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You searched for subject:(let 7). Showing records 1 – 30 of 32 total matches.

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Universitat de Valencia

1. Vega Oomen, Olivia. Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico .

Degree: 2017, Universitat de Valencia

 INTRODUCCIÓN El embarazo ectópico (EE) es una complicación precoz de la gestación en la cual un óvulo fecundado se implanta en un sitio distinto al… (more)

Subjects/Keywords: microrna; embarazo ectópico; lin28; let-7

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

APA (6th Edition):

Vega Oomen, O. (2017). Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/59541

Chicago Manual of Style (16th Edition):

Vega Oomen, Olivia. “Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico .” 2017. Doctoral Dissertation, Universitat de Valencia. Accessed January 27, 2020. http://hdl.handle.net/10550/59541.

MLA Handbook (7th Edition):

Vega Oomen, Olivia. “Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico .” 2017. Web. 27 Jan 2020.

Vancouver:

Vega Oomen O. Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2017. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10550/59541.

Council of Science Editors:

Vega Oomen O. Descripción y comparación del perfil de expresión del sistema LIN28/Let-7 y microRNAs asociados en tejido placentario sano y tejido placentario procedente de embarazo ectópico . [Doctoral Dissertation]. Universitat de Valencia; 2017. Available from: http://hdl.handle.net/10550/59541


Université Paris-Sud – Paris XI

2. Kropp, Jérémie. Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2014, Université Paris-Sud – Paris XI

A la suite d’un criblage pangénomique, nous avons montré que l’inhibition d’un miARN de la famille let-7, miR-98, entraîne une forte accélération de la différenciation… (more)

Subjects/Keywords: MicroARN; Let-7; MiR-98; Différenciation du muscle strié squelettique; E2F5; MicroRNA; Let-7; MiR-98; Skeletal muscle differenciation; E2F5

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APA (6th Edition):

Kropp, J. (2014). Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA11T090

Chicago Manual of Style (16th Edition):

Kropp, Jérémie. “Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 27, 2020. http://www.theses.fr/2014PA11T090.

MLA Handbook (7th Edition):

Kropp, Jérémie. “Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway.” 2014. Web. 27 Jan 2020.

Vancouver:

Kropp J. Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2020 Jan 27]. Available from: http://www.theses.fr/2014PA11T090.

Council of Science Editors:

Kropp J. Régulation de la différenciation du muscle strié squelettique par la voie let-7 – E2F5 : Regulation of Skeletal Muscle Differentiation by the let-7 – E2F5 Pathway. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA11T090


University of Pennsylvania

3. King, Catrina E. Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer.

Degree: 2010, University of Pennsylvania

 Lin28b is an RNA-binding protein that inhibits biogenesis of tumor-suppressive microRNAs of the let-7 family, and is involved in induction of pluripotency. Although LIN28B has… (more)

Subjects/Keywords: LIN28B let-7 colon cancer LIN28 microRNA; Cancer Biology

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APA (6th Edition):

King, C. E. (2010). Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1551

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):

King, Catrina E. “Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer.” 2010. Thesis, University of Pennsylvania. Accessed January 27, 2020. https://repository.upenn.edu/edissertations/1551.

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

MLA Handbook (7th Edition):

King, Catrina E. “Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer.” 2010. Web. 27 Jan 2020.

Vancouver:

King CE. Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2020 Jan 27]. Available from: https://repository.upenn.edu/edissertations/1551.

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

Council of Science Editors:

King CE. Lin28B, LET-7, and the Molecular Pathogenesis of Colon Cancer. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/1551

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


University of Miami

4. Joshi, Shaurya. LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2016, University of Miami

 One of the prominent causes of heart failure is atherosclerosis of the coronary arteries. Obstruction of blood flow within the coronary arteries results in inadequate… (more)

Subjects/Keywords: Ischemia-reperfusion; Apoptosis; Let-7; Lin28; AKT; PIK3IP1

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APA (6th Edition):

Joshi, S. (2016). LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1590

Chicago Manual of Style (16th Edition):

Joshi, Shaurya. “LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury.” 2016. Doctoral Dissertation, University of Miami. Accessed January 27, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/1590.

MLA Handbook (7th Edition):

Joshi, Shaurya. “LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury.” 2016. Web. 27 Jan 2020.

Vancouver:

Joshi S. LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury. [Internet] [Doctoral dissertation]. University of Miami; 2016. [cited 2020 Jan 27]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1590.

Council of Science Editors:

Joshi S. LIN28/let-7 Axis as a Regulator of Myocardial Ischemic Injury. [Doctoral Dissertation]. University of Miami; 2016. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1590


Colorado State University

5. Enriquez, Vanessa Ann. Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype.

Degree: PhD, Cell and Molecular Biology, 2007, Colorado State University

 Ovarian cancer is the fifth most deadly cancer among women in the United States and the most lethal gynecological malignancy in the world. Recent studies… (more)

Subjects/Keywords: miRNAs; exosomes; LIN28; let-7

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APA (6th Edition):

Enriquez, V. A. (2007). Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83733

Chicago Manual of Style (16th Edition):

Enriquez, Vanessa Ann. “Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype.” 2007. Doctoral Dissertation, Colorado State University. Accessed January 27, 2020. http://hdl.handle.net/10217/83733.

MLA Handbook (7th Edition):

Enriquez, Vanessa Ann. “Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype.” 2007. Web. 27 Jan 2020.

Vancouver:

Enriquez VA. Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype. [Internet] [Doctoral dissertation]. Colorado State University; 2007. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10217/83733.

Council of Science Editors:

Enriquez VA. Pluripotency factors and miRNAs in human ovarian cancer cells and their secreted exosomes regulate gene expression and phenotype. [Doctoral Dissertation]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/83733


Universidade Estadual de Campinas

6. Araujo, Hygor Nunes, 1988-. Controle molecular da função mitocondrial pelo miRNA let-7b-5p .

Degree: 2019, Universidade Estadual de Campinas

 Resumo: Através de um banco de dados público (MIRWALK) buscando a associação de microRNAs e alvos moleculares na biogênese mitocondrial. A análise bioinformática mostrou interação… (more)

Subjects/Keywords: MicroRNAs; Mitocôndria; Let-7; Gene lin28a; PPAR beta

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APA (6th Edition):

Araujo, Hygor Nunes, 1. (2019). Controle molecular da função mitocondrial pelo miRNA let-7b-5p . (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/335587

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):

Araujo, Hygor Nunes, 1988-. “Controle molecular da função mitocondrial pelo miRNA let-7b-5p .” 2019. Thesis, Universidade Estadual de Campinas. Accessed January 27, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/335587.

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

MLA Handbook (7th Edition):

Araujo, Hygor Nunes, 1988-. “Controle molecular da função mitocondrial pelo miRNA let-7b-5p .” 2019. Web. 27 Jan 2020.

Vancouver:

Araujo, Hygor Nunes 1. Controle molecular da função mitocondrial pelo miRNA let-7b-5p . [Internet] [Thesis]. Universidade Estadual de Campinas; 2019. [cited 2020 Jan 27]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/335587.

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

Council of Science Editors:

Araujo, Hygor Nunes 1. Controle molecular da função mitocondrial pelo miRNA let-7b-5p . [Thesis]. Universidade Estadual de Campinas; 2019. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/335587

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

7. Ricarte Filho, Júlio Cezar Marques. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.

Degree: PhD, Biologia Celular e Tecidual, 2009, University of São Paulo

Neste estudo, geramos ensaios de espectrometria de massa para detecção de 111 mutações nos genes RET, BRAF, NRAS, HRAS, KRAS, PIK3CA e AKT1 e avaliamos… (more)

Subjects/Keywords: AKT1; AKT1; BRAF; BRAF; Câncer tiróide; Genotipagem por espectrometria de massa; Histologia; Histology; Let-7 microRNA; Mass spectrometry genotyping; MicroRNA let-7; Neoplasias; Neoplasms; RET/PTC; RET/PTC; Thyroid cancer

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APA (6th Edition):

Ricarte Filho, J. C. M. (2009). Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;

Chicago Manual of Style (16th Edition):

Ricarte Filho, Júlio Cezar Marques. “Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.” 2009. Doctoral Dissertation, University of São Paulo. Accessed January 27, 2020. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;.

MLA Handbook (7th Edition):

Ricarte Filho, Júlio Cezar Marques. “Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.” 2009. Web. 27 Jan 2020.

Vancouver:

Ricarte Filho JCM. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2020 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;.

Council of Science Editors:

Ricarte Filho JCM. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;

8. Fuziwara, Cesar Seigi. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.

Degree: Mestrado, Biologia Celular e Tecidual, 2010, University of São Paulo

No câncer, alterações em microRNAs (miRNAs), pequenos RNAs que regulam a tradução protéica, exerce efeito oncogênico (oncomiR). Os oncomiRs regulam genes chave para a proliferação… (more)

Subjects/Keywords: Glândula tireóide; Let-7; Let-7; MicroRNA; MicroRNA; miR-17-92; miR-17-92; Neoplasias da tireóide; Proliferação RET/PTC; Proliferation; RET-PTC; Thyroid gland; Thyroid neoplasms

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APA (6th Edition):

Fuziwara, C. S. (2010). Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;

Chicago Manual of Style (16th Edition):

Fuziwara, Cesar Seigi. “Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.” 2010. Masters Thesis, University of São Paulo. Accessed January 27, 2020. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;.

MLA Handbook (7th Edition):

Fuziwara, Cesar Seigi. “Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.” 2010. Web. 27 Jan 2020.

Vancouver:

Fuziwara CS. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Jan 27]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;.

Council of Science Editors:

Fuziwara CS. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;

9. Manier, Salomon. Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation.

Degree: Docteur es, Hématologie, 2017, Université Lille II – Droit et Santé

 Le Myélome Multiple (MM) est une hémopathie maligne caractérisée par la prolifération de plasmocytes tumoraux médullaires. MYC occupe un rôle central dans l'oncogenèse du MM… (more)

Subjects/Keywords: LIN28B/let-7; Rocaglate; Traduction; Myélome multiple; MYC; Exosome; MicroARN; LIN28B/let-7; Rocaglate-scaffold; Multiple myeloma; MYC; MicroRNA; Exosomes; Rocaglates; Translation

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APA (6th Edition):

Manier, S. (2017). Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2017LIL2S012

Chicago Manual of Style (16th Edition):

Manier, Salomon. “Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation.” 2017. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed January 27, 2020. http://www.theses.fr/2017LIL2S012.

MLA Handbook (7th Edition):

Manier, Salomon. “Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation.” 2017. Web. 27 Jan 2020.

Vancouver:

Manier S. Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2017. [cited 2020 Jan 27]. Available from: http://www.theses.fr/2017LIL2S012.

Council of Science Editors:

Manier S. Ciblage de MYC par étude de l'axe LIN28B/let-7 et de l'initiation de la traduction dans le myélome multiple : Targeting MYC in multiple myeloma by interfering with the LIN28B/let-7 axis and inhibiting translation initiation. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2017. Available from: http://www.theses.fr/2017LIL2S012


University of Minnesota

10. McCulloch, Katherine Ann. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.

Degree: Molecular, Cellular, Developmental Biology and Genetics, 2013, University of Minnesota

 The heterochronic pathway of C. elegans ensures the appropriate timing of post-embryonic development. Mutations in heterochronic genes cause skipping or reiteration of larval programs, resulting… (more)

Subjects/Keywords: Heterochrony; let-7; lin-42; miRNA; Molecular, cellular, developmental biology and genetics

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APA (6th Edition):

McCulloch, K. A. (2013). Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. (Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/171448

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):

McCulloch, Katherine Ann. “Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.” 2013. Thesis, University of Minnesota. Accessed January 27, 2020. http://hdl.handle.net/11299/171448.

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

MLA Handbook (7th Edition):

McCulloch, Katherine Ann. “Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development.” 2013. Web. 27 Jan 2020.

Vancouver:

McCulloch KA. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. [Internet] [Thesis]. University of Minnesota; 2013. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/11299/171448.

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

Council of Science Editors:

McCulloch KA. Characterization of the function of the C. elegans heterochronic gene lin-42/per during larval development. [Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/171448

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


UCLA

11. Gaeta, Xavier. Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation.

Degree: Molec, Cell, & Dev Biology, 2016, UCLA

 Pluripotent Stem Cells (PSCs) have the unique ability to divide indefinitely and self-renew in vitro, as well as differentiate into all cell types of the… (more)

Subjects/Keywords: Molecular biology; Developmental biology; Neurosciences; let-7 miRNAs; nervous system development; stem cell biology

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APA (6th Edition):

Gaeta, X. (2016). Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/7b32m8rb

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):

Gaeta, Xavier. “Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation.” 2016. Thesis, UCLA. Accessed January 27, 2020. http://www.escholarship.org/uc/item/7b32m8rb.

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

MLA Handbook (7th Edition):

Gaeta, Xavier. “Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation.” 2016. Web. 27 Jan 2020.

Vancouver:

Gaeta X. Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation. [Internet] [Thesis]. UCLA; 2016. [cited 2020 Jan 27]. Available from: http://www.escholarship.org/uc/item/7b32m8rb.

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

Council of Science Editors:

Gaeta X. Multilevel regulation of the let-7 miRNAs coordinates human central nervous system developmental maturation. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/7b32m8rb

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


University of California – San Diego

12. Mondol, Vanessa. MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans.

Degree: Biology, 2015, University of California – San Diego

 MicroRNAs (miRNAs) are small non-coding RNAs, ~22 nucleotides (nt) long, with major roles in gene regulation. MiRNAs bind imperfectly to complementary sequences in the 3’… (more)

Subjects/Keywords: Biology; Molecular biology; Developmental biology; C. elegans; let-7; Microprocessor; microRNA; pri-miRNA; trans-splicing

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APA (6th Edition):

Mondol, V. (2015). MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/3f93318b

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):

Mondol, Vanessa. “MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans.” 2015. Thesis, University of California – San Diego. Accessed January 27, 2020. http://www.escholarship.org/uc/item/3f93318b.

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

MLA Handbook (7th Edition):

Mondol, Vanessa. “MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans.” 2015. Web. 27 Jan 2020.

Vancouver:

Mondol V. MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans. [Internet] [Thesis]. University of California – San Diego; 2015. [cited 2020 Jan 27]. Available from: http://www.escholarship.org/uc/item/3f93318b.

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

Council of Science Editors:

Mondol V. MicroRNAs in the Making: Post-transcriptional Regulation of MicroRNA Biogenesis in Caenorhabditis elegans. [Thesis]. University of California – San Diego; 2015. Available from: http://www.escholarship.org/uc/item/3f93318b

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


University of California – San Francisco

13. Melton, Collin Alfred. Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal.

Degree: Biomedical Sciences, 2010, University of California – San Francisco

 When an embryonic stem cell (ESC) differentiates, it must both silence the ESC self-renewal program as well as activate new tissue-specific programs. In the absence… (more)

Subjects/Keywords: Biology, General; differentiation; embryonic stem cell; ESCC; let-7; microRNA; self-renewal

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

APA (6th Edition):

Melton, C. A. (2010). Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9g6288t5

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):

Melton, Collin Alfred. “Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal.” 2010. Thesis, University of California – San Francisco. Accessed January 27, 2020. http://www.escholarship.org/uc/item/9g6288t5.

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

MLA Handbook (7th Edition):

Melton, Collin Alfred. “Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal.” 2010. Web. 27 Jan 2020.

Vancouver:

Melton CA. Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2020 Jan 27]. Available from: http://www.escholarship.org/uc/item/9g6288t5.

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

Council of Science Editors:

Melton CA. Opposing microRNAs Regulate Mouse Embryonic Stem Cell Self-Renewal. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/9g6288t5

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


University of New South Wales

14. Swaminathan, Sanjay. Understanding the critical role of microRNAs in HIV-1 pathogenesis.

Degree: Clinical School - St Vincent's Hospital, 2011, University of New South Wales

 MicroRNAs (miRNAs) are ~22 nucleotide small RNAs which are critical regulators of mRNA translation and have key roles in HIV-1 infection. We characterized miRNA changes… (more)

Subjects/Keywords: CD4+ T cells; miRNA; HIV-1; Monocytes; IL-10; Blimp-1; Let-7

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APA (6th Edition):

Swaminathan, S. (2011). Understanding the critical role of microRNAs in HIV-1 pathogenesis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9999/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Swaminathan, Sanjay. “Understanding the critical role of microRNAs in HIV-1 pathogenesis.” 2011. Doctoral Dissertation, University of New South Wales. Accessed January 27, 2020. http://handle.unsw.edu.au/1959.4/51319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9999/SOURCE02?view=true.

MLA Handbook (7th Edition):

Swaminathan, Sanjay. “Understanding the critical role of microRNAs in HIV-1 pathogenesis.” 2011. Web. 27 Jan 2020.

Vancouver:

Swaminathan S. Understanding the critical role of microRNAs in HIV-1 pathogenesis. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2020 Jan 27]. Available from: http://handle.unsw.edu.au/1959.4/51319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9999/SOURCE02?view=true.

Council of Science Editors:

Swaminathan S. Understanding the critical role of microRNAs in HIV-1 pathogenesis. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9999/SOURCE02?view=true


Texas Medical Center

15. Liu, Can. MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development.

Degree: PhD, 2012, Texas Medical Center

  Most human tumors contain a population of cells with stem cell properties, called cancer stem cells (CSCs), which are believed to be responsible for… (more)

Subjects/Keywords: microRNA; prostate cancer; cancer stem cell; miR-34a; let-7; miR-301; Biology; Cancer Biology; Medicine and Health Sciences

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APA (6th Edition):

Liu, C. (2012). MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/236

Chicago Manual of Style (16th Edition):

Liu, Can. “MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development.” 2012. Doctoral Dissertation, Texas Medical Center. Accessed January 27, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/236.

MLA Handbook (7th Edition):

Liu, Can. “MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development.” 2012. Web. 27 Jan 2020.

Vancouver:

Liu C. MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development. [Internet] [Doctoral dissertation]. Texas Medical Center; 2012. [cited 2020 Jan 27]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/236.

Council of Science Editors:

Liu C. MicroRNA Regulation of Prostate Cancer Stem/Progenitor Cells and Prostate Cancer Development. [Doctoral Dissertation]. Texas Medical Center; 2012. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/236


UCLA

16. Xie, Yuan. Defining the role of oxygen tension in cell fate decision making of human neural progenitors.

Degree: Molec, Cell, & Dev Biology, 2015, UCLA

 Human pluripotent stem cells (hPSCs) have opened up numerous avenues, including regenerative medicine and modeling development and disease. However, when compared to the fetal tissue-derived… (more)

Subjects/Keywords: Molecular biology; Neurosciences; Cellular biology; Astrogenesis; Differentiation; Hypoxia; Hypoxia inducible factor/HIF; LIN28/let-7 miRNAs; Neural progenitor cell

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APA (6th Edition):

Xie, Y. (2015). Defining the role of oxygen tension in cell fate decision making of human neural progenitors. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4jd62857

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):

Xie, Yuan. “Defining the role of oxygen tension in cell fate decision making of human neural progenitors.” 2015. Thesis, UCLA. Accessed January 27, 2020. http://www.escholarship.org/uc/item/4jd62857.

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

MLA Handbook (7th Edition):

Xie, Yuan. “Defining the role of oxygen tension in cell fate decision making of human neural progenitors.” 2015. Web. 27 Jan 2020.

Vancouver:

Xie Y. Defining the role of oxygen tension in cell fate decision making of human neural progenitors. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Jan 27]. Available from: http://www.escholarship.org/uc/item/4jd62857.

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

Council of Science Editors:

Xie Y. Defining the role of oxygen tension in cell fate decision making of human neural progenitors. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/4jd62857

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

17. Anene, Chinedu A. Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells.

Degree: PhD, 2017, University of Bradford

 Cardiovascular disease is a major cause of morbidity and mortality around the globe, which is linked to athero-thrombosis. The risk factors for atherothrombosis, thus cardiovascular… (more)

Subjects/Keywords: Cardiovascular diseases; microRNA (miRNA); Angiogenesis; Endothelial cells; Let-7a; Micro-particles; Platelet activation; Molecular mechanisms; Lethal-7

Page 1 Page 2

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APA (6th Edition):

Anene, C. A. (2017). Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/16041

Chicago Manual of Style (16th Edition):

Anene, Chinedu A. “Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells.” 2017. Doctoral Dissertation, University of Bradford. Accessed January 27, 2020. http://hdl.handle.net/10454/16041.

MLA Handbook (7th Edition):

Anene, Chinedu A. “Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells.” 2017. Web. 27 Jan 2020.

Vancouver:

Anene CA. Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells. [Internet] [Doctoral dissertation]. University of Bradford; 2017. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10454/16041.

Council of Science Editors:

Anene CA. Platelet micro-particles induce angiogenesis through the delivery of the micro-RNA Let-7a into endothelial cells. [Doctoral Dissertation]. University of Bradford; 2017. Available from: http://hdl.handle.net/10454/16041


Freie Universität Berlin

18. Fuchs, Heiko. Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung.

Degree: 2011, Freie Universität Berlin

 Zusammenfassung MicroRNAs, eine Klasse nicht kodierender RNAs mit einer Länge von ca. 22 Nukleotiden, inhibieren die Translation von messenger-RNAs durch imperfekte Bindung an bestimmte Sequenzen… (more)

Subjects/Keywords: microRNAs; let-7; miR-125; miR-124; miR-128; Lin-41; Lin-28; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Fuchs, H. (2011). Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7806

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):

Fuchs, Heiko. “Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung.” 2011. Thesis, Freie Universität Berlin. Accessed January 27, 2020. http://dx.doi.org/10.17169/refubium-7806.

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

MLA Handbook (7th Edition):

Fuchs, Heiko. “Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung.” 2011. Web. 27 Jan 2020.

Vancouver:

Fuchs H. Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2020 Jan 27]. Available from: http://dx.doi.org/10.17169/refubium-7806.

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

Council of Science Editors:

Fuchs H. Einfluss von im Gehirn angereicherten mikroRNAs auf die Neuralentwicklung. [Thesis]. Freie Universität Berlin; 2011. Available from: http://dx.doi.org/10.17169/refubium-7806

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


University of Colorado

19. Cohen, Max Louis. Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1.

Degree: PhD, 2013, University of Colorado

  The heterochronic gene network controls developmental timing in the nematode roundworm Caenorhabditis elegans. Bi-stable switch-like changes in gene expression occur during its development as… (more)

Subjects/Keywords: C. elegans; elt-1; Gene expression; heterochronic; let-7; micoRNA; Biology; Cell and Developmental Biology; Developmental Biology; Genetics; Molecular Biology

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APA (6th Edition):

Cohen, M. L. (2013). Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/mcdb_gradetds/18

Chicago Manual of Style (16th Edition):

Cohen, Max Louis. “Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1.” 2013. Doctoral Dissertation, University of Colorado. Accessed January 27, 2020. https://scholar.colorado.edu/mcdb_gradetds/18.

MLA Handbook (7th Edition):

Cohen, Max Louis. “Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1.” 2013. Web. 27 Jan 2020.

Vancouver:

Cohen ML. Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2020 Jan 27]. Available from: https://scholar.colorado.edu/mcdb_gradetds/18.

Council of Science Editors:

Cohen ML. Regulation of C. elegans Developmental Timing by the GATA Transcription Factor elt-1. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/mcdb_gradetds/18

20. WANG YU. CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA.

Degree: 2011, National University of Singapore

Subjects/Keywords: HCC; HBV; HBx; microRNA; miR-224.let-7

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APA (6th Edition):

YU, W. (2011). CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/23686

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):

YU, WANG. “CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA.” 2011. Thesis, National University of Singapore. Accessed January 27, 2020. http://scholarbank.nus.edu.sg/handle/10635/23686.

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

MLA Handbook (7th Edition):

YU, WANG. “CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA.” 2011. Web. 27 Jan 2020.

Vancouver:

YU W. CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2020 Jan 27]. Available from: http://scholarbank.nus.edu.sg/handle/10635/23686.

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

Council of Science Editors:

YU W. CHARACTERIZATION OF MICRORNA DEREGULATION IN HEPATOCELLULAR CARCINOMA. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/23686

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


Freie Universität Berlin

21. Mayr, Florian. Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese.

Degree: 2013, Freie Universität Berlin

 Lin28 ist ein essentielles RNA-Bindeprotein, welches ubiquitär in embryonalen Stammzellen exprimiert wird und mit dessen Hilfe induziert pluripotente Stammzellen (iPSC) erzeugt werden können. Seine physiologische… (more)

Subjects/Keywords: Lin28; let-7; miRNA, Dicer; cold-shock domain; zinc-knuckle domain; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie

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APA (6th Edition):

Mayr, F. (2013). Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-13727

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):

Mayr, Florian. “Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese.” 2013. Thesis, Freie Universität Berlin. Accessed January 27, 2020. http://dx.doi.org/10.17169/refubium-13727.

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

MLA Handbook (7th Edition):

Mayr, Florian. “Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese.” 2013. Web. 27 Jan 2020.

Vancouver:

Mayr F. Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Jan 27]. Available from: http://dx.doi.org/10.17169/refubium-13727.

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

Council of Science Editors:

Mayr F. Strukturelle und funktionelle Analyse der Lin28-vermittelten Blockierung der let-7 miRNA Biogenese. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-13727

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

22. Ilbay, Orkan. Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans.

Degree: Interdisciplinary Graduate Program, Molecular Medicine, 2019, U of Massachusetts : Med

  Robustness is a ubiquitous property of biological systems, however, underlying mechanisms that help reinforce the optimal phenotypes despite environmental or physiological perturbations are poorly… (more)

Subjects/Keywords: Developmental robustness; heterochronic pathway; developmental timing; microRNAs; let-7; LIN-28; pluripotency; reprogramming.; Cell and Developmental Biology; Developmental Biology; Life Sciences

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APA (6th Edition):

Ilbay, O. (2019). Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/1057

Chicago Manual of Style (16th Edition):

Ilbay, Orkan. “Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans.” 2019. Doctoral Dissertation, U of Massachusetts : Med. Accessed January 27, 2020. https://escholarship.umassmed.edu/gsbs_diss/1057.

MLA Handbook (7th Edition):

Ilbay, Orkan. “Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans.” 2019. Web. 27 Jan 2020.

Vancouver:

Ilbay O. Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2019. [cited 2020 Jan 27]. Available from: https://escholarship.umassmed.edu/gsbs_diss/1057.

Council of Science Editors:

Ilbay O. Robustness Mechanisms of Temporal Cell-Fate Progression in C. Elegans. [Doctoral Dissertation]. U of Massachusetts : Med; 2019. Available from: https://escholarship.umassmed.edu/gsbs_diss/1057

23. Μόσιαλου, Ιωάννα. Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo.

Degree: 2010, University of Crete (UOC); Πανεπιστήμιο Κρήτης

 Numerous epidemiological and clinical trials have established that High Density Lipoprotein (HDL) is a strong and independent risk factor for the development of atherosclerosis and… (more)

Subjects/Keywords: Απολιποπρωτεΐνη Μ; Πυρηνικοί υποδοχείς ορμονών; Απολιποπρωτεΐνη Ε; Αθηροσκλήρωση; Μεταγραφική ρύθμιση; Φλεγμονές; Μεταβολισμός λιπιδίων; Απολιποπρωτεΐνη Α-ΙΙ; HDL ( High Density Lipoprotein ); HNF4; RXR; Jun; Let-7; miR-122; ABCA1; HepG2

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APA (6th Edition):

Μόσιαλου, . . (2010). Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/24664

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):

Μόσιαλου, Ιωάννα. “Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo.” 2010. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed January 27, 2020. http://hdl.handle.net/10442/hedi/24664.

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

MLA Handbook (7th Edition):

Μόσιαλου, Ιωάννα. “Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo.” 2010. Web. 27 Jan 2020.

Vancouver:

Μόσιαλου . Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2010. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10442/hedi/24664.

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

Council of Science Editors:

Μόσιαλου . Μηχανισμοί μεταγραφικής ρύθμισης των γονιδίων των απoλιποπρωτεϊνών του ανθρώπου in vivo. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2010. Available from: http://hdl.handle.net/10442/hedi/24664

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


Université de Montréal

24. Desjardins, Alexandre. Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g .

Degree: 2014, Université de Montréal

 La régulation de l’expression des gènes est ce qui permet à nos cellules de s’adapter à leur environnement, de combattre les infections ou, plus généralement,… (more)

Subjects/Keywords: Lin28; let-7; microARN; régulation post-transcriptionnelle; interaction protéine-ARN; formation de complexes macromoléculaires; gels natifs; microRNA; post-transcriptional regulation; protein-RNA interaction; macromolecular complex formation; native gels

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APA (6th Edition):

Desjardins, A. (2014). Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11068

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):

Desjardins, Alexandre. “Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g .” 2014. Thesis, Université de Montréal. Accessed January 27, 2020. http://hdl.handle.net/1866/11068.

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

MLA Handbook (7th Edition):

Desjardins, Alexandre. “Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g .” 2014. Web. 27 Jan 2020.

Vancouver:

Desjardins A. Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/1866/11068.

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

Council of Science Editors:

Desjardins A. Caractérisation de l’interaction entre la protéine Lin28 et le précurseur du microARN let-7g . [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/11068

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

25. Paz, Edwin Alfredo. Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling .

Degree: 2013, University of Arizona

 Eukaryotic cells tightly regulate metabolism in order to sustain normal processes. Dysregulation of cellular metabolism is associated with multiple diseases including cancer. Polyamine metabolism is… (more)

Subjects/Keywords: DFMO; eIF5A; let-7; oncometabolite; polyamines; LIN28; Cancer Biology

…75 Figure 3.9. Polyamines regulate HMGA in a let-7 dependent manner ...............76… …82 Figure 3.13 Working model for polyamines and eIF5A regulation on LIN28/let-7… …RNAs involved in cellular responses including effects on the let-7 microRNA family. Moreover… …also suggests that MYC is able to inhibit transcription of a let-7 microRNA cluster by… …of polyamine inhibition on hsa-let-7i.......................................70 Figure 3.7… 

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

APA (6th Edition):

Paz, E. A. (2013). Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/299021

Chicago Manual of Style (16th Edition):

Paz, Edwin Alfredo. “Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling .” 2013. Doctoral Dissertation, University of Arizona. Accessed January 27, 2020. http://hdl.handle.net/10150/299021.

MLA Handbook (7th Edition):

Paz, Edwin Alfredo. “Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling .” 2013. Web. 27 Jan 2020.

Vancouver:

Paz EA. Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10150/299021.

Council of Science Editors:

Paz EA. Molecular Mechanisms of Polyamine Metabolism Affecting Oncogenic Signaling . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/299021


University of Toronto

26. Grieco, Anthony. Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis.

Degree: 2011, University of Toronto

The genes that regulate pubertal timing in the general population are not well understood. Recently, genome-wide association studies have demonstrated that genetic variants near LIN28B… (more)

Subjects/Keywords: Pubertal Timing; HPO Axis; LIN28B; Ovary; qRT-PCR; IHC; RT-PCR; LIN28A; GnRH Neuron; Single Nucleotide Polymorphisms; Genome Wide Association Studies; Let-7; Follicle; Oocyte; 0369

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APA (6th Edition):

Grieco, A. (2011). Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30616

Chicago Manual of Style (16th Edition):

Grieco, Anthony. “Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis.” 2011. Masters Thesis, University of Toronto. Accessed January 27, 2020. http://hdl.handle.net/1807/30616.

MLA Handbook (7th Edition):

Grieco, Anthony. “Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis.” 2011. Web. 27 Jan 2020.

Vancouver:

Grieco A. Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/1807/30616.

Council of Science Editors:

Grieco A. Evaluation of the Expression of LIN28A and LIN28B within the Hypothalamic-pituitary-gonadal Axis. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30616

27. Patterson, Michaela Cyr. Modeling Human Neural Development Using Pluripotent Stem Cells.

Degree: Molec, Cell, & Dev Biology, 2012, UCLA

 Human pluripotent stem cells (hPSCs) are derived from the developing blastocyst or through transcription factor based reprogramming. hPSCs have the capacity to self-renew and give… (more)

Subjects/Keywords: Developmental biology; human development; human fetal tissue; let-7; LIN28; pluripotent stem cell

…LIN28/let-7 in the developmental maturity of pluripotent stem cell derived neural progenitors… …54 CHAPTER 4: Functional role of LIN28/let-7 in the developmental maturity of pluripotent… …authors. Aim III: Establish a functional role for LIN28/let-7 in the developmental maturity of… …determined that the LIN28/let-7 pathway can correct a significant portion of the genes… …Differences between hESCs and hiPSCs - the undifferentiated state …. 7 Deriving clinically… 

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APA (6th Edition):

Patterson, M. C. (2012). Modeling Human Neural Development Using Pluripotent Stem Cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9fg436zc

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):

Patterson, Michaela Cyr. “Modeling Human Neural Development Using Pluripotent Stem Cells.” 2012. Thesis, UCLA. Accessed January 27, 2020. http://www.escholarship.org/uc/item/9fg436zc.

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

MLA Handbook (7th Edition):

Patterson, Michaela Cyr. “Modeling Human Neural Development Using Pluripotent Stem Cells.” 2012. Web. 27 Jan 2020.

Vancouver:

Patterson MC. Modeling Human Neural Development Using Pluripotent Stem Cells. [Internet] [Thesis]. UCLA; 2012. [cited 2020 Jan 27]. Available from: http://www.escholarship.org/uc/item/9fg436zc.

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

Council of Science Editors:

Patterson MC. Modeling Human Neural Development Using Pluripotent Stem Cells. [Thesis]. UCLA; 2012. Available from: http://www.escholarship.org/uc/item/9fg436zc

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

28. Thornton, James Edward. Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs.

Degree: PhD, Biological Sciences in Public Health, 2013, Harvard University

 MicroRNAs (miRNAs) are a diverse and evolutionarily conserved class of non-coding RNAs that play a multitude of roles in many branches of eukaryotic biology. The… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Developmental biology; let-7; miRNA; TUT4; TUT7; TUTase; Uridylation

…Biogenesis 5 Lin28 and let-7: A crucial developmental axis 13 Lin28 selectively inhibits let-7… …biogenesis 19 Uncovering the regulatory mechanism of Lin28 towards let-7 20 Lin28 is a stem… …The future of Lin28 and let-7 32 PAPs and TUTases 33 TUTase Identification and Early… …2: Lin28-mediated control of let-7 expression by alternative TUTases Zcchc11 (TUT4… …x22;""! LIST OF FIGURES Figure 1.1 Lin28 selectively blocks let-7 biogenesis 16… 

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APA (6th Edition):

Thornton, J. E. (2013). Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11181173

Chicago Manual of Style (16th Edition):

Thornton, James Edward. “Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs.” 2013. Doctoral Dissertation, Harvard University. Accessed January 27, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11181173.

MLA Handbook (7th Edition):

Thornton, James Edward. “Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs.” 2013. Web. 27 Jan 2020.

Vancouver:

Thornton JE. Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Jan 27]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11181173.

Council of Science Editors:

Thornton JE. Roles for Terminal Uridyl Transferases in the Post-Transcriptional Regulation of Developmental miRNAs. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11181173


Freie Universität Berlin

29. Rybak, Agnieszka. Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS.

Degree: 2009, Freie Universität Berlin

 Die Entdeckung der microRNA(miRNAs), eine Gruppe von ca. 22 Nukleotid langen regulatorischen RNAs, hat zu einer kleinen Revolution in der Biologie geführt. miRNAs sind endogen… (more)

Subjects/Keywords: MicroRNA; Stem cells; let-7; 500 Naturwissenschaften und Mathematik::540 Chemie; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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

APA (6th Edition):

Rybak, A. (2009). Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7441

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):

Rybak, Agnieszka. “Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS.” 2009. Thesis, Freie Universität Berlin. Accessed January 27, 2020. http://dx.doi.org/10.17169/refubium-7441.

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

MLA Handbook (7th Edition):

Rybak, Agnieszka. “Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS.” 2009. Web. 27 Jan 2020.

Vancouver:

Rybak A. Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS. [Internet] [Thesis]. Freie Universität Berlin; 2009. [cited 2020 Jan 27]. Available from: http://dx.doi.org/10.17169/refubium-7441.

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

Council of Science Editors:

Rybak A. Expression und Funktion der microRNA let-7 bei der Stammzelldifferenzierung und Entwicklung des ZNS. [Thesis]. Freie Universität Berlin; 2009. Available from: http://dx.doi.org/10.17169/refubium-7441

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

30. García Cruz, Roseli Marlen. The role of p19 C-H-Ras protein in metastasis and proliferative pathways.

Degree: 2013, Universitat de Barcelona

 Ras is an evolutionary and conserved family of genes present in many organisms, in humans, Ras is conformed by three members called N-Ras, K-Ras and… (more)

Subjects/Keywords: Micro RNAs; MicroRNAs; H-ras; Let-7; miR-206; Biotecnologia; Biotecnología; Biotechnology; Ciències de la Salut; 577

…Activation of PI3K/AKT/mTOr signaling pathway via let-7/Ras .. Fig. 32 Oncogenic activation of… …in cancer … Table 16. Misregulation of miR-let-7 in cancer .. Table… …Table 56. Targets of miR-let-7 … 171 LIST OF GRAPHICS Pages Graphic 1… …signaling transduction pathways Fig. 7 Ras molecular mechanism related to metastasis… …species (ROS) … Table 7. Distribution of frequency of Ras mutations in… 

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

APA (6th Edition):

García Cruz, R. M. (2013). The role of p19 C-H-Ras protein in metastasis and proliferative pathways. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/123849

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):

García Cruz, Roseli Marlen. “The role of p19 C-H-Ras protein in metastasis and proliferative pathways.” 2013. Thesis, Universitat de Barcelona. Accessed January 27, 2020. http://hdl.handle.net/10803/123849.

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

MLA Handbook (7th Edition):

García Cruz, Roseli Marlen. “The role of p19 C-H-Ras protein in metastasis and proliferative pathways.” 2013. Web. 27 Jan 2020.

Vancouver:

García Cruz RM. The role of p19 C-H-Ras protein in metastasis and proliferative pathways. [Internet] [Thesis]. Universitat de Barcelona; 2013. [cited 2020 Jan 27]. Available from: http://hdl.handle.net/10803/123849.

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

Council of Science Editors:

García Cruz RM. The role of p19 C-H-Ras protein in metastasis and proliferative pathways. [Thesis]. Universitat de Barcelona; 2013. Available from: http://hdl.handle.net/10803/123849

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

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