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You searched for subject:(Cilia). Showing records 1 – 30 of 296 total matches.

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Boston University

1. Cifuni, Justin Michael. Identification and isolation of primary cilia in the HAT-7 cell line.

Degree: MSin Dentistry, Molecular and Cell Biology, 2015, Boston University

 Primary cilia (PC) are 9+0 arranged microtubule based cellular organelles that are present on the surface of most eukaryotic cells. Their functions in various locations… (more)

Subjects/Keywords: Cilia

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APA (6th Edition):

Cifuni, J. M. (2015). Identification and isolation of primary cilia in the HAT-7 cell line. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/31778

Chicago Manual of Style (16th Edition):

Cifuni, Justin Michael. “Identification and isolation of primary cilia in the HAT-7 cell line.” 2015. Masters Thesis, Boston University. Accessed October 28, 2020. http://hdl.handle.net/2144/31778.

MLA Handbook (7th Edition):

Cifuni, Justin Michael. “Identification and isolation of primary cilia in the HAT-7 cell line.” 2015. Web. 28 Oct 2020.

Vancouver:

Cifuni JM. Identification and isolation of primary cilia in the HAT-7 cell line. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2144/31778.

Council of Science Editors:

Cifuni JM. Identification and isolation of primary cilia in the HAT-7 cell line. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/31778


Tulane University

2. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Mannan F. Singly-periodic Stokes Flow and the Simulation of Cilia. [Internet] [Thesis]. Tulane University; 2017. [cited 2020 Oct 28]. 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

3. 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 October 28, 2020. http://hdl.handle.net/1807/76125.

MLA Handbook (7th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Web. 28 Oct 2020.

Vancouver:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 28]. 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

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/1807/76193

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 October 28, 2020. http://hdl.handle.net/1807/76193.

MLA Handbook (7th Edition):

Yu, Emily Pui Yun. “Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia.” 2016. Web. 28 Oct 2020.

Vancouver:

Yu EPY. Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 28]. 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

5. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Evans SK. Somatostatin Receptors on Neuronal Cilia: Evidence for Neuroprotection. [Internet] [Thesis]. University of North Texas; 2012. [cited 2020 Oct 28]. 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 Georgia

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

Degree: 2016, 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; flagella; intraflagellar transport; tubulin

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APA (6th Edition):

Craft, J. M. (2016). Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/35047

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):

Craft, Julie Melissa. “Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii.” 2016. Thesis, University of Georgia. Accessed October 28, 2020. http://hdl.handle.net/10724/35047.

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

MLA Handbook (7th Edition):

Craft, Julie Melissa. “Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii.” 2016. Web. 28 Oct 2020.

Vancouver:

Craft JM. Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. [Internet] [Thesis]. University of Georgia; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10724/35047.

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

Council of Science Editors:

Craft JM. Cilium-autonomous regulation of tubulin transport by intraflagellar transport in Chlamydomonas reinhardtii. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/35047

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 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true

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 October 28, 2020. http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true.

MLA Handbook (7th Edition):

Shearer, Robert. “Defining the role of the E3 ubiquitin ligase UBR5 in cancer.” 2016. Web. 28 Oct 2020.

Vancouver:

Shearer R. Defining the role of the E3 ubiquitin ligase UBR5 in cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2020 Oct 28]. Available from: http://handle.unsw.edu.au/1959.4/57120 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true.

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 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42626/SOURCE02?view=true


University of Texas – Austin

8. 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 October 28, 2020. http://hdl.handle.net/2152/63460.

MLA Handbook (7th Edition):

Tu, Fan. “Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells.” 2017. Web. 28 Oct 2020.

Vancouver:

Tu F. Systematic analysis of Rfx2 target genes in vertebrate multiciliated cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Oct 28]. 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

9. 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 October 28, 2020. 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. 28 Oct 2020.

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 2020 Oct 28]. 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

10. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Ferreira RJRdSR. Cilia motility studies in zebrafish embryos. [Internet] [Thesis]. Universidade Nova; 2012. [cited 2020 Oct 28]. 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


Vanderbilt University

11. 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://hdl.handle.net/1803/14546

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 October 28, 2020. http://hdl.handle.net/1803/14546.

MLA Handbook (7th Edition):

Armour, Eric Andrew. “Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.” 2013. Web. 28 Oct 2020.

Vancouver:

Armour EA. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1803/14546.

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://hdl.handle.net/1803/14546


Queen Mary, University of London

12. O'Toole, Samuel Matthew. The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?.

Degree: PhD, 2019, Queen Mary, University of London

 Primary cilia are microtubule-based cellular organelles that project into the extracellular space. They subserve a wide range of sensory stimuli, co-ordinate and modulate a number… (more)

Subjects/Keywords: Primary cilia; tumourigenesis; phaeochromocytomas; neuroendocrine tumours

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APA (6th Edition):

O'Toole, S. M. (2019). The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/60609 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791868

Chicago Manual of Style (16th Edition):

O'Toole, Samuel Matthew. “The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?.” 2019. Doctoral Dissertation, Queen Mary, University of London. Accessed October 28, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/60609 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791868.

MLA Handbook (7th Edition):

O'Toole, Samuel Matthew. “The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?.” 2019. Web. 28 Oct 2020.

Vancouver:

O'Toole SM. The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2019. [cited 2020 Oct 28]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/60609 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791868.

Council of Science Editors:

O'Toole SM. The molecular pathogenesis and diagnosis of phaeochromocytoma : roles for primary cilia and adrenal venous sampling?. [Doctoral Dissertation]. Queen Mary, University of London; 2019. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/60609 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.791868


McMaster University

13. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Woloshansky TS. Primary Cilia Dynamics, Morphology and Acetylation are Abnormal in Huntington’s Disease Cell Models. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2020 Oct 28]. 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


Penn State University

14. Liu, Jinling. Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse.

Degree: 2014, Penn State University

 The Hedgehog (Hh) signaling is crucial for vertebrate development and physiology. The morphogen Sonic hedgehog (Shh), one of the Hh family of secreted proteins, plays… (more)

Subjects/Keywords: hedgehog; spinal cord patterning; Gli; Sufu; cilia

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APA (6th Edition):

Liu, J. (2014). Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23511

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

Chicago Manual of Style (16th Edition):

Liu, Jinling. “Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse.” 2014. Thesis, Penn State University. Accessed October 28, 2020. https://submit-etda.libraries.psu.edu/catalog/23511.

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

MLA Handbook (7th Edition):

Liu, Jinling. “Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse.” 2014. Web. 28 Oct 2020.

Vancouver:

Liu J. Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse. [Internet] [Thesis]. Penn State University; 2014. [cited 2020 Oct 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/23511.

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

Council of Science Editors:

Liu J. Genetic analyses of the cilia-dependent hedgehog signal transduction in the mouse. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23511

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


Penn State University

15. 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://submit-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 October 28, 2020. https://submit-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. 28 Oct 2020.

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 2020 Oct 28]. Available from: https://submit-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://submit-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 Cambridge

16. Hamilton, Evelyn Alexandra Waterhouse. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.

Degree: PhD, 2019, University of Cambridge

 Synchronisation is broadly defined as the coordinated action of two or more individual elements that exhibit some time periodic behaviour. It is widely observed across… (more)

Subjects/Keywords: rower model; hydrodynamic forces; synchronisation; cilia

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APA (6th Edition):

Hamilton, E. A. W. (2019). Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/299204

Chicago Manual of Style (16th Edition):

Hamilton, Evelyn Alexandra Waterhouse. “Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 28, 2020. https://www.repository.cam.ac.uk/handle/1810/299204.

MLA Handbook (7th Edition):

Hamilton, Evelyn Alexandra Waterhouse. “Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.” 2019. Web. 28 Oct 2020.

Vancouver:

Hamilton EAW. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 28]. Available from: https://www.repository.cam.ac.uk/handle/1810/299204.

Council of Science Editors:

Hamilton EAW. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/299204


University of Colorado

17. 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 https://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 October 28, 2020. https://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. 28 Oct 2020.

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 2020 Oct 28]. Available from: https://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: https://scholar.colorado.edu/chem_gradetds/54


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 October 28, 2020. 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. 28 Oct 2020.

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 2020 Oct 28]. 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. 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 October 28, 2020. http://hdl.handle.net/10871/20774.

MLA Handbook (7th Edition):

McIntosh, Kate. “The extra ciliary roles of Meckel-Gruber syndrome proteins.” 2015. Web. 28 Oct 2020.

Vancouver:

McIntosh K. The extra ciliary roles of Meckel-Gruber syndrome proteins. [Internet] [Doctoral dissertation]. University of Exeter; 2015. [cited 2020 Oct 28]. 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

20. 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 October 28, 2020. 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. 28 Oct 2020.

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 2020 Oct 28]. 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


Brandeis University

21. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Carlone M. Establishing Paramecium tetraurelia as a new genetic model system for studying ciliary structure and function. [Internet] [Thesis]. Brandeis University; 2015. [cited 2020 Oct 28]. 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 Iowa

22. 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 (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 October 28, 2020. 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. 28 Oct 2020.

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 2020 Oct 28]. 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


University of Cambridge

23. Pellicciotta, Nicola. The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia.

Degree: PhD, 2020, University of Cambridge

 Fluid flow generated by a ciliated epithelium is a fascinating evidence of collective behaviour in nature. In many organs and eukaryotic organisms, thousands of microscale… (more)

Subjects/Keywords: motile cilia; synchronisation; multiciliated cells; microfluidics

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APA (6th Edition):

Pellicciotta, N. (2020). The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303640

Chicago Manual of Style (16th Edition):

Pellicciotta, Nicola. “The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 28, 2020. https://www.repository.cam.ac.uk/handle/1810/303640.

MLA Handbook (7th Edition):

Pellicciotta, Nicola. “The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia.” 2020. Web. 28 Oct 2020.

Vancouver:

Pellicciotta N. The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 28]. Available from: https://www.repository.cam.ac.uk/handle/1810/303640.

Council of Science Editors:

Pellicciotta N. The role of hydrodynamic forces in synchronisation and alignment of mammalian motile cilia. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303640

24. 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 October 28, 2020. 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. 28 Oct 2020.

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 2020 Oct 28]. 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 Edinburgh

25. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Mali GR. Multisystem functional characterisation of motile ciliopathy genes HEATR2 and ZMYND10. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Oct 28]. 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

26. 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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

Moore DJ. Identification and characterisation of conserved ciliary genes expressed in Drosophila sensory neurons. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Oct 28]. 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


University of Edinburgh

27. 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 October 28, 2020. http://hdl.handle.net/1842/9898.

MLA Handbook (7th Edition):

Hall, Emma Andisi. “Screening for genes involved in cilia formation and function.” 2012. Web. 28 Oct 2020.

Vancouver:

Hall EA. Screening for genes involved in cilia formation and function. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Oct 28]. 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


University of North Texas

28. Hao, Yung-Chia. Primary Cilia in the Oligodendrocyte Lineage.

Degree: 2013, University of North Texas

 oligodendrocytes migrate from the corpus callosum into the overlying cortex. The incidence of cilia did not change markedly across age groups, and did not vary… (more)

Subjects/Keywords: Primary cilia; oligodendrocyte precursor cell; sonic hedgehog

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APA (6th Edition):

Hao, Y. (2013). Primary Cilia in the Oligodendrocyte Lineage. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc271828/

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):

Hao, Yung-Chia. “Primary Cilia in the Oligodendrocyte Lineage.” 2013. Thesis, University of North Texas. Accessed October 28, 2020. https://digital.library.unt.edu/ark:/67531/metadc271828/.

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

MLA Handbook (7th Edition):

Hao, Yung-Chia. “Primary Cilia in the Oligodendrocyte Lineage.” 2013. Web. 28 Oct 2020.

Vancouver:

Hao Y. Primary Cilia in the Oligodendrocyte Lineage. [Internet] [Thesis]. University of North Texas; 2013. [cited 2020 Oct 28]. Available from: https://digital.library.unt.edu/ark:/67531/metadc271828/.

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

Council of Science Editors:

Hao Y. Primary Cilia in the Oligodendrocyte Lineage. [Thesis]. University of North Texas; 2013. Available from: https://digital.library.unt.edu/ark:/67531/metadc271828/

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


University of Cambridge

29. Hamilton, Evelyn Alexandra Waterhouse. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.

Degree: PhD, 2019, University of Cambridge

 Synchronisation is broadly defined as the coordinated action of two or more individual elements that exhibit some time periodic behaviour. It is widely observed across… (more)

Subjects/Keywords: rower model; hydrodynamic forces; synchronisation; cilia

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APA (6th Edition):

Hamilton, E. A. W. (2019). Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.46269 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792964

Chicago Manual of Style (16th Edition):

Hamilton, Evelyn Alexandra Waterhouse. “Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 28, 2020. https://doi.org/10.17863/CAM.46269 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792964.

MLA Handbook (7th Edition):

Hamilton, Evelyn Alexandra Waterhouse. “Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment.” 2019. Web. 28 Oct 2020.

Vancouver:

Hamilton EAW. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 28]. Available from: https://doi.org/10.17863/CAM.46269 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792964.

Council of Science Editors:

Hamilton EAW. Controlling the collective dynamics in systems of active oscillators through geometry and hydrodynamic entrainment. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.46269 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792964

30. Wills, Brandon M. Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii.

Degree: 2019, Marquette University

Cilia and flagella are synonymous organelles that protrude above the cell surface to propel fluid and monitor signals in the environment. These functions are central… (more)

Subjects/Keywords: Chlamydomonas; Cilia; Flagella; IFT; RSP3; Trafficking; Biology

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

APA (6th Edition):

Wills, B. M. (2019). Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/theses_open/621

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):

Wills, Brandon M. “Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii.” 2019. Thesis, Marquette University. Accessed October 28, 2020. https://epublications.marquette.edu/theses_open/621.

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

MLA Handbook (7th Edition):

Wills, Brandon M. “Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii.” 2019. Web. 28 Oct 2020.

Vancouver:

Wills BM. Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii. [Internet] [Thesis]. Marquette University; 2019. [cited 2020 Oct 28]. Available from: https://epublications.marquette.edu/theses_open/621.

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

Council of Science Editors:

Wills BM. Optimizing Tools for the Investigation of Flagella Protein Trafficking in Chlamydomonas Reinhardtii. [Thesis]. Marquette University; 2019. Available from: https://epublications.marquette.edu/theses_open/621

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

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