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

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University of Minnesota

1. Johnston, Alura Lynn. Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors.

Degree: MS, Stem Cell Biology, 2013, University of Minnesota

 Spinal cord injury (SCI) is a debilitating disorder that affects numerous aspects of a person's health. After injury, oligodendrocytes (myelinating glial cells) in the damaged… (more)

Subjects/Keywords: Direct reprogramming; Oligodendrocyte; Progenitor

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APA (6th Edition):

Johnston, A. L. (2013). Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162361

Chicago Manual of Style (16th Edition):

Johnston, Alura Lynn. “Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors.” 2013. Masters Thesis, University of Minnesota. Accessed November 24, 2017. http://hdl.handle.net/11299/162361.

MLA Handbook (7th Edition):

Johnston, Alura Lynn. “Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors.” 2013. Web. 24 Nov 2017.

Vancouver:

Johnston AL. Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/11299/162361.

Council of Science Editors:

Johnston AL. Direct reprogramming of mouse embryonic fibroblasts to oligodendrocyte progenitor cells using various transcription factors. [Masters Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/162361


University of California – San Diego

2. Tsunemoto, Rachel. Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming.

Degree: Neurosciences, 2016, University of California – San Diego

 The mammalian nervous system is comprised of an unknown, but recognizably large, number of diverse neuronal subtypes. Recently, direct reprogramming (also known as transdifferentiation) has… (more)

Subjects/Keywords: Neurosciences; Direct Reprogramming; Induced Neurons; Transcription Factors

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APA (6th Edition):

Tsunemoto, R. (2016). Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/59k3t2xt

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):

Tsunemoto, Rachel. “Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming.” 2016. Thesis, University of California – San Diego. Accessed November 24, 2017. http://www.escholarship.org/uc/item/59k3t2xt.

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

MLA Handbook (7th Edition):

Tsunemoto, Rachel. “Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming.” 2016. Web. 24 Nov 2017.

Vancouver:

Tsunemoto R. Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2017 Nov 24]. Available from: http://www.escholarship.org/uc/item/59k3t2xt.

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

Council of Science Editors:

Tsunemoto R. Deciphering Transcriptional Control of Neuronal Identity and Diversity Using Direct Reprogramming. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/59k3t2xt

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


Case Western Reserve University

3. Lager, Angela Marie. Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin.

Degree: PhD, Genetics, 2015, Case Western Reserve University

 The oligodendrocyte lineage is essential for high-fidelity information transfer in neural circuits of the central nervous system. Oligodendrocytes arise from a pool of migratory progenitor… (more)

Subjects/Keywords: Developmental Biology; Genetics; myelin; oligodendrocytes; cell reprogramming; regenerative therapy; direct reprogramming; myelin repair

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APA (6th Edition):

Lager, A. M. (2015). Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1427898199

Chicago Manual of Style (16th Edition):

Lager, Angela Marie. “Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin.” 2015. Doctoral Dissertation, Case Western Reserve University. Accessed November 24, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1427898199.

MLA Handbook (7th Edition):

Lager, Angela Marie. “Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin.” 2015. Web. 24 Nov 2017.

Vancouver:

Lager AM. Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2015. [cited 2017 Nov 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1427898199.

Council of Science Editors:

Lager AM. Cell Reprogramming Technologies for Treatment and Understanding of Genetic Disorders of Myelin. [Doctoral Dissertation]. Case Western Reserve University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1427898199


University of Toronto

4. Namdar, Sogand. Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System.

Degree: 2016, University of Toronto

Organ transplantation is the treatment of choice for management of end-stage organ diseases. Graft failure due to chronic rejection is characterized by fibrosis of structures… (more)

Subjects/Keywords: chronic rejection; direct reprogramming; fibrosis; lung; myofibroblasts; PiggyBac; 0541

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APA (6th Edition):

Namdar, S. (2016). Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75962

Chicago Manual of Style (16th Edition):

Namdar, Sogand. “Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System.” 2016. Masters Thesis, University of Toronto. Accessed November 24, 2017. http://hdl.handle.net/1807/75962.

MLA Handbook (7th Edition):

Namdar, Sogand. “Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System.” 2016. Web. 24 Nov 2017.

Vancouver:

Namdar S. Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/1807/75962.

Council of Science Editors:

Namdar S. Feasibility of Direct Reprogramming of Myofibroblasts to Lung Epithelial Cells Utilizing PiggyBac Transposon System. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/75962


University of California – San Diego

5. Adamowicz, David Hideo. Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies.

Degree: Neurosciences, 2017, University of California – San Diego

 Dementia with Lewy bodies (DLB) is a neurodegenerative disease that shares clinical features with Alzheimer’s disease (dementia) and Parkinson’s disease (movement disorder). Diagnosis is confirmed… (more)

Subjects/Keywords: Neurosciences; Dementia with Lewy Bodies; Direct reprogramming; Hippocampus; Inflammation; Memory; α-synuclein

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APA (6th Edition):

Adamowicz, D. H. (2017). Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9wt947rv

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):

Adamowicz, David Hideo. “Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies.” 2017. Thesis, University of California – San Diego. Accessed November 24, 2017. http://www.escholarship.org/uc/item/9wt947rv.

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

MLA Handbook (7th Edition):

Adamowicz, David Hideo. “Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies.” 2017. Web. 24 Nov 2017.

Vancouver:

Adamowicz DH. Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2017 Nov 24]. Available from: http://www.escholarship.org/uc/item/9wt947rv.

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

Council of Science Editors:

Adamowicz DH. Elucidating the Basis for Memory Impairment in Dementia with Lewy Bodies. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/9wt947rv

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

6. Sripathy Rao, Srinidhi Rao. Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells.

Degree: MS, Stem Cell Biology, 2016, University of Minnesota

Reprogramming is the process of converting a somatic cell into a different cell type in a controlled manner without an intermediate pluripotent state, usually by… (more)

Subjects/Keywords: Beta-like cells; Direct Reprogramming; Viral Vectors

…that function similarly to pancreatic beta cells. Direct reprogramming of somatic cell types… …to the direct reprogramming of liver to pancreatic cells. During development, both the… …al. demonstrated effective in vivo direct reprogramming of amylase+/CK19–/Ins– mouse… …could be used as a potential remedy for juvenile diabetes by direct reprogramming cells of non… …and external signals was sufficient to induce direct reprogramming of a particular cell type… 

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APA (6th Edition):

Sripathy Rao, S. R. (2016). Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/185068

Chicago Manual of Style (16th Edition):

Sripathy Rao, Srinidhi Rao. “Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells.” 2016. Masters Thesis, University of Minnesota. Accessed November 24, 2017. http://hdl.handle.net/11299/185068.

MLA Handbook (7th Edition):

Sripathy Rao, Srinidhi Rao. “Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells.” 2016. Web. 24 Nov 2017.

Vancouver:

Sripathy Rao SR. Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells. [Internet] [Masters thesis]. University of Minnesota; 2016. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/11299/185068.

Council of Science Editors:

Sripathy Rao SR. Determination of Methods for Improved Reprogramming of Various Cell Types to Functional Beta-like Cells. [Masters Thesis]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/185068


Universidade Nova

7. Franco, António Duarte Zapico Bicho de Sousa. Long non-coding RNA contributes to direct conversion reprogramming.

Degree: 2016, Universidade Nova

 Over the last years, research led lncRNAs to go from transcriptional noise to important regulators of gene expression, being now known their association with many… (more)

Subjects/Keywords: LncRNA; Direct reprogramming; Multipotency; Zeb2NAT; Pnky; Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias

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APA (6th Edition):

Franco, A. D. Z. B. d. S. (2016). Long non-coding RNA contributes to direct conversion reprogramming. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19464

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):

Franco, António Duarte Zapico Bicho de Sousa. “Long non-coding RNA contributes to direct conversion reprogramming.” 2016. Thesis, Universidade Nova. Accessed November 24, 2017. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19464.

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

MLA Handbook (7th Edition):

Franco, António Duarte Zapico Bicho de Sousa. “Long non-coding RNA contributes to direct conversion reprogramming.” 2016. Web. 24 Nov 2017.

Vancouver:

Franco ADZBdS. Long non-coding RNA contributes to direct conversion reprogramming. [Internet] [Thesis]. Universidade Nova; 2016. [cited 2017 Nov 24]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19464.

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

Council of Science Editors:

Franco ADZBdS. Long non-coding RNA contributes to direct conversion reprogramming. [Thesis]. Universidade Nova; 2016. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/19464

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


University of Helsinki

8. Silfvast, Saga. The potential of direct cardiac reprogramming in cardiac regeneration.

Degree: 2016, University of Helsinki

 Heart failure is a major public health problem and a leading cause of mortality worldwide. The most common cause of heart failure is myocardial infarction.… (more)

Subjects/Keywords: direct reprogramming; cardiac regeneration; fibroblast; cardiomyocyte; drug discovery; screening; suora solujen uudelleenohjelmointi; sydämen regeneraatio; fibroblasti; sydänlihassolu; lääkekehitys; lääkeseulonta; Farmakologia; direct reprogramming; cardiac regeneration; fibroblast; cardiomyocyte; drug discovery; screening; suora solujen uudelleenohjelmointi; sydämen regeneraatio; fibroblasti; sydänlihassolu; lääkekehitys; lääkeseulonta

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APA (6th Edition):

Silfvast, S. (2016). The potential of direct cardiac reprogramming in cardiac regeneration. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/172969

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):

Silfvast, Saga. “The potential of direct cardiac reprogramming in cardiac regeneration.” 2016. Thesis, University of Helsinki. Accessed November 24, 2017. http://hdl.handle.net/10138/172969.

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

MLA Handbook (7th Edition):

Silfvast, Saga. “The potential of direct cardiac reprogramming in cardiac regeneration.” 2016. Web. 24 Nov 2017.

Vancouver:

Silfvast S. The potential of direct cardiac reprogramming in cardiac regeneration. [Internet] [Thesis]. University of Helsinki; 2016. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/10138/172969.

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

Council of Science Editors:

Silfvast S. The potential of direct cardiac reprogramming in cardiac regeneration. [Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/172969

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


Kyoto University / 京都大学

9. Katayama, Hokahiro. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製.

Degree: 博士(医学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20605号

医博第4254号

Subjects/Keywords: direct reprogramming; hepatocyte like cells; piggyBac; mesenchymal stem cells; iHeps

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APA (6th Edition):

Katayama, H. (2017). Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/226759 ; http://dx.doi.org/10.14989/doctor.k20605

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):

Katayama, Hokahiro. “Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製.” 2017. Thesis, Kyoto University / 京都大学. Accessed November 24, 2017. http://hdl.handle.net/2433/226759 ; http://dx.doi.org/10.14989/doctor.k20605.

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

MLA Handbook (7th Edition):

Katayama, Hokahiro. “Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製.” 2017. Web. 24 Nov 2017.

Vancouver:

Katayama H. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/2433/226759 ; http://dx.doi.org/10.14989/doctor.k20605.

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

Council of Science Editors:

Katayama H. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. : 非ウィルスベクターであるpiggyBac transposonを用いた挿入遺伝子の遺残のない肝細胞様細胞の作製. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/226759 ; http://dx.doi.org/10.14989/doctor.k20605

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


Kyoto University

10. Katayama, Hokahiro. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon.

Degree: 2017, Kyoto University

Subjects/Keywords: direct reprogramming; hepatocyte like cells; piggyBac; mesenchymal stem cells; iHeps

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

APA (6th Edition):

Katayama, H. (2017). Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/226759

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):

Katayama, Hokahiro. “Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. ” 2017. Thesis, Kyoto University. Accessed November 24, 2017. http://hdl.handle.net/2433/226759.

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

MLA Handbook (7th Edition):

Katayama, Hokahiro. “Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. ” 2017. Web. 24 Nov 2017.

Vancouver:

Katayama H. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. [Internet] [Thesis]. Kyoto University; 2017. [cited 2017 Nov 24]. Available from: http://hdl.handle.net/2433/226759.

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

Council of Science Editors:

Katayama H. Generation of non-viral, transgene-free hepatocyte like cells with piggyBac transposon. [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/226759

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

.