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You searched for subject:(reticulum). Showing records 1 – 30 of 531 total matches.

[1] [2] [3] [4] [5] … [18]

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Oregon State University

1. Dixon, Brian M. The aging endoplasmic reticulum.

Degree: PhD, Molecular and Cellular Biology, 2008, Oregon State University

 Hallmarks of aging include the accumulation of aberrant proteins and a lower resistance to stresses. Because the endoplasmic reticulum (ER) functions to fold proteins and… (more)

Subjects/Keywords: Endoplasmic Reticulum; Endoplasmic reticulum

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APA (6th Edition):

Dixon, B. M. (2008). The aging endoplasmic reticulum. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/8283

Chicago Manual of Style (16th Edition):

Dixon, Brian M. “The aging endoplasmic reticulum.” 2008. Doctoral Dissertation, Oregon State University. Accessed January 25, 2020. http://hdl.handle.net/1957/8283.

MLA Handbook (7th Edition):

Dixon, Brian M. “The aging endoplasmic reticulum.” 2008. Web. 25 Jan 2020.

Vancouver:

Dixon BM. The aging endoplasmic reticulum. [Internet] [Doctoral dissertation]. Oregon State University; 2008. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1957/8283.

Council of Science Editors:

Dixon BM. The aging endoplasmic reticulum. [Doctoral Dissertation]. Oregon State University; 2008. Available from: http://hdl.handle.net/1957/8283


University of Alberta

2. Coe, Helen. Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function.

Degree: PhD, Medical Sciences-Paediatrics, 2010, University of Alberta

 The endoplasmic reticulum is responsible for folding of newly synthesized proteins. Chaperone proteins, calreticulin and calnexin, with the thiol-oxidoreductase ERp57, interact with nascent proteins in… (more)

Subjects/Keywords: endoplasmic reticulum

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APA (6th Edition):

Coe, H. (2010). Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/8k71nh69m

Chicago Manual of Style (16th Edition):

Coe, Helen. “Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function.” 2010. Doctoral Dissertation, University of Alberta. Accessed January 25, 2020. https://era.library.ualberta.ca/files/8k71nh69m.

MLA Handbook (7th Edition):

Coe, Helen. “Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function.” 2010. Web. 25 Jan 2020.

Vancouver:

Coe H. Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2020 Jan 25]. Available from: https://era.library.ualberta.ca/files/8k71nh69m.

Council of Science Editors:

Coe H. Endoplasmic Reticulum Chaperone Proteins Calnexin and ERp57: Structure and Function. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/8k71nh69m


Texas A&M University

3. Wahlman, Judit. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.

Degree: 2009, Texas A&M University

 Secretory proteins that are unable to assemble into native proteins in the endoplasmic reticulum (ER) are transported back into the cytosol for degradation. Many cytosolic… (more)

Subjects/Keywords: Fluorescence; endoplasmic reticulum

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APA (6th Edition):

Wahlman, J. (2009). Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2019

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):

Wahlman, Judit. “Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.” 2009. Thesis, Texas A&M University. Accessed January 25, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2019.

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

MLA Handbook (7th Edition):

Wahlman, Judit. “Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.” 2009. Web. 25 Jan 2020.

Vancouver:

Wahlman J. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2019.

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

Council of Science Editors:

Wahlman J. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2019

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


University of Georgia

4. Patham, Bhargavi. Protein translocation across endoplasmic reticulum of a trypanosome.

Degree: PhD, Cellular Biology, 2005, University of Georgia

 Despite being recognized as an important organelle in the secretory pathway, not many aspects of endoplasmic reticulum (ER) protein import are understood in Trypanosoma brucei,… (more)

Subjects/Keywords: Endoplasmic Reticulum

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APA (6th Edition):

Patham, B. (2005). Protein translocation across endoplasmic reticulum of a trypanosome. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/patham_bhargavi_200508_phd

Chicago Manual of Style (16th Edition):

Patham, Bhargavi. “Protein translocation across endoplasmic reticulum of a trypanosome.” 2005. Doctoral Dissertation, University of Georgia. Accessed January 25, 2020. http://purl.galileo.usg.edu/uga_etd/patham_bhargavi_200508_phd.

MLA Handbook (7th Edition):

Patham, Bhargavi. “Protein translocation across endoplasmic reticulum of a trypanosome.” 2005. Web. 25 Jan 2020.

Vancouver:

Patham B. Protein translocation across endoplasmic reticulum of a trypanosome. [Internet] [Doctoral dissertation]. University of Georgia; 2005. [cited 2020 Jan 25]. Available from: http://purl.galileo.usg.edu/uga_etd/patham_bhargavi_200508_phd.

Council of Science Editors:

Patham B. Protein translocation across endoplasmic reticulum of a trypanosome. [Doctoral Dissertation]. University of Georgia; 2005. Available from: http://purl.galileo.usg.edu/uga_etd/patham_bhargavi_200508_phd


University of Alberta

5. Jung, Joanna. The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins.

Degree: PhD, Department of Biochemistry, 2011, University of Alberta

 ABSTRACT Endoplasmic reticulum (ER) plays an essential role in the proper folding, maturation and quality control of newly synthesized membrane and secretory proteins. The ER… (more)

Subjects/Keywords: Endoplasmic reticulum, calnexin, myelin glycoproteins

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APA (6th Edition):

Jung, J. (2011). The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/bg257f046

Chicago Manual of Style (16th Edition):

Jung, Joanna. “The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins.” 2011. Doctoral Dissertation, University of Alberta. Accessed January 25, 2020. https://era.library.ualberta.ca/files/bg257f046.

MLA Handbook (7th Edition):

Jung, Joanna. “The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins.” 2011. Web. 25 Jan 2020.

Vancouver:

Jung J. The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2020 Jan 25]. Available from: https://era.library.ualberta.ca/files/bg257f046.

Council of Science Editors:

Jung J. The role of endoplasmic reticulum quality control system in the biology of the major myelin glycoproteins. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/bg257f046


University of Alberta

6. Burton, Robyn-Lee. Initial Characterization of Vaccinia Virus B6.

Degree: MS, Department of Medical Microbiology and Immunology, 2014, University of Alberta

 Vaccinia virus, the prototypic poxvirus, is remarkably successful at circumventing the host immune response using an array of dedicated proteins. Studying these immune modulators and… (more)

Subjects/Keywords: Endoplasmic reticulum; Vaccinia; B6

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APA (6th Edition):

Burton, R. (2014). Initial Characterization of Vaccinia Virus B6. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/707958117

Chicago Manual of Style (16th Edition):

Burton, Robyn-Lee. “Initial Characterization of Vaccinia Virus B6.” 2014. Masters Thesis, University of Alberta. Accessed January 25, 2020. https://era.library.ualberta.ca/files/707958117.

MLA Handbook (7th Edition):

Burton, Robyn-Lee. “Initial Characterization of Vaccinia Virus B6.” 2014. Web. 25 Jan 2020.

Vancouver:

Burton R. Initial Characterization of Vaccinia Virus B6. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2020 Jan 25]. Available from: https://era.library.ualberta.ca/files/707958117.

Council of Science Editors:

Burton R. Initial Characterization of Vaccinia Virus B6. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/707958117

7. 木俣, 有紀. 小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: endoplasmic reticulum

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APA (6th Edition):

木俣, . (n.d.). 小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/8661

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

木俣, 有紀. “小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed January 25, 2020. http://hdl.handle.net/10061/8661.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

木俣, 有紀. “小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ.” Web. 25 Jan 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

木俣 . 小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2020 Jan 25]. Available from: http://hdl.handle.net/10061/8661.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

木俣 . 小胞体ストレスセンサーIre1の活性化機構の多様性に関する研究 : Membrane aberrancy and unfolded proteins activate the endoplasmic reticulum stress sensor Ire1 in different ways; ショウホウタイ ストレス センサー Ire1 ノ カッセイカ キコウ ノ タヨウセイ ニ カンスル ケンキュウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/8661

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Cornell University

8. Davis, Kristen. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .

Degree: 2015, Cornell University

 Lactation is an essential stage of mammalian life. Milk is a complex fluid that provides complete nutrition for neonates in the early stages of postnatal… (more)

Subjects/Keywords: endoplasmic reticulum; mammary gland; lactation

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APA (6th Edition):

Davis, K. (2015). Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40669

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):

Davis, Kristen. “Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .” 2015. Thesis, Cornell University. Accessed January 25, 2020. http://hdl.handle.net/1813/40669.

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

MLA Handbook (7th Edition):

Davis, Kristen. “Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .” 2015. Web. 25 Jan 2020.

Vancouver:

Davis K. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1813/40669.

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

Council of Science Editors:

Davis K. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40669

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


Cornell University

9. Manford, Andrew. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation .

Degree: 2014, Cornell University

 Endoplasmic reticulum-plasma membrane (ER-PM) contact sites are specialized stable regions of the ER that are tightly apposed to the PM. These conserved organelle junctions are… (more)

Subjects/Keywords: Phosphoinositide; Endoplasmic Reticulum; Plasma Membrane

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APA (6th Edition):

Manford, A. (2014). Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36042

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):

Manford, Andrew. “Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation .” 2014. Thesis, Cornell University. Accessed January 25, 2020. http://hdl.handle.net/1813/36042.

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

MLA Handbook (7th Edition):

Manford, Andrew. “Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation .” 2014. Web. 25 Jan 2020.

Vancouver:

Manford A. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1813/36042.

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

Council of Science Editors:

Manford A. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36042

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


Cornell University

10. Sun, Shengyi. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease .

Degree: 2015, Cornell University

 A growing epidemic of obesity and inflammatory bowel disease is threatening the health of millions of people around the world. Recent studies have established that… (more)

Subjects/Keywords: Inflammation; Endoplasmic reticulum; Disease

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APA (6th Edition):

Sun, S. (2015). The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/39422

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):

Sun, Shengyi. “The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease .” 2015. Thesis, Cornell University. Accessed January 25, 2020. http://hdl.handle.net/1813/39422.

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

MLA Handbook (7th Edition):

Sun, Shengyi. “The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease .” 2015. Web. 25 Jan 2020.

Vancouver:

Sun S. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1813/39422.

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

Council of Science Editors:

Sun S. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39422

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


Hong Kong University of Science and Technology

11. Zhang, Chao. Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1).

Degree: 2012, Hong Kong University of Science and Technology

 The endoplasmic reticulum (ER) is a continuous membrane network in eukaryotic cells composed of the nuclear envelope, the rough ER and the smooth ER. ER… (more)

Subjects/Keywords: Endoplasmic reticulum ; Membrane proteins

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APA (6th Edition):

Zhang, C. (2012). Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1). (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7512 ; https://doi.org/10.14711/thesis-b1169583 ; http://repository.ust.hk/ir/bitstream/1783.1-7512/1/th_redirect.html

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):

Zhang, Chao. “Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1).” 2012. Thesis, Hong Kong University of Science and Technology. Accessed January 25, 2020. http://repository.ust.hk/ir/Record/1783.1-7512 ; https://doi.org/10.14711/thesis-b1169583 ; http://repository.ust.hk/ir/bitstream/1783.1-7512/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhang, Chao. “Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1).” 2012. Web. 25 Jan 2020.

Vancouver:

Zhang C. Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1). [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Jan 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-7512 ; https://doi.org/10.14711/thesis-b1169583 ; http://repository.ust.hk/ir/bitstream/1783.1-7512/1/th_redirect.html.

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

Council of Science Editors:

Zhang C. Characterization of the novel protein transmembrane and coiled-coil domain family 1 (TMCC1). [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-7512 ; https://doi.org/10.14711/thesis-b1169583 ; http://repository.ust.hk/ir/bitstream/1783.1-7512/1/th_redirect.html

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


Wayne State University

12. Sleiman, Naama. Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes.

Degree: PhD, Physiology, 2014, Wayne State University

  Junctional SR is an important and unique ER subdomain in the adult myocyte that releases Ca2+ through the actions of an exclusive set of… (more)

Subjects/Keywords: Calsequestrin; Endoplasmic Reticulum; Hypertrophy; Sarcoplasmic Reticulum; Trafficking; Triadin; Cell Biology; Physiology

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APA (6th Edition):

Sleiman, N. (2014). Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1056

Chicago Manual of Style (16th Edition):

Sleiman, Naama. “Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes.” 2014. Doctoral Dissertation, Wayne State University. Accessed January 25, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1056.

MLA Handbook (7th Edition):

Sleiman, Naama. “Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes.” 2014. Web. 25 Jan 2020.

Vancouver:

Sleiman N. Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes. [Internet] [Doctoral dissertation]. Wayne State University; 2014. [cited 2020 Jan 25]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1056.

Council of Science Editors:

Sleiman N. Junctional Sarcoplasmic Reticulum Protein Processing And Trafficking In Cardiac Tissue And Primary Cultured Cardiomyocytes. [Doctoral Dissertation]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1056


IUPUI

13. Akin, Brandy Lee. Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum.

Degree: 2011, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The Ca2+ pump or Ca2+-ATPase of cardiac sarcoplasmic reticulum, SERCA2a, is regulated by phospholamban (PLB), a small inhibitory phosphoprotein that… (more)

Subjects/Keywords: Ca-ATPase; SERCA; phospholamban; calcium; sarcoplasmic reticulum; Phosphoproteins; Sarcoplasmic reticulum; Calcium

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APA (6th Edition):

Akin, B. L. (2011). Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2516

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):

Akin, Brandy Lee. “Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum.” 2011. Thesis, IUPUI. Accessed January 25, 2020. http://hdl.handle.net/1805/2516.

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

MLA Handbook (7th Edition):

Akin, Brandy Lee. “Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum.” 2011. Web. 25 Jan 2020.

Vancouver:

Akin BL. Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum. [Internet] [Thesis]. IUPUI; 2011. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1805/2516.

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

Council of Science Editors:

Akin BL. Investigating the molecular mechanism of phospholamban regulation of the Ca²-pump of cardiac sarcoplasmic reticulum. [Thesis]. IUPUI; 2011. Available from: http://hdl.handle.net/1805/2516

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


University of Hong Kong

14. 谭志佳; Tan, Zhijia. Molecular analyses of chondrocyte differentiation and adaptation to ER stress.

Degree: PhD, 2013, University of Hong Kong

 Endochondral bone development depends on the progression of chondrocyte proliferation, hypertrophy and terminal differentiation, which requires precise transcriptional regulation and signaling coordination. Disturbance of this… (more)

Subjects/Keywords: Cell differentiation; Endoplasmic reticulum; Cartilage cells

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APA (6th Edition):

谭志佳; Tan, Z. (2013). Molecular analyses of chondrocyte differentiation and adaptation to ER stress. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tan, Z. [谭志佳]. (2013). Molecular analyses of chondrocyte differentiation and adaptation to ER stress. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016250 ; http://dx.doi.org/10.5353/th_b5016250 ; http://hdl.handle.net/10722/209435

Chicago Manual of Style (16th Edition):

谭志佳; Tan, Zhijia. “Molecular analyses of chondrocyte differentiation and adaptation to ER stress.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed January 25, 2020. Tan, Z. [谭志佳]. (2013). Molecular analyses of chondrocyte differentiation and adaptation to ER stress. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016250 ; http://dx.doi.org/10.5353/th_b5016250 ; http://hdl.handle.net/10722/209435.

MLA Handbook (7th Edition):

谭志佳; Tan, Zhijia. “Molecular analyses of chondrocyte differentiation and adaptation to ER stress.” 2013. Web. 25 Jan 2020.

Vancouver:

谭志佳; Tan Z. Molecular analyses of chondrocyte differentiation and adaptation to ER stress. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2020 Jan 25]. Available from: Tan, Z. [谭志佳]. (2013). Molecular analyses of chondrocyte differentiation and adaptation to ER stress. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016250 ; http://dx.doi.org/10.5353/th_b5016250 ; http://hdl.handle.net/10722/209435.

Council of Science Editors:

谭志佳; Tan Z. Molecular analyses of chondrocyte differentiation and adaptation to ER stress. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Tan, Z. [谭志佳]. (2013). Molecular analyses of chondrocyte differentiation and adaptation to ER stress. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5016250 ; http://dx.doi.org/10.5353/th_b5016250 ; http://hdl.handle.net/10722/209435


University of Minnesota

15. O'Rourke, Allison. A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2017, University of Minnesota

 Skeletal muscle accounts for 40% of mass in adult humans. The primary function of skeletal muscle is to produce movement via contraction of the sarcomere.… (more)

Subjects/Keywords: Actin Isoforms; Mitochondria; Sarcoplasmic Reticulum; Skeletal Muscle

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APA (6th Edition):

O'Rourke, A. (2017). A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/199033

Chicago Manual of Style (16th Edition):

O'Rourke, Allison. “A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface.” 2017. Doctoral Dissertation, University of Minnesota. Accessed January 25, 2020. http://hdl.handle.net/11299/199033.

MLA Handbook (7th Edition):

O'Rourke, Allison. “A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface.” 2017. Web. 25 Jan 2020.

Vancouver:

O'Rourke A. A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/11299/199033.

Council of Science Editors:

O'Rourke A. A Role for βcyto- and γcyto Actin at the Sarco/endoplasmic Reticulum-Mitochondrial Interface. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/199033


Penn State University

16. Wei, Jianwen. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.

Degree: PhD, Genetics, 2008, Penn State University

 PERK (eukaryotic translation initiation factor 2 alpha kinase 3) is an endoplasmic reticulum (ER) resident transmembrane protein. In response to alterations of ER homeostasis, PERK… (more)

Subjects/Keywords: PERK; osteoblast; Runx2; procollagen; proliferation; endoplasmic reticulum

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APA (6th Edition):

Wei, J. (2008). PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8441

Chicago Manual of Style (16th Edition):

Wei, Jianwen. “PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.” 2008. Doctoral Dissertation, Penn State University. Accessed January 25, 2020. https://etda.libraries.psu.edu/catalog/8441.

MLA Handbook (7th Edition):

Wei, Jianwen. “PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.” 2008. Web. 25 Jan 2020.

Vancouver:

Wei J. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Jan 25]. Available from: https://etda.libraries.psu.edu/catalog/8441.

Council of Science Editors:

Wei J. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8441


Penn State University

17. Gupta, Sounak. PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY.

Degree: PhD, Molecular Medicine, 2010, Penn State University

 Loss of function mutations of Perk (EIF2AK3) in humans leads to the Wolcott-Rallison Syndrome (WRS), which is the most common cause of consanguineous cases of… (more)

Subjects/Keywords: DIABETES; TRAFFICKING; PERK; INSULINOMA; ENDOPLASMIC RETICULUM; PROINSULIN

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APA (6th Edition):

Gupta, S. (2010). PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11066

Chicago Manual of Style (16th Edition):

Gupta, Sounak. “PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY.” 2010. Doctoral Dissertation, Penn State University. Accessed January 25, 2020. https://etda.libraries.psu.edu/catalog/11066.

MLA Handbook (7th Edition):

Gupta, Sounak. “PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY.” 2010. Web. 25 Jan 2020.

Vancouver:

Gupta S. PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2020 Jan 25]. Available from: https://etda.libraries.psu.edu/catalog/11066.

Council of Science Editors:

Gupta S. PERK (EIF2AK3) REGULATES PROINSULIN TRAFFICKING AND QUALITY CONTROL IN THE SECRETORY PATHWAY. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11066


Montana Tech

18. Bentley, Marvin. Luminal calcium regulates membrane fusion in the early secretory pathway.

Degree: PhD, 2010, Montana Tech

 Calcium is an important regulatory ion which acts as a trigger or is required at a basal level for many membrane fusion events. The role… (more)

Subjects/Keywords: calcium; COPII; endoplasmic reticulum; ERGIC; Golgi; transport

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APA (6th Edition):

Bentley, M. (2010). Luminal calcium regulates membrane fusion in the early secretory pathway. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/636

Chicago Manual of Style (16th Edition):

Bentley, Marvin. “Luminal calcium regulates membrane fusion in the early secretory pathway.” 2010. Doctoral Dissertation, Montana Tech. Accessed January 25, 2020. https://scholarworks.umt.edu/etd/636.

MLA Handbook (7th Edition):

Bentley, Marvin. “Luminal calcium regulates membrane fusion in the early secretory pathway.” 2010. Web. 25 Jan 2020.

Vancouver:

Bentley M. Luminal calcium regulates membrane fusion in the early secretory pathway. [Internet] [Doctoral dissertation]. Montana Tech; 2010. [cited 2020 Jan 25]. Available from: https://scholarworks.umt.edu/etd/636.

Council of Science Editors:

Bentley M. Luminal calcium regulates membrane fusion in the early secretory pathway. [Doctoral Dissertation]. Montana Tech; 2010. Available from: https://scholarworks.umt.edu/etd/636

19. El Boustany, Charbel. Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver.

Degree: Docteur es, Biologie-Santé, 2009, Université Lille I – Sciences et Technologies

La tumeur maligne primitive du foie la plus fréquente est le carcinome hépatocellulaire. Le développement des cellules tumorales hépatiques dépend d'un influx calcique dont la… (more)

Subjects/Keywords: Protéines du reticulum endoplasmique; Homéostasie calcique

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APA (6th Edition):

El Boustany, C. (2009). Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2009LIL10038

Chicago Manual of Style (16th Edition):

El Boustany, Charbel. “Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver.” 2009. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed January 25, 2020. http://www.theses.fr/2009LIL10038.

MLA Handbook (7th Edition):

El Boustany, Charbel. “Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver.” 2009. Web. 25 Jan 2020.

Vancouver:

El Boustany C. Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2009. [cited 2020 Jan 25]. Available from: http://www.theses.fr/2009LIL10038.

Council of Science Editors:

El Boustany C. Rôle des canaux calciques de la membrane plasmique dans la prolifération des cellules tumorales hépatiques : Role of plasma membrane calcium channels in tumoral cell proliferation in human liver. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2009. Available from: http://www.theses.fr/2009LIL10038


University of the Western Cape

20. Isaacs, Rabia. The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells.

Degree: 2012, University of the Western Cape

 Cancer is defined as the abnormal growth of genetically mutated or perturbant cells. Nicotine is a known cancer promoter and an apoptotic suppressor. This alkaloid… (more)

Subjects/Keywords: Nicotine; Tunicamycin; Endoplasmic reticulum; Thapsigargin; Apoptosis

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APA (6th Edition):

Isaacs, R. (2012). The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells. (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4579

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):

Isaacs, Rabia. “The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells. ” 2012. Thesis, University of the Western Cape. Accessed January 25, 2020. http://hdl.handle.net/11394/4579.

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

MLA Handbook (7th Edition):

Isaacs, Rabia. “The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells. ” 2012. Web. 25 Jan 2020.

Vancouver:

Isaacs R. The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells. [Internet] [Thesis]. University of the Western Cape; 2012. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/11394/4579.

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

Council of Science Editors:

Isaacs R. The in vitro effects of nicotine and selected antibiotics, tunicamycin and thapsigargin on human Breast carcinoma (mcf-7) cells. [Thesis]. University of the Western Cape; 2012. Available from: http://hdl.handle.net/11394/4579

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


Texas State University – San Marcos

21. Duarte, Adam. Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus).

Degree: MS, Wildlife Ecology, 2011, Texas State University – San Marcos

 Understanding capacity and fill dynamics of the gastrointestinal tract under different environmental conditions gives insight into how herbivores meet life history demands. In female white-tailed… (more)

Subjects/Keywords: Digestive physiology; Rumen-reticulum; White-tailed deer

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APA (6th Edition):

Duarte, A. (2011). Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus). (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/4272

Chicago Manual of Style (16th Edition):

Duarte, Adam. “Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus).” 2011. Masters Thesis, Texas State University – San Marcos. Accessed January 25, 2020. https://digital.library.txstate.edu/handle/10877/4272.

MLA Handbook (7th Edition):

Duarte, Adam. “Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus).” 2011. Web. 25 Jan 2020.

Vancouver:

Duarte A. Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus). [Internet] [Masters thesis]. Texas State University – San Marcos; 2011. [cited 2020 Jan 25]. Available from: https://digital.library.txstate.edu/handle/10877/4272.

Council of Science Editors:

Duarte A. Dynamics of Rumen-Reticulum Capacity and Fill In Female White-Tailed Deer (Odocoileus Virginianus). [Masters Thesis]. Texas State University – San Marcos; 2011. Available from: https://digital.library.txstate.edu/handle/10877/4272


Drexel University

22. Lao, Taotao. OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum.

Degree: 2011, Drexel University

Hypoxia-inducible factor 1 (HIF-1) is the master regulator of oxygen homeostasis and plays critical roles in cells’ responses to multiple signaling by activating proangiogenic progress… (more)

Subjects/Keywords: Biology; Hypoxia-inducible factor; Endoplasmic reticulum

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APA (6th Edition):

Lao, T. (2011). OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/3981

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):

Lao, Taotao. “OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum.” 2011. Thesis, Drexel University. Accessed January 25, 2020. http://hdl.handle.net/1860/3981.

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

MLA Handbook (7th Edition):

Lao, Taotao. “OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum.” 2011. Web. 25 Jan 2020.

Vancouver:

Lao T. OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum. [Internet] [Thesis]. Drexel University; 2011. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/1860/3981.

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

Council of Science Editors:

Lao T. OS-9 regulates hypoxia-inducible factor 1a in the endoplasmic reticulum. [Thesis]. Drexel University; 2011. Available from: http://hdl.handle.net/1860/3981

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


University of Cambridge

23. Capatina, Nadejda. Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation.

Degree: PhD, 2019, University of Cambridge

 The project aimed to provide a mechanistic understanding of the effect of endoplasmic reticulum (ER) stress on the differentiation of trophoblast stem cells (TSCs), placental… (more)

Subjects/Keywords: endoplasmic reticulum stress; trophoblast; stem cell differentiation

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APA (6th Edition):

Capatina, N. (2019). Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/298767

Chicago Manual of Style (16th Edition):

Capatina, Nadejda. “Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 25, 2020. https://www.repository.cam.ac.uk/handle/1810/298767.

MLA Handbook (7th Edition):

Capatina, Nadejda. “Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation.” 2019. Web. 25 Jan 2020.

Vancouver:

Capatina N. Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jan 25]. Available from: https://www.repository.cam.ac.uk/handle/1810/298767.

Council of Science Editors:

Capatina N. Role of Endoplasmic Reticulum Stress in Trophoblast Stem Cell Differentiation. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/298767


University of Cape Town

24. Arendse, Michael Peter. Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle.

Degree: Image, Division of Chemical Pathology, 1979, University of Cape Town

 Mild acid treatment or incubation in the presence of Ethylene glycol bis (β-aminoethyl ether) - N,N' - tetraacetic acid inactivates calcium transport by sarcoplasmic reticulum(more)

Subjects/Keywords: Sarcoplasmic reticulum; Membranes

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APA (6th Edition):

Arendse, M. P. (1979). Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27656

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):

Arendse, Michael Peter. “Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle.” 1979. Thesis, University of Cape Town. Accessed January 25, 2020. http://hdl.handle.net/11427/27656.

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

MLA Handbook (7th Edition):

Arendse, Michael Peter. “Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle.” 1979. Web. 25 Jan 2020.

Vancouver:

Arendse MP. Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle. [Internet] [Thesis]. University of Cape Town; 1979. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/11427/27656.

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

Council of Science Editors:

Arendse MP. Membrane reconstitution studies on the irreversibility of inactivation of sarcoplasmic reticulum of rabbit skeletal muscle. [Thesis]. University of Cape Town; 1979. Available from: http://hdl.handle.net/11427/27656

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


University of Tasmania

25. Pavez, MP. STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones.

Degree: 2018, University of Tasmania

 The precise connectivity that underlies neural circuitry in the central nervous system is regulated by axon guidance. This process is regulated by a highly specialized… (more)

Subjects/Keywords: Calcium; growth cone; cytoskeleton; microtubules; endoplasmic reticulum

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APA (6th Edition):

Pavez, M. (2018). STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/29666/1/Pavez_whole_thesis.pdf

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):

Pavez, MP. “STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones.” 2018. Thesis, University of Tasmania. Accessed January 25, 2020. https://eprints.utas.edu.au/29666/1/Pavez_whole_thesis.pdf.

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

MLA Handbook (7th Edition):

Pavez, MP. “STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones.” 2018. Web. 25 Jan 2020.

Vancouver:

Pavez M. STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones. [Internet] [Thesis]. University of Tasmania; 2018. [cited 2020 Jan 25]. Available from: https://eprints.utas.edu.au/29666/1/Pavez_whole_thesis.pdf.

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

Council of Science Editors:

Pavez M. STIM1 regulates spatiotemporal calcium signals and the cytoskeleton in motile growth cones. [Thesis]. University of Tasmania; 2018. Available from: https://eprints.utas.edu.au/29666/1/Pavez_whole_thesis.pdf

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


Duke University

26. Reid, David William. Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells .

Degree: 2014, Duke University

  The partitioning of translation to the outer membrane of the endoplasmic reticulum is a problem that has been the subject of inquiry since the… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Endoplasmic reticulum; mRNA; Ribosome; Translation

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APA (6th Edition):

Reid, D. W. (2014). Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8752

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):

Reid, David William. “Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells .” 2014. Thesis, Duke University. Accessed January 25, 2020. http://hdl.handle.net/10161/8752.

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

MLA Handbook (7th Edition):

Reid, David William. “Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells .” 2014. Web. 25 Jan 2020.

Vancouver:

Reid DW. Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells . [Internet] [Thesis]. Duke University; 2014. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/10161/8752.

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

Council of Science Editors:

Reid DW. Segregation of Protein Synthesis Between the Cytoplasm and Endoplasmic Reticulum of Eukaryotic Cells . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/8752

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


Hong Kong University of Science and Technology

27. Chu, Hong. Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae.

Degree: 2012, Hong Kong University of Science and Technology

 In the secretory pathway, proteins are transported from the endoplasmic reticulum (ER) to Golgi in COPII-coated vesicles. The COPII protein complex is comprised of Sar1p,… (more)

Subjects/Keywords: Membrane proteins ; Endoplasmic reticulum ; Saccharomyces cerevisiae

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APA (6th Edition):

Chu, H. (2012). Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7643 ; https://doi.org/10.14711/thesis-b1176689 ; http://repository.ust.hk/ir/bitstream/1783.1-7643/1/th_redirect.html

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):

Chu, Hong. “Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed January 25, 2020. http://repository.ust.hk/ir/Record/1783.1-7643 ; https://doi.org/10.14711/thesis-b1176689 ; http://repository.ust.hk/ir/bitstream/1783.1-7643/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Chu, Hong. “Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae.” 2012. Web. 25 Jan 2020.

Vancouver:

Chu H. Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Jan 25]. Available from: http://repository.ust.hk/ir/Record/1783.1-7643 ; https://doi.org/10.14711/thesis-b1176689 ; http://repository.ust.hk/ir/bitstream/1783.1-7643/1/th_redirect.html.

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

Council of Science Editors:

Chu H. Sorting of ER-Golgi SNAREs by the COPII coat in saccharomyces cerevisiae. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-7643 ; https://doi.org/10.14711/thesis-b1176689 ; http://repository.ust.hk/ir/bitstream/1783.1-7643/1/th_redirect.html

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


University College Cork

28. English, Kathleen Kelly. Type 1 ryanodine receptor interactions.

Degree: 2015, University College Cork

 Excitation-contraction coupling is an essential part of skeletal muscle contraction. It encompasses the sensing of depolarisation of the plasma membrane coupled with the release of… (more)

Subjects/Keywords: Calcium signalling; Sarcoplasmic reticulum; Junctophilin; Sarcopenia; Muscle

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

APA (6th Edition):

English, K. K. (2015). Type 1 ryanodine receptor interactions. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/2238

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):

English, Kathleen Kelly. “Type 1 ryanodine receptor interactions.” 2015. Thesis, University College Cork. Accessed January 25, 2020. http://hdl.handle.net/10468/2238.

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

MLA Handbook (7th Edition):

English, Kathleen Kelly. “Type 1 ryanodine receptor interactions.” 2015. Web. 25 Jan 2020.

Vancouver:

English KK. Type 1 ryanodine receptor interactions. [Internet] [Thesis]. University College Cork; 2015. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/10468/2238.

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

Council of Science Editors:

English KK. Type 1 ryanodine receptor interactions. [Thesis]. University College Cork; 2015. Available from: http://hdl.handle.net/10468/2238

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


Michigan State University

29. Tripathy, Ashutosh. Anionic permeability of the liver ER membrane.

Degree: PhD, Department of Physiology, 1993, Michigan State University

Subjects/Keywords: Endoplasmic reticulum; Liver

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

APA (6th Edition):

Tripathy, A. (1993). Anionic permeability of the liver ER membrane. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:22578

Chicago Manual of Style (16th Edition):

Tripathy, Ashutosh. “Anionic permeability of the liver ER membrane.” 1993. Doctoral Dissertation, Michigan State University. Accessed January 25, 2020. http://etd.lib.msu.edu/islandora/object/etd:22578.

MLA Handbook (7th Edition):

Tripathy, Ashutosh. “Anionic permeability of the liver ER membrane.” 1993. Web. 25 Jan 2020.

Vancouver:

Tripathy A. Anionic permeability of the liver ER membrane. [Internet] [Doctoral dissertation]. Michigan State University; 1993. [cited 2020 Jan 25]. Available from: http://etd.lib.msu.edu/islandora/object/etd:22578.

Council of Science Editors:

Tripathy A. Anionic permeability of the liver ER membrane. [Doctoral Dissertation]. Michigan State University; 1993. Available from: http://etd.lib.msu.edu/islandora/object/etd:22578


University of Ottawa

30. Nassrallah, Wissam. Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity .

Degree: 2015, University of Ottawa

 Homeostatic synaptic plasticity (HSP) regulates synaptic strength in response to changing neuronal firing patterns. This form of plasticity is defined by neurons’ ability to sense… (more)

Subjects/Keywords: Store-Operated Responese; Homeostatic Synaptic Plasticity; AMPA Receptors; Endoplasmic Reticulum Calcium Stores; Endoplasmic Reticulum

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

APA (6th Edition):

Nassrallah, W. (2015). Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/33357

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):

Nassrallah, Wissam. “Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity .” 2015. Thesis, University of Ottawa. Accessed January 25, 2020. http://hdl.handle.net/10393/33357.

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

MLA Handbook (7th Edition):

Nassrallah, Wissam. “Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity .” 2015. Web. 25 Jan 2020.

Vancouver:

Nassrallah W. Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2020 Jan 25]. Available from: http://hdl.handle.net/10393/33357.

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

Council of Science Editors:

Nassrallah W. Store-Operated Response in CA1 Pyramidal Neurons Exhibits Features of Homeostatic Synaptic Plasticity . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/33357

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

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