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You searched for +publisher:"University of Texas Southwestern Medical Center" +contributor:("Albanesi, Joseph P."). Showing records 1 – 23 of 23 total matches.

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University of Texas Southwestern Medical Center

1. Patrick, Anna Elizabeth. Cotranslational Folding of CFTR.

Degree: 2013, University of Texas Southwestern Medical Center

 The life of the cystic fibrosis transmembrane conductance regulator (CFTR) protein in the cell is dictated by its biogenesis, cellular trafficking, regulated function, and destruction.… (more)

Subjects/Keywords: Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Protein Folding

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APA (6th Edition):

Patrick, A. E. (2013). Cotranslational Folding of CFTR. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1704

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):

Patrick, Anna Elizabeth. “Cotranslational Folding of CFTR.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/1704.

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

MLA Handbook (7th Edition):

Patrick, Anna Elizabeth. “Cotranslational Folding of CFTR.” 2013. Web. 09 Jul 2020.

Vancouver:

Patrick AE. Cotranslational Folding of CFTR. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/1704.

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

Council of Science Editors:

Patrick AE. Cotranslational Folding of CFTR. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1704

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


University of Texas Southwestern Medical Center

2. Umlauf, Benjamin J. Methods for Identifying Subcellular Targeting Ligands and Selected Applications.

Degree: 2015, University of Texas Southwestern Medical Center

 Subcellular localization plays an essential role in targeting drug therapies as generally the pro-drug or linker relies on physical conditions of a particular subcellular compartment… (more)

Subjects/Keywords: Endocytosis; Lysosomes; Peptides

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APA (6th Edition):

Umlauf, B. J. (2015). Methods for Identifying Subcellular Targeting Ligands and Selected Applications. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4228

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):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4228.

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

MLA Handbook (7th Edition):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Web. 09 Jul 2020.

Vancouver:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4228.

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

Council of Science Editors:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4228

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


University of Texas Southwestern Medical Center

3. Zaganjor, Elma 1981-. Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C.

Degree: 2013, University of Texas Southwestern Medical Center

 The kinesin-like protein KIF2A is a microtubule-associated motor protein thatauses microtubule depolymerization by inducing a conformational change in tubulin. The depolymerase function of KIF2A is… (more)

Subjects/Keywords: Cell Transformation, Neoplastic; Extracellular Signal-Regulated MAP Kinases; Kinesin

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APA (6th Edition):

Zaganjor, E. 1. (2013). Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-124

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):

Zaganjor, Elma 1981-. “Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-124.

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

MLA Handbook (7th Edition):

Zaganjor, Elma 1981-. “Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C.” 2013. Web. 09 Jul 2020.

Vancouver:

Zaganjor E1. Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-124.

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

Council of Science Editors:

Zaganjor E1. Regulation by ERK1/2 of Novel Substrates, Kinesins KIF2A and KIF2C. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-124

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


University of Texas Southwestern Medical Center

4. Estrada, Armando, III 1980-. Regulation of Cell Migration by WNK1.

Degree: 2012, University of Texas Southwestern Medical Center

 Cell motility is an immensely complex process that involves reorganization of the cytoskeleton, and consequent membrane deformation, triggered by a variety of motogenic stimuli, including… (more)

Subjects/Keywords: Cell Movement; Cytoskeleton; Protein-Serine-Threonine Kinases

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APA (6th Edition):

Estrada, Armando, I. 1. (2012). Regulation of Cell Migration by WNK1. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-65

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):

Estrada, Armando, III 1980-. “Regulation of Cell Migration by WNK1.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-65.

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

MLA Handbook (7th Edition):

Estrada, Armando, III 1980-. “Regulation of Cell Migration by WNK1.” 2012. Web. 09 Jul 2020.

Vancouver:

Estrada, Armando I1. Regulation of Cell Migration by WNK1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-65.

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

Council of Science Editors:

Estrada, Armando I1. Regulation of Cell Migration by WNK1. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-65

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


University of Texas Southwestern Medical Center

5. Kadamur Bhavani, Ganesh. Dual Regulation of Phospholipase C-beta by G betagamma.

Degree: 2016, University of Texas Southwestern Medical Center

 Agonist-bound G protein coupled receptors (GPCRs) activate G protein heterotrimers by catalyzing release of GDP and binding of GTP to the G alpha subunit (Ga),… (more)

Subjects/Keywords: GTP-Binding Protein beta Subunits; GTP-Binding Protein gamma Subunits; Phospholipase C beta

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APA (6th Edition):

Kadamur Bhavani, G. (2016). Dual Regulation of Phospholipase C-beta by G betagamma. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5297

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):

Kadamur Bhavani, Ganesh. “Dual Regulation of Phospholipase C-beta by G betagamma.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/5297.

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

MLA Handbook (7th Edition):

Kadamur Bhavani, Ganesh. “Dual Regulation of Phospholipase C-beta by G betagamma.” 2016. Web. 09 Jul 2020.

Vancouver:

Kadamur Bhavani G. Dual Regulation of Phospholipase C-beta by G betagamma. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/5297.

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

Council of Science Editors:

Kadamur Bhavani G. Dual Regulation of Phospholipase C-beta by G betagamma. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5297

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


University of Texas Southwestern Medical Center

6. Weil, Lauren Melissa. Regulation of the Cytoskeleton by Kinesins.

Degree: 2013, University of Texas Southwestern Medical Center

 Kinesins are motor proteins that associate with microtubules. The position of the motor domain has been linked to kinesin function. While amino-terminal and carboxy-terminal localization… (more)

Subjects/Keywords: Cytoskeleton; Kinesin; Microtubules; Mitosis

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APA (6th Edition):

Weil, L. M. (2013). Regulation of the Cytoskeleton by Kinesins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2731

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):

Weil, Lauren Melissa. “Regulation of the Cytoskeleton by Kinesins.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/2731.

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

MLA Handbook (7th Edition):

Weil, Lauren Melissa. “Regulation of the Cytoskeleton by Kinesins.” 2013. Web. 09 Jul 2020.

Vancouver:

Weil LM. Regulation of the Cytoskeleton by Kinesins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/2731.

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

Council of Science Editors:

Weil LM. Regulation of the Cytoskeleton by Kinesins. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2731

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


University of Texas Southwestern Medical Center

7. Medina, Frank J., III 1979-. Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF.

Degree: 2012, University of Texas Southwestern Medical Center

 RhoA plays a key role in regulation of the actin cytoskeleton, cell migration and cell shape. Rho GTPases cycle between an inactive GDP-bound state and… (more)

Subjects/Keywords: Guanine Nucleotide Exchange Factors; rhoA GTP-Binding Protein

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APA (6th Edition):

Medina, Frank J., I. 1. (2012). Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-66

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):

Medina, Frank J., III 1979-. “Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-66.

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

MLA Handbook (7th Edition):

Medina, Frank J., III 1979-. “Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF.” 2012. Web. 09 Jul 2020.

Vancouver:

Medina, Frank J. I1. Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-66.

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

Council of Science Editors:

Medina, Frank J. I1. Activated RhoA Positively Regulates Exchange Activity of PDZ-RhoGEF. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-66

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


University of Texas Southwestern Medical Center

8. Ayaz, Pelin 1983-. A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase.

Degree: 2012, University of Texas Southwestern Medical Center

 Stu2p/XMAP215/Dis1 family proteins are evolutionarily conserved regulatory factors that use alpha/beta-tubulin-interacting TOG (tumor overexpressed gene) domains to catalyze fast microtubule growth. Catalysis requires that these… (more)

Subjects/Keywords: Microtubule-Associated Proteins; Microtubules; Saccharomyces cerevisiae Proteins; Tubulin

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APA (6th Edition):

Ayaz, P. 1. (2012). A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-60

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):

Ayaz, Pelin 1983-. “A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-60.

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

MLA Handbook (7th Edition):

Ayaz, Pelin 1983-. “A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase.” 2012. Web. 09 Jul 2020.

Vancouver:

Ayaz P1. A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-60.

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

Council of Science Editors:

Ayaz P1. A TOG:αβ-Tubulin Complex Structure Reveals Conformation-Based Mechanisms for a Microtubule Polymerase. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-60

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


University of Texas Southwestern Medical Center

9. Carter, Angela Michelle. Mechanisms for Regulation of RhoA by Hormones.

Degree: 2012, University of Texas Southwestern Medical Center

 The family of RGS-RhoGEFs, which consists of p115RhoGEF, LARG, and PDZ-RhoGEF (PRG), are specific guanine nucleotide exchange factors (GEF) for the monomeric GTPase, RhoA. Like… (more)

Subjects/Keywords: Guanine Nucleotide Exchange Factors; Proto-Oncogene Proteins; Signal Transduction; rhoA GTP-Binding Protein

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APA (6th Edition):

Carter, A. M. (2012). Mechanisms for Regulation of RhoA by Hormones. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-67

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):

Carter, Angela Michelle. “Mechanisms for Regulation of RhoA by Hormones.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-67.

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

MLA Handbook (7th Edition):

Carter, Angela Michelle. “Mechanisms for Regulation of RhoA by Hormones.” 2012. Web. 09 Jul 2020.

Vancouver:

Carter AM. Mechanisms for Regulation of RhoA by Hormones. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-67.

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

Council of Science Editors:

Carter AM. Mechanisms for Regulation of RhoA by Hormones. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-12-67

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


University of Texas Southwestern Medical Center

10. McReynolds, Andrea Christine. Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding.

Degree: 2013, University of Texas Southwestern Medical Center

 The protein kinase extracellular signal-regulated kinase 2 (ERK2) has been well understood structurally for nearly twenty years. New insight is emerging about its structure and… (more)

Subjects/Keywords: DNA; Extracellular Signal-Regulated MAP Kinases; Phosphorylation

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APA (6th Edition):

McReynolds, A. C. (2013). Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2725

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):

McReynolds, Andrea Christine. “Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/2725.

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

MLA Handbook (7th Edition):

McReynolds, Andrea Christine. “Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding.” 2013. Web. 09 Jul 2020.

Vancouver:

McReynolds AC. Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/2725.

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

Council of Science Editors:

McReynolds AC. Functional Significance of Extracellular Signal Regulated Kinase (ERK2) Phosphorylation States: Implications for DNA Binding. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2725

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


University of Texas Southwestern Medical Center

11. Tu, Szu-Wei. Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking.

Degree: 2013, University of Texas Southwestern Medical Center

 <p>The file named "TU-DISSERTATION-2013.pdf" is the primary dissertation file. Twelve (12) supplemental videos are also provided (in Audio Video Interleaved format). p><p>With No Lysine (WNK)… (more)

Subjects/Keywords: Cytokinesis; Mitosis; Protein-Serine-Threonine Kinases; Spindle Apparatus

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APA (6th Edition):

Tu, S. (2013). Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1742

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):

Tu, Szu-Wei. “Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/1742.

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

MLA Handbook (7th Edition):

Tu, Szu-Wei. “Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking.” 2013. Web. 09 Jul 2020.

Vancouver:

Tu S. Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/1742.

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

Council of Science Editors:

Tu S. Investigating the Biological Functions of the Protein Kinase WNK1 in the Regulation of Cytoskeletal Structures and Membrane Trafficking. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1742

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


University of Texas Southwestern Medical Center

12. Seven, Alpay Burak. Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release.

Degree: 2015, University of Texas Southwestern Medical Center

 Neurotransmitter release is a central event in interneuronal communication. The release machinery includes three SNAREs (soluble N-ethylmaleimide sensitive factor adaptor protein receptor) and Munc18-1 as… (more)

Subjects/Keywords: Munc18 Proteins; Nerve Tissue Proteins; Neurotransmitter Agents; SNARE Proteins; Synaptic Vesicles; Synaptotagmin I

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APA (6th Edition):

Seven, A. B. (2015). Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4113

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):

Seven, Alpay Burak. “Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4113.

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

MLA Handbook (7th Edition):

Seven, Alpay Burak. “Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release.” 2015. Web. 09 Jul 2020.

Vancouver:

Seven AB. Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4113.

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

Council of Science Editors:

Seven AB. Unraveling the Functions of Synaptotagmin and Munc13 in Neurotransmitter Release. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4113

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


University of Texas Southwestern Medical Center

13. Checketts, Joshua Allen. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.

Degree: 2013, University of Texas Southwestern Medical Center

 Gene therapy is the ability to correct diseases at the DNA level and has long been a goal of science and medicine. The earliest gene… (more)

Subjects/Keywords: Gene Therapy; Gene Targeting; Severe Combined Immunodeficiency

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APA (6th Edition):

Checketts, J. A. (2013). Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1727

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):

Checketts, Joshua Allen. “Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/1727.

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

MLA Handbook (7th Edition):

Checketts, Joshua Allen. “Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.” 2013. Web. 09 Jul 2020.

Vancouver:

Checketts JA. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/1727.

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

Council of Science Editors:

Checketts JA. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1727

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


University of Texas Southwestern Medical Center

14. Semeiks, Jeremy Raymond. On Two Problems in Comparative Genomics of Eukaryotes.

Degree: 2013, University of Texas Southwestern Medical Center

 The recent advent of whole-genome sequencing allows us to use novel comparative methods to explore the genetic bases for traits of interest. Here, I present… (more)

Subjects/Keywords: Genes, Fungal; Multigene Family; Stachybotrys

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APA (6th Edition):

Semeiks, J. R. (2013). On Two Problems in Comparative Genomics of Eukaryotes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2015-05-94

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):

Semeiks, Jeremy Raymond. “On Two Problems in Comparative Genomics of Eukaryotes.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2015-05-94.

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

MLA Handbook (7th Edition):

Semeiks, Jeremy Raymond. “On Two Problems in Comparative Genomics of Eukaryotes.” 2013. Web. 09 Jul 2020.

Vancouver:

Semeiks JR. On Two Problems in Comparative Genomics of Eukaryotes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2015-05-94.

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

Council of Science Editors:

Semeiks JR. On Two Problems in Comparative Genomics of Eukaryotes. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2015-05-94

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


University of Texas Southwestern Medical Center

15. Taylor, Clinton A., IV. Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling.

Degree: 2016, University of Texas Southwestern Medical Center

 Protein-protein interactions are essential for nearly every cellular process. Within signaling pathways, such interactions carry out numerous functions such as defining substrate specificity, inhibition of… (more)

Subjects/Keywords: Mitogen-Activated Protein Kinase Kinases; Protein-Serine-Threonine Kinases; Signal Transduction; Transcription Factors

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APA (6th Edition):

Taylor, Clinton A., I. (2016). Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6152

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):

Taylor, Clinton A., IV. “Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/6152.

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

MLA Handbook (7th Edition):

Taylor, Clinton A., IV. “Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling.” 2016. Web. 09 Jul 2020.

Vancouver:

Taylor, Clinton A. I. Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/6152.

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

Council of Science Editors:

Taylor, Clinton A. I. Regulation and Dysregulation via Docking Interactions in WNK and ERK1/2 MAPK Signaling. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/6152

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


University of Texas Southwestern Medical Center

16. Ghosh, Anwesha. Studies on Cellular Nutrient Responses and Protein Degradation.

Degree: 2015, University of Texas Southwestern Medical Center

 I have worked on two projects. The first project investigates mechanisms involved in cellular responses to amino acids. Amino-acid abundance promotes protein synthesis and cell… (more)

Subjects/Keywords: Autophagy; Intercellular Signaling Peptides and Proteins; TOR Serine-Threonine Kinases; Ubiquitin-Protein Ligases

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APA (6th Edition):

Ghosh, A. (2015). Studies on Cellular Nutrient Responses and Protein Degradation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4204

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):

Ghosh, Anwesha. “Studies on Cellular Nutrient Responses and Protein Degradation.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4204.

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

MLA Handbook (7th Edition):

Ghosh, Anwesha. “Studies on Cellular Nutrient Responses and Protein Degradation.” 2015. Web. 09 Jul 2020.

Vancouver:

Ghosh A. Studies on Cellular Nutrient Responses and Protein Degradation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4204.

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

Council of Science Editors:

Ghosh A. Studies on Cellular Nutrient Responses and Protein Degradation. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4204

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


University of Texas Southwestern Medical Center

17. Cupka, Dorothy Lynn. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.

Degree: 2015, University of Texas Southwestern Medical Center

 Targeted delivery of imaging and therapeutic agents to tumors improves detection, characterization, and treatment of many types of cancers. Peptides are capable of efficient and… (more)

Subjects/Keywords: Antigens, Neoplasm; Integrins; Neoplasms; Peptides

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APA (6th Edition):

Cupka, D. L. (2015). Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4208

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):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4208.

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

MLA Handbook (7th Edition):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Web. 09 Jul 2020.

Vancouver:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4208.

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

Council of Science Editors:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4208

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


University of Texas Southwestern Medical Center

18. Peres, Yair. Role for Lipids in the Cellular Transmission of α-Synuclein.

Degree: 2015, University of Texas Southwestern Medical Center

 The presynaptic protein α-Synuclein (α-Syn) abnormally aggregates in the brains of Parkinson's Disease patients. Evidence suggest a transcellular transfer of an oligomeric form of the… (more)

Subjects/Keywords: alpha-Synuclein; Brain; Lipid Metabolism; Parkinson Disease

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APA (6th Edition):

Peres, Y. (2015). Role for Lipids in the Cellular Transmission of α-Synuclein. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4205

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):

Peres, Yair. “Role for Lipids in the Cellular Transmission of α-Synuclein.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4205.

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

MLA Handbook (7th Edition):

Peres, Yair. “Role for Lipids in the Cellular Transmission of α-Synuclein.” 2015. Web. 09 Jul 2020.

Vancouver:

Peres Y. Role for Lipids in the Cellular Transmission of α-Synuclein. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4205.

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

Council of Science Editors:

Peres Y. Role for Lipids in the Cellular Transmission of α-Synuclein. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4205

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


University of Texas Southwestern Medical Center

19. Velez, Nahir Aimee 1983-. Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog.

Degree: 2012, University of Texas Southwestern Medical Center

 Human African Trypanosomiasis (HAT) is caused by single-celled parasites, Trypanosoma brucei, which are transmitted to humans by infected tsetse flies. Trypanosomiasis has a profound impact… (more)

Subjects/Keywords: Adenosylmethionine Decarboxylase; Trypanosoma brucei brucei; Trypanosomiasis, African

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APA (6th Edition):

Velez, N. A. 1. (2012). Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-08-64

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):

Velez, Nahir Aimee 1983-. “Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-08-64.

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

MLA Handbook (7th Edition):

Velez, Nahir Aimee 1983-. “Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog.” 2012. Web. 09 Jul 2020.

Vancouver:

Velez NA1. Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-08-64.

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

Council of Science Editors:

Velez NA1. Structural Basis for the Allosteric Activation of Trypanosoma Brucei S-adenosylmethionine Decarboxylase by a Catalytically Dead Homolog. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2012-08-64

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


University of Texas Southwestern Medical Center

20. Leitz, Jeremy Thomas Sheng. Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion.

Degree: 2014, University of Texas Southwestern Medical Center

 Synaptic vesicle recycling is critical for the maintenance and proper function of neurotransmission. Neurotransmission can proceed through action-potential evoked vesicle fusion where, upon depolarization, Ca2+… (more)

Subjects/Keywords: Calcium; Endocytosis; Neurons; Synapses; Synaptic Vesicles

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APA (6th Edition):

Leitz, J. T. S. (2014). Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3576

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):

Leitz, Jeremy Thomas Sheng. “Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/3576.

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

MLA Handbook (7th Edition):

Leitz, Jeremy Thomas Sheng. “Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion.” 2014. Web. 09 Jul 2020.

Vancouver:

Leitz JTS. Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/3576.

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

Council of Science Editors:

Leitz JTS. Optical Quantal Analysis of Evoked and Spontaneous Single-Vesicle Fusion. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3576

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


University of Texas Southwestern Medical Center

21. Collins, Katie Anne. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.

Degree: 2014, University of Texas Southwestern Medical Center

 Autism is a neurological disorder characterized by repetetive behaviors, social anxiety and verbal and non-verbal communication. Fragile X Syndrome (FXS) is the most common genetic… (more)

Subjects/Keywords: Carrier Proteins; Fragile X Syndrome; Gene Expression Regulation; Receptors, Metabotropic Glutamate

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APA (6th Edition):

Collins, K. A. (2014). The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3308

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):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/3308.

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

MLA Handbook (7th Edition):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Web. 09 Jul 2020.

Vancouver:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/3308.

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

Council of Science Editors:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3308

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


University of Texas Southwestern Medical Center

22. Kuo, Yi-Chun. Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective.

Degree: 2017, University of Texas Southwestern Medical Center

 The Semaphorin-Plexin signaling is important for regulating axon guidance. Binding of Semaphorin to the Plexin receptor induces the dimerization of Plexin and stimulates its cytoplasmic… (more)

Subjects/Keywords: Cell Adhesion Molecules; Nerve Tissue Proteins; Receptors, Cell Surface; rho GTP-Binding Proteins

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APA (6th Edition):

Kuo, Y. (2017). Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7739

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):

Kuo, Yi-Chun. “Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/7739.

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

MLA Handbook (7th Edition):

Kuo, Yi-Chun. “Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective.” 2017. Web. 09 Jul 2020.

Vancouver:

Kuo Y. Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/7739.

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

Council of Science Editors:

Kuo Y. Dissecting the Function of FARP1 and Rho GTPases in Semaphorin-Plexin Signaling: Structural Perspective. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7739

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


University of Texas Southwestern Medical Center

23. Jung, Gwanghyun. Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase.

Degree: PhD, Genetics & Development, 2008, University of Texas Southwestern Medical Center

 Phosphoinositides play fundamental roles in controlling membrane-based signaling events. Phosphatidylinositol 4-kinases (PI4Ks) catalyze the production of PI4P, a major precursor in phosphoinositide biosynthesis, and consist… (more)

Subjects/Keywords: Protein Sorting Signals; Mass Spectrometry; Immunoprecipitation; Phosphatidylinositols

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

APA (6th Edition):

Jung, G. (2008). Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase. (Doctoral Dissertation). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/581

Chicago Manual of Style (16th Edition):

Jung, Gwanghyun. “Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase.” 2008. Doctoral Dissertation, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/581.

MLA Handbook (7th Edition):

Jung, Gwanghyun. “Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase.” 2008. Web. 09 Jul 2020.

Vancouver:

Jung G. Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase. [Internet] [Doctoral dissertation]. University of Texas Southwestern Medical Center; 2008. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/581.

Council of Science Editors:

Jung G. Molecular and Functional Analysis of Phosphatidylinositol 4 Kinase. [Doctoral Dissertation]. University of Texas Southwestern Medical Center; 2008. Available from: http://hdl.handle.net/2152.5/581

.