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Dates: 2000 – 2004

You searched for subject:( Protein Protein Interaktionen). Showing records 1 – 30 of 887 total matches.

[1] [2] [3] [4] [5] … [30]

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ETH Zürich

1. Koller, Daniela. Short N-terminal regions of the calcitonin-like receptor define ligand specificity.

Degree: 2004, ETH Zürich

Subjects/Keywords: CALCITONIN (HORMONE); G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); CALCITONIN (HORMONES); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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

APA (6th Edition):

Koller, D. (2004). Short N-terminal regions of the calcitonin-like receptor define ligand specificity. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/148072

Chicago Manual of Style (16th Edition):

Koller, Daniela. “Short N-terminal regions of the calcitonin-like receptor define ligand specificity.” 2004. Doctoral Dissertation, ETH Zürich. Accessed July 21, 2019. http://hdl.handle.net/20.500.11850/148072.

MLA Handbook (7th Edition):

Koller, Daniela. “Short N-terminal regions of the calcitonin-like receptor define ligand specificity.” 2004. Web. 21 Jul 2019.

Vancouver:

Koller D. Short N-terminal regions of the calcitonin-like receptor define ligand specificity. [Internet] [Doctoral dissertation]. ETH Zürich; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/20.500.11850/148072.

Council of Science Editors:

Koller D. Short N-terminal regions of the calcitonin-like receptor define ligand specificity. [Doctoral Dissertation]. ETH Zürich; 2004. Available from: http://hdl.handle.net/20.500.11850/148072


University of Georgia

2. Canseco, Miguel Angel. Protein nutrition of dairy cows fed high fat diets.

Degree: MS, Animal Science, 2002, University of Georgia

 Two experiments were conducted to determine the value of specific protein supplements in lactating dairy cows fed high fat diets. Experiment 1, six feedstuffs (wheat… (more)

Subjects/Keywords: Protein degradation

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APA (6th Edition):

Canseco, M. A. (2002). Protein nutrition of dairy cows fed high fat diets. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms

Chicago Manual of Style (16th Edition):

Canseco, Miguel Angel. “Protein nutrition of dairy cows fed high fat diets.” 2002. Masters Thesis, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms.

MLA Handbook (7th Edition):

Canseco, Miguel Angel. “Protein nutrition of dairy cows fed high fat diets.” 2002. Web. 21 Jul 2019.

Vancouver:

Canseco MA. Protein nutrition of dairy cows fed high fat diets. [Internet] [Masters thesis]. University of Georgia; 2002. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms.

Council of Science Editors:

Canseco MA. Protein nutrition of dairy cows fed high fat diets. [Masters Thesis]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/canseco_miguel_a_200208_ms

3. Akhrymuk, Alena. Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus.

Degree: 2004, Universität Dortmund

 In lebenden Zellen benötigen Proteine molekulare Chaperone um Aggregation zu vermeiden. Das molekulare Chaperon DnaK aus T.thermophilus gehört zur Hsp70-Familie. Hsp70-Proteine bestehen aus einer hochkonservierten… (more)

Subjects/Keywords: Chaperone; folding; interaction; protein; 540

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APA (6th Edition):

Akhrymuk, A. (2004). Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/2501

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):

Akhrymuk, Alena. “Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus.” 2004. Thesis, Universität Dortmund. Accessed July 21, 2019. http://hdl.handle.net/2003/2501.

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

MLA Handbook (7th Edition):

Akhrymuk, Alena. “Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus.” 2004. Web. 21 Jul 2019.

Vancouver:

Akhrymuk A. Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus. [Internet] [Thesis]. Universität Dortmund; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2003/2501.

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

Council of Science Editors:

Akhrymuk A. Studies on the interaction between the molecular chaperone DnaK and Nucleotide exchange factor GrpE from Thermus thermophilus. [Thesis]. Universität Dortmund; 2004. Available from: http://hdl.handle.net/2003/2501

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


University of Georgia

4. Sterling, Kimberly Gruwell. Dietary crude protein and lysine in broiler chicken nutrition.

Degree: PhD, Poultry Science, 2002, University of Georgia

 The effect of dietary crude protein (CP) and lysine on broiler chicken performance was investigated in this dissertation. Four studies were conducted to better understand… (more)

Subjects/Keywords: Crude Protein

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APA (6th Edition):

Sterling, K. G. (2002). Dietary crude protein and lysine in broiler chicken nutrition. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/sterling_kimberly_g_200212_phd

Chicago Manual of Style (16th Edition):

Sterling, Kimberly Gruwell. “Dietary crude protein and lysine in broiler chicken nutrition.” 2002. Doctoral Dissertation, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/sterling_kimberly_g_200212_phd.

MLA Handbook (7th Edition):

Sterling, Kimberly Gruwell. “Dietary crude protein and lysine in broiler chicken nutrition.” 2002. Web. 21 Jul 2019.

Vancouver:

Sterling KG. Dietary crude protein and lysine in broiler chicken nutrition. [Internet] [Doctoral dissertation]. University of Georgia; 2002. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/sterling_kimberly_g_200212_phd.

Council of Science Editors:

Sterling KG. Dietary crude protein and lysine in broiler chicken nutrition. [Doctoral Dissertation]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/sterling_kimberly_g_200212_phd


University of Georgia

5. Paiva, Newton Naves. Supplemental protein to enhance nutrient utilization of steers fed high fiber hay.

Degree: MS, Animal Science, 2003, University of Georgia

 incremental levels of rumen undegradable protein (RUP) on nutrient utilization of growing steers fed high fiber hay. Metabolism study: Holstein steers (n = 6, 217… (more)

Subjects/Keywords: Protein Supplementation

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APA (6th Edition):

Paiva, N. N. (2003). Supplemental protein to enhance nutrient utilization of steers fed high fiber hay. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/paiva_newton_n_200308_ms

Chicago Manual of Style (16th Edition):

Paiva, Newton Naves. “Supplemental protein to enhance nutrient utilization of steers fed high fiber hay.” 2003. Masters Thesis, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/paiva_newton_n_200308_ms.

MLA Handbook (7th Edition):

Paiva, Newton Naves. “Supplemental protein to enhance nutrient utilization of steers fed high fiber hay.” 2003. Web. 21 Jul 2019.

Vancouver:

Paiva NN. Supplemental protein to enhance nutrient utilization of steers fed high fiber hay. [Internet] [Masters thesis]. University of Georgia; 2003. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/paiva_newton_n_200308_ms.

Council of Science Editors:

Paiva NN. Supplemental protein to enhance nutrient utilization of steers fed high fiber hay. [Masters Thesis]. University of Georgia; 2003. Available from: http://purl.galileo.usg.edu/uga_etd/paiva_newton_n_200308_ms


Texas A&M University

6. Lum, Karin Tien. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.

Degree: 2004, Texas A&M University

 Directed evolution studies were done with PTE for the enhancement of hydrolysis of both sarin and soman analogs. Particular attention was focused on the toxic… (more)

Subjects/Keywords: protein engineering

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APA (6th Edition):

Lum, K. T. (2004). Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149

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):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Thesis, Texas A&M University. Accessed July 21, 2019. http://hdl.handle.net/1969.1/149.

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

MLA Handbook (7th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Web. 21 Jul 2019.

Vancouver:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Internet] [Thesis]. Texas A&M University; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1969.1/149.

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

Council of Science Editors:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Thesis]. Texas A&M University; 2004. Available from: http://hdl.handle.net/1969.1/149

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


Oregon State University

7. Merwin, Jason R. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.

Degree: PhD, Molecular and Cellular Biology, 2003, Oregon State University

 Reporter gene transactivation by human p53 is inhibited in budding yeast lacking the TRR1 gene encoding thioredoxin reductase. Thioredoxin reductase specifically catalyzes the NADPH-dependent reduction… (more)

Subjects/Keywords: p53 protein

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APA (6th Edition):

Merwin, J. R. (2003). Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/30498

Chicago Manual of Style (16th Edition):

Merwin, Jason R. “Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.” 2003. Doctoral Dissertation, Oregon State University. Accessed July 21, 2019. http://hdl.handle.net/1957/30498.

MLA Handbook (7th Edition):

Merwin, Jason R. “Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.” 2003. Web. 21 Jul 2019.

Vancouver:

Merwin JR. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. [Internet] [Doctoral dissertation]. Oregon State University; 2003. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1957/30498.

Council of Science Editors:

Merwin JR. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. [Doctoral Dissertation]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/30498


Wake Forest University

8. Hill, David Brooks. Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12.

Degree: 2003, Wake Forest University

 Motor proteins such as kinesin and dynein drive vesicle transport within cells by converting the chemical energy of ATP into mechanical work. Though isolated kinesin… (more)

Subjects/Keywords: motor protein

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APA (6th Edition):

Hill, D. B. (2003). Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/14748

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):

Hill, David Brooks. “Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12.” 2003. Thesis, Wake Forest University. Accessed July 21, 2019. http://hdl.handle.net/10339/14748.

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

MLA Handbook (7th Edition):

Hill, David Brooks. “Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12.” 2003. Web. 21 Jul 2019.

Vancouver:

Hill DB. Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12. [Internet] [Thesis]. Wake Forest University; 2003. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10339/14748.

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

Council of Science Editors:

Hill DB. Changes in the Number of Molecular Motors Driving Vesicle Transport in PC12. [Thesis]. Wake Forest University; 2003. Available from: http://hdl.handle.net/10339/14748

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


ETH Zürich

9. Gujer, Remo. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.

Degree: 2001, ETH Zürich

Subjects/Keywords: CALCITONINGEN-BEZOGENES PEPTID (BIOCHEMIE); G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); GLYKOSYLIERUNGSREAKTIONEN + GLYKOSYLIERUNG (BIOCHEMIE); CALCITONIN GENE-RELATED PEPTIDE (BIOCHEMISTRY); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); GLYCOSYLATION REACTIONS + GLYCOSYLATION (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Gujer, R. (2001). Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145067

Chicago Manual of Style (16th Edition):

Gujer, Remo. “Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.” 2001. Doctoral Dissertation, ETH Zürich. Accessed July 21, 2019. http://hdl.handle.net/20.500.11850/145067.

MLA Handbook (7th Edition):

Gujer, Remo. “Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors.” 2001. Web. 21 Jul 2019.

Vancouver:

Gujer R. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. [Internet] [Doctoral dissertation]. ETH Zürich; 2001. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/20.500.11850/145067.

Council of Science Editors:

Gujer R. Influence of receptor-activity-modifying proteins (RAMP) on the formation of functional G-protein-coupled receptors. [Doctoral Dissertation]. ETH Zürich; 2001. Available from: http://hdl.handle.net/20.500.11850/145067


ETH Zürich

10. Müller-Steiner, Sarah. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.

Degree: 2003, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); CALCITONINGEN-BEZOGENES PEPTID (BIOCHEMIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); CALCITONIN GENE-RELATED PEPTIDE (BIOCHEMISTRY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/610; Life sciences; Medical sciences, medicine

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APA (6th Edition):

Müller-Steiner, S. (2003). Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147770

Chicago Manual of Style (16th Edition):

Müller-Steiner, Sarah. “Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.” 2003. Doctoral Dissertation, ETH Zürich. Accessed July 21, 2019. http://hdl.handle.net/20.500.11850/147770.

MLA Handbook (7th Edition):

Müller-Steiner, Sarah. “Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors.” 2003. Web. 21 Jul 2019.

Vancouver:

Müller-Steiner S. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. [Internet] [Doctoral dissertation]. ETH Zürich; 2003. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/20.500.11850/147770.

Council of Science Editors:

Müller-Steiner S. Functional interaction of receptor-activity-modifying proteins (RAMP) with G protein-coupled receptors. [Doctoral Dissertation]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147770


ETH Zürich

11. Aldecoa, Amaya. Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP).

Degree: 2001, ETH Zürich

Subjects/Keywords: G-PROTEIN-GEKOPPELTE REZEPTOREN (MEMBRANBIOLOGIE); CALCITONINGEN-BEZOGENES PEPTID (BIOCHEMIE); REZEPTOR-LIGAND INTERAKTIONEN (MOLEKULARBIOLOGIE); GLYKOSYLIERUNGSREAKTIONEN + GLYKOSYLIERUNG (BIOCHEMIE); G PROTEIN COUPLED RECEPTORS (MEMBRANE BIOLOGY); CALCITONIN GENE-RELATED PEPTIDE (BIOCHEMISTRY); RECEPTOR-LIGAND INTERACTIONS (MOLECULAR BIOLOGY); GLYCOSYLATION REACTIONS + GLYCOSYLATION (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Aldecoa, A. (2001). Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP). (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145277

Chicago Manual of Style (16th Edition):

Aldecoa, Amaya. “Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP).” 2001. Doctoral Dissertation, ETH Zürich. Accessed July 21, 2019. http://hdl.handle.net/20.500.11850/145277.

MLA Handbook (7th Edition):

Aldecoa, Amaya. “Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP).” 2001. Web. 21 Jul 2019.

Vancouver:

Aldecoa A. Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP). [Internet] [Doctoral dissertation]. ETH Zürich; 2001. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/20.500.11850/145277.

Council of Science Editors:

Aldecoa A. Functional interaction of G protein-coupled receptors of the calcitonin peptide family with accessory receptor-activity-modifying proteins (RAMP). [Doctoral Dissertation]. ETH Zürich; 2001. Available from: http://hdl.handle.net/20.500.11850/145277

12. Vuolanto, Antti. Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications.

Degree: 2004, Helsinki University of Technology

 Chemical cross-linking of protein crystals form an insoluble and active protein matrix. Cross-linked protein crystals (CLPCs) have many excellent properties including high volumetric activity and… (more)

Subjects/Keywords: cross-linked protein crystal; protein crystallization; bioseparation; biocatalysis

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APA (6th Edition):

Vuolanto, A. (2004). Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications. (Thesis). Helsinki University of Technology. Retrieved from http://lib.tkk.fi/Diss/2004/isbn951227177X/

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):

Vuolanto, Antti. “Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications.” 2004. Thesis, Helsinki University of Technology. Accessed July 21, 2019. http://lib.tkk.fi/Diss/2004/isbn951227177X/.

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

MLA Handbook (7th Edition):

Vuolanto, Antti. “Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications.” 2004. Web. 21 Jul 2019.

Vancouver:

Vuolanto A. Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications. [Internet] [Thesis]. Helsinki University of Technology; 2004. [cited 2019 Jul 21]. Available from: http://lib.tkk.fi/Diss/2004/isbn951227177X/.

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

Council of Science Editors:

Vuolanto A. Cross-Linked Protein Crystal Technology in Bioseparation and Biocatalytic Applications. [Thesis]. Helsinki University of Technology; 2004. Available from: http://lib.tkk.fi/Diss/2004/isbn951227177X/

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

13. Durek, Thomas. Semi-synthesis and biological evaluation of prenylated Rab proteins.

Degree: 2004, Universität Dortmund

 Native chemical ligation (NCL) and the related technique, expressed protein ligation(EPL), have been extremely useful for the synthesis of various proteins in the past. Inparticular… (more)

Subjects/Keywords: expressed protein ligation; GDI; prenylation; protein semisynthesis; Rab; 540

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APA (6th Edition):

Durek, T. (2004). Semi-synthesis and biological evaluation of prenylated Rab proteins. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/5571

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):

Durek, Thomas. “Semi-synthesis and biological evaluation of prenylated Rab proteins.” 2004. Thesis, Universität Dortmund. Accessed July 21, 2019. http://hdl.handle.net/2003/5571.

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

MLA Handbook (7th Edition):

Durek, Thomas. “Semi-synthesis and biological evaluation of prenylated Rab proteins.” 2004. Web. 21 Jul 2019.

Vancouver:

Durek T. Semi-synthesis and biological evaluation of prenylated Rab proteins. [Internet] [Thesis]. Universität Dortmund; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2003/5571.

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

Council of Science Editors:

Durek T. Semi-synthesis and biological evaluation of prenylated Rab proteins. [Thesis]. Universität Dortmund; 2004. Available from: http://hdl.handle.net/2003/5571

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


Massey University

14. Back, Penelope Jane. The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants.

Degree: PhD, Animal Science, 2002, Massey University

 The primary aim of this thesis was to determine the role of insulin in milk protein production in pasture-fed lactating ruminants (ewes and cows), using… (more)

Subjects/Keywords: Milk protein production; Protein synthesis

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APA (6th Edition):

Back, P. J. (2002). The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/1974

Chicago Manual of Style (16th Edition):

Back, Penelope Jane. “The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants.” 2002. Doctoral Dissertation, Massey University. Accessed July 21, 2019. http://hdl.handle.net/10179/1974.

MLA Handbook (7th Edition):

Back, Penelope Jane. “The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants.” 2002. Web. 21 Jul 2019.

Vancouver:

Back PJ. The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants. [Internet] [Doctoral dissertation]. Massey University; 2002. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10179/1974.

Council of Science Editors:

Back PJ. The role of insulin in the regulation of milk protein synthesis in pasture-fed lactating ruminants. [Doctoral Dissertation]. Massey University; 2002. Available from: http://hdl.handle.net/10179/1974


University of Texas – Austin

15. Rainey, Mark Allan. A structure/function analysis of macromolecular recognition by the protein kinase ERK2.

Degree: Institute for Cellular and Molecular Biology, 2004, University of Texas – Austin

 Mitogen-activate protein kinases (MAPKs) phosphorylate protein substrates in the presence of magnesium and adenosine triphosphate in response to extracellular environmental signals to carry out signal-dependent… (more)

Subjects/Keywords: Protein kinase ERK2; Protein binding

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APA (6th Edition):

Rainey, M. A. (2004). A structure/function analysis of macromolecular recognition by the protein kinase ERK2. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1392

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):

Rainey, Mark Allan. “A structure/function analysis of macromolecular recognition by the protein kinase ERK2.” 2004. Thesis, University of Texas – Austin. Accessed July 21, 2019. http://hdl.handle.net/2152/1392.

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

MLA Handbook (7th Edition):

Rainey, Mark Allan. “A structure/function analysis of macromolecular recognition by the protein kinase ERK2.” 2004. Web. 21 Jul 2019.

Vancouver:

Rainey MA. A structure/function analysis of macromolecular recognition by the protein kinase ERK2. [Internet] [Thesis]. University of Texas – Austin; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2152/1392.

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

Council of Science Editors:

Rainey MA. A structure/function analysis of macromolecular recognition by the protein kinase ERK2. [Thesis]. University of Texas – Austin; 2004. Available from: http://hdl.handle.net/2152/1392

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


Hong Kong University of Science and Technology

16. Ng, Wai Sun. Multi-functions of the PP2A domain of axin.

Degree: 2004, Hong Kong University of Science and Technology

 Axin serves as a scaffold protein in Wnt signaling pathway to negatively regulate the stability of β-catenin, and it also facilitates the c-Jun N-terminal/stress-activated protein(more)

Subjects/Keywords: Protein-protein interactions; Protein binding; Phosphoprotein phosphatases

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APA (6th Edition):

Ng, W. S. (2004). Multi-functions of the PP2A domain of axin. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/th_redirect.html

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):

Ng, Wai Sun. “Multi-functions of the PP2A domain of axin.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed July 21, 2019. https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Ng, Wai Sun. “Multi-functions of the PP2A domain of axin.” 2004. Web. 21 Jul 2019.

Vancouver:

Ng WS. Multi-functions of the PP2A domain of axin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Jul 21]. Available from: https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/th_redirect.html.

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

Council of Science Editors:

Ng WS. Multi-functions of the PP2A domain of axin. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b839570 ; http://repository.ust.hk/ir/bitstream/1783.1-3764/1/th_redirect.html

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


Hong Kong University of Science and Technology

17. Rui, Hongliang. Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin.

Degree: 2004, Hong Kong University of Science and Technology

 Axin was originally identified from the characterization of the Fused locus, the disruption of which leads to duplication of axis and embryonic lethality. Axin is… (more)

Subjects/Keywords: Protein binding; Protein-protein interactions; Cellular signal transduction

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APA (6th Edition):

Rui, H. (2004). Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b849111 ; http://repository.ust.hk/ir/bitstream/1783.1-2316/1/th_redirect.html

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):

Rui, Hongliang. “Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed July 21, 2019. https://doi.org/10.14711/thesis-b849111 ; http://repository.ust.hk/ir/bitstream/1783.1-2316/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Rui, Hongliang. “Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin.” 2004. Web. 21 Jul 2019.

Vancouver:

Rui H. Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Jul 21]. Available from: https://doi.org/10.14711/thesis-b849111 ; http://repository.ust.hk/ir/bitstream/1783.1-2316/1/th_redirect.html.

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

Council of Science Editors:

Rui H. Regulation of MAPK/JNK signaling pathway and TGF-beta signaling pathway by axin. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b849111 ; http://repository.ust.hk/ir/bitstream/1783.1-2316/1/th_redirect.html

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


University of Sydney

18. Simpson, Raina Jui Yu. The multiple roles of zinc finger domains .

Degree: 2004, University of Sydney

 Zinc finger (ZnF) domains are prevalent in eukaryotes and play crucial roles in mediating protein-DNA and protein-protein interactions. This Thesis focuses on the molecular details… (more)

Subjects/Keywords: zinc fingers; protein-protein; protein-DNA; interactions

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APA (6th Edition):

Simpson, R. J. Y. (2004). The multiple roles of zinc finger domains . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/655

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):

Simpson, Raina Jui Yu. “The multiple roles of zinc finger domains .” 2004. Thesis, University of Sydney. Accessed July 21, 2019. http://hdl.handle.net/2123/655.

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

MLA Handbook (7th Edition):

Simpson, Raina Jui Yu. “The multiple roles of zinc finger domains .” 2004. Web. 21 Jul 2019.

Vancouver:

Simpson RJY. The multiple roles of zinc finger domains . [Internet] [Thesis]. University of Sydney; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2123/655.

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

Council of Science Editors:

Simpson RJY. The multiple roles of zinc finger domains . [Thesis]. University of Sydney; 2004. Available from: http://hdl.handle.net/2123/655

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


University of Georgia

19. Kazmierski, Michelle Nicole. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.

Degree: MS, Food Science, 2002, University of Georgia

 Despite its widespread utilization, information relating to the characterization of commercially available whey protein isolate (WPI) is limited. Further insight into its behavior in mixed… (more)

Subjects/Keywords: Whey protein isolate

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

APA (6th Edition):

Kazmierski, M. N. (2002). Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/kazmierski_michelle_n_200212_ms

Chicago Manual of Style (16th Edition):

Kazmierski, Michelle Nicole. “Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.” 2002. Masters Thesis, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/kazmierski_michelle_n_200212_ms.

MLA Handbook (7th Edition):

Kazmierski, Michelle Nicole. “Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions.” 2002. Web. 21 Jul 2019.

Vancouver:

Kazmierski MN. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. [Internet] [Masters thesis]. University of Georgia; 2002. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/kazmierski_michelle_n_200212_ms.

Council of Science Editors:

Kazmierski MN. Thermally induced aggregation of whey proteins : characterization of protein isolates and beta-lactoglobulin/ pectin interactions. [Masters Thesis]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/kazmierski_michelle_n_200212_ms


University of Georgia

20. Hill, Kimberley Temeca. Pharmacokinetic analysis and formulation development of therapeutic proteins.

Degree: PhD, Pharmacy (Pharmaceutics), 2004, University of Georgia

 Overcoming the challenges of protein drug delivery requires an integrated partnership between well-established concepts in drug delivery and a bit of the avant-garde, with the… (more)

Subjects/Keywords: protein drug delivery

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APA (6th Edition):

Hill, K. T. (2004). Pharmacokinetic analysis and formulation development of therapeutic proteins. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/hill_kimberley_t_200412_phd

Chicago Manual of Style (16th Edition):

Hill, Kimberley Temeca. “Pharmacokinetic analysis and formulation development of therapeutic proteins.” 2004. Doctoral Dissertation, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/hill_kimberley_t_200412_phd.

MLA Handbook (7th Edition):

Hill, Kimberley Temeca. “Pharmacokinetic analysis and formulation development of therapeutic proteins.” 2004. Web. 21 Jul 2019.

Vancouver:

Hill KT. Pharmacokinetic analysis and formulation development of therapeutic proteins. [Internet] [Doctoral dissertation]. University of Georgia; 2004. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/hill_kimberley_t_200412_phd.

Council of Science Editors:

Hill KT. Pharmacokinetic analysis and formulation development of therapeutic proteins. [Doctoral Dissertation]. University of Georgia; 2004. Available from: http://purl.galileo.usg.edu/uga_etd/hill_kimberley_t_200412_phd


University of Utah

21. Doak, Thomas Graeme. Transposons in ciliated protozoa;.

Degree: PhD, Oncological Sciences;, 2001, University of Utah

 Ciliated protozoa carry two types of nuclei in each cell. One is an undifferentiated “germline” micronucleus; the other is a nucleus that has undergone a… (more)

Subjects/Keywords: Protein-Coding; Genes

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APA (6th Edition):

Doak, T. G. (2001). Transposons in ciliated protozoa;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/912/rec/1423

Chicago Manual of Style (16th Edition):

Doak, Thomas Graeme. “Transposons in ciliated protozoa;.” 2001. Doctoral Dissertation, University of Utah. Accessed July 21, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/912/rec/1423.

MLA Handbook (7th Edition):

Doak, Thomas Graeme. “Transposons in ciliated protozoa;.” 2001. Web. 21 Jul 2019.

Vancouver:

Doak TG. Transposons in ciliated protozoa;. [Internet] [Doctoral dissertation]. University of Utah; 2001. [cited 2019 Jul 21]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/912/rec/1423.

Council of Science Editors:

Doak TG. Transposons in ciliated protozoa;. [Doctoral Dissertation]. University of Utah; 2001. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/912/rec/1423


Hong Kong University of Science and Technology

22. Cheung, Po Yan. Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation.

Degree: 2002, Hong Kong University of Science and Technology

 Activation of MAPKs by their upstream MAPKKs has long been thought to be a direct process with direct binding and concomitant phosphorylation of MAPKs without… (more)

Subjects/Keywords: Protein kinases; Tubulins

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APA (6th Edition):

Cheung, P. Y. (2002). Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b776185 ; http://repository.ust.hk/ir/bitstream/1783.1-3750/1/th_redirect.html

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):

Cheung, Po Yan. “Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation.” 2002. Thesis, Hong Kong University of Science and Technology. Accessed July 21, 2019. https://doi.org/10.14711/thesis-b776185 ; http://repository.ust.hk/ir/bitstream/1783.1-3750/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Cheung, Po Yan. “Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation.” 2002. Web. 21 Jul 2019.

Vancouver:

Cheung PY. Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2002. [cited 2019 Jul 21]. Available from: https://doi.org/10.14711/thesis-b776185 ; http://repository.ust.hk/ir/bitstream/1783.1-3750/1/th_redirect.html.

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

Council of Science Editors:

Cheung PY. Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation. [Thesis]. Hong Kong University of Science and Technology; 2002. Available from: https://doi.org/10.14711/thesis-b776185 ; http://repository.ust.hk/ir/bitstream/1783.1-3750/1/th_redirect.html

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


McGill University

23. Stewart, Deborah. P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing.

Degree: PhD, Institute of Parasitology., 2004, McGill University

In normal cells, the p53 tumour suppressor induces cell cycle arrest or apoptosis in response to a variety of stresses, including DNA damage and ectopic… (more)

Subjects/Keywords: Papillomaviruses.; p53 protein.

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APA (6th Edition):

Stewart, D. (2004). P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile85651.pdf

Chicago Manual of Style (16th Edition):

Stewart, Deborah. “P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing.” 2004. Doctoral Dissertation, McGill University. Accessed July 21, 2019. http://digitool.library.mcgill.ca/thesisfile85651.pdf.

MLA Handbook (7th Edition):

Stewart, Deborah. “P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing.” 2004. Web. 21 Jul 2019.

Vancouver:

Stewart D. P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing. [Internet] [Doctoral dissertation]. McGill University; 2004. [cited 2019 Jul 21]. Available from: http://digitool.library.mcgill.ca/thesisfile85651.pdf.

Council of Science Editors:

Stewart D. P53 regulatory mechanisms by human papillomavirus (HPV) E6 and alternative splicing. [Doctoral Dissertation]. McGill University; 2004. Available from: http://digitool.library.mcgill.ca/thesisfile85651.pdf


Oregon State University

24. Doneanu, Catalin E. Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes.

Degree: PhD, Chemistry, 2002, Oregon State University

Subjects/Keywords: DNA-protein interactions

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APA (6th Edition):

Doneanu, C. E. (2002). Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/31851

Chicago Manual of Style (16th Edition):

Doneanu, Catalin E. “Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes.” 2002. Doctoral Dissertation, Oregon State University. Accessed July 21, 2019. http://hdl.handle.net/1957/31851.

MLA Handbook (7th Edition):

Doneanu, Catalin E. “Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes.” 2002. Web. 21 Jul 2019.

Vancouver:

Doneanu CE. Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes. [Internet] [Doctoral dissertation]. Oregon State University; 2002. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1957/31851.

Council of Science Editors:

Doneanu CE. Mass spectrometric analysis of UV-crosslinked protein-nucleic acid complexes. [Doctoral Dissertation]. Oregon State University; 2002. Available from: http://hdl.handle.net/1957/31851


Michigan State University

25. Vacratsis, Panayiotis Orestes. Molecular mechanisms regulating the mixed lineage kinase MLK3.

Degree: PhD, Department of Biochemistry and Molecular Biology, 2001, Michigan State University

Subjects/Keywords: Protein kinases; Phosphorylation

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APA (6th Edition):

Vacratsis, P. O. (2001). Molecular mechanisms regulating the mixed lineage kinase MLK3. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:31083

Chicago Manual of Style (16th Edition):

Vacratsis, Panayiotis Orestes. “Molecular mechanisms regulating the mixed lineage kinase MLK3.” 2001. Doctoral Dissertation, Michigan State University. Accessed July 21, 2019. http://etd.lib.msu.edu/islandora/object/etd:31083.

MLA Handbook (7th Edition):

Vacratsis, Panayiotis Orestes. “Molecular mechanisms regulating the mixed lineage kinase MLK3.” 2001. Web. 21 Jul 2019.

Vancouver:

Vacratsis PO. Molecular mechanisms regulating the mixed lineage kinase MLK3. [Internet] [Doctoral dissertation]. Michigan State University; 2001. [cited 2019 Jul 21]. Available from: http://etd.lib.msu.edu/islandora/object/etd:31083.

Council of Science Editors:

Vacratsis PO. Molecular mechanisms regulating the mixed lineage kinase MLK3. [Doctoral Dissertation]. Michigan State University; 2001. Available from: http://etd.lib.msu.edu/islandora/object/etd:31083


University of Adelaide

26. Fotia, Andrew B. Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2.

Degree: 2004, University of Adelaide

Protein modification by ubiquitination regulates protein abundance, function and localisation. Specificity of ubiquitination is largely determined by ubiquitinprotein ligases (E3s). The Nedd4–family proteins are a… (more)

Subjects/Keywords: protein; ubiquitin; hypertension

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APA (6th Edition):

Fotia, A. B. (2004). Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/37956

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):

Fotia, Andrew B. “Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2.” 2004. Thesis, University of Adelaide. Accessed July 21, 2019. http://hdl.handle.net/2440/37956.

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

MLA Handbook (7th Edition):

Fotia, Andrew B. “Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2.” 2004. Web. 21 Jul 2019.

Vancouver:

Fotia AB. Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2. [Internet] [Thesis]. University of Adelaide; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2440/37956.

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

Council of Science Editors:

Fotia AB. Regulation of sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2. [Thesis]. University of Adelaide; 2004. Available from: http://hdl.handle.net/2440/37956

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


Hong Kong University of Science and Technology

27. Wong, Chung Kai. The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms.

Degree: 2004, Hong Kong University of Science and Technology

 Axin, Ccd1 (coiled-coil – DIX1), and Dishevelled (Dvl or Dsh) are three known DIX domain proteins that play important roles in Wnt signaling. In addition, Dvl… (more)

Subjects/Keywords: Proteins; Protein-protein interactions; Gene expression

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APA (6th Edition):

Wong, C. K. (2004). The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b839562 ; http://repository.ust.hk/ir/bitstream/1783.1-3763/1/th_redirect.html

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):

Wong, Chung Kai. “The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed July 21, 2019. https://doi.org/10.14711/thesis-b839562 ; http://repository.ust.hk/ir/bitstream/1783.1-3763/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wong, Chung Kai. “The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms.” 2004. Web. 21 Jul 2019.

Vancouver:

Wong CK. The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Jul 21]. Available from: https://doi.org/10.14711/thesis-b839562 ; http://repository.ust.hk/ir/bitstream/1783.1-3763/1/th_redirect.html.

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

Council of Science Editors:

Wong CK. The DIX domain protein Ccd1 inhibits JNK activation by axin and dishevelled through distinct mechanisms. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b839562 ; http://repository.ust.hk/ir/bitstream/1783.1-3763/1/th_redirect.html

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


University of Texas – Austin

28. Cox, James Colin, 1974-. Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection.

Degree: Cellular and Molecular Biology, 2004, University of Texas – Austin

 RNA binding proteins play a crucial role in normal cellular functions. However, little work has been successful in developing a code of recognition that may… (more)

Subjects/Keywords: Nucleoproteins; RNA-protein interactions; Protein engineering

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APA (6th Edition):

Cox, James Colin, 1. (2004). Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1217

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):

Cox, James Colin, 1974-. “Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection.” 2004. Thesis, University of Texas – Austin. Accessed July 21, 2019. http://hdl.handle.net/2152/1217.

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

MLA Handbook (7th Edition):

Cox, James Colin, 1974-. “Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection.” 2004. Web. 21 Jul 2019.

Vancouver:

Cox, James Colin 1. Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection. [Internet] [Thesis]. University of Texas – Austin; 2004. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2152/1217.

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

Council of Science Editors:

Cox, James Colin 1. Probing specificity of RNA : ribonucleoprotein interactions through in vitro selection. [Thesis]. University of Texas – Austin; 2004. Available from: http://hdl.handle.net/2152/1217

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


The Ohio State University

29. Jovanovic, Milan. Structure-function relationships in the protein subunit of bacterial ribonuclease P.

Degree: PhD, Ohio State Biochemistry Program, 2004, The Ohio State University

 Ribonuclease P (RNase P) is a ribonucleoprotein involved in tRNA biosynthesis in all living organisms. Bacterial RNase P is comprised of a catalytic RNA subunit… (more)

Subjects/Keywords: Chemistry, Biochemistry; Bacterial RNase; RNase; C5 protein; C5; PROTEIN; F18A/F22A; PROTEIN SUBUNIT

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

APA (6th Edition):

Jovanovic, M. (2004). Structure-function relationships in the protein subunit of bacterial ribonuclease P. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1092422670

Chicago Manual of Style (16th Edition):

Jovanovic, Milan. “Structure-function relationships in the protein subunit of bacterial ribonuclease P.” 2004. Doctoral Dissertation, The Ohio State University. Accessed July 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1092422670.

MLA Handbook (7th Edition):

Jovanovic, Milan. “Structure-function relationships in the protein subunit of bacterial ribonuclease P.” 2004. Web. 21 Jul 2019.

Vancouver:

Jovanovic M. Structure-function relationships in the protein subunit of bacterial ribonuclease P. [Internet] [Doctoral dissertation]. The Ohio State University; 2004. [cited 2019 Jul 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1092422670.

Council of Science Editors:

Jovanovic M. Structure-function relationships in the protein subunit of bacterial ribonuclease P. [Doctoral Dissertation]. The Ohio State University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1092422670


The Ohio State University

30. Li, Hongyuan. Structure of KI67 FHA domain and its binding to HNIFK.

Degree: PhD, Biochemistry, 2003, The Ohio State University

 The Ki67 protein is a 359 kDa nuclear protein whose existence is strictly associated with the cell cycle and has been used extensively as a… (more)

Subjects/Keywords: FHA domain; NMR structure; protein-protein interaction; phospho-protein recognition

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

APA (6th Edition):

Li, H. (2003). Structure of KI67 FHA domain and its binding to HNIFK. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1060882032

Chicago Manual of Style (16th Edition):

Li, Hongyuan. “Structure of KI67 FHA domain and its binding to HNIFK.” 2003. Doctoral Dissertation, The Ohio State University. Accessed July 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1060882032.

MLA Handbook (7th Edition):

Li, Hongyuan. “Structure of KI67 FHA domain and its binding to HNIFK.” 2003. Web. 21 Jul 2019.

Vancouver:

Li H. Structure of KI67 FHA domain and its binding to HNIFK. [Internet] [Doctoral dissertation]. The Ohio State University; 2003. [cited 2019 Jul 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1060882032.

Council of Science Editors:

Li H. Structure of KI67 FHA domain and its binding to HNIFK. [Doctoral Dissertation]. The Ohio State University; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1060882032

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