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You searched for subject:(Cellular biology). Showing records 1 – 30 of 2993 total matches.

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Wright State University

1. Battini, Vishnu Priya Chowdary. Accurate splicing of HDAC6 requires Son.

Degree: MS, Biological Sciences, 2013, Wright State University

 Pre-mRNA splicing requires proper splice site selection mediated by many factors including snRNPs and serine-arginine rich (SR) splicing factors. Son is the largest known SR… (more)

Subjects/Keywords: Cellular Biology; cellular biology

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APA (6th Edition):

Battini, V. P. C. (2013). Accurate splicing of HDAC6 requires Son. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1390306890

Chicago Manual of Style (16th Edition):

Battini, Vishnu Priya Chowdary. “Accurate splicing of HDAC6 requires Son.” 2013. Masters Thesis, Wright State University. Accessed November 21, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=wright1390306890.

MLA Handbook (7th Edition):

Battini, Vishnu Priya Chowdary. “Accurate splicing of HDAC6 requires Son.” 2013. Web. 21 Nov 2018.

Vancouver:

Battini VPC. Accurate splicing of HDAC6 requires Son. [Internet] [Masters thesis]. Wright State University; 2013. [cited 2018 Nov 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1390306890.

Council of Science Editors:

Battini VPC. Accurate splicing of HDAC6 requires Son. [Masters Thesis]. Wright State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1390306890


Duke University

2. McClure, Allison Wolff. Pheromone Gradient Tracking Mechanisms During Yeast Mating .

Degree: 2014, Duke University

  Many cell types are remarkably adept at tracking chemical gradients, but they use different mechanisms in order to properly migrate or grow up-gradient. Bacteria… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

McClure, A. W. (2014). Pheromone Gradient Tracking Mechanisms During Yeast Mating . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9419

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):

McClure, Allison Wolff. “Pheromone Gradient Tracking Mechanisms During Yeast Mating .” 2014. Thesis, Duke University. Accessed November 21, 2018. http://hdl.handle.net/10161/9419.

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

MLA Handbook (7th Edition):

McClure, Allison Wolff. “Pheromone Gradient Tracking Mechanisms During Yeast Mating .” 2014. Web. 21 Nov 2018.

Vancouver:

McClure AW. Pheromone Gradient Tracking Mechanisms During Yeast Mating . [Internet] [Thesis]. Duke University; 2014. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/10161/9419.

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

Council of Science Editors:

McClure AW. Pheromone Gradient Tracking Mechanisms During Yeast Mating . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/9419

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


Duke University

3. Chen, Hsin. Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis .

Degree: 2012, Duke University

  The cells of the budding yeast Saccharomyces cerevisiae undergo a robust morphological cycle, involving reorganization of the actin cytoskeleton, septin ring formation, and polarized… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Chen, H. (2012). Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5494

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

Chicago Manual of Style (16th Edition):

Chen, Hsin. “Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis .” 2012. Thesis, Duke University. Accessed November 21, 2018. http://hdl.handle.net/10161/5494.

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

MLA Handbook (7th Edition):

Chen, Hsin. “Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis .” 2012. Web. 21 Nov 2018.

Vancouver:

Chen H. Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis . [Internet] [Thesis]. Duke University; 2012. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/10161/5494.

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

Council of Science Editors:

Chen H. Cytoskeletal Dynamics and the Temporal Control of Yeast Morphogenesis . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/5494

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


Duke University

4. Gemberling, Matthew P. Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration .

Degree: 2014, Duke University

  Heart disease is the leading cause of death in the developed world. Adult mammals cannot replace lost cardiac tissue after injury, leading to reduced… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Gemberling, M. P. (2014). Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9412

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):

Gemberling, Matthew P. “Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration .” 2014. Thesis, Duke University. Accessed November 21, 2018. http://hdl.handle.net/10161/9412.

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

MLA Handbook (7th Edition):

Gemberling, Matthew P. “Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration .” 2014. Web. 21 Nov 2018.

Vancouver:

Gemberling MP. Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration . [Internet] [Thesis]. Duke University; 2014. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/10161/9412.

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

Council of Science Editors:

Gemberling MP. Mechanisms that drive cardiomyocyte proliferation during zebrafish heart regeneration . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/9412

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


Temple University

5. Frara, Nagat. THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR.

Degree: PhD, 2015, Temple University

Cell Biology

Osteoactivin (OA) is a novel osteogenic and repair factor. It has the ability to regulate cell proliferation, adhesion, differentiation, and synthesis and regulation… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Frara, N. (2015). THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,336629

Chicago Manual of Style (16th Edition):

Frara, Nagat. “THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR.” 2015. Doctoral Dissertation, Temple University. Accessed November 21, 2018. http://digital.library.temple.edu/u?/p245801coll10,336629.

MLA Handbook (7th Edition):

Frara, Nagat. “THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR.” 2015. Web. 21 Nov 2018.

Vancouver:

Frara N. THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2018 Nov 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,336629.

Council of Science Editors:

Frara N. THE ROLE OF OSTEOACTIVIN IN MUSCULOSKELETAL TISSUES AS A REPAIR AND ANABOLIC FACTOR. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,336629


University of Kansas

6. Hung, Wei-Ting. EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS.

Degree: PhD, Molecular & Integrative Physiology, 2016, University of Kansas

 Formation of the follicular fluid antrum within the ovarian follicle provides a unique environment for the developing oocyte. Follicular fluid contains factors including nucleic acids,… (more)

Subjects/Keywords: Cellular biology

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

APA (6th Edition):

Hung, W. (2016). EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/24810

Chicago Manual of Style (16th Edition):

Hung, Wei-Ting. “EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS.” 2016. Doctoral Dissertation, University of Kansas. Accessed November 21, 2018. http://hdl.handle.net/1808/24810.

MLA Handbook (7th Edition):

Hung, Wei-Ting. “EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS.” 2016. Web. 21 Nov 2018.

Vancouver:

Hung W. EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/1808/24810.

Council of Science Editors:

Hung W. EXTRACELLULAR VESICLES IN OVARIAN ANTRAL FOLLICLES: CHARACTERIZATION AND FUNCTIONS. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/24810


The Ohio State University

7. Sever, Nurettin Ilter. Investigation of the Role of Different Regions of the Cbl Protein in its Function.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2013, The Ohio State University

 The duration and amplitude of any signal transduction pathway should be tightly regulated for the maintenance of homeostasis in any organism. Cbl protein is one… (more)

Subjects/Keywords: Cellular Biology

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APA (6th Edition):

Sever, N. I. (2013). Investigation of the Role of Different Regions of the Cbl Protein in its Function. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1386059140

Chicago Manual of Style (16th Edition):

Sever, Nurettin Ilter. “Investigation of the Role of Different Regions of the Cbl Protein in its Function.” 2013. Doctoral Dissertation, The Ohio State University. Accessed November 21, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1386059140.

MLA Handbook (7th Edition):

Sever, Nurettin Ilter. “Investigation of the Role of Different Regions of the Cbl Protein in its Function.” 2013. Web. 21 Nov 2018.

Vancouver:

Sever NI. Investigation of the Role of Different Regions of the Cbl Protein in its Function. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2018 Nov 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1386059140.

Council of Science Editors:

Sever NI. Investigation of the Role of Different Regions of the Cbl Protein in its Function. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1386059140


University of Cincinnati

8. WILLIAMS, JON. EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS.

Degree: PhD, Medicine : Neuroscience/Medical Science Scholars Interdisiplinary, 2008, University of Cincinnati

 This dissertation contains three independent studies involving the developmental cell biology of neural crest-derived glial lineage cells in the context of neurofibromatosis, type 1 (NF1).… (more)

Subjects/Keywords: Cellular Biology

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APA (6th Edition):

WILLIAMS, J. (2008). EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212181112

Chicago Manual of Style (16th Edition):

WILLIAMS, JON. “EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS.” 2008. Doctoral Dissertation, University of Cincinnati. Accessed November 21, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212181112.

MLA Handbook (7th Edition):

WILLIAMS, JON. “EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS.” 2008. Web. 21 Nov 2018.

Vancouver:

WILLIAMS J. EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS. [Internet] [Doctoral dissertation]. University of Cincinnati; 2008. [cited 2018 Nov 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212181112.

Council of Science Editors:

WILLIAMS J. EFFECTS OF LOSS OF NF1 GENE ON PERIPHERAL NERVOUS SYSTEM PROGENITORS AND TUMORIGENESIS. [Doctoral Dissertation]. University of Cincinnati; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212181112


The Ohio State University

9. Yang, Jennifer. Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2016, The Ohio State University

 Biliary tract cancer (BTC) represents a rare but deadly disease due to difficulties in diagnosis and identifying effective treatment regimens. Even with continual improvement in… (more)

Subjects/Keywords: Cellular Biology

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APA (6th Edition):

Yang, J. (2016). Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1461777433

Chicago Manual of Style (16th Edition):

Yang, Jennifer. “Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia.” 2016. Doctoral Dissertation, The Ohio State University. Accessed November 21, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1461777433.

MLA Handbook (7th Edition):

Yang, Jennifer. “Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia.” 2016. Web. 21 Nov 2018.

Vancouver:

Yang J. Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2018 Nov 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461777433.

Council of Science Editors:

Yang J. Targeted Therapeutics against Biliary Cancer Elicit Concurrent Tumor Extrinsic Effects on Immune Suppression and Cancer Cachexia. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1461777433

10. Berk-Rauch, Hanna E. FMRP Regulates the Expression of Axonal Messages In Vivo.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2013, Brown University

 Fragile X syndrome, a leading cause of autism and the most common form of inherited intellectual disability, results from the loss of Fragile X mental… (more)

Subjects/Keywords: cellular biology

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APA (6th Edition):

Berk-Rauch, H. E. (2013). FMRP Regulates the Expression of Axonal Messages In Vivo. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320509/

Chicago Manual of Style (16th Edition):

Berk-Rauch, Hanna E. “FMRP Regulates the Expression of Axonal Messages In Vivo.” 2013. Doctoral Dissertation, Brown University. Accessed November 21, 2018. https://repository.library.brown.edu/studio/item/bdr:320509/.

MLA Handbook (7th Edition):

Berk-Rauch, Hanna E. “FMRP Regulates the Expression of Axonal Messages In Vivo.” 2013. Web. 21 Nov 2018.

Vancouver:

Berk-Rauch HE. FMRP Regulates the Expression of Axonal Messages In Vivo. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2018 Nov 21]. Available from: https://repository.library.brown.edu/studio/item/bdr:320509/.

Council of Science Editors:

Berk-Rauch HE. FMRP Regulates the Expression of Axonal Messages In Vivo. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320509/


Rice University

11. Amin, Shivas Rajni. Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program.

Degree: 2010, Rice University

 Vertebrate development requires that cell proliferation be properly coordinated with morphogenesis, the process by which an embryo acquires form, and cell specification, the process by… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Amin, S. R. (2010). Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program. (Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/62038

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):

Amin, Shivas Rajni. “Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program.” 2010. Thesis, Rice University. Accessed November 21, 2018. http://hdl.handle.net/1911/62038.

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

MLA Handbook (7th Edition):

Amin, Shivas Rajni. “Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program.” 2010. Web. 21 Nov 2018.

Vancouver:

Amin SR. Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program. [Internet] [Thesis]. Rice University; 2010. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/1911/62038.

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

Council of Science Editors:

Amin SR. Investigation of mechanisms regulating cell proliferation in the zebrafish developmental program. [Thesis]. Rice University; 2010. Available from: http://hdl.handle.net/1911/62038

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


University of California – Berkeley

12. Acosta, Jamie. Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice.

Degree: Comparative Biochemistry, 2015, University of California – Berkeley

 Tissues exist in a highly ordered three dimensional structure that is critical to inform function. When cells are explanted into culture, the tissue-specific functions are… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Acosta, J. (2015). Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1zk6s482

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):

Acosta, Jamie. “Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice.” 2015. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/1zk6s482.

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

MLA Handbook (7th Edition):

Acosta, Jamie. “Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice.” 2015. Web. 21 Nov 2018.

Vancouver:

Acosta J. Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/1zk6s482.

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

Council of Science Editors:

Acosta J. Integrating form and function in the mammary gland: crosstalk of extracellular matrix, extracellular matrix degrading enzymes and epithelial cells in 3D cultures and engineered mice. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/1zk6s482

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


University of California – Berkeley

13. Helmke, Kara. Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture.

Degree: Molecular & Cell Biology, 2014, University of California – Berkeley

 The function of the spindle to faithfully segregate chromosomes is universal among eukaryotes. A common feature of metaphase spindles is their self-organizing, bipolar structure, with… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Helmke, K. (2014). Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8vz146zw

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):

Helmke, Kara. “Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture.” 2014. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/8vz146zw.

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

MLA Handbook (7th Edition):

Helmke, Kara. “Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture.” 2014. Web. 21 Nov 2018.

Vancouver:

Helmke K. Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/8vz146zw.

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

Council of Science Editors:

Helmke K. Interspecies Comparisons of Xenopus Egg Extracts Reveal Mechanisms for Modulating Meiotic Spindle Size and Architecture. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/8vz146zw

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


University of California – Riverside

14. Truong, Tan Minh. Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids.

Degree: Cell, Molecular and Developmental Biology, 2017, University of California – Riverside

 Phage display is a powerful screening method capable of potentially screening over 1011 unique peptide sequences for protein-protein or protein-DNA interactions. It has been extensively… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Truong, T. M. (2017). Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/46s2552t

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):

Truong, Tan Minh. “Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids.” 2017. Thesis, University of California – Riverside. Accessed November 21, 2018. http://www.escholarship.org/uc/item/46s2552t.

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

MLA Handbook (7th Edition):

Truong, Tan Minh. “Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids.” 2017. Web. 21 Nov 2018.

Vancouver:

Truong TM. Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids. [Internet] [Thesis]. University of California – Riverside; 2017. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/46s2552t.

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

Council of Science Editors:

Truong TM. Development of a Phage Display System for Engineering Peptide Inhibitors Containing Multiple Non-Canonical Amino Acids. [Thesis]. University of California – Riverside; 2017. Available from: http://www.escholarship.org/uc/item/46s2552t

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


University of California – Berkeley

15. Limbad, Chandani Bhupendrabhai. Characterizing Senescence in Astrocytes and its Effect on Neurons.

Degree: Comparative Biochemistry, 2017, University of California – Berkeley

Cellular senescence, characterized by a permanent cell cycle arrest and an inflammatory phenotype called the senescence-associated secretory phenotype (SASP), has been described during aging and… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Limbad, C. B. (2017). Characterizing Senescence in Astrocytes and its Effect on Neurons. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4887v9f6

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):

Limbad, Chandani Bhupendrabhai. “Characterizing Senescence in Astrocytes and its Effect on Neurons.” 2017. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/4887v9f6.

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

MLA Handbook (7th Edition):

Limbad, Chandani Bhupendrabhai. “Characterizing Senescence in Astrocytes and its Effect on Neurons.” 2017. Web. 21 Nov 2018.

Vancouver:

Limbad CB. Characterizing Senescence in Astrocytes and its Effect on Neurons. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/4887v9f6.

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

Council of Science Editors:

Limbad CB. Characterizing Senescence in Astrocytes and its Effect on Neurons. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/4887v9f6

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


UCLA

16. Sullivan, William Juster. Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation.

Degree: Molecular and Medical Pharmacology, 2017, UCLA

 The metabolic state of a cell can be determined by cell-extrinsic factors, including nutrient availability and growth factor signaling. Here, we define extracellular matrix (ECM)… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Sullivan, W. J. (2017). Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4fj8f40n

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):

Sullivan, William Juster. “Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation.” 2017. Thesis, UCLA. Accessed November 21, 2018. http://www.escholarship.org/uc/item/4fj8f40n.

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

MLA Handbook (7th Edition):

Sullivan, William Juster. “Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation.” 2017. Web. 21 Nov 2018.

Vancouver:

Sullivan WJ. Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation. [Internet] [Thesis]. UCLA; 2017. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/4fj8f40n.

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

Council of Science Editors:

Sullivan WJ. Hyaluronidase Promotes Glucose Metabolism: Identification of the Extracellular Matrix as a Node of Cell-Extrinsic Metabolic Regulation. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/4fj8f40n

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


University of California – San Diego

17. Ravi, Ritesh. Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells.

Degree: Biology, 2017, University of California – San Diego

 Coiled-Coil Domain Containing 90B (CCDC90B) is a protein of unknown function, which has three functional transcripts according to Ensembl genome browser. In this project, we… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Ravi, R. (2017). Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/7xj8n5xk

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):

Ravi, Ritesh. “Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells.” 2017. Thesis, University of California – San Diego. Accessed November 21, 2018. http://www.escholarship.org/uc/item/7xj8n5xk.

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

MLA Handbook (7th Edition):

Ravi, Ritesh. “Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells.” 2017. Web. 21 Nov 2018.

Vancouver:

Ravi R. Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/7xj8n5xk.

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

Council of Science Editors:

Ravi R. Effects of T1-CCDC90Bon the Mitochondria in Human Mammary Epithelial Cells. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/7xj8n5xk

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


University of California – Berkeley

18. Carroll, Susheela Yogini. Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae.

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

 K28 is an A/B toxin that targets yeast cells and depends on endocytosis and retrograde trafficking for toxicity. Knowledge of the specific proteins, lipids, and… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Carroll, S. Y. (2010). Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7gz0d3vf

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):

Carroll, Susheela Yogini. “Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae.” 2010. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/7gz0d3vf.

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

MLA Handbook (7th Edition):

Carroll, Susheela Yogini. “Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae.” 2010. Web. 21 Nov 2018.

Vancouver:

Carroll SY. Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/7gz0d3vf.

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

Council of Science Editors:

Carroll SY. Uptake of Toxin K28 and Early Endocytic Site Formation in S. cerevisiae. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/7gz0d3vf

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


University of California – Berkeley

19. Joyner, Ryan Preston. The Dynamic Organization of the Yeast Genome.

Degree: Molecular & Cell Biology, 2014, University of California – Berkeley

 Regardless of size, shape, or function, all cells must rapidly respond to a changing environment, especially in adverse conditions. Various environmental stresses including heat shock,… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Joyner, R. P. (2014). The Dynamic Organization of the Yeast Genome. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3565x0kc

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):

Joyner, Ryan Preston. “The Dynamic Organization of the Yeast Genome.” 2014. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/3565x0kc.

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

MLA Handbook (7th Edition):

Joyner, Ryan Preston. “The Dynamic Organization of the Yeast Genome.” 2014. Web. 21 Nov 2018.

Vancouver:

Joyner RP. The Dynamic Organization of the Yeast Genome. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/3565x0kc.

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

Council of Science Editors:

Joyner RP. The Dynamic Organization of the Yeast Genome. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/3565x0kc

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


University of California – Santa Cruz

20. Lim, Angeline. Axonal Transport Of Neuropeptides In Drosophila Axons.

Degree: Molecular Cell and Developmental Biology, 2014, University of California – Santa Cruz

 Microtubule motor proteins are known to drive long distance organelle transport in neurons, but there are many motor species and many organelle types, so specific… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Lim, A. (2014). Axonal Transport Of Neuropeptides In Drosophila Axons. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/3v52j5rs

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):

Lim, Angeline. “Axonal Transport Of Neuropeptides In Drosophila Axons.” 2014. Thesis, University of California – Santa Cruz. Accessed November 21, 2018. http://www.escholarship.org/uc/item/3v52j5rs.

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

MLA Handbook (7th Edition):

Lim, Angeline. “Axonal Transport Of Neuropeptides In Drosophila Axons.” 2014. Web. 21 Nov 2018.

Vancouver:

Lim A. Axonal Transport Of Neuropeptides In Drosophila Axons. [Internet] [Thesis]. University of California – Santa Cruz; 2014. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/3v52j5rs.

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

Council of Science Editors:

Lim A. Axonal Transport Of Neuropeptides In Drosophila Axons. [Thesis]. University of California – Santa Cruz; 2014. Available from: http://www.escholarship.org/uc/item/3v52j5rs

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


Harvard University

21. Oak, Youbean. Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility.

Degree: PhD, Biology, Molecular and Cellular, 2014, Harvard University

 Fascin is an actin bundling protein whose overexpression has in recent years been systematically linked to increased metastasis and poor outcome in cancer patients. It… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Oak, Y. (2014). Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13104236

Chicago Manual of Style (16th Edition):

Oak, Youbean. “Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility.” 2014. Doctoral Dissertation, Harvard University. Accessed November 21, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13104236.

MLA Handbook (7th Edition):

Oak, Youbean. “Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility.” 2014. Web. 21 Nov 2018.

Vancouver:

Oak Y. Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2018 Nov 21]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13104236.

Council of Science Editors:

Oak Y. Filopodia-independent roles of the actin bundling protein fascin in promoting cell motility. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13104236


University of California – San Diego

22. Farber-Katz, Suzette Elena. DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK.

Degree: Biomedical Sciences, 2012, University of California – San Diego

 Golgi morphology and function has fascinated scientists for decades; however, it was unclear how the two were related. Our research delving into the function of… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Farber-Katz, S. E. (2012). DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0p0476db

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):

Farber-Katz, Suzette Elena. “DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK.” 2012. Thesis, University of California – San Diego. Accessed November 21, 2018. http://www.escholarship.org/uc/item/0p0476db.

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

MLA Handbook (7th Edition):

Farber-Katz, Suzette Elena. “DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK.” 2012. Web. 21 Nov 2018.

Vancouver:

Farber-Katz SE. DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK. [Internet] [Thesis]. University of California – San Diego; 2012. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/0p0476db.

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

Council of Science Editors:

Farber-Katz SE. DNA Damage Triggers Golgi Dispersal via GOLPH3 and DNA-PK. [Thesis]. University of California – San Diego; 2012. Available from: http://www.escholarship.org/uc/item/0p0476db

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


University of California – Berkeley

23. Smoligovets, Alexander Alexandrovich. From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors.

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

 The actin cytoskeleton has for decades been known to be important in the process of T-cell recognition of antigen. Upon receiving stimulus from T-cell receptors… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Smoligovets, A. A. (2012). From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0cn4f9zp

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):

Smoligovets, Alexander Alexandrovich. “From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors.” 2012. Thesis, University of California – Berkeley. Accessed November 21, 2018. http://www.escholarship.org/uc/item/0cn4f9zp.

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

MLA Handbook (7th Edition):

Smoligovets, Alexander Alexandrovich. “From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors.” 2012. Web. 21 Nov 2018.

Vancouver:

Smoligovets AA. From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/0cn4f9zp.

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

Council of Science Editors:

Smoligovets AA. From actin to Zap70: the outcomes of the interaction of the actin cytoskeleton with T-cell receptors. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/0cn4f9zp

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


University of California – San Diego

24. Williams, Wesley. Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha.

Degree: Biology (Joint Doctoral SDSU), 2017, University of California – San Diego

 Hepatitis C Virus (HCV) is a blood-borne virus found worldwide, though most prevalent in third world countries. Currently, there is no vaccine and chronic infection… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Williams, W. (2017). Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/8cd809c3

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):

Williams, Wesley. “Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha.” 2017. Thesis, University of California – San Diego. Accessed November 21, 2018. http://www.escholarship.org/uc/item/8cd809c3.

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

MLA Handbook (7th Edition):

Williams, Wesley. “Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha.” 2017. Web. 21 Nov 2018.

Vancouver:

Williams W. Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/8cd809c3.

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

Council of Science Editors:

Williams W. Elucidating Hepatitis C Virus Core Interactions with the Host Environment, Specifically Phosphorylated IkappaB-alpha. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/8cd809c3

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


Temple University

25. Michael, James. Regulation of Ras signaling and oncogenesis by plasma membrane microdomains.

Degree: PhD, 2016, Temple University

Cell Biology

In this study, we assessed the contributions of plasma membrane (PM) microdomain targeting to the functions of H-Ras and R-Ras. These paralogues have… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Michael, J. (2016). Regulation of Ras signaling and oncogenesis by plasma membrane microdomains. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,377230

Chicago Manual of Style (16th Edition):

Michael, James. “Regulation of Ras signaling and oncogenesis by plasma membrane microdomains.” 2016. Doctoral Dissertation, Temple University. Accessed November 21, 2018. http://digital.library.temple.edu/u?/p245801coll10,377230.

MLA Handbook (7th Edition):

Michael, James. “Regulation of Ras signaling and oncogenesis by plasma membrane microdomains.” 2016. Web. 21 Nov 2018.

Vancouver:

Michael J. Regulation of Ras signaling and oncogenesis by plasma membrane microdomains. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2018 Nov 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,377230.

Council of Science Editors:

Michael J. Regulation of Ras signaling and oncogenesis by plasma membrane microdomains. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,377230

26. Zinno, John Peter. The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay.

Degree: 2018, State University of New York at Stony Brook

  The regulation and mechanism of outer membrane (OM) lysis during spore wall assembly is not well understood. Although the timing of OM lysis has… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Zinno, J. P. (2018). The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay. (Thesis). State University of New York at Stony Brook. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10686038

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):

Zinno, John Peter. “The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay.” 2018. Thesis, State University of New York at Stony Brook. Accessed November 21, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10686038.

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

MLA Handbook (7th Edition):

Zinno, John Peter. “The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay.” 2018. Web. 21 Nov 2018.

Vancouver:

Zinno JP. The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay. [Internet] [Thesis]. State University of New York at Stony Brook; 2018. [cited 2018 Nov 21]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10686038.

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

Council of Science Editors:

Zinno JP. The in vivo Detection of Outer Membrane Lysis during Spore Wall Assembly in Saccharomyces Cerevisiae Using a Novel Split GFP Assay. [Thesis]. State University of New York at Stony Brook; 2018. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10686038

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


UCLA

27. Krall, Abigail. Metabolite Signaling Mediates Cellular Homeostasis and Proliferation.

Degree: Molecular and Medical Pharmacology, 2018, UCLA

 Nutrients and metabolites can both positively and negatively regulate cell signaling and anabolic metabolism. These signaling properties suggest that metabolites can influence both proliferation and… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Krall, A. (2018). Metabolite Signaling Mediates Cellular Homeostasis and Proliferation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/95k478zn

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):

Krall, Abigail. “Metabolite Signaling Mediates Cellular Homeostasis and Proliferation.” 2018. Thesis, UCLA. Accessed November 21, 2018. http://www.escholarship.org/uc/item/95k478zn.

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

MLA Handbook (7th Edition):

Krall, Abigail. “Metabolite Signaling Mediates Cellular Homeostasis and Proliferation.” 2018. Web. 21 Nov 2018.

Vancouver:

Krall A. Metabolite Signaling Mediates Cellular Homeostasis and Proliferation. [Internet] [Thesis]. UCLA; 2018. [cited 2018 Nov 21]. Available from: http://www.escholarship.org/uc/item/95k478zn.

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

Council of Science Editors:

Krall A. Metabolite Signaling Mediates Cellular Homeostasis and Proliferation. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/95k478zn

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

28. Witte, Kristen. Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae.

Degree: 2017, The University of Chicago

  Cell polarization underlies many cellular and organismal functions. The GTPase Cdc42 orchestrates polarization in many contexts. In budding yeast, polarization is associated with a… (more)

Subjects/Keywords: Cellular biology

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APA (6th Edition):

Witte, K. (2017). Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae. (Thesis). The University of Chicago. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=10282229

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):

Witte, Kristen. “Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae.” 2017. Thesis, The University of Chicago. Accessed November 21, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10282229.

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

MLA Handbook (7th Edition):

Witte, Kristen. “Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae.” 2017. Web. 21 Nov 2018.

Vancouver:

Witte K. Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae. [Internet] [Thesis]. The University of Chicago; 2017. [cited 2018 Nov 21]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10282229.

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

Council of Science Editors:

Witte K. Optogenetic Investigation Reveals Robust Symmetry Breaking Mechanisms in Saccharomyces cerevisiae. [Thesis]. The University of Chicago; 2017. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=10282229

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


Boston University

29. Laflamme, Collette. Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion.

Degree: PhD, Medical Nutritional Sciences, 2015, Boston University

 Our laboratory identified Adiporedoxin (Adrx), an endoplasmic reticulum localized oxidoreductase whose expression in adipose tissue is many fold greater than other tissues. In gain and… (more)

Subjects/Keywords: Cellular biology

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

APA (6th Edition):

Laflamme, C. (2015). Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15062

Chicago Manual of Style (16th Edition):

Laflamme, Collette. “Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion.” 2015. Doctoral Dissertation, Boston University. Accessed November 21, 2018. http://hdl.handle.net/2144/15062.

MLA Handbook (7th Edition):

Laflamme, Collette. “Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion.” 2015. Web. 21 Nov 2018.

Vancouver:

Laflamme C. Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/2144/15062.

Council of Science Editors:

Laflamme C. Adiporedoxin, an upstream modulator of endoplasmic reticulum oxidative folding and protein secretion. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/15062


Boston University

30. Vakhshoorzadeh, Jasmine. Defining YAP/TAZ-dependency in human breast cancer cells.

Degree: MS, Medical Sciences, 2016, Boston University

 OVERVIEW: Hyperactivation and amplification of the oncogenic transcriptional co-factors YAP and TAZ are common in breast cancer. However, it is unknown if breast cancer cells… (more)

Subjects/Keywords: Cellular biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vakhshoorzadeh, J. (2016). Defining YAP/TAZ-dependency in human breast cancer cells. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/17028

Chicago Manual of Style (16th Edition):

Vakhshoorzadeh, Jasmine. “Defining YAP/TAZ-dependency in human breast cancer cells.” 2016. Masters Thesis, Boston University. Accessed November 21, 2018. http://hdl.handle.net/2144/17028.

MLA Handbook (7th Edition):

Vakhshoorzadeh, Jasmine. “Defining YAP/TAZ-dependency in human breast cancer cells.” 2016. Web. 21 Nov 2018.

Vancouver:

Vakhshoorzadeh J. Defining YAP/TAZ-dependency in human breast cancer cells. [Internet] [Masters thesis]. Boston University; 2016. [cited 2018 Nov 21]. Available from: http://hdl.handle.net/2144/17028.

Council of Science Editors:

Vakhshoorzadeh J. Defining YAP/TAZ-dependency in human breast cancer cells. [Masters Thesis]. Boston University; 2016. Available from: http://hdl.handle.net/2144/17028

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