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Dept: Biochemistry

You searched for subject:( Espaces priv s). Showing records 1 – 19 of 19 total matches.

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Case Western Reserve University

1. Peng, Yi. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.

Degree: PhD, Biochemistry, 2009, Case Western Reserve University

S-adenosylmethionine-dependent methyltransferases (AdoMet-dependent MTases) are a main subfamily of MTases, which play critical roles in diverse methylation reactions in many significant biological processes. AdoMet-dependent… (more)

Subjects/Keywords: Biochemistry; S-adenosylmethionine-dependent methyltransferase

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APA (6th Edition):

Peng, Y. (2009). Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254

Chicago Manual of Style (16th Edition):

Peng, Yi. “Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254.

MLA Handbook (7th Edition):

Peng, Yi. “Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.” 2009. Web. 16 Jun 2019.

Vancouver:

Peng Y. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254.

Council of Science Editors:

Peng Y. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254


Vilnius University

2. Bielskienė, Kristina. Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes.

Degree: PhD, Biochemistry, 2009, Vilnius University

Despite a great deal of research, the functional significance of tightly bound DNA-protein complexes is not yet clear, therefore these complexes are perfect object for… (more)

Subjects/Keywords: Tightly bound DNA-protein complexes; Nuclear matrix; S/MAR sequences; Tvirti DNR-baltymų kompleksai; Branduolio matriksas; S/MAR sekos

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APA (6th Edition):

Bielskienė, K. (2009). Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_111955-77123 ;

Chicago Manual of Style (16th Edition):

Bielskienė, Kristina. “Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes.” 2009. Doctoral Dissertation, Vilnius University. Accessed June 16, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_111955-77123 ;.

MLA Handbook (7th Edition):

Bielskienė, Kristina. “Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes.” 2009. Web. 16 Jun 2019.

Vancouver:

Bielskienė K. Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes. [Internet] [Doctoral dissertation]. Vilnius University; 2009. [cited 2019 Jun 16]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_111955-77123 ;.

Council of Science Editors:

Bielskienė K. Analysis of the barley (Hordeum vulgare) tightly bound DNA-protein complexes. [Doctoral Dissertation]. Vilnius University; 2009. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_111955-77123 ;


Vilnius University

3. Bielskienė, Kristina. Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas.

Degree: Dissertation, Biochemistry, 2009, Vilnius University

Žinoma, kad pastovi nehistoninių polipetidų frakcija yra išgryninama kartu su eukariotine DNR ir sudaro labai tvirtus (galbūt kovalentinius) kompleksus tarp branduolio baltymų ir DNR. Nustatyta,… (more)

Subjects/Keywords: Tvirti DNR-baltymų kompleksai; Branduolio matriksas; S/MAR sekos; Tightly bound DNA-protein complexes; Nuclear matrix; S/MAR sequences

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APA (6th Edition):

Bielskienė, K. (2009). Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_112036-51456 ;

Chicago Manual of Style (16th Edition):

Bielskienė, Kristina. “Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas.” 2009. Doctoral Dissertation, Vilnius University. Accessed June 16, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_112036-51456 ;.

MLA Handbook (7th Edition):

Bielskienė, Kristina. “Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas.” 2009. Web. 16 Jun 2019.

Vancouver:

Bielskienė K. Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas. [Internet] [Doctoral dissertation]. Vilnius University; 2009. [cited 2019 Jun 16]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_112036-51456 ;.

Council of Science Editors:

Bielskienė K. Miežių (Hordeum vulgare) tvirtų DNR-baltymų kompleksų tyrimas. [Doctoral Dissertation]. Vilnius University; 2009. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2009~D_20091202_112036-51456 ;


University of Pretoria

4. Smit, Salome. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria presents a global health risk that is becoming increasingly difficult to treat due to increased resistance of both the parasite and mosquito to all… (more)

Subjects/Keywords: Methionine metabolism; Malaria; S-adenosylmethionine decarboxylase; Mosquito; Parasite; UCTD

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APA (6th Edition):

Smit, S. (2011). Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25743

Chicago Manual of Style (16th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Doctoral Dissertation, University of Pretoria. Accessed June 16, 2019. http://hdl.handle.net/2263/25743.

MLA Handbook (7th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Web. 16 Jun 2019.

Vancouver:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/2263/25743.

Council of Science Editors:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/25743


University of Pretoria

5. Coertzen, Dina. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.

Degree: PhD, Biochemistry, 2015, University of Pretoria

 Malaria is considered the most prevailing human parasitic disease. Despite various chemotherapeutic interventions being available, the parasite responsible for the most lethal form of malaria,… (more)

Subjects/Keywords: UCTD; S-adenosylmethionine decarboxylase; Plasmodium falciparum; Parasite Specific Inserts; Polyamines

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APA (6th Edition):

Coertzen, D. (2015). Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/46163

Chicago Manual of Style (16th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2015. Doctoral Dissertation, University of Pretoria. Accessed June 16, 2019. http://hdl.handle.net/2263/46163.

MLA Handbook (7th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2015. Web. 16 Jun 2019.

Vancouver:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2015. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/2263/46163.

Council of Science Editors:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2015. Available from: http://hdl.handle.net/2263/46163


The Ohio State University

6. Luo, Wen-I. The Role of Chaperones in Iron-Sulfur Cluster Biogenesis.

Degree: PhD, Biochemistry, 2011, The Ohio State University

  Iron-sulfur (Fe-S) clusters are crucial co-factors that participate in several key biological events such as mitochondrial respiration, photosynthesis and nitrogen fixation. In eukaryotes, Fe-S(more)

Subjects/Keywords: Biochemistry; Mortalin; Hsp70 chaperone; ISU; Fe-S cluster

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APA (6th Edition):

Luo, W. (2011). The Role of Chaperones in Iron-Sulfur Cluster Biogenesis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1325168796

Chicago Manual of Style (16th Edition):

Luo, Wen-I. “The Role of Chaperones in Iron-Sulfur Cluster Biogenesis.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1325168796.

MLA Handbook (7th Edition):

Luo, Wen-I. “The Role of Chaperones in Iron-Sulfur Cluster Biogenesis.” 2011. Web. 16 Jun 2019.

Vancouver:

Luo W. The Role of Chaperones in Iron-Sulfur Cluster Biogenesis. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325168796.

Council of Science Editors:

Luo W. The Role of Chaperones in Iron-Sulfur Cluster Biogenesis. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1325168796


Stellenbosch University

7. van Rensburg, Wilma. Characterization of natural antimicrobial peptides adsorbed to different matrices.

Degree: MSc, Biochemistry, 2015, Stellenbosch University

 ENGLISH ABSTRACT: Biofouling is the attachment and biofilm formation that leads to negative repercussions such as persistent post-harvest infections, infections obtained from medical implants and… (more)

Subjects/Keywords: Tyrocidines; Gramicidin S; Solid surface activity; Antimicrobial peptides; Antimicrobial surfaces; UCTD

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APA (6th Edition):

van Rensburg, W. (2015). Characterization of natural antimicrobial peptides adsorbed to different matrices. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/97929

Chicago Manual of Style (16th Edition):

van Rensburg, Wilma. “Characterization of natural antimicrobial peptides adsorbed to different matrices.” 2015. Masters Thesis, Stellenbosch University. Accessed June 16, 2019. http://hdl.handle.net/10019.1/97929.

MLA Handbook (7th Edition):

van Rensburg, Wilma. “Characterization of natural antimicrobial peptides adsorbed to different matrices.” 2015. Web. 16 Jun 2019.

Vancouver:

van Rensburg W. Characterization of natural antimicrobial peptides adsorbed to different matrices. [Internet] [Masters thesis]. Stellenbosch University; 2015. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10019.1/97929.

Council of Science Editors:

van Rensburg W. Characterization of natural antimicrobial peptides adsorbed to different matrices. [Masters Thesis]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/97929


Virginia Tech

8. Miller, Danielle Virginia. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.

Degree: PhD, Biochemistry, 2017, Virginia Tech

S-Adenosyl-L-methionine (SAM) is an essential metabolite for all domains of life. SAM- dependent reactions result in three major metabolites: S-adenosyl-L-homocysteine (SAH), methylthioadenosine (MTA), and 5'-deoxyadenosine… (more)

Subjects/Keywords: S-adenosyl-L-methionine; SAM; recycling; 6-deoxy-5-ketofructose 1-phosphate; aromatic amino acids; methionine salvage; 5'-deoxyadenosine; S-adenosylhomoysteine; methylthioadenosine

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APA (6th Edition):

Miller, D. V. (2017). Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77520

Chicago Manual of Style (16th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Doctoral Dissertation, Virginia Tech. Accessed June 16, 2019. http://hdl.handle.net/10919/77520.

MLA Handbook (7th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Web. 16 Jun 2019.

Vancouver:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10919/77520.

Council of Science Editors:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/77520

9. Panneerselvam, Vijayaraj. Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -.

Degree: Biochemistry, 2011, Bharathidasan University

The present study is the first report of 4-(methyl nitrosamino)-1-(3-pyridyl)-1- butanone (NNK) and N-nitrosonornicotine (NNN) on phospholipid metabolism using two different model systems. Tobacco specific… (more)

Subjects/Keywords: Tobacco specific nitrosamines; N-nitrosonornicotine; S. cerevisiae; Pulmonary surfactant; Phospholipid; Phospholipase A2; Acyltransferases; Fatty acid

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APA (6th Edition):

Panneerselvam, V. (2011). Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -. (Thesis). Bharathidasan University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4767

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):

Panneerselvam, Vijayaraj. “Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -.” 2011. Thesis, Bharathidasan University. Accessed June 16, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/4767.

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

MLA Handbook (7th Edition):

Panneerselvam, Vijayaraj. “Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -.” 2011. Web. 16 Jun 2019.

Vancouver:

Panneerselvam V. Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -. [Internet] [Thesis]. Bharathidasan University; 2011. [cited 2019 Jun 16]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4767.

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

Council of Science Editors:

Panneerselvam V. Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system; -. [Thesis]. Bharathidasan University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4767

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


Case Western Reserve University

10. Magner, William John. Analysis of the functional domains of the 1.3 S subunit of transcarboxylase.

Degree: PhD, Biochemistry, 1994, Case Western Reserve University

 Transcarboxylase is a complex, multi-subunit enzyme found in Propionibacterium shermanii which serves as a model for the family of biotin dependent carboxylases. The enzyme is… (more)

Subjects/Keywords: Chemistry, Biochemistry; Transcarboxylase; 1.3 S subunit

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APA (6th Edition):

Magner, W. J. (1994). Analysis of the functional domains of the 1.3 S subunit of transcarboxylase. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1061559282

Chicago Manual of Style (16th Edition):

Magner, William John. “Analysis of the functional domains of the 1.3 S subunit of transcarboxylase.” 1994. Doctoral Dissertation, Case Western Reserve University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1061559282.

MLA Handbook (7th Edition):

Magner, William John. “Analysis of the functional domains of the 1.3 S subunit of transcarboxylase.” 1994. Web. 16 Jun 2019.

Vancouver:

Magner WJ. Analysis of the functional domains of the 1.3 S subunit of transcarboxylase. [Internet] [Doctoral dissertation]. Case Western Reserve University; 1994. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1061559282.

Council of Science Editors:

Magner WJ. Analysis of the functional domains of the 1.3 S subunit of transcarboxylase. [Doctoral Dissertation]. Case Western Reserve University; 1994. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1061559282


Virginia Tech

11. O'Carroll, Ina Puleri. Assembly of Iron-Sulfur Clusters In Vivo.

Degree: PhD, Biochemistry, 2009, Virginia Tech

 Iron-sulfur [Fe-S] clusters are protein cofactors that facilitate various life-sustaining biological processes. Their in vivo assembly is accomplished by three different systems known to date.… (more)

Subjects/Keywords: ISC; [Fe-S] clusters; Azotobacter vinelandii

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APA (6th Edition):

O'Carroll, I. P. (2009). Assembly of Iron-Sulfur Clusters In Vivo. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/26289

Chicago Manual of Style (16th Edition):

O'Carroll, Ina Puleri. “Assembly of Iron-Sulfur Clusters In Vivo.” 2009. Doctoral Dissertation, Virginia Tech. Accessed June 16, 2019. http://hdl.handle.net/10919/26289.

MLA Handbook (7th Edition):

O'Carroll, Ina Puleri. “Assembly of Iron-Sulfur Clusters In Vivo.” 2009. Web. 16 Jun 2019.

Vancouver:

O'Carroll IP. Assembly of Iron-Sulfur Clusters In Vivo. [Internet] [Doctoral dissertation]. Virginia Tech; 2009. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10919/26289.

Council of Science Editors:

O'Carroll IP. Assembly of Iron-Sulfur Clusters In Vivo. [Doctoral Dissertation]. Virginia Tech; 2009. Available from: http://hdl.handle.net/10919/26289


University of KwaZulu-Natal

12. [No author]. A study of the role of redox potential in lysosomal function.

Degree: Biochemistry, 2013, University of KwaZulu-Natal

No abstract available. Advisors/Committee Members: Dennison, Clive (advisor).

Subjects/Keywords: Lysosomes.; Cathepsin B.; Cathepsin S.; Glucosidases.; Biochemistry.

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APA (6th Edition):

author], [. (2013). A study of the role of redox potential in lysosomal function. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/9727

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):

author], [No. “A study of the role of redox potential in lysosomal function. ” 2013. Thesis, University of KwaZulu-Natal. Accessed June 16, 2019. http://hdl.handle.net/10413/9727.

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

MLA Handbook (7th Edition):

author], [No. “A study of the role of redox potential in lysosomal function. ” 2013. Web. 16 Jun 2019.

Vancouver:

author] [. A study of the role of redox potential in lysosomal function. [Internet] [Thesis]. University of KwaZulu-Natal; 2013. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10413/9727.

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

Council of Science Editors:

author] [. A study of the role of redox potential in lysosomal function. [Thesis]. University of KwaZulu-Natal; 2013. Available from: http://hdl.handle.net/10413/9727

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


University of Pretoria

13. Williams, Marni. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria is prevalent in over 100 countries which is populated by half of the world’s population and culminates in approximately one million deaths per annum,… (more)

Subjects/Keywords: Protein-protein interactions; Polyamines; Plasmodium falciparum; Malaria; X-ray crystallography; Structure-based drug design; S-adenosylmethionine decarboxylase/ornithine de; UCTD

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APA (6th Edition):

Williams, M. (2011). Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/26237

Chicago Manual of Style (16th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Doctoral Dissertation, University of Pretoria. Accessed June 16, 2019. http://hdl.handle.net/2263/26237.

MLA Handbook (7th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Web. 16 Jun 2019.

Vancouver:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/2263/26237.

Council of Science Editors:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/26237


The Ohio State University

14. Nuth, Manunya. Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold.

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

 Of the transition metals, iron is the metal of choice for cells (with the exception of a few <i>Lactobacillus</i> species) found mainly in heme and… (more)

Subjects/Keywords: Chemistry, Biochemistry; Fe-S; iron-sulfur; IscU; IscS; NifS

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APA (6th Edition):

Nuth, M. (2004). Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1092856116

Chicago Manual of Style (16th Edition):

Nuth, Manunya. “Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold.” 2004. Doctoral Dissertation, The Ohio State University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1092856116.

MLA Handbook (7th Edition):

Nuth, Manunya. “Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold.” 2004. Web. 16 Jun 2019.

Vancouver:

Nuth M. Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold. [Internet] [Doctoral dissertation]. The Ohio State University; 2004. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1092856116.

Council of Science Editors:

Nuth M. Mechanism of Fe-S cluster biosynthesis: the [2Fe-2S] IscU as a model scaffold. [Doctoral Dissertation]. The Ohio State University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1092856116


Virginia Tech

15. Johnson, Deborah Cumaraswamy. Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii.

Degree: PhD, Biochemistry, 2006, Virginia Tech

 A system was developed for the controlled expression of genes in Azotobacter vinelandii by using genomic fusions to the sucrose catabolic regulon. This system was… (more)

Subjects/Keywords: Nif; Isc; [Fe-S] cluster biosynthesis; Azotobacter vinelandii

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APA (6th Edition):

Johnson, D. C. (2006). Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/27755

Chicago Manual of Style (16th Edition):

Johnson, Deborah Cumaraswamy. “Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii.” 2006. Doctoral Dissertation, Virginia Tech. Accessed June 16, 2019. http://hdl.handle.net/10919/27755.

MLA Handbook (7th Edition):

Johnson, Deborah Cumaraswamy. “Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii.” 2006. Web. 16 Jun 2019.

Vancouver:

Johnson DC. Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii. [Internet] [Doctoral dissertation]. Virginia Tech; 2006. [cited 2019 Jun 16]. Available from: http://hdl.handle.net/10919/27755.

Council of Science Editors:

Johnson DC. Controlled Expression and Functional Analysis of the Iron-Sulfur Cluster Biosynthetic Machinery in Azotobacter vinelandii. [Doctoral Dissertation]. Virginia Tech; 2006. Available from: http://hdl.handle.net/10919/27755


Vilnius University

16. Čiplys, Evaldas. Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells.

Degree: PhD, Biochemistry, 2011, Vilnius University

The aims of the study were to determine the reasons for unsuccessful expression of measles virus hemaglutinin (MeH) in the yeast cells and to generate… (more)

Subjects/Keywords: Measles virus hemaglutinin; Yeast S. cerevisiae and P. pastoris; Cytoplasmic unfolded protein response; Humanization of yeast; Tymų viruso hemgaliutininas; Mielės S. cerevisiae ir P. pastroris; Citoplazminis nesusivyniojusių baltymų atsakas; Mielių humanizavimas

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APA (6th Edition):

Čiplys, Evaldas. (2011). Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092012-09066 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Čiplys, Evaldas. “Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells.” 2011. Doctoral Dissertation, Vilnius University. Accessed June 16, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092012-09066 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Čiplys, Evaldas. “Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells.” 2011. Web. 16 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Čiplys, Evaldas. Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells. [Internet] [Doctoral dissertation]. Vilnius University; 2011. [cited 2019 Jun 16]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092012-09066 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Čiplys, Evaldas. Analysis of maturation of measles virus hemaglutinin in yeast S. cerevisiae and P. pastoris secretory pathway and humanization of yeast cells. [Doctoral Dissertation]. Vilnius University; 2011. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092012-09066 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Vilnius University

17. Čiplys, Evaldas. Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas.

Degree: Dissertation, Biochemistry, 2011, Vilnius University

Baigiamojo darbo tikslai – nustatyti neefektyvios žmogaus virusų glikobaltymų raiškos mielėse priežastis ir sukurti mielių kamienus su integruotais žmogaus ląstelių sekrecinio kelio genais bei ištirti… (more)

Subjects/Keywords: Tymų viruso hemgaliutininas; Mielės S. cerevisiae ir P. pastroris; Citoplazminis nesusivyniojusių baltymų atsakas; Mielių humanizavimas; Measles virus hemaglutinin; Yeast S. cerevisiae and P. pastoris; Cytoplasmic unfolded protein response; Humanization of yeast

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APA (6th Edition):

Čiplys, Evaldas. (2011). Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092023-35961 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Čiplys, Evaldas. “Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas.” 2011. Doctoral Dissertation, Vilnius University. Accessed June 16, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092023-35961 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Čiplys, Evaldas. “Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas.” 2011. Web. 16 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Čiplys, Evaldas. Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas. [Internet] [Doctoral dissertation]. Vilnius University; 2011. [cited 2019 Jun 16]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092023-35961 ;.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Čiplys, Evaldas. Tymų viruso hemagliutinino baltymo brendimo procesų mielių S. cerevisiae ir P. pastoris ląstelių sekreciniame kelyje tyrimas ir mielių humanizavimas. [Doctoral Dissertation]. Vilnius University; 2011. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20111227_092023-35961 ;

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

18. Carter-O'Connell, Ian O’Brien. Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe.

Degree: PhD, Biochemistry, 2012, Harvard University

 Inorganic phosphate is an essential nutrient required by all organisms for optimal growth. During phosphate starvation, Saccharomyces cerevisiae induces a set of genes responsible for… (more)

Subjects/Keywords: S. pombe; biochemistry; systematic biology; PHO pathway; whole genome

…66 Identification of the PHO Responsive Genes in S. pombe… …66 pho7+ and csk1+ Regulate a Core Subset of the PHO Response in S. pombe… …High-Throughput Sequencing of the S. pombe Transcriptome (RNA-Seq).......125… …128 CHAPTER 4: CONCLUSIONS REGARDING THE S. CEREVISIAE PHO85-PHO80 STRUCTURE AND THE PHO… …PATHWAY IN S. POMBE...........................................135 STRUCTURE AND FUNCTION OF THE… 

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APA (6th Edition):

Carter-O'Connell, I. O. (2012). Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9414562

Chicago Manual of Style (16th Edition):

Carter-O'Connell, Ian O’Brien. “Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe.” 2012. Doctoral Dissertation, Harvard University. Accessed June 16, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9414562.

MLA Handbook (7th Edition):

Carter-O'Connell, Ian O’Brien. “Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe.” 2012. Web. 16 Jun 2019.

Vancouver:

Carter-O'Connell IO. Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2019 Jun 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9414562.

Council of Science Editors:

Carter-O'Connell IO. Structural Analysis of the CDK-Cyclin Complex of Pho85-Pho80 and Genome-Wide Characterization of the Phosphate Starvation Response in Schizosaccharomyces pombe. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9414562


The Ohio State University

19. Tong, Grace C. Characterization of Cys-34 in serum albumin.

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

 The Cys-34 thiol of serum albumin has been suggested to be a carrier and stabilizer of nitric oxide in plasma. The pKa of the Cys-34… (more)

Subjects/Keywords: acrylamide; cooperative binding; cys-34; fatty acid binding; nitric oxide; nitrosation of cysteine; nitrosation of tryptophan; redox state of thiol; pKa of protein thiol; serum albumin; S-nitrosothiol; thiol reactivity

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APA (6th Edition):

Tong, G. C. (2003). Characterization of Cys-34 in serum albumin. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1061473878

Chicago Manual of Style (16th Edition):

Tong, Grace C. “Characterization of Cys-34 in serum albumin.” 2003. Doctoral Dissertation, The Ohio State University. Accessed June 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1061473878.

MLA Handbook (7th Edition):

Tong, Grace C. “Characterization of Cys-34 in serum albumin.” 2003. Web. 16 Jun 2019.

Vancouver:

Tong GC. Characterization of Cys-34 in serum albumin. [Internet] [Doctoral dissertation]. The Ohio State University; 2003. [cited 2019 Jun 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1061473878.

Council of Science Editors:

Tong GC. Characterization of Cys-34 in serum albumin. [Doctoral Dissertation]. The Ohio State University; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1061473878

.