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You searched for subject:(Polarity proteins). Showing records 1 – 15 of 15 total matches.

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University of New South Wales

1. Abu Siniyeh, Ahmed. Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae.

Degree: Centre for Vascular Research, 2014, University of New South Wales

 The composition and structure of plasma membranes is critical for many cell functions. The plasma membrane of polarized epithelial cells can be divided into two… (more)

Subjects/Keywords: Zebrafish; Membrane order; Polarity proteins; Lipid rafts proteins

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APA (6th Edition):

Abu Siniyeh, A. (2014). Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53724 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12419/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Abu Siniyeh, Ahmed. “Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae.” 2014. Doctoral Dissertation, University of New South Wales. Accessed October 24, 2020. http://handle.unsw.edu.au/1959.4/53724 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12419/SOURCE02?view=true.

MLA Handbook (7th Edition):

Abu Siniyeh, Ahmed. “Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae.” 2014. Web. 24 Oct 2020.

Vancouver:

Abu Siniyeh A. Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2020 Oct 24]. Available from: http://handle.unsw.edu.au/1959.4/53724 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12419/SOURCE02?view=true.

Council of Science Editors:

Abu Siniyeh A. Characterizing and quantifying membrane order of polarized epithelial cells in zebrafish larvae. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53724 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12419/SOURCE02?view=true


University of Cambridge

2. Dzafic, Edo. Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT.

Degree: PhD, 2020, University of Cambridge

 Knowing the localisation and spatial organisation of proteins is crucial for understanding their function. The development of super-resolution imaging has improved our ability to garner… (more)

Subjects/Keywords: super-resolution imaging; DNA-PAINT; qPAINT; cell polarity; polarity proteins; aPKC; Par6; Crumbs; protein clustering; quantitative imaging; Drosophila melanogaster; fruit fly; single-molecule localisation microscopy; molecular counting

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APA (6th Edition):

Dzafic, E. (2020). Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/304024

Chicago Manual of Style (16th Edition):

Dzafic, Edo. “Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 24, 2020. https://www.repository.cam.ac.uk/handle/1810/304024.

MLA Handbook (7th Edition):

Dzafic, Edo. “Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT.” 2020. Web. 24 Oct 2020.

Vancouver:

Dzafic E. Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 24]. Available from: https://www.repository.cam.ac.uk/handle/1810/304024.

Council of Science Editors:

Dzafic E. Quantitative super-resolution imaging of cell polarity proteins using DNA-PAINT. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/304024


IUPUI

3. Ranahan, William P. The oncogenic properties of Amot80 in mammary epithelia.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

While breast cancer is the second most commonly diagnosed cancer worldwide, its causes and natural history are not well defined.… (more)

Subjects/Keywords: Amot, Angiomotin, Breast Cancer, Epithelia, Polarity; Epithelium  – Differentiation; Epithelium  – Growth; Epithelial cells; Breast  – Cancer; Cancer cells  – Growth  – Regulation; Polarity (Biology)  – Research; Mammals  – Development; Cellular signal transduction; Cancer cells  – Research; Transcription factors; Tumor suppressor proteins; Oncogenes  – Research; Cancer  – Endocrine aspects; Pathology, Molecular

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APA (6th Edition):

Ranahan, W. P. (2014). The oncogenic properties of Amot80 in mammary epithelia. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/4082

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):

Ranahan, William P. “The oncogenic properties of Amot80 in mammary epithelia.” 2014. Thesis, IUPUI. Accessed October 24, 2020. http://hdl.handle.net/1805/4082.

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

MLA Handbook (7th Edition):

Ranahan, William P. “The oncogenic properties of Amot80 in mammary epithelia.” 2014. Web. 24 Oct 2020.

Vancouver:

Ranahan WP. The oncogenic properties of Amot80 in mammary epithelia. [Internet] [Thesis]. IUPUI; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1805/4082.

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

Council of Science Editors:

Ranahan WP. The oncogenic properties of Amot80 in mammary epithelia. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/4082

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

4. Hung, Hui-Fang. Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2016, U of Massachusetts : Med

  Epithelial cells are necessary building blocks of the organs they line. Their apicalbasolateral polarity, characterized by an asymmetric distribution of cell components along their… (more)

Subjects/Keywords: Heat-Shock Proteins; Cell Division; Cell Movement; Cell Polarity; Centrioles; Centrosome; Endosomes; Epithelial Cells; Microtubule-Organizing Center; Microtubules; Cenexin; Cell Biology; Cellular and Molecular Physiology

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APA (6th Edition):

Hung, H. (2016). Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/842

Chicago Manual of Style (16th Edition):

Hung, Hui-Fang. “Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 24, 2020. http://escholarship.umassmed.edu/gsbs_diss/842.

MLA Handbook (7th Edition):

Hung, Hui-Fang. “Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation.” 2016. Web. 24 Oct 2020.

Vancouver:

Hung H. Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2020 Oct 24]. Available from: http://escholarship.umassmed.edu/gsbs_diss/842.

Council of Science Editors:

Hung H. Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/842


University of Michigan

5. Karnak, David Michael. Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity.

Degree: PhD, Pure Sciences, 2004, University of Michigan

 Asymmetric distribution of proteins and other molecules within cells allows for efficient completion of myriad complex tasks necessary for life. In mammalian epithelia, apical and… (more)

Subjects/Keywords: Biochemical; Cell Polarity; Dimerization; Domain; Important; L27; Lin; Linking; Proteins; Structural; Studies

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APA (6th Edition):

Karnak, D. M. (2004). Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/124447

Chicago Manual of Style (16th Edition):

Karnak, David Michael. “Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity.” 2004. Doctoral Dissertation, University of Michigan. Accessed October 24, 2020. http://hdl.handle.net/2027.42/124447.

MLA Handbook (7th Edition):

Karnak, David Michael. “Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity.” 2004. Web. 24 Oct 2020.

Vancouver:

Karnak DM. Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity. [Internet] [Doctoral dissertation]. University of Michigan; 2004. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2027.42/124447.

Council of Science Editors:

Karnak DM. Biochemical and structural studies of the LIN-2 and 7 (L27) dimerization domain: Linking proteins important to cell polarity. [Doctoral Dissertation]. University of Michigan; 2004. Available from: http://hdl.handle.net/2027.42/124447


Boston College

6. Alford, Lea Marie. Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos.

Degree: PhD, Biology, 2009, Boston College

Polarity established by the first cleavages in sea urchin embryos was investigated in this thesis revealing precocious embryonic polarity. Studies of embryonic polarity have focused… (more)

Subjects/Keywords: cell polarity; membrane domain; myosin II; PAR proteins; sea urchin

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APA (6th Edition):

Alford, L. M. (2009). Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101295

Chicago Manual of Style (16th Edition):

Alford, Lea Marie. “Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos.” 2009. Doctoral Dissertation, Boston College. Accessed October 24, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101295.

MLA Handbook (7th Edition):

Alford, Lea Marie. “Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos.” 2009. Web. 24 Oct 2020.

Vancouver:

Alford LM. Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos. [Internet] [Doctoral dissertation]. Boston College; 2009. [cited 2020 Oct 24]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101295.

Council of Science Editors:

Alford LM. Identification and Spatiotemporal Control of the Asymmetrical Membrane Cortex in Cleavage Stage Sea Urchin Embryos. [Doctoral Dissertation]. Boston College; 2009. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101295

7. Kim, Soyoung. A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation.

Degree: Interdisciplinary Graduate Program, RNA Therapeutics Institute, 2008, U of Massachusetts : Med

  Asymmetric cell divisions constitute a basic foundation of animal development, providing a mechanism for placing specific cell types at defined positions in a developing… (more)

Subjects/Keywords: Cell Polarity; Caenorhabditis elegans Proteins; Cytoskeletal Proteins; Body Patterning; Cell Differentiation; Digestive System; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Digestive System; Embryonic Structures

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APA (6th Edition):

Kim, S. (2008). A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/385

Chicago Manual of Style (16th Edition):

Kim, Soyoung. “A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 24, 2020. https://escholarship.umassmed.edu/gsbs_diss/385.

MLA Handbook (7th Edition):

Kim, Soyoung. “A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation.” 2008. Web. 24 Oct 2020.

Vancouver:

Kim S. A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2020 Oct 24]. Available from: https://escholarship.umassmed.edu/gsbs_diss/385.

Council of Science Editors:

Kim S. A Study of Cell Polarity and Fate Specification in Early C. Elegans Embryos: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/385

8. Galván Ampudia, Carlos Samuel. Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis.

Degree: 2009, Molecular & Developmental Genetics, Institute of Biology (IBL), Faculty of Science, Leiden University

 In view of their predominant sessile lifestyle, plants need to be able to adapt to changes in their environment. Environmental signals such as light and… (more)

Subjects/Keywords: AGC kinases; Arabidopsis; Auxin; Calcium binding proteins; Cell polarity; PIN auxin efflux carriers; Plant development; Polar auxin transport; AGC kinases; Arabidopsis; Auxin; Calcium binding proteins; Cell polarity; PIN auxin efflux carriers; Plant development; Polar auxin transport

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APA (6th Edition):

Galván Ampudia, C. S. (2009). Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis. (Doctoral Dissertation). Molecular & Developmental Genetics, Institute of Biology (IBL), Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/14506

Chicago Manual of Style (16th Edition):

Galván Ampudia, Carlos Samuel. “Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis.” 2009. Doctoral Dissertation, Molecular & Developmental Genetics, Institute of Biology (IBL), Faculty of Science, Leiden University. Accessed October 24, 2020. http://hdl.handle.net/1887/14506.

MLA Handbook (7th Edition):

Galván Ampudia, Carlos Samuel. “Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis.” 2009. Web. 24 Oct 2020.

Vancouver:

Galván Ampudia CS. Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis. [Internet] [Doctoral dissertation]. Molecular & Developmental Genetics, Institute of Biology (IBL), Faculty of Science, Leiden University; 2009. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1887/14506.

Council of Science Editors:

Galván Ampudia CS. Plant AGC protein kinases orient auxin-mediated differential growth and organogenesis. [Doctoral Dissertation]. Molecular & Developmental Genetics, Institute of Biology (IBL), Faculty of Science, Leiden University; 2009. Available from: http://hdl.handle.net/1887/14506

9. Martzoukou, Olga. A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools.

Degree: 2018, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 In eukaryotic cells, transmembrane proteins are co-translationally inserted in the lipid bilayer of the Endoplasmic Reticulum (ER). In order for these proteins to exit the… (more)

Subjects/Keywords: Ενδοκυτταρική διακίνηση; Πολική αύξηση; Νηματοειδής μύκητας; Σύμπλοκα προσαρμογέων AP; Κυτταρική βιολογία; Ενδοκύτωση; Εξωκύτωση; Κλαθρίνη; Ολιγομερισμός μεταφορέων πουρινών; Κυτταροσκελετός; Cell biology; Membrane endocytosis - trafficking; Endocytosis; Exocytosis; Adaptor proteins; Filamentous fungi; Polarity; Clathrin; Oligomerization of purine transporters; Cytoskeleton

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APA (6th Edition):

Martzoukou, O. (2018). A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/43936

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):

Martzoukou, Olga. “A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools.” 2018. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 24, 2020. http://hdl.handle.net/10442/hedi/43936.

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

MLA Handbook (7th Edition):

Martzoukou, Olga. “A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools.” 2018. Web. 24 Oct 2020.

Vancouver:

Martzoukou O. A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10442/hedi/43936.

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

Council of Science Editors:

Martzoukou O. A study of membrane protein trafficking, endocytosis and degradation through the development of new genetic and biochemical tools. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. Available from: http://hdl.handle.net/10442/hedi/43936

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


Vanderbilt University

10. Davis, Michael Alan. Loss of p120ctn : its effect on cadherin levels, development, and tumor progression.

Degree: PhD, Cancer Biology, 2005, Vanderbilt University

 p120 binds and is thought to regulate the cell-cell adhesion molecule E-cadherin. Experiments in a p120-deficient carcinoma cell line suggest a critical role for p120… (more)

Subjects/Keywords: p120; p120 ctn; cadherin; tumor progression; salivary; siRNA; polarity; knockdown; Cadherins; Tumor suppressor proteins; Salivary glands  – Growth

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APA (6th Edition):

Davis, M. A. (2005). Loss of p120ctn : its effect on cadherin levels, development, and tumor progression. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11884

Chicago Manual of Style (16th Edition):

Davis, Michael Alan. “Loss of p120ctn : its effect on cadherin levels, development, and tumor progression.” 2005. Doctoral Dissertation, Vanderbilt University. Accessed October 24, 2020. http://hdl.handle.net/1803/11884.

MLA Handbook (7th Edition):

Davis, Michael Alan. “Loss of p120ctn : its effect on cadherin levels, development, and tumor progression.” 2005. Web. 24 Oct 2020.

Vancouver:

Davis MA. Loss of p120ctn : its effect on cadherin levels, development, and tumor progression. [Internet] [Doctoral dissertation]. Vanderbilt University; 2005. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1803/11884.

Council of Science Editors:

Davis MA. Loss of p120ctn : its effect on cadherin levels, development, and tumor progression. [Doctoral Dissertation]. Vanderbilt University; 2005. Available from: http://hdl.handle.net/1803/11884

11. Rocheleau, Christian Ernest. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.

Degree: Cell Biology, RNA Therapeutics Institute, 1999, U of Massachusetts : Med

  During embryonic development of the nematode Caenorhabditis elegans, cell fates are specified by asymmetric segregation of cell fate determinants and via cell-cell signaling events.… (more)

Subjects/Keywords: Cell Polarity; Caenorhabditis elegans; Cell Differentiation; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Embryonic Structures; Enzymes and Coenzymes

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APA (6th Edition):

Rocheleau, C. E. (1999). Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/46

Chicago Manual of Style (16th Edition):

Rocheleau, Christian Ernest. “Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 24, 2020. https://escholarship.umassmed.edu/gsbs_diss/46.

MLA Handbook (7th Edition):

Rocheleau, Christian Ernest. “Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.” 1999. Web. 24 Oct 2020.

Vancouver:

Rocheleau CE. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2020 Oct 24]. Available from: https://escholarship.umassmed.edu/gsbs_diss/46.

Council of Science Editors:

Rocheleau CE. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/46


University of Oregon

12. Nipper, Rick William Jr., 1978-. Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts.

Degree: 2007, University of Oregon

 Asymmetric cell division (ACD) is a unique mechanism employed during development to achieve cellular diversity from a small number of progenitor cells. Cells undergoing ACD… (more)

Subjects/Keywords: G-proteins; Partner of inscuteable; Neuroblast; Asymmetric cell division; Cell polarity; Mud; Biochemistry; Pins

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APA (6th Edition):

Nipper, Rick William Jr., 1. (2007). Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/6194

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):

Nipper, Rick William Jr., 1978-. “Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts.” 2007. Thesis, University of Oregon. Accessed October 24, 2020. http://hdl.handle.net/1794/6194.

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

MLA Handbook (7th Edition):

Nipper, Rick William Jr., 1978-. “Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts.” 2007. Web. 24 Oct 2020.

Vancouver:

Nipper, Rick William Jr. 1. Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts. [Internet] [Thesis]. University of Oregon; 2007. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1794/6194.

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

Council of Science Editors:

Nipper, Rick William Jr. 1. Molecular function of the cell polarity protein partner of inscuteable in Drosophila neuroblasts. [Thesis]. University of Oregon; 2007. Available from: http://hdl.handle.net/1794/6194

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

13. Lee, Chan-jae. The roles of Shroom family proteins during Xenopus development.

Degree: PhD, Cell and Molecular Biology, 2009, University of Texas – Austin

 The Shroom family of proteins is currently comprised of four members, Shroom1, 2, 3 and 4. Since Shroom3 was shown to be a critical protein… (more)

Subjects/Keywords: Shroom family proteins; Xenopus development; Shroom3; Shroom2; Cell morphogenesis; Polarization; Pigment polarity

…involved in signaling for neural induction? .......39 CHAPTER III SHROOM FAMILY PROTEINS PLAY A… …III. 2. 3. All Shroom family proteins are able to control γ-tubulin distribution… …Shroom proteins control apicobasal cell elongation in epithelia… …proteins. .......................................................................61 viii III. 3… …proteins may be involved in cell heightening67 III. 3. 3. What is the function of the leucine… 

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APA (6th Edition):

Lee, C. (2009). The roles of Shroom family proteins during Xenopus development. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/6544

Chicago Manual of Style (16th Edition):

Lee, Chan-jae. “The roles of Shroom family proteins during Xenopus development.” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed October 24, 2020. http://hdl.handle.net/2152/6544.

MLA Handbook (7th Edition):

Lee, Chan-jae. “The roles of Shroom family proteins during Xenopus development.” 2009. Web. 24 Oct 2020.

Vancouver:

Lee C. The roles of Shroom family proteins during Xenopus development. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2152/6544.

Council of Science Editors:

Lee C. The roles of Shroom family proteins during Xenopus development. [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/6544

14. Geng, Cuiyun. Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis.

Degree: PhD, Molecular Biology, 2006, University of Texas – Austin

 Establishment of cell polarity requires the involvement of several posttranscriptional regulatory mechanisms, including mRNA localization and translational control. A family of highly conserved RNA binding… (more)

Subjects/Keywords: Cell polarity; MRNA localization; VICKZ proteins; Imp; MRNA translational control; Drosophila; Binding protein; Oogenesis

…17 VICKZ FAMILY PROTEINS ..20 VICKZ proteins involve in mRNA… …localization and translational control...20 Imp is a Drosophila homologue of VICKZ proteins… …hnRNP proteins Sqd and Hrp48 …....42 Imp is concentrated at the site of grk mRNA… …Overexpression of Imp alters dorsovental polarity and expression of grk …..47… …Imp overexpression disrupts oocyte polarity and expression of osk .49 DISCUSSION… 

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

APA (6th Edition):

Geng, C. (2006). Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/29593

Chicago Manual of Style (16th Edition):

Geng, Cuiyun. “Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis.” 2006. Doctoral Dissertation, University of Texas – Austin. Accessed October 24, 2020. http://hdl.handle.net/2152/29593.

MLA Handbook (7th Edition):

Geng, Cuiyun. “Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis.” 2006. Web. 24 Oct 2020.

Vancouver:

Geng C. Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2006. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2152/29593.

Council of Science Editors:

Geng C. Functional characterization of the role of Imp, a Drosophila mRNA binding protein, during oogenesis. [Doctoral Dissertation]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/29593


ETH Zürich

15. Bachmann, Stephan Jan. Development of Models for Biomolecular Simulation: Polarisability and Solvation.

Degree: 2014, ETH Zürich

Subjects/Keywords: POLARITÄT, HYDROPHILE UND LIPOPHOBE MOLEKÜLE UND INTERAKTIONEN (BIOPHYSIKALISCHE CHEMIE); MOLEKÜLDYNAMIK + MOLEKÜLMOBILITÄT + MOLEKÜLMOTILITÄT (BIOMOLEKÜLE); PROTEINE + POLYPEPTIDE (BIOCHEMIE); LÖSUNGSMITTELEINFLÜSSE + SOLVATATION + SOLVOLYSE (PHYSIKALISCHE CHEMIE); MOLEKULARE DYNAMIK (MOLEKÜLPHYSIK); POLARITY, HYDROPHILIC AND LIPOPHOBIC MOLECULES AND INTERACTIONS (BIOPHYSICAL CHEMISTRY); MOLECULAR DYNAMICS + MOLECULAR MOBILITY + MOLECULAR MOTILITY (BIOMOLECULES); PROTEINS + POLYPEPTIDES (BIOCHEMISTRY); SOLVENT EFFECTS + SOLVATATION + SOLVOLYSIS (PHYSICAL CHEMISTRY); MOLECULAR DYNAMICS (MOLECULAR PHYSICS); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/540; Life sciences; Chemistry

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

APA (6th Edition):

Bachmann, S. J. (2014). Development of Models for Biomolecular Simulation: Polarisability and Solvation. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154680

Chicago Manual of Style (16th Edition):

Bachmann, Stephan Jan. “Development of Models for Biomolecular Simulation: Polarisability and Solvation.” 2014. Doctoral Dissertation, ETH Zürich. Accessed October 24, 2020. http://hdl.handle.net/20.500.11850/154680.

MLA Handbook (7th Edition):

Bachmann, Stephan Jan. “Development of Models for Biomolecular Simulation: Polarisability and Solvation.” 2014. Web. 24 Oct 2020.

Vancouver:

Bachmann SJ. Development of Models for Biomolecular Simulation: Polarisability and Solvation. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/20.500.11850/154680.

Council of Science Editors:

Bachmann SJ. Development of Models for Biomolecular Simulation: Polarisability and Solvation. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/154680

.