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You searched for subject:(IMPDH). Showing records 1 – 10 of 10 total matches.

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Brandeis University

1. Mints, Yuliya. Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?.

Degree: 2011, Brandeis University

Retinitis pigmentosa (RP) is one of the leading causes of retinal degeneration worldwide. Many inherited forms exist, and treatment is limited due to a lack… (more)

Subjects/Keywords: transcription; IMPDH; retinitis pigmentosa; inosine monophosphate dehydrogenase

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APA (6th Edition):

Mints, Y. (2011). Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/24371

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):

Mints, Yuliya. “Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?.” 2011. Thesis, Brandeis University. Accessed April 18, 2021. http://hdl.handle.net/10192/24371.

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

MLA Handbook (7th Edition):

Mints, Yuliya. “Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?.” 2011. Web. 18 Apr 2021.

Vancouver:

Mints Y. Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?. [Internet] [Thesis]. Brandeis University; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10192/24371.

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

Council of Science Editors:

Mints Y. Inosine Monophosphate Dehydrogenase and Transcription: a mechanism for retinitis pigmentosa?. [Thesis]. Brandeis University; 2011. Available from: http://hdl.handle.net/10192/24371

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


University of Georgia

2. Bonsu, Eric Osei-Tutu. Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase.

Degree: 2014, University of Georgia

IMPDH is a key enzyme in the de novo biosynthesis of purine nucleotides. It catalyzes the conversion of inosine monophosphate (IMP) to xanthosine monophosphate (XMP)… (more)

Subjects/Keywords: IMPDH; Stille Coupling,Michael Acceptors,Antiviral

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APA (6th Edition):

Bonsu, E. O. (2014). Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/22303

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):

Bonsu, Eric Osei-Tutu. “Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase.” 2014. Thesis, University of Georgia. Accessed April 18, 2021. http://hdl.handle.net/10724/22303.

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

MLA Handbook (7th Edition):

Bonsu, Eric Osei-Tutu. “Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase.” 2014. Web. 18 Apr 2021.

Vancouver:

Bonsu EO. Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10724/22303.

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

Council of Science Editors:

Bonsu EO. Synthesis of C-2 and C-6 functionalized ribofuranosylpurine analogues as potential antiviral agents targeting inhibition of inosine monophosphate dehydrogenase. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/22303

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

3. Citterio-Quentin, Antony. Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology.

Degree: Docteur es, Pharmacologie, 2016, Lyon

Cette étude a pour objectifs 1) d'évaluer l'activité érythrocytaire de l'inosine triphosphate pyrophosphatase (ITPA) et de l'inosine monophosphate deshydrogénase (IMPDH) en lien avec le suivi… (more)

Subjects/Keywords: ITPA; IMPDH; Phénotype; Érythrocytes; Azathioprine; Métabolites thiopuriques; Gastro-entérologie; ITPA; IMPDH; Phenotype; Red blood cells; Azathioprine; Thiopurine metabolites; Gastro-enterology; 615

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APA (6th Edition):

Citterio-Quentin, A. (2016). Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSE1225

Chicago Manual of Style (16th Edition):

Citterio-Quentin, Antony. “Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology.” 2016. Doctoral Dissertation, Lyon. Accessed April 18, 2021. http://www.theses.fr/2016LYSE1225.

MLA Handbook (7th Edition):

Citterio-Quentin, Antony. “Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology.” 2016. Web. 18 Apr 2021.

Vancouver:

Citterio-Quentin A. Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2021 Apr 18]. Available from: http://www.theses.fr/2016LYSE1225.

Council of Science Editors:

Citterio-Quentin A. Étude phénotypique des enzymes du métabolisme des thiopurines (ITPA, IMPDH), lien avec les métabolites thiopuriques et optimisation thérapeutique en gastro-entérologie : Phenotypic study of enzymes involved in thiopurine metabolism (ITPA, IMPDH), relationship with thiopurine metabolites and therapeutic optimization in gastro-enterology. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSE1225


University of Southern California

4. Wang, Jian. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.

Degree: PhD, Molecular Pharmacology & Toxicology, 2009, University of Southern California

 Tacrolimus and mycophenolic acid (MPA) are commonly used in clinic to prevent rejection in transplant recipients. The influence of ABCB1 polymorphisms on tacrolimus dosing has… (more)

Subjects/Keywords: pharmacogenetics; ABCB1; IMPDH; transplantation; polymorphism

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APA (6th Edition):

Wang, J. (2009). ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458

Chicago Manual of Style (16th Edition):

Wang, Jian. “ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.” 2009. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458.

MLA Handbook (7th Edition):

Wang, Jian. “ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.” 2009. Web. 18 Apr 2021.

Vancouver:

Wang J. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458.

Council of Science Editors:

Wang J. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458

5. Zerhouni, Marwa. Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds.

Degree: Docteur es, Sciences de la vie et de la santé, 2020, Université Côte d'Azur

Le mélanome cutané métastatique et les syndromes myélodysplasiques (SMD) sont deux cancers incurables développant des résistances à leurs traitements antitumoraux de référence. Les cellules résistantes… (more)

Subjects/Keywords: Thérapie ciblée; Leucémie; Mélanome; Résistance acquise; Inhibiteur covalent; Glycolyse; PKM2; Synthèse des purines; IMPDH; Targeted therapy; Leukemia; Melanoma; Acquired resistance; Covalent inhibitor; Glycolysis; PKM2; Purine synthesis; IMPDH

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APA (6th Edition):

Zerhouni, M. (2020). Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds. (Doctoral Dissertation). Université Côte d'Azur. Retrieved from http://www.theses.fr/2020COAZ6008

Chicago Manual of Style (16th Edition):

Zerhouni, Marwa. “Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds.” 2020. Doctoral Dissertation, Université Côte d'Azur. Accessed April 18, 2021. http://www.theses.fr/2020COAZ6008.

MLA Handbook (7th Edition):

Zerhouni, Marwa. “Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds.” 2020. Web. 18 Apr 2021.

Vancouver:

Zerhouni M. Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds. [Internet] [Doctoral dissertation]. Université Côte d'Azur; 2020. [cited 2021 Apr 18]. Available from: http://www.theses.fr/2020COAZ6008.

Council of Science Editors:

Zerhouni M. Mécanismes de résistance aux thérapies ciblées dans le mélanome cutané métastatique et les syndromes myélodysplasiques : Caractérisation et validation préclinique de composés innovants : Mechanisms of resistance to targeted therapies in cutaneous metastatic melanoma and myelodysplastic syndromes : Characterization and preclinical validation of innovative compounds. [Doctoral Dissertation]. Université Côte d'Azur; 2020. Available from: http://www.theses.fr/2020COAZ6008


Freie Universität Berlin

6. Markmann, Denise. Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation.

Degree: 2015, Freie Universität Berlin

 Background Mycophenolic acid (MPA) is a part of standard immunosuppressive therapy after renal transplantation. There are only spare prospective studies investigating different dose schemes of… (more)

Subjects/Keywords: mycophenolate mofetil; therapeutic drug monitoring; IMPDH; renal transplantation; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Markmann, D. (2015). Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12687

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):

Markmann, Denise. “Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation.” 2015. Thesis, Freie Universität Berlin. Accessed April 18, 2021. https://refubium.fu-berlin.de/handle/fub188/12687.

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

MLA Handbook (7th Edition):

Markmann, Denise. “Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation.” 2015. Web. 18 Apr 2021.

Vancouver:

Markmann D. Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 18]. Available from: https://refubium.fu-berlin.de/handle/fub188/12687.

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

Council of Science Editors:

Markmann D. Investigations of pharmacokinetics and pharmacodynamics of mycophenolate mofetil in the first year after renal transplantation. [Thesis]. Freie Universität Berlin; 2015. Available from: https://refubium.fu-berlin.de/handle/fub188/12687

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

7. Dang, Yifan. IMPDH forms complexes with RNA polymerase and ribosome.

Degree: 2014, Brandeis University

 Inosine 5’-monophosphate dehydrogenase (IMPDH) is a purine biosynthetic enzyme that catalyzes oxidation of inosine monophosphate (IMP) to xanthosine monophosphate (XMP). This enzyme is a homotetramer,… (more)

Subjects/Keywords: IMPDH; RNA polymerase; ribosome; binding; complex

…Introduction Inosine 5’-monophosphate dehydrogenase (IMPDH) is an important… …x28;GMP) synthesis (Whitby et al. 1997). IMPDH oxidizes inosine 5… …a precursor of guanosine monophosphate (GMP). Therefore IMPDH controls the… …x29; IMPDH is a homotetramer, and each monomer is composed of a catalytic domain and a… …no effect on enzymatic activity of IMPDH (Pimkin and Markham 2008). CBS domain of… 

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APA (6th Edition):

Dang, Y. (2014). IMPDH forms complexes with RNA polymerase and ribosome. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/27236

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):

Dang, Yifan. “IMPDH forms complexes with RNA polymerase and ribosome.” 2014. Thesis, Brandeis University. Accessed April 18, 2021. http://hdl.handle.net/10192/27236.

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

MLA Handbook (7th Edition):

Dang, Yifan. “IMPDH forms complexes with RNA polymerase and ribosome.” 2014. Web. 18 Apr 2021.

Vancouver:

Dang Y. IMPDH forms complexes with RNA polymerase and ribosome. [Internet] [Thesis]. Brandeis University; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10192/27236.

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

Council of Science Editors:

Dang Y. IMPDH forms complexes with RNA polymerase and ribosome. [Thesis]. Brandeis University; 2014. Available from: http://hdl.handle.net/10192/27236

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


University of Oslo

8. Bremer, Sara. IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling.

Degree: 2004, University of Oslo

 Mykofenolat mofetil (MMF) (CellCept®) brukes etter transplantasjoner for å hindre avstøtning av det transplanterte organet. MMF er et prodrug som raskt omdannes til mykofenolat (MPA).… (more)

Subjects/Keywords: inosinmonofosfat dehydrogenase mRNA reverstranskriptase mykofenolat sanntids PCR LightCycler MagnaPure IMPDH; VDP::568

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APA (6th Edition):

Bremer, S. (2004). IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-11409 ; https://www.duo.uio.no/handle/10852/12073

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):

Bremer, Sara. “IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling.” 2004. Thesis, University of Oslo. Accessed April 18, 2021. http://urn.nb.no/URN:NBN:no-11409 ; https://www.duo.uio.no/handle/10852/12073.

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

MLA Handbook (7th Edition):

Bremer, Sara. “IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling.” 2004. Web. 18 Apr 2021.

Vancouver:

Bremer S. IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling. [Internet] [Thesis]. University of Oslo; 2004. [cited 2021 Apr 18]. Available from: http://urn.nb.no/URN:NBN:no-11409 ; https://www.duo.uio.no/handle/10852/12073.

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

Council of Science Editors:

Bremer S. IMPDH type I og II ekspresjon i blodceller: Utvikling, validering og etablering av relativ kvantitativ RT-PCR analyse : Ekspresjonsendringer hos nyretransplanterte under mykofenolatbehandling. [Thesis]. University of Oslo; 2004. Available from: http://urn.nb.no/URN:NBN:no-11409 ; https://www.duo.uio.no/handle/10852/12073

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


University of Oslo

9. Rasmussen, Ingrid. Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling.

Degree: 2005, University of Oslo

 Mykofenolatmofetil (MMF) benyttes i kombinasjon med andre immunsuppressive legemidler for å hindre avstøtningsreaksjon etter organtransplantasjon. MMF er et prodrug som etter peroralt inntak metaboliseres presystemisk… (more)

Subjects/Keywords: mykofenolat immunsuppresjon transplantasjon genuttrykk inosin monofosfat dehydrogenase IMPDH; VDP::568

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APA (6th Edition):

Rasmussen, I. (2005). Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-11385 ; https://www.duo.uio.no/handle/10852/12093 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12093/1/HOVEDFAG_IR.pdf

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):

Rasmussen, Ingrid. “Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling.” 2005. Thesis, University of Oslo. Accessed April 18, 2021. http://urn.nb.no/URN:NBN:no-11385 ; https://www.duo.uio.no/handle/10852/12093 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12093/1/HOVEDFAG_IR.pdf.

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

MLA Handbook (7th Edition):

Rasmussen, Ingrid. “Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling.” 2005. Web. 18 Apr 2021.

Vancouver:

Rasmussen I. Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling. [Internet] [Thesis]. University of Oslo; 2005. [cited 2021 Apr 18]. Available from: http://urn.nb.no/URN:NBN:no-11385 ; https://www.duo.uio.no/handle/10852/12093 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12093/1/HOVEDFAG_IR.pdf.

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

Council of Science Editors:

Rasmussen I. Ekspresjon av IMPDH type I og II i retikulocytter hos nyretransplanterte under mykofenolatbehandling. [Thesis]. University of Oslo; 2005. Available from: http://urn.nb.no/URN:NBN:no-11385 ; https://www.duo.uio.no/handle/10852/12093 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12093/1/HOVEDFAG_IR.pdf

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


University of Queensland

10. Bajaj, Megha. Development of novel anti-infective drugs targeting microbial proteins.

Degree: Institute for Molecular Bioscience, 2015, University of Queensland

Subjects/Keywords: Virulence factor; Substrate-binding protein; PsaA; Conformational flexibility; Fragment based drug discovery; Purine metabolic pathway; IMPDH; 0304 Medicinal and Biomolecular Chemistry; 0307 Theoretical and Computational Chemistry

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APA (6th Edition):

Bajaj, M. (2015). Development of novel anti-infective drugs targeting microbial proteins. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:375524

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):

Bajaj, Megha. “Development of novel anti-infective drugs targeting microbial proteins.” 2015. Thesis, University of Queensland. Accessed April 18, 2021. http://espace.library.uq.edu.au/view/UQ:375524.

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

MLA Handbook (7th Edition):

Bajaj, Megha. “Development of novel anti-infective drugs targeting microbial proteins.” 2015. Web. 18 Apr 2021.

Vancouver:

Bajaj M. Development of novel anti-infective drugs targeting microbial proteins. [Internet] [Thesis]. University of Queensland; 2015. [cited 2021 Apr 18]. Available from: http://espace.library.uq.edu.au/view/UQ:375524.

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

Council of Science Editors:

Bajaj M. Development of novel anti-infective drugs targeting microbial proteins. [Thesis]. University of Queensland; 2015. Available from: http://espace.library.uq.edu.au/view/UQ:375524

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

.