pincus D. Homeostasis in the Unfolded Protein Response. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/0mh706n8

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


University of California – San Francisco

2. Currie, Erin. Proteins at the Saccharomyces cerevisiae Lipid Droplet.

Degree: Cell Biology, 2014, University of California – San Francisco

 Lipid droplets (LDs) are ubiquitous and dynamic organelles whose major functions are in lipid metabolism. They are unique among organelles because they have a phospholipid… (more)

Subjects/Keywords: Cellular biology

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

APA (6th Edition):

Currie, E. (2014). Proteins at the Saccharomyces cerevisiae Lipid Droplet. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/56s679fb

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):

Currie, Erin. “Proteins at the Saccharomyces cerevisiae Lipid Droplet.” 2014. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/56s679fb.

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

MLA Handbook (7th Edition):

Currie, Erin. “Proteins at the Saccharomyces cerevisiae Lipid Droplet.” 2014. Web. 17 Aug 2019.

Vancouver:

Currie E. Proteins at the Saccharomyces cerevisiae Lipid Droplet. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/56s679fb.

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

Council of Science Editors:

Currie E. Proteins at the Saccharomyces cerevisiae Lipid Droplet. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/56s679fb

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


University of California – San Francisco

3. Genuth, Miriam A. Chick cranial neural crest cell migration.

Degree: Cell Biology, 2017, University of California – San Francisco

 This thesis presents work toward understanding how chick neural crest cells polarize their protrusions to achieve directed motility. There are multiple strategies that cells can… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Genuth, M. A. (2017). Chick cranial neural crest cell migration. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/15m058xj

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):

Genuth, Miriam A. “Chick cranial neural crest cell migration.” 2017. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/15m058xj.

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

MLA Handbook (7th Edition):

Genuth, Miriam A. “Chick cranial neural crest cell migration.” 2017. Web. 17 Aug 2019.

Vancouver:

Genuth MA. Chick cranial neural crest cell migration. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/15m058xj.

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

Council of Science Editors:

Genuth MA. Chick cranial neural crest cell migration. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/15m058xj

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


University of California – San Francisco

4. Carbone, Catherine Bianca. In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase.

Degree: Cell Biology, 2018, University of California – San Francisco

 One of the most important cellular decisions made by the immune system is whether or not a T cell will activate after contacting and antigen… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Carbone, C. B. (2018). In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4270r9b6

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):

Carbone, Catherine Bianca. “In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase.” 2018. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/4270r9b6.

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

MLA Handbook (7th Edition):

Carbone, Catherine Bianca. “In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase.” 2018. Web. 17 Aug 2019.

Vancouver:

Carbone CB. In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/4270r9b6.

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

Council of Science Editors:

Carbone CB. In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/4270r9b6

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


University of California – San Francisco

5. Millius, Arthur. WAVE-mediated Actin Assembly.

Degree: Cell Biology, 2011, University of California – San Francisco

 This thesis presents work toward understanding the biophysical mechanisms that control polarized cell movement.  Many cells move in response to external cues, and this directed… (more)

Subjects/Keywords: Cellular biology; Biochemistry

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APA (6th Edition):

Millius, A. (2011). WAVE-mediated Actin Assembly. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4t0664vv

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):

Millius, Arthur. “WAVE-mediated Actin Assembly.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/4t0664vv.

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

MLA Handbook (7th Edition):

Millius, Arthur. “WAVE-mediated Actin Assembly.” 2011. Web. 17 Aug 2019.

Vancouver:

Millius A. WAVE-mediated Actin Assembly. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/4t0664vv.

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

Council of Science Editors:

Millius A. WAVE-mediated Actin Assembly. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/4t0664vv

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


University of California – San Francisco

6. Pemble, Hayley. Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions.

Degree: Cell Biology, 2014, University of California – San Francisco

 Proper chromosome segregation requires dynamic regulation of kinetochore-microtubule attachments throughout mitosis. Multiple kinetochore proteins display microtubule-binding activity, yet how exactly these proteins are spatially and… (more)

Subjects/Keywords: Cellular biology; Molecular biology

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APA (6th Edition):

Pemble, H. (2014). Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4500k6cw

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):

Pemble, Hayley. “Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions.” 2014. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/4500k6cw.

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

MLA Handbook (7th Edition):

Pemble, Hayley. “Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions.” 2014. Web. 17 Aug 2019.

Vancouver:

Pemble H. Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/4500k6cw.

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

Council of Science Editors:

Pemble H. Role of CLASP2 phosphorylation in regulating kinetochore-microtubule interactions. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/4500k6cw

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


University of California – San Francisco

7. Loveless, Theresa Berens. Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase.

Degree: Cell Biology, 2015, University of California – San Francisco

 When DNA is damaged, or DNA replication goes awry, cells activate checkpoints to allow time for damage to be repaired and replication to complete. In… (more)

Subjects/Keywords: Biology; Cellular biology; Biochemistry

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APA (6th Edition):

Loveless, T. B. (2015). Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/09s756t8

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):

Loveless, Theresa Berens. “Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase.” 2015. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/09s756t8.

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

MLA Handbook (7th Edition):

Loveless, Theresa Berens. “Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase.” 2015. Web. 17 Aug 2019.

Vancouver:

Loveless TB. Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/09s756t8.

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

Council of Science Editors:

Loveless TB. Artificial activation of the DNA replication checkpoint and 11 new substrates of the beta-TRCP ubiquitin ligase. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/09s756t8

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


University of California – San Francisco

8. Stanley, Robert. The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry.

Degree: Cell Biology, 2016, University of California – San Francisco

 The Role of Wnt Signaling Proteins in Neurodevelopment and Psychiatric SusceptibilityRobert StanleyAbstractProper regulation of cell signaling pathways is required for normal neurodevelopment. Dysfunction in signaling… (more)

Subjects/Keywords: Neurosciences; Cellular biology; Developmental biology

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APA (6th Edition):

Stanley, R. (2016). The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3xm9k6fn

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):

Stanley, Robert. “The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry.” 2016. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/3xm9k6fn.

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

MLA Handbook (7th Edition):

Stanley, Robert. “The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry.” 2016. Web. 17 Aug 2019.

Vancouver:

Stanley R. The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/3xm9k6fn.

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

Council of Science Editors:

Stanley R. The Role of Wnt Signaling Proteins in Neurodevelopement and Psychiatry. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/3xm9k6fn

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


Harvard University

9. Dempsey, Jamie Michelle. SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing.

Degree: PhD, Cell Biology, 2012, Harvard University

 The mechanisms through which a cell controls its proliferation, differentiation, metabolism, motility, and ultimate survival in response to extracellular cues are largely controlled by the… (more)

Subjects/Keywords: mTORC1; RSK; S6K; SRPK2; cellular biology

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APA (6th Edition):

Dempsey, J. M. (2012). SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817664

Chicago Manual of Style (16th Edition):

Dempsey, Jamie Michelle. “SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing.” 2012. Doctoral Dissertation, Harvard University. Accessed August 17, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817664.

MLA Handbook (7th Edition):

Dempsey, Jamie Michelle. “SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing.” 2012. Web. 17 Aug 2019.

Vancouver:

Dempsey JM. SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2019 Aug 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817664.

Council of Science Editors:

Dempsey JM. SRPK2 Phosphorylation by the AGC Kinases, and mTORC1 Regulation of Alternative Splicing. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817664


University of California – San Francisco

10. Temkin, Paul. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.

Degree: Cell Biology, 2011, University of California – San Francisco

 This thesis addresses the endosomal sorting of the beta-2 adrenergic receptor (B2AR), a "typical" (family A) member of the large superfamily of seven-transmembrane signaling receptors,… (more)

Subjects/Keywords: Cellular biology; adrb2; B2AR; GPCR; Retromer; SNX27

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

APA (6th Edition):

Temkin, P. (2011). Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7zc0j3wd

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):

Temkin, Paul. “Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/7zc0j3wd.

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

MLA Handbook (7th Edition):

Temkin, Paul. “Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor.” 2011. Web. 17 Aug 2019.

Vancouver:

Temkin P. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/7zc0j3wd.

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

Council of Science Editors:

Temkin P. Elucidating the Post-Endocytic Sorting Mechanism of the Beta-2 Adrenergic Receptor. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/7zc0j3wd

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


University of California – San Francisco

11. Houk, Andrew. The Spatial Patterning of Signals during Neutrophil Migration.

Degree: Cell Biology, 2011, University of California – San Francisco

 Cells must migrate for neurons to make connections with distant partners, immune cells to find their prey and cancer cells to metastasize. Actin filament assembly… (more)

Subjects/Keywords: Cellular biology; Biochemistry; Biophysics; Actin; Chemotaxis; Rac

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APA (6th Edition):

Houk, A. (2011). The Spatial Patterning of Signals during Neutrophil Migration. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/23g5n3bp

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):

Houk, Andrew. “The Spatial Patterning of Signals during Neutrophil Migration.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/23g5n3bp.

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

MLA Handbook (7th Edition):

Houk, Andrew. “The Spatial Patterning of Signals during Neutrophil Migration.” 2011. Web. 17 Aug 2019.

Vancouver:

Houk A. The Spatial Patterning of Signals during Neutrophil Migration. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/23g5n3bp.

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

Council of Science Editors:

Houk A. The Spatial Patterning of Signals during Neutrophil Migration. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/23g5n3bp

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


University of California – San Francisco

12. Henry, Anastasia Gail. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.

Degree: Cell Biology, 2012, University of California – San Francisco

 This dissertation examines the role of ubiquitination in regulating the endocytic trafficking of opioid receptors, members of the large superfamily of seven-transmembrane receptors (7TMRs). The… (more)

Subjects/Keywords: Cellular biology; endocytosis; GPCR; signaling; ubiquitin

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APA (6th Edition):

Henry, A. G. (2012). Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5zj8675c

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):

Henry, Anastasia Gail. “Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.” 2012. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/5zj8675c.

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

MLA Handbook (7th Edition):

Henry, Anastasia Gail. “Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors.” 2012. Web. 17 Aug 2019.

Vancouver:

Henry AG. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/5zj8675c.

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

Council of Science Editors:

Henry AG. Elucidating the role of ubiquitin in controlling the endocytic trafficking of opioid receptors. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/5zj8675c

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


University of California – San Francisco

13. Foss, Sarah. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.

Degree: Cell Biology, 2012, University of California – San Francisco

 Three vesicular glutamate transporters (VGLUT1, -2, and -3) are found in the mammalian central nervous system. The transporters are expressed in different brain regions in… (more)

Subjects/Keywords: Neurosciences; Cellular biology; endocytosis; synaptic vesicle

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APA (6th Edition):

Foss, S. (2012). Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/66j3k3qw

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):

Foss, Sarah. “Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.” 2012. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/66j3k3qw.

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

MLA Handbook (7th Edition):

Foss, Sarah. “Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.” 2012. Web. 17 Aug 2019.

Vancouver:

Foss S. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/66j3k3qw.

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

Council of Science Editors:

Foss S. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/66j3k3qw

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


Harvard University

14. Sarraf, Shireen Akhavan. Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction.

Degree: PhD, Cell Biology, 2013, Harvard University

 Parkinson's disease (PD) is a progressive neurological disorder resulting from loss of dopaminergic neurons of the substantia nigra, in part due to mitochondrial dysfunction. The… (more)

Subjects/Keywords: Cellular biology; Molecular biology; diGly; Parkin; Parkinson's; Pink1; Proteomics; Ubiquitin

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APA (6th Edition):

Sarraf, S. A. (2013). Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11110427

Chicago Manual of Style (16th Edition):

Sarraf, Shireen Akhavan. “Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction.” 2013. Doctoral Dissertation, Harvard University. Accessed August 17, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11110427.

MLA Handbook (7th Edition):

Sarraf, Shireen Akhavan. “Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction.” 2013. Web. 17 Aug 2019.

Vancouver:

Sarraf SA. Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2019 Aug 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11110427.

Council of Science Editors:

Sarraf SA. Defining the Landscape of the PARKIN- and PINK1-Dependent Ubiquitin-Modified Proteome in Response to Mitochondrial Dysfunction. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11110427


University of California – San Francisco

15. Kline, Ahnika. The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A.

Degree: Cell Biology, 2011, University of California – San Francisco

 Integrins are heterodimeric membrane proteins that mediate cell adhesion, migration and proliferation in a number of physiologic processes, including angiogenesis. The integrin α9β1 binds to… (more)

Subjects/Keywords: Cellular Biology; Biology; alpha9beta1; angiogenesis; integrin; matrigel; pericyte; VEGF-A

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APA (6th Edition):

Kline, A. (2011). The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6md630vt

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):

Kline, Ahnika. “The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/6md630vt.

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

MLA Handbook (7th Edition):

Kline, Ahnika. “The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A.” 2011. Web. 17 Aug 2019.

Vancouver:

Kline A. The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/6md630vt.

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

Council of Science Editors:

Kline A. The Role of Integrin Alpha9Beta1 During Angiogenesis Induced by VEGF-A. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/6md630vt

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


University of California – San Francisco

16. Leaf, Alison Emily. Elucidating the cellular targeting of signaling receptors to primary cilia.

Degree: Cell Biology, 2015, University of California – San Francisco

 This dissertation explores how members of the largest class of signaling receptors, seven-transmembrane receptors (7TMRs), are targeted to the primary cilium, a protrusion of the… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Biochemistry; cilia; membrane trafficking; signaling receptors

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APA (6th Edition):

Leaf, A. E. (2015). Elucidating the cellular targeting of signaling receptors to primary cilia. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6t52s7b4

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):

Leaf, Alison Emily. “Elucidating the cellular targeting of signaling receptors to primary cilia.” 2015. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/6t52s7b4.

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

MLA Handbook (7th Edition):

Leaf, Alison Emily. “Elucidating the cellular targeting of signaling receptors to primary cilia.” 2015. Web. 17 Aug 2019.

Vancouver:

Leaf AE. Elucidating the cellular targeting of signaling receptors to primary cilia. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/6t52s7b4.

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

Council of Science Editors:

Leaf AE. Elucidating the cellular targeting of signaling receptors to primary cilia. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/6t52s7b4

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


University of California – San Francisco

17. Slabodnick, Mark Maddock. Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein.

Degree: Cell Biology, 2014, University of California – San Francisco

 Over the last few decades scientists have often turned to one of a handful of well-established model systems in order to address a number of… (more)

Subjects/Keywords: Biology; Cellular biology; Molecular biology; ciliate; Heterotrich; Mob1; morphogenesis; RNA interference; Stentor coeruleus

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APA (6th Edition):

Slabodnick, M. M. (2014). Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6tb3c3h1

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):

Slabodnick, Mark Maddock. “Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein.” 2014. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/6tb3c3h1.

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

MLA Handbook (7th Edition):

Slabodnick, Mark Maddock. “Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein.” 2014. Web. 17 Aug 2019.

Vancouver:

Slabodnick MM. Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/6tb3c3h1.

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

Council of Science Editors:

Slabodnick MM. Reviving Stentor coeruleus as a Modern Model for Morphogenesis: RNA interference reveals Mob1 as an asymmetrically localized polarity protein. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/6tb3c3h1

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


University of California – San Francisco

18. Berry, Emily Corine. Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease.

Degree: Cell Biology, 2015, University of California – San Francisco

 Cardiac development requires that multiple progenitor cell types undergo complex cell fate and morphological changes cooperatively to generate the four-chambered heart. Orchestration of this process… (more)

Subjects/Keywords: Cellular biology; Developmental biology; Molecular biology; cardiac; cardiac development; miRNA; myocardial infarction; reprogramming; smooth muscle

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APA (6th Edition):

Berry, E. C. (2015). Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/15k3k7h7

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):

Berry, Emily Corine. “Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease.” 2015. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/15k3k7h7.

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

MLA Handbook (7th Edition):

Berry, Emily Corine. “Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease.” 2015. Web. 17 Aug 2019.

Vancouver:

Berry EC. Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/15k3k7h7.

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

Council of Science Editors:

Berry EC. Leveraging Factors Important During Cardiac Development to Disrupt Acquired Cardiovascular Disease. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/15k3k7h7

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


University of California – San Francisco

19. Strong, Isaac Jon Thomas. Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio.

Degree: Cell Biology, 2015, University of California – San Francisco

 Rapid and synchronous syncytial mitotic cycles without gap phases characterize the initial phase of Drosophila embryogenesis. Starting at cell cycle 10, incremental and progressive increases… (more)

Subjects/Keywords: Biology; Cellular biology; Developmental biology; cell cycle; cyclin:Cdk; Drosophila; MBT; nuclear to cytoplasmic ratio

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APA (6th Edition):

Strong, I. J. T. (2015). Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7783979m

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):

Strong, Isaac Jon Thomas. “Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio.” 2015. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/7783979m.

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

MLA Handbook (7th Edition):

Strong, Isaac Jon Thomas. “Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio.” 2015. Web. 17 Aug 2019.

Vancouver:

Strong IJT. Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/7783979m.

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

Council of Science Editors:

Strong IJT. Inhibiting cyclin:Cdk in the Drosophila early embryo uncouples the mid blastula transition from the nuclear to cytoplasmic ratio. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/7783979m

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


Case Western Reserve University

20. Undurti, Arundhati. Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function.

Degree: PhD, Cell Biology, 2010, Case Western Reserve University

 High levels of high density lipoprotein (HDL) are associated with a decreased risk of cardiovascular disease (CVD). The atheroprotective function of HDL has been attributed… (more)

Subjects/Keywords: Cellular Biology; High Density Lipoprotein; Myeloperoxidase; Cardiovascular Disease

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APA (6th Edition):

Undurti, A. (2010). Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1279209478

Chicago Manual of Style (16th Edition):

Undurti, Arundhati. “Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1279209478.

MLA Handbook (7th Edition):

Undurti, Arundhati. “Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function.” 2010. Web. 17 Aug 2019.

Vancouver:

Undurti A. Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1279209478.

Council of Science Editors:

Undurti A. Role of Myeloperoxidase Mediated Oxidative Modification and Apolipoprotein Composition in High Density Lipoprotein Function. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1279209478


Harvard University

21. Grady, Joshua Terrence Wilson. Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale.

Degree: PhD, Cell Biology, 2013, Harvard University

 Liquid chromatography coupled tandem mass spectrometry (LC-MS/MS) has become the preferred method for large-scale peptide and phosphopeptide identification and quantification. The dominance of LC-MS/MS is… (more)

Subjects/Keywords: Cellular biology; Mass Spectrometry; Multiplexing; Phosphorylation; Proteomics; Quantitative

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APA (6th Edition):

Grady, J. T. W. (2013). Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129110

Chicago Manual of Style (16th Edition):

Grady, Joshua Terrence Wilson. “Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale.” 2013. Doctoral Dissertation, Harvard University. Accessed August 17, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129110.

MLA Handbook (7th Edition):

Grady, Joshua Terrence Wilson. “Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale.” 2013. Web. 17 Aug 2019.

Vancouver:

Grady JTW. Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2019 Aug 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129110.

Council of Science Editors:

Grady JTW. Adapting Quantitative Protein and Phosphorylation Analyses to a Proteome-Wide Scale. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129110

22. Tukachinsky, Hanna. Mechanistic Studies of Vertebrate Hedgehog Signaling.

Degree: PhD, Cell Biology, 2012, Harvard University

 Metazoans use Hedgehog signaling to direct many stages of embryonic development, and deregulation of this pathway is implicated in many types of cancer. I investigated… (more)

Subjects/Keywords: Cellular biology; Hedgehog signaling

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APA (6th Edition):

Tukachinsky, H. (2012). Mechanistic Studies of Vertebrate Hedgehog Signaling. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10403678

Chicago Manual of Style (16th Edition):

Tukachinsky, Hanna. “Mechanistic Studies of Vertebrate Hedgehog Signaling.” 2012. Doctoral Dissertation, Harvard University. Accessed August 17, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10403678.

MLA Handbook (7th Edition):

Tukachinsky, Hanna. “Mechanistic Studies of Vertebrate Hedgehog Signaling.” 2012. Web. 17 Aug 2019.

Vancouver:

Tukachinsky H. Mechanistic Studies of Vertebrate Hedgehog Signaling. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2019 Aug 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10403678.

Council of Science Editors:

Tukachinsky H. Mechanistic Studies of Vertebrate Hedgehog Signaling. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10403678


University of California – San Francisco

23. Kuhn, Jonathan Alexander. The control of mitotic progression by kinetochore-microtubule attachments.

Degree: Cell Biology, 2019, University of California – San Francisco

 To maintain genomic integrity, the Spindle Assembly Checkpoint (SAC) prevents anaphase onset until all chromosomes attach to the mitotic spindle in a bioriented fashion. The… (more)

Subjects/Keywords: Cellular biology; Biophysics; Cell Cycle; Checkpoint; Kinetochore; Mitosis

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APA (6th Edition):

Kuhn, J. A. (2019). The control of mitotic progression by kinetochore-microtubule attachments. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9p9863jd

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):

Kuhn, Jonathan Alexander. “The control of mitotic progression by kinetochore-microtubule attachments.” 2019. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/9p9863jd.

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

MLA Handbook (7th Edition):

Kuhn, Jonathan Alexander. “The control of mitotic progression by kinetochore-microtubule attachments.” 2019. Web. 17 Aug 2019.

Vancouver:

Kuhn JA. The control of mitotic progression by kinetochore-microtubule attachments. [Internet] [Thesis]. University of California – San Francisco; 2019. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/9p9863jd.

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

Council of Science Editors:

Kuhn JA. The control of mitotic progression by kinetochore-microtubule attachments. [Thesis]. University of California – San Francisco; 2019. Available from: http://www.escholarship.org/uc/item/9p9863jd

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


University of California – San Francisco

24. Merksamer, Philip Ian. The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells.

Degree: Cell Biology, 2010, University of California – San Francisco

 In eukaryotic cells, secreted and membrane proteins fold within the endoplasmic reticulum (ER). Various physiological or pathophysiological conditions can disrupt ER protein folding homeostasis and… (more)

Subjects/Keywords: Cellular Biology; endoplasmic reticulum stress; fluorescent protein reporters; unfolded protein response

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APA (6th Edition):

Merksamer, P. I. (2010). The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1dw4d3hd

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):

Merksamer, Philip Ian. “The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells.” 2010. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/1dw4d3hd.

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

MLA Handbook (7th Edition):

Merksamer, Philip Ian. “The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells.” 2010. Web. 17 Aug 2019.

Vancouver:

Merksamer PI. The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/1dw4d3hd.

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

Council of Science Editors:

Merksamer PI. The Development and Application of Fluorescent Protein Reporters to Measure Endoplasmic Reticulum Stress in Single Cells. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/1dw4d3hd

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


University of California – San Francisco

25. Nehil, Michael. Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection.

Degree: Cell Biology, 2011, University of California – San Francisco

 High mobility group box 1 (HMGB1) is a nuclear protein first discovered nearly 30 years ago. It was described to aid in transcription by forming… (more)

Subjects/Keywords: Cellular biology; Virology; adenovirus; cancer; chromatin; epigenetic; hmgb1; sema3a

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APA (6th Edition):

Nehil, M. (2011). Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/478704h8

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):

Nehil, Michael. “Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/478704h8.

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

MLA Handbook (7th Edition):

Nehil, Michael. “Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection.” 2011. Web. 17 Aug 2019.

Vancouver:

Nehil M. Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/478704h8.

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

Council of Science Editors:

Nehil M. Novel roles for HMGB1 in cancer and its mechanisms of release during Adenovirus infection. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/478704h8

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


University of California – San Francisco

26. Engel, Benjamin David. Regulation of Flagellar Length by Intraflagellar Transport.

Degree: Cell Biology, 2011, University of California – San Francisco

 Eukaryotic flagella (also referred to as cilia) are microtubule-based organelles that protrude from the cell body into the extracellular environment. In addition to powering cell… (more)

Subjects/Keywords: Cellular Biology; Biochemistry; Chlamydomonas; cilia; flagella; IFT; intraflagellar transport; TIRF

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APA (6th Edition):

Engel, B. D. (2011). Regulation of Flagellar Length by Intraflagellar Transport. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4929p0qd

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):

Engel, Benjamin David. “Regulation of Flagellar Length by Intraflagellar Transport.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/4929p0qd.

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

MLA Handbook (7th Edition):

Engel, Benjamin David. “Regulation of Flagellar Length by Intraflagellar Transport.” 2011. Web. 17 Aug 2019.

Vancouver:

Engel BD. Regulation of Flagellar Length by Intraflagellar Transport. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/4929p0qd.

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

Council of Science Editors:

Engel BD. Regulation of Flagellar Length by Intraflagellar Transport. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/4929p0qd

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


University of California – San Francisco

27. Kannegaard, Elisa Sandoval. Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii.

Degree: Cell Biology, 2011, University of California – San Francisco

 How the complex spatial organization of a eukaryotic cell is achieved is an enduring and fundamental question in cell biology. The size and arrangement of… (more)

Subjects/Keywords: Cellular Biology; Genetics; Chlamydomonas; cilia; flagella; katanin; length control; PF15

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APA (6th Edition):

Kannegaard, E. S. (2011). Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7h16z7ws

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):

Kannegaard, Elisa Sandoval. “Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/7h16z7ws.

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

MLA Handbook (7th Edition):

Kannegaard, Elisa Sandoval. “Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii.” 2011. Web. 17 Aug 2019.

Vancouver:

Kannegaard ES. Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/7h16z7ws.

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

Council of Science Editors:

Kannegaard ES. Analysis of length control in short flagella mutants of Chlamydomonas reinhardtii. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/7h16z7ws

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


University of California – San Francisco

28. Wemmer, Kimberly A. Architecture and Assembly of Chlamydomonas Flagella.

Degree: Cell Biology, 2011, University of California – San Francisco

 Eukaryotic cilia and flagella play crucial roles in development, signaling, and motility, and their proper function is essential to many organisms, including all vertebrates. Cilia… (more)

Subjects/Keywords: Cellular biology; central pair; Chlamydomonas; cilia; flagella; length control; noise

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

APA (6th Edition):

Wemmer, K. A. (2011). Architecture and Assembly of Chlamydomonas Flagella. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/41v540tt

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):

Wemmer, Kimberly A. “Architecture and Assembly of Chlamydomonas Flagella.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/41v540tt.

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

MLA Handbook (7th Edition):

Wemmer, Kimberly A. “Architecture and Assembly of Chlamydomonas Flagella.” 2011. Web. 17 Aug 2019.

Vancouver:

Wemmer KA. Architecture and Assembly of Chlamydomonas Flagella. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/41v540tt.

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

Council of Science Editors:

Wemmer KA. Architecture and Assembly of Chlamydomonas Flagella. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/41v540tt

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


University of California – San Francisco

29. Goodwin, Sarah. Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends.

Degree: Cell Biology, 2011, University of California – San Francisco

 Microtubules are the principle scaffold of the mitotic spindle, serve as tracks for intracellular transport of proteins and mRNAs, and also participate in signaling functions.… (more)

Subjects/Keywords: Cellular biology; Drosophila; microtubule; microtubule dynamics; microtubule stability; minus end; mitosis

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

APA (6th Edition):

Goodwin, S. (2011). Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6kn9g5hm

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):

Goodwin, Sarah. “Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends.” 2011. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/6kn9g5hm.

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

MLA Handbook (7th Edition):

Goodwin, Sarah. “Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends.” 2011. Web. 17 Aug 2019.

Vancouver:

Goodwin S. Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/6kn9g5hm.

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

Council of Science Editors:

Goodwin S. Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/6kn9g5hm

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


University of California – San Francisco

30. Callahan, Joseph Aaron. Roles of Ubiquitin Sensor ABIN-1 In The Immune System.

Degree: Cell Biology, 2013, University of California – San Francisco

 Heterologous expression of ABIN-1 (A20 Binding and Inhibitor of NF-kB-1, gene name Tnip1), like A20, was suggested to restrict TNF-induced inflammation and cell death. ABIN-1's… (more)

Subjects/Keywords: Cellular biology; Physiology; Immunology; A20; ABIN; inflammation; NFkB; Psoriasis; ubiquitin

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

APA (6th Edition):

Callahan, J. A. (2013). Roles of Ubiquitin Sensor ABIN-1 In The Immune System. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7170r00x

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):

Callahan, Joseph Aaron. “Roles of Ubiquitin Sensor ABIN-1 In The Immune System.” 2013. Thesis, University of California – San Francisco. Accessed August 17, 2019. http://www.escholarship.org/uc/item/7170r00x.

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

MLA Handbook (7th Edition):

Callahan, Joseph Aaron. “Roles of Ubiquitin Sensor ABIN-1 In The Immune System.” 2013. Web. 17 Aug 2019.

Vancouver:

Callahan JA. Roles of Ubiquitin Sensor ABIN-1 In The Immune System. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/7170r00x.

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

Council of Science Editors:

Callahan JA. Roles of Ubiquitin Sensor ABIN-1 In The Immune System. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/7170r00x

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

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