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You searched for subject:(Envelope Proteins). Showing records 1 – 30 of 35 total matches.

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University of Leicester

1. Shak, Caroline. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.

Degree: PhD, 2020, University of Leicester

 Several stages of nuclear movement and positioning occur during the differentiation of myoblasts into myotubes and myofibres, allowing nuclei to be spread along the cell… (more)

Subjects/Keywords: Centrosomal Proteins; nuclear envelope; myogenesis

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APA (6th Edition):

Shak, C. (2020). Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. (Doctoral Dissertation). University of Leicester. Retrieved from https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213

Chicago Manual of Style (16th Edition):

Shak, Caroline. “Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.” 2020. Doctoral Dissertation, University of Leicester. Accessed December 02, 2020. https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213.

MLA Handbook (7th Edition):

Shak, Caroline. “Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.” 2020. Web. 02 Dec 2020.

Vancouver:

Shak C. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. [Internet] [Doctoral dissertation]. University of Leicester; 2020. [cited 2020 Dec 02]. Available from: https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213.

Council of Science Editors:

Shak C. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. [Doctoral Dissertation]. University of Leicester; 2020. Available from: https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213


University of Edinburgh

2. Robson, Michael Ian. NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis.

Degree: PhD, 2015, University of Edinburgh

 Gene positioning changes with respect to the nuclear periphery correlate with their activation in a number of tissues during development. However, the determination of the… (more)

Subjects/Keywords: 572.8; nuclear envelope transmembrane proteins; NETs; genome organisation; gene expression; development; myogenesis; DamID; FISH

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APA (6th Edition):

Robson, M. I. (2015). NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17914

Chicago Manual of Style (16th Edition):

Robson, Michael Ian. “NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 02, 2020. http://hdl.handle.net/1842/17914.

MLA Handbook (7th Edition):

Robson, Michael Ian. “NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis.” 2015. Web. 02 Dec 2020.

Vancouver:

Robson MI. NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1842/17914.

Council of Science Editors:

Robson MI. NETS coordinate genome organisation and gene expression changes in T-cells and during myogenesis. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/17914

3. Farnsworth, Aaron Quinn. The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress.

Degree: PhD, 2007, Oregon Health Sciences University

Subjects/Keywords: Simplexvirus; Glycoproteins; Viral Envelope Proteins; Biological Transport

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APA (6th Edition):

Farnsworth, A. Q. (2007). The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4MS3QR1 ; http://digitalcommons.ohsu.edu/etd/800

Chicago Manual of Style (16th Edition):

Farnsworth, Aaron Quinn. “The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress.” 2007. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 02, 2020. doi:10.6083/M4MS3QR1 ; http://digitalcommons.ohsu.edu/etd/800.

MLA Handbook (7th Edition):

Farnsworth, Aaron Quinn. “The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress.” 2007. Web. 02 Dec 2020.

Vancouver:

Farnsworth AQ. The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2007. [cited 2020 Dec 02]. Available from: doi:10.6083/M4MS3QR1 ; http://digitalcommons.ohsu.edu/etd/800.

Council of Science Editors:

Farnsworth AQ. The role of herpes simplex virus glycoprotein gE/gI in virus envelopment and egress. [Doctoral Dissertation]. Oregon Health Sciences University; 2007. Available from: doi:10.6083/M4MS3QR1 ; http://digitalcommons.ohsu.edu/etd/800

4. Fish, Kenneth N. Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages.

Degree: PhD, 1998, Oregon Health Sciences University

Subjects/Keywords: Cytomegalovirus; Virus Replication; Brain  – virology; Macrophages; Viral Envelope Proteins

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APA (6th Edition):

Fish, K. N. (1998). Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M42V2DB8 ; http://digitalcommons.ohsu.edu/etd/2569

Chicago Manual of Style (16th Edition):

Fish, Kenneth N. “Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages.” 1998. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 02, 2020. doi:10.6083/M42V2DB8 ; http://digitalcommons.ohsu.edu/etd/2569.

MLA Handbook (7th Edition):

Fish, Kenneth N. “Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages.” 1998. Web. 02 Dec 2020.

Vancouver:

Fish KN. Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1998. [cited 2020 Dec 02]. Available from: doi:10.6083/M42V2DB8 ; http://digitalcommons.ohsu.edu/etd/2569.

Council of Science Editors:

Fish KN. Mechanisms of human cytomegalovirus persistence in monocyte-derived macrophages. [Doctoral Dissertation]. Oregon Health Sciences University; 1998. Available from: doi:10.6083/M42V2DB8 ; http://digitalcommons.ohsu.edu/etd/2569


Harvard University

5. Markovski, Monica. Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors.

Degree: PhD, Microbiology and Molecular Genetics, 2012, Harvard University

 To fortify their cytoplasmic membrane and protect it from osmotic rupture, most bacteria surround themselves with a peptidoglycan (PG) exoskeleton. The PG synthases that build… (more)

Subjects/Keywords: cell envelope; Gram-negative; penicillin-binding proteins; peptidoglycan; peptidoglycan synthesis; peptidoglycan synthetic complex; microbiology; molecular biology; genetics

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APA (6th Edition):

Markovski, M. (2012). Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9547905

Chicago Manual of Style (16th Edition):

Markovski, Monica. “Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors.” 2012. Doctoral Dissertation, Harvard University. Accessed December 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9547905.

MLA Handbook (7th Edition):

Markovski, Monica. “Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors.” 2012. Web. 02 Dec 2020.

Vancouver:

Markovski M. Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2020 Dec 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9547905.

Council of Science Editors:

Markovski M. Bacterial Cell Wall Synthases Require Outer Membrane Lipoprotein Cofactors. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9547905

6. Celigoy, Jessica G. NMR Studies of Viral Envelope Proteins.

Degree: 2012, University of Illinois – Chicago

 Detailed structural information about viral envelope proteins is necessary for a better understanding of the viral entry mechanism, as well as for the development of… (more)

Subjects/Keywords: NMR; envelope proteins; HIV-1; SARS-CoV

…ABSTRACT Detailed structural information about viral envelope proteins is necessary for a… …NMR techniques to gather more information on the structure of the envelope proteins of SARS… …is found attached to many proteins on the cell surface. After receptor binding envelope… …shown in Table 1.1. The cleavage of the envelope proteins is a necessary step for viral entry… …SARS-CoV and Ebola) the proteolytic processing of the envelope proteins is a step… 

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APA (6th Edition):

Celigoy, J. G. (2012). NMR Studies of Viral Envelope Proteins. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/8949

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):

Celigoy, Jessica G. “NMR Studies of Viral Envelope Proteins.” 2012. Thesis, University of Illinois – Chicago. Accessed December 02, 2020. http://hdl.handle.net/10027/8949.

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

MLA Handbook (7th Edition):

Celigoy, Jessica G. “NMR Studies of Viral Envelope Proteins.” 2012. Web. 02 Dec 2020.

Vancouver:

Celigoy JG. NMR Studies of Viral Envelope Proteins. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10027/8949.

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

Council of Science Editors:

Celigoy JG. NMR Studies of Viral Envelope Proteins. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/8949

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


University of Illinois – Urbana-Champaign

7. Agrawal, Utsav. Probing surface protein patterning in biological systems using fluorescence nanoscopy.

Degree: PhD, Chemical Engineering, 2015, University of Illinois – Urbana-Champaign

 A complete understanding of biological substructures is often obscured by the diffraction limit of visible light in conventional fluorescence microscopy. Recently developed fluorescence nanoscopy techniques… (more)

Subjects/Keywords: fluorescence nanoscopy; stochastic optical reconstruction microscopy (STORM); B. subtilis; human immunodeficiency virus (HIV); chemotaxis; McpB; envelope proteins; clustering

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APA (6th Edition):

Agrawal, U. (2015). Probing surface protein patterning in biological systems using fluorescence nanoscopy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88273

Chicago Manual of Style (16th Edition):

Agrawal, Utsav. “Probing surface protein patterning in biological systems using fluorescence nanoscopy.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 02, 2020. http://hdl.handle.net/2142/88273.

MLA Handbook (7th Edition):

Agrawal, Utsav. “Probing surface protein patterning in biological systems using fluorescence nanoscopy.” 2015. Web. 02 Dec 2020.

Vancouver:

Agrawal U. Probing surface protein patterning in biological systems using fluorescence nanoscopy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2142/88273.

Council of Science Editors:

Agrawal U. Probing surface protein patterning in biological systems using fluorescence nanoscopy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88273

8. TANG XUHUA. Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV).

Degree: 2007, National University of Singapore

Subjects/Keywords: white spot syndrome virus; envelope proteins; structure

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APA (6th Edition):

XUHUA, T. (2007). Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV). (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/23054

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):

XUHUA, TANG. “Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV).” 2007. Thesis, National University of Singapore. Accessed December 02, 2020. http://scholarbank.nus.edu.sg/handle/10635/23054.

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

MLA Handbook (7th Edition):

XUHUA, TANG. “Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV).” 2007. Web. 02 Dec 2020.

Vancouver:

XUHUA T. Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV). [Internet] [Thesis]. National University of Singapore; 2007. [cited 2020 Dec 02]. Available from: http://scholarbank.nus.edu.sg/handle/10635/23054.

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

Council of Science Editors:

XUHUA T. Structural determination and characterization of the envelope proteins of shrimp white spot syndrome virus (WSSV). [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/23054

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

9. Gliniak, Brian C. Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration.

Degree: PhD, 1988, Oregon Health Sciences University

Subjects/Keywords: Leukemia, Erythroblastic, Acute; Retroviridae Infections; Viral Envelope Proteins; Proto-Oncogene Proteins

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APA (6th Edition):

Gliniak, B. C. (1988). Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4Z31WS0 ; http://digitalcommons.ohsu.edu/etd/1974

Chicago Manual of Style (16th Edition):

Gliniak, Brian C. “Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration.” 1988. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 02, 2020. doi:10.6083/M4Z31WS0 ; http://digitalcommons.ohsu.edu/etd/1974.

MLA Handbook (7th Edition):

Gliniak, Brian C. “Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration.” 1988. Web. 02 Dec 2020.

Vancouver:

Gliniak BC. Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1988. [cited 2020 Dec 02]. Available from: doi:10.6083/M4Z31WS0 ; http://digitalcommons.ohsu.edu/etd/1974.

Council of Science Editors:

Gliniak BC. Friend virus-induced erythroleukemia : relationship to viral env expression, cellular oncogene expression and proviral integration. [Doctoral Dissertation]. Oregon Health Sciences University; 1988. Available from: doi:10.6083/M4Z31WS0 ; http://digitalcommons.ohsu.edu/etd/1974

10. Xiang, Yang. Regulation of protein traffic in the TGN.

Degree: PhD, 2000, Oregon Health Sciences University

Subjects/Keywords: Endosomes; Membrane Proteins; Golgi Apparatus; Serine Endopeptidases; Viral Envelope Proteins

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APA (6th Edition):

Xiang, Y. (2000). Regulation of protein traffic in the TGN. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M46Q1VHC ; http://digitalcommons.ohsu.edu/etd/3312

Chicago Manual of Style (16th Edition):

Xiang, Yang. “Regulation of protein traffic in the TGN.” 2000. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 02, 2020. doi:10.6083/M46Q1VHC ; http://digitalcommons.ohsu.edu/etd/3312.

MLA Handbook (7th Edition):

Xiang, Yang. “Regulation of protein traffic in the TGN.” 2000. Web. 02 Dec 2020.

Vancouver:

Xiang Y. Regulation of protein traffic in the TGN. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2000. [cited 2020 Dec 02]. Available from: doi:10.6083/M46Q1VHC ; http://digitalcommons.ohsu.edu/etd/3312.

Council of Science Editors:

Xiang Y. Regulation of protein traffic in the TGN. [Doctoral Dissertation]. Oregon Health Sciences University; 2000. Available from: doi:10.6083/M46Q1VHC ; http://digitalcommons.ohsu.edu/etd/3312

11. Saiz Ros, Natalia. Herpes virus egress through the nuclear envelope and host response against infections.

Degree: PhD, 2017, University of Edinburgh

 The nuclear envelope is a highly organised double membrane system that separates the activities of the nuclear and cytoplasmic compartments in eukaryotic systems. The wide… (more)

Subjects/Keywords: herpesviruses; cellular proteins; nuclear envelope; NET23/STING; vesicle fusion proteins

…and ONM, contain unique sets of integral membrane proteins called Nuclear Envelope… …Abstract The nuclear envelope is a highly organised double membrane system that separates… …proteins associated with this cellular structure indicates that it is a major signalling node for… …2) What is the nuclear envelope role of NET23/STING in the activation of immune… …proteins would disperse into the ER during infection. I identified a group of vesicle fusion… 

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APA (6th Edition):

Saiz Ros, N. (2017). Herpes virus egress through the nuclear envelope and host response against infections. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28892

Chicago Manual of Style (16th Edition):

Saiz Ros, Natalia. “Herpes virus egress through the nuclear envelope and host response against infections.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed December 02, 2020. http://hdl.handle.net/1842/28892.

MLA Handbook (7th Edition):

Saiz Ros, Natalia. “Herpes virus egress through the nuclear envelope and host response against infections.” 2017. Web. 02 Dec 2020.

Vancouver:

Saiz Ros N. Herpes virus egress through the nuclear envelope and host response against infections. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1842/28892.

Council of Science Editors:

Saiz Ros N. Herpes virus egress through the nuclear envelope and host response against infections. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28892

12. Krzyzaniak, Magdalena Anna. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).

Degree: PhD, 2008, University of Alabama – Birmingham

HCMV consists of a dsDNA genome enclosed by, an icosahedral capsid surrounded by a layer of tegument proteins; the virion structure is enclosed in a… (more)

Subjects/Keywords: Cytomegalovirus  – physiology <; br>; Glycoproteins  – metabolism <; br>; Protein Sorting Signals <; br>; Viral Envelope Proteins  – metabolism <; br>; Virus Assembly <; br>; Virus Replication

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APA (6th Edition):

Krzyzaniak, M. A. (2008). Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,231

Chicago Manual of Style (16th Edition):

Krzyzaniak, Magdalena Anna. “Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 02, 2020. http://contentdm.mhsl.uab.edu/u?/etd,231.

MLA Handbook (7th Edition):

Krzyzaniak, Magdalena Anna. “Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV).” 2008. Web. 02 Dec 2020.

Vancouver:

Krzyzaniak MA. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2020 Dec 02]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,231.

Council of Science Editors:

Krzyzaniak MA. Role of the gM/gN glycoprotein complex in the final assembly and egress of the human cytomegalovirus (HCMV). [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,231

13. Zhang, Fan. A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2013, U of Massachusetts : Med

  Transposon silencing is required to maintain genome stability. The non-coding piRNAs effectively suppress of transposon activity during germline development. In the Drosophila female germline,… (more)

Subjects/Keywords: DEAD-box RNA Helicases; DNA Transposable Elements; Drosophila Proteins; Drosophila melanogaster; Germ Cells; Nuclear Envelope; Small Interfering RNA; Biochemistry; Genetics; Genomics; Molecular Biology; Molecular Genetics

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APA (6th Edition):

Zhang, F. (2013). A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/685

Chicago Manual of Style (16th Edition):

Zhang, Fan. “A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 02, 2020. http://escholarship.umassmed.edu/gsbs_diss/685.

MLA Handbook (7th Edition):

Zhang, Fan. “A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation.” 2013. Web. 02 Dec 2020.

Vancouver:

Zhang F. A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2020 Dec 02]. Available from: http://escholarship.umassmed.edu/gsbs_diss/685.

Council of Science Editors:

Zhang F. A Novel Role of UAP56 in piRNA Mediated Transposon Silencing: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/685

14. Manat, Guillaume. Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope.

Degree: Docteur es, Biochimie et biologie structurale, 2016, Université Paris-Saclay (ComUE)

Chez les bactéries, l’undécaprényl-phosphate (C55-P) est utilisé comme transporteur lipidique de sous-unités glycanes à travers la membrane plasmique. Après la synthèse de son précurseur (C55-PP)… (more)

Subjects/Keywords: Undécaprényl-Phosphate; Phosphatases; Protéines membranaires; Enveloppe bactérienne; Système à deux composants; Antibio-Résistance; Undecaprenyl-Phosphate; Phosphatases; Integral membrane proteins; Bacterial envelope; Two-Component system; Antibiotic resistance

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APA (6th Edition):

Manat, G. (2016). Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS098

Chicago Manual of Style (16th Edition):

Manat, Guillaume. “Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed December 02, 2020. http://www.theses.fr/2016SACLS098.

MLA Handbook (7th Edition):

Manat, Guillaume. “Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope.” 2016. Web. 02 Dec 2020.

Vancouver:

Manat G. Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Dec 02]. Available from: http://www.theses.fr/2016SACLS098.

Council of Science Editors:

Manat G. Etude fonctionnelle des undécaprényl-pyrophosphate phosphatases BacA et LpxT, enzymes membranaires impliquées dans la biogenèse de l’enveloppe bactérienne : Functional characterization of undecaprenyl-pyrophosphate phosphatases BacA and LpxT, integral membrane proteins involved in the biogenesis of the bacterial envelope. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS098

15. Moustafa, Rehab. Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C.

Degree: Docteur es, Virologie, 2019, Université Lille II – Droit et Santé

 Aujourd’hui, le Virus de l'Hépatite C (VHC) infecte plus 70 millions de personnes dans le monde. L’Organisation mondiale de la santé prévoit l’élimination du virus… (more)

Subjects/Keywords: Hépatite C; Glycoprotéine; Entrée virale; Protéines d'enveloppe; Assemblée virale; Ectodomaine E1; Hepatitis C; Viral assembly; Glycoprotein; Viral entry; E1 ectodomain; Viral entry; Envelope proteins

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

APA (6th Edition):

Moustafa, R. (2019). Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2019LIL2S002

Chicago Manual of Style (16th Edition):

Moustafa, Rehab. “Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C.” 2019. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed December 02, 2020. http://www.theses.fr/2019LIL2S002.

MLA Handbook (7th Edition):

Moustafa, Rehab. “Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C.” 2019. Web. 02 Dec 2020.

Vancouver:

Moustafa R. Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2019. [cited 2020 Dec 02]. Available from: http://www.theses.fr/2019LIL2S002.

Council of Science Editors:

Moustafa R. Characterization of functional determinants in the C-terminal part of hepatitis C virus E1 glycoprotein ectodomain : Caractérisation de déterminants fonctionnels dans la partie C-terminale de l'ectodomaine de la glycoprotéine E1 du virus de l'hépatite C. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2019. Available from: http://www.theses.fr/2019LIL2S002


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

16. Κουβάτσης, Βλάσιος. Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1).

Degree: 2011, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 Hepatitis C virus (HCV) is a major cause of liver diseases, including chronic hepatitis, cirrhosis, and hepatocellular carcinoma. HCV is a small enveloped virus that… (more)

Subjects/Keywords: Ιός ηπατίτιδας C (HCV); Γλυκοπρωτείνης ιικού φακέλου; Χιμαιρικές πρωτεϊνες; Ανασυνδυασμένοι ερπητοϊοί; Hepatitis C virus (HCV); Viral envelope glycoproteins; Chimeric proteins; Recombinant herpesviruses

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APA (6th Edition):

Κουβάτσης, . . (2011). Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1). (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/27129

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):

Κουβάτσης, Βλάσιος. “Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1).” 2011. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed December 02, 2020. http://hdl.handle.net/10442/hedi/27129.

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

MLA Handbook (7th Edition):

Κουβάτσης, Βλάσιος. “Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1).” 2011. Web. 02 Dec 2020.

Vancouver:

Κουβάτσης . Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1). [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10442/hedi/27129.

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

Council of Science Editors:

Κουβάτσης . Κλωνοποίηση, έκφραση και χαρακτηριστμός γλυκοπρωτεϊνών του ιού Hepatitis C (HCV) με τη χρήση ανασυνδυασμένων ιικών φορέων βασισμένων στον ιό Hespes simplex 1 (HSV-1). [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2011. Available from: http://hdl.handle.net/10442/hedi/27129

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


University of Florida

17. Liu, Qian. Protein Interactions at the Inner Nuclear Membrane.

Degree: PhD, Medical Sciences - Molecular Cell Biology (IDP), 2008, University of Florida

 Physical connections between the nucleoskeleton and cytoskeleton were recently uncovered, which we have previously defined as LINC (linker of nucleoskeleton and cytoskeleton) complex. They form… (more)

Subjects/Keywords: Antibodies; Cells; Chromatin; Lamins; Membrane proteins; Nuclear lamina; Nuclear membrane; Nuclear pore; Progeria; Proteins; envelope, inner, lamin, linc, membrane, nuclear

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

APA (6th Edition):

Liu, Q. (2008). Protein Interactions at the Inner Nuclear Membrane. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0023960

Chicago Manual of Style (16th Edition):

Liu, Qian. “Protein Interactions at the Inner Nuclear Membrane.” 2008. Doctoral Dissertation, University of Florida. Accessed December 02, 2020. https://ufdc.ufl.edu/UFE0023960.

MLA Handbook (7th Edition):

Liu, Qian. “Protein Interactions at the Inner Nuclear Membrane.” 2008. Web. 02 Dec 2020.

Vancouver:

Liu Q. Protein Interactions at the Inner Nuclear Membrane. [Internet] [Doctoral dissertation]. University of Florida; 2008. [cited 2020 Dec 02]. Available from: https://ufdc.ufl.edu/UFE0023960.

Council of Science Editors:

Liu Q. Protein Interactions at the Inner Nuclear Membrane. [Doctoral Dissertation]. University of Florida; 2008. Available from: https://ufdc.ufl.edu/UFE0023960

18. Santana, Vinicius Canato. Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas.

Degree: PhD, Alergia e Imunopatologia, 2014, University of São Paulo

A formulação HIVBr18, previamente desenvolvida e testada, é uma vacina de DNA que codifica 18 epítopos CD4, promíscuos e conservados do HIV-1, e que após… (more)

Subjects/Keywords: Adjuvantes imunológicos; Adjuvants immunologic; Aids vaccines; Camundongos endogâmicos BALB C; Citocinas; Cytokines; Fator estimulador de colônias de granulócitos e macrófagos; Granulocyte-macrophage colony-stimulating factor; Herpesvirus 1 human; Herpesvirus humano 1; HIV-1; HIV-1; Mice inbred BALB C; Proteínas do envelope viral; Vaccines DNA; Vacinas contra a aids; Vacinas de DNA; Viral envelope proteins

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APA (6th Edition):

Santana, V. C. (2014). Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5146/tde-23092014-091246/ ;

Chicago Manual of Style (16th Edition):

Santana, Vinicius Canato. “Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas.” 2014. Doctoral Dissertation, University of São Paulo. Accessed December 02, 2020. http://www.teses.usp.br/teses/disponiveis/5/5146/tde-23092014-091246/ ;.

MLA Handbook (7th Edition):

Santana, Vinicius Canato. “Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas.” 2014. Web. 02 Dec 2020.

Vancouver:

Santana VC. Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Dec 02]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-23092014-091246/ ;.

Council of Science Editors:

Santana VC. Desenvolvimento de estratégias para aumento da imunogenicidade da vacina de DNA HIVBr18 baseadas na fusão com a glicoproteína D do herpes vírus humano tipo 1 e na coadministração de citocinas. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-23092014-091246/ ;

19. Wang, Q. Structural and functional analysis of the baculovirus envelope fusion protein F.

Degree: 2015, Wageningen University

  Baculoviruses are enveloped, double-stranded DNA viruses that are pathogenic predominantly to insects. Insects, such as caterpillars, become infected by oral feeding on proteinaceous occlusion… (more)

Subjects/Keywords: baculovirus; envelopeiwitten; fusie-eiwitten; virusmorfologie; virale structurele eiwitten; Virussen van ongewervelden; baculovirus; envelope proteins; fusion proteins; viral morphology; viral structural proteins; Viruses of Invertebrates

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APA (6th Edition):

Wang, Q. (2015). Structural and functional analysis of the baculovirus envelope fusion protein F. (Doctoral Dissertation). Wageningen University. Retrieved from http://library.wur.nl/WebQuery/wurpubs/493047 ; urn:nbn:nl:ui:32-493047 ; urn:nbn:nl:ui:32-493047 ; http://library.wur.nl/WebQuery/wurpubs/493047

Chicago Manual of Style (16th Edition):

Wang, Q. “Structural and functional analysis of the baculovirus envelope fusion protein F.” 2015. Doctoral Dissertation, Wageningen University. Accessed December 02, 2020. http://library.wur.nl/WebQuery/wurpubs/493047 ; urn:nbn:nl:ui:32-493047 ; urn:nbn:nl:ui:32-493047 ; http://library.wur.nl/WebQuery/wurpubs/493047.

MLA Handbook (7th Edition):

Wang, Q. “Structural and functional analysis of the baculovirus envelope fusion protein F.” 2015. Web. 02 Dec 2020.

Vancouver:

Wang Q. Structural and functional analysis of the baculovirus envelope fusion protein F. [Internet] [Doctoral dissertation]. Wageningen University; 2015. [cited 2020 Dec 02]. Available from: http://library.wur.nl/WebQuery/wurpubs/493047 ; urn:nbn:nl:ui:32-493047 ; urn:nbn:nl:ui:32-493047 ; http://library.wur.nl/WebQuery/wurpubs/493047.

Council of Science Editors:

Wang Q. Structural and functional analysis of the baculovirus envelope fusion protein F. [Doctoral Dissertation]. Wageningen University; 2015. Available from: http://library.wur.nl/WebQuery/wurpubs/493047 ; urn:nbn:nl:ui:32-493047 ; urn:nbn:nl:ui:32-493047 ; http://library.wur.nl/WebQuery/wurpubs/493047


University of Florida

20. Yaswen, Linda Ruth. Cloning and characterization of Epstein-Barr virus glycoprotein gp85.

Degree: 1993, University of Florida

Subjects/Keywords: Research ( mesh ); Herpesvirus 4, Human ( mesh ); Viral Envelope Proteins  – genetics ( mesh ); Viral Envelope Proteins  – chemistry ( mesh ); Membrane Proteins  – genetics ( mesh ); Membrane Proteins  – chemistry ( mesh ); Glycoproteins  – genetics ( mesh ); Glycoproteins  – chemistry ( mesh ); Molecular Sequence Data ( mesh ); Amino Acid Sequence ( mesh ); Department of Pathology and Laboratory Medicine thesis Ph.D ( mesh )

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APA (6th Edition):

Yaswen, L. R. (1993). Cloning and characterization of Epstein-Barr virus glycoprotein gp85. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00066674

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):

Yaswen, Linda Ruth. “Cloning and characterization of Epstein-Barr virus glycoprotein gp85.” 1993. Thesis, University of Florida. Accessed December 02, 2020. https://ufdc.ufl.edu/AA00066674.

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

MLA Handbook (7th Edition):

Yaswen, Linda Ruth. “Cloning and characterization of Epstein-Barr virus glycoprotein gp85.” 1993. Web. 02 Dec 2020.

Vancouver:

Yaswen LR. Cloning and characterization of Epstein-Barr virus glycoprotein gp85. [Internet] [Thesis]. University of Florida; 1993. [cited 2020 Dec 02]. Available from: https://ufdc.ufl.edu/AA00066674.

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

Council of Science Editors:

Yaswen LR. Cloning and characterization of Epstein-Barr virus glycoprotein gp85. [Thesis]. University of Florida; 1993. Available from: https://ufdc.ufl.edu/AA00066674

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

21. Richards, Kathryn H. Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2008, U of Massachusetts : Med

  The Human Immunodeficiency Virus (HIV) is able to infect CD4<sup>+</sup> T cells as well as macrophages. Macrophage-tropism has been linked to determinants in the… (more)

Subjects/Keywords: HIV-1; HIV Infections; Tropism; Viral Envelope Proteins; Macrophages; Human Immunodeficiency Virus Proteins; Viral Regulatory and Accessory Proteins; Virus Replication; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Hemic and Immune Systems; Viruses

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APA (6th Edition):

Richards, K. H. (2008). Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/378

Chicago Manual of Style (16th Edition):

Richards, Kathryn H. “Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 02, 2020. https://escholarship.umassmed.edu/gsbs_diss/378.

MLA Handbook (7th Edition):

Richards, Kathryn H. “Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation.” 2008. Web. 02 Dec 2020.

Vancouver:

Richards KH. Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2020 Dec 02]. Available from: https://escholarship.umassmed.edu/gsbs_diss/378.

Council of Science Editors:

Richards KH. Mutations in the vpu and env Genes of HIV-1 Can Adversely Impact Infectivity: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/378

22. Murawski, Matthew R. Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation.

Degree: Immunology and Microbiology, Medicine, 2009, U of Massachusetts : Med

  Respiratory syncytial virus (RSV) causes a common infection that is associated with a range of respiratory illnesses from common cold-like symptoms to serious lower… (more)

Subjects/Keywords: Respiratory Syncytial Virus Vaccines; Respiratory Syncytial Viruses; Immunity; Innate; Immunity; Active; Toll-Like Receptor 2; Vaccines; Virosome; Viral Envelope Proteins; Respiratory Syncytial Virus Infections; Hemic and Immune Systems; Virus Diseases; Viruses

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APA (6th Edition):

Murawski, M. R. (2009). Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/432

Chicago Manual of Style (16th Edition):

Murawski, Matthew R. “Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 02, 2020. https://escholarship.umassmed.edu/gsbs_diss/432.

MLA Handbook (7th Edition):

Murawski, Matthew R. “Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation.” 2009. Web. 02 Dec 2020.

Vancouver:

Murawski MR. Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2020 Dec 02]. Available from: https://escholarship.umassmed.edu/gsbs_diss/432.

Council of Science Editors:

Murawski MR. Respiratory Syncytial Virus (RSV) Induces Innate Immunity through Toll-Like Receptors and Acquired Immunity via the RSV G Protein: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/432

23. Schaefer, Kaitlin. The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases.

Degree: PhD, 2018, Harvard University

The Gram-positive cell wall is a massive macromolecule composed primarily of two polymers: peptidoglycan (PG) and cell wall glycopolymers. Wall teichoic acid (WTA) is the… (more)

Subjects/Keywords: cell wall; glycopolymers; wall teichoic acid; peptidoglycan; antibiotics; cell envelope; LCP proteins; Staphylococcus aureus

…found three proteins belonging to a family of cell-envelope implicated proteins called LytR… …envelope proteins Initially identified in the 1990s, LCP family proteins were annotated as cell… …envelope membrane proteins that are present primarily in Gram-positive bacteria,110-114 though… …108 4.1.7 LCP proteins determine the proper PG substrate through steric exclusion ......110… …12 Chapter 2: Are LCP proteins ligases… 

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

APA (6th Edition):

Schaefer, K. (2018). The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42015372

Chicago Manual of Style (16th Edition):

Schaefer, Kaitlin. “The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases.” 2018. Doctoral Dissertation, Harvard University. Accessed December 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42015372.

MLA Handbook (7th Edition):

Schaefer, Kaitlin. “The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases.” 2018. Web. 02 Dec 2020.

Vancouver:

Schaefer K. The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases. [Internet] [Doctoral dissertation]. Harvard University; 2018. [cited 2020 Dec 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42015372.

Council of Science Editors:

Schaefer K. The Reconstitution of Mature Cell Wall Polymer and the Roles of LCP Ligases. [Doctoral Dissertation]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42015372


University of Florida

24. Kim, Daein. Identification and Characterization of Nuclear Envelope Proteins.

Degree: PhD, Medical Sciences - Molecular Cell Biology (IDP), 2012, University of Florida

Subjects/Keywords: Cells; Chromosomes; Diseases; Genetic mutation; Lamins; Nuclear lamina; Nuclear membrane; Prophase; Proteins; Telomeres; envelope; nuclear

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

APA (6th Edition):

Kim, D. (2012). Identification and Characterization of Nuclear Envelope Proteins. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0043567

Chicago Manual of Style (16th Edition):

Kim, Daein. “Identification and Characterization of Nuclear Envelope Proteins.” 2012. Doctoral Dissertation, University of Florida. Accessed December 02, 2020. https://ufdc.ufl.edu/UFE0043567.

MLA Handbook (7th Edition):

Kim, Daein. “Identification and Characterization of Nuclear Envelope Proteins.” 2012. Web. 02 Dec 2020.

Vancouver:

Kim D. Identification and Characterization of Nuclear Envelope Proteins. [Internet] [Doctoral dissertation]. University of Florida; 2012. [cited 2020 Dec 02]. Available from: https://ufdc.ufl.edu/UFE0043567.

Council of Science Editors:

Kim D. Identification and Characterization of Nuclear Envelope Proteins. [Doctoral Dissertation]. University of Florida; 2012. Available from: https://ufdc.ufl.edu/UFE0043567

25. Rizzotto, Andrea. Targeting nuclear size for therapeutic intervention in cancer.

Degree: PhD, 2019, University of Edinburgh

 Nuclear size normally scales with cell size and is maintained throughout the cell cycle, but in cancer this karyoplasmic ratio, the ratio between the cytoplasm… (more)

Subjects/Keywords: Nuclear Envelope Transmembrane proteins; NETs; nuclear size changes; karyoplasmic ratio; nuclear size defects

…specific nuclear envelope transmembrane proteins (NETs) and separately a small molecule… …envelope proteins affecting nuclear size. 64 Figure 13 Nuclear size and fluorescence intensity… …transmembrane proteins, but there are hundreds of other Nuclear Envelope Transmembrane proteins (… …outer and inner nuclear envelope membranes called nuclear envelope transmembrane proteins… …National Center for Biotechnology information NE nuclear envelope NET nuclear envelope… 

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APA (6th Edition):

Rizzotto, A. (2019). Targeting nuclear size for therapeutic intervention in cancer. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/36097

Chicago Manual of Style (16th Edition):

Rizzotto, Andrea. “Targeting nuclear size for therapeutic intervention in cancer.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed December 02, 2020. http://hdl.handle.net/1842/36097.

MLA Handbook (7th Edition):

Rizzotto, Andrea. “Targeting nuclear size for therapeutic intervention in cancer.” 2019. Web. 02 Dec 2020.

Vancouver:

Rizzotto A. Targeting nuclear size for therapeutic intervention in cancer. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1842/36097.

Council of Science Editors:

Rizzotto A. Targeting nuclear size for therapeutic intervention in cancer. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/36097


Rockefeller University

26. Niepel, Mario. Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope.

Degree: 2005, Rockefeller University

 The nuclear envelope (NE) separates the genetic material from the rest of the cell, delimits and defines the nucleus, organizes the intranuclear architecture and serves… (more)

Subjects/Keywords: nuclear envelope; Mlp proteins; nuclear transport; nuclear pore complex; yeast; spindle pole body; Life Sciences

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

APA (6th Edition):

Niepel, M. (2005). Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope. (Masters Thesis). Rockefeller University. Retrieved from https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/92

Chicago Manual of Style (16th Edition):

Niepel, Mario. “Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope.” 2005. Masters Thesis, Rockefeller University. Accessed December 02, 2020. https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/92.

MLA Handbook (7th Edition):

Niepel, Mario. “Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope.” 2005. Web. 02 Dec 2020.

Vancouver:

Niepel M. Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope. [Internet] [Masters thesis]. Rockefeller University; 2005. [cited 2020 Dec 02]. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/92.

Council of Science Editors:

Niepel M. Myosin-Like Proteins in S. cerevisiae: Multifunctional, Structural Components of the Nuclear Envelope. [Masters Thesis]. Rockefeller University; 2005. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/92

27. Hulten, van, M.C.W. Virion composition and genomics of white spot syndrome virus of shrimp.

Degree: 2001, NARCIS

  Since its first discovery in Taiwan in 1992, White spot syndrome virus (WSSV) has caused major economic damage to shrimp culture. The virus has… (more)

Subjects/Keywords: penaeus monodon; dierenvirussen; garnalen; genomen; eiwitten; taxonomie; envelopeiwitten; genexpressieanalyse; Virussen van ongewervelden; shrimps; penaeus monodon; animal viruses; genomes; proteins; envelope proteins; taxonomy; genomics; Viruses of Invertebrates

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APA (6th Edition):

Hulten, van, M. C. W. (2001). Virion composition and genomics of white spot syndrome virus of shrimp. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/110728 ; urn:nbn:nl:ui:32-110728 ; urn:nbn:nl:ui:32-110728 ; http://library.wur.nl/WebQuery/wurpubs/110728

Chicago Manual of Style (16th Edition):

Hulten, van, M C W. “Virion composition and genomics of white spot syndrome virus of shrimp.” 2001. Doctoral Dissertation, NARCIS. Accessed December 02, 2020. http://library.wur.nl/WebQuery/wurpubs/110728 ; urn:nbn:nl:ui:32-110728 ; urn:nbn:nl:ui:32-110728 ; http://library.wur.nl/WebQuery/wurpubs/110728.

MLA Handbook (7th Edition):

Hulten, van, M C W. “Virion composition and genomics of white spot syndrome virus of shrimp.” 2001. Web. 02 Dec 2020.

Vancouver:

Hulten, van MCW. Virion composition and genomics of white spot syndrome virus of shrimp. [Internet] [Doctoral dissertation]. NARCIS; 2001. [cited 2020 Dec 02]. Available from: http://library.wur.nl/WebQuery/wurpubs/110728 ; urn:nbn:nl:ui:32-110728 ; urn:nbn:nl:ui:32-110728 ; http://library.wur.nl/WebQuery/wurpubs/110728.

Council of Science Editors:

Hulten, van MCW. Virion composition and genomics of white spot syndrome virus of shrimp. [Doctoral Dissertation]. NARCIS; 2001. Available from: http://library.wur.nl/WebQuery/wurpubs/110728 ; urn:nbn:nl:ui:32-110728 ; urn:nbn:nl:ui:32-110728 ; http://library.wur.nl/WebQuery/wurpubs/110728


University of Florida

28. Crisp, Melissa Lynn. The LINC Complex and Nucleo-Cytoplasmic Coupling.

Degree: PhD, Medical Sciences - Molecular Cell Biology (IDP), 2008, University of Florida

Subjects/Keywords: Antibodies; Cells; Centrosomes; Hela cells; Lamins; Membrane proteins; Microtubules; Nuclear lamina; Nuclear membrane; Proteins; envelope, epithelial, giant, kinesin, linc, nesprin, nuclear, nucleus, sun, sun1, sun2

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

APA (6th Edition):

Crisp, M. L. (2008). The LINC Complex and Nucleo-Cytoplasmic Coupling. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0022079

Chicago Manual of Style (16th Edition):

Crisp, Melissa Lynn. “The LINC Complex and Nucleo-Cytoplasmic Coupling.” 2008. Doctoral Dissertation, University of Florida. Accessed December 02, 2020. https://ufdc.ufl.edu/UFE0022079.

MLA Handbook (7th Edition):

Crisp, Melissa Lynn. “The LINC Complex and Nucleo-Cytoplasmic Coupling.” 2008. Web. 02 Dec 2020.

Vancouver:

Crisp ML. The LINC Complex and Nucleo-Cytoplasmic Coupling. [Internet] [Doctoral dissertation]. University of Florida; 2008. [cited 2020 Dec 02]. Available from: https://ufdc.ufl.edu/UFE0022079.

Council of Science Editors:

Crisp ML. The LINC Complex and Nucleo-Cytoplasmic Coupling. [Doctoral Dissertation]. University of Florida; 2008. Available from: https://ufdc.ufl.edu/UFE0022079

29. Shanks, Melissa Christine. Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway.

Degree: School of Chemistry and Molecular Biosciences, 2015, University of Queensland

Subjects/Keywords: DENV-2; Dengue fever; Flavivirus; Virus Fusion; Structural Proteins; Envelope Proteins; 030406 Proteins and Peptides; 0601 Biochemistry and Cell Biology; 060108 Protein Trafficking

…particles with Dengue envelope proteins [6]. Sanofi-Pasteur has created a tetravalent… …x5B;46, 48-50]. Many class I viral envelope proteins have been characterised including… …of a variety of virus envelope proteins such as Hepatitis C [72, 73], Ebola [… …proteins 22 Figure 9. Proposed fusion process of homotrimer E, Class I & Class II proteins 25… …location in the envelope glycoprotein 28 Figure 15. Amino acid substitutions of the E2 α-helix 30… 

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APA (6th Edition):

Shanks, M. C. (2015). Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:363952

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):

Shanks, Melissa Christine. “Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway.” 2015. Thesis, University of Queensland. Accessed December 02, 2020. http://espace.library.uq.edu.au/view/UQ:363952.

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

MLA Handbook (7th Edition):

Shanks, Melissa Christine. “Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway.” 2015. Web. 02 Dec 2020.

Vancouver:

Shanks MC. Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway. [Internet] [Thesis]. University of Queensland; 2015. [cited 2020 Dec 02]. Available from: http://espace.library.uq.edu.au/view/UQ:363952.

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

Council of Science Editors:

Shanks MC. Site-directed mutagenesis of the membrane-proximal (MPER) α-helical E2 region of DENV E to characterise the significance of individual residues in protein expression and migration through the secretory pathway. [Thesis]. University of Queensland; 2015. Available from: http://espace.library.uq.edu.au/view/UQ:363952

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

30. ΠΥΡΠΑΣΟΠΟΥΛΟΥ, ΑΘΗΝΑ. ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ.

Degree: 1997, University of Crete (UOC); Πανεπιστήμιο Κρήτης

MORPHOLOGICAL STUDIES HAVE ESTABLISHED A CLOSE ASSOCIATION OF PERIPHERAL HETEROCHROMATIN WITH THE NUCLEAR ENVELOPE, WHICH HAS BEEN ATTRIBUTED BOTH TO NUCLEAR LAMIN AND LAMIN -… (more)

Subjects/Keywords: ΑΝΟΣΟΑΦΑΙΡΕΣΗ; ΔΙΑΛΥΤΟΙ ΠΑΡΑΓΟΝΤΕΣ ΚΥΤΤΑΡΟΠΛΑΣΜΑΤΟΣ; Διαμεμβρανικές πρωτεΐνες; ΕΠΑΝΑΣΧΗΜΑΤΙΣΜΟΣ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ; Λαμινίνες; Πυρηνικός φάκελος; Χρωματίνη; Chromatine; IMMUNODEPLETION; INTERGRAL MEMBRANE PROTEINS; Lamins; Nuclear envelope; NUCLEAR REASSEMBLY; SOLUBLE FACTORS

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APA (6th Edition):

ΠΥΡΠΑΣΟΠΟΥΛΟΥ, . . (1997). ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/8743

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):

ΠΥΡΠΑΣΟΠΟΥΛΟΥ, ΑΘΗΝΑ. “ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ.” 1997. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed December 02, 2020. http://hdl.handle.net/10442/hedi/8743.

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

MLA Handbook (7th Edition):

ΠΥΡΠΑΣΟΠΟΥΛΟΥ, ΑΘΗΝΑ. “ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ.” 1997. Web. 02 Dec 2020.

Vancouver:

ΠΥΡΠΑΣΟΠΟΥΛΟΥ . ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 1997. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10442/hedi/8743.

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

Council of Science Editors:

ΠΥΡΠΑΣΟΠΟΥΛΟΥ . ΑΛΛΗΛΕΠΙΔΡΑΣΕΙΣ ΤΟΥ ΠΥΡΗΝΙΚΟΥ ΦΑΚΕΛΟΥ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ: ΒΙΟΧΗΜΙΚΟΣ ΧΑΡΑΚΤΗΡΙΣΜΟΣ ΠΑΡΑΓΟΝΤΩΝ ΠΟΥ ΣΥΝΔΕΟΥΝ ΤΗΝ ΕΣΩ ΠΥΡΗΝΙΚΗ ΜΕΜΒΡΑΝΗ ΜΕ ΤΗ ΧΡΩΜΑΤΙΝΗ. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 1997. Available from: http://hdl.handle.net/10442/hedi/8743

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

[1] [2]

.