Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Genetic mutation). Showing records 1 – 30 of 318 total matches.

[1] [2] [3] [4] [5] … [11]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Florida

1. Salomon,Matthew P. Genetic Variation in Caenorhabditid Nematode Worms.

Degree: PhD, Zoology - Biology, 2011, University of Florida

 When we observe the natural world we cannot help but notice the amount of variation all around us. Where does this variation come from? What… (more)

Subjects/Keywords: Genetic loci; Genetic mutation; Genetic variance; Genetic variation; Genomes; Microsatellites; Species; Statistical discrepancies; Taxa; Worms; caenorhabditis  – evolution  – genetic  – microsatellite  – mutation  – nematode

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

P, S. (2011). Genetic Variation in Caenorhabditid Nematode Worms. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0043343

Chicago Manual of Style (16th Edition):

P, Salomon,Matthew. “Genetic Variation in Caenorhabditid Nematode Worms.” 2011. Doctoral Dissertation, University of Florida. Accessed July 21, 2019. http://ufdc.ufl.edu/UFE0043343.

MLA Handbook (7th Edition):

P, Salomon,Matthew. “Genetic Variation in Caenorhabditid Nematode Worms.” 2011. Web. 21 Jul 2019.

Vancouver:

P S. Genetic Variation in Caenorhabditid Nematode Worms. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2019 Jul 21]. Available from: http://ufdc.ufl.edu/UFE0043343.

Council of Science Editors:

P S. Genetic Variation in Caenorhabditid Nematode Worms. [Doctoral Dissertation]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0043343

2. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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


University of Edinburgh

3. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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


Cornell University

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

Degree: 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population .” 2014. Thesis, Cornell University. Accessed July 21, 2019. http://hdl.handle.net/1813/36147.

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

MLA Handbook (7th Edition):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population .” 2014. Web. 21 Jul 2019.

Vancouver:

Goldstein O. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population . [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1813/36147.

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

Council of Science Editors:

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

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


Université de Montréal

5. Girard, Simon L. Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie .

Degree: 2014, Université de Montréal

 La schizophrénie est une maladie psychiatrique grave qui affecte approximativement 1 % de la population. Il est clairement établi que la maladie possède une composante… (more)

Subjects/Keywords: Schizophrénie; Génétique; Mutation de novo; Variation génétique; Effet de l'âge parental; Schizophrenia; Genetic; De novo mutation; Genetic variation; Parental age effect

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Girard, S. L. (2014). Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/10875

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):

Girard, Simon L. “Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie .” 2014. Thesis, Université de Montréal. Accessed July 21, 2019. http://hdl.handle.net/1866/10875.

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

MLA Handbook (7th Edition):

Girard, Simon L. “Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie .” 2014. Web. 21 Jul 2019.

Vancouver:

Girard SL. Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1866/10875.

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

Council of Science Editors:

Girard SL. Étude sur le rôle des mutations de novo dans l’étiologie génétique de la schizophrénie . [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/10875

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

6. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. http://escholarship.umassmed.edu/gsbs_diss/667.

MLA Handbook (7th Edition):

Hietpas, Ryan T. “Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.” 2013. Web. 21 Jul 2019.

Vancouver:

Hietpas RT. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Jul 21]. 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

7. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. http://hdl.handle.net/10138/236398.

MLA Handbook (7th Edition):

Mikkola, Annamari. “Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa.” 2018. Web. 21 Jul 2019.

Vancouver:

Mikkola A. Hampaiden kovakudosten perinnöllinen sairaus suomalaisessa suvussa. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2019 Jul 21]. 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


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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


Universiteit Utrecht

9. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Francioli LC. Inherited and de novo variation in human genomes. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2019 Jul 21]. 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

10. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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/ ;

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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

12. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Erkko H(. TOPBP1, CLSPN and PALB2 genes in familial breast cancer susceptibility. [Internet] [Doctoral dissertation]. University of Oulu; 2008. [cited 2019 Jul 21]. 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

13. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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 Edinburgh

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

Degree: 1987, University of Edinburgh

Subjects/Keywords: 572.8; Genetic mutation studies

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. http://hdl.handle.net/1842/14296.

MLA Handbook (7th Edition):

Roberts, Jacqueline Lucy. “A study of replicating instabilities in Schizosaccharomyces pombe.” 1987. Web. 21 Jul 2019.

Vancouver:

Roberts JL. A study of replicating instabilities in Schizosaccharomyces pombe. [Internet] [Doctoral dissertation]. University of Edinburgh; 1987. [cited 2019 Jul 21]. 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


Université de Montréal

15. Tarabeux, Julien. Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique .

Degree: 2013, Université de Montréal

 Les troubles schizophréniques (SCZ) ont une forte héritabilité, de l’ordre de 80%, mais, une très faible part du risque génétique a été identifiée. La plupart… (more)

Subjects/Keywords: génétique; schizophrénie; de novo; nmda; glutamate; mutation; genetic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tarabeux, J. (2013). Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12796

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):

Tarabeux, Julien. “Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique .” 2013. Thesis, Université de Montréal. Accessed July 21, 2019. http://hdl.handle.net/1866/12796.

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

MLA Handbook (7th Edition):

Tarabeux, Julien. “Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique .” 2013. Web. 21 Jul 2019.

Vancouver:

Tarabeux J. Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1866/12796.

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

Council of Science Editors:

Tarabeux J. Etude des déterminants génétiques des psychoses à début précoce. Génétique de la schizophrénie et hypothèse glutamatergique . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/12796

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


East Carolina University

16. Manne, Akarsh. Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II.

Degree: 2010, East Carolina University

 Photosynthesis is the process by which cyanobacteria, algae, and higher plants convert light energy to chemical energy via the biosynthesis of carbohydrates. Photosystem II is… (more)

Subjects/Keywords: Biology, Molecular; Molecular biology; Photosynthesis – Genetic aspects; Mutation (Biology)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Manne, A. (2010). Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/2878

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):

Manne, Akarsh. “Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II.” 2010. Thesis, East Carolina University. Accessed July 21, 2019. http://hdl.handle.net/10342/2878.

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

MLA Handbook (7th Edition):

Manne, Akarsh. “Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II.” 2010. Web. 21 Jul 2019.

Vancouver:

Manne A. Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II. [Internet] [Thesis]. East Carolina University; 2010. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10342/2878.

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

Council of Science Editors:

Manne A. Characterization of Site-Directed Mutants in the Cytochrome c-550 Protein of Photosystem II. [Thesis]. East Carolina University; 2010. Available from: http://hdl.handle.net/10342/2878

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


University of Hong Kong

17. 王雪; Wang, Xue. Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies.

Degree: PhD, 2013, University of Hong Kong

 Hedgehogs are important morphogens essential for regulating a wide range of developmental processes. Mutations in IHH lead to digit abnormalities and skeletal defects such as… (more)

Subjects/Keywords: Cellular signal transduction; Mutation (Biology); Fingers - Abnormalities - Genetic aspects

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

王雪; Wang, X. (2013). Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wang, X. [王雪]. (2013). Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387943. ; http://dx.doi.org/10.5353/th_b5387943 ; http://hdl.handle.net/10722/238556

Chicago Manual of Style (16th Edition):

王雪; Wang, Xue. “Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed July 21, 2019. Wang, X. [王雪]. (2013). Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387943. ; http://dx.doi.org/10.5353/th_b5387943 ; http://hdl.handle.net/10722/238556.

MLA Handbook (7th Edition):

王雪; Wang, Xue. “Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies.” 2013. Web. 21 Jul 2019.

Vancouver:

王雪; Wang X. Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Jul 21]. Available from: Wang, X. [王雪]. (2013). Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387943. ; http://dx.doi.org/10.5353/th_b5387943 ; http://hdl.handle.net/10722/238556.

Council of Science Editors:

王雪; Wang X. Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Wang, X. [王雪]. (2013). Molecular and cellular consequences of Indian hedgehog mutations causing brachydactylies. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5387943. ; http://dx.doi.org/10.5353/th_b5387943 ; http://hdl.handle.net/10722/238556


Ryerson University

18. 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)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Tarlarini C. MOLECULAR AND GENETIC CHARACTERIZATION OF ALS PATIENTS. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2019 Jul 21]. 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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

WANG M. Description and Application of Genetic Algorithm. [Internet] [Thesis]. , School of Engineering; 2012. [cited 2019 Jul 21]. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Basham CE. Characterizing the vegetative phenotype of fzt maize mutant. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2019 Jul 21]. 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


George Mason University

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Tran KD. Simultaneous Application of Chromosomal Microarray Analysis and Polymerase Chain Reaction Genetic Disease Detection . [Internet] [Thesis]. George Mason University; 2014. [cited 2019 Jul 21]. 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


Vanderbilt University

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Huang, X. (2014). Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11232014-230859/ ;

Chicago Manual of Style (16th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed July 21, 2019. http://etd.library.vanderbilt.edu/available/etd-11232014-230859/ ;.

MLA Handbook (7th Edition):

Huang, Xuan. “Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities.” 2014. Web. 21 Jul 2019.

Vancouver:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Jul 21]. Available from: http://etd.library.vanderbilt.edu/available/etd-11232014-230859/ ;.

Council of Science Editors:

Huang X. Epilepsy-associated mutations in GABRG2: characterization and therapeutic opportunities. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-11232014-230859/ ;


Montana State University

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

Degree: 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).

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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):

Goel, Anupam. “NMR investigations of the role of intrinsic flexibility of the tryptophan repressor.” 2012. Thesis, Montana State University. Accessed July 21, 2019. https://scholarworks.montana.edu/xmlui/handle/1/1346.

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

MLA Handbook (7th Edition):

Goel, Anupam. “NMR investigations of the role of intrinsic flexibility of the tryptophan repressor.” 2012. Web. 21 Jul 2019.

Vancouver:

Goel A. NMR investigations of the role of intrinsic flexibility of the tryptophan repressor. [Internet] [Thesis]. Montana State University; 2012. [cited 2019 Jul 21]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1346.

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

Council of Science Editors:

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

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


University of North Texas

25. 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.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

Vancouver:

Adhikari B. Identification and Characterization of an Arabidopsis thaliana Mutant with Tolerance to N-lauroylethanolamine. [Internet] [Thesis]. University of North Texas; 2015. [cited 2019 Jul 21]. 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


Florida Atlantic University

26. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 July 21, 2019. 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. 21 Jul 2019.

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 2019 Jul 21]. 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


University of Florida

27. Policht, Tyler. Fine mapping of the maize rough endosperm4 mutation.

Degree: 2010, University of Florida

 The yield of maize is important for the food supply of the world. Targeted crop improvement requires an understanding of genes that are necessary for… (more)

Subjects/Keywords: Alleles; Chromosomes; Corn; Endosperm; Genetic mapping; Genetic mutation; Genomes; Phenotypes; Polymerase chain reaction; Seedlings; Corn; Gene mapping; Genetic markers; Mutagenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Policht, T. (2010). Fine mapping of the maize rough endosperm4 mutation. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060595

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):

Policht, Tyler. “Fine mapping of the maize rough endosperm4 mutation.” 2010. Thesis, University of Florida. Accessed July 21, 2019. http://ufdc.ufl.edu/AA00060595.

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

MLA Handbook (7th Edition):

Policht, Tyler. “Fine mapping of the maize rough endosperm4 mutation.” 2010. Web. 21 Jul 2019.

Vancouver:

Policht T. Fine mapping of the maize rough endosperm4 mutation. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Jul 21]. Available from: http://ufdc.ufl.edu/AA00060595.

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

Council of Science Editors:

Policht T. Fine mapping of the maize rough endosperm4 mutation. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00060595

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


University of Florida

28. Pattamatta, Amrutha. Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein.

Degree: MS, Biomedical Engineering, 2013, University of Florida

 Prion diseases are a rare group of neurodegenerativedisorders caused by the misfolding of the Prion protein (PrP). Currently thereare no treatment options available for these… (more)

Subjects/Keywords: Antibodies; Digestion; Diseases; Disulfides; Drosophila; Epitopes; Genetic mutation; Mushroom bodies; Prion diseases; Prions; d201n  – drosophila  – helix-3  – mutation  – neurodegeneration  – prion  – q211p

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pattamatta, A. (2013). Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045560

Chicago Manual of Style (16th Edition):

Pattamatta, Amrutha. “Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein.” 2013. Masters Thesis, University of Florida. Accessed July 21, 2019. http://ufdc.ufl.edu/UFE0045560.

MLA Handbook (7th Edition):

Pattamatta, Amrutha. “Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein.” 2013. Web. 21 Jul 2019.

Vancouver:

Pattamatta A. Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein. [Internet] [Masters thesis]. University of Florida; 2013. [cited 2019 Jul 21]. Available from: http://ufdc.ufl.edu/UFE0045560.

Council of Science Editors:

Pattamatta A. Using Drosophila to Evaluate the Neurotoxicity and Misfolding Induced by Two Pathogenic Mutations on Helix-3 of the Prion Protein. [Masters Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045560


University of Florida

29. Cadavid, Felipe. The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms.

Degree: 2010, University of Florida

 C. elegans contains an insertion bias at di-nucleotide microsatellite regions of the genome; a trend that is not shared by C. briggsae which has a… (more)

Subjects/Keywords: DNA; Genetic mutation; Genome size; Genomes; Microsatellites; Nucleotides; Population size; Roundworms; Species; Worms; Caenorhabditis elegans; Mutation (Biology); Nematodes; Nematodes – Evolution

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cadavid, F. (2010). The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060013

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):

Cadavid, Felipe. “The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms.” 2010. Thesis, University of Florida. Accessed July 21, 2019. http://ufdc.ufl.edu/AA00060013.

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

MLA Handbook (7th Edition):

Cadavid, Felipe. “The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms.” 2010. Web. 21 Jul 2019.

Vancouver:

Cadavid F. The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Jul 21]. Available from: http://ufdc.ufl.edu/AA00060013.

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

Council of Science Editors:

Cadavid F. The Evolution of Insertion-Deletion Mutations in Microsatellite Regions of Caenorhabditid Nematode Worms. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00060013

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


Halmstad University

30. Sandberg, Anna. Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos.

Degree: Health and Welfare, 2018, Halmstad University

Det föreligger en ökad risk för att utveckla bröst- och äggstockscancer om kvinnan bär på mutation i BRöstCAncergen1 eller BRöstCAncergen2. Kvinnan ställs inför svåra… (more)

Subjects/Keywords: BRCA1; BRCA2; women; woman; mutation; nursing; experience; genetic; BRCA1; BRCA2; kvinna; kvinnor; mutation; omvårdnad; upplevelse; ärftlig; Nursing; Omvårdnad

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sandberg, A. (2018). Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos. (Thesis). Halmstad University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-36728

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):

Sandberg, Anna. “Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos.” 2018. Thesis, Halmstad University. Accessed July 21, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-36728.

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

MLA Handbook (7th Edition):

Sandberg, Anna. “Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos.” 2018. Web. 21 Jul 2019.

Vancouver:

Sandberg A. Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos. [Internet] [Thesis]. Halmstad University; 2018. [cited 2019 Jul 21]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-36728.

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

Council of Science Editors:

Sandberg A. Kvinnors upplevelse av att leva med ärftlig risk för bröst- och äggstockscancer : Att vänta på en cancerdiagnos. [Thesis]. Halmstad University; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-36728

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

[1] [2] [3] [4] [5] … [11]

.