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You searched for subject:( c terminal kinesin). Showing records 1 – 30 of 11221 total matches.

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Queens University

1. Duan, Da. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .

Degree: Biochemistry, 2013, Queens University

 The kinesin-14 Kar3 from Saccharomyces cerevisiae (Sc) is a C-terminal motor that forms a heterodimer with the kinesin-accessory protein Vik1. Although Vik1 possesses a typical… (more)

Subjects/Keywords: motility; Candida glabrata; Ashbya gossypii; N-C termini interaction; Saccharomyces cerevisiae; c-terminal kinesin; heterodimer; minus-end directed motility; kinesin; microtubules; mitosis

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APA (6th Edition):

Duan, D. (2013). UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8118

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):

Duan, Da. “UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .” 2013. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/8118.

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

MLA Handbook (7th Edition):

Duan, Da. “UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .” 2013. Web. 22 Aug 2019.

Vancouver:

Duan D. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/8118.

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

Council of Science Editors:

Duan D. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8118

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


University of Alberta

2. Han, Xue. Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation.

Degree: PhD, Department of Biological Sciences, 2014, University of Alberta

 Regulation of microtubule dynamics is essential for many cellular processes, including proper assembly and function of the mitotic spindle. One mechanism for temporal and spatial… (more)

Subjects/Keywords: kinesin; microtubule dynamics; phosphorylation; C. elegans

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APA (6th Edition):

Han, X. (2014). Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ccv43nx063

Chicago Manual of Style (16th Edition):

Han, Xue. “Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation.” 2014. Doctoral Dissertation, University of Alberta. Accessed August 22, 2019. https://era.library.ualberta.ca/files/ccv43nx063.

MLA Handbook (7th Edition):

Han, Xue. “Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation.” 2014. Web. 22 Aug 2019.

Vancouver:

Han X. Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2019 Aug 22]. Available from: https://era.library.ualberta.ca/files/ccv43nx063.

Council of Science Editors:

Han X. Regulation of Caenorhabditis elegans MCAK by Aurora Kinase Phosphorylation. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/ccv43nx063


University of Rochester

3. Caterino, Tamara. Molecular Determinants of Linker Histone Binding to Nucleosomes.

Degree: PhD, 2011, University of Rochester

 Linker histones are multi-functional proteins that are involved in a myriad of processes ranging from the stabilization of folding and condensation of chromatin to playing… (more)

Subjects/Keywords: Linker Histone; Nucleosome; C-terminal Domain

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APA (6th Edition):

Caterino, T. (2011). Molecular Determinants of Linker Histone Binding to Nucleosomes. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14612

Chicago Manual of Style (16th Edition):

Caterino, Tamara. “Molecular Determinants of Linker Histone Binding to Nucleosomes.” 2011. Doctoral Dissertation, University of Rochester. Accessed August 22, 2019. http://hdl.handle.net/1802/14612.

MLA Handbook (7th Edition):

Caterino, Tamara. “Molecular Determinants of Linker Histone Binding to Nucleosomes.” 2011. Web. 22 Aug 2019.

Vancouver:

Caterino T. Molecular Determinants of Linker Histone Binding to Nucleosomes. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1802/14612.

Council of Science Editors:

Caterino T. Molecular Determinants of Linker Histone Binding to Nucleosomes. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14612


Colorado State University

4. Seidel, Erik. Assessing histone H2A.Z and the H2A tails in chromatin structure.

Degree: MS(M.S.), Biochemistry and Molecular Biology, 2018, Colorado State University

 Deoxyribose nucleic acid (DNA) is a negatively charged macromolecule that encodes life's genetic material. In organisms, it is bound to net positively charged histone proteins… (more)

Subjects/Keywords: H2A C-Terminal Tail; H2A.Z; Chromatin; Micrococcal Nuclease; H2A N-Terminal Tail

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APA (6th Edition):

Seidel, E. (2018). Assessing histone H2A.Z and the H2A tails in chromatin structure. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/189392

Chicago Manual of Style (16th Edition):

Seidel, Erik. “Assessing histone H2A.Z and the H2A tails in chromatin structure.” 2018. Masters Thesis, Colorado State University. Accessed August 22, 2019. http://hdl.handle.net/10217/189392.

MLA Handbook (7th Edition):

Seidel, Erik. “Assessing histone H2A.Z and the H2A tails in chromatin structure.” 2018. Web. 22 Aug 2019.

Vancouver:

Seidel E. Assessing histone H2A.Z and the H2A tails in chromatin structure. [Internet] [Masters thesis]. Colorado State University; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10217/189392.

Council of Science Editors:

Seidel E. Assessing histone H2A.Z and the H2A tails in chromatin structure. [Masters Thesis]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/189392

5. Marcel Marín Villa. Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection.

Degree: 2006, Fundação Oswaldo Cruz

 O objetivo do presente trabalho foi o estudo das características do domínio pre, pro e C-terminal da cisteína proteinase 2 (Lpcys2) de L. pifanoi e… (more)

Subjects/Keywords: Leishmania pifanoi; Cisteína Proteinase; Domínio C-terminal; Infecção; PARASITOLOGIA; Leishmania pifanoi; Cysteine proteinasew; C-terminal Domain; Infection

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APA (6th Edition):

Villa, M. M. (2006). Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection. (Thesis). Fundação Oswaldo Cruz. Retrieved from http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=82

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):

Villa, Marcel Marín. “Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection.” 2006. Thesis, Fundação Oswaldo Cruz. Accessed August 22, 2019. http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=82.

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

MLA Handbook (7th Edition):

Villa, Marcel Marín. “Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection.” 2006. Web. 22 Aug 2019.

Vancouver:

Villa MM. Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection. [Internet] [Thesis]. Fundação Oswaldo Cruz; 2006. [cited 2019 Aug 22]. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=82.

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

Council of Science Editors:

Villa MM. Characterization of the pre, pro and CTE domains of the cysteine proteinase 2 (Lpcys2) of Leishmania pifanoi: paper in lysosomal targeting and infection. [Thesis]. Fundação Oswaldo Cruz; 2006. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=82

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

6. Oladosu, Oyindamola. Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration.

Degree: Docteur es, Biophysique et biologie structurale, 2017, Université de Strasbourg

L’Integrase du VIH est une ADN recombinase catalysant deux réactions qui permettent l'intégration de l'ADN viral dans l'ADN hôte. L’intégrase du VIH comprend 3 domaines… (more)

Subjects/Keywords: Integrase du VIH; Domaine C-terminal; Chromatine; Coévolution; Multimerisation; HIV Integrase; C-terminal domain; Chromatin; Coevolution; Multimerization; 572.8; 616.97

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APA (6th Edition):

Oladosu, O. (2017). Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ025

Chicago Manual of Style (16th Edition):

Oladosu, Oyindamola. “Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed August 22, 2019. http://www.theses.fr/2017STRAJ025.

MLA Handbook (7th Edition):

Oladosu, Oyindamola. “Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration.” 2017. Web. 22 Aug 2019.

Vancouver:

Oladosu O. Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Aug 22]. Available from: http://www.theses.fr/2017STRAJ025.

Council of Science Editors:

Oladosu O. Structures et fonctions du domaine C-Terminal de l'intégrase du VIH-1 : Structures and functions of the C-Terminal domain of HIV-1 integration. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ025


Université de Sherbrooke

7. Blain, Jennifer. Mécanismes de régulation de la voie NOTCH1 .

Degree: 2017, Université de Sherbrooke

 La voie NOTCH est activée de manière aberrante dans de nombreux cancers. Son activation implique la liaison d’un récepteur transmembranaire NOTCH à son ligand, engendrant… (more)

Subjects/Keywords: NIC1; MAML1; Domaine C-terminal; Endocytose; Transcription; Phosphorylation

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APA (6th Edition):

Blain, J. (2017). Mécanismes de régulation de la voie NOTCH1 . (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/11519

Chicago Manual of Style (16th Edition):

Blain, Jennifer. “Mécanismes de régulation de la voie NOTCH1 .” 2017. Doctoral Dissertation, Université de Sherbrooke. Accessed August 22, 2019. http://hdl.handle.net/11143/11519.

MLA Handbook (7th Edition):

Blain, Jennifer. “Mécanismes de régulation de la voie NOTCH1 .” 2017. Web. 22 Aug 2019.

Vancouver:

Blain J. Mécanismes de régulation de la voie NOTCH1 . [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11143/11519.

Council of Science Editors:

Blain J. Mécanismes de régulation de la voie NOTCH1 . [Doctoral Dissertation]. Université de Sherbrooke; 2017. Available from: http://hdl.handle.net/11143/11519

8. Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.

Degree: 博士(医学), 2015, Nara Medical University / 奈良県立医科大学

Acute aortic dissection (AAD) is a life-threating disease; however, there is almost no effective pharmacotherapy for it. An increase in c-Jun N-terminal kinase (JNK) phosphorylation… (more)

Subjects/Keywords: Stretch; c-Jun N-terminal kinase; p38; Acute aortic dissection; Olmesartan

Page 1

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APA (6th Edition):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, K. (2015). Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2939

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):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. “Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.” 2015. Thesis, Nara Medical University / 奈良県立医科大学. Accessed August 22, 2019. http://hdl.handle.net/10564/2939.

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

MLA Handbook (7th Edition):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. “Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.” 2015. Web. 22 Aug 2019.

Vancouver:

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama K. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10564/2939.

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

Council of Science Editors:

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama K. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. Available from: http://hdl.handle.net/10564/2939

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


Georgia State University

9. Zhang, Han. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.

Degree: PhD, Biology, 2013, Georgia State University

  Multi-drug resistance (MDR) has become a serious clinical problem for both cancer and infectious disease treatment. One of the leading causes of MDR is… (more)

Subjects/Keywords: Multi-drug resistance; C-terminal domain; ABC transporter; Membrane protein

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APA (6th Edition):

Zhang, H. (2013). Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/125

Chicago Manual of Style (16th Edition):

Zhang, Han. “Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.” 2013. Doctoral Dissertation, Georgia State University. Accessed August 22, 2019. https://scholarworks.gsu.edu/biology_diss/125.

MLA Handbook (7th Edition):

Zhang, Han. “Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.” 2013. Web. 22 Aug 2019.

Vancouver:

Zhang H. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2019 Aug 22]. Available from: https://scholarworks.gsu.edu/biology_diss/125.

Council of Science Editors:

Zhang H. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/biology_diss/125


University of Minnesota

10. Wang, Yen-Chih. Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Protein prenylation is a common post-translational modification of specific protein-derived cysteine residues in eukaryotic cells. To study the substrate specificity of these enzymes, the primary… (more)

Subjects/Keywords: Combinatorial synthesis; C-terminal peptide library; Farnesyltransferase; Prenylation

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APA (6th Edition):

Wang, Y. (2014). Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/165843

Chicago Manual of Style (16th Edition):

Wang, Yen-Chih. “Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase.” 2014. Doctoral Dissertation, University of Minnesota. Accessed August 22, 2019. http://hdl.handle.net/11299/165843.

MLA Handbook (7th Edition):

Wang, Yen-Chih. “Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase.” 2014. Web. 22 Aug 2019.

Vancouver:

Wang Y. Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11299/165843.

Council of Science Editors:

Wang Y. Solid-phase synthesis of C-Terminal peptide Libraries for studying the specificity of protein farnesyltransferase. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/165843

11. Maxfield, Dane Arthur. Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars.

Degree: PhD, Biology, 2014, University of Utah

 The cellular processes that govern neuronal function are highly complex and tightly regulated in order to perform the elaborate information processing achieved by the brain.… (more)

Subjects/Keywords: AMPAR; C. elegans; Kinesin; Synapse; Trafficking

…x28;Stern-Bach et al., 1994), and the C-terminal domain mediates receptor localization… …19 1.5 The C. elegans locomotory control circuit… …when coexpressed in C. elegans AVA neurons..............122 A.9 CNI-1 modifies neuron… …123 A.S1 C. elegans cni-1 encodes a member of the family of cornichon proteins… …products and pathways that regulate synaptic strength in C. elegans by using genetic, molecular… 

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APA (6th Edition):

Maxfield, D. A. (2014). Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2963/rec/1453

Chicago Manual of Style (16th Edition):

Maxfield, Dane Arthur. “Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars.” 2014. Doctoral Dissertation, University of Utah. Accessed August 22, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2963/rec/1453.

MLA Handbook (7th Edition):

Maxfield, Dane Arthur. “Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars.” 2014. Web. 22 Aug 2019.

Vancouver:

Maxfield DA. Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2019 Aug 22]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2963/rec/1453.

Council of Science Editors:

Maxfield DA. Kinesin-1 regulates synaptic strength by mediating delivery, removal and redistribution of ampars. [Doctoral Dissertation]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2963/rec/1453


University of Georgia

12. Darne, Chetan Padmakar. Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs.

Degree: MS, Chemistry, 2005, University of Georgia

 Cell division and intracellular functions are dependent on kinesin motor proteins. These proteins convey their cellular cargos by “walking” along the microtubule tracks. Specific inhibitors… (more)

Subjects/Keywords: kinesin

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APA (6th Edition):

Darne, C. P. (2005). Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/darne_chetan_p_200505_ms

Chicago Manual of Style (16th Edition):

Darne, Chetan Padmakar. “Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs.” 2005. Masters Thesis, University of Georgia. Accessed August 22, 2019. http://purl.galileo.usg.edu/uga_etd/darne_chetan_p_200505_ms.

MLA Handbook (7th Edition):

Darne, Chetan Padmakar. “Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs.” 2005. Web. 22 Aug 2019.

Vancouver:

Darne CP. Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs. [Internet] [Masters thesis]. University of Georgia; 2005. [cited 2019 Aug 22]. Available from: http://purl.galileo.usg.edu/uga_etd/darne_chetan_p_200505_ms.

Council of Science Editors:

Darne CP. Kinesin motor protein inhibitors: toward the synthesis of adociasulfate analogs. [Masters Thesis]. University of Georgia; 2005. Available from: http://purl.galileo.usg.edu/uga_etd/darne_chetan_p_200505_ms

13. Fallesen, Todd Landon. KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE.

Degree: 2010, Wake Forest University

 Conventional kinesin is a motor protein capable of converting the chemical energy of ATP into mechanical work. In the cell, this is used to actively… (more)

Subjects/Keywords: kinesin

…Asbury, C. (2005). "Kinesin: World's Tiniest Biped." Current Opinion… …was engineered with six histidine residues at the C-terminal end, which are used to aid in… …thiogalactopyranoside kB Boltzmann’s Constant KHC Kinesin Heavy Chain M Molar m magnetization M270… …measure of fit vii LIST OF FIGURES Page 1.1 Conventional Kinesin… …2 1.2 Microtubule with kinesin attached… 

Page 1 Page 2 Page 3 Page 4 Page 5

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

APA (6th Edition):

Fallesen, T. L. (2010). KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/30429

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):

Fallesen, Todd Landon. “KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE.” 2010. Thesis, Wake Forest University. Accessed August 22, 2019. http://hdl.handle.net/10339/30429.

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

MLA Handbook (7th Edition):

Fallesen, Todd Landon. “KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE.” 2010. Web. 22 Aug 2019.

Vancouver:

Fallesen TL. KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE. [Internet] [Thesis]. Wake Forest University; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10339/30429.

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

Council of Science Editors:

Fallesen TL. KINESIN-MICROTUBULE INTERACTIONS DURING GLIDING ASSAYS UNDER MAGNETIC FORCE. [Thesis]. Wake Forest University; 2010. Available from: http://hdl.handle.net/10339/30429

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


Penn State University

14. Mickolajczyk, Keith. MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY.

Degree: 2018, Penn State University

Kinesin motor proteins drive numerous active processes the cell, including vesicle transport, DNA and organelle repositioning, intraflagellar transport, and mitotic spindle organization. There are 45… (more)

Subjects/Keywords: Kinesin; iSCAT

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APA (6th Edition):

Mickolajczyk, K. (2018). MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY. (Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/15517kjm378

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):

Mickolajczyk, Keith. “MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY.” 2018. Thesis, Penn State University. Accessed August 22, 2019. https://etda.libraries.psu.edu/catalog/15517kjm378.

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

MLA Handbook (7th Edition):

Mickolajczyk, Keith. “MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY.” 2018. Web. 22 Aug 2019.

Vancouver:

Mickolajczyk K. MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY. [Internet] [Thesis]. Penn State University; 2018. [cited 2019 Aug 22]. Available from: https://etda.libraries.psu.edu/catalog/15517kjm378.

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

Council of Science Editors:

Mickolajczyk K. MECHANOCHEMICAL BASIS OF FUNCTIONAL DIVERSITY IN THE KINESIN SUPERFAMILY. [Thesis]. Penn State University; 2018. Available from: https://etda.libraries.psu.edu/catalog/15517kjm378

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


University of Kansas

15. Saito, Chieko. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Acetaminophen (APAP) is a widely used analgesic, which is safe at therapeutic levels. APAP is mainly conjugated with glucuronic acid and sulfate to form water-soluble,… (more)

Subjects/Keywords: Health sciences; Toxicology; Acetaminophen; C-jun n-terminal kinase; Glutathione; Metallothionein; N-acetylcysteine

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APA (6th Edition):

Saito, C. (2010). PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6369

Chicago Manual of Style (16th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Doctoral Dissertation, University of Kansas. Accessed August 22, 2019. http://hdl.handle.net/1808/6369.

MLA Handbook (7th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Web. 22 Aug 2019.

Vancouver:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1808/6369.

Council of Science Editors:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6369

16. Syed, Ali Awais. Agent based simulation for C-AGVs at Intermodal Terminal.

Degree: 2009, , School of Computing

In recent history there has been a steady increase in container traffic worldwide. As a result modern western Container Terminal ports are turning towards… (more)

Subjects/Keywords: Agents; Automated Container Terminal; C-AGV; MAS; NetLogo.; Computer Sciences; Datavetenskap (datalogi); Telecommunications; Telekommunikation

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APA (6th Edition):

Syed, A. A. (2009). Agent based simulation for C-AGVs at Intermodal Terminal. (Thesis). , School of Computing. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1133

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):

Syed, Ali Awais. “Agent based simulation for C-AGVs at Intermodal Terminal.” 2009. Thesis, , School of Computing. Accessed August 22, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1133.

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

MLA Handbook (7th Edition):

Syed, Ali Awais. “Agent based simulation for C-AGVs at Intermodal Terminal.” 2009. Web. 22 Aug 2019.

Vancouver:

Syed AA. Agent based simulation for C-AGVs at Intermodal Terminal. [Internet] [Thesis]. , School of Computing; 2009. [cited 2019 Aug 22]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1133.

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

Council of Science Editors:

Syed AA. Agent based simulation for C-AGVs at Intermodal Terminal. [Thesis]. , School of Computing; 2009. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:bth-1133

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


University of Oxford

17. Kuznetsova, Olga. Regulation of human RNA polymerase II CTD modifications.

Degree: PhD, 2015, University of Oxford

 Transcription of human protein-coding genes and most small nuclear RNA genes is mediated by RNA Polymerase II (Pol II). During a cycle of transcription, Pol… (more)

Subjects/Keywords: 572.8; Medical Sciences; Pathology; RNA Polymerase; Transcription; Gene regulation; C-terminal domain; Integrator

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APA (6th Edition):

Kuznetsova, O. (2015). Regulation of human RNA polymerase II CTD modifications. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e745b5b6-8a4a-4b7a-81d7-499bca8bfea1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647692

Chicago Manual of Style (16th Edition):

Kuznetsova, Olga. “Regulation of human RNA polymerase II CTD modifications.” 2015. Doctoral Dissertation, University of Oxford. Accessed August 22, 2019. http://ora.ox.ac.uk/objects/uuid:e745b5b6-8a4a-4b7a-81d7-499bca8bfea1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647692.

MLA Handbook (7th Edition):

Kuznetsova, Olga. “Regulation of human RNA polymerase II CTD modifications.” 2015. Web. 22 Aug 2019.

Vancouver:

Kuznetsova O. Regulation of human RNA polymerase II CTD modifications. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Aug 22]. Available from: http://ora.ox.ac.uk/objects/uuid:e745b5b6-8a4a-4b7a-81d7-499bca8bfea1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647692.

Council of Science Editors:

Kuznetsova O. Regulation of human RNA polymerase II CTD modifications. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:e745b5b6-8a4a-4b7a-81d7-499bca8bfea1 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647692


University of Illinois – Chicago

18. Lowry, Jessica L. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.

Degree: 2013, University of Illinois – Chicago

 High levels of nitric oxide (NO) generated in the vasculature under inflammatory conditions are usually attributed to inducible nitric oxide synthase (iNOS), but the role… (more)

Subjects/Keywords: Nitric Oxide; c-Jun-N-Terminal Kinase; endothelial nitric oxide synthase; inflammation; migration

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APA (6th Edition):

Lowry, J. L. (2013). A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10054

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):

Lowry, Jessica L. “A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.” 2013. Thesis, University of Illinois – Chicago. Accessed August 22, 2019. http://hdl.handle.net/10027/10054.

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

MLA Handbook (7th Edition):

Lowry, Jessica L. “A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.” 2013. Web. 22 Aug 2019.

Vancouver:

Lowry JL. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10027/10054.

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

Council of Science Editors:

Lowry JL. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10054

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


University of Washington

19. Kuhar, Jamie Rose. Mechanisms of Opioid Receptor Desensitization.

Degree: PhD, 2015, University of Washington

 Agonists targeting MOR are effective analgesics, but their clinical use is hindered by side effects, including tolerance and addiction. KOR agonists also produce analgesia, but… (more)

Subjects/Keywords: Arrestin; c-Jun N-terminal kinase; Fentanyl; Morphine; Opioid; p38; Pharmacology; pharmacology

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APA (6th Edition):

Kuhar, J. R. (2015). Mechanisms of Opioid Receptor Desensitization. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/34122

Chicago Manual of Style (16th Edition):

Kuhar, Jamie Rose. “Mechanisms of Opioid Receptor Desensitization.” 2015. Doctoral Dissertation, University of Washington. Accessed August 22, 2019. http://hdl.handle.net/1773/34122.

MLA Handbook (7th Edition):

Kuhar, Jamie Rose. “Mechanisms of Opioid Receptor Desensitization.” 2015. Web. 22 Aug 2019.

Vancouver:

Kuhar JR. Mechanisms of Opioid Receptor Desensitization. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1773/34122.

Council of Science Editors:

Kuhar JR. Mechanisms of Opioid Receptor Desensitization. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/34122

20. 김, 진수. The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell.

Degree: 2014, Ajou University

Parkinson's disease(PD) is the progressive neurodegenerative disorder that profoundly affects movement, and is characterized by dopaminergic neuronal loss in the substantia nigra, midbrain. Symtoms of… (more)

Subjects/Keywords: 파킨슨병; UCH-L1(Ubiquitin C-terminal Hydrolase-L1); 지질 래프트; 타이로신-인산화 반응

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APA (6th Edition):

김, . (2014). The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/10868 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000017411

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):

김, 진수. “The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell.” 2014. Thesis, Ajou University. Accessed August 22, 2019. http://repository.ajou.ac.kr/handle/201003/10868 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000017411.

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

MLA Handbook (7th Edition):

김, 진수. “The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell.” 2014. Web. 22 Aug 2019.

Vancouver:

김 . The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell. [Internet] [Thesis]. Ajou University; 2014. [cited 2019 Aug 22]. Available from: http://repository.ajou.ac.kr/handle/201003/10868 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000017411.

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

Council of Science Editors:

김 . The localization of UCH-L1(Ubiquitin C-terminaHydrolase-L1) in lipid rafts of neuronal cell. [Thesis]. Ajou University; 2014. Available from: http://repository.ajou.ac.kr/handle/201003/10868 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000017411

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


Oklahoma State University

21. Szabla, Kristen Lynn. HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins.

Degree: Department of Biochemistry and Molecular Biology, 2010, Oklahoma State University

 Heat shock protein 90 (Hsp90) is a highly conserved, eukaryotic, molecular chaperone which stabilizes an assortment of oncogenic proteins. Currently, novobiocin and related coumarins are… (more)

Subjects/Keywords: chlorobiocin; coumermycin; c-terminal domain binding site; hsp90; novobiocin; surface plasmon resonance

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APA (6th Edition):

Szabla, K. L. (2010). HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins. (Thesis). Oklahoma State University. Retrieved from http://hdl.handle.net/11244/8941

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):

Szabla, Kristen Lynn. “HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins.” 2010. Thesis, Oklahoma State University. Accessed August 22, 2019. http://hdl.handle.net/11244/8941.

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

MLA Handbook (7th Edition):

Szabla, Kristen Lynn. “HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins.” 2010. Web. 22 Aug 2019.

Vancouver:

Szabla KL. HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins. [Internet] [Thesis]. Oklahoma State University; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11244/8941.

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

Council of Science Editors:

Szabla KL. HSP90 C-terminal Domain Binding Site For Novobiocin and Related Coumarins. [Thesis]. Oklahoma State University; 2010. Available from: http://hdl.handle.net/11244/8941

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


University of Arizona

22. Nyberg, Joel Benjamin. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .

Degree: 2013, University of Arizona

 The melanocortin 3 and 4 receptors share 58% overall amino acid identity and 76% similarity. This high level of similarity between the MC3R and the… (more)

Subjects/Keywords: Melancortins; Melanocortin 3; Melanocortin 3 selective ligands; Peptides; Chemistry; C-terminal modification

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APA (6th Edition):

Nyberg, J. B. (2013). Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/283606

Chicago Manual of Style (16th Edition):

Nyberg, Joel Benjamin. “Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .” 2013. Doctoral Dissertation, University of Arizona. Accessed August 22, 2019. http://hdl.handle.net/10150/283606.

MLA Handbook (7th Edition):

Nyberg, Joel Benjamin. “Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .” 2013. Web. 22 Aug 2019.

Vancouver:

Nyberg JB. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10150/283606.

Council of Science Editors:

Nyberg JB. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/283606


University of Adelaide

23. Armstrong, Heather Krista. Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer.

Degree: 2016, University of Adelaide

 One of the most common causes of cancer-related deaths for men in the developed world is prostate cancer (PCa), occurring in 1 in 5 men… (more)

Subjects/Keywords: Hsp90; prostate cancer; molecular chaperone; heat shock protein; AUY922; C-terminal; inhibitors; drug resistance; cytoskeleton

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APA (6th Edition):

Armstrong, H. K. (2016). Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/119552

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):

Armstrong, Heather Krista. “Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer.” 2016. Thesis, University of Adelaide. Accessed August 22, 2019. http://hdl.handle.net/2440/119552.

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

MLA Handbook (7th Edition):

Armstrong, Heather Krista. “Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer.” 2016. Web. 22 Aug 2019.

Vancouver:

Armstrong HK. Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2440/119552.

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

Council of Science Editors:

Armstrong HK. Elucidating the molecular action of synthetic heat shock protein 90 inhibitors in prostate cancer. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/119552

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

24. Zubillaga, Jose Antonio. Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project.

Degree: MS, Civil Engineering, 2008, North Carolina State University

Subjects/Keywords: RDU Terminal C; Bertsche System

…76 Figure 5.1 – Rendering of proposed Terminal C [Fentress]… …Terminal C. Part of the plan is to demolish the old terminal and create a newer, more… …Terminal C will almost triple in size and it will feature a larger airline check-in, security… …description of Terminal C project construction will be given. Every truss is a combination of glue… …contractor for the redevelopment of the Terminal C. The contract required the general contractor to… 

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APA (6th Edition):

Zubillaga, J. A. (2008). Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/580

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):

Zubillaga, Jose Antonio. “Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project.” 2008. Thesis, North Carolina State University. Accessed August 22, 2019. http://www.lib.ncsu.edu/resolver/1840.16/580.

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

MLA Handbook (7th Edition):

Zubillaga, Jose Antonio. “Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project.” 2008. Web. 22 Aug 2019.

Vancouver:

Zubillaga JA. Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project. [Internet] [Thesis]. North Carolina State University; 2008. [cited 2019 Aug 22]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/580.

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

Council of Science Editors:

Zubillaga JA. Erection and Strength Aspects of the Roof Trusses for RDU Airport Terminal C Project. [Thesis]. North Carolina State University; 2008. Available from: http://www.lib.ncsu.edu/resolver/1840.16/580

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


University of Notre Dame

25. Anthony E Clemons. Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>.

Degree: PhD, Biological Sciences, 2014, University of Notre Dame

  Gene expression during embryogenesis impacts adult mosquito fitness, the ability of an organism to survive and transmit its genotype to offspring as compared to… (more)

Subjects/Keywords: Aeded aegypti; Puckered; C-Jun N-terminal Kinase; insulin signaling pathway; stress signaling pathway

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APA (6th Edition):

Clemons, A. E. (2014). Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/w089280462m

Chicago Manual of Style (16th Edition):

Clemons, Anthony E. “Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>.” 2014. Doctoral Dissertation, University of Notre Dame. Accessed August 22, 2019. https://curate.nd.edu/show/w089280462m.

MLA Handbook (7th Edition):

Clemons, Anthony E. “Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>.” 2014. Web. 22 Aug 2019.

Vancouver:

Clemons AE. Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2014. [cited 2019 Aug 22]. Available from: https://curate.nd.edu/show/w089280462m.

Council of Science Editors:

Clemons AE. Conserved Developmental Cues of Aedes aegypti and their Impact on the Mosquito Vector</h1>. [Doctoral Dissertation]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/w089280462m


University of Toronto

26. Michalec, Ola Michelle. Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons.

Degree: 2017, University of Toronto

Teneurin C-terminal associated peptides (TCAPs) are a family of 40-41 amino acid peptides located at the C-terminus of each of the four teneurin type II… (more)

Subjects/Keywords: Astrocyte-neuron co-cultures; Astrocytes; Calcium; Evolution; Neurons; Teneurin C-terminal associated peptide (TCAP); 0379

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APA (6th Edition):

Michalec, O. M. (2017). Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79095

Chicago Manual of Style (16th Edition):

Michalec, Ola Michelle. “Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons.” 2017. Masters Thesis, University of Toronto. Accessed August 22, 2019. http://hdl.handle.net/1807/79095.

MLA Handbook (7th Edition):

Michalec, Ola Michelle. “Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons.” 2017. Web. 22 Aug 2019.

Vancouver:

Michalec OM. Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1807/79095.

Council of Science Editors:

Michalec OM. Teneurin C-terminal Associated Peptides (TCAPs): Evolutionary Origins and the Role of TCAP-1 on Calcium Flux in Astrocyte Monocultures and in Astrocytes Co-cultured with Neurons. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79095


University of Southern Mississippi

27. Chen, Qichuan. The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival.

Degree: MS, Biological Sciences, 2014, University of Southern Mississippi

  From a genetic and allelic modifier screen, we report that the Drosophila melanogaster T-box transcription factor midline (mid), a homolog to the human TBX20… (more)

Subjects/Keywords: mid; midline; Tbx20; dFOXO; C-Jun-N-terminal kinase; insulin receptor; Developmental Biology

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APA (6th Edition):

Chen, Q. (2014). The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival. (Masters Thesis). University of Southern Mississippi. Retrieved from https://aquila.usm.edu/masters_theses/76

Chicago Manual of Style (16th Edition):

Chen, Qichuan. “The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival.” 2014. Masters Thesis, University of Southern Mississippi. Accessed August 22, 2019. https://aquila.usm.edu/masters_theses/76.

MLA Handbook (7th Edition):

Chen, Qichuan. “The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival.” 2014. Web. 22 Aug 2019.

Vancouver:

Chen Q. The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival. [Internet] [Masters thesis]. University of Southern Mississippi; 2014. [cited 2019 Aug 22]. Available from: https://aquila.usm.edu/masters_theses/76.

Council of Science Editors:

Chen Q. The <i>Drosophila</i> T-box Transcription Factor Midline Functions within the Insulin/AKT and c-Jun-N-terminal Kinase Signaling Pathways to Regulate Interomatidial Bristle Formation and Cell Survival. [Masters Thesis]. University of Southern Mississippi; 2014. Available from: https://aquila.usm.edu/masters_theses/76


University of Waterloo

28. Brefo-Mensah, Eric K. Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity.

Degree: 2018, University of Waterloo

 CAMP factor is a well-known pore-forming toxin secreted by Streptococcus agalactiae that forms discrete pores on susceptible membranes whether natural or artificial. This work reports… (more)

Subjects/Keywords: CAMP factor; Streptococcus agalactiae; N-terminal domain; C-terminal domain; Fluorescence; Cholesterol; Membrane lipid composition; Oligomerization; Lipid acyl chain length; Degree of saturation; Pore formation; Cysteine mutant; Membrane permeabilization

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APA (6th Edition):

Brefo-Mensah, E. K. (2018). Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/13341

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):

Brefo-Mensah, Eric K. “Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity.” 2018. Thesis, University of Waterloo. Accessed August 22, 2019. http://hdl.handle.net/10012/13341.

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

MLA Handbook (7th Edition):

Brefo-Mensah, Eric K. “Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity.” 2018. Web. 22 Aug 2019.

Vancouver:

Brefo-Mensah EK. Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10012/13341.

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

Council of Science Editors:

Brefo-Mensah EK. Streptococcus agalactiae CAMP factor: Functional Roles of N- and C-terminal Domains & Target Membrane Effect on Toxin Activity. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/13341

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


Rice University

29. Tsao, David. Investigations of macromolecular complex functions in living cells.

Degree: PhD, Engineering, 2017, Rice University

 Characterizing the collective functions of cytoskeletal motors is critical to understanding mechanisms that regulate the internal organization of eukaryotic cells as well as the roles… (more)

Subjects/Keywords: IQGAP1; kinesin; myosin

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APA (6th Edition):

Tsao, D. (2017). Investigations of macromolecular complex functions in living cells. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/96154

Chicago Manual of Style (16th Edition):

Tsao, David. “Investigations of macromolecular complex functions in living cells.” 2017. Doctoral Dissertation, Rice University. Accessed August 22, 2019. http://hdl.handle.net/1911/96154.

MLA Handbook (7th Edition):

Tsao, David. “Investigations of macromolecular complex functions in living cells.” 2017. Web. 22 Aug 2019.

Vancouver:

Tsao D. Investigations of macromolecular complex functions in living cells. [Internet] [Doctoral dissertation]. Rice University; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1911/96154.

Council of Science Editors:

Tsao D. Investigations of macromolecular complex functions in living cells. [Doctoral Dissertation]. Rice University; 2017. Available from: http://hdl.handle.net/1911/96154


University of California – San Francisco

30. Jonsson, Erik. Mechanisms of Kinesin Processivity.

Degree: Biophysics, 2015, University of California – San Francisco

 Kinesins are molecular motors that convert chemical energy, stored in the bonds of ATP, into productive work. They form one of the three branches of… (more)

Subjects/Keywords: Biophysics; Gating; Kinesin; Kinesin-1; Kinesin-14; Processivity

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

APA (6th Edition):

Jonsson, E. (2015). Mechanisms of Kinesin Processivity. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/17c615bv

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):

Jonsson, Erik. “Mechanisms of Kinesin Processivity.” 2015. Thesis, University of California – San Francisco. Accessed August 22, 2019. http://www.escholarship.org/uc/item/17c615bv.

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

MLA Handbook (7th Edition):

Jonsson, Erik. “Mechanisms of Kinesin Processivity.” 2015. Web. 22 Aug 2019.

Vancouver:

Jonsson E. Mechanisms of Kinesin Processivity. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/17c615bv.

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

Council of Science Editors:

Jonsson E. Mechanisms of Kinesin Processivity. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/17c615bv

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

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