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You searched for subject:(Genetic mutation). Showing records 1 – 30 of 301 total matches.

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1. Boubaker, Chokri. Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers.

Degree: Docteur es, Pathologie humaine. Génétique humaine, 2013, Aix-Marseille; Institut supérieur de biotechnologie (Monastir, Tunisie)

La maladie de Charcot-Marie-Tooth représente un groupe hétérogène de maladies tant sur le plan clinique que sur le plan génétique. A ce jour, on dénombre… (more)

Subjects/Keywords: Maladie,Génétique,CMT,Mutation,Consanguinité; Disease,Genetic,CMT,Mutation, Consanguinity

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APA (6th Edition):

Boubaker, C. (2013). Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers. (Doctoral Dissertation). Aix-Marseille; Institut supérieur de biotechnologie (Monastir, Tunisie). Retrieved from http://www.theses.fr/2013AIXM5010

Chicago Manual of Style (16th Edition):

Boubaker, Chokri. “Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers.” 2013. Doctoral Dissertation, Aix-Marseille; Institut supérieur de biotechnologie (Monastir, Tunisie). Accessed March 01, 2021. http://www.theses.fr/2013AIXM5010.

MLA Handbook (7th Edition):

Boubaker, Chokri. “Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers.” 2013. Web. 01 Mar 2021.

Vancouver:

Boubaker C. Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers. [Internet] [Doctoral dissertation]. Aix-Marseille; Institut supérieur de biotechnologie (Monastir, Tunisie); 2013. [cited 2021 Mar 01]. Available from: http://www.theses.fr/2013AIXM5010.

Council of Science Editors:

Boubaker C. Etude génétique de familles consanguines atteintes de diverses formes de la maladie de Charcot-Marie-Tooth : Enzymatic oligomerization of flavonoids and evaluation of the biological activities of synthesized oligomers. [Doctoral Dissertation]. Aix-Marseille; Institut supérieur de biotechnologie (Monastir, Tunisie); 2013. Available from: http://www.theses.fr/2013AIXM5010


Cornell University

2. Goldstein, Orly. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population.

Degree: PhD, Veterinary Medicine, 2014, Cornell University

 As of October 2013, around 285 million people are visually impaired worldwide. For an important subset of these, this visual impairment is genetic. That is,… (more)

Subjects/Keywords: Retinal degeneration; Genetic mutation; Canine PRA

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APA (6th Edition):

Goldstein, O. (2014). Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36147

Chicago Manual of Style (16th Edition):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population.” 2014. Doctoral Dissertation, Cornell University. Accessed March 01, 2021. http://hdl.handle.net/1813/36147.

MLA Handbook (7th Edition):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population.” 2014. Web. 01 Mar 2021.

Vancouver:

Goldstein O. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1813/36147.

Council of Science Editors:

Goldstein O. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36147


University of Melbourne

3. Webster, Wesley Andrew James. Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum.

Degree: 2013, University of Melbourne

 Methods to alter gene function in Plasmodium are barely out of infancy, with much growth occurring within the past five years via adaptation of protocols… (more)

Subjects/Keywords: malaria; Plasmodium falciparum; mutation; genetic manipulation

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APA (6th Edition):

Webster, W. A. J. (2013). Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39837

Chicago Manual of Style (16th Edition):

Webster, Wesley Andrew James. “Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum.” 2013. Masters Thesis, University of Melbourne. Accessed March 01, 2021. http://hdl.handle.net/11343/39837.

MLA Handbook (7th Edition):

Webster, Wesley Andrew James. “Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum.” 2013. Web. 01 Mar 2021.

Vancouver:

Webster WAJ. Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum. [Internet] [Masters thesis]. University of Melbourne; 2013. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/11343/39837.

Council of Science Editors:

Webster WAJ. Establishing and elucidating conditional genetic manipulation of the malaria parasite, Plasmodium falciparum. [Masters Thesis]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/39837


University of Edinburgh

4. McKenzie, Rod. Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae.

Degree: PhD, 1989, University of Edinburgh

Subjects/Keywords: 572.8; Genetic mutation

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APA (6th Edition):

McKenzie, R. (1989). Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/12632

Chicago Manual of Style (16th Edition):

McKenzie, Rod. “Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae.” 1989. Doctoral Dissertation, University of Edinburgh. Accessed March 01, 2021. http://hdl.handle.net/1842/12632.

MLA Handbook (7th Edition):

McKenzie, Rod. “Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae.” 1989. Web. 01 Mar 2021.

Vancouver:

McKenzie R. Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Edinburgh; 1989. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1842/12632.

Council of Science Editors:

McKenzie R. Molecular structure of the bifunctional purine biosynthesis pathway genes : Ade1 in Schizosaccharomyces pombe and Ade5, 7 in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Edinburgh; 1989. Available from: http://hdl.handle.net/1842/12632

5. Hietpas, Ryan T. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  Evolution is the single cohesive logical framework in which all biological processes may exist simultaneously. Incremental changes in phenotype over imperceptibly large timescales have… (more)

Subjects/Keywords: Molecular Evolution; Mutation; Genetic Fitness; Genetic Techniques; Point Mutation; Saccharomyces cerevisiae Proteins; Computational Biology; Evolution; Molecular Genetics

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APA (6th Edition):

Hietpas, R. T. (2013). Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/667

Chicago Manual of Style (16th Edition):

Hietpas, Ryan T. “Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed March 01, 2021. http://escholarship.umassmed.edu/gsbs_diss/667.

MLA Handbook (7th Edition):

Hietpas, Ryan T. “Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.” 2013. Web. 01 Mar 2021.

Vancouver:

Hietpas RT. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2021 Mar 01]. Available from: http://escholarship.umassmed.edu/gsbs_diss/667.

Council of Science Editors:

Hietpas RT. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/667


University of Helsinki

6. Mikkola, Annamari. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.

Degree: Medicinska fakulteten, 2018, University of Helsinki

 Tutkimuksen kohteena on suomalainen suku, jossa esiintyy hampaiden kovakudosten perinnöllinen kehityshäiriö. Aikaisemmissa tutkimuksissa kehityshäiriön aiheuttava mutaatio on paikallistettu kromosomiin 15, ja kahden näytteen eksomisekvensoinnilla on… (more)

Subjects/Keywords: Tooth abnormalities; genetic disorder; mutation; PCR; DNA Sequencing; Tooth abnormalities; genetic disorder; mutation; PCR; DNA Sequencing

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APA (6th Edition):

Mikkola, A. (2018). Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/236398

Chicago Manual of Style (16th Edition):

Mikkola, Annamari. “Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.” 2018. Masters Thesis, University of Helsinki. Accessed March 01, 2021. http://hdl.handle.net/10138/236398.

MLA Handbook (7th Edition):

Mikkola, Annamari. “Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.” 2018. Web. 01 Mar 2021.

Vancouver:

Mikkola A. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10138/236398.

Council of Science Editors:

Mikkola A. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. [Masters Thesis]. University of Helsinki; 2018. Available from: http://hdl.handle.net/10138/236398

7. Cheek, David Michael. Mutation frequencies in a birth-death branching process.

Degree: PhD, 2019, University of Edinburgh

 A growing population of cells accumulates genetic mutations. We study stochastic models of this process. Cells divide and die as a branching process, and a… (more)

Subjects/Keywords: genetic data; tumour trajectory; mutation frequencies; genetic sequence; power-law distribution; quantitative relationships

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APA (6th Edition):

Cheek, D. M. (2019). Mutation frequencies in a birth-death branching process. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/36163

Chicago Manual of Style (16th Edition):

Cheek, David Michael. “Mutation frequencies in a birth-death branching process.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed March 01, 2021. http://hdl.handle.net/1842/36163.

MLA Handbook (7th Edition):

Cheek, David Michael. “Mutation frequencies in a birth-death branching process.” 2019. Web. 01 Mar 2021.

Vancouver:

Cheek DM. Mutation frequencies in a birth-death branching process. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1842/36163.

Council of Science Editors:

Cheek DM. Mutation frequencies in a birth-death branching process. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/36163


University of Utah

8. Appel, Bruce. Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;.

Degree: PhD, Human Genetics;, 1993, University of Utah

 During animal development, different regions of an embryo acquire distinct identities. In Drosophila melanogaster, morphological distinctions along the anterior-posterior axis require the function of homeotic… (more)

Subjects/Keywords: Mutation; Proteins; Transcription, Genetic

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APA (6th Edition):

Appel, B. (1993). Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/299/rec/620

Chicago Manual of Style (16th Edition):

Appel, Bruce. “Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;.” 1993. Doctoral Dissertation, University of Utah. Accessed March 01, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/299/rec/620.

MLA Handbook (7th Edition):

Appel, Bruce. “Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;.” 1993. Web. 01 Mar 2021.

Vancouver:

Appel B. Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;. [Internet] [Doctoral dissertation]. University of Utah; 1993. [cited 2021 Mar 01]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/299/rec/620.

Council of Science Editors:

Appel B. Homeotic genes and regional specification in Drosophila: characterization of the abdominalA gene and mechanisms of transcriptional control by homeotic proteins;. [Doctoral Dissertation]. University of Utah; 1993. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/299/rec/620


Ryerson University

9. Naqvi, Haider Z. Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans.

Degree: 2009, Ryerson University

 Novel genetic enhancer screens were conducted targeting mutants involved in the guidance of axons of the DA and DB classes of motor neurons in C.… (more)

Subjects/Keywords: Caenorhabditis elegans; Axonal transport; Genetic translation; Mutation (Biology)

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APA (6th Edition):

Naqvi, H. Z. (2009). Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A1646

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):

Naqvi, Haider Z. “Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans.” 2009. Thesis, Ryerson University. Accessed March 01, 2021. https://digital.library.ryerson.ca/islandora/object/RULA%3A1646.

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

MLA Handbook (7th Edition):

Naqvi, Haider Z. “Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans.” 2009. Web. 01 Mar 2021.

Vancouver:

Naqvi HZ. Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans. [Internet] [Thesis]. Ryerson University; 2009. [cited 2021 Mar 01]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A1646.

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

Council of Science Editors:

Naqvi HZ. Identification Of A Novel Gene Altered In The RQ1 Mutant Strain Affecting Motor Axon Migration In Caenorhabditis Elegans. [Thesis]. Ryerson University; 2009. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A1646

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


Universiteit Utrecht

10. Francioli, L.C. Inherited and de novo variation in human genomes.

Degree: 2015, Universiteit Utrecht

 Most human traits, ranging from physical appearance to behavior and disease susceptibility, are in part inherited through genetic material. Whole-genome sequencing has enabled the complete… (more)

Subjects/Keywords: dutch genetic mutation; variation; insertion; deletion; population rate; haplotype; genome

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APA (6th Edition):

Francioli, L. C. (2015). Inherited and de novo variation in human genomes. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/310736

Chicago Manual of Style (16th Edition):

Francioli, L C. “Inherited and de novo variation in human genomes.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed March 01, 2021. http://dspace.library.uu.nl:8080/handle/1874/310736.

MLA Handbook (7th Edition):

Francioli, L C. “Inherited and de novo variation in human genomes.” 2015. Web. 01 Mar 2021.

Vancouver:

Francioli LC. Inherited and de novo variation in human genomes. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Mar 01]. Available from: http://dspace.library.uu.nl:8080/handle/1874/310736.

Council of Science Editors:

Francioli LC. Inherited and de novo variation in human genomes. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/310736

11. Brasil, Amanda Salem. Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like.

Degree: Mestrado, Pediatria, 2009, University of São Paulo

 INTRODUÇÃO: a síndrome de Noonan apresenta herança autossômica dominante e é considerada uma doença relativamente frequente na população, com uma incidência estimada entre 1/1000 e… (more)

Subjects/Keywords: Mutação; Mutation; Noonan syndrome; Polimorfismo genético; Polymorphism genetic; Síndrome de Noonan

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APA (6th Edition):

Brasil, A. S. (2009). Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5141/tde-25022010-140048/ ;

Chicago Manual of Style (16th Edition):

Brasil, Amanda Salem. “Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like.” 2009. Masters Thesis, University of São Paulo. Accessed March 01, 2021. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-25022010-140048/ ;.

MLA Handbook (7th Edition):

Brasil, Amanda Salem. “Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like.” 2009. Web. 01 Mar 2021.

Vancouver:

Brasil AS. Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2021 Mar 01]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-25022010-140048/ ;.

Council of Science Editors:

Brasil AS. Estudo dos genes PTPN11 e KRAS em pacientes afetados pela síndrome de Noonan e pelas síndromes Noonan-like. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-25022010-140048/ ;

12. Klaver, Stefanie Gomes. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.

Degree: Mestrado, Imunologia, 2011, University of São Paulo

A síndrome de HIGM é uma imunodeficiência, caracterizada por níveis séricos normais ou elevados de IgM associados com baixos níveis de IgG, IgA e IgE.… (more)

Subjects/Keywords: Genetic mutation; Genética molecular; Immunogenetics; Imunogenética; Molecular genetics; Mutação genética

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APA (6th Edition):

Klaver, S. G. (2011). Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;

Chicago Manual of Style (16th Edition):

Klaver, Stefanie Gomes. “Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.” 2011. Masters Thesis, University of São Paulo. Accessed March 01, 2021. http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;.

MLA Handbook (7th Edition):

Klaver, Stefanie Gomes. “Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica.” 2011. Web. 01 Mar 2021.

Vancouver:

Klaver SG. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2021 Mar 01]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;.

Council of Science Editors:

Klaver SG. Defeitos genético-moleculares e aspectos clínicos de pacientes com síndrome de hiper IgM autossômica. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/42/42133/tde-09022012-124352/ ;


University of Oulu

13. Erkko, H. (Hannele). TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.

Degree: 2008, University of Oulu

 Abstract The currently known susceptibility genes account for approximately 25% of familial breast cancer predisposition. Additional factors contributing to the pathogenesis of breast cancer are,… (more)

Subjects/Keywords: CLSPN; Genetic predisposition to disease; PALB2; TOPBP1; breast neoplasms; mutation; penetrance

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APA (6th Edition):

Erkko, H. (. (2008). TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789514289682

Chicago Manual of Style (16th Edition):

Erkko, H (Hannele). “TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.” 2008. Doctoral Dissertation, University of Oulu. Accessed March 01, 2021. http://urn.fi/urn:isbn:9789514289682.

MLA Handbook (7th Edition):

Erkko, H (Hannele). “TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility.” 2008. Web. 01 Mar 2021.

Vancouver:

Erkko H(. TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. [Internet] [Doctoral dissertation]. University of Oulu; 2008. [cited 2021 Mar 01]. Available from: http://urn.fi/urn:isbn:9789514289682.

Council of Science Editors:

Erkko H(. TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. [Doctoral Dissertation]. University of Oulu; 2008. Available from: http://urn.fi/urn:isbn:9789514289682


Nelson Mandela Metropolitan University

14. Suleman, Essa. Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus.

Degree: PhD, Faculty of Science, 2011, Nelson Mandela Metropolitan University

 It is generally known that media containing simple sugars (sucrose, glucose) and organic nitrogen sources (ammonium) when buffered to acidic pH stimulates aflatoxin production in… (more)

Subjects/Keywords: Mutation (Biology); Genetic regulation; Proteins  – Synthesis; Microbiological synthesis

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APA (6th Edition):

Suleman, E. (2011). Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus. (Doctoral Dissertation). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/d1012683

Chicago Manual of Style (16th Edition):

Suleman, Essa. “Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus.” 2011. Doctoral Dissertation, Nelson Mandela Metropolitan University. Accessed March 01, 2021. http://hdl.handle.net/10948/d1012683.

MLA Handbook (7th Edition):

Suleman, Essa. “Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus.” 2011. Web. 01 Mar 2021.

Vancouver:

Suleman E. Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus. [Internet] [Doctoral dissertation]. Nelson Mandela Metropolitan University; 2011. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10948/d1012683.

Council of Science Editors:

Suleman E. Mutational analysis of the PacC binding sites within the aflR promoter in Aspergillus flavus. [Doctoral Dissertation]. Nelson Mandela Metropolitan University; 2011. Available from: http://hdl.handle.net/10948/d1012683


University of North Texas

15. Adhikari, Bikash. Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine.

Degree: 2015, University of North Texas

 N-Acylethanolamines (NAEs) are fatty acid derivatives in plants that negatively influence seedling growth. N-Lauroylethanolamine (NAE 12:0), one type of NAE, inhibits root length, increases radial… (more)

Subjects/Keywords: Arabidopsis; n-acylethanolamines; genetic screening; Arabidopsis thaliana.; Mutation (Biology); Plant lipids.

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APA (6th Edition):

Adhikari, B. (2015). Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc822833/

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):

Adhikari, Bikash. “Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine.” 2015. Thesis, University of North Texas. Accessed March 01, 2021. https://digital.library.unt.edu/ark:/67531/metadc822833/.

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

MLA Handbook (7th Edition):

Adhikari, Bikash. “Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine.” 2015. Web. 01 Mar 2021.

Vancouver:

Adhikari B. Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine. [Internet] [Thesis]. University of North Texas; 2015. [cited 2021 Mar 01]. Available from: https://digital.library.unt.edu/ark:/67531/metadc822833/.

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

Council of Science Editors:

Adhikari B. Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc822833/

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

16. C. Tarlarini. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.

Degree: 2014, Università degli Studi di Milano

 Amyotrophic lateral sclerosis (ALS) is an adult‑onset, rapidly progressive and ultimately fatal neurodegenerative disorder characterised by degeneration of upper and lower motor neurons. This leads… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; ALS; genetic; mutation; Settore BIO/10 - Biochimica

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APA (6th Edition):

Tarlarini, C. (2014). MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/232574

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):

Tarlarini, C.. “MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.” 2014. Thesis, Università degli Studi di Milano. Accessed March 01, 2021. http://hdl.handle.net/2434/232574.

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

MLA Handbook (7th Edition):

Tarlarini, C.. “MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS.” 2014. Web. 01 Mar 2021.

Vancouver:

Tarlarini C. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/2434/232574.

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

Council of Science Editors:

Tarlarini C. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/232574

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


Georgia Tech

17. Karunakaran, Kirti A. Analysis of the impact of a p53 mutation in a homogeneous genetic background.

Degree: MS, Biology, 2020, Georgia Tech

 In more than 50% of cancers, p53, a tumor suppressor gene involved cell cycle arrest and apoptosis, has been seen to be heavily mutated making… (more)

Subjects/Keywords: p53; Genetic background; CRISPR Cas 9; LOF mutation

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APA (6th Edition):

Karunakaran, K. A. (2020). Analysis of the impact of a p53 mutation in a homogeneous genetic background. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62822

Chicago Manual of Style (16th Edition):

Karunakaran, Kirti A. “Analysis of the impact of a p53 mutation in a homogeneous genetic background.” 2020. Masters Thesis, Georgia Tech. Accessed March 01, 2021. http://hdl.handle.net/1853/62822.

MLA Handbook (7th Edition):

Karunakaran, Kirti A. “Analysis of the impact of a p53 mutation in a homogeneous genetic background.” 2020. Web. 01 Mar 2021.

Vancouver:

Karunakaran KA. Analysis of the impact of a p53 mutation in a homogeneous genetic background. [Internet] [Masters thesis]. Georgia Tech; 2020. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1853/62822.

Council of Science Editors:

Karunakaran KA. Analysis of the impact of a p53 mutation in a homogeneous genetic background. [Masters Thesis]. Georgia Tech; 2020. Available from: http://hdl.handle.net/1853/62822


George Mason University

18. Tran, Khoa D. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .

Degree: 2014, George Mason University

 This thesis demonstrates the successful integration and application of chromosomal microarray analysis (CMA) and mutation-specific polymerase chain reaction (PCR) within 24 hours for the detection… (more)

Subjects/Keywords: Chromosomal Microarray Analysis; genetic disease mutation; fertility; PGD

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APA (6th Edition):

Tran, K. D. (2014). Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8995

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):

Tran, Khoa D. “Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .” 2014. Thesis, George Mason University. Accessed March 01, 2021. http://hdl.handle.net/1920/8995.

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

MLA Handbook (7th Edition):

Tran, Khoa D. “Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection .” 2014. Web. 01 Mar 2021.

Vancouver:

Tran KD. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . [Internet] [Thesis]. George Mason University; 2014. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1920/8995.

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

Council of Science Editors:

Tran KD. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . [Thesis]. George Mason University; 2014. Available from: http://hdl.handle.net/1920/8995

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


Florida Atlantic University

19. Karri, Jagadeshwari. Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features.

Degree: M.S.C.S., 2012, Florida Atlantic University

Summary: Cytogenetics is a study on the genetic considerations associated with structural and functional aspects of the cells with reference to chromosomal inclusions. Chromosomes are… (more)

Subjects/Keywords: Medical genetics; Chromosome abnormalities; Cancer – Genetic aspects; Mutation (Biology); DNA damage

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APA (6th Edition):

Karri, J. (2012). Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features. (Masters Thesis). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3358597

Chicago Manual of Style (16th Edition):

Karri, Jagadeshwari. “Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features.” 2012. Masters Thesis, Florida Atlantic University. Accessed March 01, 2021. http://purl.flvc.org/FAU/3358597.

MLA Handbook (7th Edition):

Karri, Jagadeshwari. “Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features.” 2012. Web. 01 Mar 2021.

Vancouver:

Karri J. Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features. [Internet] [Masters thesis]. Florida Atlantic University; 2012. [cited 2021 Mar 01]. Available from: http://purl.flvc.org/FAU/3358597.

Council of Science Editors:

Karri J. Cytogenic bioinformatics of chromosomal aberrations and genetic disorders: data-mining of relevant biostatistical features. [Masters Thesis]. Florida Atlantic University; 2012. Available from: http://purl.flvc.org/FAU/3358597

20. WANG, MIN. Description and Application of Genetic Algorithm.

Degree: 2012, , School of Engineering

Genetic Algorithm (GA) as a class of Evolutionary Algorithm (EA) is a search algorithm based on the mechanics of natural selection and natural genetics.… (more)

Subjects/Keywords: Genetic Algorithm (GA); Time Table Problem (TTP); Selection; Crossover; Mutation

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APA (6th Edition):

WANG, M. (2012). Description and Application of Genetic Algorithm. (Thesis). , School of Engineering. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:bth-2362

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):

WANG, MIN. “Description and Application of Genetic Algorithm.” 2012. Thesis, , School of Engineering. Accessed March 01, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:bth-2362.

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

MLA Handbook (7th Edition):

WANG, MIN. “Description and Application of Genetic Algorithm.” 2012. Web. 01 Mar 2021.

Vancouver:

WANG M. Description and Application of Genetic Algorithm. [Internet] [Thesis]. , School of Engineering; 2012. [cited 2021 Mar 01]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:bth-2362.

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

Council of Science Editors:

WANG M. Description and Application of Genetic Algorithm. [Thesis]. , School of Engineering; 2012. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:bth-2362

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


East Carolina University

21. Basham, Christine Elizabeth. Characterizing the vegetative phenotype of fzt maize mutant.

Degree: 2012, East Carolina University

 microRNAs are short non-coding RNA strands that regulate gene expression post-transcriptionally in all multicellular organisms. miRNAs begin as a hairpin in the nucleus. The primary… (more)

Subjects/Keywords: Corn – Mutation breeding; Corn – Anatomy; RNA; Gene expression; Genetic regulation

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APA (6th Edition):

Basham, C. E. (2012). Characterizing the vegetative phenotype of fzt maize mutant. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13887

Chicago Manual of Style (16th Edition):

Basham, Christine Elizabeth. “Characterizing the vegetative phenotype of fzt maize mutant.” 2012. Masters Thesis, East Carolina University. Accessed March 01, 2021. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13887.

MLA Handbook (7th Edition):

Basham, Christine Elizabeth. “Characterizing the vegetative phenotype of fzt maize mutant.” 2012. Web. 01 Mar 2021.

Vancouver:

Basham CE. Characterizing the vegetative phenotype of fzt maize mutant. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2021 Mar 01]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13887.

Council of Science Editors:

Basham CE. Characterizing the vegetative phenotype of fzt maize mutant. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13887


Montana State University

22. Goel, Anupam. NMR investigations of the role of intrinsic flexibility of the tryptophan repressor.

Degree: PhD, College of Letters & Science, 2012, Montana State University

 The tryptophan repressor protein regulates intracellular concentration of Tryptophan in Escherichia coli by binding to DNA operators and is activated in the presence of high… (more)

Subjects/Keywords: Tryptophan.; Repressors, Genetic.; Nuclear magnetic resonance.; Mutation (Biology).

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APA (6th Edition):

Goel, A. (2012). NMR investigations of the role of intrinsic flexibility of the tryptophan repressor. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/1346

Chicago Manual of Style (16th Edition):

Goel, Anupam. “NMR investigations of the role of intrinsic flexibility of the tryptophan repressor.” 2012. Doctoral Dissertation, Montana State University. Accessed March 01, 2021. https://scholarworks.montana.edu/xmlui/handle/1/1346.

MLA Handbook (7th Edition):

Goel, Anupam. “NMR investigations of the role of intrinsic flexibility of the tryptophan repressor.” 2012. Web. 01 Mar 2021.

Vancouver:

Goel A. NMR investigations of the role of intrinsic flexibility of the tryptophan repressor. [Internet] [Doctoral dissertation]. Montana State University; 2012. [cited 2021 Mar 01]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1346.

Council of Science Editors:

Goel A. NMR investigations of the role of intrinsic flexibility of the tryptophan repressor. [Doctoral Dissertation]. Montana State University; 2012. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1346


University of Edinburgh

23. Roberts, Jacqueline Lucy. A study of replicating instabilities in Schizosaccharomyces pombe.

Degree: PhD, 1987, University of Edinburgh

Subjects/Keywords: 572.8; Genetic mutation studies

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APA (6th Edition):

Roberts, J. L. (1987). A study of replicating instabilities in Schizosaccharomyces pombe. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/14296

Chicago Manual of Style (16th Edition):

Roberts, Jacqueline Lucy. “A study of replicating instabilities in Schizosaccharomyces pombe.” 1987. Doctoral Dissertation, University of Edinburgh. Accessed March 01, 2021. http://hdl.handle.net/1842/14296.

MLA Handbook (7th Edition):

Roberts, Jacqueline Lucy. “A study of replicating instabilities in Schizosaccharomyces pombe.” 1987. Web. 01 Mar 2021.

Vancouver:

Roberts JL. A study of replicating instabilities in Schizosaccharomyces pombe. [Internet] [Doctoral dissertation]. University of Edinburgh; 1987. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1842/14296.

Council of Science Editors:

Roberts JL. A study of replicating instabilities in Schizosaccharomyces pombe. [Doctoral Dissertation]. University of Edinburgh; 1987. Available from: http://hdl.handle.net/1842/14296

24. Teller, Melissa M. Effect of age on ABRs in mice with EphA4 mutations.

Degree: 2017, James Madison University

 It is known that EphA4 can influence the establishment of tonotopic pathways in the auditory system. This can be measured by an increase in thresholds… (more)

Subjects/Keywords: auditory brainstem response; EphA4; genetic mutation; mice; Speech Pathology and Audiology

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APA (6th Edition):

Teller, M. M. (2017). Effect of age on ABRs in mice with EphA4 mutations. (Doctoral Dissertation). James Madison University. Retrieved from https://commons.lib.jmu.edu/diss201019/144

Chicago Manual of Style (16th Edition):

Teller, Melissa M. “Effect of age on ABRs in mice with EphA4 mutations.” 2017. Doctoral Dissertation, James Madison University. Accessed March 01, 2021. https://commons.lib.jmu.edu/diss201019/144.

MLA Handbook (7th Edition):

Teller, Melissa M. “Effect of age on ABRs in mice with EphA4 mutations.” 2017. Web. 01 Mar 2021.

Vancouver:

Teller MM. Effect of age on ABRs in mice with EphA4 mutations. [Internet] [Doctoral dissertation]. James Madison University; 2017. [cited 2021 Mar 01]. Available from: https://commons.lib.jmu.edu/diss201019/144.

Council of Science Editors:

Teller MM. Effect of age on ABRs in mice with EphA4 mutations. [Doctoral Dissertation]. James Madison University; 2017. Available from: https://commons.lib.jmu.edu/diss201019/144


Vanderbilt University

25. Huang, Xuan. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.

Degree: PhD, Neuroscience, 2014, Vanderbilt University

 Epilepsy is a neurological disorder affecting almost one percent of the population, and genetic epilepsy are those caused by a presumed or unknown genetic factor(s).… (more)

Subjects/Keywords: GABA(A) receptors; GABRG2; genetic epilepsy; mutation; therapy

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APA (6th Edition):

Huang, X. (2014). Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14755

Chicago Manual of Style (16th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed March 01, 2021. http://hdl.handle.net/1803/14755.

MLA Handbook (7th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Web. 01 Mar 2021.

Vancouver:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/1803/14755.

Council of Science Editors:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14755


Michigan State University

26. Nadakuduti, Satya Swathi. Forward genetics to unravel novel genes and their functions in tomato fruit development.

Degree: 2014, Michigan State University

Thesis Ph. D. Michigan State University. Plant Breeding, Genetics and Biotechnology-Horticulture 2014.

Tomato (Solanum lycopersicum) is a member of the large and phenotypically diverse Solanaceae… (more)

Subjects/Keywords: Tomatoes – Genetics; Fruit – Development – Genetic aspects; Plant mutation; Phenotype; Horticulture

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APA (6th Edition):

Nadakuduti, S. S. (2014). Forward genetics to unravel novel genes and their functions in tomato fruit development. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:2622

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):

Nadakuduti, Satya Swathi. “Forward genetics to unravel novel genes and their functions in tomato fruit development.” 2014. Thesis, Michigan State University. Accessed March 01, 2021. http://etd.lib.msu.edu/islandora/object/etd:2622.

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

MLA Handbook (7th Edition):

Nadakuduti, Satya Swathi. “Forward genetics to unravel novel genes and their functions in tomato fruit development.” 2014. Web. 01 Mar 2021.

Vancouver:

Nadakuduti SS. Forward genetics to unravel novel genes and their functions in tomato fruit development. [Internet] [Thesis]. Michigan State University; 2014. [cited 2021 Mar 01]. Available from: http://etd.lib.msu.edu/islandora/object/etd:2622.

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

Council of Science Editors:

Nadakuduti SS. Forward genetics to unravel novel genes and their functions in tomato fruit development. [Thesis]. Michigan State University; 2014. Available from: http://etd.lib.msu.edu/islandora/object/etd:2622

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


Université Paris-Sud – Paris XI

27. Bergthold, Guillaume. Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques.

Degree: Docteur es, Cancérologie, 2015, Université Paris-Sud – Paris XI

Les gliomes de bas-grade représentent la tumeur cérébrale la plus fréquente chez l’enfant. Elles sont caractérisées par un large spectre de sous-types tumoraux, très hétérogènes.… (more)

Subjects/Keywords: Gliomes de bas-grade; Enfant; Mutation; Génétique; Transcriptome; ?; Low-grade gliomas; Children; Mutation; Genetic; Transcriptomic; Single-cell

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APA (6th Edition):

Bergthold, G. (2015). Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA11T053

Chicago Manual of Style (16th Edition):

Bergthold, Guillaume. “Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed March 01, 2021. http://www.theses.fr/2015PA11T053.

MLA Handbook (7th Edition):

Bergthold, Guillaume. “Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques.” 2015. Web. 01 Mar 2021.

Vancouver:

Bergthold G. Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2021 Mar 01]. Available from: http://www.theses.fr/2015PA11T053.

Council of Science Editors:

Bergthold G. Genomic Profiling of Pediatric Low-Grade Gliomas : Etude des profils génétiques des gliomes de bas-grade pédiatriques. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA11T053

28. Ghaleb, Youmna. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.

Degree: Docteur es, Développement, 2017, Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth)

L’hypercholestérolémie familiale à transmission autosomique dominante (ADH), caractérisée par une élévation des taux plasmatiques en cholestérol total et LDL-C, est due à des altérations de… (more)

Subjects/Keywords: LRP6; Score génétique; Phénocopies; Mutation libanaise; GRS; Familial hypercholesterolemia; Cardiovascular diseases; Genetic studies; LRP6; Polygenic hypercholesterolemia; Genetic risk score; Phenocopy; Lebanese mutation; GRS

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APA (6th Edition):

Ghaleb, Y. (2017). Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. (Doctoral Dissertation). Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth). Retrieved from http://www.theses.fr/2017USPCC270

Chicago Manual of Style (16th Edition):

Ghaleb, Youmna. “Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.” 2017. Doctoral Dissertation, Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth). Accessed March 01, 2021. http://www.theses.fr/2017USPCC270.

MLA Handbook (7th Edition):

Ghaleb, Youmna. “Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.” 2017. Web. 01 Mar 2021.

Vancouver:

Ghaleb Y. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth); 2017. [cited 2021 Mar 01]. Available from: http://www.theses.fr/2017USPCC270.

Council of Science Editors:

Ghaleb Y. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. [Doctoral Dissertation]. Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth); 2017. Available from: http://www.theses.fr/2017USPCC270


Universidade do Rio Grande do Sul

29. Baja, Karine Gehlen. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.

Degree: 2013, Universidade do Rio Grande do Sul

 A P-glicoproteína (P-gp) é uma transportadora transmembrana de múltiplos fármacos, produto do gene MDR1 (ABCB1). A P-gp contribui para a função de barreira de vários… (more)

Subjects/Keywords: Tramadol; MDR1; P-glycoprotein; Farmacocinética; Genetic mutation; Farmacogenética; Gogs; Genes MDR; Cães; Sustained release tramadol

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

APA (6th Edition):

Baja, K. G. (2013). Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/79520

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):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Thesis, Universidade do Rio Grande do Sul. Accessed March 01, 2021. http://hdl.handle.net/10183/79520.

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

MLA Handbook (7th Edition):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Web. 01 Mar 2021.

Vancouver:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2013. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10183/79520.

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

Council of Science Editors:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Thesis]. Universidade do Rio Grande do Sul; 2013. Available from: http://hdl.handle.net/10183/79520

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


University of Hong Kong

30. Leon, Yuk-yu. Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients.

Degree: 2007, University of Hong Kong

Subjects/Keywords: Mutation (Biology); Hirschsprung's disease - Genetic aspects.

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

APA (6th Edition):

Leon, Y. (2007). Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/52781

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):

Leon, Yuk-yu. “Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients.” 2007. Thesis, University of Hong Kong. Accessed March 01, 2021. http://hdl.handle.net/10722/52781.

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

MLA Handbook (7th Edition):

Leon, Yuk-yu. “Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients.” 2007. Web. 01 Mar 2021.

Vancouver:

Leon Y. Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients. [Internet] [Thesis]. University of Hong Kong; 2007. [cited 2021 Mar 01]. Available from: http://hdl.handle.net/10722/52781.

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

Council of Science Editors:

Leon Y. Functional analysis of RET mutations in Chinese Hirschsprung's diseasepatients. [Thesis]. University of Hong Kong; 2007. Available from: http://hdl.handle.net/10722/52781

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

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