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You searched for +publisher:"California State University – Sacramento" +contributor:("Carter, Rosalee C."). Showing records 1 – 23 of 23 total matches.

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California State University – Sacramento

1. Olney, Laura. Targeted integrin activation on human mesenchymal stem cells.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Human mesenchymal stem cells (MSCs) have the capacity for self-renewal, immune evasion and suppression, and differentiation. These characteristics have brought MSCs to the forefront of… (more)

Subjects/Keywords: LLP2A; LXW7; Differentiation; Bone marrow

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APA (6th Edition):

Olney, L. (2015). Targeted integrin activation on human mesenchymal stem cells. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139353

Chicago Manual of Style (16th Edition):

Olney, Laura. “Targeted integrin activation on human mesenchymal stem cells.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/139353.

MLA Handbook (7th Edition):

Olney, Laura. “Targeted integrin activation on human mesenchymal stem cells.” 2015. Web. 19 Oct 2020.

Vancouver:

Olney L. Targeted integrin activation on human mesenchymal stem cells. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/139353.

Council of Science Editors:

Olney L. Targeted integrin activation on human mesenchymal stem cells. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139353


California State University – Sacramento

2. Ryzhuk, Volodymyr. Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Mesenchymal stem cell (MSC) based therapy has been suggested for a wide range of tissue damage, from spinal cord injuries to diabetes. Many of the… (more)

Subjects/Keywords: Stem cell; Biomaterials; Hydrogels

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APA (6th Edition):

Ryzhuk, V. (2015). Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/138780

Chicago Manual of Style (16th Edition):

Ryzhuk, Volodymyr. “Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/138780.

MLA Handbook (7th Edition):

Ryzhuk, Volodymyr. “Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications.” 2015. Web. 19 Oct 2020.

Vancouver:

Ryzhuk V. Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/138780.

Council of Science Editors:

Ryzhuk V. Optimizing delivery vehicle for human placenta derived mesenchymal stem cells for regenerative medicine applications. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/138780


California State University – Sacramento

3. Meyer, Nathaniel Paul. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.

Degree: MA, Biology (Stem Cell, 2015, California State University – Sacramento

 The histone variant protein H3.3 plays necessary roles in embryogenesis, spermatogenesis, and transcription.H3.3 is encoded for by two genes: H3F3A and H3F3B in humans and… (more)

Subjects/Keywords: H3f3a; H3.3; Neural stem cells; Histone proteins

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APA (6th Edition):

Meyer, N. P. (2015). Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139193

Chicago Manual of Style (16th Edition):

Meyer, Nathaniel Paul. “Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/139193.

MLA Handbook (7th Edition):

Meyer, Nathaniel Paul. “Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.” 2015. Web. 19 Oct 2020.

Vancouver:

Meyer NP. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/139193.

Council of Science Editors:

Meyer NP. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139193


California State University – Sacramento

4. Copaciu, Raul S. Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Dysfunction of the heart???s physiological pacemaker, the sinoatrial node (SAN), contributes to the onset of cardiac arrhythmias. Conventional treatment is accomplished by implantation of an… (more)

Subjects/Keywords: Heart; Isl1; Differentiation; Arrhythmia; SK channel; EBIO; Sinoatrial node

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APA (6th Edition):

Copaciu, R. S. (2015). Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139374

Chicago Manual of Style (16th Edition):

Copaciu, Raul S. “Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/139374.

MLA Handbook (7th Edition):

Copaciu, Raul S. “Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells.” 2015. Web. 19 Oct 2020.

Vancouver:

Copaciu RS. Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/139374.

Council of Science Editors:

Copaciu RS. Induction of an augmented pacemaking cardiomyocyte population from human induced pluripotent stem cell-derived cardiac progenitor cells. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139374


California State University – Sacramento

5. Knudson, Alisha. miRNA analysis of hMSC-derived exosomes compared across isolation techniques.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Exosomes are a class of nano-sized extracellular vesicles, typically 40-150 nm in diameter, that are released from endocytic multivesicular bodies. Exosomal contents are unique to… (more)

Subjects/Keywords: microRNA; Mesenchymal stem cells; Extracellular vesicles; Ultracentrifugation

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APA (6th Edition):

Knudson, A. (2015). miRNA analysis of hMSC-derived exosomes compared across isolation techniques. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139409

Chicago Manual of Style (16th Edition):

Knudson, Alisha. “miRNA analysis of hMSC-derived exosomes compared across isolation techniques.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/139409.

MLA Handbook (7th Edition):

Knudson, Alisha. “miRNA analysis of hMSC-derived exosomes compared across isolation techniques.” 2015. Web. 19 Oct 2020.

Vancouver:

Knudson A. miRNA analysis of hMSC-derived exosomes compared across isolation techniques. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/139409.

Council of Science Editors:

Knudson A. miRNA analysis of hMSC-derived exosomes compared across isolation techniques. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139409


California State University – Sacramento

6. Croteau, Christopher. Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development.

Degree: MA, Biological Science, 2016, California State University – Sacramento

 Canavan disease (CD) is an autosomal recessive neurodegenerative disorder that begins in infancy and causes death by early childhood. CD is typified by a loss… (more)

Subjects/Keywords: Canavan disease; Central nervous system myelination; Oligodendrocytes

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APA (6th Edition):

Croteau, C. (2016). Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171323

Chicago Manual of Style (16th Edition):

Croteau, Christopher. “Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171323.

MLA Handbook (7th Edition):

Croteau, Christopher. “Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development.” 2016. Web. 19 Oct 2020.

Vancouver:

Croteau C. Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171323.

Council of Science Editors:

Croteau C. Inducing ASPA expression in astroglia and the role of SOX2 in glial cell development. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171323


California State University – Sacramento

7. Cicchetto, Andrew C. Genetically modified multipotent stromal cells for the treatment of osteoarthritis.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Osteoarthritis (OA) is a degenerative joint disease estimated to affect 630 million people worldwide. OA is characterized by the progressive loss of articular cartilage, damage… (more)

Subjects/Keywords: Interleukin-10; Gene Therapy; Cell Therapy; Lentivirus

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APA (6th Edition):

Cicchetto, A. C. (2016). Genetically modified multipotent stromal cells for the treatment of osteoarthritis. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171158

Chicago Manual of Style (16th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171158.

MLA Handbook (7th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Web. 19 Oct 2020.

Vancouver:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171158.

Council of Science Editors:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171158


California State University – Sacramento

8. Clark, Kaitlin. Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Degenerative lesions of the equine foot and hoof, which include laminitis, navicular and deep digital flexor tendon (DDFT) injuries, are common debilitating diseases in horses.… (more)

Subjects/Keywords: Equine adipose stem cells; Biomarkers; Degenerative disease; Pathology; Therapy; Veterinary medicine

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APA (6th Edition):

Clark, K. (2016). Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171177

Chicago Manual of Style (16th Edition):

Clark, Kaitlin. “Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171177.

MLA Handbook (7th Edition):

Clark, Kaitlin. “Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy.” 2016. Web. 19 Oct 2020.

Vancouver:

Clark K. Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171177.

Council of Science Editors:

Clark K. Identification of blood biomarkers and monitoring of degenerative disorders of the equine foot in response to autologous mesenchymal stem cell therapy. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171177


California State University – Sacramento

9. Walker, Scott. Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Spina bifida is a congenital anomaly that is caused by incomplete closure of the neural tube before birth and it affects as many as 1… (more)

Subjects/Keywords: Mesenchymal stem cell; Secretome; P-MSC; AF-MSC

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APA (6th Edition):

Walker, S. (2016). Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171262

Chicago Manual of Style (16th Edition):

Walker, Scott. “Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171262.

MLA Handbook (7th Edition):

Walker, Scott. “Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection.” 2016. Web. 19 Oct 2020.

Vancouver:

Walker S. Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171262.

Council of Science Editors:

Walker S. Comparison of same donor placental and amniotic fluid mesenchymal stem cells in secretion, exosomes and neuroprotection. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171262


California State University – Sacramento

10. Wada, Christina Hoang Anh. Investigating Procr as an alternative breast cancer stem cell surface marker to CD44.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Breast cancer has one of the highest mortality rates among cancers afflicting women. Despite six decades of cancer treatment using chemotherapeutic drugs and hormonal and… (more)

Subjects/Keywords: CD201; CD49f; CD29; CD24

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APA (6th Edition):

Wada, C. H. A. (2016). Investigating Procr as an alternative breast cancer stem cell surface marker to CD44. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171250

Chicago Manual of Style (16th Edition):

Wada, Christina Hoang Anh. “Investigating Procr as an alternative breast cancer stem cell surface marker to CD44.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171250.

MLA Handbook (7th Edition):

Wada, Christina Hoang Anh. “Investigating Procr as an alternative breast cancer stem cell surface marker to CD44.” 2016. Web. 19 Oct 2020.

Vancouver:

Wada CHA. Investigating Procr as an alternative breast cancer stem cell surface marker to CD44. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171250.

Council of Science Editors:

Wada CHA. Investigating Procr as an alternative breast cancer stem cell surface marker to CD44. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171250


California State University – Sacramento

11. Martinez, Joshua D. Buccal biopsies as an epithelial cell source for tracheal tissue engineering.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Human tracheal disorders severely compromise a patient???s quality of life and can be life threatening. Ex vivo tracheal reconstruction using biological or a bioartificial composite… (more)

Subjects/Keywords: Tissue engineering; Epithelial cell culture; Translational research

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APA (6th Edition):

Martinez, J. D. (2016). Buccal biopsies as an epithelial cell source for tracheal tissue engineering. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171140

Chicago Manual of Style (16th Edition):

Martinez, Joshua D. “Buccal biopsies as an epithelial cell source for tracheal tissue engineering.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/171140.

MLA Handbook (7th Edition):

Martinez, Joshua D. “Buccal biopsies as an epithelial cell source for tracheal tissue engineering.” 2016. Web. 19 Oct 2020.

Vancouver:

Martinez JD. Buccal biopsies as an epithelial cell source for tracheal tissue engineering. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/171140.

Council of Science Editors:

Martinez JD. Buccal biopsies as an epithelial cell source for tracheal tissue engineering. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171140


California State University – Sacramento

12. Fox, Hannah. Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Diabetes, a disease increasingly affecting the U.S. population, puts patients at risk for chronic wound development. Chronic wounds respond poorly to available treatments and burden… (more)

Subjects/Keywords: Integrin; Alpha 4; MSC; LLP2A; Peptide; Wound healing; Mesenchymal stem cell; Bone

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APA (6th Edition):

Fox, H. (2016). Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/179903

Chicago Manual of Style (16th Edition):

Fox, Hannah. “Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/179903.

MLA Handbook (7th Edition):

Fox, Hannah. “Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A.” 2016. Web. 19 Oct 2020.

Vancouver:

Fox H. Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/179903.

Council of Science Editors:

Fox H. Evaluation of mesenchymal stem cell response to [alpha]4 integrin specific peptide, LLP2A. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/179903


California State University – Sacramento

13. Sturgill, Ian. Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Of all of the types of primary brain tumors, glioblastoma multiforme (GBM) is both the most common and most aggressive. As a direct result of… (more)

Subjects/Keywords: Cancer stem cell; Immunotherapy; Glioblastoma

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APA (6th Edition):

Sturgill, I. (2017). Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190572

Chicago Manual of Style (16th Edition):

Sturgill, Ian. “Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/190572.

MLA Handbook (7th Edition):

Sturgill, Ian. “Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity.” 2017. Web. 19 Oct 2020.

Vancouver:

Sturgill I. Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/190572.

Council of Science Editors:

Sturgill I. Combined impact of the proteasome inhibitor bortezomib and ex vivo-activated natural killer cells on human glioma stem cell targeting and cytotoxicity. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190572


California State University – Sacramento

14. Hammerstad, Bruce. Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Autism Spectrum Disorder (ASD) affects an estimated 21.7 million individuals globally with an estimated annual cost to the United States of $35 billion. Manifestations of… (more)

Subjects/Keywords: Autism; Developmental disorders; Neurons

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APA (6th Edition):

Hammerstad, B. (2017). Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190543

Chicago Manual of Style (16th Edition):

Hammerstad, Bruce. “Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/190543.

MLA Handbook (7th Edition):

Hammerstad, Bruce. “Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid.” 2017. Web. 19 Oct 2020.

Vancouver:

Hammerstad B. Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/190543.

Council of Science Editors:

Hammerstad B. Quantification of cortical parvalbumin, calbindin, and calretinin expressing interneurons in rats after treatment with valproic acid. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190543


California State University – Sacramento

15. Aguilar, Vanessa J. Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Pediatric lung disorders are a leading cause of illness and death in infants and children. These diseases are poorly understood and there are few treatment… (more)

Subjects/Keywords: Pediatrics; Prematurity; Lung disease; Surfactant protein b deficiency; hiPSC

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APA (6th Edition):

Aguilar, V. J. (2017). Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190746

Chicago Manual of Style (16th Edition):

Aguilar, Vanessa J. “Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/190746.

MLA Handbook (7th Edition):

Aguilar, Vanessa J. “Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells.” 2017. Web. 19 Oct 2020.

Vancouver:

Aguilar VJ. Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/190746.

Council of Science Editors:

Aguilar VJ. Optimizing differentiation of alveolar epithelial cells from human induced pluripotent stem cells. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190746


California State University – Sacramento

16. Cortez-Toledo, Elizabeth Jasmin. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Hemophilia A (HA) is a genetic disorder resulting from deficient levels of the coagulation protein factor VIII. HA is inherited through an X-linked recessive pattern… (more)

Subjects/Keywords: Stem cells; Factor VIII; Hemophilia A; Liver organoids

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APA (6th Edition):

Cortez-Toledo, E. J. (2017). Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190683

Chicago Manual of Style (16th Edition):

Cortez-Toledo, Elizabeth Jasmin. “Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/190683.

MLA Handbook (7th Edition):

Cortez-Toledo, Elizabeth Jasmin. “Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII.” 2017. Web. 19 Oct 2020.

Vancouver:

Cortez-Toledo EJ. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/190683.

Council of Science Editors:

Cortez-Toledo EJ. Generation of liver organoids using IPSC derived hepatocyte and endothelial cells for persistent secretion of factor VIII. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190683


California State University – Sacramento

17. Palka, Jessica. Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients.

Degree: MA, Biological Science (Stem Cell, 2017, California State University – Sacramento

 Craniosynostosis is a condition caused by premature fusion of one or more cranial sutures during fetal development. Inappropriate suture fusion can lead to abnormal skull… (more)

Subjects/Keywords: Mesenchymal stem cells; Craniosynostosis; Suture; Nonsyndromic craniosynostosis; Alizarin red assay; ALP assay; qPCR; Bone; Fused suture; Open suture

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APA (6th Edition):

Palka, J. (2017). Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/190680

Chicago Manual of Style (16th Edition):

Palka, Jessica. “Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients.” 2017. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/190680.

MLA Handbook (7th Edition):

Palka, Jessica. “Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients.” 2017. Web. 19 Oct 2020.

Vancouver:

Palka J. Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients. [Internet] [Masters thesis]. California State University – Sacramento; 2017. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/190680.

Council of Science Editors:

Palka J. Molecular analysis of mesenchymal stem cells from prematurely closed and open sutures from nonsyndromic single suture craniosynostosis patients. [Masters Thesis]. California State University – Sacramento; 2017. Available from: http://hdl.handle.net/10211.3/190680

18. Adams, Andrew E. The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Diabetic foot ulcers (DFU) are chronic, non-healing wounds on the feet of diabetic individuals and are the leading cause of non-traumatic amputations in the United… (more)

Subjects/Keywords: Mesenchymal stem cells; Beta-adrenergic receptor; Beta-blocker; Chronic wounds; Diabetes; Diabetic foot ulcer; Timolol

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APA (6th Edition):

Adams, A. E. (2015). The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/140049

Chicago Manual of Style (16th Edition):

Adams, Andrew E. “The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/140049.

MLA Handbook (7th Edition):

Adams, Andrew E. “The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model.” 2015. Web. 19 Oct 2020.

Vancouver:

Adams AE. The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/140049.

Council of Science Editors:

Adams AE. The safety and efficacy of timolol treated mesenchymal stem cells in a scaffold on an in vivo diabetic wound model. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/140049

19. Dighe, Pratiksha Atul. Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 Neurodevelopmental disorders, in general, and particularly autism and schizophrenia are associated with altered brain organization and structure resulting as a consequence of aberrant neurogenesis. Embryonic… (more)

Subjects/Keywords: Fetal brain development; Neurodevelopment; Embyonic neurogenesis; Microglia and their interaction with neural precursor cells

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APA (6th Edition):

Dighe, P. A. (2015). Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139788

Chicago Manual of Style (16th Edition):

Dighe, Pratiksha Atul. “Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/139788.

MLA Handbook (7th Edition):

Dighe, Pratiksha Atul. “Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?.” 2015. Web. 19 Oct 2020.

Vancouver:

Dighe PA. Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/139788.

Council of Science Editors:

Dighe PA. Fetal microglia aid in defining the proliferative zones of neural stem cells in the developing cerebral cortex?. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139788

20. Howard, Katie. Revascularization of acellular bladder grafts.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 The urinary bladder is a hollow organ comprised of multiple tissue layers that serve to store and void urine from the body. There are a… (more)

Subjects/Keywords: Tissue engineering; Progenitor cell; Blood vessel; Neuropathic bladder; Urologic research

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APA (6th Edition):

Howard, K. (2015). Revascularization of acellular bladder grafts. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/140048

Chicago Manual of Style (16th Edition):

Howard, Katie. “Revascularization of acellular bladder grafts.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/140048.

MLA Handbook (7th Edition):

Howard, Katie. “Revascularization of acellular bladder grafts.” 2015. Web. 19 Oct 2020.

Vancouver:

Howard K. Revascularization of acellular bladder grafts. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/140048.

Council of Science Editors:

Howard K. Revascularization of acellular bladder grafts. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/140048

21. Horton, Kayla C. Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 The central nervous system (CNS), consisting of the brain and spinal cord, is a complex network of neuronal and non-neuronal cells that are responsible for… (more)

Subjects/Keywords: Spinal cord injuries; Neurogenesis; Central nervous system cell therapy; Mesenchymal stem cells

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APA (6th Edition):

Horton, K. C. (2015). Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/140477

Chicago Manual of Style (16th Edition):

Horton, Kayla C. “Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/140477.

MLA Handbook (7th Edition):

Horton, Kayla C. “Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics.” 2015. Web. 19 Oct 2020.

Vancouver:

Horton KC. Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/140477.

Council of Science Editors:

Horton KC. Mesenchymal stem cell delivery, survival and migration in a non-invasive system for central nervous system therapeutics. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/140477

22. Hammond, Elizabeth. The role of TCF7l2 in the generation of oligodendrocytes during development.

Degree: MA, Biological Science (Stem Cell, 2015, California State University – Sacramento

 One of the major obstacles to myelin repair in multiple sclerosis is the failure of endogenous oligodendrocyte progenitor cells (OPCs) to differentiate into mature oligodendrocytes… (more)

Subjects/Keywords: TCF7l2; Wnt; Neural stem cells; Oligodendrogenesis

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APA (6th Edition):

Hammond, E. (2015). The role of TCF7l2 in the generation of oligodendrocytes during development. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/145928

Chicago Manual of Style (16th Edition):

Hammond, Elizabeth. “The role of TCF7l2 in the generation of oligodendrocytes during development.” 2015. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/145928.

MLA Handbook (7th Edition):

Hammond, Elizabeth. “The role of TCF7l2 in the generation of oligodendrocytes during development.” 2015. Web. 19 Oct 2020.

Vancouver:

Hammond E. The role of TCF7l2 in the generation of oligodendrocytes during development. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/145928.

Council of Science Editors:

Hammond E. The role of TCF7l2 in the generation of oligodendrocytes during development. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/145928

23. Nguyen, Amanda Waber. Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?.

Degree: MS, Biological Science (Stem Cell, 2014, California State University – Sacramento

 Understanding the underlying factors that regulate early neurogenesis is essential to identifying inducers of aberrant neurodevelopment linked to autism and schizophrenia. Determination of these factors… (more)

Subjects/Keywords: Autism; Stem cells; Neurodevelopment; Immunology; Schizophrenia

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APA (6th Edition):

Nguyen, A. W. (2014). Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/131535

Chicago Manual of Style (16th Edition):

Nguyen, Amanda Waber. “Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?.” 2014. Masters Thesis, California State University – Sacramento. Accessed October 19, 2020. http://hdl.handle.net/10211.3/131535.

MLA Handbook (7th Edition):

Nguyen, Amanda Waber. “Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?.” 2014. Web. 19 Oct 2020.

Vancouver:

Nguyen AW. Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?. [Internet] [Masters thesis]. California State University – Sacramento; 2014. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10211.3/131535.

Council of Science Editors:

Nguyen AW. Expression of Toll-like Receptors 3 and 4 (TLR3/4) on neural progenitor cells (radial glial cells): is direct immune activation possible in rat embryonic brain with maternal immune activation?. [Masters Thesis]. California State University – Sacramento; 2014. Available from: http://hdl.handle.net/10211.3/131535

.