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You searched for +publisher:"Cornell University" +contributor:("Qian, Shu-Bing"). Showing records 1 – 9 of 9 total matches.

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Cornell University

1. Liu, Botao. Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation.

Degree: PhD, Genetics, 2014, Cornell University

 Cell survival in changing environments requires appropriate regulation of gene expression, including translational control. Multiple stress signaling pathways converge on several key translation factors and… (more)

Subjects/Keywords: Translation; Stress response; Ribosome profiling

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APA (6th Edition):

Liu, B. (2014). Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37029

Chicago Manual of Style (16th Edition):

Liu, Botao. “Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation.” 2014. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/37029.

MLA Handbook (7th Edition):

Liu, Botao. “Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation.” 2014. Web. 28 Nov 2020.

Vancouver:

Liu B. Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/37029.

Council of Science Editors:

Liu B. Investigating Translational Reprogramming In Cellular Stress Response By Elongation Pausing And Alternative Initiation. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37029


Cornell University

2. Ludwicki, Morgan Baltz. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC.

Degree: PhD, Chemical Engineering, 2019, Cornell University

 Manipulation of the ubiquitin-proteasome pathway to achieve targeted silencing of cellular proteins has emerged as a reliable and customizable strategy for remodeling the mammalian proteome.… (more)

Subjects/Keywords: Chemical engineering; E3 ubiquitin ligase; Ubiquibody; IpaH9.8; Protein knockdown; Targeted protein silencing; Bioengineering

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APA (6th Edition):

Ludwicki, M. B. (2019). BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67803

Chicago Manual of Style (16th Edition):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC.” 2019. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/67803.

MLA Handbook (7th Edition):

Ludwicki, Morgan Baltz. “BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC.” 2019. Web. 28 Nov 2020.

Vancouver:

Ludwicki MB. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/67803.

Council of Science Editors:

Ludwicki MB. BROAD-SPECTRUM PROTEOME EDITING WITH AN ENGINEERED BACTERIAL UBIQUITIN LIGASE MIMIC. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67803


Cornell University

3. Sullivan, Peter Mayo. Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

 Intronic hexanucleotide repeat expansion in the C9orf72 gene is a leading cause of frontotemporal lobar degeneration (FTLD) with amyotrophic lateral sclerosis (ALS). Among several hypotheses,… (more)

Subjects/Keywords: ALS; C9orf72; FTLD; Lysosome; SMCR8; WDR41; Cellular biology; Molecular biology

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APA (6th Edition):

Sullivan, P. M. (2017). Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/57003

Chicago Manual of Style (16th Edition):

Sullivan, Peter Mayo. “Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72.” 2017. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/57003.

MLA Handbook (7th Edition):

Sullivan, Peter Mayo. “Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72.” 2017. Web. 28 Nov 2020.

Vancouver:

Sullivan PM. Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/57003.

Council of Science Editors:

Sullivan PM. Elucidating the disease relevance and function of the ALS/FTLD-associated protein C9orf72. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/57003


Cornell University

4. Pareja, Kristeen Alcaide. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.

Degree: PhD, Pharmacology, 2018, Cornell University

 Excessive cellular reactive oxygen species (ROS), or oxidative stress, can lead to cell damage and is implicated in diseases such as cancer, aging and neurodegenerative… (more)

Subjects/Keywords: Cellular biology; Pharmacology

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APA (6th Edition):

Pareja, K. A. (2018). A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59801

Chicago Manual of Style (16th Edition):

Pareja, Kristeen Alcaide. “A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.” 2018. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/59801.

MLA Handbook (7th Edition):

Pareja, Kristeen Alcaide. “A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.” 2018. Web. 28 Nov 2020.

Vancouver:

Pareja KA. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/59801.

Council of Science Editors:

Pareja KA. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59801


Cornell University

5. Zhao, Yingying. A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast.

Degree: PhD, Physiology, 2013, Cornell University

 A UBIQUITIN-DEPENDENT SURVEILLANCE SYSTEM MEDIATES PLASMA  MEMBRANE PROTEIN QUALITY CONTROL IN YEAST    Yingying Zhao, Ph. D.  Cornell University 2013    A key function of the ubiquitin-proteasome system is targeting of misfolded proteins  for degradation. In the cytosol, specialized E3 ligases target soluble misfolded  proteins for ubiquitination and subsequent proteasomal degradation. However, the  case is more complicated for integral membrane proteins. Following co- translational insertion in the ER membrane, proteins that fail to fold properly in the  ER are subject to ER-assisted degradation (ERAD), which involves  retrotranslocation of proteins back into the cytosol followed by ubiquitin- dependent proteasomal degradation. Properly folded PM proteins, such as signaling  receptors, ion channels, and nutrient transporters, exit the ER and traffic through  the Golgi to the cell surface where they mediate their specific functions.  Maintenance of proper PM proteostasis, particularly with respect to ion channels  and nutrient transporters, is crucial to prevent loss of PM integrity and dissipation  of essential ion and chemical gradients. As such, when PM resident proteins become  damaged or misfolded, they must be recognized, removed by endocytosis and  delivered to the lysosome for degradation. Thus, cells maintain a "cradle to grave"  quality monitoring system for integral membrane proteins, yet the mechanisms of    iii  quality surveillance, particularly at the PM, remain poorly understood. … (more)

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APA (6th Edition):

Zhao, Y. (2013). A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33968

Chicago Manual of Style (16th Edition):

Zhao, Yingying. “A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast.” 2013. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/33968.

MLA Handbook (7th Edition):

Zhao, Yingying. “A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast.” 2013. Web. 28 Nov 2020.

Vancouver:

Zhao Y. A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/33968.

Council of Science Editors:

Zhao Y. A Ubiquitin-Dependent Surveillance System Mediates Plasma Membrane Protein Quality Control In Yeast. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33968


Cornell University

6. Chen, Hong. The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast.

Degree: PhD, Nutrition, 2012, Cornell University

 The genetic basis underlying how organisms adapt to different environments and evolve new life style is a central issue of molecular evolution. The evolution of… (more)

Subjects/Keywords: aerobic fermentation; gene duplication; pyruvate kinase

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APA (6th Edition):

Chen, H. (2012). The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31040

Chicago Manual of Style (16th Edition):

Chen, Hong. “The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast.” 2012. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/31040.

MLA Handbook (7th Edition):

Chen, Hong. “The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast.” 2012. Web. 28 Nov 2020.

Vancouver:

Chen H. The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/31040.

Council of Science Editors:

Chen H. The Role Of Gene Duplication During The Evolution Of Aerobic Fermentation In Yeast. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31040

7. Liao, Juiyun. SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA.

Degree: PhD, Plant Biology, 2019, Cornell University

 The caseinolytic proteolytic machinery (CLP) is an essential and abundant protease of the chloroplast protease network. It is composed of multiple components (a proteolytic core… (more)

Subjects/Keywords: CLP; subtrate; trapping; Proteolysis; Biochemistry; Botany; protease; Plant sciences

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APA (6th Edition):

Liao, J. (2019). SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67299

Chicago Manual of Style (16th Edition):

Liao, Juiyun. “SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA.” 2019. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/67299.

MLA Handbook (7th Edition):

Liao, Juiyun. “SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA.” 2019. Web. 28 Nov 2020.

Vancouver:

Liao J. SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/67299.

Council of Science Editors:

Liao J. SUBSTRATES, STRUCTURES, AND FUNCTIONS OF THE CHLOROPLAST CLP PROTEASE SYSTEM IN ARABIDOPSIS THALIANA. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67299

8. Conn, Crystal. Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis.

Degree: PhD, Genetics, 2013, Cornell University

 The proper balance between protein synthesis, maturation, and degradation is crucial for an organism to survive and prosper. Each of these processes is coupled to… (more)

Subjects/Keywords: Protein Synthesis; mTOR; Protein Homeostasis

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APA (6th Edition):

Conn, C. (2013). Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34159

Chicago Manual of Style (16th Edition):

Conn, Crystal. “Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis.” 2013. Doctoral Dissertation, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/34159.

MLA Handbook (7th Edition):

Conn, Crystal. “Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis.” 2013. Web. 28 Nov 2020.

Vancouver:

Conn C. Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/34159.

Council of Science Editors:

Conn C. Elucidating The Regulatory Mechanisms Of The Mammalian Target Of Rapamycin Complex 1 (Mtorc1) In Protein Homeostasis. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34159

9. Sun, Tao. Novel application of microalgae in animal nutrition and human health.

Degree: M.S., Animal Science, Animal Science, 2018, Cornell University

 World population is estimated to reach 8.6 billion by 2030. The increasing population caused huge pressure on food supply which relies on staple crop production… (more)

Subjects/Keywords: amino acid; astaxanthin; DHA; growth performance; meat quality; microalgae; Animal sciences

…protocol was approved by the Institutional Animal Care and Use Committee of Cornell University… …Experimental protocol was approved by the Institution of Animal Care and Use Committee of Cornell… …University. 2.3.2 Growth Performance and Collection of Excreta and Digesta Body weight was… 

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APA (6th Edition):

Sun, T. (2018). Novel application of microalgae in animal nutrition and human health. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59762

Chicago Manual of Style (16th Edition):

Sun, Tao. “Novel application of microalgae in animal nutrition and human health.” 2018. Masters Thesis, Cornell University. Accessed November 28, 2020. http://hdl.handle.net/1813/59762.

MLA Handbook (7th Edition):

Sun, Tao. “Novel application of microalgae in animal nutrition and human health.” 2018. Web. 28 Nov 2020.

Vancouver:

Sun T. Novel application of microalgae in animal nutrition and human health. [Internet] [Masters thesis]. Cornell University; 2018. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1813/59762.

Council of Science Editors:

Sun T. Novel application of microalgae in animal nutrition and human health. [Masters Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59762

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