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You searched for subject:( Mutation Missense 60). Showing records 1 – 30 of 5490 total matches.

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1. Lee, Seung-Ah. Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism.

Degree: PhD, 2008, University of Alabama – Birmingham

Retinol dehydrogenase 12 (RDH12) is a member of the microsomal short-chain dehydrogenase/reductase superfamily of proteins that is highly expressed in photorecep-tor cells. Mutations in RDH12… (more)

Subjects/Keywords: Alcohol Oxidoreductases  – metabolism<; br>; Genetic Diseases, Inborn  – enzymology<; br>; Lipid Peroxidation<; br>; Mutation, Missense<; br>; Photoreceptor Cells  – enzymology<; br>; Retinal Diseases  – enzymology<; br>; Retinaldehyde  – metabolism<; br>; Retinoids  – metabolism<; br>; Tretinoin  – metabolism

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

APA (6th Edition):

Lee, S. (2008). Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,814

Chicago Manual of Style (16th Edition):

Lee, Seung-Ah. “Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,814.

MLA Handbook (7th Edition):

Lee, Seung-Ah. “Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism.” 2008. Web. 19 Sep 2019.

Vancouver:

Lee S. Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,814.

Council of Science Editors:

Lee S. Function of human retinol dehydrogenase 12 (RDH12) in retinoid metabolism. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,814

2. Nelson, Michael Paul. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.

Degree: PhD, 2012, University of Alabama – Birmingham

Pneumonia caused by the fungal pathogen Pneumocystis continues to be the leading cause of morbidity and mortality in AIDS patients. In addition, there are a… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes – immunology.<; br>; Cell Differentiation – genetics<; br>; Evolution, Molecular.<; br>; Genome, Viral<; br>; HIV Infections<; br>; HIV-1 – immunology<; br>; Immune Evasion.<; br>; Mutation, Missense<; br>; Phenotype<; br>; T-Box Domain Proteins – genetics.<; br>; Viral Proteins – immunology.

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APA (6th Edition):

Nelson, M. P. (2012). Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1409

Chicago Manual of Style (16th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1409.

MLA Handbook (7th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Web. 19 Sep 2019.

Vancouver:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409.

Council of Science Editors:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409


Indian Institute of Science

3. Balasubramanyam, Rashmi. Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods.

Degree: 2017, Indian Institute of Science

Missense mutations account for more than 50% of the mutations known to be involved in human inherited diseases. Missense classification is a challenging task that… (more)

Subjects/Keywords: Missense Classification; Supervised Classification; Ensemble Learning Methods; Missense Mutation Classification; Missense Classifiers; Missense Mutations; Computer Science

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APA (6th Edition):

Balasubramanyam, R. (2017). Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3804 ; http://etd.iisc.ernet.in/abstracts/4674/G28613-Abs.pdf

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

Chicago Manual of Style (16th Edition):

Balasubramanyam, Rashmi. “Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods.” 2017. Thesis, Indian Institute of Science. Accessed September 19, 2019. http://etd.iisc.ernet.in/2005/3804 ; http://etd.iisc.ernet.in/abstracts/4674/G28613-Abs.pdf.

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

MLA Handbook (7th Edition):

Balasubramanyam, Rashmi. “Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods.” 2017. Web. 19 Sep 2019.

Vancouver:

Balasubramanyam R. Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods. [Internet] [Thesis]. Indian Institute of Science; 2017. [cited 2019 Sep 19]. Available from: http://etd.iisc.ernet.in/2005/3804 ; http://etd.iisc.ernet.in/abstracts/4674/G28613-Abs.pdf.

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

Council of Science Editors:

Balasubramanyam R. Supervised Classification of Missense Mutations as Pathogenic or Tolerated using Ensemble Learning Methods. [Thesis]. Indian Institute of Science; 2017. Available from: http://etd.iisc.ernet.in/2005/3804 ; http://etd.iisc.ernet.in/abstracts/4674/G28613-Abs.pdf

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

4. Masyukova, Svetlana V. Analysis of NPHP complex genetic interactions associated with human cilia disorders.

Degree: PhD, 2011, University of Alabama – Birmingham

Primary cilia are antenna-like organelles that extend from the surface of almost all mammalian cell types. They regulate many signaling pathways and sense physical and… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins – metabolism.<; br>; Cilia – metabolism.<; br>; Membrane Proteins – metabolism<; br>; Mutation, Missense – physiology.<; br>; Proteins – genetics<; br>; Proteins – metabolism

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

APA (6th Edition):

Masyukova, S. V. (2011). Analysis of NPHP complex genetic interactions associated with human cilia disorders. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1352

Chicago Manual of Style (16th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1352.

MLA Handbook (7th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Web. 19 Sep 2019.

Vancouver:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352.

Council of Science Editors:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352


University of Pennsylvania

5. Clark, Elisia. Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation.

Degree: 2018, University of Pennsylvania

 Friedreich’s Ataxia (FRDA) is an incurable neurodegenerative disease caused by mutations in the frataxin (FXN) gene, resulting in decreased expression of the mitochondrial protein FXN.… (more)

Subjects/Keywords: frataxin; Friedreich ataxia; missense mutation; Molecular Biology; Neuroscience and Neurobiology; Pharmacology

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APA (6th Edition):

Clark, E. (2018). Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2964

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):

Clark, Elisia. “Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation.” 2018. Thesis, University of Pennsylvania. Accessed September 19, 2019. https://repository.upenn.edu/edissertations/2964.

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

MLA Handbook (7th Edition):

Clark, Elisia. “Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation.” 2018. Web. 19 Sep 2019.

Vancouver:

Clark E. Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2019 Sep 19]. Available from: https://repository.upenn.edu/edissertations/2964.

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

Council of Science Editors:

Clark E. Investigating Molecular Mechanisms Underlying Mild Phenotype In Friedreich Ataxia Patients With G130v Missense Mutation. [Thesis]. University of Pennsylvania; 2018. Available from: https://repository.upenn.edu/edissertations/2964

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


University of Texas Southwestern Medical Center

6. Rodriguez, Andrea Christine. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.

Degree: 2015, University of Texas Southwestern Medical Center

 O-linked β-N-acetylglucosamine (O-GlcNAc) is an abundant post-translational modification that is regulated by two enzymes, O-GlcNAc transferase (OGT) and O-GlcNAc hydrolase (OGA). While it is elusive… (more)

Subjects/Keywords: Acetylglucosamine; Mutation, Missense; N-Acetylglucosaminyltransferases; Nuclear Pore Complex Proteins

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APA (6th Edition):

Rodriguez, A. C. (2015). Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4449

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):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed September 19, 2019. http://hdl.handle.net/2152.5/4449.

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

MLA Handbook (7th Edition):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Web. 19 Sep 2019.

Vancouver:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2152.5/4449.

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

Council of Science Editors:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4449

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


University of Minnesota

7. Talsness, Dana. Biophysical, cellular, and animal models of dystrophin missense mutations.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 The 427kDa protein dystrophin is expressed in skeletal muscle where it localizes to the costamere and physically links the interior of muscle fibers to the… (more)

Subjects/Keywords: DMD; Duchenne; Dystrophin; Missense mutation; Protein misfolding; Molecular, cellular, developmental biology and genetics

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

APA (6th Edition):

Talsness, D. (2014). Biophysical, cellular, and animal models of dystrophin missense mutations. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/171764

Chicago Manual of Style (16th Edition):

Talsness, Dana. “Biophysical, cellular, and animal models of dystrophin missense mutations.” 2014. Doctoral Dissertation, University of Minnesota. Accessed September 19, 2019. http://hdl.handle.net/11299/171764.

MLA Handbook (7th Edition):

Talsness, Dana. “Biophysical, cellular, and animal models of dystrophin missense mutations.” 2014. Web. 19 Sep 2019.

Vancouver:

Talsness D. Biophysical, cellular, and animal models of dystrophin missense mutations. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/11299/171764.

Council of Science Editors:

Talsness D. Biophysical, cellular, and animal models of dystrophin missense mutations. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/171764


Tampere University

8. Khan, Sofia. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2010, Tampere University

 Valkuaisaineet eli proteiinit ovat välttämättömiä elämää ylläpitäviä molekyylejä. Kaikkien proteiinien rakennusohjeet ovat perimässä ja ne rakentuvat 20 erilaisesta aminohaposta, joiden ominaisuudet ja järjestys määrittelevät proteiinin… (more)

Subjects/Keywords: mutaatio; proteiini; proteiinirakenne; stabiilisuus; homologiamallinnus; missense mutation; protein structure; stability; homology modeling

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APA (6th Edition):

Khan, S. (2010). Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66579

Chicago Manual of Style (16th Edition):

Khan, Sofia. “Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .” 2010. Doctoral Dissertation, Tampere University. Accessed September 19, 2019. https://trepo.tuni.fi/handle/10024/66579.

MLA Handbook (7th Edition):

Khan, Sofia. “Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models .” 2010. Web. 19 Sep 2019.

Vancouver:

Khan S. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . [Internet] [Doctoral dissertation]. Tampere University; 2010. [cited 2019 Sep 19]. Available from: https://trepo.tuni.fi/handle/10024/66579.

Council of Science Editors:

Khan S. Mutational effects on protein structures: Knowledge gained from databases, predictions and protein models . [Doctoral Dissertation]. Tampere University; 2010. Available from: https://trepo.tuni.fi/handle/10024/66579


Indian Institute of Science

9. Lakhotia, Smita. Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer.

Degree: 2006, Indian Institute of Science

 Breast Cancer susceptibility gene 1 (BRCA1) & Breast Cancer Breast cancer is one of the most common malignancies affecting women worldwide. About 5-10% of all… (more)

Subjects/Keywords: Breast Cancer; Malignant Tumor; Gene; Breast Cancer Susceptibility Gene - Mutation; Novel Missense Mutation; BRCAI Protein; Biochemical Genetics

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APA (6th Edition):

Lakhotia, S. (2006). Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/456

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):

Lakhotia, Smita. “Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer.” 2006. Thesis, Indian Institute of Science. Accessed September 19, 2019. http://hdl.handle.net/2005/456.

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

MLA Handbook (7th Edition):

Lakhotia, Smita. “Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer.” 2006. Web. 19 Sep 2019.

Vancouver:

Lakhotia S. Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer. [Internet] [Thesis]. Indian Institute of Science; 2006. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2005/456.

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

Council of Science Editors:

Lakhotia S. Breast Cancer Susceptibility Gene 1 (BRCA1) And Breast Cancer. [Thesis]. Indian Institute of Science; 2006. Available from: http://hdl.handle.net/2005/456

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

10. Liu, Zhaoping. Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1).

Degree: MS, 2001, Oregon Health Sciences University

Subjects/Keywords: Cerebellar Ataxia; Mutation, Missense; Potassium Channels; Ion Channel Gating

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APA (6th Edition):

Liu, Z. (2001). Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1). (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4R20ZNF ; http://digitalcommons.ohsu.edu/etd/3246

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):

Liu, Zhaoping. “Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1).” 2001. Thesis, Oregon Health Sciences University. Accessed September 19, 2019. doi:10.6083/M4R20ZNF ; http://digitalcommons.ohsu.edu/etd/3246.

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

MLA Handbook (7th Edition):

Liu, Zhaoping. “Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1).” 2001. Web. 19 Sep 2019.

Vancouver:

Liu Z. Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1). [Internet] [Thesis]. Oregon Health Sciences University; 2001. [cited 2019 Sep 19]. Available from: doi:10.6083/M4R20ZNF ; http://digitalcommons.ohsu.edu/etd/3246.

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

Council of Science Editors:

Liu Z. Single-channel properties of episodic ataxia type 1 (EA-1) mutations in the human voltage-gated potassium channels (hKv1.1). [Thesis]. Oregon Health Sciences University; 2001. Available from: doi:10.6083/M4R20ZNF ; http://digitalcommons.ohsu.edu/etd/3246

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


University of Tennessee – Knoxville

11. Adebali, Ogun. Applications of Evolutionary Bioinformatics in Basic and Biomedical Research.

Degree: 2015, University of Tennessee – Knoxville

 With the revolutionary progress in sequencing technologies, computational biology emerged as a game-changing field which is applied in understanding molecular events of life for not… (more)

Subjects/Keywords: protein domain; phylogenetic profiling; missense mutation prediction; orthologs and paralogs; phylogenetics; Bioinformatics; Computational Biology; Genomics; Other Genetics and Genomics

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

APA (6th Edition):

Adebali, O. (2015). Applications of Evolutionary Bioinformatics in Basic and Biomedical Research. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/3540

Chicago Manual of Style (16th Edition):

Adebali, Ogun. “Applications of Evolutionary Bioinformatics in Basic and Biomedical Research.” 2015. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed September 19, 2019. https://trace.tennessee.edu/utk_graddiss/3540.

MLA Handbook (7th Edition):

Adebali, Ogun. “Applications of Evolutionary Bioinformatics in Basic and Biomedical Research.” 2015. Web. 19 Sep 2019.

Vancouver:

Adebali O. Applications of Evolutionary Bioinformatics in Basic and Biomedical Research. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2015. [cited 2019 Sep 19]. Available from: https://trace.tennessee.edu/utk_graddiss/3540.

Council of Science Editors:

Adebali O. Applications of Evolutionary Bioinformatics in Basic and Biomedical Research. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2015. Available from: https://trace.tennessee.edu/utk_graddiss/3540

12. Field, Matthew Arnell. Computational analysis of genetic variation .

Degree: 2015, Australian National University

 High throughput sequences are generating increasingly detailed catalogues of genetic variation both in human disease and within the larger population. To effectively utilise this rich… (more)

Subjects/Keywords: bioinformatics; genetic variation; human disease; VASP; DeepSNVMiner; melanoma; variant prioritisation; missense mutation; high-throughput; genome; variant prioritization

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APA (6th Edition):

Field, M. A. (2015). Computational analysis of genetic variation . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/106398

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):

Field, Matthew Arnell. “Computational analysis of genetic variation .” 2015. Thesis, Australian National University. Accessed September 19, 2019. http://hdl.handle.net/1885/106398.

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

MLA Handbook (7th Edition):

Field, Matthew Arnell. “Computational analysis of genetic variation .” 2015. Web. 19 Sep 2019.

Vancouver:

Field MA. Computational analysis of genetic variation . [Internet] [Thesis]. Australian National University; 2015. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1885/106398.

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

Council of Science Editors:

Field MA. Computational analysis of genetic variation . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/106398

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


Georgia Tech

13. Preeprem, Thanawadee. Functional assessments of amino acid variation in human genomes.

Degree: PhD, Biology, 2014, Georgia Tech

 The Human Genome Project, initiated in 1990, creates an enormous amount of excitement in human genetics—a field of study that seeks answers to the understanding… (more)

Subjects/Keywords: Human genome variations; Single nucleotide polymorphisms; Missense mutations; Amino acid mutations; Integrative analysis; Functional assessment; Functional genomics; Computer simulation; Mutation (Biology); Amino acids

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

APA (6th Edition):

Preeprem, T. (2014). Functional assessments of amino acid variation in human genomes. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51869

Chicago Manual of Style (16th Edition):

Preeprem, Thanawadee. “Functional assessments of amino acid variation in human genomes.” 2014. Doctoral Dissertation, Georgia Tech. Accessed September 19, 2019. http://hdl.handle.net/1853/51869.

MLA Handbook (7th Edition):

Preeprem, Thanawadee. “Functional assessments of amino acid variation in human genomes.” 2014. Web. 19 Sep 2019.

Vancouver:

Preeprem T. Functional assessments of amino acid variation in human genomes. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/1853/51869.

Council of Science Editors:

Preeprem T. Functional assessments of amino acid variation in human genomes. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/51869

14. Xayarath, Bobbi. Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence.

Degree: PhD, 2007, University of Alabama – Birmingham

 The polysaccharide capsules of Streptococcus pneumoniae represent the most important virulence determinant produced by this organism. Ninety-one different serotypes have been identified, but only a… (more)

Subjects/Keywords: Bacterial Capsules  – metabolism <; br>; Cell Wall  – metabolism <; br>; Genes, Essential <; br>; Mutation <; br>; Polysaccharides, Bacterial  – metabolism <; br>; Streptococcus pneumoniae  – physiology

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

APA (6th Edition):

Xayarath, B. (2007). Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,190

Chicago Manual of Style (16th Edition):

Xayarath, Bobbi. “Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,190.

MLA Handbook (7th Edition):

Xayarath, Bobbi. “Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence.” 2007. Web. 19 Sep 2019.

Vancouver:

Xayarath B. Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,190.

Council of Science Editors:

Xayarath B. Effects of specific alterations in capsule structure on Streptococcus pneumoniae capsule assembly and virulence. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,190

15. Douglas, Chanel Catherine. A study into the protein/protein interactions involved in HIV-1 capsid assembly.

Degree: PhD, 2007, University of Alabama – Birmingham

The aim of this work was to build an understanding of the protein/protein interactions involved in HIV-1 capsid assembly as it relates to the condensation… (more)

Subjects/Keywords: Capsid Proteins  – chemistry <; br>; HIV-1  – chemistry <; br>; Mutation  – genetics <; br>; Protein Binding <; br>; Static Electricity <; br>; Virus Assembly

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APA (6th Edition):

Douglas, C. C. (2007). A study into the protein/protein interactions involved in HIV-1 capsid assembly. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,363

Chicago Manual of Style (16th Edition):

Douglas, Chanel Catherine. “A study into the protein/protein interactions involved in HIV-1 capsid assembly.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,363.

MLA Handbook (7th Edition):

Douglas, Chanel Catherine. “A study into the protein/protein interactions involved in HIV-1 capsid assembly.” 2007. Web. 19 Sep 2019.

Vancouver:

Douglas CC. A study into the protein/protein interactions involved in HIV-1 capsid assembly. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,363.

Council of Science Editors:

Douglas CC. A study into the protein/protein interactions involved in HIV-1 capsid assembly. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,363

16. Yu, Wanfeng. Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I.

Degree: PhD, 2007, University of Alabama – Birmingham

The features of tRNALys,3 that dictate why human immunodeficiency virus exclu-sively selects this tRNA as the primer for initiation of reverse transcription is unknown. The… (more)

Subjects/Keywords: HIV-1  – genetics <; br>; HIV-1  – physiology <; br>; Mutation  – genetics <; br>; RNA, Transfer, Amino Acyl  – genetics <; br>; Virus Replication  – genetics

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APA (6th Edition):

Yu, W. (2007). Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,306

Chicago Manual of Style (16th Edition):

Yu, Wanfeng. “Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,306.

MLA Handbook (7th Edition):

Yu, Wanfeng. “Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I.” 2007. Web. 19 Sep 2019.

Vancouver:

Yu W. Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,306.

Council of Science Editors:

Yu W. Importance of tRNALys,3 structure and use in gag translation for primer selection required for replication of human immunodeficiency virus type I. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,306

17. Kho, Eun-Young. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.

Degree: 2012, University of Alabama – Birmingham

The large family of human papillomaviruses (HPVs) infects the cutaneous or mucosal epithelia causing benign hyper proliferative diseases. Infections by the high-risk (HR) HPV genotypes… (more)

Subjects/Keywords: DNA; Viral – metabolism DNA-Binding Proteins – genetics Genes; p53 Human papillomavirus 18 – genetics. Mutation Mutation; Missense Oncogene Proteins; Viral – genetics.

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

APA (6th Edition):

Kho, E. (2012). Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1730

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):

Kho, Eun-Young. “Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.” 2012. Thesis, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1730.

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

MLA Handbook (7th Edition):

Kho, Eun-Young. “Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?.” 2012. Web. 19 Sep 2019.

Vancouver:

Kho E. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1730.

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

Council of Science Editors:

Kho E. Is P53 A Target Of Hpv-18 E6 In The Viral Life Cycle?. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1730

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

18. Drace, Kevin. Microbial biofilm attachment to Caenorhabditis elegans.

Degree: PhD, 2008, University of Alabama – Birmingham

The closely related bacterial species Xenorhabdus nematophila, Yersinia pestis and Y. pseudotuberculosis make biofilms capable of adhering to the head of the model nematode Caenorhabditis… (more)

Subjects/Keywords: Bacterial Adhesion  – physiology <; br>; Biofilms <; br>; Caenorhabditis elegans  – microbiology <; br>; Insect Vectors  – microbiology <; br>; Mutation  – genetics <; br>; Yersinia  – physiology <; br>; Yersinia pestis  – physiology

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APA (6th Edition):

Drace, K. (2008). Microbial biofilm attachment to Caenorhabditis elegans. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,198

Chicago Manual of Style (16th Edition):

Drace, Kevin. “Microbial biofilm attachment to Caenorhabditis elegans.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,198.

MLA Handbook (7th Edition):

Drace, Kevin. “Microbial biofilm attachment to Caenorhabditis elegans.” 2008. Web. 19 Sep 2019.

Vancouver:

Drace K. Microbial biofilm attachment to Caenorhabditis elegans. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,198.

Council of Science Editors:

Drace K. Microbial biofilm attachment to Caenorhabditis elegans. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,198

19. Hollingsworth, T.j. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.

Degree: 2013, University of Alabama – Birmingham

Retinitis pigmentosa is one of the most common inherited blinding disorders, affecting 1 in 4000 individuals world-wide. Approximately 30% of retinitis pigmentosa cases are dominantly… (more)

Subjects/Keywords: Genes, Dominant – genetics.<; br>; Mutant Proteins – metabolism.<; br>; Mutation – genetics<; br>; Retinal Degeneration – metabolism.<; br>; Retinal Rod Photoreceptor Cells<; br>; Retinitis Pigmentosa<; br>; Rhodopsin – metabolism.

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

APA (6th Edition):

Hollingsworth, T. j. (2013). The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1785

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):

Hollingsworth, T j. “The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.” 2013. Thesis, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1785.

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

MLA Handbook (7th Edition):

Hollingsworth, T j. “The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.” 2013. Web. 19 Sep 2019.

Vancouver:

Hollingsworth Tj. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. [Internet] [Thesis]. University of Alabama – Birmingham; 2013. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1785.

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

Council of Science Editors:

Hollingsworth Tj. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. [Thesis]. University of Alabama – Birmingham; 2013. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1785

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


University of Georgia

20. Gresham, Cory Sands. The oocyte as a transmitter and mediator of genetic damage to offspring.

Degree: PhD, Toxicology, 2013, University of Georgia

 Although numerous chemical germ cell mutagens have been identified in research animals, no chemical mutagens have been positively identified in human germ cells. The paucity… (more)

Subjects/Keywords: Mutation

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APA (6th Edition):

Gresham, C. S. (2013). The oocyte as a transmitter and mediator of genetic damage to offspring. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/gresham_cory_s_201312_phd

Chicago Manual of Style (16th Edition):

Gresham, Cory Sands. “The oocyte as a transmitter and mediator of genetic damage to offspring.” 2013. Doctoral Dissertation, University of Georgia. Accessed September 19, 2019. http://purl.galileo.usg.edu/uga_etd/gresham_cory_s_201312_phd.

MLA Handbook (7th Edition):

Gresham, Cory Sands. “The oocyte as a transmitter and mediator of genetic damage to offspring.” 2013. Web. 19 Sep 2019.

Vancouver:

Gresham CS. The oocyte as a transmitter and mediator of genetic damage to offspring. [Internet] [Doctoral dissertation]. University of Georgia; 2013. [cited 2019 Sep 19]. Available from: http://purl.galileo.usg.edu/uga_etd/gresham_cory_s_201312_phd.

Council of Science Editors:

Gresham CS. The oocyte as a transmitter and mediator of genetic damage to offspring. [Doctoral Dissertation]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/gresham_cory_s_201312_phd

21. Cani, Carolina Maria Gomes. Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1.

Degree: PhD, Endocrinologia, 2010, University of São Paulo

 Os craniofaringiomas são os tumores mais frequentes da região hipotálamohipofisária na faixa etária pediátrica. Apesar de serem histologicamente benignos, sua tendência infiltrativa e seu comportamento… (more)

Subjects/Keywords: Adamantinomatous craniopharyngioma; Beta catenin; Beta catenina; Craniofaringioma adamantinomatoso; Expressão gênica; Fator de transcrição PIT-1/genética; Gene expression; Homeodomain proteins/genetics; Mutação de sentido incorreto; Mutation missense; Proteínas de homeodomínio/genética; Sela túrcica/patologia; Sella turcica/pathology; Transcription factor PIT-1/genetics

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APA (6th Edition):

Cani, C. M. G. (2010). Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-20122010-103438/ ;

Chicago Manual of Style (16th Edition):

Cani, Carolina Maria Gomes. “Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1.” 2010. Doctoral Dissertation, University of São Paulo. Accessed September 19, 2019. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-20122010-103438/ ;.

MLA Handbook (7th Edition):

Cani, Carolina Maria Gomes. “Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1.” 2010. Web. 19 Sep 2019.

Vancouver:

Cani CMG. Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2019 Sep 19]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-20122010-103438/ ;.

Council of Science Editors:

Cani CMG. Análise da expressão dos genes PROP1 e CTNNB1 em craniofaringiomas adamantinomatosos com e sem mutação somática no CTNNB1. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-20122010-103438/ ;

22. Oliver, Melissa Beth. Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity.

Degree: 2013, University of Alabama – Birmingham

<italic>Streptococcus pneumoniae <italic> (pneumococcus) is an important human pathogen that expresses a capsular polysaccharide (PS) to shield underlying antigenic structures from complement-mediated opsonophagocytosis. Thus, capsular… (more)

Subjects/Keywords: Bacterial Capsules – enzymology.<; br>; Bacterial Proteins – metabolism<; br>; Genetic Loci – physiology.<; br>; Glycosyltransferases – metabolism.<; br>; Mutation, Missense<; br>; Polysaccharides, Bacterial – biosynthesis<; br>; Streptococcus pneumoniae – enzymology<; br>; Streptococcus pneumoniae – metabolism

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APA (6th Edition):

Oliver, M. B. (2013). Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1802

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):

Oliver, Melissa Beth. “Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity.” 2013. Thesis, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1802.

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

MLA Handbook (7th Edition):

Oliver, Melissa Beth. “Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity.” 2013. Web. 19 Sep 2019.

Vancouver:

Oliver MB. Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity. [Internet] [Thesis]. University of Alabama – Birmingham; 2013. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1802.

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

Council of Science Editors:

Oliver MB. Microevolution Of Capsule Synthesis Genes Contributes To Pneumococcal Capsule Diversity. [Thesis]. University of Alabama – Birmingham; 2013. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1802

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

23. Desviat, Lourdes Ruiz. Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man.

Degree: 2018, Public Library of Science

Subjects/Keywords: Animal model; Enzyme activity; Exon; Missense mutation; Ornithine transcarbamylase deficiency; Biología y Biomedicina / Biología

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APA (6th Edition):

Desviat, L. R. (2018). Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man. (Thesis). Public Library of Science. Retrieved from http://hdl.handle.net/10486/673377

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):

Desviat, Lourdes Ruiz. “Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man.” 2018. Thesis, Public Library of Science. Accessed September 19, 2019. http://hdl.handle.net/10486/673377.

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

MLA Handbook (7th Edition):

Desviat, Lourdes Ruiz. “Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man.” 2018. Web. 19 Sep 2019.

Vancouver:

Desviat LR. Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man. [Internet] [Thesis]. Public Library of Science; 2018. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10486/673377.

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

Council of Science Editors:

Desviat LR. Functional characterization of the spf/ash splicing variation in OTC deficiency of mice and man. [Thesis]. Public Library of Science; 2018. Available from: http://hdl.handle.net/10486/673377

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

24. 町田, 正晴. 日本における肥大型心筋症の遺伝学的異質性.

Degree: 博士(医学), 医学, 1994, Hokkaido University

Subjects/Keywords: hypertrophic cardiomyopathy; missense mutation; β-myosin heavy chain gene; PCR-SSCP analysis; linkage analysis; genetical heterogeneity

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APA (6th Edition):

町田, . (1994). 日本における肥大型心筋症の遺伝学的異質性. (Doctoral Dissertation). Hokkaido University. Retrieved from http://hdl.handle.net/2115/51190

Chicago Manual of Style (16th Edition):

町田, 正晴. “日本における肥大型心筋症の遺伝学的異質性.” 1994. Doctoral Dissertation, Hokkaido University. Accessed September 19, 2019. http://hdl.handle.net/2115/51190.

MLA Handbook (7th Edition):

町田, 正晴. “日本における肥大型心筋症の遺伝学的異質性.” 1994. Web. 19 Sep 2019.

Vancouver:

町田 . 日本における肥大型心筋症の遺伝学的異質性. [Internet] [Doctoral dissertation]. Hokkaido University; 1994. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/2115/51190.

Council of Science Editors:

町田 . 日本における肥大型心筋症の遺伝学的異質性. [Doctoral Dissertation]. Hokkaido University; 1994. Available from: http://hdl.handle.net/2115/51190


University of Missouri – Columbia

25. Schuckmann, Matthew M. Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I.

Degree: 2011, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Connection subdomain mutations are a recently discovered class of reverse transcriptase (RT) drug resistance mutations… (more)

Subjects/Keywords: viral drug resistance; retroviral inhibitors; enzymology; DNA polymerase; RNase H; Drug Resistance, Viral  – drug effects; HIV-1  – drug effects; HIV Reverse Transcriptase; Reverse Transcriptase Inhibitors; Ribonuclease H; Nevirapine; Mutation, Missense; Drug Resistance, Viral  – genetics

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APA (6th Edition):

Schuckmann, M. M. (2011). Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/14917

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):

Schuckmann, Matthew M. “Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I.” 2011. Thesis, University of Missouri – Columbia. Accessed September 19, 2019. https://doi.org/10.32469/10355/14917.

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

MLA Handbook (7th Edition):

Schuckmann, Matthew M. “Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I.” 2011. Web. 19 Sep 2019.

Vancouver:

Schuckmann MM. Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2019 Sep 19]. Available from: https://doi.org/10.32469/10355/14917.

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

Council of Science Editors:

Schuckmann MM. Characterization of HIV-1 reverse transcriptase drug resistance connection subdomain mutation N348I. [Thesis]. University of Missouri – Columbia; 2011. Available from: https://doi.org/10.32469/10355/14917

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


University of Oxford

26. Rodgers, Jessica. Functional characterisation of key residues in the photopigment melanopsin.

Degree: PhD, 2016, University of Oxford

 Melanopsin (Opn4) is the opsin photopigment of intrinsically photosensitive retinal ganglion cells (ipRGCs). It has a conserved opsin structure and activation mechanism, yet demonstrates unusual… (more)

Subjects/Keywords: 573.8; Opsins; Retina; Biological Rhythms; Optogenetics; G-protein coupled receptor; Opn4; Missense Mutation; ipRGC; Circadian Rhythms; Adeno-associated virus; Spectral Tuning; Single Nucleotide Polymorphism; Photopigment; Melanopsin; Opsin; Pupillometry; Multi-electrode array

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APA (6th Edition):

Rodgers, J. (2016). Functional characterisation of key residues in the photopigment melanopsin. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:d1184150-9b61-4cc9-94ad-2cc13a3d21ce ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730276

Chicago Manual of Style (16th Edition):

Rodgers, Jessica. “Functional characterisation of key residues in the photopigment melanopsin.” 2016. Doctoral Dissertation, University of Oxford. Accessed September 19, 2019. http://ora.ox.ac.uk/objects/uuid:d1184150-9b61-4cc9-94ad-2cc13a3d21ce ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730276.

MLA Handbook (7th Edition):

Rodgers, Jessica. “Functional characterisation of key residues in the photopigment melanopsin.” 2016. Web. 19 Sep 2019.

Vancouver:

Rodgers J. Functional characterisation of key residues in the photopigment melanopsin. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2019 Sep 19]. Available from: http://ora.ox.ac.uk/objects/uuid:d1184150-9b61-4cc9-94ad-2cc13a3d21ce ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730276.

Council of Science Editors:

Rodgers J. Functional characterisation of key residues in the photopigment melanopsin. [Doctoral Dissertation]. University of Oxford; 2016. Available from: http://ora.ox.ac.uk/objects/uuid:d1184150-9b61-4cc9-94ad-2cc13a3d21ce ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730276

27. Γεωργίου, Θεόδωρος. GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων.

Degree: 2003, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Subjects/Keywords: GM1 γαγγλιοζίτωση; β-γαλακτοζιτάση; Επιδημιολογική μελέτη; Συχνότητα φορέων; Σημειακή παρερμηνευτική μετάλλαξη; Μη νοηματική μετάλλαξη; Μετάλλαξη ματίσματος; Μελέτες έκφρασης; GM1 gangliosidosis; β-galactosidase; Epidemiological study; Frequency of carriers; Missense mutation; Nonsense mutation; Splicing mutation; Expression studies

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

APA (6th Edition):

Γεωργίου, . . (2003). GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/19789

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):

Γεωργίου, Θεόδωρος. “GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων.” 2003. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed September 19, 2019. http://hdl.handle.net/10442/hedi/19789.

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

MLA Handbook (7th Edition):

Γεωργίου, Θεόδωρος. “GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων.” 2003. Web. 19 Sep 2019.

Vancouver:

Γεωργίου . GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2003. [cited 2019 Sep 19]. Available from: http://hdl.handle.net/10442/hedi/19789.

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

Council of Science Editors:

Γεωργίου . GM1 γαγγλιοζίτωση. Επιδημιολογική μελέτη στο χωριό Πελένδρι της Κύπρου και χαρακτηρισμός μεταλλάξεων. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2003. Available from: http://hdl.handle.net/10442/hedi/19789

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

28. Jurkuvenaite, Asta. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).

Degree: PhD, 2008, University of Alabama – Birmingham

Cystic fibrosis (CF) is a genetic disease resulting from mutations in the cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel that functions at… (more)

Subjects/Keywords: Biotinylation. Cell Membrane  – metabolism<; br>; Cystic Fibrosis Transmembrane Conductance Regulator  – chemistry<; br>; Cystic Fibrosis Transmembrane Conductance Regulator  – metabolism<; br>; Mutation<; br>; Protein Structure, Tertiary

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

APA (6th Edition):

Jurkuvenaite, A. (2008). Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,601

Chicago Manual of Style (16th Edition):

Jurkuvenaite, Asta. “Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed September 19, 2019. http://contentdm.mhsl.uab.edu/u?/etd,601.

MLA Handbook (7th Edition):

Jurkuvenaite, Asta. “Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR).” 2008. Web. 19 Sep 2019.

Vancouver:

Jurkuvenaite A. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Sep 19]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,601.

Council of Science Editors:

Jurkuvenaite A. Biogenesis, trafficking, and function of wild-type and mutant cystic fibrosis transmembrane conductance regulator (CFTR). [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,601

29. Zhang, Zhe. IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING.

Degree: PhD, Physics and Astronomy, 2013, Clemson University

 Single-point mutation in genome, for example, single-nucleotide polymorphism (SNP) or rare genetic mutation, is the change of a single nucleotide for another in the genome… (more)

Subjects/Keywords: drug design; Missense Mutation; protein-protein interaction; protein stability; small molecules binding; virtual screening; Biological and Chemical Physics

…92 4.7 The effects on H-bond network due to the missense mutation Y328C ....... 93 5.1… …produce truncated, usually nonfunctional proteins [4]. Missense mutation, on the other… …others [13-22]. The ability of predicting whether a given missense mutation is… …x5D; (Chapter 3). Following Chapter 3, recently a new missense mutation Y328C was… …mutability of disease-causing missense mutation sites in spermine synthase. PLoS One 6: e20373. 7… 

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

APA (6th Edition):

Zhang, Z. (2013). IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1126

Chicago Manual of Style (16th Edition):

Zhang, Zhe. “IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING.” 2013. Doctoral Dissertation, Clemson University. Accessed September 19, 2019. https://tigerprints.clemson.edu/all_dissertations/1126.

MLA Handbook (7th Edition):

Zhang, Zhe. “IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING.” 2013. Web. 19 Sep 2019.

Vancouver:

Zhang Z. IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING. [Internet] [Doctoral dissertation]. Clemson University; 2013. [cited 2019 Sep 19]. Available from: https://tigerprints.clemson.edu/all_dissertations/1126.

Council of Science Editors:

Zhang Z. IN SILICO MODELING THE EFFECT OF SINGLE POINT MUTATIONS AND RESCUING THE EFFECT BY SMALL MOLECULES BINDING. [Doctoral Dissertation]. Clemson University; 2013. Available from: https://tigerprints.clemson.edu/all_dissertations/1126

30. Bertola, Débora Romeo. Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan.

Degree: PhD, Pediatria, 2006, University of São Paulo

INTRODUÇÃO: A síndrome de Noonan é uma doença autossômica dominante caracterizada por baixa estatura, dismorfismos faciais (hipertelorismo ocular, inclinação para baixo das fendas palpebrais, ptose… (more)

Subjects/Keywords: Fosfatase proteína-tirosina; LEOPARD syndrome; Mutação; Mutação de sentido incorreto; Mutation; Mutation missense; Noonan syndrome/etiology; Noonan syndrome/genetics; Protein-tyrosine-phosphatase; Síndrome de LEOPARD; Síndrome de Noonan/etiologia; Síndrome de Noonan/genética

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

APA (6th Edition):

Bertola, D. R. (2006). Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5141/tde-12042006-110700/ ;

Chicago Manual of Style (16th Edition):

Bertola, Débora Romeo. “Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan.” 2006. Doctoral Dissertation, University of São Paulo. Accessed September 19, 2019. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-12042006-110700/ ;.

MLA Handbook (7th Edition):

Bertola, Débora Romeo. “Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan.” 2006. Web. 19 Sep 2019.

Vancouver:

Bertola DR. Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan. [Internet] [Doctoral dissertation]. University of São Paulo; 2006. [cited 2019 Sep 19]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-12042006-110700/ ;.

Council of Science Editors:

Bertola DR. Estudo do gene PTPN11 nos pacientes afetados pela síndrome de Noonan. [Doctoral Dissertation]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-12042006-110700/ ;

[1] [2] [3] [4] [5] … [183]

.