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

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Universiteit Utrecht

1. Penders, A.F. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.

Degree: 2010, Universiteit Utrecht

 Long term complications in diabetes patients are a consequence of the constantly high blood glucose levels, hyperglycemia. In patients with type 1 diabetes hyperglycemia is… (more)

Subjects/Keywords: Geneeskunde; diabetes; hyperglycemia; insulin; beta-cell replacement therapy; stem cell transplantation

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APA (6th Edition):

Penders, A. F. (2010). Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/40071

Chicago Manual of Style (16th Edition):

Penders, A F. “Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.” 2010. Masters Thesis, Universiteit Utrecht. Accessed October 20, 2019. http://dspace.library.uu.nl:8080/handle/1874/40071.

MLA Handbook (7th Edition):

Penders, A F. “Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.” 2010. Web. 20 Oct 2019.

Vancouver:

Penders AF. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2019 Oct 20]. Available from: http://dspace.library.uu.nl:8080/handle/1874/40071.

Council of Science Editors:

Penders AF. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/40071


University of Manchester

2. Saif, Muhammad A. Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation.

Degree: Thesis (M.D.), 2013, University of Manchester

 Lysosomal storage disorders (LSDs) are caused by defective lysosomal degradation of macromolecules resulting in accumulation of substrates in various tissues. This gradually leads to organ… (more)

Subjects/Keywords: Stem cell transplantation; Lysosomal storage disorders; Enzyme replacement therapy

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APA (6th Edition):

Saif, M. A. (2013). Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/immune-responses-in-patients-withlysosomal-storage-disorders-treated-with-enzyme-replacement-therapy-and-haemopoietic-stem-cell-transplantation(e745df5b-44d5-4803-bbe1-db31ad9e6f75).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740242

Chicago Manual of Style (16th Edition):

Saif, Muhammad A. “Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 20, 2019. https://www.research.manchester.ac.uk/portal/en/theses/immune-responses-in-patients-withlysosomal-storage-disorders-treated-with-enzyme-replacement-therapy-and-haemopoietic-stem-cell-transplantation(e745df5b-44d5-4803-bbe1-db31ad9e6f75).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740242.

MLA Handbook (7th Edition):

Saif, Muhammad A. “Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation.” 2013. Web. 20 Oct 2019.

Vancouver:

Saif MA. Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Oct 20]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/immune-responses-in-patients-withlysosomal-storage-disorders-treated-with-enzyme-replacement-therapy-and-haemopoietic-stem-cell-transplantation(e745df5b-44d5-4803-bbe1-db31ad9e6f75).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740242.

Council of Science Editors:

Saif MA. Immune responses in patients with lysosomal storage disorders treated with enzyme replacement therapy and haemopoietic stem cell transplantation. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/immune-responses-in-patients-withlysosomal-storage-disorders-treated-with-enzyme-replacement-therapy-and-haemopoietic-stem-cell-transplantation(e745df5b-44d5-4803-bbe1-db31ad9e6f75).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740242


University of Manchester

3. Saif, Muhammad. Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation.

Degree: 2013, University of Manchester

Lysosomal storage disorders (LSDs) are caused by defective lysosomal degradation of macromolecules resulting in accumulation of substrates in various tissues. This gradually leads to organ… (more)

Subjects/Keywords: Enzyme replacement therapy; Lysosomal storage disorders; Stem cell transplantation

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APA (6th Edition):

Saif, M. (2013). Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:190335

Chicago Manual of Style (16th Edition):

Saif, Muhammad. “Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 20, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:190335.

MLA Handbook (7th Edition):

Saif, Muhammad. “Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation.” 2013. Web. 20 Oct 2019.

Vancouver:

Saif M. Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Oct 20]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:190335.

Council of Science Editors:

Saif M. Immune responses in patients withLysosomal Storage Disorders treated with Enzyme Replacement Therapy and Haemopoietic Stem Cell Transplantation. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:190335


University of Technology, Sydney

4. Gerace, Dario. Gene and stem cell therapy for type 1 diabetes mellitus.

Degree: 2017, University of Technology, Sydney

 Type 1 diabetes (T1D) results from the autoimmune destruction of the insulin-producing pancreatic β-cells. As a result, people with T1D suffer from high blood glucose… (more)

Subjects/Keywords: Cell replacement therapy for diabetes.; Mesenchymal stem cells.; Diabetes.

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APA (6th Edition):

Gerace, D. (2017). Gene and stem cell therapy for type 1 diabetes mellitus. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/120253

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):

Gerace, Dario. “Gene and stem cell therapy for type 1 diabetes mellitus.” 2017. Thesis, University of Technology, Sydney. Accessed October 20, 2019. http://hdl.handle.net/10453/120253.

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

MLA Handbook (7th Edition):

Gerace, Dario. “Gene and stem cell therapy for type 1 diabetes mellitus.” 2017. Web. 20 Oct 2019.

Vancouver:

Gerace D. Gene and stem cell therapy for type 1 diabetes mellitus. [Internet] [Thesis]. University of Technology, Sydney; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10453/120253.

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

Council of Science Editors:

Gerace D. Gene and stem cell therapy for type 1 diabetes mellitus. [Thesis]. University of Technology, Sydney; 2017. Available from: http://hdl.handle.net/10453/120253

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


University of Manitoba

5. Dyck, Scott. Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury.

Degree: Physiology and Pathophysiology, 2015, University of Manitoba

 Populations of oligodendrocytes are susceptible to cell death following spinal cord injury (SCI), which results in axon demyelination. Multipotent resident neural precursor cells (NPCs) and… (more)

Subjects/Keywords: Spinal cord injury; Glial scar; Astrogliosis; CSPGs; Chondroitin sulfate proteoglycans; Cell replacement; Oligodendrocyte replacement; Oligodendrogenesis; Neuroinflammation

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APA (6th Edition):

Dyck, S. (2015). Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/32952

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):

Dyck, Scott. “Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury.” 2015. Thesis, University of Manitoba. Accessed October 20, 2019. http://hdl.handle.net/1993/32952.

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

MLA Handbook (7th Edition):

Dyck, Scott. “Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury.” 2015. Web. 20 Oct 2019.

Vancouver:

Dyck S. Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury. [Internet] [Thesis]. University of Manitoba; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1993/32952.

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

Council of Science Editors:

Dyck S. Elucidating the role and mechanisms of CSPGs in modulating endogenous repair processes in spinal cord injury. [Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/32952

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

6. Moriarty, Niamh. The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease.

Degree: 2018, NUI Galway

 Extensive pre-clinical and clinical assessment has shown that, when transplanted into the Parkinsonian brain, primary dopaminergic neurons can survive, integrate with the host system, produce… (more)

Subjects/Keywords: Parkinson's Disease; Cell Replacement Therapy; Biomaterials; Neurotrophic Support; Medicine; Pharmacology and Therapeutics

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APA (6th Edition):

Moriarty, N. (2018). The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/14576

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):

Moriarty, Niamh. “The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease.” 2018. Thesis, NUI Galway. Accessed October 20, 2019. http://hdl.handle.net/10379/14576.

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

MLA Handbook (7th Edition):

Moriarty, Niamh. “The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease.” 2018. Web. 20 Oct 2019.

Vancouver:

Moriarty N. The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease. [Internet] [Thesis]. NUI Galway; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10379/14576.

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

Council of Science Editors:

Moriarty N. The potential of injectable collagen hydrogels to enhance dopaminergic cell replacement therapies for Parkinson's disease. [Thesis]. NUI Galway; 2018. Available from: http://hdl.handle.net/10379/14576

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

7. Del Greco, Elizabeth. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.

Degree: MS, Biological Sciences, 2017, Dominican University of California

  Recombinant proteins have revolutionized the biomedical industry, providing therapeutics for life-threatening diseases and protein reagents for research applications. BioMarin Pharmaceutical Inc. develops recombinant protein… (more)

Subjects/Keywords: recombinant protein production; protein expression; cell line development; enzyme replacement therapy; lysosomal storage disorder; SP2/0 cell line; Biotechnology

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APA (6th Edition):

Del Greco, E. (2017). Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. (Masters Thesis). Dominican University of California. Retrieved from https://scholar.dominican.edu/masters-theses/283

Chicago Manual of Style (16th Edition):

Del Greco, Elizabeth. “Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.” 2017. Masters Thesis, Dominican University of California. Accessed October 20, 2019. https://scholar.dominican.edu/masters-theses/283.

MLA Handbook (7th Edition):

Del Greco, Elizabeth. “Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications.” 2017. Web. 20 Oct 2019.

Vancouver:

Del Greco E. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. [Internet] [Masters thesis]. Dominican University of California; 2017. [cited 2019 Oct 20]. Available from: https://scholar.dominican.edu/masters-theses/283.

Council of Science Editors:

Del Greco E. Mammalian Cell Line Development Platform for Recombinant Protein Production: Expanding the Protein Expression Toolbox for Research and Drug Discovery Applications. [Masters Thesis]. Dominican University of California; 2017. Available from: https://scholar.dominican.edu/masters-theses/283


University of Delaware

8. Kubaski, Francyne. Diagnosis and therapies for mucopolysaccharidoses .

Degree: 2017, University of Delaware

 Mucopolysaccharidoses (MPS) are lysosomal storage disorders characterized by progressive accumulation of glycosaminoglycans (GAGs) due to deficiency of specific lysosomal enzymes. MPS are classified according to… (more)

Subjects/Keywords: Pure sciences; Biological sciences; Enzyme replacement therapy; Glycosaminoglycans; Hematopoietic stem cell transplantation; Mucopolysaccharidoses; Newborn screening; Tandem mass spectrometry

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APA (6th Edition):

Kubaski, F. (2017). Diagnosis and therapies for mucopolysaccharidoses . (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/21745

Chicago Manual of Style (16th Edition):

Kubaski, Francyne. “Diagnosis and therapies for mucopolysaccharidoses .” 2017. Doctoral Dissertation, University of Delaware. Accessed October 20, 2019. http://udspace.udel.edu/handle/19716/21745.

MLA Handbook (7th Edition):

Kubaski, Francyne. “Diagnosis and therapies for mucopolysaccharidoses .” 2017. Web. 20 Oct 2019.

Vancouver:

Kubaski F. Diagnosis and therapies for mucopolysaccharidoses . [Internet] [Doctoral dissertation]. University of Delaware; 2017. [cited 2019 Oct 20]. Available from: http://udspace.udel.edu/handle/19716/21745.

Council of Science Editors:

Kubaski F. Diagnosis and therapies for mucopolysaccharidoses . [Doctoral Dissertation]. University of Delaware; 2017. Available from: http://udspace.udel.edu/handle/19716/21745


University of California – San Francisco

9. Singla, Veena. Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length.

Degree: Cell Biology, 2010, University of California – San Francisco

 We describe here a resource of mouse embryonic stem (ES) cell lines that contain gene trap insertions capable of post-insertional modification. We demonstrate Floxin technology… (more)

Subjects/Keywords: Biology, Cell; Biology, Genetics; Biology, Molecular; centrosome; embryonic stem cells; gene knockout; gene replacement; Orofaciodigital syndrome type I; primary cilia

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APA (6th Edition):

Singla, V. (2010). Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/8jm9613g

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):

Singla, Veena. “Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length.” 2010. Thesis, University of California – San Francisco. Accessed October 20, 2019. http://www.escholarship.org/uc/item/8jm9613g.

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

MLA Handbook (7th Edition):

Singla, Veena. “Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length.” 2010. Web. 20 Oct 2019.

Vancouver:

Singla V. Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2019 Oct 20]. Available from: http://www.escholarship.org/uc/item/8jm9613g.

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

Council of Science Editors:

Singla V. Application of the Floxin gene targeting technology reveals that Ofd1 controls centriole length. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/8jm9613g

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

10. Edgar, Yuji Egawa. Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料.

Degree: 博士(工学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19009号

工博第4051号

Subjects/Keywords: neural stem cell; collagen; recombinant protein; scaffold; cell replacement therapy

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APA (6th Edition):

Edgar, Y. E. (2015). Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/199333 ; http://dx.doi.org/10.14989/doctor.k19009

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):

Edgar, Yuji Egawa. “Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料.” 2015. Thesis, Kyoto University / 京都大学. Accessed October 20, 2019. http://hdl.handle.net/2433/199333 ; http://dx.doi.org/10.14989/doctor.k19009.

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

MLA Handbook (7th Edition):

Edgar, Yuji Egawa. “Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料.” 2015. Web. 20 Oct 2019.

Vancouver:

Edgar YE. Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2433/199333 ; http://dx.doi.org/10.14989/doctor.k19009.

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

Council of Science Editors:

Edgar YE. Biomaterials for neural cells replacement therapy : 神経細胞の移植治療に用いる生体材料. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/199333 ; http://dx.doi.org/10.14989/doctor.k19009

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

11. Edgar, Yuji Egawa. Biomaterials for neural cells replacement therapy .

Degree: 2015, Kyoto University

Subjects/Keywords: neural stem cell; collagen; recombinant protein; scaffold; cell replacement therapy

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Edgar, Y. E. (2015). Biomaterials for neural cells replacement therapy . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/199333

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):

Edgar, Yuji Egawa. “Biomaterials for neural cells replacement therapy .” 2015. Thesis, Kyoto University. Accessed October 20, 2019. http://hdl.handle.net/2433/199333.

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

MLA Handbook (7th Edition):

Edgar, Yuji Egawa. “Biomaterials for neural cells replacement therapy .” 2015. Web. 20 Oct 2019.

Vancouver:

Edgar YE. Biomaterials for neural cells replacement therapy . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2433/199333.

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

Council of Science Editors:

Edgar YE. Biomaterials for neural cells replacement therapy . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/199333

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


University of Lund

12. Cardoso, Tiago. Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair.

Degree: 2018, University of Lund

 The derivation of dopamine neurons from human embryonic stem cells (hESCs) now offers a promising alternative to fetal tissue for cell replacement therapy (CRT) in… (more)

Subjects/Keywords: Biomedicinsk laboratorievetenskap/teknologi; Rabies-based tracing; Parkinson's disease cell therapy; Cell Replacement Therapy; Human embryonic stem cells; Dopamine neuron; Synaptic integration; circuitry repair

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APA (6th Edition):

Cardoso, T. (2018). Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/024fd2e2-8bc0-4bea-a735-c8467f2b0b0a ; http://portal.research.lu.se/ws/files/53569001/avhTC_v8_copy.pdf

Chicago Manual of Style (16th Edition):

Cardoso, Tiago. “Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair.” 2018. Doctoral Dissertation, University of Lund. Accessed October 20, 2019. http://lup.lub.lu.se/record/024fd2e2-8bc0-4bea-a735-c8467f2b0b0a ; http://portal.research.lu.se/ws/files/53569001/avhTC_v8_copy.pdf.

MLA Handbook (7th Edition):

Cardoso, Tiago. “Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair.” 2018. Web. 20 Oct 2019.

Vancouver:

Cardoso T. Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair. [Internet] [Doctoral dissertation]. University of Lund; 2018. [cited 2019 Oct 20]. Available from: http://lup.lub.lu.se/record/024fd2e2-8bc0-4bea-a735-c8467f2b0b0a ; http://portal.research.lu.se/ws/files/53569001/avhTC_v8_copy.pdf.

Council of Science Editors:

Cardoso T. Cell Replacement Therapy for Parkinson's Disease: Potential for Circuitry Repair. [Doctoral Dissertation]. University of Lund; 2018. Available from: http://lup.lub.lu.se/record/024fd2e2-8bc0-4bea-a735-c8467f2b0b0a ; http://portal.research.lu.se/ws/files/53569001/avhTC_v8_copy.pdf

13. DO DANG VINH. The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth.

Degree: 2009, National University of Singapore

Subjects/Keywords: Delayed tooth replantation; cell sheet; cell dipping; ankylosis; replacement resorption

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APA (6th Edition):

VINH, D. D. (2009). The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/17675

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):

VINH, DO DANG. “The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth.” 2009. Thesis, National University of Singapore. Accessed October 20, 2019. http://scholarbank.nus.edu.sg/handle/10635/17675.

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

MLA Handbook (7th Edition):

VINH, DO DANG. “The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth.” 2009. Web. 20 Oct 2019.

Vancouver:

VINH DD. The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2019 Oct 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/17675.

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

Council of Science Editors:

VINH DD. The Effect of Periodontal Cell Sheet Wrapping and Cell Dipping Co-Culturing Techniques in Delayed Replanted Canine Teeth. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/17675

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

14. Cogliati, Tiziana Paola. Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells.

Degree: 2012, Department Moleculaire Celbiologie, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 This thesis reports the isolation, characterization and allotransplantation in porcine retina of ciliary epithelium (CE)-derived cells, also known as retinal stem cells (RSCs). The self-renewal… (more)

Subjects/Keywords: CE; Cell replacement; Ciliary epithelium; Retina transplantation; Retinal stem cell; Transplantation; CE; Cell replacement; Ciliary epithelium; Retina transplantation; Retinal stem cell; Transplantation

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APA (6th Edition):

Cogliati, T. P. (2012). Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells. (Doctoral Dissertation). Department Moleculaire Celbiologie, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/19856

Chicago Manual of Style (16th Edition):

Cogliati, Tiziana Paola. “Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells.” 2012. Doctoral Dissertation, Department Moleculaire Celbiologie, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed October 20, 2019. http://hdl.handle.net/1887/19856.

MLA Handbook (7th Edition):

Cogliati, Tiziana Paola. “Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells.” 2012. Web. 20 Oct 2019.

Vancouver:

Cogliati TP. Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells. [Internet] [Doctoral dissertation]. Department Moleculaire Celbiologie, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1887/19856.

Council of Science Editors:

Cogliati TP. Study and retina allotransplantation of porcine ciliary epithelium (CE)-derived cells. [Doctoral Dissertation]. Department Moleculaire Celbiologie, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2012. Available from: http://hdl.handle.net/1887/19856


University of Oulu

15. Kellokoski, E. (Eija). Ghrelin and atherosclerosis:human, experimental animal and cell culture studies.

Degree: 2009, University of Oulu

Abstract Atherosclerosis is the major cause of cardiovascular diseases and the leading cause of death globally. Atherosclerosis is a complex, chronic disease characterized by lipid… (more)

Subjects/Keywords: atherosclerosis; cell adhesion molecules; endothelial cells; estrogen replacement therapy; ghrelin; macrophages; mouse model of atherosclerosis; obesity; vaccination; adheesiomolekyylit; ateroskleroosi; eläinmalli; endoteelisolut; estrogeenihoito; greliini; kaulavaltimot; lihavuus; rokote; syöjäsolut

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APA (6th Edition):

Kellokoski, E. (. (2009). Ghrelin and atherosclerosis:human, experimental animal and cell culture studies. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514292590

Chicago Manual of Style (16th Edition):

Kellokoski, E (Eija). “Ghrelin and atherosclerosis:human, experimental animal and cell culture studies.” 2009. Doctoral Dissertation, University of Oulu. Accessed October 20, 2019. http://urn.fi/urn:isbn:9789514292590.

MLA Handbook (7th Edition):

Kellokoski, E (Eija). “Ghrelin and atherosclerosis:human, experimental animal and cell culture studies.” 2009. Web. 20 Oct 2019.

Vancouver:

Kellokoski E(. Ghrelin and atherosclerosis:human, experimental animal and cell culture studies. [Internet] [Doctoral dissertation]. University of Oulu; 2009. [cited 2019 Oct 20]. Available from: http://urn.fi/urn:isbn:9789514292590.

Council of Science Editors:

Kellokoski E(. Ghrelin and atherosclerosis:human, experimental animal and cell culture studies. [Doctoral Dissertation]. University of Oulu; 2009. Available from: http://urn.fi/urn:isbn:9789514292590


Université du Luxembourg

16. Hemmer, Kathrin. IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES.

Degree: 2015, Université du Luxembourg

 The seminal discovery that somatic cells can be reprogrammed into induced pluripotent stem cells (iPSCs) opens new horizons for future personalised cell replacement therapies. This… (more)

Subjects/Keywords: neural stem cells; in vivo analysis; cell replacement therapies; Life sciences :: Multidisciplinary, general & others [F99]; Sciences du vivant :: Multidisciplinaire, généralités & autres [F99]

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APA (6th Edition):

Hemmer, K. (2015). IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES. (Doctoral Dissertation). Université du Luxembourg. Retrieved from http://orbilu.uni.lu/handle/10993/21576

Chicago Manual of Style (16th Edition):

Hemmer, Kathrin. “IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES.” 2015. Doctoral Dissertation, Université du Luxembourg. Accessed October 20, 2019. http://orbilu.uni.lu/handle/10993/21576.

MLA Handbook (7th Edition):

Hemmer, Kathrin. “IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES.” 2015. Web. 20 Oct 2019.

Vancouver:

Hemmer K. IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES. [Internet] [Doctoral dissertation]. Université du Luxembourg; 2015. [cited 2019 Oct 20]. Available from: http://orbilu.uni.lu/handle/10993/21576.

Council of Science Editors:

Hemmer K. IN VIVO ANALYSIS OF STEM CELLS AS A PREREQUISITE FOR AUTOLOGOUS CELL REPLACEMENT THERAPIES. [Doctoral Dissertation]. Université du Luxembourg; 2015. Available from: http://orbilu.uni.lu/handle/10993/21576

17. Somaa, Fahad. Cell based restoration of motor function in rodent models of Parkinson's disease and stroke.

Degree: 2015, University of Melbourne

 Parkinson`s disease (PD) and Ischemic stroke are common disorders in our aging population. Although a large body of basic research highlights the potential of cell(more)

Subjects/Keywords: cell replacement therapy; brain injury; stroke; Parkinson`s disease

…5 1.1.2 Cell replacement therapy for PD… …12 1.2.2 Cell replacement therapy for stroke… …16 1.2.7 Cell therapies for stoke: protection, replacement or both… …Central nervous system CRT - Cell replacement therapy CXCR-4 - Chemokine (C-X-C Motif… …cell replacement therapy for I) Parkinson’s disease and II) stroke. Each of these… 

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APA (6th Edition):

Somaa, F. (2015). Cell based restoration of motor function in rodent models of Parkinson's disease and stroke. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/116122

Chicago Manual of Style (16th Edition):

Somaa, Fahad. “Cell based restoration of motor function in rodent models of Parkinson's disease and stroke.” 2015. Doctoral Dissertation, University of Melbourne. Accessed October 20, 2019. http://hdl.handle.net/11343/116122.

MLA Handbook (7th Edition):

Somaa, Fahad. “Cell based restoration of motor function in rodent models of Parkinson's disease and stroke.” 2015. Web. 20 Oct 2019.

Vancouver:

Somaa F. Cell based restoration of motor function in rodent models of Parkinson's disease and stroke. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/11343/116122.

Council of Science Editors:

Somaa F. Cell based restoration of motor function in rodent models of Parkinson's disease and stroke. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/116122

18. Callahan, Justin. Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade.

Degree: 2013, University of South Florida

 When foundations are designed on weak clay layers, it is a common practice to modify the subgrade by installing stone columns. Currently used methods for… (more)

Subjects/Keywords: Flexible Foundation; Ground Modification; Replacement Ratio; Unit Cell; Civil Engineering

…settlement reduction. Figure 1 Diagram of a Unit Cell 1 Several methods are available to… …uniform load as well as a rigid 2 foundation on a single unit cell (Figure 1) which… …and the concept of a unit cell with respect to the performance of a stone-column modified… …stone columns, a mixture of the hardening soil model and the unit-cell stone 9 column… …loading or unloading. 2.2.2 Stone-Column Unit Cell When a stone column is installed in the… 

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APA (6th Edition):

Callahan, J. (2013). Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4450

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):

Callahan, Justin. “Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade.” 2013. Thesis, University of South Florida. Accessed October 20, 2019. https://scholarcommons.usf.edu/etd/4450.

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

MLA Handbook (7th Edition):

Callahan, Justin. “Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade.” 2013. Web. 20 Oct 2019.

Vancouver:

Callahan J. Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade. [Internet] [Thesis]. University of South Florida; 2013. [cited 2019 Oct 20]. Available from: https://scholarcommons.usf.edu/etd/4450.

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

Council of Science Editors:

Callahan J. Prediction of the Performance of a Flexible Footing on a Stone-Column Modified Subgrade. [Thesis]. University of South Florida; 2013. Available from: https://scholarcommons.usf.edu/etd/4450

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


University of Lund

19. Kurowska, Zuzanna. Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons.

Degree: 2012, University of Lund

 Parkinson’s disease (PD) is currently the second most common neurodegenerative disorder (after Alzheimer’s disease). PD is diagnosed on its motor symptoms, which include akinesia, bradykinesia,… (more)

Subjects/Keywords: Neurovetenskaper; LUHMES cells; substantia nigra pars compacta; microarray; heparan sulphate 3-O-sulfotransferase; neurocan; midbrain dopaminergic neurons; grafting; embryonic stem cells; proteoglycans; glycosaminoglycans; Nogo-A; cell replacement therapy; Parkinson’s disease

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APA (6th Edition):

Kurowska, Z. (2012). Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/3044164 ; http://portal.research.lu.se/ws/files/3933912/3044184.pdf

Chicago Manual of Style (16th Edition):

Kurowska, Zuzanna. “Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons.” 2012. Doctoral Dissertation, University of Lund. Accessed October 20, 2019. http://lup.lub.lu.se/record/3044164 ; http://portal.research.lu.se/ws/files/3933912/3044184.pdf.

MLA Handbook (7th Edition):

Kurowska, Zuzanna. “Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons.” 2012. Web. 20 Oct 2019.

Vancouver:

Kurowska Z. Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons. [Internet] [Doctoral dissertation]. University of Lund; 2012. [cited 2019 Oct 20]. Available from: http://lup.lub.lu.se/record/3044164 ; http://portal.research.lu.se/ws/files/3933912/3044184.pdf.

Council of Science Editors:

Kurowska Z. Towards cell replacement therapy in Parkinson’s disease. Proteoglycans and Nogo-A as modulators of axonal growth in midbrain dopaminergic neurons. [Doctoral Dissertation]. University of Lund; 2012. Available from: http://lup.lub.lu.se/record/3044164 ; http://portal.research.lu.se/ws/files/3933912/3044184.pdf


University of Western Ontario

20. Wong, Michael Ka Chun. Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro.

Degree: 2015, University of Western Ontario

 Nicotine exposure during pregnancy leads to adverse health outcomes, including compromised placental development. Although the molecular mechanisms remain elusive, recent studies identified that endoplasmic reticulum… (more)

Subjects/Keywords: ER stress; unfolded protein response; PERK; TUDCA; nicotine replacement therapy; Biochemical Phenomena, Metabolism, and Nutrition; Biological Phenomena, Cell Phenomena, and Immunity; Developmental Biology; Laboratory and Basic Science Research; Medical Cell Biology; Medical Molecular Biology; Medical Physiology; Medical Toxicology; Reproductive and Urinary Physiology

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APA (6th Edition):

Wong, M. K. C. (2015). Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2997

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):

Wong, Michael Ka Chun. “Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro.” 2015. Thesis, University of Western Ontario. Accessed October 20, 2019. https://ir.lib.uwo.ca/etd/2997.

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

MLA Handbook (7th Edition):

Wong, Michael Ka Chun. “Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro.” 2015. Web. 20 Oct 2019.

Vancouver:

Wong MKC. Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2019 Oct 20]. Available from: https://ir.lib.uwo.ca/etd/2997.

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

Council of Science Editors:

Wong MKC. Characterization of the nicotine-induced endoplasmic reticulum stress response in the rat placenta in vivo and in vitro. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/2997

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


McMaster University

21. Gleave, Jacqueline. Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease.

Degree: PhD, 2009, McMaster University

Cell therapy for Parkinson's disease will greatly benefit from progress in methods aimed at visualizing the dopamine system and cell replacement techniques. Currently, cell(more)

Subjects/Keywords: Cell Therapy; Parkinson's; Disease; dopamine system; cell replacement; transplantation; NSPCs; Neural stem/progenitor cells; technetium-99m; cells; photon; SPECT; DNA

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APA (6th Edition):

Gleave, J. (2009). Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/17291

Chicago Manual of Style (16th Edition):

Gleave, Jacqueline. “Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease.” 2009. Doctoral Dissertation, McMaster University. Accessed October 20, 2019. http://hdl.handle.net/11375/17291.

MLA Handbook (7th Edition):

Gleave, Jacqueline. “Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease.” 2009. Web. 20 Oct 2019.

Vancouver:

Gleave J. Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease. [Internet] [Doctoral dissertation]. McMaster University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/11375/17291.

Council of Science Editors:

Gleave J. Correlative Spect Imaging Of Neural Stem/Progenitor Cell Transplants In A Rat Model Of Parkinson's Disease. [Doctoral Dissertation]. McMaster University; 2009. Available from: http://hdl.handle.net/11375/17291

22. Mourtzi, Theodora. Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20.

Degree: 2019, University of Patras; Πανεπιστήμιο Πατρών

 Neurotrophic factors are among the most promising therapeutic candidates against Parkinson's disease (PD), but their clinical use is limited due to their inability to cross… (more)

Subjects/Keywords: Νευρογένεση στον ενήλικο; Νόσος του Parkinson; Μυς "weaver"; Θεραπεία κυτταρικής αποκατάστασης; Μέλαινα ουσία; BDNF; Μικρονευροτροφίνες; ΒΝΝ-20; Νευροπροστασία; Ενήλικη νευρογένεση; Νευροτροφικοί παράγοντες; Νευροτροφίνες; Adult neurogenesis; Parkinson's disease; "Weaver" mouse; Substantia nigra; Cell replacement therapy; Neuroprotection; Microneurotrophins; BNN-20; BDNF; Neurotrophic factors; Neurotrophins

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APA (6th Edition):

Mourtzi, T. (2019). Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/45367

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):

Mourtzi, Theodora. “Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20.” 2019. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed October 20, 2019. http://hdl.handle.net/10442/hedi/45367.

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

MLA Handbook (7th Edition):

Mourtzi, Theodora. “Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20.” 2019. Web. 20 Oct 2019.

Vancouver:

Mourtzi T. Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2019. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10442/hedi/45367.

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

Council of Science Editors:

Mourtzi T. Διερεύνηση της επαγωγής ενήλικης ντοπαμινεργικής νευρογένεσης στη μέλαινα ουσία του παρκινσονικού μοντέλου μυός "Weaver", υπό τη χρόνια χορήγηση της μικρομοριακής νευροτροφίνης BNN-20. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2019. Available from: http://hdl.handle.net/10442/hedi/45367

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


Erasmus University Rotterdam

23. MacKenzie, Katherine. Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden.

Degree: 2019, Erasmus University Rotterdam

 textabstractThe work of this thesis investigates the development of, and treatment options for, Hirschsprung disease (HSCR). We explore the missing heritability that is seen in… (more)

Subjects/Keywords: Hirschsprung disease; enteric nervous system; neural crest; somatic mutations; copy number variation; Goldberg-Shprintzen syndrome; KIF1BP; missense variations; cell replacement therapy

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APA (6th Edition):

MacKenzie, K. (2019). Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/116709

Chicago Manual of Style (16th Edition):

MacKenzie, Katherine. “Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden.” 2019. Doctoral Dissertation, Erasmus University Rotterdam. Accessed October 20, 2019. http://hdl.handle.net/1765/116709.

MLA Handbook (7th Edition):

MacKenzie, Katherine. “Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden.” 2019. Web. 20 Oct 2019.

Vancouver:

MacKenzie K. Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2019. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1765/116709.

Council of Science Editors:

MacKenzie K. Hirschsprung Disease: development & treatment avenues: De ziekte van Hirschsprung: ontwikkeling & behandelingsmogelijkheden. [Doctoral Dissertation]. Erasmus University Rotterdam; 2019. Available from: http://hdl.handle.net/1765/116709


University of Lund

24. Andersson, Elin. Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2.

Degree: 2005, University of Lund

 Parkinsons disease (PD) is a neurodegenerative disorder where dopaminergic neurons of the substantia nigra (SNc) in the mesencephalon are progressively eliminated. The ensuing loss of… (more)

Subjects/Keywords: Medicinska grundvetenskaper; Medicine (human and vertebrates); Medicin (människa och djur); cell replacement; Parkinson?s; dopamine; neuronal specification; development; mesencephalon; TH; neuronal differentiation; proneural genes; transcription factors; bHLH; neurospheres; stem cell; progenitor cell

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APA (6th Edition):

Andersson, E. (2005). Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/545931 ; http://portal.research.lu.se/ws/files/4382510/545933.pdf

Chicago Manual of Style (16th Edition):

Andersson, Elin. “Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2.” 2005. Doctoral Dissertation, University of Lund. Accessed October 20, 2019. http://lup.lub.lu.se/record/545931 ; http://portal.research.lu.se/ws/files/4382510/545933.pdf.

MLA Handbook (7th Edition):

Andersson, Elin. “Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2.” 2005. Web. 20 Oct 2019.

Vancouver:

Andersson E. Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2. [Internet] [Doctoral dissertation]. University of Lund; 2005. [cited 2019 Oct 20]. Available from: http://lup.lub.lu.se/record/545931 ; http://portal.research.lu.se/ws/files/4382510/545933.pdf.

Council of Science Editors:

Andersson E. Generation of midbrain dopaminergic neurons in vivo and in vitro: the role of Neurogenin2. [Doctoral Dissertation]. University of Lund; 2005. Available from: http://lup.lub.lu.se/record/545931 ; http://portal.research.lu.se/ws/files/4382510/545933.pdf

25. Zhang, Chuyuan. Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon.

Degree: 2013, University of Saskatchewan

 A whole-cell DHA-rich algal product (A-DHA, provided by Evonik Industries) that is rich in DHA (125 mg DHA/g dry matter) is a possible replacement for… (more)

Subjects/Keywords: Whole-cell DHA-rich algae (A-DHA); Fish oil replacement; Digestibility; Growth performance; Fatty acid retention; Rainbow trout; Atlantic salmon

…24 3. Determination of the Chemical Composition and Digestibility of a Whole-Cell DHA… …41 4. Effects of Dietary Fish Oil Replacement with Canola Oil and DHA-Rich Algal… …OF ABBREVIATIONS ADC = Apparent Digestibility Coefficient A-DHA = Whole-Cell DHA-Rich… …replacement with vegetable oils, either partially or totally, in fish feeds results in significantly… …component: carotenoids and vitamins, and the lipids are protected by algal cell wall (Patil… 

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APA (6th Edition):

Zhang, C. (2013). Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-03-948

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):

Zhang, Chuyuan. “Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon.” 2013. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2013-03-948.

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

MLA Handbook (7th Edition):

Zhang, Chuyuan. “Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon.” 2013. Web. 20 Oct 2019.

Vancouver:

Zhang C. Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2013-03-948.

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

Council of Science Editors:

Zhang C. Determination of the Digestibility of a Whole-Cell DHA-Rich Algal Product and Its Effect on the Lipid Composition of Rainbow Trout and Atlantic Salmon. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-03-948

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


Washington University in St. Louis

26. Au, Leslie. Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications.

Degree: PhD, Biomedical Engineering, 2009, Washington University in St. Louis

 This research investigated the synthesis and optical properties of Au nanostructures with an aim to use them as imaging agents and photothermal transducers for the… (more)

Subjects/Keywords: Engineering; Biomedical; Chemistry; General; Biology; Cell; Galvanic Replacement Reaction; Gold Nanocages; Gold Nanostructures; Localized Surface Plasmon Resonance; Optical Imaging Agent; Photothermal Therapy

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

APA (6th Edition):

Au, L. (2009). Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/881

Chicago Manual of Style (16th Edition):

Au, Leslie. “Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications.” 2009. Doctoral Dissertation, Washington University in St. Louis. Accessed October 20, 2019. https://openscholarship.wustl.edu/etd/881.

MLA Handbook (7th Edition):

Au, Leslie. “Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications.” 2009. Web. 20 Oct 2019.

Vancouver:

Au L. Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2009. [cited 2019 Oct 20]. Available from: https://openscholarship.wustl.edu/etd/881.

Council of Science Editors:

Au L. Engineering the Optical Properties of Gold Nanostructures for Biomedical Applications. [Doctoral Dissertation]. Washington University in St. Louis; 2009. Available from: https://openscholarship.wustl.edu/etd/881


Brno University of Technology

27. Tatíček, Vojtěch. Konstrukce transportního vozíku s robotem nebo nosičem palet .

Degree: 2019, Brno University of Technology

 Cílem práce bylo navrhnout konstrukci dopravního zařízení pod průmyslový robot, nosič palet či jiné zařízení. Tímto dopravním zařízením lze pohybovat v jedné ose na pevně… (more)

Subjects/Keywords: Manipulace s obrobky; manipulace s nástroji; lineární výrobní systém; dopravní zařízení pro robot; transportní zařízení pro robot; dopravní zařízení pro nosič palet; automatická výměna obrobků; lineární výrobní buňka; rozšíření pracovního prostoru robotu; sedmá osa robotu; přídavná pohybová osa robotu; automatizace výměny obrobků ve výrobní buňce; bezobslužný provoz výrobní buňky.; Workpiece handling; workpiece manipulation; tool handling; tool manipulation; linear manufacturing system; robot conveying equipment; transport equipment for robot; transport equipment for pallet holder; automatic workpiece replacement; linear production cell; robot workspace extension; seventh robot axis; additional robot motion axis; automation of workpiece exchange in manufacturing cell; unattended production cell operation.

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

APA (6th Edition):

Tatíček, V. (2019). Konstrukce transportního vozíku s robotem nebo nosičem palet . (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/179404

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):

Tatíček, Vojtěch. “Konstrukce transportního vozíku s robotem nebo nosičem palet .” 2019. Thesis, Brno University of Technology. Accessed October 20, 2019. http://hdl.handle.net/11012/179404.

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

MLA Handbook (7th Edition):

Tatíček, Vojtěch. “Konstrukce transportního vozíku s robotem nebo nosičem palet .” 2019. Web. 20 Oct 2019.

Vancouver:

Tatíček V. Konstrukce transportního vozíku s robotem nebo nosičem palet . [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/11012/179404.

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

Council of Science Editors:

Tatíček V. Konstrukce transportního vozíku s robotem nebo nosičem palet . [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/179404

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


University of Debrecen

28. Agyare, Eunice. Neuronal Differentiation of mouse embryonic stem cells .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 The major goal of this study is to differentiate mouse ESCs into neural progenitor cells (NPCs) and investigate the inducibility of a reporter transgene during… (more)

Subjects/Keywords: BMP Bone Morphogenetic Proteins; bFGF Basic Fibroblast Growth Factor; CNS Central Nervous System; DOX Doxycycline; DMEM Dulbecco's Modified Eagle Medium; DMSO Dimethyl Sulfoxide; EGFP Green Fluorescence Protein; ESCs Embryonic Stem cells; FACS Fluorescence Activated Cell Sorting; FBS Fetal Bovine Serum; FGF Fibroblast Growth Factor; GFAP Glial Fibrillary Acidic Protein; G418 Genetic; HSCs Hematopoietic Stem Cells; hESCs Human Embryonic Stem Cells; ICM Inner Cell Mass; iPSCs Induced Pluripotent Stem Cells; IKMC International Knockout Mouse Consortium; KSR Knockout Serum Replacement; LIF Leukemia Inhibitory Factor; mESCs Mouse Embryonic Stem Cells; MEF Mouse Embryonic Fibroblast; N2B27 Neurobasal plus B27 supplement; NPCs Neuro Progenitor Cells; PBS Phosphate Buffered Saline; Q- PCR Quantitative Polymerase Chain Reaction; RGPs Radial Glial Progenitor; TA Transactivator

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

APA (6th Edition):

Agyare, E. (n.d.). Neuronal Differentiation of mouse embryonic stem cells . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/269914

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Agyare, Eunice. “Neuronal Differentiation of mouse embryonic stem cells .” Thesis, University of Debrecen. Accessed October 20, 2019. http://hdl.handle.net/2437/269914.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Agyare, Eunice. “Neuronal Differentiation of mouse embryonic stem cells .” Web. 20 Oct 2019.

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

Vancouver:

Agyare E. Neuronal Differentiation of mouse embryonic stem cells . [Internet] [Thesis]. University of Debrecen; [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2437/269914.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Agyare E. Neuronal Differentiation of mouse embryonic stem cells . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/269914

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

.