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You searched for subject:( Cilia). Showing records 1 – 30 of 260 total matches.

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1. Craft, Julie Melissa. Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii.

Degree: PhD, Cellular Biology, 2015, University of Georgia

 The microtubule-based axoneme is the defining characteristic of all eukaryotic flagella and cilia. Assembly of this structure during ciliogenesis requires a vast translocation of the… (more)

Subjects/Keywords: cilia

Cilia: Conserved organelles with diverse functions ................... 1 1.2 Intraflagellar… …Transport .............................................................. 7 1.3 Cilia in human… …22 2.4 Tubulin enters cilia by IFT and diffusion .................................. 24 2.5… …The frequency of tubulin transport of IFT is regulated by the assembly status of cilia… …tubulin is increased in growing cilia… 

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APA (6th Edition):

Craft, J. M. (2015). Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/craft_julie_m_201512_phd

Chicago Manual of Style (16th Edition):

Craft, Julie Melissa. “Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii.” 2015. Doctoral Dissertation, University of Georgia. Accessed December 05, 2019. http://purl.galileo.usg.edu/uga_etd/craft_julie_m_201512_phd.

MLA Handbook (7th Edition):

Craft, Julie Melissa. “Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii.” 2015. Web. 05 Dec 2019.

Vancouver:

Craft JM. Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. [Internet] [Doctoral dissertation]. University of Georgia; 2015. [cited 2019 Dec 05]. Available from: http://purl.galileo.usg.edu/uga_etd/craft_julie_m_201512_phd.

Council of Science Editors:

Craft JM. Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. [Doctoral Dissertation]. University of Georgia; 2015. Available from: http://purl.galileo.usg.edu/uga_etd/craft_julie_m_201512_phd


University of Hong Kong

2. 徐强; Xu, Qiang. Modeling the deformation of primary cilium.

Degree: M. Phil., 2011, University of Hong Kong

In this thesis we developed a new mechanics model of the primary cilium and analyzed its bending behavior. The primary cilium that extends from the… (more)

Subjects/Keywords: Cilia and ciliary motion.

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APA (6th Edition):

徐强; Xu, Q. (2011). Modeling the deformation of primary cilium. (Masters Thesis). University of Hong Kong. Retrieved from Xu, Q. [徐强]. (2011). Modeling the deformation of primary cilium. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725000 ; http://dx.doi.org/10.5353/th_b4725000 ; http://hdl.handle.net/10722/173860

Chicago Manual of Style (16th Edition):

徐强; Xu, Qiang. “Modeling the deformation of primary cilium.” 2011. Masters Thesis, University of Hong Kong. Accessed December 05, 2019. Xu, Q. [徐强]. (2011). Modeling the deformation of primary cilium. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725000 ; http://dx.doi.org/10.5353/th_b4725000 ; http://hdl.handle.net/10722/173860.

MLA Handbook (7th Edition):

徐强; Xu, Qiang. “Modeling the deformation of primary cilium.” 2011. Web. 05 Dec 2019.

Vancouver:

徐强; Xu Q. Modeling the deformation of primary cilium. [Internet] [Masters thesis]. University of Hong Kong; 2011. [cited 2019 Dec 05]. Available from: Xu, Q. [徐强]. (2011). Modeling the deformation of primary cilium. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725000 ; http://dx.doi.org/10.5353/th_b4725000 ; http://hdl.handle.net/10722/173860.

Council of Science Editors:

徐强; Xu Q. Modeling the deformation of primary cilium. [Masters Thesis]. University of Hong Kong; 2011. Available from: Xu, Q. [徐强]. (2011). Modeling the deformation of primary cilium. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4725000 ; http://dx.doi.org/10.5353/th_b4725000 ; http://hdl.handle.net/10722/173860


Tulane University

3. Mannan, Forest. Singly-periodic Stokes Flow and the Simulation of Cilia.

Degree: 2017, Tulane University

1

Forest Mannan

Advisors/Committee Members: Cortez, Ricardo (Thesis advisor), School of Science & Engineering Mathematics (Degree granting institution).

Subjects/Keywords: Cilia Simulation

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APA (6th Edition):

Mannan, F. (2017). Singly-periodic Stokes Flow and the Simulation of Cilia. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:75417

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):

Mannan, Forest. “Singly-periodic Stokes Flow and the Simulation of Cilia.” 2017. Thesis, Tulane University. Accessed December 05, 2019. https://digitallibrary.tulane.edu/islandora/object/tulane:75417.

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

MLA Handbook (7th Edition):

Mannan, Forest. “Singly-periodic Stokes Flow and the Simulation of Cilia.” 2017. Web. 05 Dec 2019.

Vancouver:

Mannan F. Singly-periodic Stokes Flow and the Simulation of Cilia. [Internet] [Thesis]. Tulane University; 2017. [cited 2019 Dec 05]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:75417.

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

Council of Science Editors:

Mannan F. Singly-periodic Stokes Flow and the Simulation of Cilia. [Thesis]. Tulane University; 2017. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:75417

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


University of Toronto

4. Yu, Emily Pui Yun. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.

Degree: 2016, University of Toronto

Primary ciliary dyskinesia (PCD) is a disease that affects the function of respiratory cilia that helps protect against airway infections. Diagnosis is difficult with current… (more)

Subjects/Keywords: cilia; PCD; spdl1; zebrafish; 0758

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APA (6th Edition):

Yu, E. P. Y. (2016). Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76125

Chicago Manual of Style (16th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Masters Thesis, University of Toronto. Accessed December 05, 2019. http://hdl.handle.net/1807/76125.

MLA Handbook (7th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Web. 05 Dec 2019.

Vancouver:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1807/76125.

Council of Science Editors:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76125


University of Toronto

5. Yu, Emily Pui Yun. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.

Degree: 2016, University of Toronto

Primary ciliary dyskinesia (PCD) is a disease that affects the function of respiratory cilia that helps protect against airway infections. Diagnosis is difficult with current… (more)

Subjects/Keywords: cilia; PCD; spdl1; zebrafish; 0758

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APA (6th Edition):

Yu, E. P. Y. (2016). Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76193

Chicago Manual of Style (16th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Masters Thesis, University of Toronto. Accessed December 05, 2019. http://hdl.handle.net/1807/76193.

MLA Handbook (7th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Web. 05 Dec 2019.

Vancouver:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1807/76193.

Council of Science Editors:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76193


University of North Texas

6. Evans, Shakila K. Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection.

Degree: 2012, University of North Texas

 Primary cilia are essential in brain development, as mediators of sonic hedgehog signaling. However, their role in mature neurons remains elusive. One means to elucidate… (more)

Subjects/Keywords: Somatostatin; neuronal cilia; neuroprotection

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APA (6th Edition):

Evans, S. K. (2012). Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc177195/

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):

Evans, Shakila K. “Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection.” 2012. Thesis, University of North Texas. Accessed December 05, 2019. https://digital.library.unt.edu/ark:/67531/metadc177195/.

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

MLA Handbook (7th Edition):

Evans, Shakila K. “Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection.” 2012. Web. 05 Dec 2019.

Vancouver:

Evans SK. Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection. [Internet] [Thesis]. University of North Texas; 2012. [cited 2019 Dec 05]. Available from: https://digital.library.unt.edu/ark:/67531/metadc177195/.

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

Council of Science Editors:

Evans SK. Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection. [Thesis]. University of North Texas; 2012. Available from: https://digital.library.unt.edu/ark:/67531/metadc177195/

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


University of New South Wales

7. Shearer, Robert. Defining the role of the E3 ubiquitin ligase UBR5 in cancer.

Degree: Clinical School - St Vincent's Hospital, 2016, University of New South Wales

 Despite recent advances, breast cancer remains a major burden on the healthcare system in Australia and abroad. Of particular concern are cancer subtypes that currently… (more)

Subjects/Keywords: Ubiquitin; Cancer; Cilia; UBR5

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APA (6th Edition):

Shearer, R. (2016). Defining the role of the E3 ubiquitin ligase UBR5 in cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57120

Chicago Manual of Style (16th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Doctoral Dissertation, University of New South Wales. Accessed December 05, 2019. http://handle.unsw.edu.au/1959.4/57120.

MLA Handbook (7th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Web. 05 Dec 2019.

Vancouver:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2019 Dec 05]. Available from: http://handle.unsw.edu.au/1959.4/57120.

Council of Science Editors:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/57120


University of Saskatchewan

8. Waddell, Brandon 1993-. Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans.

Degree: 2019, University of Saskatchewan

 Across eukaryotic species, Shugoshin proteins perform several critical functions in meiotic and mitotic cells that ensures faithful chromosome segregation and the preservation of genomic stability.… (more)

Subjects/Keywords: Shugoshin; C. elegans; cilia

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APA (6th Edition):

Waddell, B. 1. (2019). Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12196

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):

Waddell, Brandon 1993-. “Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans.” 2019. Thesis, University of Saskatchewan. Accessed December 05, 2019. http://hdl.handle.net/10388/12196.

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

MLA Handbook (7th Edition):

Waddell, Brandon 1993-. “Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans.” 2019. Web. 05 Dec 2019.

Vancouver:

Waddell B1. Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10388/12196.

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

Council of Science Editors:

Waddell B1. Initial Characterisation of a Novel Role of Shugoshin in Ciliated Neurons of Caenorhabditis elegans. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12196

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


University of Texas – Austin

9. Tu, Fan. Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells.

Degree: PhD, Cell and Molecular Biology, 2017, University of Texas – Austin

 Multiciliated cells (MCCs) drive directional fluid flow in diverse tubular organs and are essential for development and homeostasis of the vertebrate central nervous system, airway,… (more)

Subjects/Keywords: Cilia; Myo5C; Arhgef18; Dennd2b; Actin

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APA (6th Edition):

Tu, F. (2017). Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63460

Chicago Manual of Style (16th Edition):

Tu, Fan. “Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed December 05, 2019. http://hdl.handle.net/2152/63460.

MLA Handbook (7th Edition):

Tu, Fan. “Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells.” 2017. Web. 05 Dec 2019.

Vancouver:

Tu F. Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/2152/63460.

Council of Science Editors:

Tu F. Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/63460


Princeton University

10. Morante, Nicholas Morante. The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease .

Degree: PhD, 2017, Princeton University

 Motile cilia are microtubule based cellular projections that are important for the generation of fluid flow and cell propulsion in many tissues in vertebrates. Cilia(more)

Subjects/Keywords: Cilia; Primary ciliary dyskinesia; Scoliosis

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APA (6th Edition):

Morante, N. M. (2017). The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01g158bk79v

Chicago Manual of Style (16th Edition):

Morante, Nicholas Morante. “The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease .” 2017. Doctoral Dissertation, Princeton University. Accessed December 05, 2019. http://arks.princeton.edu/ark:/88435/dsp01g158bk79v.

MLA Handbook (7th Edition):

Morante, Nicholas Morante. “The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease .” 2017. Web. 05 Dec 2019.

Vancouver:

Morante NM. The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Dec 05]. Available from: http://arks.princeton.edu/ark:/88435/dsp01g158bk79v.

Council of Science Editors:

Morante NM. The Virtues of Self-Flagellation: Forward and Reverse Genetics to Probe the Roles of Motile Cilia in Vertebrate Development and Human Disease . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01g158bk79v


Universidade Nova

11. Ferreira, Rita Joana Rodrigues da Silva Rua. Cilia motility studies in zebrafish embryos.

Degree: 2012, Universidade Nova

A thesis submitted in fulfilment of the requirements for the degree of Masters in Molecular Genetics and Biomedicine

Motile ciliary dysfunctions cause specific Ciliopathies that… (more)

Subjects/Keywords: Kupffer’s vesicle; Motile cilia; Cilia beat frequency; Fluid-flow; DeltaD-/- mutants

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APA (6th Edition):

Ferreira, R. J. R. d. S. R. (2012). Cilia motility studies in zebrafish embryos. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7984

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):

Ferreira, Rita Joana Rodrigues da Silva Rua. “Cilia motility studies in zebrafish embryos.” 2012. Thesis, Universidade Nova. Accessed December 05, 2019. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7984.

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

MLA Handbook (7th Edition):

Ferreira, Rita Joana Rodrigues da Silva Rua. “Cilia motility studies in zebrafish embryos.” 2012. Web. 05 Dec 2019.

Vancouver:

Ferreira RJRdSR. Cilia motility studies in zebrafish embryos. [Internet] [Thesis]. Universidade Nova; 2012. [cited 2019 Dec 05]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7984.

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

Council of Science Editors:

Ferreira RJRdSR. Cilia motility studies in zebrafish embryos. [Thesis]. Universidade Nova; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/7984

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


University of Toledo Health Science Campus

12. Gibson, Hayley. The Effect of Muscarinic Modulators on Cilia Structure and Function.

Degree: MS, Pharmaceutical Sciences (Pharmacology/Toxicology), 2017, University of Toledo Health Science Campus

 Primary endothelial cilia are microtubule-based organelles that act as mechano-sensors to help detect and respond to changes in the extracellular environment. One of these responses… (more)

Subjects/Keywords: Pharmacology; Polycystic kidney disease; acetylcholine muscarinic 1 receptor; primary endothelial cilia; blood pressure; hypertension; cilia length; cilia function

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APA (6th Edition):

Gibson, H. (2017). The Effect of Muscarinic Modulators on Cilia Structure and Function. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1499104909617105

Chicago Manual of Style (16th Edition):

Gibson, Hayley. “The Effect of Muscarinic Modulators on Cilia Structure and Function.” 2017. Masters Thesis, University of Toledo Health Science Campus. Accessed December 05, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1499104909617105.

MLA Handbook (7th Edition):

Gibson, Hayley. “The Effect of Muscarinic Modulators on Cilia Structure and Function.” 2017. Web. 05 Dec 2019.

Vancouver:

Gibson H. The Effect of Muscarinic Modulators on Cilia Structure and Function. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2017. [cited 2019 Dec 05]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1499104909617105.

Council of Science Editors:

Gibson H. The Effect of Muscarinic Modulators on Cilia Structure and Function. [Masters Thesis]. University of Toledo Health Science Campus; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1499104909617105


University of Colorado

13. Vonderfecht, Tyson. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.

Degree: PhD, Chemistry & Biochemistry, 2012, University of Colorado

  The basal body is a microtubule-organizing center responsible for nucleating the cilium, a cellular structure important for a wide variety of cellular functions such… (more)

Subjects/Keywords: basal body; centrin; cilia; Tetrahymena; Cell Biology

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APA (6th Edition):

Vonderfecht, T. (2012). The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/54

Chicago Manual of Style (16th Edition):

Vonderfecht, Tyson. “The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.” 2012. Doctoral Dissertation, University of Colorado. Accessed December 05, 2019. http://scholar.colorado.edu/chem_gradetds/54.

MLA Handbook (7th Edition):

Vonderfecht, Tyson. “The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies.” 2012. Web. 05 Dec 2019.

Vancouver:

Vonderfecht T. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2019 Dec 05]. Available from: http://scholar.colorado.edu/chem_gradetds/54.

Council of Science Editors:

Vonderfecht T. The two human centrin homologues in Tetrahymena have similar but distinct functions at basal bodies. [Doctoral Dissertation]. University of Colorado; 2012. Available from: http://scholar.colorado.edu/chem_gradetds/54


Miami University

14. Subramanian, Aswati. p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila.

Degree: PhD, Zoology, 2014, Miami University

 Axonemal dyneins are molecular motors composed of heavy chains, intermediate chains and light chains. Dynein light chains that are associated with the heavy chains help… (more)

Subjects/Keywords: Biology; Tetrahymena, p28 dynein light chains, cilia

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APA (6th Edition):

Subramanian, A. (2014). p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1389719903

Chicago Manual of Style (16th Edition):

Subramanian, Aswati. “p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila.” 2014. Doctoral Dissertation, Miami University. Accessed December 05, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1389719903.

MLA Handbook (7th Edition):

Subramanian, Aswati. “p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila.” 2014. Web. 05 Dec 2019.

Vancouver:

Subramanian A. p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila. [Internet] [Doctoral dissertation]. Miami University; 2014. [cited 2019 Dec 05]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1389719903.

Council of Science Editors:

Subramanian A. p28 DYNEIN LIGHT CHAINS AND CILIARY MOTILITY IN Tetrahymena thermophila. [Doctoral Dissertation]. Miami University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1389719903


University of Edinburgh

15. Hall, Emma Andisi. Screening for genes involved in cilia formation and function.

Degree: PhD, 2012, University of Edinburgh

Cilia are small microtubule based structures found on the surface of almost all mammalian cells, enclosed in a highly specialised extension of the cell membrane.… (more)

Subjects/Keywords: 572.8; cilia; Azi1; RNAi; RNA interference

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APA (6th Edition):

Hall, E. A. (2012). Screening for genes involved in cilia formation and function. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9898

Chicago Manual of Style (16th Edition):

Hall, Emma Andisi. “Screening for genes involved in cilia formation and function.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2019. http://hdl.handle.net/1842/9898.

MLA Handbook (7th Edition):

Hall, Emma Andisi. “Screening for genes involved in cilia formation and function.” 2012. Web. 05 Dec 2019.

Vancouver:

Hall EA. Screening for genes involved in cilia formation and function. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1842/9898.

Council of Science Editors:

Hall EA. Screening for genes involved in cilia formation and function. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/9898

16. McIntosh, Kate. The extra ciliary roles of Meckel-Gruber syndrome proteins.

Degree: PhD, 2015, University of Exeter

 Meckel-Gruber syndrome (MKS) is a recessive genetic disease that is uniformly lethal in affected children due to resultant developmental defects in the kidney and brain.… (more)

Subjects/Keywords: 500; MKS; actin; cilia; ciliopathy; microtubules; ROCK

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APA (6th Edition):

McIntosh, K. (2015). The extra ciliary roles of Meckel-Gruber syndrome proteins. (Doctoral Dissertation). University of Exeter. Retrieved from http://hdl.handle.net/10871/20774

Chicago Manual of Style (16th Edition):

McIntosh, Kate. “The extra ciliary roles of Meckel-Gruber syndrome proteins.” 2015. Doctoral Dissertation, University of Exeter. Accessed December 05, 2019. http://hdl.handle.net/10871/20774.

MLA Handbook (7th Edition):

McIntosh, Kate. “The extra ciliary roles of Meckel-Gruber syndrome proteins.” 2015. Web. 05 Dec 2019.

Vancouver:

McIntosh K. The extra ciliary roles of Meckel-Gruber syndrome proteins. [Internet] [Doctoral dissertation]. University of Exeter; 2015. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10871/20774.

Council of Science Editors:

McIntosh K. The extra ciliary roles of Meckel-Gruber syndrome proteins. [Doctoral Dissertation]. University of Exeter; 2015. Available from: http://hdl.handle.net/10871/20774


University of Manchester

17. Boylan, Michael. A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse.

Degree: PhD, 2015, University of Manchester

 Human congenital heart disease (CHD) is the most common cause of non-infectious neonatal death affecting 1-2% of live births (Hoffman and Kaplan, 2002). Treatment of… (more)

Subjects/Keywords: 616.1; Prpf8; Cilia; Mouse; Left Right Axis

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APA (6th Edition):

Boylan, M. (2015). A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-novel-point-mutation-in-prpf8-causes-defects-in-leftright-axis-establishment-in-the-mouse(3d547ed3-ecc3-472c-8703-cb6a84270ba4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674710

Chicago Manual of Style (16th Edition):

Boylan, Michael. “A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse.” 2015. Doctoral Dissertation, University of Manchester. Accessed December 05, 2019. https://www.research.manchester.ac.uk/portal/en/theses/a-novel-point-mutation-in-prpf8-causes-defects-in-leftright-axis-establishment-in-the-mouse(3d547ed3-ecc3-472c-8703-cb6a84270ba4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674710.

MLA Handbook (7th Edition):

Boylan, Michael. “A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse.” 2015. Web. 05 Dec 2019.

Vancouver:

Boylan M. A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Dec 05]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-novel-point-mutation-in-prpf8-causes-defects-in-leftright-axis-establishment-in-the-mouse(3d547ed3-ecc3-472c-8703-cb6a84270ba4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674710.

Council of Science Editors:

Boylan M. A novel point mutation in Prpf8 causes defects in left-right axis establishment in the mouse. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-novel-point-mutation-in-prpf8-causes-defects-in-leftright-axis-establishment-in-the-mouse(3d547ed3-ecc3-472c-8703-cb6a84270ba4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674710


University of Illinois – Chicago

18. Appelbe, Oliver. Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1.

Degree: 2013, University of Illinois – Chicago

 Mouse genetics in development: the Juvenile hydrocephalus mouse and conditional deletion of Delta-like 1 Oliver Katsumi Appelbe Biological Sciences University of Illinois at Chicago Chicago,… (more)

Subjects/Keywords: hydrocephalus; cilia; Jhy; Dlk1; conditional deletion

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APA (6th Edition):

Appelbe, O. (2013). Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9776

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):

Appelbe, Oliver. “Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1.” 2013. Thesis, University of Illinois – Chicago. Accessed December 05, 2019. http://hdl.handle.net/10027/9776.

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

MLA Handbook (7th Edition):

Appelbe, Oliver. “Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1.” 2013. Web. 05 Dec 2019.

Vancouver:

Appelbe O. Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10027/9776.

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

Council of Science Editors:

Appelbe O. Mouse Genetics in Development: The Juvenile Hydrocephalus Mouse and Conditional Deletion of Delta-like 1. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/9776

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

19. Wilson, Kate. Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure.

Degree: PhD, Mechanical Engineering & Materials Science, 2015, Washington University in St. Louis

Cilia and flagella are subcellular organelles used to generate fluid flow or propel the cell. These long cylindrical structures are composed of cytoskeletal elements… (more)

Subjects/Keywords: Axoneme; Chlamydomonas; Cilia; Flagella; Modeling; Viscosity; Engineering

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APA (6th Edition):

Wilson, K. (2015). Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/eng_etds/102

Chicago Manual of Style (16th Edition):

Wilson, Kate. “Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure.” 2015. Doctoral Dissertation, Washington University in St. Louis. Accessed December 05, 2019. https://openscholarship.wustl.edu/eng_etds/102.

MLA Handbook (7th Edition):

Wilson, Kate. “Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure.” 2015. Web. 05 Dec 2019.

Vancouver:

Wilson K. Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2015. [cited 2019 Dec 05]. Available from: https://openscholarship.wustl.edu/eng_etds/102.

Council of Science Editors:

Wilson K. Probing Mechanical Forces in Flagella by Manipulation of Media Viscosity and Axonemal Structure. [Doctoral Dissertation]. Washington University in St. Louis; 2015. Available from: https://openscholarship.wustl.edu/eng_etds/102


University of Manchester

20. Boylan, Michael. A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse.

Degree: 2015, University of Manchester

Human congenital heart disease (CHD) is the most common cause of non-infectious neonatal death affecting 1-2% of live births (Hoffman and Kaplan, 2002). Treatment of… (more)

Subjects/Keywords: Prpf8; Cilia; Mouse; Left Right Axis

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APA (6th Edition):

Boylan, M. (2015). A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277226

Chicago Manual of Style (16th Edition):

Boylan, Michael. “A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse.” 2015. Doctoral Dissertation, University of Manchester. Accessed December 05, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277226.

MLA Handbook (7th Edition):

Boylan, Michael. “A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse.” 2015. Web. 05 Dec 2019.

Vancouver:

Boylan M. A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Dec 05]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277226.

Council of Science Editors:

Boylan M. A Novel Point Mutation in Prpf8 Causes Defects in Left-Right Axis Establishment in the Mouse. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:277226


McMaster University

21. Woloshansky, Tanya S. Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models.

Degree: MSc, 2014, McMaster University

The primary cilium is a singular signaling organelle found on most mammalian cell types. Dysfunction of the primary cilium or associated structures form a… (more)

Subjects/Keywords: Primary Cilia; Huntington's disease; Huntingtin; Acetylation

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APA (6th Edition):

Woloshansky, T. S. (2014). Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15357

Chicago Manual of Style (16th Edition):

Woloshansky, Tanya S. “Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models.” 2014. Masters Thesis, McMaster University. Accessed December 05, 2019. http://hdl.handle.net/11375/15357.

MLA Handbook (7th Edition):

Woloshansky, Tanya S. “Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models.” 2014. Web. 05 Dec 2019.

Vancouver:

Woloshansky TS. Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/11375/15357.

Council of Science Editors:

Woloshansky TS. Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15357


University of Edinburgh

22. Mali, Girish Ram. Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10.

Degree: PhD, 2015, University of Edinburgh

Cilia are polarized extensions of the cells microtubule-based cytoskeleton dedicated to sensory, signaling and motility-related functions. In mammals, there are two main types of cilia,… (more)

Subjects/Keywords: 571.6; motile cilia; dynein assembly; CRISPR

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APA (6th Edition):

Mali, G. R. (2015). Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/21683

Chicago Manual of Style (16th Edition):

Mali, Girish Ram. “Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2019. http://hdl.handle.net/1842/21683.

MLA Handbook (7th Edition):

Mali, Girish Ram. “Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10.” 2015. Web. 05 Dec 2019.

Vancouver:

Mali GR. Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1842/21683.

Council of Science Editors:

Mali GR. Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/21683


University of Edinburgh

23. Moore, Daniel John. Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons.

Degree: PhD, 2014, University of Edinburgh

 Drosophila provide an excellent model organism in which to study cilia as there are only two ciliated cell types; the sensory neurons and sperm cells.… (more)

Subjects/Keywords: 612.8; cilia; Drosophila; Primary Ciliary Dyskinesia; PCD

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APA (6th Edition):

Moore, D. J. (2014). Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17918

Chicago Manual of Style (16th Edition):

Moore, Daniel John. “Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2019. http://hdl.handle.net/1842/17918.

MLA Handbook (7th Edition):

Moore, Daniel John. “Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons.” 2014. Web. 05 Dec 2019.

Vancouver:

Moore DJ. Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/1842/17918.

Council of Science Editors:

Moore DJ. Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/17918


Wright State University

24. Magley, Robert Alan. A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis.

Degree: MS, Biological Sciences, 2018, Wright State University

 Tubulin comprises the structural element of microtubules and Tau is one ofmany microtubule-associated proteins. Tau Tubulin Kinase (TTBK)phosphorylates both Tau and Tubulin and is required… (more)

Subjects/Keywords: Biology; Planarian; Schmitdea mediterranea; cilia; sperm

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APA (6th Edition):

Magley, R. A. (2018). A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright153546883070243

Chicago Manual of Style (16th Edition):

Magley, Robert Alan. “A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis.” 2018. Masters Thesis, Wright State University. Accessed December 05, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright153546883070243.

MLA Handbook (7th Edition):

Magley, Robert Alan. “A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis.” 2018. Web. 05 Dec 2019.

Vancouver:

Magley RA. A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis. [Internet] [Masters thesis]. Wright State University; 2018. [cited 2019 Dec 05]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright153546883070243.

Council of Science Editors:

Magley RA. A planarian Tau Tubulin Kinase homolog is required for spermatogenesis and epithelial ciliogenesis. [Masters Thesis]. Wright State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright153546883070243


Vanderbilt University

25. Armour, Eric Andrew. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 Tuberous Sclerosis Complex (TSC) is a multi-organ hamartomatous disease caused by loss of function mutations in either the TSC1 or TSC2 genes. Despite involvement of… (more)

Subjects/Keywords: TSC; pluripotency; Tuberous Sclerosis; cilia; cystogenesis; mTOR

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APA (6th Edition):

Armour, E. A. (2013). Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11162013-142310/ ;

Chicago Manual of Style (16th Edition):

Armour, Eric Andrew. “Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 05, 2019. http://etd.library.vanderbilt.edu/available/etd-11162013-142310/ ;.

MLA Handbook (7th Edition):

Armour, Eric Andrew. “Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.” 2013. Web. 05 Dec 2019.

Vancouver:

Armour EA. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Dec 05]. Available from: http://etd.library.vanderbilt.edu/available/etd-11162013-142310/ ;.

Council of Science Editors:

Armour EA. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-11162013-142310/ ;


Brandeis University

26. Carlone, Michael. Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function.

Degree: 2015, Brandeis University

 Paramecium tetraurelia is a ciliate that has long been used for a variety of different scientific studies, but has yet to be established as a… (more)

Subjects/Keywords: Paramecium; tetraurelia; cilia; microscopy; electron; tomography

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APA (6th Edition):

Carlone, M. (2015). Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/30511

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):

Carlone, Michael. “Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function.” 2015. Thesis, Brandeis University. Accessed December 05, 2019. http://hdl.handle.net/10192/30511.

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

MLA Handbook (7th Edition):

Carlone, Michael. “Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function.” 2015. Web. 05 Dec 2019.

Vancouver:

Carlone M. Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function. [Internet] [Thesis]. Brandeis University; 2015. [cited 2019 Dec 05]. Available from: http://hdl.handle.net/10192/30511.

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

Council of Science Editors:

Carlone M. Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function. [Thesis]. Brandeis University; 2015. Available from: http://hdl.handle.net/10192/30511

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


University of New Mexico

27. Sun, Xiaobo. Transcriptional networks of lung airway epithelial ciliogenesis.

Degree: Biomedical Sciences Graduate Program, 2009, University of New Mexico

 Motile cilia of the mammalian airway play an essential role in innate defense. The coordinated transcriptional regulation of cilial axoneme genes remains to be elucidated.… (more)

Subjects/Keywords: Transcriptional Regulation; Lung Airway Epithelium; Cilia; Ciliogenesis

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APA (6th Edition):

Sun, X. (2009). Transcriptional networks of lung airway epithelial ciliogenesis. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/107

Chicago Manual of Style (16th Edition):

Sun, Xiaobo. “Transcriptional networks of lung airway epithelial ciliogenesis.” 2009. Masters Thesis, University of New Mexico. Accessed December 05, 2019. https://digitalrepository.unm.edu/biom_etds/107.

MLA Handbook (7th Edition):

Sun, Xiaobo. “Transcriptional networks of lung airway epithelial ciliogenesis.” 2009. Web. 05 Dec 2019.

Vancouver:

Sun X. Transcriptional networks of lung airway epithelial ciliogenesis. [Internet] [Masters thesis]. University of New Mexico; 2009. [cited 2019 Dec 05]. Available from: https://digitalrepository.unm.edu/biom_etds/107.

Council of Science Editors:

Sun X. Transcriptional networks of lung airway epithelial ciliogenesis. [Masters Thesis]. University of New Mexico; 2009. Available from: https://digitalrepository.unm.edu/biom_etds/107


Rochester Institute of Technology

28. Norton, Michael M. Modeling problems in mucus viscoelasticity and mucociliary clearance.

Degree: Mechanical Engineering, 2009, Rochester Institute of Technology

 From the common cold and allergies to severe chronic and acute respiratory impairments, the function of the body's mucociliary clearance mechanism plays a primary defense… (more)

Subjects/Keywords: Cilia; Clearance; Maxwell; Model; Mucus; Viscoelastic

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APA (6th Edition):

Norton, M. M. (2009). Modeling problems in mucus viscoelasticity and mucociliary clearance. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/7181

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):

Norton, Michael M. “Modeling problems in mucus viscoelasticity and mucociliary clearance.” 2009. Thesis, Rochester Institute of Technology. Accessed December 05, 2019. https://scholarworks.rit.edu/theses/7181.

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

MLA Handbook (7th Edition):

Norton, Michael M. “Modeling problems in mucus viscoelasticity and mucociliary clearance.” 2009. Web. 05 Dec 2019.

Vancouver:

Norton MM. Modeling problems in mucus viscoelasticity and mucociliary clearance. [Internet] [Thesis]. Rochester Institute of Technology; 2009. [cited 2019 Dec 05]. Available from: https://scholarworks.rit.edu/theses/7181.

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

Council of Science Editors:

Norton MM. Modeling problems in mucus viscoelasticity and mucociliary clearance. [Thesis]. Rochester Institute of Technology; 2009. Available from: https://scholarworks.rit.edu/theses/7181

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


Penn State University

29. Yang, Xiaoxu. Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system.

Degree: 2017, Penn State University

 The Hedgehog (Hh) signaling pathway is crucial for various developmental processes such as proliferation, differentiation and cell migration. Primary cilia are critical for Hh signaling… (more)

Subjects/Keywords: Hh signaling; Sufu; Gli2; primary cilia

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APA (6th Edition):

Yang, X. (2017). Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system. (Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/14719xzy112

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):

Yang, Xiaoxu. “Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system.” 2017. Thesis, Penn State University. Accessed December 05, 2019. https://etda.libraries.psu.edu/catalog/14719xzy112.

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

MLA Handbook (7th Edition):

Yang, Xiaoxu. “Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system.” 2017. Web. 05 Dec 2019.

Vancouver:

Yang X. Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system. [Internet] [Thesis]. Penn State University; 2017. [cited 2019 Dec 05]. Available from: https://etda.libraries.psu.edu/catalog/14719xzy112.

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

Council of Science Editors:

Yang X. Investigating the roles of primary cilium in Gli protein activation and Hedgehog signaling pathway using Sufu/Gli ciliary recruitment system. [Thesis]. Penn State University; 2017. Available from: https://etda.libraries.psu.edu/catalog/14719xzy112

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


University of Iowa

30. Scott, Charles Anthony. Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease.

Degree: PhD, Biology, 2017, University of Iowa

  Mutations in BBS6 cause two clinically distinct syndromes, Bardet-Biedl syndrome (BBS), a syndrome caused by defects in cilia transport and function, as well as… (more)

Subjects/Keywords: bardet-biedl; cilia; heart; zebrafish; Biology

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

APA (6th Edition):

Scott, C. A. (2017). Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5848

Chicago Manual of Style (16th Edition):

Scott, Charles Anthony. “Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease.” 2017. Doctoral Dissertation, University of Iowa. Accessed December 05, 2019. https://ir.uiowa.edu/etd/5848.

MLA Handbook (7th Edition):

Scott, Charles Anthony. “Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease.” 2017. Web. 05 Dec 2019.

Vancouver:

Scott CA. Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2019 Dec 05]. Available from: https://ir.uiowa.edu/etd/5848.

Council of Science Editors:

Scott CA. Novel mechanisms of Bardet-Biedl syndrome proteins: implications in blindness and congenital heart disease. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5848

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