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University: The Ohio State University

You searched for subject:(Molecular Genetics). Showing records 1 – 30 of 73 total matches.

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The Ohio State University

1. Ouseph, Madhu Micheal. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.

Degree: PhD, Biochemistry Program, Ohio State, 2012, The Ohio State University

  Coordinated activation and repression of E2F-responsive genes is believed to be pivotal for progression of normal cell cycle. Studies using lower organisms and mammalian… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Ouseph, M. M. (2012). Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740

Chicago Manual of Style (16th Edition):

Ouseph, Madhu Micheal. “Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.” 2012. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740.

MLA Handbook (7th Edition):

Ouseph, Madhu Micheal. “Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.” 2012. Web. 07 Jul 2020.

Vancouver:

Ouseph MM. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740.

Council of Science Editors:

Ouseph MM. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740


The Ohio State University

2. Stephan, Joseph. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2008, The Ohio State University

  A cell in its natural environment spends its time in a quiescent state known as G0. A challenge the cell faces is to determine… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Stephan, J. (2008). An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573

Chicago Manual of Style (16th Edition):

Stephan, Joseph. “An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573.

MLA Handbook (7th Edition):

Stephan, Joseph. “An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.” 2008. Web. 07 Jul 2020.

Vancouver:

Stephan J. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573.

Council of Science Editors:

Stephan J. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573


The Ohio State University

3. Ghosh, Sankha. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2014, The Ohio State University

 Vascular remodeling is a necessary process not only for embryonic development but also for specific physiological and pathological conditions in adult. Several growth factors are… (more)

Subjects/Keywords: Molecular Biology; Developmental Biology; Genetics

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APA (6th Edition):

Ghosh, S. (2014). REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955

Chicago Manual of Style (16th Edition):

Ghosh, Sankha. “REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955.

MLA Handbook (7th Edition):

Ghosh, Sankha. “REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.” 2014. Web. 07 Jul 2020.

Vancouver:

Ghosh S. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955.

Council of Science Editors:

Ghosh S. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955


The Ohio State University

4. Jowdy, Casey C. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.

Degree: PhD, Molecular Genetics, 2010, The Ohio State University

  During development the precise wiring of the nervous system is dependent on thecorrect repertoire of axon guidance molecules being expressed at the right time… (more)

Subjects/Keywords: Biology; Genetics; Molecular Biology

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APA (6th Edition):

Jowdy, C. C. (2010). The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382

Chicago Manual of Style (16th Edition):

Jowdy, Casey C. “The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382.

MLA Handbook (7th Edition):

Jowdy, Casey C. “The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.” 2010. Web. 07 Jul 2020.

Vancouver:

Jowdy CC. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382.

Council of Science Editors:

Jowdy CC. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382


The Ohio State University

5. Zhang, Bo. COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE.

Degree: PhD, Molecular Genetics, 2017, The Ohio State University

 RNA-protein (RNP) granules are non-membrane-bound organelles that function to compartmentalize the cytoplasm of eukaryotic cells. There are a number of distinct RNP granules, including the… (more)

Subjects/Keywords: Genetics; Molecular Biology; Cellular Biology

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APA (6th Edition):

Zhang, B. (2017). COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1494291288298218

Chicago Manual of Style (16th Edition):

Zhang, Bo. “COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE.” 2017. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1494291288298218.

MLA Handbook (7th Edition):

Zhang, Bo. “COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE.” 2017. Web. 07 Jul 2020.

Vancouver:

Zhang B. COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE. [Internet] [Doctoral dissertation]. The Ohio State University; 2017. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1494291288298218.

Council of Science Editors:

Zhang B. COMPARTMENTS WITHOUT BORDERS—DISSECTING THE ROLES FOR P-BODIES THROUGH HRR25 PROTEIN KINASE. [Doctoral Dissertation]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1494291288298218


The Ohio State University

6. Tseng, Rong-Jeng. Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2008, The Ohio State University

  <i>Pax</i> genes are important in organogenesis during animal development. These genes affect the development of a range of different cell types, and promote cell… (more)

Subjects/Keywords: Biology; Cellular Biology; Genetics; Molecular Biology

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APA (6th Edition):

Tseng, R. (2008). Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1213384889

Chicago Manual of Style (16th Edition):

Tseng, Rong-Jeng. “Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1213384889.

MLA Handbook (7th Edition):

Tseng, Rong-Jeng. “Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>.” 2008. Web. 07 Jul 2020.

Vancouver:

Tseng R. Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213384889.

Council of Science Editors:

Tseng R. Identification and characterization of factors functioning with EGL-38 PAX to regulate <i>lin-48</i> in <i>Caenorhabditis elegans</i>. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213384889


The Ohio State University

7. Nuthikattu, Saivageethi. Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana.

Degree: PhD, Plant Cellular and Molecular Biology, 2014, The Ohio State University

 Transposable elements (TEs) are jumping genes, which when active move from one part of the genome to another and cause mutations and genome instability in… (more)

Subjects/Keywords: Molecular Biology; Genetics; Biology; Plant Biology

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APA (6th Edition):

Nuthikattu, S. (2014). Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1417685369

Chicago Manual of Style (16th Edition):

Nuthikattu, Saivageethi. “Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1417685369.

MLA Handbook (7th Edition):

Nuthikattu, Saivageethi. “Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana.” 2014. Web. 07 Jul 2020.

Vancouver:

Nuthikattu S. Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1417685369.

Council of Science Editors:

Nuthikattu S. Diverse mechanisms of Athila retrotransposon epigenetic silencing in Arabidopsis thaliana. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1417685369


The Ohio State University

8. Carver, Laura. Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members.

Degree: PhD, Molecular Genetics, 2011, The Ohio State University

  The field of axon guidance is concerned with deciphering how axons use temporal and spatial cues to pattern a precise trajectory. We use the… (more)

Subjects/Keywords: Developmental Biology; Genetics; Molecular Biology; Neurobiology; Axon guidance; Commissureless; Roundabout; Drosophila melanogaster; neurobiology; molecular biology; genetics; developmental biology

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APA (6th Edition):

Carver, L. (2011). Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1316455618

Chicago Manual of Style (16th Edition):

Carver, Laura. “Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members.” 2011. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1316455618.

MLA Handbook (7th Edition):

Carver, Laura. “Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members.” 2011. Web. 07 Jul 2020.

Vancouver:

Carver L. Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1316455618.

Council of Science Editors:

Carver L. Regulation of Slit-Robo Signaling by Commissureless and Comm Family Members. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1316455618


The Ohio State University

9. Miller, Antony J. Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis.

Degree: PhD, Molecular Genetics, 2014, The Ohio State University

 The Notch signaling pathway is a cell-to-cell signal transduction mechanism utilized throughout the kingdom metazoa. While we have a strong understanding of the mechanism by… (more)

Subjects/Keywords: Molecular Biology; Genetics; Developmental Biology; Notch Signaling; Fringe Genes; Development; Differentiation

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APA (6th Edition):

Miller, A. J. (2014). Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1420667621

Chicago Manual of Style (16th Edition):

Miller, Antony J. “Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1420667621.

MLA Handbook (7th Edition):

Miller, Antony J. “Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis.” 2014. Web. 07 Jul 2020.

Vancouver:

Miller AJ. Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1420667621.

Council of Science Editors:

Miller AJ. Regulation of Ligand-Mediated Notch Activation in Mammalian Development and Homeostasis. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1420667621


The Ohio State University

10. Tangeman, Larissa J. Regulation of BLM Nucleolar Localization.

Degree: MS, Biomedical Sciences, 2017, The Ohio State University

 Defects in coordinated ribosomal RNA (rRNA) transcription in the nucleolus cause cellular and organismal growth deficiencies. Bloom’s syndrome, an autosomal recessive human disorder caused by… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; Genetics; Regulation, BLM Nucleolar Localization

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APA (6th Edition):

Tangeman, L. J. (2017). Regulation of BLM Nucleolar Localization. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817

Chicago Manual of Style (16th Edition):

Tangeman, Larissa J. “Regulation of BLM Nucleolar Localization.” 2017. Masters Thesis, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817.

MLA Handbook (7th Edition):

Tangeman, Larissa J. “Regulation of BLM Nucleolar Localization.” 2017. Web. 07 Jul 2020.

Vancouver:

Tangeman LJ. Regulation of BLM Nucleolar Localization. [Internet] [Masters thesis]. The Ohio State University; 2017. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817.

Council of Science Editors:

Tangeman LJ. Regulation of BLM Nucleolar Localization. [Masters Thesis]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817


The Ohio State University

11. Santanam, Urmila. Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2010, The Ohio State University

  B-cell chronic lymphocytic leukemia (B-CLL), the most common human leukemia in the world, is a malignancy of mature B-lymphocytes. Deregulation of the TCL1 oncogene… (more)

Subjects/Keywords: Biomedical Research; Genetics; Molecular Biology; CLL; microRNA; transgenic mice; PXDN

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APA (6th Edition):

Santanam, U. (2010). Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1281447982

Chicago Manual of Style (16th Edition):

Santanam, Urmila. “Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1281447982.

MLA Handbook (7th Edition):

Santanam, Urmila. “Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia.” 2010. Web. 07 Jul 2020.

Vancouver:

Santanam U. Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281447982.

Council of Science Editors:

Santanam U. Role of microRNA-29 in the Pathogenesis of B-Cell Chronic Lymphocytic Leukemia. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281447982


The Ohio State University

12. Srinivasan, Ruchika. ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2009, The Ohio State University

  High cell growth rates during embryogenesis and adult-pathological conditions require high nutrient supply and hence, extensive vascular remodeling or angiogenesis. Since, the molecules and… (more)

Subjects/Keywords: Adult Education; Cellular Biology; Genetics; Molecular Biology; Erk embryonic angiogenesis

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APA (6th Edition):

Srinivasan, R. (2009). ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1252946298

Chicago Manual of Style (16th Edition):

Srinivasan, Ruchika. “ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS.” 2009. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1252946298.

MLA Handbook (7th Edition):

Srinivasan, Ruchika. “ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS.” 2009. Web. 07 Jul 2020.

Vancouver:

Srinivasan R. ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1252946298.

Council of Science Editors:

Srinivasan R. ERK1/2 AND THEIR DOWNSTREAM EFFECTOR ETS1/2 PLAY A REDUNDANT ENDOTHELIAL CELL-AUTONOMOUS ROLE DURING MOUSE EMBRYONIC ANGIOGENESIS. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1252946298


The Ohio State University

13. Fries, Anthony Charles. The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes.

Degree: MS, Evolution, Ecology, and Organismal Biology, 2009, The Ohio State University

 Differences in organismal life-history characteristics are often related to variation in an organisms’ energy expenditure. For example, tropical bird species show a significantly slower “pace… (more)

Subjects/Keywords: Biology; Genetics; Molecular Biology; Evolution; birds; mitochondria; positive selection; oxidative phosphorylation

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APA (6th Edition):

Fries, A. C. (2009). The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1258557488

Chicago Manual of Style (16th Edition):

Fries, Anthony Charles. “The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes.” 2009. Masters Thesis, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1258557488.

MLA Handbook (7th Edition):

Fries, Anthony Charles. “The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes.” 2009. Web. 07 Jul 2020.

Vancouver:

Fries AC. The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes. [Internet] [Masters thesis]. The Ohio State University; 2009. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1258557488.

Council of Science Editors:

Fries AC. The molecular evolution of mitochondrial oxidative phosphorylation genes in the Order Passeriformes. [Masters Thesis]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1258557488


The Ohio State University

14. Li, Jing. Biological function of E2F7 and E2F8 is essential for embryo development.

Degree: PhD, Molecular Genetics, 2009, The Ohio State University

  The novel E2F7 and E2F8 family members are thought to function as transcriptional repressors important for the control of cell proliferation in vitro. However,… (more)

Subjects/Keywords: Genetics; Molecular Biology; E2F; embryo development; apoptosis; cell cycle; transcriptional regulation

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APA (6th Edition):

Li, J. (2009). Biological function of E2F7 and E2F8 is essential for embryo development. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018

Chicago Manual of Style (16th Edition):

Li, Jing. “Biological function of E2F7 and E2F8 is essential for embryo development.” 2009. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018.

MLA Handbook (7th Edition):

Li, Jing. “Biological function of E2F7 and E2F8 is essential for embryo development.” 2009. Web. 07 Jul 2020.

Vancouver:

Li J. Biological function of E2F7 and E2F8 is essential for embryo development. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018.

Council of Science Editors:

Li J. Biological function of E2F7 and E2F8 is essential for embryo development. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018


The Ohio State University

15. Pringle, Daphne R. Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2013, The Ohio State University

 Thyroid cancer is the most commone endocrine malignancy in the population and incidence rates continue to rise. The two most common types of thyroid cancer,… (more)

Subjects/Keywords: Molecular Biology; Oncology; Genetics; Thyroid cancer, PKA, mouse models

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APA (6th Edition):

Pringle, D. R. (2013). Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1373732842

Chicago Manual of Style (16th Edition):

Pringle, Daphne R. “Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA.” 2013. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1373732842.

MLA Handbook (7th Edition):

Pringle, Daphne R. “Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA.” 2013. Web. 07 Jul 2020.

Vancouver:

Pringle DR. Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA. [Internet] [Doctoral dissertation]. The Ohio State University; 2013. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1373732842.

Council of Science Editors:

Pringle DR. Mechanisms of Follicular Thyroid Cancer Development and Progression in the Context of Dysregulated PKA. [Doctoral Dissertation]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1373732842


The Ohio State University

16. Paul, Litty. Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2008, The Ohio State University

  Epidermal growth factor receptor (EGFR) signaling regulates cell survival, migration, proliferation and cell fate specification in animals. The receptor undergoes dimerization and autophosphorylation upon… (more)

Subjects/Keywords: Genetics; Molecular Biology; Epidermal growth factor receptor; Drosophila

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APA (6th Edition):

Paul, L. (2008). Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1213277951

Chicago Manual of Style (16th Edition):

Paul, Litty. “Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1213277951.

MLA Handbook (7th Edition):

Paul, Litty. “Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster.” 2008. Web. 07 Jul 2020.

Vancouver:

Paul L. Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213277951.

Council of Science Editors:

Paul L. Ligand mediated regulation of Epidermal Growth Factor Receptor signaling in Drosophila melanogaster. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1213277951


The Ohio State University

17. Berbari, Nicolas F. Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome.

Degree: PhD, Integrated Biomedical Science, 2008, The Ohio State University

  Cilia are hair-like microtubule based cellular appendages that extend 5-30 microns from the surface of most vertebrate cells. Since their initial discovery over a… (more)

Subjects/Keywords: Biomedical Research; Cellular Biology; Genetics; Molecular Biology; cilia; Bardet-Biedl Syndrome

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APA (6th Edition):

Berbari, N. F. (2008). Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1203443295

Chicago Manual of Style (16th Edition):

Berbari, Nicolas F. “Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1203443295.

MLA Handbook (7th Edition):

Berbari, Nicolas F. “Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome.” 2008. Web. 07 Jul 2020.

Vancouver:

Berbari NF. Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1203443295.

Council of Science Editors:

Berbari NF. Investigations into Neuronal Cilia Utilizing Mouse Models of Bardet-Biedl Syndrome. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1203443295


The Ohio State University

18. Ratnam, Nivedita Mohan. NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2017, The Ohio State University

 Macrophages are attracted to developing tumors and can participate in immune surveillance to eliminate neoplastic cells. In response, neoplastic cells utilize NF-kB to suppress this… (more)

Subjects/Keywords: Biology; Cellular Biology; Genetics; Immunology; Molecular Biology; Oncology

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APA (6th Edition):

Ratnam, N. M. (2017). NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1505306161707059

Chicago Manual of Style (16th Edition):

Ratnam, Nivedita Mohan. “NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development.” 2017. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1505306161707059.

MLA Handbook (7th Edition):

Ratnam, Nivedita Mohan. “NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development.” 2017. Web. 07 Jul 2020.

Vancouver:

Ratnam NM. NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development. [Internet] [Doctoral dissertation]. The Ohio State University; 2017. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1505306161707059.

Council of Science Editors:

Ratnam NM. NF-kB Regulates GDF-15 to Suppress Macrophage Surveillance During Early Tumor Development. [Doctoral Dissertation]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1505306161707059


The Ohio State University

19. Liu, Yi-Hsuan. Identifying novel genes involved in zinc homeostasis using a fission yeast model.

Degree: MS, Human Ecology: Human Nutrition, 2015, The Ohio State University

 Metals, such as iron, zinc, copper, and manganese are needed to maintain normal biological and cellular functions and are therefore essential for all organisms. Zinc… (more)

Subjects/Keywords: Nutrition; Molecular Biology; Genetics; zinc; gene regulation; mitochondrial zinc; yeast

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APA (6th Edition):

Liu, Y. (2015). Identifying novel genes involved in zinc homeostasis using a fission yeast model. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1428660969

Chicago Manual of Style (16th Edition):

Liu, Yi-Hsuan. “Identifying novel genes involved in zinc homeostasis using a fission yeast model.” 2015. Masters Thesis, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1428660969.

MLA Handbook (7th Edition):

Liu, Yi-Hsuan. “Identifying novel genes involved in zinc homeostasis using a fission yeast model.” 2015. Web. 07 Jul 2020.

Vancouver:

Liu Y. Identifying novel genes involved in zinc homeostasis using a fission yeast model. [Internet] [Masters thesis]. The Ohio State University; 2015. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1428660969.

Council of Science Editors:

Liu Y. Identifying novel genes involved in zinc homeostasis using a fission yeast model. [Masters Thesis]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1428660969


The Ohio State University

20. Luo, Yuqun. Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees.

Degree: PhD, Graduate School, 2002, The Ohio State University

Subjects/Keywords: Biology; Molecular genetics; Medical genetics; Gene mapping

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APA (6th Edition):

Luo, Y. (2002). Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486549482668451

Chicago Manual of Style (16th Edition):

Luo, Yuqun. “Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees.” 2002. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486549482668451.

MLA Handbook (7th Edition):

Luo, Yuqun. “Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees.” 2002. Web. 07 Jul 2020.

Vancouver:

Luo Y. Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486549482668451.

Council of Science Editors:

Luo Y. Incorporation of genetic marker information in estimating model parameters for complex traits with data from large complex pedigrees. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486549482668451


The Ohio State University

21. Sanford, Jonathan Christian. Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment.

Degree: PhD, Integrated Biomedical Science Graduate Program, 2014, The Ohio State University

 Regulatory variants, less well characterized than coding polymorphisms, have the potential to serve as clinically relevant biomarkers for determining drug efficacy or toxicity. This study… (more)

Subjects/Keywords: Genetics; Molecular Biology; Pharmacology; pharmacogenetics; genetics; cytochrome; drug metabolism; angiotensin; carboxylesterase; CYP2C19; ACE; CES1; cardiovascular; allele; polymorphism; SNP; clopidogrel

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APA (6th Edition):

Sanford, J. C. (2014). Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1405518187

Chicago Manual of Style (16th Edition):

Sanford, Jonathan Christian. “Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405518187.

MLA Handbook (7th Edition):

Sanford, Jonathan Christian. “Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment.” 2014. Web. 07 Jul 2020.

Vancouver:

Sanford JC. Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405518187.

Council of Science Editors:

Sanford JC. Pharmacogenetics of Drug Metabolizing Enzymes Involved in Cardiovascular Drug Treatment. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405518187


The Ohio State University

22. Pucker, Andrew David. Mechanotransduction in the Ciliary Muscle.

Degree: PhD, Vision Science, 2016, The Ohio State University

 Introduction: Thicker ciliary muscles have been associated with more myopic refractive errors. The mechanism leading to thicker ciliary muscles in myopic subjects is currently unknown.… (more)

Subjects/Keywords: Ophthalmology; Molecular Biology; Genetics; Histology; Ciliary Body; Ciliary Muscle; Myopia; Accommodation; Aging; Guinea Pigs; Histology; Molecular Biology

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APA (6th Edition):

Pucker, A. D. (2016). Mechanotransduction in the Ciliary Muscle. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1460647729

Chicago Manual of Style (16th Edition):

Pucker, Andrew David. “Mechanotransduction in the Ciliary Muscle.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1460647729.

MLA Handbook (7th Edition):

Pucker, Andrew David. “Mechanotransduction in the Ciliary Muscle.” 2016. Web. 07 Jul 2020.

Vancouver:

Pucker AD. Mechanotransduction in the Ciliary Muscle. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1460647729.

Council of Science Editors:

Pucker AD. Mechanotransduction in the Ciliary Muscle. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1460647729


The Ohio State University

23. Stoerker, Jay. Molecular genetics of the Epstein-Barr virus.

Degree: PhD, Graduate School, 1983, The Ohio State University

Subjects/Keywords: Biology; Epstein-Barr virus; Molecular genetics

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APA (6th Edition):

Stoerker, J. (1983). Molecular genetics of the Epstein-Barr virus. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487240083947294

Chicago Manual of Style (16th Edition):

Stoerker, Jay. “Molecular genetics of the Epstein-Barr virus.” 1983. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487240083947294.

MLA Handbook (7th Edition):

Stoerker, Jay. “Molecular genetics of the Epstein-Barr virus.” 1983. Web. 07 Jul 2020.

Vancouver:

Stoerker J. Molecular genetics of the Epstein-Barr virus. [Internet] [Doctoral dissertation]. The Ohio State University; 1983. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487240083947294.

Council of Science Editors:

Stoerker J. Molecular genetics of the Epstein-Barr virus. [Doctoral Dissertation]. The Ohio State University; 1983. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487240083947294


The Ohio State University

24. Mustafa, Mufaddal. Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer.

Degree: MS, Pathology, 2013, The Ohio State University

 Hepatocellular carcinoma (HCC) is the third most common cause of cancer-related death worldwide. There are a limited number of therapeutic options currently available to delay… (more)

Subjects/Keywords: Oncology; Biology; Molecular Biology; Genetics; 5-hmC; methylation; hydroxymethylation; HCC; liver; cancer

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APA (6th Edition):

Mustafa, M. (2013). Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1366115027

Chicago Manual of Style (16th Edition):

Mustafa, Mufaddal. “Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer.” 2013. Masters Thesis, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1366115027.

MLA Handbook (7th Edition):

Mustafa, Mufaddal. “Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer.” 2013. Web. 07 Jul 2020.

Vancouver:

Mustafa M. Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer. [Internet] [Masters thesis]. The Ohio State University; 2013. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1366115027.

Council of Science Editors:

Mustafa M. Alterations in Genomic 5-Hydroxymethylcytosine Level in Hepatocellular Cancer. [Masters Thesis]. The Ohio State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1366115027


The Ohio State University

25. Williams, Dustin R. Regulation of Notch Activation by Lunatic Fringe During Somitogenesis.

Degree: PhD, Molecular Genetics, 2014, The Ohio State University

 During somitogenesis, paired somites periodically bud from the presomitic mesoderm (PSM) located at the caudal end of the embryo. These somites will give rise to… (more)

Subjects/Keywords: Molecular Biology; Genetics; Biology; Notch pathway, Lunatic fringe; somitogenesis; somite; segmentation clock

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APA (6th Edition):

Williams, D. R. (2014). Regulation of Notch Activation by Lunatic Fringe During Somitogenesis. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1397756440

Chicago Manual of Style (16th Edition):

Williams, Dustin R. “Regulation of Notch Activation by Lunatic Fringe During Somitogenesis.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1397756440.

MLA Handbook (7th Edition):

Williams, Dustin R. “Regulation of Notch Activation by Lunatic Fringe During Somitogenesis.” 2014. Web. 07 Jul 2020.

Vancouver:

Williams DR. Regulation of Notch Activation by Lunatic Fringe During Somitogenesis. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397756440.

Council of Science Editors:

Williams DR. Regulation of Notch Activation by Lunatic Fringe During Somitogenesis. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397756440


The Ohio State University

26. Madabusi, Narasimhan Kandaye. Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy.

Degree: MS, Molecular, Cellular and Developmental Biology, 2012, The Ohio State University

  Spinal Muscular Atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of lower motor neurons and muscle atrophy. It is caused due… (more)

Subjects/Keywords: Biochemistry; Genetics; Molecular Biology; Spinal Muscular Atrophy; SMN; missense mutations; mouse models

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APA (6th Edition):

Madabusi, N. K. (2012). Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1339442849

Chicago Manual of Style (16th Edition):

Madabusi, Narasimhan Kandaye. “Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy.” 2012. Masters Thesis, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1339442849.

MLA Handbook (7th Edition):

Madabusi, Narasimhan Kandaye. “Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy.” 2012. Web. 07 Jul 2020.

Vancouver:

Madabusi NK. Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy. [Internet] [Masters thesis]. The Ohio State University; 2012. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1339442849.

Council of Science Editors:

Madabusi NK. Characterization of three SMN missense mutations using mouse models of Spinal Muscular Atrophy. [Masters Thesis]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1339442849

27. Grierson, Patrick Michael. The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription.

Degree: PhD, Integrated Biomedical Science Graduate Program, 2012, The Ohio State University

  The BLM helicase is a DNA repair protein mutated in the hereditary condition Bloom’s syndrome (BS). BLM is best known for its roles in… (more)

Subjects/Keywords: Biochemistry; Biology; Genetics; Molecular Biology

…CHAPTER ONE Literature Review The clinical presentation and genetics of Bloom’s syndrome… 

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APA (6th Edition):

Grierson, P. M. (2012). The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1337865492

Chicago Manual of Style (16th Edition):

Grierson, Patrick Michael. “The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription.” 2012. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1337865492.

MLA Handbook (7th Edition):

Grierson, Patrick Michael. “The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription.” 2012. Web. 07 Jul 2020.

Vancouver:

Grierson PM. The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337865492.

Council of Science Editors:

Grierson PM. The BLM helicase facilitates RNA polymerase I-mediated ribosomal RNA transcription. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1337865492

28. Wahi, Kanu, Wahi. EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK.

Degree: PhD, Molecular Genetics, 2016, The Ohio State University

 Somitogenesis is a developmental process in vertebrates involving periodic formation of somites that bud from an unsegmented region known as the pre-somitic mesoderm (PSM) and… (more)

Subjects/Keywords: Developmental Biology; Genetics; Molecular Biology

…Graduate Fellow, Department of Molecular Genetics, The Ohio State University Publications 1… …Fields of Study Major Field: Molecular Genetics viii Table of Contents Abstract… …understand the molecular basis of oscillatory expression of clock genes. A transcript or protein… 

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APA (6th Edition):

Wahi, Kanu, W. (2016). EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1469108634

Chicago Manual of Style (16th Edition):

Wahi, Kanu, Wahi. “EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK.” 2016. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1469108634.

MLA Handbook (7th Edition):

Wahi, Kanu, Wahi. “EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK.” 2016. Web. 07 Jul 2020.

Vancouver:

Wahi, Kanu W. EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK. [Internet] [Doctoral dissertation]. The Ohio State University; 2016. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1469108634.

Council of Science Editors:

Wahi, Kanu W. EXAMINING THE POST-TRANSCRIPTIONAL REGULATION OF LUNATIC FRINGE (Lfng) IN THE MOUSE SEGMENTATION CLOCK. [Doctoral Dissertation]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1469108634


The Ohio State University

29. Sawant, Dwitiya B. The Role of Mps1 and Centrin 3 in Centriole Assembly.

Degree: PhD, Molecular Genetics, 2015, The Ohio State University

 Centrosomes are membrane-free structures that function as microtubule organizing centers in most eukaryotes. Through this ability of organizing microtubules, they are mainly involved in interphase… (more)

Subjects/Keywords: Cellular Biology; Genetics; Molecular Biology; Centrosomes; Centrioles; Centrin 2; Centrin 3; Mps1; Breast Cancer

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APA (6th Edition):

Sawant, D. B. (2015). The Role of Mps1 and Centrin 3 in Centriole Assembly. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1429857356

Chicago Manual of Style (16th Edition):

Sawant, Dwitiya B. “The Role of Mps1 and Centrin 3 in Centriole Assembly.” 2015. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1429857356.

MLA Handbook (7th Edition):

Sawant, Dwitiya B. “The Role of Mps1 and Centrin 3 in Centriole Assembly.” 2015. Web. 07 Jul 2020.

Vancouver:

Sawant DB. The Role of Mps1 and Centrin 3 in Centriole Assembly. [Internet] [Doctoral dissertation]. The Ohio State University; 2015. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1429857356.

Council of Science Editors:

Sawant DB. The Role of Mps1 and Centrin 3 in Centriole Assembly. [Doctoral Dissertation]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1429857356


The Ohio State University

30. Hamilton, Paul Theodore. Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element.

Degree: PhD, Graduate School, 1984, The Ohio State University

Subjects/Keywords: Biology; Nucleotide sequence; Molecular cloning; Escherichia coli – Genetics

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

APA (6th Edition):

Hamilton, P. T. (1984). Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487257452615065

Chicago Manual of Style (16th Edition):

Hamilton, Paul Theodore. “Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element.” 1984. Doctoral Dissertation, The Ohio State University. Accessed July 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487257452615065.

MLA Handbook (7th Edition):

Hamilton, Paul Theodore. “Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element.” 1984. Web. 07 Jul 2020.

Vancouver:

Hamilton PT. Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element. [Internet] [Doctoral dissertation]. The Ohio State University; 1984. [cited 2020 Jul 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487257452615065.

Council of Science Editors:

Hamilton PT. Structure of genes from Methanobrevibacter smithii : evidence for ribosome binding sites, an operon, and an insertion element. [Doctoral Dissertation]. The Ohio State University; 1984. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487257452615065

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