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You searched for +publisher:"Temple University" +contributor:("Rothberg, Brad S."). Showing records 1 – 8 of 8 total matches.

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Temple University

1. Doonan, Patrick John. Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics.

Degree: PhD, 2012, Temple University

Biochemistry

Mitochondrial calcium (Ca2+) uptake has been studied for over five decades, with crucial insights into its underlying mechanisms enabled by development of the chemi-osmotic… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Calcium; LETM1; MICU1; Mitochondria; Mitochondria Calcium Uniporter; Uniporter

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APA (6th Edition):

Doonan, P. J. (2012). Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,214818

Chicago Manual of Style (16th Edition):

Doonan, Patrick John. “Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics.” 2012. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,214818.

MLA Handbook (7th Edition):

Doonan, Patrick John. “Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics.” 2012. Web. 24 Sep 2020.

Vancouver:

Doonan PJ. Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,214818.

Council of Science Editors:

Doonan PJ. Mitochondrial Calcium Uptake: LETM1 and MICU1 Are Mitochondrial Proteins That Regulate Mitochondrial Calcium Homeostasis and Cellular Bioenergetics. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,214818


Temple University

2. Thomson, Andrew Shane. Voltage-dependent gating at the selectivity filter of the MthK K+ channel.

Degree: PhD, 2013, Temple University

Biochemistry

Voltage-dependent K+ channels can undergo a gating process known as C-type inactivation. This type of gating consists of entry into a nonconducting state that… (more)

Subjects/Keywords: Biochemistry; Channel; Inactivation; MthK; Potassium

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APA (6th Edition):

Thomson, A. S. (2013). Voltage-dependent gating at the selectivity filter of the MthK K+ channel. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,214824

Chicago Manual of Style (16th Edition):

Thomson, Andrew Shane. “Voltage-dependent gating at the selectivity filter of the MthK K+ channel.” 2013. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,214824.

MLA Handbook (7th Edition):

Thomson, Andrew Shane. “Voltage-dependent gating at the selectivity filter of the MthK K+ channel.” 2013. Web. 24 Sep 2020.

Vancouver:

Thomson AS. Voltage-dependent gating at the selectivity filter of the MthK K+ channel. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,214824.

Council of Science Editors:

Thomson AS. Voltage-dependent gating at the selectivity filter of the MthK K+ channel. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,214824


Temple University

3. Smith, Frank J. Structural and Functional Analysis of the MthK K+ Channel RCK Domain.

Degree: PhD, 2013, Temple University

Biochemistry

Regulator of K+ conductance (RCK) domains control the activity of a variety of K+ channels and transporters, including the prokaryotic TrkA/H K+ transport complex… (more)

Subjects/Keywords: Biochemistry; Biophysics;

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APA (6th Edition):

Smith, F. J. (2013). Structural and Functional Analysis of the MthK K+ Channel RCK Domain. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,230546

Chicago Manual of Style (16th Edition):

Smith, Frank J. “Structural and Functional Analysis of the MthK K+ Channel RCK Domain.” 2013. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,230546.

MLA Handbook (7th Edition):

Smith, Frank J. “Structural and Functional Analysis of the MthK K+ Channel RCK Domain.” 2013. Web. 24 Sep 2020.

Vancouver:

Smith FJ. Structural and Functional Analysis of the MthK K+ Channel RCK Domain. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,230546.

Council of Science Editors:

Smith FJ. Structural and Functional Analysis of the MthK K+ Channel RCK Domain. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,230546


Temple University

4. HENDRON, EUNAN. Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function.

Degree: PhD, 2013, Temple University

Biochemistry

In an effort to dissect the mechanism of SOCe activation, I used two novel 2-APB analogs (DPB162-AE and DPB163-AE) which are ~50-100 times more… (more)

Subjects/Keywords: Biochemistry;

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APA (6th Edition):

HENDRON, E. (2013). Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,235040

Chicago Manual of Style (16th Edition):

HENDRON, EUNAN. “Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function.” 2013. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,235040.

MLA Handbook (7th Edition):

HENDRON, EUNAN. “Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function.” 2013. Web. 24 Sep 2020.

Vancouver:

HENDRON E. Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,235040.

Council of Science Editors:

HENDRON E. Potent and specific actions of 2-Aminoethoxydiphenyl borate (2-APB) derivatives on Orai channel function. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,235040


Temple University

5. Daswani, Varsha. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.

Degree: PhD, 2015, Temple University

Biomedical Sciences

Combretastatin A4 phosphate (CA4P) is a potent vascular disrupting agent utilized in the treatment of cancer. The observed rapid vascular shutdown post administration… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry;

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APA (6th Edition):

Daswani, V. (2015). Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,334013

Chicago Manual of Style (16th Edition):

Daswani, Varsha. “Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.” 2015. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,334013.

MLA Handbook (7th Edition):

Daswani, Varsha. “Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes.” 2015. Web. 24 Sep 2020.

Vancouver:

Daswani V. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,334013.

Council of Science Editors:

Daswani V. Fluorescence and aggregation properties of the anti-cancer drug, CA4P, in archaeal liposomes. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,334013


Temple University

6. Ayesa, Umme. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.

Degree: PhD, 2016, Temple University

Biochemistry

One of earlier challenges in treating cancer was utilizing drugs that are powerful yet do not cause severe toxicity to patients. Although the use… (more)

Subjects/Keywords: Biophysics

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

APA (6th Edition):

Ayesa, U. (2016). CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,368614

Chicago Manual of Style (16th Edition):

Ayesa, Umme. “CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.” 2016. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,368614.

MLA Handbook (7th Edition):

Ayesa, Umme. “CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE.” 2016. Web. 24 Sep 2020.

Vancouver:

Ayesa U. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,368614.

Council of Science Editors:

Ayesa U. CHARACTERIZATION OF THERMOSENSITIVE HYBRID ARCHAEOSOMES AND DPA-CY3[22,22]/POPC LIPOSOMES AND IN VITRO EVALUATION OF THEIR POTENTIAL USEFULNESS IN TARGETED DELIVERY AND CONTROLLED RELEASE. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,368614


Temple University

7. Feather, Danielle. GLT-1 dysfunction as an underlying cause of cerebral palsy.

Degree: PhD, 2016, Temple University

Biochemistry

Cerebral Palsy (CP) is an umbrella term that describes abnormal motor movements that is caused by damage in the brain and, depending on the… (more)

Subjects/Keywords: Neurosciences; Biology

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APA (6th Edition):

Feather, D. (2016). GLT-1 dysfunction as an underlying cause of cerebral palsy. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,409354

Chicago Manual of Style (16th Edition):

Feather, Danielle. “GLT-1 dysfunction as an underlying cause of cerebral palsy.” 2016. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,409354.

MLA Handbook (7th Edition):

Feather, Danielle. “GLT-1 dysfunction as an underlying cause of cerebral palsy.” 2016. Web. 24 Sep 2020.

Vancouver:

Feather D. GLT-1 dysfunction as an underlying cause of cerebral palsy. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,409354.

Council of Science Editors:

Feather D. GLT-1 dysfunction as an underlying cause of cerebral palsy. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,409354


Temple University

8. Samakai, Elsie. TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS.

Degree: PhD, 2017, Temple University

Biochemistry

Antigen presentation to T cells results in their activation through T Cell Receptor (TCR) stimulation, resulting in sustained elevation of cytosolic Ca2+ concentration critical… (more)

Subjects/Keywords: Biochemistry; Immunology;

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

APA (6th Edition):

Samakai, E. (2017). TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,466164

Chicago Manual of Style (16th Edition):

Samakai, Elsie. “TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS.” 2017. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,466164.

MLA Handbook (7th Edition):

Samakai, Elsie. “TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS.” 2017. Web. 24 Sep 2020.

Vancouver:

Samakai E. TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,466164.

Council of Science Editors:

Samakai E. TRANSCRIPTIONAL CONTROL OF Ca2+ SIGNALING IN T CELLS. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,466164

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