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You searched for subject:(heterozygote). Showing records 1 – 12 of 12 total matches.

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Boston University

1. Rajapakse, Thanna. Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures.

Degree: MS, Biomedical Forensic Sciences, 2014, Boston University

 Reliable detection of low template DNA (LTDNA) is dependent on reproducible allelic peaks and use of appropriately set thresholds. Analyzing LTDNA at different thresholds than… (more)

Subjects/Keywords: Molecular biology; DNA; Heterozygote balance; Low template; Mixture; Post-amplification purification

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APA (6th Edition):

Rajapakse, T. (2014). Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/15373

Chicago Manual of Style (16th Edition):

Rajapakse, Thanna. “Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures.” 2014. Masters Thesis, Boston University. Accessed October 31, 2020. http://hdl.handle.net/2144/15373.

MLA Handbook (7th Edition):

Rajapakse, Thanna. “Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures.” 2014. Web. 31 Oct 2020.

Vancouver:

Rajapakse T. Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures. [Internet] [Masters thesis]. Boston University; 2014. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2144/15373.

Council of Science Editors:

Rajapakse T. Fidelity of heterozygote balance and contributor proportions before and after post-PCR purification of low template two-person mixtures. [Masters Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15373


Brandeis University

2. Thompson, Chelsea Anne. Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers.

Degree: 2016, Brandeis University

 Ornithine transcarbamylase deficiency (OTCD) is an inborn error of metabolism and the most common urea cycle disorder. Affected individuals may experience hyperammonemia, which can be… (more)

Subjects/Keywords: Ornithine Transcarbamylase Deficiency; OTC; OTCD; Urea Cycle Disorder; Carrier; Heterozygote; Partial OTCD; Genetic Counseling

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APA (6th Edition):

Thompson, C. A. (2016). Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/31814

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):

Thompson, Chelsea Anne. “Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers.” 2016. Thesis, Brandeis University. Accessed October 31, 2020. http://hdl.handle.net/10192/31814.

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

MLA Handbook (7th Edition):

Thompson, Chelsea Anne. “Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers.” 2016. Web. 31 Oct 2020.

Vancouver:

Thompson CA. Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers. [Internet] [Thesis]. Brandeis University; 2016. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10192/31814.

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

Council of Science Editors:

Thompson CA. Hidden on the X: Psychosocial Implications of Ornithine Transcarbamylase Deficiency in Female Carriers. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/31814

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


University of Georgia

3. Lindsay, Cheryl Beth. Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp.

Degree: 2014, University of Georgia

 The polyembryonic parasitoid wasp, Copidosoma floridanum, has evolved a caste system, consisting of soldiers and reproductives. Prior studies suggest soldiers have evolved in response to… (more)

Subjects/Keywords: Copidosoma floridanum; Gpi; soldiers; heterozygote advantage; partial local mate competition; life-history trade-offs

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APA (6th Edition):

Lindsay, C. B. (2014). Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/25866

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):

Lindsay, Cheryl Beth. “Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp.” 2014. Thesis, University of Georgia. Accessed October 31, 2020. http://hdl.handle.net/10724/25866.

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

MLA Handbook (7th Edition):

Lindsay, Cheryl Beth. “Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp.” 2014. Web. 31 Oct 2020.

Vancouver:

Lindsay CB. Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10724/25866.

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

Council of Science Editors:

Lindsay CB. Factors affecting caste development, brood type, and sex ratios of a polyembryonic wasp. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/25866

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

4. Mulcahy, EM. Peripheral immune cell abnormalities associated with cystic fibrosis.

Degree: 2017, University of Tasmania

 Cystic fibrosis (CF) is the most common life-limiting single-gene disease. It is caused by mutations to the cystic fibrosis transmembrane conductance regulator (CFTR) gene that… (more)

Subjects/Keywords: Cystic fibrosis; peripheral blood; T cell; dendritic cell; natural killer cell; myeloid derived suppressor cell; monocyte; CFTR heterozygote

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APA (6th Edition):

Mulcahy, E. (2017). Peripheral immune cell abnormalities associated with cystic fibrosis. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/23874/1/Mulchay_whole_thesis.pdf

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

Chicago Manual of Style (16th Edition):

Mulcahy, EM. “Peripheral immune cell abnormalities associated with cystic fibrosis.” 2017. Thesis, University of Tasmania. Accessed October 31, 2020. https://eprints.utas.edu.au/23874/1/Mulchay_whole_thesis.pdf.

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

MLA Handbook (7th Edition):

Mulcahy, EM. “Peripheral immune cell abnormalities associated with cystic fibrosis.” 2017. Web. 31 Oct 2020.

Vancouver:

Mulcahy E. Peripheral immune cell abnormalities associated with cystic fibrosis. [Internet] [Thesis]. University of Tasmania; 2017. [cited 2020 Oct 31]. Available from: https://eprints.utas.edu.au/23874/1/Mulchay_whole_thesis.pdf.

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

Council of Science Editors:

Mulcahy E. Peripheral immune cell abnormalities associated with cystic fibrosis. [Thesis]. University of Tasmania; 2017. Available from: https://eprints.utas.edu.au/23874/1/Mulchay_whole_thesis.pdf

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


University of Oslo

5. Fosaas, Kristina. Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine.

Degree: 2006, University of Oslo

 Introduction: Both risperidone and venlafaxine are metabolized by Cytochrome P450 2D6 (CYP2D6). Genetic polymorphism in this enzyme may contribute to the significant variation in pharmacokinetics… (more)

Subjects/Keywords: venlafaksin risperidon CYP2D6 heterozygote mutasjoner; VDP::568

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APA (6th Edition):

Fosaas, K. (2006). Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine. (Thesis). University of Oslo. Retrieved from http://urn.nb.no/URN:NBN:no-13978 ; https://www.duo.uio.no/handle/10852/12139 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12139/1/endeligeoppgavenpdf.pdf

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

Chicago Manual of Style (16th Edition):

Fosaas, Kristina. “Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine.” 2006. Thesis, University of Oslo. Accessed October 31, 2020. http://urn.nb.no/URN:NBN:no-13978 ; https://www.duo.uio.no/handle/10852/12139 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12139/1/endeligeoppgavenpdf.pdf.

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

MLA Handbook (7th Edition):

Fosaas, Kristina. “Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine.” 2006. Web. 31 Oct 2020.

Vancouver:

Fosaas K. Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine. [Internet] [Thesis]. University of Oslo; 2006. [cited 2020 Oct 31]. Available from: http://urn.nb.no/URN:NBN:no-13978 ; https://www.duo.uio.no/handle/10852/12139 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12139/1/endeligeoppgavenpdf.pdf.

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

Council of Science Editors:

Fosaas K. Effect of heterozygous mutations in CYP2D6 on serum concentration of risperidone and venlafaxine. [Thesis]. University of Oslo; 2006. Available from: http://urn.nb.no/URN:NBN:no-13978 ; https://www.duo.uio.no/handle/10852/12139 ; Fulltext https://www.duo.uio.no/bitstream/handle/10852/12139/1/endeligeoppgavenpdf.pdf

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


Freie Universität Berlin

6. Schöfisch, Karina. Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse.

Degree: 2013, Freie Universität Berlin

 Non-Mendelian inheritance of the t-haplotype from heterozygous male mice to their offspring is also known as transmission ratio distortion. The t-haplotype, a variant form of… (more)

Subjects/Keywords: haplotypes; t-complex genome region; heterozygote; sperm motility; gene expression regulation; inheritance patterns/genetics; mi; 600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft::630 Landwirtschaft und verwandte Bereiche

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APA (6th Edition):

Schöfisch, K. (2013). Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12814

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):

Schöfisch, Karina. “Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse.” 2013. Thesis, Freie Universität Berlin. Accessed October 31, 2020. https://refubium.fu-berlin.de/handle/fub188/12814.

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

MLA Handbook (7th Edition):

Schöfisch, Karina. “Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse.” 2013. Web. 31 Oct 2020.

Vancouver:

Schöfisch K. Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Oct 31]. Available from: https://refubium.fu-berlin.de/handle/fub188/12814.

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

Council of Science Editors:

Schöfisch K. Investigations on the haploid specificity of the t-complex responder in non- Mendelian inheritance in the mouse. [Thesis]. Freie Universität Berlin; 2013. Available from: https://refubium.fu-berlin.de/handle/fub188/12814

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


University of Florida

7. Scocco, Christopher M. Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.).

Degree: PhD, Entomology and Nematology, 2018, University of Florida

 The ghost ant, Tapinoma melanocephalum (F.) (Hymenoptera: Formicidae: Dolichoderinae) is major cosmopolitan urban and agricultural pest ant, capable of invading homes and agricultural greenhouses in… (more)

Subjects/Keywords: 18s  – 28s  – 6-fam  – allele  – ants  – co1  – coi  – cox1  – coxi  – dolichoderinae  – electrophoresis  – formicidae  – heterozygosity  – heterozygote  – invasive  – microsatellites  – mtdna  – page  – pcr  – phylogenetics  – polyacrylamide  – rdna

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APA (6th Edition):

Scocco, C. M. (2018). Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.). (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0052681

Chicago Manual of Style (16th Edition):

Scocco, Christopher M. “Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.).” 2018. Doctoral Dissertation, University of Florida. Accessed October 31, 2020. https://ufdc.ufl.edu/UFE0052681.

MLA Handbook (7th Edition):

Scocco, Christopher M. “Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.).” 2018. Web. 31 Oct 2020.

Vancouver:

Scocco CM. Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.). [Internet] [Doctoral dissertation]. University of Florida; 2018. [cited 2020 Oct 31]. Available from: https://ufdc.ufl.edu/UFE0052681.

Council of Science Editors:

Scocco CM. Genetic Investigation of the Invasive Ghost Ant, Tapinoma melanocephalum (F.). [Doctoral Dissertation]. University of Florida; 2018. Available from: https://ufdc.ufl.edu/UFE0052681


University of Lund

8. Sawangproh, Weerachon. Gene transfer by interspecific hybridization in bryophytes.

Degree: 2019, University of Lund

 The role of hybridization in evolution has been debated for more than a century regarding bryophytes (mosses, liverworts, and hornworts) as well as most other… (more)

Subjects/Keywords: Ecology; homozygote; heterozygote; admixture; single nucleotide polymorphism; STRUCTURE; PCoA; hybrid index; inbreeding; outbreeding; hybrid depression; heterosis; phylogeny; purging selection; genetic purging; genotype; phenotype; sympatry; allopatry

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APA (6th Edition):

Sawangproh, W. (2019). Gene transfer by interspecific hybridization in bryophytes. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/df204693-bfc0-489b-b662-5a8cde94171c ; https://portal.research.lu.se/ws/files/62786159/LUP_weerachon.pdf

Chicago Manual of Style (16th Edition):

Sawangproh, Weerachon. “Gene transfer by interspecific hybridization in bryophytes.” 2019. Doctoral Dissertation, University of Lund. Accessed October 31, 2020. https://lup.lub.lu.se/record/df204693-bfc0-489b-b662-5a8cde94171c ; https://portal.research.lu.se/ws/files/62786159/LUP_weerachon.pdf.

MLA Handbook (7th Edition):

Sawangproh, Weerachon. “Gene transfer by interspecific hybridization in bryophytes.” 2019. Web. 31 Oct 2020.

Vancouver:

Sawangproh W. Gene transfer by interspecific hybridization in bryophytes. [Internet] [Doctoral dissertation]. University of Lund; 2019. [cited 2020 Oct 31]. Available from: https://lup.lub.lu.se/record/df204693-bfc0-489b-b662-5a8cde94171c ; https://portal.research.lu.se/ws/files/62786159/LUP_weerachon.pdf.

Council of Science Editors:

Sawangproh W. Gene transfer by interspecific hybridization in bryophytes. [Doctoral Dissertation]. University of Lund; 2019. Available from: https://lup.lub.lu.se/record/df204693-bfc0-489b-b662-5a8cde94171c ; https://portal.research.lu.se/ws/files/62786159/LUP_weerachon.pdf


Universiteit Utrecht

9. Thompson, P.N. Congenital myasthenic syndrome of Brahman cattle.

Degree: 2006, Universiteit Utrecht

 The postsynaptic congenital myasthenic syndrome that is the subject of this thesis is caused by a deficiency of nAChR at the neuromuscular junction, resulting from… (more)

Subjects/Keywords: Diergeneeskunde; Brahman cattle; South Africa; inherited disease; congenital myasthenic syndrome; acetylcholine receptor; lethal recessive mutation; heterozygote advantage; gene frequency; pedigree analysis; control programme

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APA (6th Edition):

Thompson, P. N. (2006). Congenital myasthenic syndrome of Brahman cattle. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/13353

Chicago Manual of Style (16th Edition):

Thompson, P N. “Congenital myasthenic syndrome of Brahman cattle.” 2006. Doctoral Dissertation, Universiteit Utrecht. Accessed October 31, 2020. http://dspace.library.uu.nl:8080/handle/1874/13353.

MLA Handbook (7th Edition):

Thompson, P N. “Congenital myasthenic syndrome of Brahman cattle.” 2006. Web. 31 Oct 2020.

Vancouver:

Thompson PN. Congenital myasthenic syndrome of Brahman cattle. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2006. [cited 2020 Oct 31]. Available from: http://dspace.library.uu.nl:8080/handle/1874/13353.

Council of Science Editors:

Thompson PN. Congenital myasthenic syndrome of Brahman cattle. [Doctoral Dissertation]. Universiteit Utrecht; 2006. Available from: http://dspace.library.uu.nl:8080/handle/1874/13353

10. Thompson, P.N. Congenital myasthenic syndrome of Brahman cattle.

Degree: 2006, University Utrecht

 The postsynaptic congenital myasthenic syndrome that is the subject of this thesis is caused by a deficiency of nAChR at the neuromuscular junction, resulting from… (more)

Subjects/Keywords: Brahman cattle; South Africa; inherited disease; congenital myasthenic syndrome; acetylcholine receptor; lethal recessive mutation; heterozygote advantage; gene frequency; pedigree analysis; control programme

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

APA (6th Edition):

Thompson, P. N. (2006). Congenital myasthenic syndrome of Brahman cattle. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/13353 ; URN:NBN:NL:UI:10-1874-13353 ; urn:isbn:0-620-37081-5 ; URN:NBN:NL:UI:10-1874-13353 ; https://dspace.library.uu.nl/handle/1874/13353

Chicago Manual of Style (16th Edition):

Thompson, P N. “Congenital myasthenic syndrome of Brahman cattle.” 2006. Doctoral Dissertation, University Utrecht. Accessed October 31, 2020. https://dspace.library.uu.nl/handle/1874/13353 ; URN:NBN:NL:UI:10-1874-13353 ; urn:isbn:0-620-37081-5 ; URN:NBN:NL:UI:10-1874-13353 ; https://dspace.library.uu.nl/handle/1874/13353.

MLA Handbook (7th Edition):

Thompson, P N. “Congenital myasthenic syndrome of Brahman cattle.” 2006. Web. 31 Oct 2020.

Vancouver:

Thompson PN. Congenital myasthenic syndrome of Brahman cattle. [Internet] [Doctoral dissertation]. University Utrecht; 2006. [cited 2020 Oct 31]. Available from: https://dspace.library.uu.nl/handle/1874/13353 ; URN:NBN:NL:UI:10-1874-13353 ; urn:isbn:0-620-37081-5 ; URN:NBN:NL:UI:10-1874-13353 ; https://dspace.library.uu.nl/handle/1874/13353.

Council of Science Editors:

Thompson PN. Congenital myasthenic syndrome of Brahman cattle. [Doctoral Dissertation]. University Utrecht; 2006. Available from: https://dspace.library.uu.nl/handle/1874/13353 ; URN:NBN:NL:UI:10-1874-13353 ; urn:isbn:0-620-37081-5 ; URN:NBN:NL:UI:10-1874-13353 ; https://dspace.library.uu.nl/handle/1874/13353

11. Sovec, Igor. Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov.

Degree: 2013, Univerza v Mariboru

Kronično vnetna črevesna bolezen (KVČB) je kompleksna avtoimunska bolezen, na razvoj katere vplivajo številni dejavniki, med njimi tudi polimorfizmi v številnih genih. Namen magistrskega dela… (more)

Subjects/Keywords: kronično vnetna črevesna bolezen (KVČB); Crohnova bolezen (CB); refraktorna oblika Crohnove bolezni (CBr); ulcerozni kolitis (UC); genetski profil; diagnostični test; polimofizem posameznega nukleotida; genotip; homozigot; heterozigot; alel; asociacijska analiza; prag; inflammatory bowel disease (IBD); Crohn’s disease (CD); refractory Crohn’s disease (CDr); ulcerative colitis (UC); genetic profile; diagnostic test; single nucleotide polymorphism; genotype; homozygote; heterozygote; allele; association analysis; cutoff point; info:eu-repo/classification/udc/616.34-002(043.2)

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APA (6th Edition):

Sovec, I. (2013). Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov. (Masters Thesis). Univerza v Mariboru. Retrieved from https://dk.um.si/IzpisGradiva.php?id=40212 ; https://dk.um.si/Dokument.php?id=54957&dn= ; https://plus.si.cobiss.net/opac7/bib/1901476?lang=sl

Chicago Manual of Style (16th Edition):

Sovec, Igor. “Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov.” 2013. Masters Thesis, Univerza v Mariboru. Accessed October 31, 2020. https://dk.um.si/IzpisGradiva.php?id=40212 ; https://dk.um.si/Dokument.php?id=54957&dn= ; https://plus.si.cobiss.net/opac7/bib/1901476?lang=sl.

MLA Handbook (7th Edition):

Sovec, Igor. “Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov.” 2013. Web. 31 Oct 2020.

Vancouver:

Sovec I. Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov. [Internet] [Masters thesis]. Univerza v Mariboru; 2013. [cited 2020 Oct 31]. Available from: https://dk.um.si/IzpisGradiva.php?id=40212 ; https://dk.um.si/Dokument.php?id=54957&dn= ; https://plus.si.cobiss.net/opac7/bib/1901476?lang=sl.

Council of Science Editors:

Sovec I. Primerjava med porazdelitvijo izbranih genetskih profilov pri bolnikih s kronično vnetno črevesno boleznijo in pri kontrolni skupini zdravih posameznikov. [Masters Thesis]. Univerza v Mariboru; 2013. Available from: https://dk.um.si/IzpisGradiva.php?id=40212 ; https://dk.um.si/Dokument.php?id=54957&dn= ; https://plus.si.cobiss.net/opac7/bib/1901476?lang=sl


University of Canterbury

12. Collins, Patrick. The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana.

Degree: MS, Plant Biotechnology, 2013, University of Canterbury

 The nuclear pore complex (NPC) is perhaps the largest protein complex in the eukaryotic cell, and controls the movement of molecules across the nuclear envelope.… (more)

Subjects/Keywords: Arabidopsis thaliana; transformation; insert; transient expression; epidermal cells; root cells; gene; protein; plant; bolting; flowering; root growth; knockout; ndc1; gp210; At1g73240; At5g40480; SALK; SAIL; Columbia; seed; germination; DNA sequencing; agarose gel electrophoresis confocal microscopy; light microscopy; stereo-fluorescence microscopy; DNA extraction; cell; nucleus; cytoplasm; nucleoplasm; nuclear pore complex; nucleoporin; nuclear envelope; putative; nuclear pore-anchoring protein; leptomycin B; gene gun; particle bombardment; agrobacterium; T-DNA; fasciation; rhodococcus fascians; cross; reverse genetics; nucleocytoplasmic transport; cross; self; synergistic; silique; transmembrane ring; dihybrid; pumilo homology domain protein; GFP; YFP; RFP; PCR; homozygote; heterozygote; inhibition

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

APA (6th Edition):

Collins, P. (2013). The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana. (Masters Thesis). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/9042

Chicago Manual of Style (16th Edition):

Collins, Patrick. “The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana.” 2013. Masters Thesis, University of Canterbury. Accessed October 31, 2020. http://dx.doi.org/10.26021/9042.

MLA Handbook (7th Edition):

Collins, Patrick. “The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana.” 2013. Web. 31 Oct 2020.

Vancouver:

Collins P. The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana. [Internet] [Masters thesis]. University of Canterbury; 2013. [cited 2020 Oct 31]. Available from: http://dx.doi.org/10.26021/9042.

Council of Science Editors:

Collins P. The Characterisation of Putative Nuclear Pore-Anchoring Proteins in Arabidopsis thaliana. [Masters Thesis]. University of Canterbury; 2013. Available from: http://dx.doi.org/10.26021/9042

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