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You searched for +publisher:"IUPUI" +contributor:("Dai, Guoli"). Showing records 1 – 9 of 9 total matches.

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IUPUI

1. Kumar, Sudhanshu. Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

During pregnancy, maternal liver exhibits robust growth to meet the metabolic demands of the developing placenta and fetus. Although hepatocyte… (more)

Subjects/Keywords: Ascl1, Liver, Regeneration, Pregnancy; Liver  – Pregnancy  – Research  – Methodology; Pregnancy in animals  – Research; Liver  – Regeneration  – Research; Liver  – Growth  – Research; Liver  – Anatomy; Liver cells  – Differentiation; Transcription factors  – Research  – Methodology  – Analysis; DNA microarrays  – Research; Mice as laboratory animals  – Pregnancy  – Testing; Gene expression  – Research; Hepatocyte growth factor  – Research; Protein microarrays; Developmental neurobiology; Tamoxifen  – Research

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

APA (6th Edition):

Kumar, S. (2014). Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/4844

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):

Kumar, Sudhanshu. “Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy.” 2014. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/4844.

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

MLA Handbook (7th Edition):

Kumar, Sudhanshu. “Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy.” 2014. Web. 17 Aug 2019.

Vancouver:

Kumar S. Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/4844.

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

Council of Science Editors:

Kumar S. Identification and characterization of Ascl1-expressing cells in maternal liver during pregnancy. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/4844

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


IUPUI

2. Lee, Joonyong. The function of ASCL1 in pregnancy-induced maternal liver growth.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The maternal liver shows marked growth during pregnancy to accommodate the development and metabolic needs of the placenta and fetus.… (more)

Subjects/Keywords: Pregnancy  – Research; Hepatocyte growth factor  – Research; Liver  – Growth  – Research; Maternal-fetal exchange; Hyperplasia; Liver  – Hypertrophy; Transcription factors  – Research  – Evaluation  – Analysis; Gene expression  – Research; Developmental neurobiology; Fetal liver cells; Liver  – Regeneration; Stem cells  – Research; Nerves, Peripheral

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APA (6th Edition):

Lee, J. (2014). The function of ASCL1 in pregnancy-induced maternal liver growth. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/5971

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):

Lee, Joonyong. “The function of ASCL1 in pregnancy-induced maternal liver growth.” 2014. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/5971.

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

MLA Handbook (7th Edition):

Lee, Joonyong. “The function of ASCL1 in pregnancy-induced maternal liver growth.” 2014. Web. 17 Aug 2019.

Vancouver:

Lee J. The function of ASCL1 in pregnancy-induced maternal liver growth. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/5971.

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

Council of Science Editors:

Lee J. The function of ASCL1 in pregnancy-induced maternal liver growth. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/5971

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


IUPUI

3. Nambiar, Shashank Manohar. Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

To cope with the high metabolic demands of the body during pregnancy, the maternal liver adapts by increasing its mass… (more)

Subjects/Keywords: Liver  – Hypertrophy  – Research  – Evaluation; Hepatocyte growth factor  – Research  – Evaluation  – Analysis; Liver  – Growth  – Research; Hyperplasia  – Research; Gene expression  – Research; Pregnancy  – Research; Liver  – Regeneration; Transcription factors  – Research  – Evaluation; Neural stem cells  – Research; Green fluorescent protein  – Research  – Analysis; Messenger RNA; Stem cells  – Research; Animal models in research

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

APA (6th Edition):

Nambiar, S. M. (2014). Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/6016

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):

Nambiar, Shashank Manohar. “Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy.” 2014. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/6016.

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

MLA Handbook (7th Edition):

Nambiar, Shashank Manohar. “Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy.” 2014. Web. 17 Aug 2019.

Vancouver:

Nambiar SM. Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/6016.

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

Council of Science Editors:

Nambiar SM. Lineage tracing of Ascl1-expressing cells in the maternal liver during pregnancy. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/6016

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


IUPUI

4. Culver, Alexander. TGF-beta signaling in an in vivo model of NASH.

Degree: 2016, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

A burgeoning area of focus within liver disease research is centered on the concomitant muscle atrophy present in end stage… (more)

Subjects/Keywords: NASH; Activin; Nonalcoholic steatohepatitis; liver; fibrosis; gdf8

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APA (6th Edition):

Culver, A. (2016). TGF-beta signaling in an in vivo model of NASH. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/11829

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):

Culver, Alexander. “TGF-beta signaling in an in vivo model of NASH.” 2016. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/11829.

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

MLA Handbook (7th Edition):

Culver, Alexander. “TGF-beta signaling in an in vivo model of NASH.” 2016. Web. 17 Aug 2019.

Vancouver:

Culver A. TGF-beta signaling in an in vivo model of NASH. [Internet] [Thesis]. IUPUI; 2016. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/11829.

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

Council of Science Editors:

Culver A. TGF-beta signaling in an in vivo model of NASH. [Thesis]. IUPUI; 2016. Available from: http://hdl.handle.net/1805/11829

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


IUPUI

5. Wang, Shukun. Inflammation in the early pathogenesis of diabetic retinopathy.

Degree: 2018, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Introduction – Diabetes is a growing health concern. Diabetic retinopathy (DR), is a complication resulting from long-term diabetes and is… (more)

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

APA (6th Edition):

Wang, S. (2018). Inflammation in the early pathogenesis of diabetic retinopathy. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/17001

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):

Wang, Shukun. “Inflammation in the early pathogenesis of diabetic retinopathy.” 2018. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/17001.

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

MLA Handbook (7th Edition):

Wang, Shukun. “Inflammation in the early pathogenesis of diabetic retinopathy.” 2018. Web. 17 Aug 2019.

Vancouver:

Wang S. Inflammation in the early pathogenesis of diabetic retinopathy. [Internet] [Thesis]. IUPUI; 2018. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/17001.

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

Council of Science Editors:

Wang S. Inflammation in the early pathogenesis of diabetic retinopathy. [Thesis]. IUPUI; 2018. Available from: http://hdl.handle.net/1805/17001

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


IUPUI

6. Hamang, Matthew J. The Roles of Activin A and B in Liver Inflammation and Fibrosis.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Liver fibrosis is the result of different types of chronic liver diseases, such as cholestatic liver disease and nonalcoholic steatohepatitis,… (more)

Subjects/Keywords: Activin; Inflammation; Liver fibrosis

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

APA (6th Edition):

Hamang, M. J. (2019). The Roles of Activin A and B in Liver Inflammation and Fibrosis. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/19008

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):

Hamang, Matthew J. “The Roles of Activin A and B in Liver Inflammation and Fibrosis.” 2019. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/19008.

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

MLA Handbook (7th Edition):

Hamang, Matthew J. “The Roles of Activin A and B in Liver Inflammation and Fibrosis.” 2019. Web. 17 Aug 2019.

Vancouver:

Hamang MJ. The Roles of Activin A and B in Liver Inflammation and Fibrosis. [Internet] [Thesis]. IUPUI; 2019. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/19008.

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

Council of Science Editors:

Hamang MJ. The Roles of Activin A and B in Liver Inflammation and Fibrosis. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/19008

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


IUPUI

7. Priddy, Carlie. Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The Keap1-Nrf2 pathway regulates a wide range of cytoprotective genes, and has been found to serve a protective and beneficial… (more)

Subjects/Keywords: Nrf2; Keap1; mechanotransduction; bone remodeling; bone; bone homeostasis; antioxidant; cytoprotective; aging; mouse; loading induced bone formation

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APA (6th Edition):

Priddy, C. (2019). Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/19985

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):

Priddy, Carlie. “Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway.” 2019. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/19985.

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

MLA Handbook (7th Edition):

Priddy, Carlie. “Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway.” 2019. Web. 17 Aug 2019.

Vancouver:

Priddy C. Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway. [Internet] [Thesis]. IUPUI; 2019. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/19985.

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

Council of Science Editors:

Priddy C. Mechanotransduction in Living Bone: Effects of the Keap1-Nrf2 Pathway. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/19985

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


IUPUI

8. Kolb, Alexander. Studies on hydrodynamic delivery as a treatment for acute kidney injury.

Degree: 2017, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Hydrodynamic delivery is a powerful tool that allows delivery of macromolecules to the kidney culminating in gene expression. This finding… (more)

Subjects/Keywords: Ischemic Preconditioning; Acute Kidney Injury; IDH2

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APA (6th Edition):

Kolb, A. (2017). Studies on hydrodynamic delivery as a treatment for acute kidney injury. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/13600

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):

Kolb, Alexander. “Studies on hydrodynamic delivery as a treatment for acute kidney injury.” 2017. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/13600.

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

MLA Handbook (7th Edition):

Kolb, Alexander. “Studies on hydrodynamic delivery as a treatment for acute kidney injury.” 2017. Web. 17 Aug 2019.

Vancouver:

Kolb A. Studies on hydrodynamic delivery as a treatment for acute kidney injury. [Internet] [Thesis]. IUPUI; 2017. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/13600.

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

Council of Science Editors:

Kolb A. Studies on hydrodynamic delivery as a treatment for acute kidney injury. [Thesis]. IUPUI; 2017. Available from: http://hdl.handle.net/1805/13600

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


IUPUI

9. Wang, Yan. Activin B Promotes Hepatic Fibrogenesis.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Liver fibrosis is a common consequence of various chronic liver diseases. Although transforming growth factor β 1 (TGFβ1) expression is… (more)

Subjects/Keywords: Activin B; Hepatocytes; Macrophages; Hepatic stellate cells; Liver fibrosis

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

APA (6th Edition):

Wang, Y. (2019). Activin B Promotes Hepatic Fibrogenesis. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/19921

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):

Wang, Yan. “Activin B Promotes Hepatic Fibrogenesis.” 2019. Thesis, IUPUI. Accessed August 17, 2019. http://hdl.handle.net/1805/19921.

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

MLA Handbook (7th Edition):

Wang, Yan. “Activin B Promotes Hepatic Fibrogenesis.” 2019. Web. 17 Aug 2019.

Vancouver:

Wang Y. Activin B Promotes Hepatic Fibrogenesis. [Internet] [Thesis]. IUPUI; 2019. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1805/19921.

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

Council of Science Editors:

Wang Y. Activin B Promotes Hepatic Fibrogenesis. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/19921

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

.