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You searched for +publisher:"Georgia Tech" +contributor:("Harish Radhakrishna"). Showing records 1 – 10 of 10 total matches.

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Georgia Tech

1. Nguyen, Giang Huong. A functional analysis of the human LPA₁G protein coupled receptor.

Degree: MS, Biology, 2004, Georgia Tech

Subjects/Keywords: Lysophospholipids; Protein kinases; Proteins

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APA (6th Edition):

Nguyen, G. H. (2004). A functional analysis of the human LPA₁G protein coupled receptor. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/36542

Chicago Manual of Style (16th Edition):

Nguyen, Giang Huong. “A functional analysis of the human LPA₁G protein coupled receptor.” 2004. Masters Thesis, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/36542.

MLA Handbook (7th Edition):

Nguyen, Giang Huong. “A functional analysis of the human LPA₁G protein coupled receptor.” 2004. Web. 24 Jan 2021.

Vancouver:

Nguyen GH. A functional analysis of the human LPA₁G protein coupled receptor. [Internet] [Masters thesis]. Georgia Tech; 2004. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/36542.

Council of Science Editors:

Nguyen GH. A functional analysis of the human LPA₁G protein coupled receptor. [Masters Thesis]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/36542


Georgia Tech

2. Schlicher, Robyn Kathryn. Mechanistic Features of Ultrasound-Mediated Bioeffects.

Degree: PhD, Biomedical Engineering, 2005, Georgia Tech

 The inability to transport molecules efficiently and easily into cells and across tissues is one of the major limitations of developing drug delivery systems. A… (more)

Subjects/Keywords: Ultrasound; Sonication; Bioeffects; Bioengineering; Ultrasonics in medicine; Ultrasonic waves Therapeutic use

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APA (6th Edition):

Schlicher, R. K. (2005). Mechanistic Features of Ultrasound-Mediated Bioeffects. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14149

Chicago Manual of Style (16th Edition):

Schlicher, Robyn Kathryn. “Mechanistic Features of Ultrasound-Mediated Bioeffects.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/14149.

MLA Handbook (7th Edition):

Schlicher, Robyn Kathryn. “Mechanistic Features of Ultrasound-Mediated Bioeffects.” 2005. Web. 24 Jan 2021.

Vancouver:

Schlicher RK. Mechanistic Features of Ultrasound-Mediated Bioeffects. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/14149.

Council of Science Editors:

Schlicher RK. Mechanistic Features of Ultrasound-Mediated Bioeffects. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/14149


Georgia Tech

3. Urs, Aarti N. Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17.

Degree: MS, Biology, 2005, Georgia Tech

 Steroidogenic factor (SF1) is an orphan nuclear receptor that is essential for steroid hormone-biosynthesis and endocrine development. Recent studies have demonstrated that phospholipids are ligands… (more)

Subjects/Keywords: CYP17; Sphingosine; Phosphatidic acids; Steroidogenic factor 1; Transcription factors; Steroid hormones Synthesis; Sphingosine; Pregnenolone; Phospholipids; Ligands

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APA (6th Edition):

Urs, A. N. (2005). Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7638

Chicago Manual of Style (16th Edition):

Urs, Aarti N. “Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17.” 2005. Masters Thesis, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/7638.

MLA Handbook (7th Edition):

Urs, Aarti N. “Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17.” 2005. Web. 24 Jan 2021.

Vancouver:

Urs AN. Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17. [Internet] [Masters thesis]. Georgia Tech; 2005. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/7638.

Council of Science Editors:

Urs AN. Reciprocal binding of sphingosine and phosphatidic acid to steroidogenic factor 1 regulates the transcription of CYP17. [Masters Thesis]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7638


Georgia Tech

4. Keselowsky, Benjamin George. Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation.

Degree: PhD, Biomedical Engineering, 2004, Georgia Tech

 Cell adhesion to proteins adsorbed onto implanted surfaces is particularly important to host responses in biomedical and tissue engineering applications. Biomaterial surface properties influence the… (more)

Subjects/Keywords: Protein adsorption; Osteoblast; Cell adhesion; Surface chemistry; Integrin; Fibronectin

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APA (6th Edition):

Keselowsky, B. G. (2004). Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/8092

Chicago Manual of Style (16th Edition):

Keselowsky, Benjamin George. “Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation.” 2004. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/8092.

MLA Handbook (7th Edition):

Keselowsky, Benjamin George. “Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation.” 2004. Web. 24 Jan 2021.

Vancouver:

Keselowsky BG. Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/8092.

Council of Science Editors:

Keselowsky BG. Engineering surfaces to direct integrin binding and signaling to promote osteoblast differentiation. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/8092


Georgia Tech

5. Salim, Samer. "Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides.

Degree: PhD, Chemistry and Biochemistry, 2004, Georgia Tech

 It has recently been shown that the binding site of SAHase, an enzyme critical in the replication mechanism of viruses, is quite flexible and exhibits… (more)

Subjects/Keywords: Flexible enzymes; Flexible inhibitors; Nucleosides Synthesis

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APA (6th Edition):

Salim, S. (2004). "Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/4867

Chicago Manual of Style (16th Edition):

Salim, Samer. “"Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides.” 2004. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/4867.

MLA Handbook (7th Edition):

Salim, Samer. “"Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides.” 2004. Web. 24 Jan 2021.

Vancouver:

Salim S. "Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/4867.

Council of Science Editors:

Salim S. "Molecular Chameleons": Design and Synthesis of a Second Series of Flexible Nucleosides. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/4867


Georgia Tech

6. Gokhale, Kavita Chandan. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.

Degree: PhD, Biology, 2005, Georgia Tech

 Poly-Q expanded exon 1 of huntingtin (Q103) fused to GFP is toxic to yeast cells containing endogenous yeast prions, [PIN+] ([RNQ+]) and/or [PSI+], which presumably… (more)

Subjects/Keywords: Chaperones; Glutamine; Molecular chaperones; Prions; Yeast

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APA (6th Edition):

Gokhale, K. C. (2005). Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6856

Chicago Manual of Style (16th Edition):

Gokhale, Kavita Chandan. “Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/6856.

MLA Handbook (7th Edition):

Gokhale, Kavita Chandan. “Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model.” 2005. Web. 24 Jan 2021.

Vancouver:

Gokhale KC. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/6856.

Council of Science Editors:

Gokhale KC. Interactions between endogenous prions, chaperones and polyglutamine proteins in the yeast model. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6856


Georgia Tech

7. Krishna, Delfi. Investigation of the role of target cell factors in retrovirus transduction.

Degree: PhD, Chemical Engineering, 2005, Georgia Tech

 Gene therapy is the intracellular delivery of genetic material for a therapeutic effect and is currently being used in clinical trials for the treatment of… (more)

Subjects/Keywords: Retrovirus; Gene therapy

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APA (6th Edition):

Krishna, D. (2005). Investigation of the role of target cell factors in retrovirus transduction. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7537

Chicago Manual of Style (16th Edition):

Krishna, Delfi. “Investigation of the role of target cell factors in retrovirus transduction.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/7537.

MLA Handbook (7th Edition):

Krishna, Delfi. “Investigation of the role of target cell factors in retrovirus transduction.” 2005. Web. 24 Jan 2021.

Vancouver:

Krishna D. Investigation of the role of target cell factors in retrovirus transduction. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/7537.

Council of Science Editors:

Krishna D. Investigation of the role of target cell factors in retrovirus transduction. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7537


Georgia Tech

8. Mouw, Janna Kay. Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling.

Degree: PhD, Bioengineering, 2005, Georgia Tech

 In pathological states such as osteoarthritis, the complex metabolic balance of cartilage is disrupted, leading to a loss in the integrity and biomechanical function of… (more)

Subjects/Keywords: Chondrogenesis; Chondrocyte; Stromal cells; Cell differentiation; Tissue engineering; Articular cartilage; Biomechanics; Cartilage cells

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APA (6th Edition):

Mouw, J. K. (2005). Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7550

Chicago Manual of Style (16th Edition):

Mouw, Janna Kay. “Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling.” 2005. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/7550.

MLA Handbook (7th Edition):

Mouw, Janna Kay. “Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling.” 2005. Web. 24 Jan 2021.

Vancouver:

Mouw JK. Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/7550.

Council of Science Editors:

Mouw JK. Mechanoregulation of chondrocytes and chondroprogenitors: the role of TGF-BETA and SMAD signaling. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7550


Georgia Tech

9. Hurst-Kennedy, Jennifer Lynne. Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation.

Degree: PhD, Biology, 2009, Georgia Tech

 Lysophosphatidic acid (LPA) is the simplest of the glycerol lipids and regulates a number of cellular processes such as morphological changes, migration, proliferation, and inhibition… (more)

Subjects/Keywords: Vitamin D metabolites; Lysophosphatidic acid; P53; Growth plate chondrocytes; Apoptosis; Lysophospholipids; Cell death

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APA (6th Edition):

Hurst-Kennedy, J. L. (2009). Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31833

Chicago Manual of Style (16th Edition):

Hurst-Kennedy, Jennifer Lynne. “Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation.” 2009. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/31833.

MLA Handbook (7th Edition):

Hurst-Kennedy, Jennifer Lynne. “Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation.” 2009. Web. 24 Jan 2021.

Vancouver:

Hurst-Kennedy JL. Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/31833.

Council of Science Editors:

Hurst-Kennedy JL. Lysophosphatidic acid, vitamin D, and p53: a novel signaling axis in cell death and differentiation. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/31833


Georgia Tech

10. Jones, Kymry Thereasa. The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor.

Degree: PhD, Biology, 2007, Georgia Tech

 The muscarinic acetylcholine type 2 receptor (M2 mAChR), a member of the GPCR superfamily, is found throughout the parasympathetic nervous system where it controls pulmonary,… (more)

Subjects/Keywords: Muscarinic; GPCR; Receptor trafficking; Ubiquitination; Internalization; Down-regulation; Muscarinic receptors; Acetylcholine Receptors; Biological control systems

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APA (6th Edition):

Jones, K. T. (2007). The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/24815

Chicago Manual of Style (16th Edition):

Jones, Kymry Thereasa. “The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor.” 2007. Doctoral Dissertation, Georgia Tech. Accessed January 24, 2021. http://hdl.handle.net/1853/24815.

MLA Handbook (7th Edition):

Jones, Kymry Thereasa. “The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor.” 2007. Web. 24 Jan 2021.

Vancouver:

Jones KT. The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1853/24815.

Council of Science Editors:

Jones KT. The role of beta-arrestin in regulating the muscarinic acetylcholine type II receptor. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/24815

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