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You searched for subject:(Protein Engineering). Showing records 901 – 920 of 920 total matches.

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901. Wang, Qinzhe. Developing Approaches to Treat Canavan Disease.

Degree: PhD, Chemistry, 2017, University of Toledo

 Canavan disease is a progressive, fatal neurological disorder that is caused by defects in the human ASPA gene, which leads to an interruption in the… (more)

Subjects/Keywords: Chemistry; Biochemistry; Analytical Chemistry; Canavan Disease; N-acetylaspartic acid; NAA; Aspartoacylase; ASPA; Aspartate N-acetyltransferase; ANAT; Asp-NAT; NAT8L; Glycosylation; MALDI; metabolism; therapy; detergent; Protein engineering; Dual Affinity Purification; inhibitor; membrane; SPEG; DTNB

…35 2.8 Mass spectrometry based protein sequencing… …65 3.7 Purification of MBP-ANAT-H6 fusion protein… …3-6 Chromatograms of two affinity purification steps for MBP-ANAT-his fusion protein 67… …terminal PEGylation reaction of ASPA 122 B-1 Hydrodynamic radius of MBP-ANAT-His fusion protein… …Assisted Laser Desorption/Ionization MBP €¦ €¦ €¦â€¦...….Maltose binding protein Mega-9… 

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APA (6th Edition):

Wang, Q. (2017). Developing Approaches to Treat Canavan Disease. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1493301078219765

Chicago Manual of Style (16th Edition):

Wang, Qinzhe. “Developing Approaches to Treat Canavan Disease.” 2017. Doctoral Dissertation, University of Toledo. Accessed July 08, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1493301078219765.

MLA Handbook (7th Edition):

Wang, Qinzhe. “Developing Approaches to Treat Canavan Disease.” 2017. Web. 08 Jul 2020.

Vancouver:

Wang Q. Developing Approaches to Treat Canavan Disease. [Internet] [Doctoral dissertation]. University of Toledo; 2017. [cited 2020 Jul 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1493301078219765.

Council of Science Editors:

Wang Q. Developing Approaches to Treat Canavan Disease. [Doctoral Dissertation]. University of Toledo; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1493301078219765

902. Vert Company, Anna. Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed.

Degree: Departament de Biologia, 2014, Universitat de Girona

 Les ribonucleases citotòxiques són proteïnes amb un gran potencial per ser utilitzades en el tractament del càncer. El nostre grup va descriure una variant citotòxica… (more)

Subjects/Keywords: Human pancreatic ribonuclease; Ribonucleasa pancreàtica humana; Ribonucleasa pancreática humana; Nuclear delivery; Localització nuclear; Localización nuclear; Cytotoxicity; Citotoxicitat; Citotoxicidad; Protein engineering; Enginyeria de proteïnes; Ingeniería de proteínas; Antitumor drugs; Drogues antitumorals; Drogas antitumorales; Microarray; Xip; Chip; 577

…bcl-2-associated X protein BCAT1… …breast cancer resistant protein BNIP3L… …BCL2/adenovirus E1B 19kDa interacting protein 3-like BS-RNase… …cAMP responsive element binding protein 5 DHCR24… …extracellular matrix protein 1 EGFR… 

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APA (6th Edition):

Vert Company, A. (2014). Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed. (Thesis). Universitat de Girona. Retrieved from http://hdl.handle.net/10803/283575

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):

Vert Company, Anna. “Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed.” 2014. Thesis, Universitat de Girona. Accessed July 08, 2020. http://hdl.handle.net/10803/283575.

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

MLA Handbook (7th Edition):

Vert Company, Anna. “Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed.” 2014. Web. 08 Jul 2020.

Vancouver:

Vert Company A. Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed. [Internet] [Thesis]. Universitat de Girona; 2014. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/10803/283575.

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

Council of Science Editors:

Vert Company A. Molecular mechanism of PE5-induced cytotoxicity and generation of new cytotoxic nuclear-directed. [Thesis]. Universitat de Girona; 2014. Available from: http://hdl.handle.net/10803/283575

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

903. Gobeil, Sophie. Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 .

Degree: 2017, Université de Montréal

Subjects/Keywords: β-lactamases; chimères; évolution; ingénierie des protéines; analyse structure-fonction-dynamique; cristallographie par diffraction de rayons X; cinétique enzymatique; résonnance magnétique nucléaire; simulation de dynamique moléculaire in silico; chimeras; evolution; protein engineering; structure-function-dynamic analysis; X-ray crystallography; enzymatic kinetics; nuclear magnetic resonance; in silico molecular dynamic simulations

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APA (6th Edition):

Gobeil, S. (2017). Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18543

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):

Gobeil, Sophie. “Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 .” 2017. Thesis, Université de Montréal. Accessed July 08, 2020. http://hdl.handle.net/1866/18543.

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

MLA Handbook (7th Edition):

Gobeil, Sophie. “Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 .” 2017. Web. 08 Jul 2020.

Vancouver:

Gobeil S. Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/1866/18543.

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

Council of Science Editors:

Gobeil S. Vérification de la corrélation entre la fonction, la structure et la dynamique sur un chemin évolutif recombinant les β-lactamases TEM-1 et PSE-4 . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18543

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


Uppsala University

904. Kalman, Grim Elison. Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea.

Degree: Structural Biology, 2019, Uppsala University

  This report summarizes the work on the cloning, expression, and purification of PerR, a metal sensing regulator from Saccharopolyspora erythraea and the subsequent characterization… (more)

Subjects/Keywords: structural biology; cell culture; protein expression; genetic engineering; spectroscopy; X-ray crystallography; small angle X-ray scattering; SAXS; transcription factor; PerR; metal binding; antibiotics; Saccharopolyspora erythraea; S. erythraea; soil bacterium; actinobacteria; actinomycetes; oxidative stress; peroxide stress; structure determination; characterization; stabilization; peroxide sensor; iron sensor; manganese sensor; metalloprotein; metal ion homeostasis; metal ion; prokaryotic; strukturbiologi; cellodling; proteinuttryck; genteknik; spektroskopi; röntgenkristallografi; småvinkel-röntgenspridning; SAXS; transkriptionsfaktor; PerR; metallbindande; antibiotika; Saccharopolyspora erythraea; S. erythraea; jordartsbakterie; Aktinobakterier; Actinobacteria; Actinomycetes; oxidativ stress; peroxid stress; strukturbestämning; karaktärisering; stabilisering; peroxidsensor; järnsensor; mangansensor; metalljonshomeostas; metalljoner; prokaryot; Structural Biology; Strukturbiologi

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APA (6th Edition):

Kalman, G. E. (2019). Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387943

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):

Kalman, Grim Elison. “Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea.” 2019. Thesis, Uppsala University. Accessed July 08, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387943.

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

MLA Handbook (7th Edition):

Kalman, Grim Elison. “Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea.” 2019. Web. 08 Jul 2020.

Vancouver:

Kalman GE. Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea. [Internet] [Thesis]. Uppsala University; 2019. [cited 2020 Jul 08]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387943.

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

Council of Science Editors:

Kalman GE. Purification, functional characterization and crystallization of the PerR peroxide sensor from Saccharopolyspora erythraea. [Thesis]. Uppsala University; 2019. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387943

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


ETH Zürich

905. Adhiambo Owiti, Judith. Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation.

Degree: 2009, ETH Zürich

Subjects/Keywords: MANIOK (PFLANZENBAU); NACHERNTE-PHYSIOLOGIE (AGRARPRODUKTE); PFLANZLICHE PROTEINE + PFLANZLICHE PEPTIDE (PFLANZENCHEMIE); PROTEINKATABOLISMUS + PEPTIDKATABOLISMUS (METABOLISMUS); PROTEOMIK (PROTEINE UND PEPTIDE); CASSAVA (CROP PRODUCTION); POST-HARVEST PHYSIOLOGY (AGRICULTURAL PRODUCTS); PLANT PROTEINS + PLANT PEPTIDES (PHYTOCHEMISTRY); PROTEIN CATABOLISM + PEPTIDE CATABOLISM (METABOLISM); PROTEOMICS (PROTEINS AND PEPTIDES); info:eu-repo/classification/ddc/660; Chemical engineering

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APA (6th Edition):

Adhiambo Owiti, J. (2009). Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/151817

Chicago Manual of Style (16th Edition):

Adhiambo Owiti, Judith. “Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation.” 2009. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/151817.

MLA Handbook (7th Edition):

Adhiambo Owiti, Judith. “Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation.” 2009. Web. 08 Jul 2020.

Vancouver:

Adhiambo Owiti J. Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation. [Internet] [Doctoral dissertation]. ETH Zürich; 2009. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/151817.

Council of Science Editors:

Adhiambo Owiti J. Molecular and biochemical understanding of post-harvest physiological deterioration in cassava roots and approaches for its modulation. [Doctoral Dissertation]. ETH Zürich; 2009. Available from: http://hdl.handle.net/20.500.11850/151817


ETH Zürich

906. Bańko, Monika I. Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines.

Degree: 2015, ETH Zürich

Subjects/Keywords: FLUORESZIERENDE PROTEINE; PROTEIN COMPLEXES; GENTECHNOLOGIE; FLUORESCENT PROTEINS; FLUORESZENZMARKIERUNG (BIOLOGIE); STRUCTURAL DYNAMICS, STRUCTURAL AND CONFORMATIONAL CHANGES (BIOMOLECULES); GENETIC ENGINEERING; CELL FUNCTION + CELL ACTIVITY (CYTOLOGY); GTPASES (ENZYMES); STRUKTURDYNAMIK, STRUKTUR- UND KONFORMATIONSVERÄNDERUNGEN (BIOMOLEKÜLE); CYTOSKELETTPROTEINE; ZELLFUNKTIONEN + ZELLAKTIVITÄTEN (CYTOLOGIE); FLUORESCENCE LABELLING (BIOLOGY); PROTEINKOMPLEXE; CYTOSKELETAL PROTEINS; GTPASEN (ENZYME); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

BaÅ„ko, M. I. (2015). Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/100436

Chicago Manual of Style (16th Edition):

BaÅ„ko, Monika I. “Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines.” 2015. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/100436.

MLA Handbook (7th Edition):

BaÅ„ko, Monika I. “Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines.” 2015. Web. 08 Jul 2020.

Vancouver:

BaÅ„ko MI. Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/100436.

Council of Science Editors:

BaÅ„ko MI. Chromosomal integration of EGFP into the SEPT2 locus allows for study on endogenous septin complex in mammalian cell lines. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/100436


University of Florida

907. Chen, Pei, 1962-. Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology.

Degree: 1996, University of Florida

Subjects/Keywords: Analgesics; Brain; Chemicals; Enzymes; Esters; Opioid analgesics; Rats; Receptors; Room temperature; Solvents; Arginine  – pharmacology ( mesh ); Brain  – drug effects ( mesh ); Drug Delivery Systems ( mesh ); Drug Design ( mesh ); Endorphins  – analogs &; derivatives ( mesh ); Endorphins  – chemical synthesis ( mesh ); Endorphins  – pharmacology ( mesh ); Lysine  – pharmacology ( mesh ); Protein Engineering ( mesh ); Tyrosine ( mesh )

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APA (6th Edition):

Chen, Pei, 1. (1996). Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology. (Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/AA00011190

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):

Chen, Pei, 1962-. “Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology.” 1996. Thesis, University of Florida. Accessed July 08, 2020. https://ufdc.ufl.edu/AA00011190.

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

MLA Handbook (7th Edition):

Chen, Pei, 1962-. “Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology.” 1996. Web. 08 Jul 2020.

Vancouver:

Chen, Pei 1. Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology. [Internet] [Thesis]. University of Florida; 1996. [cited 2020 Jul 08]. Available from: https://ufdc.ufl.edu/AA00011190.

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

Council of Science Editors:

Chen, Pei 1. Delivery of a kyotorphin analog into the central nervous system by molecular packing and sequential metabolism design, synthesis and pharmacology. [Thesis]. University of Florida; 1996. Available from: https://ufdc.ufl.edu/AA00011190

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


ETH Zürich

908. Billerbeck, Sonja. Orthogonalization of complex cell-free production systems.

Degree: 2013, ETH Zürich

Subjects/Keywords: BIOCHEMISCHE BIOTECHNOLOGIE; ZELLFREIE TRANSLATION, IN-VITRO PROTEINBIOSYNTHESE (MOLEKULARE GENETIK); SYNTHETISCHE BIOLOGIE; CELL FREE TRANSLATION, IN VITRO PROTEIN BIOSYNTHESIS (MOLECULAR GENETICS); ORTHOGONALSYSTEME + ORTHOGONALREIHEN (FUNKTIONENSYSTEME); ORTHOGONAL SYSTEMS + ORTHOGONAL SERIES (FUNCTION SYSTEMS); PEPTIDE HYDROLASES, PROTEASES (ENZYMES); BIOCHEMICAL ENGINEERING; SYNTHETIC BIOLOGY; PEPTIDHYDROLASEN, PROTEASEN (ENZYME); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Billerbeck, S. (2013). Orthogonalization of complex cell-free production systems. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/69027

Chicago Manual of Style (16th Edition):

Billerbeck, Sonja. “Orthogonalization of complex cell-free production systems.” 2013. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/69027.

MLA Handbook (7th Edition):

Billerbeck, Sonja. “Orthogonalization of complex cell-free production systems.” 2013. Web. 08 Jul 2020.

Vancouver:

Billerbeck S. Orthogonalization of complex cell-free production systems. [Internet] [Doctoral dissertation]. ETH Zürich; 2013. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/69027.

Council of Science Editors:

Billerbeck S. Orthogonalization of complex cell-free production systems. [Doctoral Dissertation]. ETH Zürich; 2013. Available from: http://hdl.handle.net/20.500.11850/69027

909. Rousaki, Aikaterini. Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance.

Degree: PhD, Biophysics, 2011, University of Michigan

 Chaperone proteins and their cochaperones are perhaps one of the most intriguing systems for investigation. Ubiquitous in nature, they can be found in every organism… (more)

Subjects/Keywords: NMR; Protein; Drug; Small Molecule; Ligand; Chaperone; Biomedical Engineering; Chemical Engineering; Computer Science; Engineering (General); Materials Science and Engineering; Nuclear Engineering and Radiological Sciences; Biological Chemistry; Complementary and Alternative Medicine; Dentistry; Genetics; Medicine (General); Microbiology and Immunology; Molecular, Cellular and Developmental Biology; Neurosciences; Pathology; Pharmacy and Pharmacology; Physical Medicine and Rehabilitation; Public Health; Chemistry; Ecology and Evolutionary Biology; Mathematics; Natural Resources and Environment; Physics; Science (General); Statistics and Numeric Data; Engineering; Health Sciences; Science

…142 VIII.6.1 Protein preparation 142 VIII.6.2 NMR assignments 143… …154 IX.3.1 Protein Preparation 154 IX.4 Results 154… …References ix 168 List of Tables Table II.1. The protein… …14 Figure II. 5: The Hsp70 protein folding cycle 16 Figure II.6: The… …experiments for the ATP and ADP state of the protein 30 Figure III.1.1… 

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APA (6th Edition):

Rousaki, A. (2011). Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86521

Chicago Manual of Style (16th Edition):

Rousaki, Aikaterini. “Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance.” 2011. Doctoral Dissertation, University of Michigan. Accessed July 08, 2020. http://hdl.handle.net/2027.42/86521.

MLA Handbook (7th Edition):

Rousaki, Aikaterini. “Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance.” 2011. Web. 08 Jul 2020.

Vancouver:

Rousaki A. Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/2027.42/86521.

Council of Science Editors:

Rousaki A. Hsp70 chaperone Proteins and their Interactions with Various Drugs as Studied by Nuclear Magnetic Resonance. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86521

910. Parola, Cristina. Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery.

Degree: 2019, ETH Zürich

 Monoclonal antibodies (mAbs) are the most promising and dominant class of biotherapeutics, due to the strategical combination of their targeting power with diverse effector functions.… (more)

Subjects/Keywords: Immunology; Protein engineering; Antibody; Genome editing; CRISPR-Cas9; Antibody engineering; antibody discovery; Antibody library; Affinity maturation; Cell engineering; info:eu-repo/classification/ddc/610; info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/600; Medical sciences, medicine; Life sciences; Technology (applied sciences)

…ever since for its use in protein engineering and discovery, with the first therapeutic… …finally allowing the discovery and engineering of recombinant antibodies of synthetic and… …effettrici. In questa tesi viene presentata la realizzazione, tramite ingegneria immunogenomica di… …ingegneria, abbiamo messo a punto un saggio per lo screening di library immuni in cui molteplici… …of contacting the antigen once the protein is correctly folded, are called complementarity… 

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APA (6th Edition):

Parola, C. (2019). Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/352141

Chicago Manual of Style (16th Edition):

Parola, Cristina. “Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery.” 2019. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/352141.

MLA Handbook (7th Edition):

Parola, Cristina. “Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery.” 2019. Web. 08 Jul 2020.

Vancouver:

Parola C. Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery. [Internet] [Doctoral dissertation]. ETH Zürich; 2019. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/352141.

Council of Science Editors:

Parola C. Immunogenomic engineering of a mammalian display platform for antibody expression, screening and discovery. [Doctoral Dissertation]. ETH Zürich; 2019. Available from: http://hdl.handle.net/20.500.11850/352141


ETH Zürich

911. Villiger, Thomas K. Bioprocess Engineering Framework to Control Protein N-linked Glycosylation.

Degree: 2015, ETH Zürich

Subjects/Keywords: PROTEINBIOTECHNOLOGIE + ENZYMBIOTECHNOLOGIE; PROTEINE, POLYPEPTIDE, ENZYME, ENZYMINHIBITOREN, PEPTIDE (PHARMAZIE); GLYKOSYLIERUNGSREAKTIONEN + GLYKOSYLIERUNG (BIOCHEMIE); MONOKLONALE ANTIKÖRPER (IMMUNOLOGISCHE TECHNIKEN); ZELLKULTUREN + GEWEBEKULTUREN (ZOOLOGIE); BIOLOGISCHE REAKTOREN (BIOTECHNOLOGIE); MODELLRECHNUNG IN DER TECHNISCHEN CHEMIE UND VERFAHRENSTECHNIK; PROTEIN ENGINEERING + ENZYME ENGINEERING; PROTEINS, POLYPEPTIDES, ENZYMES, ENZYME INHIBITORS, PEPTIDES (PHARMACY); GLYCOSYLATION REACTIONS + GLYCOSYLATION (BIOCHEMISTRY); MONOCLONAL ANTIBODIES (IMMUNOLOGICAL TECHNIQUES); CELL CULTURES + TISSUE CULTURES (ZOOLOGY); BIOLOGICAL REACTORS (BIOTECHNOLOGY); MATHEMATICAL MODELING IN TECHNICAL CHEMISTRY AND PROCESS ENGINEERING; info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/610; Life sciences; Medical sciences, medicine

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APA (6th Edition):

Villiger, T. K. (2015). Bioprocess Engineering Framework to Control Protein N-linked Glycosylation. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155315

Chicago Manual of Style (16th Edition):

Villiger, Thomas K. “Bioprocess Engineering Framework to Control Protein N-linked Glycosylation.” 2015. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/155315.

MLA Handbook (7th Edition):

Villiger, Thomas K. “Bioprocess Engineering Framework to Control Protein N-linked Glycosylation.” 2015. Web. 08 Jul 2020.

Vancouver:

Villiger TK. Bioprocess Engineering Framework to Control Protein N-linked Glycosylation. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/155315.

Council of Science Editors:

Villiger TK. Bioprocess Engineering Framework to Control Protein N-linked Glycosylation. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155315

912. Reaver, Nathan George Frederick. Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins.

Degree: MSin Bioengineering, Bioengineering, 2013, University of Toledo

 The concentration ratio of glycated to non-glycated forms of various blood proteins can be used as a diagnostic measure in diabetes to determine a history… (more)

Subjects/Keywords: Biomedical Research; Biochemistry; Chemistry; Engineering; Health Care; Health Sciences; Medicine; Molecular Chemistry; Optics; Organic Chemistry; Technology; Biomedical Engineering; aptamer; aptamers; surface plasmon resonance; SPR; diabetes mellitus; glycated protein; biosensor; hemoglobin; glycated hemoglobin; SELEX; Systematic Evolution of Ligands by Exponential Enrichment; fibrinogen; non-enzymatic glycosylation; plasmonics

…139 A SELEX Protocol A.1 Coupling Target Protein to Magnetic Beads (MB)… …17 2-4 The Glucose(t) function with solved glycated protein level profiles… …98 4-4 Response from initial protein injection and injection of same concentration after… …100 4-6 Response from initial protein injection and injection of same concentration after… …101 4-8 Response from initial protein injection and injection of same concentration after… 

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APA (6th Edition):

Reaver, N. G. F. (2013). Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1373319138

Chicago Manual of Style (16th Edition):

Reaver, Nathan George Frederick. “Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins.” 2013. Masters Thesis, University of Toledo. Accessed July 08, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1373319138.

MLA Handbook (7th Edition):

Reaver, Nathan George Frederick. “Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins.” 2013. Web. 08 Jul 2020.

Vancouver:

Reaver NGF. Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins. [Internet] [Masters thesis]. University of Toledo; 2013. [cited 2020 Jul 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1373319138.

Council of Science Editors:

Reaver NGF. Development and Characterization of Aptamers for the use in Surface Plasmon Resonance Sensors for the Detection of Glycated Blood Proteins. [Masters Thesis]. University of Toledo; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1373319138


University of Otago

913. May, Adam Stephen Gary. In vitro meat: protein for twelve billion? .

Degree: 2013, University of Otago

 This thesis provides the background for the creative component of this MSciComm – entitled ‘Meating Expectations’ - a 25 minute documentary produced with Rodney August.… (more)

Subjects/Keywords: in vitro meat; cultured meat; lab meat; franken steak; meat production; meat grown from stem cells; Conventional meat production; meat consumption; sustainable meat; humane meat; Meat without slaughter; victimless meat; embryonic stem cells; adult stem cells; protein; somatic stem cells; Dedifferentiation; differentiation; Entomophagy; Fibroblasts; Hypertrophy; in vivo; in vitro; Myoblast; myofibre; myofiber; muscle fibre; myofibril; myotube; myogenesis; Myogenic contraction; Myosatellite cells; quorn; Surimi; tempeh; tofu; Transdifferentiation; agriculture; population growth; diminishing natural resources; limited land; declining grain stocks; rising meat demand; malnourished people; rising affluence; biofuels; higher food prices; global food insecurity; meat disadvantages; history of in vitro meat; muscle development; proliferation; proliferative capacity; tissue restoration; skeletal muscle regeneration; skeletal muscle; tissue engineering; muscle; engineering; culture media; bioreactors; ground meat; processed meat; scaffold based techniques; scaffold; self organizing techniques; structured meat; disease; disease control

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APA (6th Edition):

May, A. S. G. (2013). In vitro meat: protein for twelve billion? . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/4101

Chicago Manual of Style (16th Edition):

May, Adam Stephen Gary. “In vitro meat: protein for twelve billion? .” 2013. Masters Thesis, University of Otago. Accessed July 08, 2020. http://hdl.handle.net/10523/4101.

MLA Handbook (7th Edition):

May, Adam Stephen Gary. “In vitro meat: protein for twelve billion? .” 2013. Web. 08 Jul 2020.

Vancouver:

May ASG. In vitro meat: protein for twelve billion? . [Internet] [Masters thesis]. University of Otago; 2013. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/10523/4101.

Council of Science Editors:

May ASG. In vitro meat: protein for twelve billion? . [Masters Thesis]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4101

914. Jäger, Linda. Investigating Catalytic Promiscuity in AroQ Enzymes.

Degree: 2017, ETH Zürich

 A fundamental goal of chemical biology is the design of novel enzymes. Due to our limited understanding of protein folding, however, novel enzymes are typically… (more)

Subjects/Keywords: Biological chemistry; Biochemistry; Chemical biology; Molecular evolution; Isochorismate pyruvate lyase; Chorismate mutase; Directed evolution; Neutral drift; Ancestral sequence reconstruction; Next generation sequencing (NGS); Evolvability; De novo enzyme design; Protein engineering; Enzyme engineering; Enzyme catalysis; info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/540; Life sciences; Chemistry

…this is that protein engineering experiments are largely carried out by amino acid… …evolutionary origin, meaning that these activities presumably emerged from a common ancestral protein… …laboratory. In our second evolutionary engineering approach, presented in Chapter 5, we describe… …funktionellen Enzyms sehr viele Protein-Variationen geprüft werden. Vielfach ist dementsprechend das… …Enzym-Engineering auf die Entwicklung von Hochdurchsatzverfahren für die Selektion oder auf… 

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APA (6th Edition):

Jäger, L. (2017). Investigating Catalytic Promiscuity in AroQ Enzymes. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/214336

Chicago Manual of Style (16th Edition):

Jäger, Linda. “Investigating Catalytic Promiscuity in AroQ Enzymes.” 2017. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/214336.

MLA Handbook (7th Edition):

Jäger, Linda. “Investigating Catalytic Promiscuity in AroQ Enzymes.” 2017. Web. 08 Jul 2020.

Vancouver:

Jäger L. Investigating Catalytic Promiscuity in AroQ Enzymes. [Internet] [Doctoral dissertation]. ETH Zürich; 2017. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/214336.

Council of Science Editors:

Jäger L. Investigating Catalytic Promiscuity in AroQ Enzymes. [Doctoral Dissertation]. ETH Zürich; 2017. Available from: http://hdl.handle.net/20.500.11850/214336

915. Jeschek, Markus. Engineering Escherichia coli for non-natural metabolism.

Degree: 2016, ETH Zürich

Subjects/Keywords: BAKTERIOLOGIE/MIKROBIOTECHNOLOGIE; ESCHERICHIA (MIKROBIOLOGIE); STOFFWECHSELWEGE UND STOFFWECHSELZYKLEN (BIOCHEMIE); PROTEINBIOTECHNOLOGIE + ENZYMBIOTECHNOLOGIE; METABOLISMUS (MIKROORGANISMEN); BIOLOGISCHE INFORMATIK UND COMPUTERANWENDUNG IN DER BIOLOGIE; BACTERIOLOGY/MICROBIOTECHNOLOGY; ESCHERICHIA (MICROBIOLOGY); METABOLIC PATHWAYS + METABOLIC CYCLES (BIOCHEMISTRY); PROTEIN ENGINEERING + ENZYME ENGINEERING; METABOLISM (MICROORGANISMS); BIOLOGICAL INFORMATICS AND COMPUTER APPLICATIONS IN BIOLOGY; info:eu-repo/classification/ddc/570; Life sciences

…proteins and enzymes and is therefore largely overlapping with fields such as protein engineering… …ZUSAMMENFASSUNG Das Forschungsgebiet des „Metabolic Engineering“ entstand innerhalb der… …befasst sich das Gebiet des „vertikalen“ Metabolic Engineering mit der zielgerichteten… …vertikale Metabolic Engineering in Richtung von Biokatalysatoren, die immer stärker von ihren… …an das Engineering von metabolischen Netzwerken bis hin zu ganzen Zellen heranzutasten. In… 

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APA (6th Edition):

Jeschek, M. (2016). Engineering Escherichia coli for non-natural metabolism. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155862

Chicago Manual of Style (16th Edition):

Jeschek, Markus. “Engineering Escherichia coli for non-natural metabolism.” 2016. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/155862.

MLA Handbook (7th Edition):

Jeschek, Markus. “Engineering Escherichia coli for non-natural metabolism.” 2016. Web. 08 Jul 2020.

Vancouver:

Jeschek M. Engineering Escherichia coli for non-natural metabolism. [Internet] [Doctoral dissertation]. ETH Zürich; 2016. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/155862.

Council of Science Editors:

Jeschek M. Engineering Escherichia coli for non-natural metabolism. [Doctoral Dissertation]. ETH Zürich; 2016. Available from: http://hdl.handle.net/20.500.11850/155862


Université de Montréal

916. Rousseau, Olivier. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .

Degree: 2019, Université de Montréal

Subjects/Keywords: Analyse de composantes indépendantes du temps et de la structure; analyse statistique; automatisation; biocatalyse; cétone de framboise; criblage à haut débit; cytochrome P450 BM3; dynamique moléculaire; indigo; ingénierie de protéines; modélisation; mutagénèse; oxydation; séquençage nouvelle génération; Automation; Biocatalysis; High-throughput screening; Modeling; Molecular dynamics; Mutagenesis; Next-generation sequencing; Oxidation; Protein engineering; Raspberry ketone; Statistical analysis; Time-structure independent component analysis

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APA (6th Edition):

Rousseau, O. (2019). Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21949

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):

Rousseau, Olivier. “Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .” 2019. Thesis, Université de Montréal. Accessed July 08, 2020. http://hdl.handle.net/1866/21949.

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

MLA Handbook (7th Edition):

Rousseau, Olivier. “Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .” 2019. Web. 08 Jul 2020.

Vancouver:

Rousseau O. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/1866/21949.

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

Council of Science Editors:

Rousseau O. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/21949

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

917. Walker, Chandler L. Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Human traumatic spinal cord injuries (SCI) are primarily incomplete contusion or compression injuries at the cervical spinal level, causing immediate… (more)

Subjects/Keywords: Spinal cord injury, PTEN, mTOR, Schwann cells, transplantation, neuroprotection; Spinal cord  – Wounds and injuries  – Treatment  – Animal models; Spinal cord  – Regeneration; Tissue engineering; Cervical vertebrae  – Wounds and injuries; Apoptosis; Autophagic vacuoles; Cell death; Cellular signal transduction; Cell transplantation; Neuroprotective agents; Central nervous system  – Regeneration; Drug targeting; Proteins  – Synthesis; Protein-tyrosine phosphatase; Rats as laboratory animals

…Figure 15. Effects of bpV(pic) on mTOR and autophagic protein analysis 1d post-SCI… …84 Figure 22. Injury and bpV-mediated effects on Akt and ribosomal protein S6… …x29;/Akt and mitogen-activated protein kinase (MAPK) pathways. These cascades are… …protein light chain 3 (LC3 II) is a widely accepted marker of autophagosomes (… …reversed this accumulation and reduced LC3 II protein levels (Walker et al., 2012)… 

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APA (6th Edition):

Walker, C. L. (2014). Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/4210

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):

Walker, Chandler L. “Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats.” 2014. Thesis, IUPUI. Accessed July 08, 2020. http://hdl.handle.net/1805/4210.

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

MLA Handbook (7th Edition):

Walker, Chandler L. “Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats.” 2014. Web. 08 Jul 2020.

Vancouver:

Walker CL. Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats. [Internet] [Thesis]. IUPUI; 2014. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/1805/4210.

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

Council of Science Editors:

Walker CL. Targeting acute phosphatase PTEN inhibition and investigation of a novel combination treatment with Schwann cell transplantation to promote spinal cord injury repair in rats. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/4210

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

918. Farré Guasch, Elisabet. Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering.

Degree: Departament d'Odontologia, 2011, Universitat Internacional de Catalunya

 ABSTRACT Background and Objective: Stem cells offer an interesting tool for tissue engineering, but the clinical applications are limited by donor site morbidity and low… (more)

Subjects/Keywords: Cèl•lules mare de teixit adipós (ASC); Células madre de tejido adiposo; Adipose stem cells; bola adiposa de Bichat (BFP); buccal fat pad; enginyeria tisul•lar òssia; bone tissue engineering; proteïna morfogenètica òssia-2 (BMP-2); bone morphogenetic protein-2; biomaterials; scaffolds; Medicina, Odontologia; 61; 616.3

…you. Jenny, Trish, Michael, Parth and colleagues from the Tissue Engineering lab, thanks to… …104 3.6. Bone tissue engineering… …POTENTIAL FOR OSTEOCHONDRAL TISSUE ENGINEERING................................149 5.1.1. ASC… …POTENTIAL FOR OSTEOCHONDRAL TISSUE ENGINEERING................................165 6.1.1. ASC… 

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APA (6th Edition):

Farré Guasch, E. (2011). Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering. (Thesis). Universitat Internacional de Catalunya. Retrieved from http://hdl.handle.net/10803/31987

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):

Farré Guasch, Elisabet. “Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering.” 2011. Thesis, Universitat Internacional de Catalunya. Accessed July 08, 2020. http://hdl.handle.net/10803/31987.

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

MLA Handbook (7th Edition):

Farré Guasch, Elisabet. “Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering.” 2011. Web. 08 Jul 2020.

Vancouver:

Farré Guasch E. Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering. [Internet] [Thesis]. Universitat Internacional de Catalunya; 2011. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/10803/31987.

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

Council of Science Editors:

Farré Guasch E. Adipose Stem Cells from Buccal Fat Pad and Abdominal Adipose Tissue for Bone tissue Engineering. [Thesis]. Universitat Internacional de Catalunya; 2011. Available from: http://hdl.handle.net/10803/31987

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


ETH Zürich

919. Eugster-Meier, Elisabeth. Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen.

Degree: 2001, ETH Zürich

Subjects/Keywords: LEBENSMITTELEMULSIONEN (LEBENSMITTELINDUSTRIE); MILCHPROTEINE + PROTEINGEHALT DER MILCH (MILCHPRODUKTION); MILCHFETT + FETTGEHALT DER MILCH (MILCHPRODUKTION); STABILISIERUNG VON LEBENSMITTELN + LEBENSMITTELSTABILISATOREN (LEBENSMITTELINDUSTRIE); ADSORPTIONSMECHANISMUS (PHYSIKALISCHE CHEMIE); GRENZFLÄCHE/FLÜSSIG-FLÜSSIG (TOPOCHEMIE); FOOD EMULSIONS (FOOD INDUSTRY); MILK PROTEINS + PROTEIN CONTENT OF MILK (DAIRYING); MILK FAT + FAT CONTENT OF MILK (DAIRYING); STABILISATION OF FOODS + FOOD STABILISERS (FOOD INDUSTRY); ADSORPTION MECHANISM (PHYSICAL CHEMISTRY); INTERFACE/LIQUID-LIQUID (TOPOCHEMISTRY); info:eu-repo/classification/ddc/660; Chemical engineering

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APA (6th Edition):

Eugster-Meier, E. (2001). Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/145072

Chicago Manual of Style (16th Edition):

Eugster-Meier, Elisabeth. “Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen.” 2001. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/145072.

MLA Handbook (7th Edition):

Eugster-Meier, Elisabeth. “Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen.” 2001. Web. 08 Jul 2020.

Vancouver:

Eugster-Meier E. Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen. [Internet] [Doctoral dissertation]. ETH Zürich; 2001. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/145072.

Council of Science Editors:

Eugster-Meier E. Adsorptionsverhalten von Proteinen und niedermolekularen Lipiden der Milch an Phasengrenzflächen. [Doctoral Dissertation]. ETH Zürich; 2001. Available from: http://hdl.handle.net/20.500.11850/145072


ETH Zürich

920. Kumar, Karthik. Treatise on the formation and sensing of lipid structures on nanofabricated arrays.

Degree: 2010, ETH Zürich

Subjects/Keywords: MEMBRANPROTEINE UND PROTEINSTRUKTUR BIOLOGISCHER MEMBRANEN; DOPPELSCHICHT-LIPIDMEMBRANEN (MEMBRANBIOLOGIE); MIKROARRAY TECHNOLOGIE (MOLEKULARGENETISCHE TECHNIKEN); LITHOGRAPHIE + MIKROLITHOGRAPHIE + NANOLITHOGRAPHIE (MIKROELEKTRONIK); BIOSENSOREN (BIOTECHNOLOGIE); MEMBRANE PROTEINS AND PROTEIN STRUCTURE OF MEMBRANES; BILAYER LIPID MEMBRANES (MEMBRANE BIOLOGY); MICROARRAY TECHNOLOGY (MOLECULAR GENETIC TECHNIQUES); LITHOGRAPHY + MICROLITHOGRAPHY + NANOLITHOGRAPHY (MICROELECTRONICS); BIOSENSORS (BIOTECHNOLOGY); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/620; Life sciences; Engineering & allied operations

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

APA (6th Edition):

Kumar, K. (2010). Treatise on the formation and sensing of lipid structures on nanofabricated arrays. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152482

Chicago Manual of Style (16th Edition):

Kumar, Karthik. “Treatise on the formation and sensing of lipid structures on nanofabricated arrays.” 2010. Doctoral Dissertation, ETH Zürich. Accessed July 08, 2020. http://hdl.handle.net/20.500.11850/152482.

MLA Handbook (7th Edition):

Kumar, Karthik. “Treatise on the formation and sensing of lipid structures on nanofabricated arrays.” 2010. Web. 08 Jul 2020.

Vancouver:

Kumar K. Treatise on the formation and sensing of lipid structures on nanofabricated arrays. [Internet] [Doctoral dissertation]. ETH Zürich; 2010. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/20.500.11850/152482.

Council of Science Editors:

Kumar K. Treatise on the formation and sensing of lipid structures on nanofabricated arrays. [Doctoral Dissertation]. ETH Zürich; 2010. Available from: http://hdl.handle.net/20.500.11850/152482

[1] … [26] [27] [28] [29] [30] [31]

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