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You searched for subject:( azole). Showing records 1 – 28 of 28 total matches.

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Texas Tech University

1. -1795-3767. Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications.

Degree: PhD, Chemistry, 2016, Texas Tech University

 In this study we investigate the amoebacidal activity of 10 steroidal inhibitors which block sterol C24-methylation, and compare its efficacy to 5 medical azoles which… (more)

Subjects/Keywords: Acanthamoeba; sterol; azole; ergosterol; keratitis; encephalitis

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APA (6th Edition):

-1795-3767. (2016). Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72340

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

Chicago Manual of Style (16th Edition):

-1795-3767. “Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications.” 2016. Doctoral Dissertation, Texas Tech University. Accessed February 17, 2020. http://hdl.handle.net/2346/72340.

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

MLA Handbook (7th Edition):

-1795-3767. “Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications.” 2016. Web. 17 Feb 2020.

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

Vancouver:

-1795-3767. Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/2346/72340.

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

Council of Science Editors:

-1795-3767. Mechanism-based inhibition of ergosterol biosynthesis in Acanthamoeba castellanii and its therapeutic implications. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72340

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


University of Sydney

2. Talbot, Jessica Jane. Common and cryptic Aspergillus species – one health pathogens .

Degree: 2018, University of Sydney

 Fungal Aspergillus species cause invasive and chronic disease in humans and other animals. This thesis investigated cryptic and common Aspergillus species in A. section Fumigati;… (more)

Subjects/Keywords: Aspergillus; aspergillosis; Aspergillus frankstonensis; azole resistance

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APA (6th Edition):

Talbot, J. J. (2018). Common and cryptic Aspergillus species – one health pathogens . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19930

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):

Talbot, Jessica Jane. “Common and cryptic Aspergillus species – one health pathogens .” 2018. Thesis, University of Sydney. Accessed February 17, 2020. http://hdl.handle.net/2123/19930.

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

MLA Handbook (7th Edition):

Talbot, Jessica Jane. “Common and cryptic Aspergillus species – one health pathogens .” 2018. Web. 17 Feb 2020.

Vancouver:

Talbot JJ. Common and cryptic Aspergillus species – one health pathogens . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/2123/19930.

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

Council of Science Editors:

Talbot JJ. Common and cryptic Aspergillus species – one health pathogens . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19930

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

3. Caudle, Kelly E. Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata.

Degree: PhD, Pharmaceutical Sciences, 2010, University of Tennessee Health Science Center

Azole antifungal resistance has emerged as a significant problem in the management of infections caused by fungi including Candida species. In recent years, Candida… (more)

Subjects/Keywords: azole resistance; azole tolerance; Candida glabrata; fluconazole; pdr1; Bacterial Infections and Mycoses; Fungi; Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Caudle, K. E. (2010). Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/39

Chicago Manual of Style (16th Edition):

Caudle, Kelly E. “Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata.” 2010. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/39.

MLA Handbook (7th Edition):

Caudle, Kelly E. “Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata.” 2010. Web. 17 Feb 2020.

Vancouver:

Caudle KE. Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2010. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/39.

Council of Science Editors:

Caudle KE. Transcriptional Regulation of Azole Antifungal Resistance and Tolerance in Candida Glabrata. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2010. Available from: https://dc.uthsc.edu/dissertations/39

4. Goel, Ruchi. Synthesis and biological stydy of some new a_amidoalkylated azole and azine;.

Degree: Chemistry, 2010, Chaudhary Charan Singh University

None newline

Summary p. 1-6

Advisors/Committee Members: Sharma, P K.

Subjects/Keywords: Biological Study; Amidoalkylated Azole; Azine

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APA (6th Edition):

Goel, R. (2010). Synthesis and biological stydy of some new a_amidoalkylated azole and azine;. (Thesis). Chaudhary Charan Singh University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/34139

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):

Goel, Ruchi. “Synthesis and biological stydy of some new a_amidoalkylated azole and azine;.” 2010. Thesis, Chaudhary Charan Singh University. Accessed February 17, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/34139.

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

MLA Handbook (7th Edition):

Goel, Ruchi. “Synthesis and biological stydy of some new a_amidoalkylated azole and azine;.” 2010. Web. 17 Feb 2020.

Vancouver:

Goel R. Synthesis and biological stydy of some new a_amidoalkylated azole and azine;. [Internet] [Thesis]. Chaudhary Charan Singh University; 2010. [cited 2020 Feb 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34139.

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

Council of Science Editors:

Goel R. Synthesis and biological stydy of some new a_amidoalkylated azole and azine;. [Thesis]. Chaudhary Charan Singh University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/34139

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


University of Manchester

5. Fernandez, Christine. CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS.

Degree: 2011, University of Manchester

 Tuberculosis (TB) affects nearly a third of the world’s population and has been termed a ‘Global Emergency’ by the WHO. The emergence of multi/extensively drug… (more)

Subjects/Keywords: Mycobacterium tuberculosis; azole drugs; CYP51; sterol demethylase; antifungals

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APA (6th Edition):

Fernandez, C. (2011). CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:132661

Chicago Manual of Style (16th Edition):

Fernandez, Christine. “CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS.” 2011. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:132661.

MLA Handbook (7th Edition):

Fernandez, Christine. “CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS.” 2011. Web. 17 Feb 2020.

Vancouver:

Fernandez C. CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Feb 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:132661.

Council of Science Editors:

Fernandez C. CHARACTERISATION OF CYTOCHROME P450 AZOLE DRUG-RESISTANT STEROL DEMETHYLASE CYP51B1 AND EXPRESSION OF CYP123 AND CYP136 FROM MYCOBACTERIUM TUBERCULOSIS. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:132661


University of Edinburgh

6. Stephen, Jennifer Lea. Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids.

Degree: PhD, 2015, University of Edinburgh

 Some interesting, biologically active natural products have been found to contain poly-azole fragments within their core. These fragments are linked through the 2- position of… (more)

Subjects/Keywords: 547; decarboxylation; palladium; cross-coupling; azole; CH activation

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APA (6th Edition):

Stephen, J. L. (2015). Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/18011

Chicago Manual of Style (16th Edition):

Stephen, Jennifer Lea. “Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed February 17, 2020. http://hdl.handle.net/1842/18011.

MLA Handbook (7th Edition):

Stephen, Jennifer Lea. “Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids.” 2015. Web. 17 Feb 2020.

Vancouver:

Stephen JL. Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1842/18011.

Council of Science Editors:

Stephen JL. Studies towards the decarboxylative cross-coupling of azole-4-carboxylic acids. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/18011


University of Manchester

7. Fernandez, Christine Cheryl. Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis.

Degree: PhD, 2011, University of Manchester

 Tuberculosis (TB) affects nearly a third of the world's population and has been termed a 'Global Emergency' by the WHO. The emergence of multi/extensively drug… (more)

Subjects/Keywords: 616.99; antifungals; sterol demethylase; CYP51; Mycobacterium tuberculosis; azole drugs

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APA (6th Edition):

Fernandez, C. C. (2011). Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-cytochrome-p450-azole-drugresistant-sterol-demethylase-cyp51b1-and-expression-of-cyp123-and-cyp136-from-mycobacterium-tuberculosis(dfc1e25e-2e14-43c1-b478-8cc820cdacd2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606870

Chicago Manual of Style (16th Edition):

Fernandez, Christine Cheryl. “Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis.” 2011. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-cytochrome-p450-azole-drugresistant-sterol-demethylase-cyp51b1-and-expression-of-cyp123-and-cyp136-from-mycobacterium-tuberculosis(dfc1e25e-2e14-43c1-b478-8cc820cdacd2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606870.

MLA Handbook (7th Edition):

Fernandez, Christine Cheryl. “Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis.” 2011. Web. 17 Feb 2020.

Vancouver:

Fernandez CC. Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Feb 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-cytochrome-p450-azole-drugresistant-sterol-demethylase-cyp51b1-and-expression-of-cyp123-and-cyp136-from-mycobacterium-tuberculosis(dfc1e25e-2e14-43c1-b478-8cc820cdacd2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606870.

Council of Science Editors:

Fernandez CC. Characterisation of cytochrome P450 azole drug-resistant sterol demethylase CYP51B1 and expression of CYP123 and CYP136 from Mycobacterium tuberculosis. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/characterisation-of-cytochrome-p450-azole-drugresistant-sterol-demethylase-cyp51b1-and-expression-of-cyp123-and-cyp136-from-mycobacterium-tuberculosis(dfc1e25e-2e14-43c1-b478-8cc820cdacd2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.606870


Queens University

8. Hum, Maaike. Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression .

Degree: Pharmacology and Toxicology, 2014, Queens University

 Heme oxygenase (HO) is the enzyme that breaks down heme to form carbon monoxide, free iron, and biliverdin. The two major isoforms, HO-1 (inducible) and… (more)

Subjects/Keywords: azole-based inhibitors; AC2M2 breast cancer; Heme Oxygenase

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APA (6th Edition):

Hum, M. (2014). Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12565

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):

Hum, Maaike. “Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression .” 2014. Thesis, Queens University. Accessed February 17, 2020. http://hdl.handle.net/1974/12565.

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

MLA Handbook (7th Edition):

Hum, Maaike. “Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression .” 2014. Web. 17 Feb 2020.

Vancouver:

Hum M. Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression . [Internet] [Thesis]. Queens University; 2014. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1974/12565.

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

Council of Science Editors:

Hum M. Heme Oxygenase Modulates AC2M2 Mouse Breast Cancer Growth and Progression . [Thesis]. Queens University; 2014. Available from: http://hdl.handle.net/1974/12565

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


Université Paris-Sud – Paris XI

9. El Hammi, Emna. Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics.

Degree: Docteur es, Chimie, 2011, Université Paris-Sud – Paris XI

Les flavohémoglobines (FlavoHbs) sont des protéines fixant l’oxygène qui possèdent un domaine globine N-terminal lié de manière covalente à un domaine C-terminal réductase contenant une… (more)

Subjects/Keywords: Flavohémoglobine; Heme; Fad; Azole; NO dioxygénase; Cristallographie; Fhp; Hmp; Yhb; Shb; Lipide; Flavohemoglobin; Heme; Fad; Azole; NO dioxygenase; Crystallography; Fhp; Hmp; Yhb; Shb; Lipid

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APA (6th Edition):

El Hammi, E. (2011). Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112051

Chicago Manual of Style (16th Edition):

El Hammi, Emna. “Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed February 17, 2020. http://www.theses.fr/2011PA112051.

MLA Handbook (7th Edition):

El Hammi, Emna. “Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics.” 2011. Web. 17 Feb 2020.

Vancouver:

El Hammi E. Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Feb 17]. Available from: http://www.theses.fr/2011PA112051.

Council of Science Editors:

El Hammi E. Les flavohemoglobines comme cibles potentielles des antibiotiques : Flavohemoglobins as potential targets of antibiotics. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112051

10. Nishimoto, Andrew T. An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Tennessee Health Science Center

  "Candida albicans is a commensal organism commonly colonizing the human gut and skin. As an opportunistic pathogen, it can cause persistent and serious infections… (more)

Subjects/Keywords: Azole; Candida albicans; ERG11; ERG3; MRR2; Resistance; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

Nishimoto, A. T. (2019). An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/493

Chicago Manual of Style (16th Edition):

Nishimoto, Andrew T. “An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans.” 2019. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/493.

MLA Handbook (7th Edition):

Nishimoto, Andrew T. “An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans.” 2019. Web. 17 Feb 2020.

Vancouver:

Nishimoto AT. An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2019. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/493.

Council of Science Editors:

Nishimoto AT. An Investigation into Clinically Relevant Determinants of Azole Resistance in Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2019. Available from: https://dc.uthsc.edu/dissertations/493


University of Alabama

11. Drab, David Martin. A versatile design platform for multi-heterocyclic ionic liquid synthesis.

Degree: 2011, University of Alabama

 Ionic liquids (ILs, briefly defined as salts exhibiting melting points below 100 degrees centrigrade) have been extensively researched in the past few decades, where properties… (more)

Subjects/Keywords: Electronic Thesis or Dissertation;  – thesis; Organic Chemistry; Inorganic Chemistry; Azole; Click Chemistry; Cyanoalkyl; Energetic Materials; Heterocycle; Ionic Liquid

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APA (6th Edition):

Drab, D. M. (2011). A versatile design platform for multi-heterocyclic ionic liquid synthesis. (Thesis). University of Alabama. Retrieved from http://purl.lib.ua.edu/34990

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):

Drab, David Martin. “A versatile design platform for multi-heterocyclic ionic liquid synthesis.” 2011. Thesis, University of Alabama. Accessed February 17, 2020. http://purl.lib.ua.edu/34990.

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

MLA Handbook (7th Edition):

Drab, David Martin. “A versatile design platform for multi-heterocyclic ionic liquid synthesis.” 2011. Web. 17 Feb 2020.

Vancouver:

Drab DM. A versatile design platform for multi-heterocyclic ionic liquid synthesis. [Internet] [Thesis]. University of Alabama; 2011. [cited 2020 Feb 17]. Available from: http://purl.lib.ua.edu/34990.

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

Council of Science Editors:

Drab DM. A versatile design platform for multi-heterocyclic ionic liquid synthesis. [Thesis]. University of Alabama; 2011. Available from: http://purl.lib.ua.edu/34990

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

12. CASTILLO CASTAÑEDA, ADRIANA CATHERINE. Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo .

Degree: 2015, Universidad de los Andes

 Fusarium spp. son hongos patógenos de humanos y plantas. Fusarium oxysporum y Fusarium solani son especies importantes aisladas de infecciones como onicomicosis, queratitis, infecciones invasivas… (more)

Subjects/Keywords: Antifungal resistance; azole; polyene; Fusarium spp.; RNA-seq; transcriptomic

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APA (6th Edition):

CASTILLO CASTAÑEDA, A. C. (2015). Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo . (Thesis). Universidad de los Andes. Retrieved from https://documentodegrado.uniandes.edu.co/documentos/8416.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):

CASTILLO CASTAÑEDA, ADRIANA CATHERINE. “Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo .” 2015. Thesis, Universidad de los Andes. Accessed February 17, 2020. https://documentodegrado.uniandes.edu.co/documentos/8416.pdf.

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

MLA Handbook (7th Edition):

CASTILLO CASTAÑEDA, ADRIANA CATHERINE. “Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo .” 2015. Web. 17 Feb 2020.

Vancouver:

CASTILLO CASTAÑEDA AC. Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo . [Internet] [Thesis]. Universidad de los Andes; 2015. [cited 2020 Feb 17]. Available from: https://documentodegrado.uniandes.edu.co/documentos/8416.pdf.

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

Council of Science Editors:

CASTILLO CASTAÑEDA AC. Transcriptomic analyses of Fusarium oxysporum and Fusarium solani challenged with antifungal compounds both in vitro and in vivo . [Thesis]. Universidad de los Andes; 2015. Available from: https://documentodegrado.uniandes.edu.co/documentos/8416.pdf

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

13. Vasicek, Erin M. Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans.

Degree: PhD, Biomedical Sciences, 2013, University of Tennessee Health Science Center

  Candida albicans is the most prevalent human fungal pathogen, found as a commensal organism in the mucosa, gastrointestinal, and urogenital tracts of humans. This… (more)

Subjects/Keywords: Antifungal; azole; Candida albicans; Rrsistance; transcriptional regulation; Bacterial Infections and Mycoses; Diseases; Fungi; Medicine and Health Sciences; Organisms

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APA (6th Edition):

Vasicek, E. M. (2013). Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/288

Chicago Manual of Style (16th Edition):

Vasicek, Erin M. “Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans.” 2013. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/288.

MLA Handbook (7th Edition):

Vasicek, Erin M. “Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans.” 2013. Web. 17 Feb 2020.

Vancouver:

Vasicek EM. Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2013. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/288.

Council of Science Editors:

Vasicek EM. Signal Transduction and Transcriptional Regulation Pathways Essential for Azole Resistance in Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2013. Available from: https://dc.uthsc.edu/dissertations/288


University of South Florida

14. Holloway, Mary Jolene Patricia. Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans.

Degree: 2011, University of South Florida

 The opportunistic fungus Candida albicans is a commensal member of the human microflora and is the most common causative agent of fungal-related disease with particular… (more)

Subjects/Keywords: azole resistance; Candida albicans; cytochrome b5 reductase; ergosterol biosynthesis; American Studies; Arts and Humanities; Biochemistry; Microbiology; Molecular Biology

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APA (6th Edition):

Holloway, M. J. P. (2011). Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/3730

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):

Holloway, Mary Jolene Patricia. “Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans.” 2011. Thesis, University of South Florida. Accessed February 17, 2020. https://scholarcommons.usf.edu/etd/3730.

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

MLA Handbook (7th Edition):

Holloway, Mary Jolene Patricia. “Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans.” 2011. Web. 17 Feb 2020.

Vancouver:

Holloway MJP. Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans. [Internet] [Thesis]. University of South Florida; 2011. [cited 2020 Feb 17]. Available from: https://scholarcommons.usf.edu/etd/3730.

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

Council of Science Editors:

Holloway MJP. Biochemical and Pharmacological Characterization of Cytochrome b5 Reductase as a Potential Novel Therapeutic Target in Candida albicans. [Thesis]. University of South Florida; 2011. Available from: https://scholarcommons.usf.edu/etd/3730

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

15. Riedrich, Matthias. Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse.

Degree: 2009, Technische Universität Dortmund

Subjects/Keywords: Aza-Wittig-Reaktion; Azole; Naturstoffe; Nosiheptid; Thiopeptidantibiotika; Totalsynthese; Zyklisierungen; 570

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APA (6th Edition):

Riedrich, M. (2009). Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/26074

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):

Riedrich, Matthias. “Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse.” 2009. Thesis, Technische Universität Dortmund. Accessed February 17, 2020. http://hdl.handle.net/2003/26074.

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

MLA Handbook (7th Edition):

Riedrich, Matthias. “Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse.” 2009. Web. 17 Feb 2020.

Vancouver:

Riedrich M. Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse. [Internet] [Thesis]. Technische Universität Dortmund; 2009. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/2003/26074.

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

Council of Science Editors:

Riedrich M. Aufbau von 5-Ring-Heterozyklen durch Aza-Witting-Ringschlüsse. [Thesis]. Technische Universität Dortmund; 2009. Available from: http://hdl.handle.net/2003/26074

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


University of Manchester

16. Bueid, Ahmed. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.

Degree: PhD, 2012, University of Manchester

 Although A. fumigatus strains are generally susceptible to azoles, recently, acquired resistance to a number of antifungal compounds has been reported, especially to triazoles possibly… (more)

Subjects/Keywords: 579.5; Aspergillus fumigatus, antifungal drug resistance, mechanisms of azole resistance, Cyp51A mutation, gene expression; the ITS, ß-tubulin, actin and calmodulin gene

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APA (6th Edition):

Bueid, A. (2012). Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/laboratory-epidemiology-and-mechanisms-of-azole-resistance-in-aspergillus-fumigatus(cfaa6ee2-36d5-473c-9531-816d9578ff17).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555566

Chicago Manual of Style (16th Edition):

Bueid, Ahmed. “Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.” 2012. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. https://www.research.manchester.ac.uk/portal/en/theses/laboratory-epidemiology-and-mechanisms-of-azole-resistance-in-aspergillus-fumigatus(cfaa6ee2-36d5-473c-9531-816d9578ff17).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555566.

MLA Handbook (7th Edition):

Bueid, Ahmed. “Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.” 2012. Web. 17 Feb 2020.

Vancouver:

Bueid A. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Feb 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/laboratory-epidemiology-and-mechanisms-of-azole-resistance-in-aspergillus-fumigatus(cfaa6ee2-36d5-473c-9531-816d9578ff17).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555566.

Council of Science Editors:

Bueid A. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/laboratory-epidemiology-and-mechanisms-of-azole-resistance-in-aspergillus-fumigatus(cfaa6ee2-36d5-473c-9531-816d9578ff17).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555566

17. Siopi, Maria. Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model.

Degree: 2018, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 The emergence of azole resistance raises concerns about first-line voriconazole treatment in high-risk patients with suspected invasive aspergillosis. Alternative therapeutic options are limited. A treatment… (more)

Subjects/Keywords: Αζολο-ανθεκτική ασπεργίλλωση; Βορικοναζόλη; Συνδυαστική θεραπεία; In vitro φαρμακοκινητικό/φαρμακοδυναμικό μοντέλο; Azole-resistant aspergillosis; Voriconazole; Combination therapy; In vitro pharmacokinetic/pharmacodynamic model

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APA (6th Edition):

Siopi, M. (2018). Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/43538

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):

Siopi, Maria. “Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model.” 2018. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed February 17, 2020. http://hdl.handle.net/10442/hedi/43538.

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

MLA Handbook (7th Edition):

Siopi, Maria. “Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model.” 2018. Web. 17 Feb 2020.

Vancouver:

Siopi M. Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10442/hedi/43538.

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

Council of Science Editors:

Siopi M. Optimizing antifungal therapy against azole-resistant Aspergillus fumigatus isolates using an in vitro pharmacokinetic/pharmacodynamic simulation model. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. Available from: http://hdl.handle.net/10442/hedi/43538

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


University of Manchester

18. Chishimba, Livingstone. Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis.

Degree: 2016, University of Manchester

 Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis, a Thesis submitted toThe University of Manchester for the Degree of… (more)

Subjects/Keywords: Severe asthma; Severe asthma with fungal sensitisation; Immunopathonegesis; Airway inflammation; Asthma phenotyping; Interleukin 17 (IL-17); Bonchoalveolar lavage (BAL); Azole antifungals; ABPA; Fungal asthma; IgE; Nebulised Amphotericin B; ImmunoCAP; Microbiome

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

APA (6th Edition):

Chishimba, L. (2016). Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298758

Chicago Manual of Style (16th Edition):

Chishimba, Livingstone. “Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis.” 2016. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298758.

MLA Handbook (7th Edition):

Chishimba, Livingstone. “Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis.” 2016. Web. 17 Feb 2020.

Vancouver:

Chishimba L. Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Feb 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298758.

Council of Science Editors:

Chishimba L. Immunopathogenesis and antifungal therapy for Severe Asthma with Fungal Sensitization and Allergic Bronchopulmonary Aspergillosis. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:298758


University of Manchester

19. Chishimba, Livingstone. Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis.

Degree: PhD, 2016, University of Manchester

 Introduction: The pathogenesis and treatment of allergic bronchopulmonary aspergillosis (ABPA), severe asthma-non fungal sensitised (SANFS) and severe asthma with fungal sensitization (SAFS) is poorly understood.… (more)

Subjects/Keywords: Microbiome; ImmunoCAP; Nebulised Amphotericin B; IgE; Fungal asthma; ABPA; Azole antifungals; Interleukin 17 (IL-17); Asthma phenotyping; Airway inflammation; Immunopathonegesis; Severe asthma with fungal sensitisation; Severe asthma; Bonchoalveolar lavage (BAL)

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

APA (6th Edition):

Chishimba, L. (2016). Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/immunopathogenesis-and-antifungal-therapy-for-severe-asthma-with-fungal-sensitization-and-allergic-bronchopulmonary-aspergillosis(1c5a49f2-2830-4567-9e5b-5ec5691b170c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764481

Chicago Manual of Style (16th Edition):

Chishimba, Livingstone. “Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis.” 2016. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. https://www.research.manchester.ac.uk/portal/en/theses/immunopathogenesis-and-antifungal-therapy-for-severe-asthma-with-fungal-sensitization-and-allergic-bronchopulmonary-aspergillosis(1c5a49f2-2830-4567-9e5b-5ec5691b170c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764481.

MLA Handbook (7th Edition):

Chishimba, Livingstone. “Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis.” 2016. Web. 17 Feb 2020.

Vancouver:

Chishimba L. Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Feb 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/immunopathogenesis-and-antifungal-therapy-for-severe-asthma-with-fungal-sensitization-and-allergic-bronchopulmonary-aspergillosis(1c5a49f2-2830-4567-9e5b-5ec5691b170c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764481.

Council of Science Editors:

Chishimba L. Immunopathogenesis and antifungal therapy for severe asthma with fungal sensitization and allergic bronchopulmonary aspergillosis. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/immunopathogenesis-and-antifungal-therapy-for-severe-asthma-with-fungal-sensitization-and-allergic-bronchopulmonary-aspergillosis(1c5a49f2-2830-4567-9e5b-5ec5691b170c).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764481


University of Gothenburg / Göteborgs Universitet

20. Hegelund Myrbäck, Tove 1971-. Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution.

Degree: 2003, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: cytochrome P450; CYP3A; tissue specific expression; inhibition; induction; azole fungicides; gene evolution; fish

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APA (6th Edition):

Hegelund Myrbäck, T. 1. (2003). Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/15915

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):

Hegelund Myrbäck, Tove 1971-. “Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution.” 2003. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed February 17, 2020. http://hdl.handle.net/2077/15915.

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

MLA Handbook (7th Edition):

Hegelund Myrbäck, Tove 1971-. “Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution.” 2003. Web. 17 Feb 2020.

Vancouver:

Hegelund Myrbäck T1. Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2003. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/2077/15915.

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

Council of Science Editors:

Hegelund Myrbäck T1. Characterization of CYP3A in fish - expression, inhibition, induction and analyses of gene evolution. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2003. Available from: http://hdl.handle.net/2077/15915

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

21. Flowers, Stephanie Ann. ERG11-Mediated Azole Resistance in Candida albicans.

Degree: PhD, Biomedical Sciences, 2013, University of Tennessee Health Science Center

  Although many medically important Candida species are commensal to the gut or colonizers of the skin, these organisms have the propensity to cause disease… (more)

Subjects/Keywords: albicans; azole; Candida; fluconazole; resistance; Bacterial Infections and Mycoses; Chemicals and Drugs; Diseases; Fungi; Medical Immunology; Medical Sciences; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Organisms; Pharmaceutical Preparations; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Flowers, S. A. (2013). ERG11-Mediated Azole Resistance in Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/335

Chicago Manual of Style (16th Edition):

Flowers, Stephanie Ann. “ERG11-Mediated Azole Resistance in Candida albicans.” 2013. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/335.

MLA Handbook (7th Edition):

Flowers, Stephanie Ann. “ERG11-Mediated Azole Resistance in Candida albicans.” 2013. Web. 17 Feb 2020.

Vancouver:

Flowers SA. ERG11-Mediated Azole Resistance in Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2013. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/335.

Council of Science Editors:

Flowers SA. ERG11-Mediated Azole Resistance in Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2013. Available from: https://dc.uthsc.edu/dissertations/335

22. Whaley, Sarah Garland. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.

Degree: PhD, Pharmaceutical Sciences, 2018, University of Tennessee Health Science Center

  Despite the scientific and medical communities’ best efforts, the incidence of fungal infections in susceptible populations continues to rise. The most common cause of… (more)

Subjects/Keywords: antifungal; azole resistance; Candida; Candida albicans; Candida glabrata; fluconazole; Bacterial Infections and Mycoses; Diseases; Medical Biochemistry; Medical Sciences; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Whaley, S. G. (2018). Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/453

Chicago Manual of Style (16th Edition):

Whaley, Sarah Garland. “Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.” 2018. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/453.

MLA Handbook (7th Edition):

Whaley, Sarah Garland. “Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.” 2018. Web. 17 Feb 2020.

Vancouver:

Whaley SG. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2018. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/453.

Council of Science Editors:

Whaley SG. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2018. Available from: https://dc.uthsc.edu/dissertations/453

23. Μπιστόλα, Ουρανία. Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες.

Degree: 2015, University of Patras

Η παρούσα Διπλωματική Εργασία επικεντρώνεται σε προσπάθειες σύνθεσης και χαρακτηρισμού νέων συμπλόκων ενώσεων του In(III) με τη χρήση 2-πυρίδυλο οξιμών, αζολίων, 2-ακετυλοπυριδίνης υδραζόνης, δι-2-πυρίδυλο κετόνης… (more)

Subjects/Keywords: Αζόλια ως υποκαταστάτες; Βάσεις schiff ως υποκαταστάτες; Δι-2-πυρίδιλο κετόνη ως υποκαταστάτης; Κρυσταλλογραφία ακτίνων Χ μονοκρυστάλλου; 2-πυρίδυλο οξίμες ως υποκαταστάτες; Ραδιοφάρμακα; Σύμπλοκα ινδίου(ΙΙΙ); Φασματοσκοπικές τεχνικές; 546.677; Azole ligands; Di-2-pyridyl ketone ligand; Indium(ΙΙΙ) complexes; 2-pyridyl oximes ligands; Radiopharmaceuticals; Schiff bases as ligands; Single-crystal X- ray cystallography; Spectroscopic techniques

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APA (6th Edition):

Μπιστόλα, . (2015). Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8797

Chicago Manual of Style (16th Edition):

Μπιστόλα, Ουρανία. “Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες.” 2015. Masters Thesis, University of Patras. Accessed February 17, 2020. http://hdl.handle.net/10889/8797.

MLA Handbook (7th Edition):

Μπιστόλα, Ουρανία. “Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες.” 2015. Web. 17 Feb 2020.

Vancouver:

Μπιστόλα . Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες. [Internet] [Masters thesis]. University of Patras; 2015. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10889/8797.

Council of Science Editors:

Μπιστόλα . Σύνθεση και χαρακτηρισμός συμπλόκων ενώσεων του Ιn(III) με υποκαταστάτες 2- πυρίδυλο οξίμες, αζόλια, δι-2-πυρίδυλο κετόνη, 2-ακετυλοπυριδίνη υδραζόνη και βάσεις Schiff για χρήση τους ως ραδιοφάρμακα και ιχνηθέτες. [Masters Thesis]. University of Patras; 2015. Available from: http://hdl.handle.net/10889/8797

24. Liu, Teresa T. Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans.

Degree: PhD, Interdisciplinary Program, 2008, University of Tennessee Health Science Center

  Candida albicans is a pathogenic fungi found in the mucosa, gastrointestinal, and urogenital tracts of humans. Oropharyngeal candidiasis (OPC), an opportunistic mucosal infection caused… (more)

Subjects/Keywords: azole resistance; CDR1; CDR2; TAC1; MDR1; MRR1; ERG11; UPC2; transcription factor; Bacterial Infections and Mycoses; Chemicals and Drugs; Diseases; Fungi; Medicine and Health Sciences; Organisms; Pharmaceutical Preparations

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

APA (6th Edition):

Liu, T. T. (2008). Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/156

Chicago Manual of Style (16th Edition):

Liu, Teresa T. “Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans.” 2008. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed February 17, 2020. https://dc.uthsc.edu/dissertations/156.

MLA Handbook (7th Edition):

Liu, Teresa T. “Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans.” 2008. Web. 17 Feb 2020.

Vancouver:

Liu TT. Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2008. [cited 2020 Feb 17]. Available from: https://dc.uthsc.edu/dissertations/156.

Council of Science Editors:

Liu TT. Transcriptional Regulation of Azole Antifungal Resistance in Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2008. Available from: https://dc.uthsc.edu/dissertations/156


University of Waikato

25. Stahlhut, Dirk. Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance .

Degree: 2008, University of Waikato

 Leaky buildings are those that show elevated moisture contents of the framing timber, which can subsequently lead to the establishment of fungal and bacterial decay.… (more)

Subjects/Keywords: Leaky Buildings; Pinus radiata; PCR-polymerase chain reaction; colony forming units; aerial spores; brown rot; Oligoporus placenta; Gloeophyllum sp.; Antrodia sinuosa; Copper azole; boron; IPBC; Tebuconazole/Propiconazole; decay micromorphology

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

APA (6th Edition):

Stahlhut, D. (2008). Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance . (Doctoral Dissertation). University of Waikato. Retrieved from http://hdl.handle.net/10289/2637

Chicago Manual of Style (16th Edition):

Stahlhut, Dirk. “Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance .” 2008. Doctoral Dissertation, University of Waikato. Accessed February 17, 2020. http://hdl.handle.net/10289/2637.

MLA Handbook (7th Edition):

Stahlhut, Dirk. “Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance .” 2008. Web. 17 Feb 2020.

Vancouver:

Stahlhut D. Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance . [Internet] [Doctoral dissertation]. University of Waikato; 2008. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10289/2637.

Council of Science Editors:

Stahlhut D. Decay Fungi from New Zealand Leaky Buildings: Isolation, Identification and Preservative Resistance . [Doctoral Dissertation]. University of Waikato; 2008. Available from: http://hdl.handle.net/10289/2637

26. Bueid, Ahmed. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.

Degree: 2012, University of Manchester

 Although A. fumigatus strains are generally susceptible to azoles, recently, acquired resistance to a number of antifungal compounds has been reported, especially to triazoles possibly… (more)

Subjects/Keywords: Aspergillus fumigatus, antifungal drug resistance, mechanisms of azole resistance, Cyp51A mutation, gene expression; the ITS, β-tubulin, actin and calmodulin gene

…1.3 Mapping of substitutions in AF-CYP51A that cause azole resistance..... 65 1.4… …3.1 Azole resistance frequency in A. fumigatus by patient 1997 – 2009........ 119 3.2… …2.9 3.1 45 3.2 MIC values for azole resistant A. fumigatus clinical isolates in 2008… …120 3.3 MIC values for azole resistant A. fumigatus clinical isolates in 2009...... 121… …195 7.4 Log10 of relative expression of 10 genes in azole resistant and susceptible… 

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

APA (6th Edition):

Bueid, A. (2012). Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164264

Chicago Manual of Style (16th Edition):

Bueid, Ahmed. “Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.” 2012. Doctoral Dissertation, University of Manchester. Accessed February 17, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164264.

MLA Handbook (7th Edition):

Bueid, Ahmed. “Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus.” 2012. Web. 17 Feb 2020.

Vancouver:

Bueid A. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Feb 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164264.

Council of Science Editors:

Bueid A. Laboratory epidemiology and mechanisms of azole resistance in Aspergillus fumigatus. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:164264

27. Li, Jin. Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans .

Degree: 2018, Université de Montréal

Subjects/Keywords: Candida albicans; Résistance aux azoles; Recombinaison homologue; TAC1; MRR1; Fluphénazine; Régulation positive; Azole resistance; Homologous recombination; Transcription factor; Fluphenazine; Upregulation; Facteur de transcription

…8 Figure 2. Major zinc cluster transcription factors mediating azole resistance in C… …The azole drugs are categorized into two groups: the triazoles and the imidazoles. The… …and mucosal Candida infections [11, 23]. 1.3. Azole resistance in C. albicans Due… …to the extensive clinical application as well as the fungistatic nature of the azole drugs… …and the fast adaptation capability of C. albicans, azole resistance in C. albicans has… 

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

APA (6th Edition):

Li, J. (2018). Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20399

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):

Li, Jin. “Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans .” 2018. Thesis, Université de Montréal. Accessed February 17, 2020. http://hdl.handle.net/1866/20399.

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

MLA Handbook (7th Edition):

Li, Jin. “Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans .” 2018. Web. 17 Feb 2020.

Vancouver:

Li J. Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans . [Internet] [Thesis]. Université de Montréal; 2018. [cited 2020 Feb 17]. Available from: http://hdl.handle.net/1866/20399.

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

Council of Science Editors:

Li J. Studying cross-talk between different transcriptional pathways controlling azole resistance in Candida albicans . [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20399

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


University of Otago

28. Huschmann, Franziska Ulrike. Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) .

Degree: University of Otago

 Infectious diseases are a worldwide health problem. The lack of effective and affordable medications for infections such as AIDS and systemic fungal infections poses a… (more)

Subjects/Keywords: infectious; diseases; resistance; AIDS; HIV; Erg11p; CYP51; cytochrome; P450; CYPs; cloning; expression; purification; crystallization; structure; X-ray; inhibitor; membrane; protein; mycoses; drug; design; azole; target; crystallography; three-dimensional; Candida; albicans; glabrata; Saccharomyces; cerevisiae; binding; assay; protease; HIV-1-PR; refinement; discovery; mutation; membrane-anchored; chromatography

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

APA (6th Edition):

Huschmann, F. U. (n.d.). Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4924

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Huschmann, Franziska Ulrike. “Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) .” Doctoral Dissertation, University of Otago. Accessed February 17, 2020. http://hdl.handle.net/10523/4924.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Huschmann, Franziska Ulrike. “Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) .” Web. 17 Feb 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Huschmann FU. Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) . [Internet] [Doctoral dissertation]. University of Otago; [cited 2020 Feb 17]. Available from: http://hdl.handle.net/10523/4924.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Huschmann FU. Investigating resistance in infectious diseases: Functional and structural characterization of the HIV-1 protease and the fungal lanosterol 14α-demethylase(Erg11p) . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/4924

Note: this citation may be lacking information needed for this citation format:
No year of publication.

.