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You searched for subject:(Heterodimer). Showing records 1 – 24 of 24 total matches.

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1. Santoshi, Seneha. Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -.

Degree: Bioinformatics, 2014, Jaypee University of Information Technology, Solan

Microtubules are major cytoskeletal structures responsible for maintaining genetic stability during cell division The dynamics of these polymers are absolutely crucial for this function that… (more)

Subjects/Keywords: Cytoskeletal; Heterodimer; Immunosuppression; Microtubules; Noscapinoids

Page 1

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APA (6th Edition):

Santoshi, S. (2014). Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -. (Thesis). Jaypee University of Information Technology, Solan. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/26902

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):

Santoshi, Seneha. “Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -.” 2014. Thesis, Jaypee University of Information Technology, Solan. Accessed July 17, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/26902.

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

MLA Handbook (7th Edition):

Santoshi, Seneha. “Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -.” 2014. Web. 17 Jul 2019.

Vancouver:

Santoshi S. Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -. [Internet] [Thesis]. Jaypee University of Information Technology, Solan; 2014. [cited 2019 Jul 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26902.

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

Council of Science Editors:

Santoshi S. Computer aided design of novel noscapinoids and their experimental evaluation as tubulin binding anti cancer drugs; -. [Thesis]. Jaypee University of Information Technology, Solan; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26902

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


Rice University

2. Zhang, Chao. Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces.

Degree: PhD, Engineering, 2018, Rice University

 Surface plasmon is the collective oscillation of free electrons in metallic nanoparticles. When two plasmonic nanoparticles are brought close together as a plasmonic dimer, their… (more)

Subjects/Keywords: Plasmonics; Photocatalysis; Heterodimer; Optical force

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APA (6th Edition):

Zhang, C. (2018). Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105850

Chicago Manual of Style (16th Edition):

Zhang, Chao. “Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces.” 2018. Doctoral Dissertation, Rice University. Accessed July 17, 2019. http://hdl.handle.net/1911/105850.

MLA Handbook (7th Edition):

Zhang, Chao. “Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces.” 2018. Web. 17 Jul 2019.

Vancouver:

Zhang C. Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1911/105850.

Council of Science Editors:

Zhang C. Plasmonic Heterodimers: Antenna-Reactor Effect and Optical Forces. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105850


University of Illinois – Urbana-Champaign

3. Ghasem pur, Salehe. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).

Degree: PhD, 0318, 2015, University of Illinois – Urbana-Champaign

 Genomic era begins with development of sequencing methods. Genome sequencing is now cost-effective and fast, giving rise to increasing amounts of genomic data. However, the… (more)

Subjects/Keywords: Enolase; L-lyxonate; Heterodimer; Heterospecies; D-Glucarate

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APA (6th Edition):

Ghasem pur, S. (2015). Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73056

Chicago Manual of Style (16th Edition):

Ghasem pur, Salehe. “Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/73056.

MLA Handbook (7th Edition):

Ghasem pur, Salehe. “Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD).” 2015. Web. 17 Jul 2019.

Vancouver:

Ghasem pur S. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/73056.

Council of Science Editors:

Ghasem pur S. Mining the enolase superfamily for new functions: investigations of D-glucarate dehydratase related proteins (GlucDRP) and L-lyxonate dehydratase proteins (LyxD). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73056


University of Colorado

4. Dalby, Andrew Benjamin. The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  Telomeres are the nucleoprotein endcaps of linear chromosomes. Telomeres shorten with each cell division, limiting the capacity of telomeres to protect chromosomal DNA. The… (more)

Subjects/Keywords: Ku heterodimer; POT1; Recrutiment; Telomerase; Telomere; TPP1; Biochemistry; Genetics and Genomics

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APA (6th Edition):

Dalby, A. B. (2014). The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/136

Chicago Manual of Style (16th Edition):

Dalby, Andrew Benjamin. “The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans.” 2014. Doctoral Dissertation, University of Colorado. Accessed July 17, 2019. http://scholar.colorado.edu/chem_gradetds/136.

MLA Handbook (7th Edition):

Dalby, Andrew Benjamin. “The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans.” 2014. Web. 17 Jul 2019.

Vancouver:

Dalby AB. The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2019 Jul 17]. Available from: http://scholar.colorado.edu/chem_gradetds/136.

Council of Science Editors:

Dalby AB. The Molecular Interfaces of Telomerase and Telomere Proteins in Yeast and Humans. [Doctoral Dissertation]. University of Colorado; 2014. Available from: http://scholar.colorado.edu/chem_gradetds/136


University of Toledo

5. Aravelli, Sandeep. Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study.

Degree: MSin Electrical Engineering, College of Engineering, University of Toledo

 GaAs (001)–c(4 × 4) reconstruction surface is one of the frequently encountered surfaces during growth in molecular beam epitaxy (MBE) under As-rich conditions. It has… (more)

Subjects/Keywords: Binding sites; c(4x4) heterodimer

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APA (6th Edition):

Aravelli, S. (n.d.). Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1324929790

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

Chicago Manual of Style (16th Edition):

Aravelli, Sandeep. “Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study.” Masters Thesis, University of Toledo. Accessed July 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1324929790.

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

MLA Handbook (7th Edition):

Aravelli, Sandeep. “Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study.” Web. 17 Jul 2019.

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

Vancouver:

Aravelli S. Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study. [Internet] [Masters thesis]. University of Toledo; [cited 2019 Jul 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1324929790.

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

Council of Science Editors:

Aravelli S. Identification of Binding Sites and Determination of Binding Energies of a Ga Adatom on the GaAs(001)–c(4 × 4) –Heterodimer Surface: A First-Principles Study. [Masters Thesis]. University of Toledo; Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1324929790

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

6. Jacqueroud, Laurent. Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells.

Degree: Docteur es, Biologie moléculaire et cellulaire, 2015, Université Claude Bernard – Lyon I

Dans ce manuscrit, nous démontrons par le biais de dimères forcés que toutes les propriétés oncogéniques de la protéine TWIST1, telles qu'évaluées par le biais… (more)

Subjects/Keywords: TWIST1; Hétérodimère; Sénescence; EMT; TWIST1; Heterodimer; Senescence; EMT; 572.8

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APA (6th Edition):

Jacqueroud, L. (2015). Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2015LYO10054

Chicago Manual of Style (16th Edition):

Jacqueroud, Laurent. “Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells.” 2015. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 17, 2019. http://www.theses.fr/2015LYO10054.

MLA Handbook (7th Edition):

Jacqueroud, Laurent. “Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells.” 2015. Web. 17 Jul 2019.

Vancouver:

Jacqueroud L. Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2015. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2015LYO10054.

Council of Science Editors:

Jacqueroud L. Identification et caractérisation des complexes transcriptionnels de la protéine TWIST1 essentiels à la progression tumorale : The heterodimeric TWIST1-E12 complex drives the oncogenic potential of TWIST1 in human mammary epithelial cells. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2015. Available from: http://www.theses.fr/2015LYO10054


Vilnius University

7. Balevičius, Vytautas. Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose.

Degree: PhD, Physics, 2013, Vilnius University

Disertacijos santraukoje reziumuojamas sužadinimo energijos pernašos eksitoniniame dimere tyrimas. Nagrinėjamas kvantinio koherentiškumo vaidmuo energijos pernašos procesų hierarchijoje: virpesinėje relaksacijoje, sužadinimo pernašoje vieneksitoninėje juostoje bei relaksacijoje… (more)

Subjects/Keywords: Eksitonai; Kvantinis koherentiškumas; Heterodimeras; Excitons; Quantum coherence; Heterodimer

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APA (6th Edition):

Balevičius, V. (2013). Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133859-60573 ;

Chicago Manual of Style (16th Edition):

Balevičius, Vytautas. “Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose.” 2013. Doctoral Dissertation, Vilnius University. Accessed July 17, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133859-60573 ;.

MLA Handbook (7th Edition):

Balevičius, Vytautas. “Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose.” 2013. Web. 17 Jul 2019.

Vancouver:

Balevičius V. Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose. [Internet] [Doctoral dissertation]. Vilnius University; 2013. [cited 2019 Jul 17]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133859-60573 ;.

Council of Science Editors:

Balevičius V. Kvantinis koherentiškumas molekulių sužadinimo energijos pernašos ir relaksacijos vyksmuose. [Doctoral Dissertation]. Vilnius University; 2013. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133859-60573 ;


Vilnius University

8. Balevičius, Vytautas. Quantum coherence in molecular excitation energy transfer and relaxation.

Degree: Dissertation, Physics, 2013, Vilnius University

In the dissertation, excitation energy transfer was studied in an excitonic dimer under various conditions of inter-chromophore resonance interaction and in different regimes of the… (more)

Subjects/Keywords: Excitons; Quantum coherence; Heterodimer; Eksitonai; Kvantinis koherentiškumas; Heterodimeras

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APA (6th Edition):

Balevičius, V. (2013). Quantum coherence in molecular excitation energy transfer and relaxation. (Doctoral Dissertation). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133913-37583 ;

Chicago Manual of Style (16th Edition):

Balevičius, Vytautas. “Quantum coherence in molecular excitation energy transfer and relaxation.” 2013. Doctoral Dissertation, Vilnius University. Accessed July 17, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133913-37583 ;.

MLA Handbook (7th Edition):

Balevičius, Vytautas. “Quantum coherence in molecular excitation energy transfer and relaxation.” 2013. Web. 17 Jul 2019.

Vancouver:

Balevičius V. Quantum coherence in molecular excitation energy transfer and relaxation. [Internet] [Doctoral dissertation]. Vilnius University; 2013. [cited 2019 Jul 17]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133913-37583 ;.

Council of Science Editors:

Balevičius V. Quantum coherence in molecular excitation energy transfer and relaxation. [Doctoral Dissertation]. Vilnius University; 2013. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20131125_133913-37583 ;


Johannes Gutenberg Universität Mainz

9. Weichert, Anna. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.

Degree: 2012, Johannes Gutenberg Universität Mainz

Die Erkrankung Amyotrophe Lateralsklerose (ALS) ist gekennzeichnet durch eine progressive Degeneration der Motoneurone. Die hierdurch im Patienten hervorgerufene fortschreitende Paralyse kann von wenigen Wochen über… (more)

Subjects/Keywords: Amyotrophe Lateralsklerose, ALS, Superoxiddismutase, SOD1, Heterodimer, Homodimer, Stabilität, Konformation, A4V, G37R, G41D, G41S, G85R, G93C; amyotrophic lateral sclerosis, superoxide dismutase, heterodimer, homodimer, stability, conformation; Natural sciences and mathematics

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APA (6th Edition):

Weichert, A. (2012). Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/

Chicago Manual of Style (16th Edition):

Weichert, Anna. “Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed July 17, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/.

MLA Handbook (7th Edition):

Weichert, Anna. “Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere.” 2012. Web. 17 Jul 2019.

Vancouver:

Weichert A. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2019 Jul 17]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/.

Council of Science Editors:

Weichert A. Der Einfluss einer wildtypischen SOD1-Untereinheit auf Konformation und Stabilität mutanter SOD1-Heterodimere. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3561/


University of Otago

10. Foglizzo, Martina. Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 .

Degree: University of Otago

 The covalent attachment of ubiquitin to substrate proteins, a process known as ubiquitylation, is a post-translational modification that modulates protein degradation and cell signalling pathways.… (more)

Subjects/Keywords: ubiquitin; nucleosomes; RING; DUBs; heterodimer; Ube2B

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APA (6th Edition):

Foglizzo, M. (n.d.). Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/6864

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

Chicago Manual of Style (16th Edition):

Foglizzo, Martina. “Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 .” Doctoral Dissertation, University of Otago. Accessed July 17, 2019. http://hdl.handle.net/10523/6864.

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

MLA Handbook (7th Edition):

Foglizzo, Martina. “Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 .” Web. 17 Jul 2019.

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

Vancouver:

Foglizzo M. Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 . [Internet] [Doctoral dissertation]. University of Otago; [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10523/6864.

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

Council of Science Editors:

Foglizzo M. Ubiquitin transfer and deubiquitylation by RNF20 and BAP1 . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/6864

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

11. DAO HOANG THIEN, KIM. Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究.

Degree: 博士(学術), 2015, Kyoto Institute of Technology / 京都工芸繊維大学

 Of eight inherited porphyria diseases in the heme-biosynthetic pathway, my study provides an understanding of a very rare disease which is the first description of… (more)

Subjects/Keywords: Congenital Erythropoietic Porphyria; deficiency; mutation; photosensitivity; uroporphyrinogen III cosynthase; Coproporphyria; coproporphyrinogen oxidase; harderoporphyria; heterodimer; homodimer

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APA (6th Edition):

DAO HOANG THIEN, K. (2015). Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究. (Thesis). Kyoto Institute of Technology / 京都工芸繊維大学. Retrieved from http://hdl.handle.net/10212/2190

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):

DAO HOANG THIEN, KIM. “Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究.” 2015. Thesis, Kyoto Institute of Technology / 京都工芸繊維大学. Accessed July 17, 2019. http://hdl.handle.net/10212/2190.

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

MLA Handbook (7th Edition):

DAO HOANG THIEN, KIM. “Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究.” 2015. Web. 17 Jul 2019.

Vancouver:

DAO HOANG THIEN K. Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究. [Internet] [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10212/2190.

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

Council of Science Editors:

DAO HOANG THIEN K. Basic and clinical investigations on patients with porphyrias: Congenital Erythropoietic Porphyria, Hereditary Coproporphyria and Harderoporphyria : ポルフィリア症患者の分子異変に関する基礎的及び臨床的研究. [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2015. Available from: http://hdl.handle.net/10212/2190

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


University of Arizona

12. Olson, Keith Mathew. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .

Degree: 2017, University of Arizona

 Most clinical opioids produce analgesia through the Mu Opioid Receptor (MOR) providing the only effective treatment for chronic pain patients. These studies explore three pre-clinical… (more)

Subjects/Keywords: Bivalent; Delta Opioid Receptor; Functional Selectivity; MDOR Heterodimer; Mu Opioid Receptor; Opioid Signaling

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APA (6th Edition):

Olson, K. M. (2017). Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/626669

Chicago Manual of Style (16th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Doctoral Dissertation, University of Arizona. Accessed July 17, 2019. http://hdl.handle.net/10150/626669.

MLA Handbook (7th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Web. 17 Jul 2019.

Vancouver:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2017. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10150/626669.

Council of Science Editors:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Doctoral Dissertation]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/626669

13. Vincent, Karla Kristine. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.

Degree: PhD, Biology, 2009, Georgia Tech

 Although a long standing convention maintained that G Protein Coupled Receptors (GPCRs) exist in the plasma membrane solely as monomers, substantial work over the last… (more)

Subjects/Keywords: Electrophysiology; Heterodimer; GPCR; G proteins; Membrane proteins

HETERODIMER CHAPTER 6 – Characterization of the Bradykinin Receptor/Beta 2 Adrenergic Receptor… …Heterodimer: Effects of other Bk2R-specific ligands on transactivation and agonist induced changes… …in heterodimer abundance 77 CHAPTER 7 – MATERIALS AND METHODS 80 7.1: Reagents 80 7.2… …exposure does not affect the relative amount of heterodimer 83 8.2: β2AR transactivation does… …physically associate 70 Figure 16: Relative amounts of Bk2R/β2AR heterodimer do not change for up… 

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APA (6th Edition):

Vincent, K. K. (2009). Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37117

Chicago Manual of Style (16th Edition):

Vincent, Karla Kristine. “Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.” 2009. Doctoral Dissertation, Georgia Tech. Accessed July 17, 2019. http://hdl.handle.net/1853/37117.

MLA Handbook (7th Edition):

Vincent, Karla Kristine. “Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization.” 2009. Web. 17 Jul 2019.

Vancouver:

Vincent KK. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1853/37117.

Council of Science Editors:

Vincent KK. Transactivation of Beta 2 Adrenergic Receptor by Bradykinin type 2 Receptor via heterodimerization. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/37117


University of Florida

14. Akhtar, Tariq. A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism.

Degree: PhD, Plant Molecular and Cellular Biology, 2010, University of Florida

 Animals cannot synthesize the B-vitamin folate and depend mainly on plants to supply them with this essential cofactor. The majority of plant folates, like those… (more)

Subjects/Keywords: Complementary DNA; Dimers; Enzymes; Metabolism; Monomers; Polymerase chain reaction; Protein isoforms; Signals; Tomatoes; Vacuoles; folate, gamma, heterodimer, polyglutamate, tomato, vacuole

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APA (6th Edition):

Akhtar, T. (2010). A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0041594

Chicago Manual of Style (16th Edition):

Akhtar, Tariq. “A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism.” 2010. Doctoral Dissertation, University of Florida. Accessed July 17, 2019. http://ufdc.ufl.edu/UFE0041594.

MLA Handbook (7th Edition):

Akhtar, Tariq. “A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism.” 2010. Web. 17 Jul 2019.

Vancouver:

Akhtar T. A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Jul 17]. Available from: http://ufdc.ufl.edu/UFE0041594.

Council of Science Editors:

Akhtar T. A Central Role for Gamma-Glutamyl Hydrolases in Plant Folate Metabolism. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0041594

15. Dooley, Scott R. Investigation of the Effect of Dimerization on Human α-Galactosidase Activity.

Degree: MS(M.S.), Biochemistry, 2014, U of Massachusetts : Masters

  Fabry disease is an X-linked lysosomal storage disease that results from a deficiency in the enzyme α-galactosidase (α-GAL). α-GAL hydrolyzes α-galactosides, and patients with… (more)

Subjects/Keywords: α-Galactosidase; activity; monomer; heterodimer; dimerization; Biochemistry; Molecular Biology; Other Biochemistry, Biophysics, and Structural Biology; Structural Biology

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APA (6th Edition):

Dooley, S. R. (2014). Investigation of the Effect of Dimerization on Human α-Galactosidase Activity. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1177

Chicago Manual of Style (16th Edition):

Dooley, Scott R. “Investigation of the Effect of Dimerization on Human α-Galactosidase Activity.” 2014. Masters Thesis, U of Massachusetts : Masters. Accessed July 17, 2019. http://scholarworks.umass.edu/theses/1177.

MLA Handbook (7th Edition):

Dooley, Scott R. “Investigation of the Effect of Dimerization on Human α-Galactosidase Activity.” 2014. Web. 17 Jul 2019.

Vancouver:

Dooley SR. Investigation of the Effect of Dimerization on Human α-Galactosidase Activity. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2019 Jul 17]. Available from: http://scholarworks.umass.edu/theses/1177.

Council of Science Editors:

Dooley SR. Investigation of the Effect of Dimerization on Human α-Galactosidase Activity. [Masters Thesis]. U of Massachusetts : Masters; 2014. Available from: http://scholarworks.umass.edu/theses/1177


University College Cork

16. Foley, Kate. Characterisation of the non-muscle α-actinins.

Degree: 2013, University College Cork

 Actinins are cytoskeleton proteins that cross-link actin filaments. Evolution of the actinin family resulted in the formation of Ca++-insensitive muscle isoforms (actinin-2 and- 3) and… (more)

Subjects/Keywords: Actinin-1; Actinin-4; Non-muscle actinin; Actin-binding / bundling; Actinin heterodimer; Cytoskeleton; Cancer – Molecular aspects; Cytology

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APA (6th Edition):

Foley, K. (2013). Characterisation of the non-muscle α-actinins. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/1180

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):

Foley, Kate. “Characterisation of the non-muscle α-actinins.” 2013. Thesis, University College Cork. Accessed July 17, 2019. http://hdl.handle.net/10468/1180.

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

MLA Handbook (7th Edition):

Foley, Kate. “Characterisation of the non-muscle α-actinins.” 2013. Web. 17 Jul 2019.

Vancouver:

Foley K. Characterisation of the non-muscle α-actinins. [Internet] [Thesis]. University College Cork; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10468/1180.

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

Council of Science Editors:

Foley K. Characterisation of the non-muscle α-actinins. [Thesis]. University College Cork; 2013. Available from: http://hdl.handle.net/10468/1180

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


University of Texas Medical Branch – Galveston

17. [No author]. Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions .

Degree: University of Texas Medical Branch – Galveston

 Platelet-derived chemokine CXCL7 (NAP-2) plays a critical role in mediating the crosstalk between platelets and neutrophils for initiating repair during vascular injury. CXCL7 function is… (more)

Subjects/Keywords: Chemokine; CXCL7; heterodimer; NMR; Glycosaminoglycan; heparin; CXCR2;

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

APA (6th Edition):

author], [. (n.d.). Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/10737

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):

author], [No. “Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions .” Thesis, University of Texas Medical Branch – Galveston. Accessed July 17, 2019. http://hdl.handle.net/2152.3/10737.

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):

author], [No. “Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions .” Web. 17 Jul 2019.

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

Vancouver:

author] [. Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2152.3/10737.

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:

author] [. Chemokine CXCL7 Monomer, Homodimer, and Heterodimer: Structural Insights, CXCR2 Receptor Function, and Glycosaminoglycan Interactions . [Thesis]. University of Texas Medical Branch – Galveston; Available from: http://hdl.handle.net/2152.3/10737

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


University of Illinois – Urbana-Champaign

18. Kanamaluru, Deepthi. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.

Degree: PhD, 0318, 2011, University of Illinois – Urbana-Champaign

 Small Heterodimer Partner (SHP, NR0B2), a member of the nuclear receptor superfamily, is an orphan receptor that lacks a DNA binding domain but contains a… (more)

Subjects/Keywords: Small Heterodimer Partner (SHP); Protein Arinine Methyltransferase 5 (PRMT5); arginine methylation; phosphorylation; protein kinase C zeta (PKC zeta); obesity and diabetes

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APA (6th Edition):

Kanamaluru, D. (2011). Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24491

Chicago Manual of Style (16th Edition):

Kanamaluru, Deepthi. “Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/24491.

MLA Handbook (7th Edition):

Kanamaluru, Deepthi. “Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications.” 2011. Web. 17 Jul 2019.

Vancouver:

Kanamaluru D. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/24491.

Council of Science Editors:

Kanamaluru D. Modulation of the activity of a key metabolic regulator Small Heterodimer Partner by post-translational modifications. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24491


Queens University

19. Duan, Da. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .

Degree: Biochemistry, 2013, Queens University

 The kinesin-14 Kar3 from Saccharomyces cerevisiae (Sc) is a C-terminal motor that forms a heterodimer with the kinesin-accessory protein Vik1. Although Vik1 possesses a typical… (more)

Subjects/Keywords: motility; Candida glabrata; Ashbya gossypii; N-C termini interaction; Saccharomyces cerevisiae; c-terminal kinesin; heterodimer; minus-end directed motility; kinesin; microtubules; mitosis

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APA (6th Edition):

Duan, D. (2013). UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8118

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):

Duan, Da. “UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .” 2013. Thesis, Queens University. Accessed July 17, 2019. http://hdl.handle.net/1974/8118.

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

MLA Handbook (7th Edition):

Duan, Da. “UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 .” 2013. Web. 17 Jul 2019.

Vancouver:

Duan D. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1974/8118.

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

Council of Science Editors:

Duan D. UNDERSTANDING THE MECHANISM OF MOTILITY OF THE HETERODIMERIC KINESIN-14 KAR3VIK1 . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8118

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


Vanderbilt University

20. Palmisano, Brian T. Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice.

Degree: PhD, Molecular Physiology and Biophysics, 2016, Vanderbilt University

 Elevated plasma triglycerides (TGs) increase risk of cardiovascular disease, especially in women. Estrogen treatment raises plasma TGs in women, but molecular mechanisms remain poorly understood.… (more)

Subjects/Keywords: CETP; beta-oxidation; Low Density Lipoprotein Receptor; LDLR; ER alpha; Estrogen Receptor alpha; SHP; Small Heterodimer Partner; VLDL; Estrogen; TGs; Triglycerides; Cholesteryl Ester Transfer Protein

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APA (6th Edition):

Palmisano, B. T. (2016). Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-08192016-161224/ ;

Chicago Manual of Style (16th Edition):

Palmisano, Brian T. “Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed July 17, 2019. http://etd.library.vanderbilt.edu//available/etd-08192016-161224/ ;.

MLA Handbook (7th Edition):

Palmisano, Brian T. “Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice.” 2016. Web. 17 Jul 2019.

Vancouver:

Palmisano BT. Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Jul 17]. Available from: http://etd.library.vanderbilt.edu//available/etd-08192016-161224/ ;.

Council of Science Editors:

Palmisano BT. Cholesteryl Ester Transfer Protein Modulates Liver Sex Hormone Signaling to Alter Triglyceride Metabolism in Male and Female Transgenic Mice. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu//available/etd-08192016-161224/ ;


University of Illinois – Urbana-Champaign

21. Fang, Sungsoon. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.

Degree: PhD, Molecular & Integrative Physiology, 2008, University of Illinois – Urbana-Champaign

 Bile acids, the end-product of cholesterol catabolism, are important for absorption and solubilization of lipids in the intestine because of their detergent properties. In addition… (more)

Subjects/Keywords: Bile acids; Bile acid signaling; Farnesoid X receptor (FXR); Small heterodimer partner (SHP)

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APA (6th Edition):

Fang, S. (2008). The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/47090

Chicago Manual of Style (16th Edition):

Fang, Sungsoon. “The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.” 2008. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/47090.

MLA Handbook (7th Edition):

Fang, Sungsoon. “The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.” 2008. Web. 17 Jul 2019.

Vancouver:

Fang S. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2008. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/47090.

Council of Science Editors:

Fang S. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2008. Available from: http://hdl.handle.net/2142/47090


Texas Medical Center

22. Edwards, Maryann A. ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL.

Degree: MS, 2012, Texas Medical Center

  Allergen-induced asthma is the leading form of asthma and a chronic condition worldwide. Common allergens are known to contribute to the pathogenesis of this… (more)

Subjects/Keywords: allergen-induced asthma; ovalbumin (OVA); TH2-specific cells; IgE antibodies; TH2-specific cytokines; airway eosinophilia; CpG oligodeoxynucleotides (ODNs); synthetic ligand; PUL-042 (TLR agonists); TLR2/6 heterodimer and TLR9; Immunology and Infectious Disease; Life Sciences; Medicine and Health Sciences

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APA (6th Edition):

Edwards, M. A. (2012). ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL. (Masters Thesis). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/251

Chicago Manual of Style (16th Edition):

Edwards, Maryann A. “ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL.” 2012. Masters Thesis, Texas Medical Center. Accessed July 17, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/251.

MLA Handbook (7th Edition):

Edwards, Maryann A. “ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL.” 2012. Web. 17 Jul 2019.

Vancouver:

Edwards MA. ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL. [Internet] [Masters thesis]. Texas Medical Center; 2012. [cited 2019 Jul 17]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/251.

Council of Science Editors:

Edwards MA. ALLERGEN SENSITIZATION AND IMMUNOMODULATION BY SYNTHETIC LIGANDS, PUL-042, IN AN ALLERGEN-INDUCED ASTHMA MURINE MODEL. [Masters Thesis]. Texas Medical Center; 2012. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/251


Virginia Tech

23. MacQuarrie, Stephanie Lee. Design and Synthesis of Novel Benzodiazepines.

Degree: PhD, Chemistry, 2005, Virginia Tech

  Bivalent drug design is an efficient strategy for increasing potency and selectivity of many drugs. We devised a strategy to prepare agonist-benzodiazepine heterodimers that… (more)

Subjects/Keywords: 4-Benzodiazepin-1; 5-dione; Density Functional Theory; Memory of Chirality; Agonist; Asymmetric Synthesis; 1; Benzodiazepine; Bivalent Ligand; GABAA Receptor; Heterodimer

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APA (6th Edition):

MacQuarrie, S. L. (2005). Design and Synthesis of Novel Benzodiazepines. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/30209

Chicago Manual of Style (16th Edition):

MacQuarrie, Stephanie Lee. “Design and Synthesis of Novel Benzodiazepines.” 2005. Doctoral Dissertation, Virginia Tech. Accessed July 17, 2019. http://hdl.handle.net/10919/30209.

MLA Handbook (7th Edition):

MacQuarrie, Stephanie Lee. “Design and Synthesis of Novel Benzodiazepines.” 2005. Web. 17 Jul 2019.

Vancouver:

MacQuarrie SL. Design and Synthesis of Novel Benzodiazepines. [Internet] [Doctoral dissertation]. Virginia Tech; 2005. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10919/30209.

Council of Science Editors:

MacQuarrie SL. Design and Synthesis of Novel Benzodiazepines. [Doctoral Dissertation]. Virginia Tech; 2005. Available from: http://hdl.handle.net/10919/30209


University of Miami

24. Kozloski, Goldi Attias. Muc4 Modulation of Ligand-Independent ErbB2 Signaling.

Degree: PhD, Biochemistry and Molecular Biology (Medicine), 2009, University of Miami

 The membrane mucin Muc4 is a heterodimer, bi-functional glycoprotein complex that is normally expressed in epithelial tissue. Functional studies on the extracellular mucin subunit of… (more)

Subjects/Keywords: Ligand-independent Activity; Microarray Screen; Heregulin; Anti-adhesion; Heterodimer; Phosphorylation; ErbB2 Signaling; Receptor Tyrosine Kinase; Membrane Mucin; Muc4; Epidermal Growth Factor Receptor

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

APA (6th Edition):

Kozloski, G. A. (2009). Muc4 Modulation of Ligand-Independent ErbB2 Signaling. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/253

Chicago Manual of Style (16th Edition):

Kozloski, Goldi Attias. “Muc4 Modulation of Ligand-Independent ErbB2 Signaling.” 2009. Doctoral Dissertation, University of Miami. Accessed July 17, 2019. https://scholarlyrepository.miami.edu/oa_dissertations/253.

MLA Handbook (7th Edition):

Kozloski, Goldi Attias. “Muc4 Modulation of Ligand-Independent ErbB2 Signaling.” 2009. Web. 17 Jul 2019.

Vancouver:

Kozloski GA. Muc4 Modulation of Ligand-Independent ErbB2 Signaling. [Internet] [Doctoral dissertation]. University of Miami; 2009. [cited 2019 Jul 17]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/253.

Council of Science Editors:

Kozloski GA. Muc4 Modulation of Ligand-Independent ErbB2 Signaling. [Doctoral Dissertation]. University of Miami; 2009. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/253

.