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Dissertations / Theses on the topic 'Chromosome variation'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Gregory, Simon Gray. "Chromosome 1 map, sequence and variation." Thesis, Open University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.272971.

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2

Carr, Martin. "Genetic variation on the fourth chromosome of Drosophila melanogaster." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324481.

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3

Anagnostopoulos, Theodore. "Investigation of sequence variation on the human X chromosome." Thesis, King's College London (University of London), 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405805.

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4

SSEKIMPI, PUPULIO SSEMOMBWE NKUNA ABBY. "CHROMOSOME VARIATION IN DROSOPHILA SPECIES OF THE MULLERI COMPLEX." Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/183809.

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Drosophila species in mulleri complex show five rod-shaped and one pair of dot-shaped chromosome. The sex-chromosomes represent the largest pair in the female, but are heteromorphic in the male, the Y-chromosome being shorter than the X-chromosome. The purpose of the research presented here is to determine whether chromosomes in the mulleri cluster species are longer than in the mojavensis cluster. The length of X-, Y-chromosomes and the rod-like autosomes were compared among the ten species studied. All the rod-like chromosomes were measured in 30 or more brain cells in each of the ten specie

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5

Stavrides, George Stavros. "Human chromosome 20q12-13.2 : structural, comparative and sequence variation studies." Thesis, University of Cambridge, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.619575.

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6

Rootsi, Siiri. "Human Y-chromosomal variation in European populations /." Tartu : Tartu University Press, 2004. http://dspace.utlib.ee/dspace/bitstream/10062/1252/5/rootsi.pdf.

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7

Plaster, C. A. "Variation in Y chromosome, mitochondrial DNA and labels of identity on Ethiopia." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1331901/.

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There is a paucity of genetic studies of Ethiopia. This thesis aims to establish the extent and distribution of variation in NRY and mtDNA genetic markers as well as ethnic and linguistic labels of identity 45 ethnic groups. A wide range of NRY and mtDNA haplogroups were observed, including both those typically observed in Africa and those more frequently observed outside Africa. Significant correlations were revealed between NRY and mtDNA diversity. Nearly all ethnic groups were significantly differentiated from each other, although the pattern of similarities indicates some recent gene flow

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8

Lu, Wenqing. "Phenotypic impact of inversions in yeast genome." Electronic Thesis or Diss., Sorbonne université, 2021. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2021SORUS514.pdf.

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Les génomes sont des structures hautement dynamiques et les grandes variations structurelles (SVs) des chromosomes, telles que les inversions, contribuent à l'évolution des génomes et à l'adaptation des espèces. Il est essentiel de comprendre l'impact fonctionnel des inversions sur la diversité phénotypique, car il existe de plus en plus de preuves que les inversions joueraient un rôle important dans les variations phénotypiques. Afin d'expliquer l'impact phénotypique des inversions, nous avons choisi la levure de boulangerie comme modèle eucaryote unicellulaire dans notre travail. Sur la base

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9

Ferreira, Irma. "Sequence variation of the amelogenin gene on the Y-chromosome / by Irma Ferreira." North-West University, 2010. http://hdl.handle.net/10394/4412.

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The accurate determination of gender of biological samples has valuable applications in medical and forensic investigations. Gender determination based on length variations in the X-Y homologous amelogenin gene, is part of most commercial multiplex DNA profiling kits. The first report of a failure of the amelogenin sex test was in 1998 when two normal males were typed as female. Subsequently, several amelogenin Y (AMELY) negative males have been reported. This study represents the first report of this phenomenon in the black South African population. This study determined the size of t

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10

Latham, Krista Erin. "Assessing Y-Chromosome Variation in the South Pacific Using Newly Detected NRY Markers." Diss., Temple University Libraries, 2008. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/5736.

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Anthropology<br>Ph.D.<br>The South Pacific is a region of incredible biological, cultural and linguistic diversity, reflecting its early settlement by human populations. It has been a region of interest to scholars because of this diversity, as well as its unique geography and settlement history. Current evidence suggests there was an initial settlement of Near Oceania during the Pleistocene by Papuan-speaking foragers, followed by a later Holocene settlement of Remote Oceania by Oceanic-speaking agriculturalists. Previous studies of human biological variation have been used to illuminate the

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11

Marshall-Shapiro, Adele H. "Variation at two hypervariable loci on chromosome 16p in the multicultural population of Montreal." Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=59409.

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The purpose of this study was to analyze the frequency distributions of alleles at the 3$ sp prime$HVR (hypervariable region) and 5$ sp prime$HVR, two highly polymorphic regions on chromosome 16p. About 300 DNA samples from individuals of East Asian, French Canadian, Greek, Italian, Jewish and Middle Eastern origin were analyzed by hybridization to probes for the 3$ sp prime$HVR and 5$ sp prime$HVR.<br>The distributions of alleles at both loci are skewed with the long tail towards the larger alleles. The observed heterozygosity at the 3$ sp prime$HVR locus for 281 individuals was 0.91, ranging

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12

Espinoza, Babilon Jose Ronald. "A study of the molecular basis of the chromosome size variation in Leishmania peruviana." Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627149.

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13

Revenikioti, Maria. "Life history and reproductive fitness variation associated with the Y chromosome in Callosobruchus maculatus." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-435099.

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In the seed beetle Callosobruchus maculatus, the female is the larger sex and the male is the smaller sex. However, males that are almost as large as females can also occur, which is due to a specific Y chromosome haplotype. This Y chromosome polymorphism is not expected since the Y chromosome does not recombine and has lost genetic variation as a consequence. Nevertheless, the Y chromosome manages to maintain this polymorphism. Thus, the questions asked are how this occurs and how the large male Y haplotype persists to exist since previous studies have shown how small males have the higher fi

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14

Varney, Robin Lynne. "Assessment of nuclear DNA variation and population structure in the eastern oyster, Crassostrea virginica, through discovery and analysis of single nucleotide polymorphisms (SNPs)." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 216 p, 2009. http://proquest.umi.com/pqdweb?did=1891582831&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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15

Brooks, Samantha Ann. "STUDIES OF GENETIC VARIATION AT THE KIT LOCUS AND WHITE SPOTTING PATTERNS IN THE HORSE." UKnowledge, 2006. http://uknowledge.uky.edu/gradschool_diss/479.

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There are numerous different white spotting patterns in the horse, including two of particular interest tobiano and sabino. In the mouse, genetic variation in the gene KIT causes many white spotting patterns. Due to the phenotypic similarity among white spotting patterns in horses and mice, KIT was investigated as the cause of the tobiano and sabino spotting patterns in horses. Initially, the KIT cDNA sequences from horses with several spotting patterns were compared. Three single nucleotide polymorphisms (SNPs) were identified, though none were associated with a spotting pattern. Three novel

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16

Bacha, Jamil. "Studies of the effects of promoter sequence variation on gene expression in human chromosome 22." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612707.

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17

Trotter, Meridith V., and n/a. "Frequency-dependent selection and the maintenance of genetic variation." University of Otago. Department of Zoology, 2008. http://adt.otago.ac.nz./public/adt-NZDU20081114.120926.

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Frequency-dependent selection has long been a popular heuristic explanation for the maintenance of genetic diversity in natural populations. Indeed, a large body of theoretical and empirical work has already gone into elucidating the causes and consequences of frequency-dependent selection. Most theoretical work, to date, has focused either on the diallelic case, or dealt with only very specific forms of frequency-dependence. A general model of the maintenance of multiallelic genetic diversity has been lacking. Here we extend a flexible general model of frequency-dependent selection, the pairw

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18

Roos-Araujo, Deidré. "Investigation of Xq chromosomal variation in relation to migraine." Thesis, Queensland University of Technology, 2019. https://eprints.qut.edu.au/128579/1/__qut.edu.au_Documents_StaffHome_StaffGroupH%24_halla_Desktop_Deidr%C3%A9%20Roos-Araujo%20Thesis.pdf.

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This research was conducted to expand the understanding of the role of the X chromosome in common and familial typical migraine. The primary objective of this study was to identify new X chromosomal genetic targets that cause migraine. Overall this research has identified nine genetic targets of interest. Various obstacles were encountered throughout this study, but the knowledge gained for overcoming these obstacles are invaluable for implementation and improvement of future genetic studies investigating the X chromosome.

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19

Martin, Gabriel. "Facteurs de risques de développer une maladie auto-immune chez les hommes? : cas particulier de la polyarthrite rhumatoïde." Thesis, Aix-Marseille, 2017. http://www.theses.fr/2017AIXM0562/document.

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Peu d’hommes sont touchés par les maladies auto-immunes (MAI), maladies où la réponse immune est très forte et attaque l’hôte. La polyarthrite rhumatoïde (PR), une maladie inflammatoire chronique, suit cette règle avec 3 femmes pour 1 homme atteint. Dans cette thèse, nous analysons les différences en fonction du sexe et les raisons d’un tel biais. D’après des observations chez l’animal, nous nous sommes demandés si les rares hommes atteints de PR ont une augmentation du nombre de copies d’un gène impliqué dans la réponse immune et porté par le chromosome (Chr) X. Contrairement aux femmes, les

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20

Cottrell, Catherine Elise. "Genetic variation and complex disease the examination of an X-linked disorder and a multifactorial disease /." Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1196182829.

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21

Modin, Helena. "Multiple sclerosis : linkage analysis and DNA variation in a complex trait /." Stockholm, 2004. http://diss.kib.ki.se/2004/91-7349-792-4/.

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22

Guinet, Françoise. "Chromosome 12 de P. Falciparum : caractérisation d'une mutation du développement sexué et identification d'un locus impliqué dans la variation antigénique." Paris 7, 1997. http://www.theses.fr/1997PA077351.

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Des études génétiques dans le parasite Plasmodium falciparum ont été rendues possibles par la réalisation et la caractérisation de croisements en laboratoire (Walliker et al. , Science (1987) 236:1661; Wellems et al. , Nature (1990) 345:253). L'utilisation de l'approche génétique a conduit à l'identification des gènes var d'importance fondamentale pour la pathogénicité et le cycle de transmission de parasite, ainsi qu'à la définition d'un locus lié au développement sexué mâle du parasite. Une région de 300 kb liée à la chloroquino-résistance avait été définie sur le chromosome 7 de P. Falcipar

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23

Duvefelt, Kristina. "Genetic variations influencing susceptibility to multiple sclerosis /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-573-9/.

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24

Rajendran, Raphael Samuel [Verfasser]. "Numerical Chromosome Variation and Mitotic Segregation Defects in Cells Generated in the Adult Brain of Teleost Fish / Raphael Samuel Rajendran." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2012. http://d-nb.info/1035267217/34.

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25

Kanaan, Sami barna. "Facteurs de risque liés au chromosome X à l'origine de la prédominance des femmes dans la polyarthrite rhumatoïde." Thesis, Aix-Marseille, 2013. http://www.theses.fr/2013AIXM4112/document.

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Comme dans la plupart des maladies auto-immunes une prédominance féminine est observée dans la polyarthrite rhumatoïde (PR). Le chromosome X, présent en 2 exemplaires chez la femme, est intéressant puisque beaucoup de gènes à fonctions immunitaires y sont localisés. Dans ce travail, nous montrons que certains de ces gènes peuvent augmenter leur nombre de copies quand l'individu vieillit. En outre, cette variation est spécifique au sexe avec une augmentation chez les hommes et l'inverse chez les femmes. D’autre part, alors que généralement les femmes inactivent aléatoirement (50:50) le chromoso

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26

Cottrell, Catherine E. "Genetic variation and complex disease: the examination of an X-linked disorder and a multifactorial disease." The Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=osu1196182829.

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27

Athanasiadis, Georgios. "Genetic variation of the X chromosome and the genomic regions of Coagulation Factors VII and XII in human populations: Epidemiological and evolutionary considerations." Doctoral thesis, Universitat de Barcelona, 2010. http://hdl.handle.net/10803/111091.

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In this work we have analyzed the variation of (i) several X chromosome polymorphic Alu insertions and (ii) several SNPs and microsatellites within and around the genomic regions of the genes coding for coagulation factors VII and XII (F7 and F12 respectively) in different human populations - mainly Mediterranean, but also from other geographic regions. Alu polymorphisms are very useful for anthropological studies to investigate the origin and genetic relationships between different human populations. In addition, there are certain mutations in the F7 and F12 genes that affect plasma levels o

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28

Silva, Laura Helena Hafner da. "Variação morfologica em populações brasileiras de Drosophila melanogaster : variação latitudinal e temporal, herdabilidade e associação com inversões cromossomicas." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316970.

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Orientador: Louis Bernard Klaczko<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia<br>Made available in DSpace on 2018-08-08T02:56:34Z (GMT). No. of bitstreams: 1 Silva_LauraHelenaHafnerda_M.pdf: 2141945 bytes, checksum: 17c00d0d744de62b04cc274305caedb5 (MD5) Previous issue date: 2006<br>Resumo: O presente trabalho tem como objetivo caracterizar a variação do tamanho e forma das asas de populações de Drosophila melanogaster em três pontos ao longo de uma grande amplitude latitudinal na costa brasileira. O trabalho foi feito a partir de coletas realizadas n

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29

Le, Roy Isabelle. "Cartographie chromosomique de QTLS impliqués dans la variation des comportements ou de leurs corrélats neuronaux chez la souris." Paris 5, 1997. http://www.theses.fr/1997PA05S016.

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La localisation des quantitative trait loci (QTLS) se situe dans une perspective de génétique inversé qui permet la localisation de gène(s) sur un chromosome à son (leur) identification, soit par marche sur le chromosome, soit par co-detections avec des gènes antérieurement identifies. Les différents traits neuronaux et comportementaux analyses dans cette thèse chez les souris parentales consanguines nzb/blnj. Gnc et c57bl/jby (lignées montrant un fort polymorphisme pour ces traits), les deux hybrides f 1s et les quatre intercroisements f 2s sont : le développement sensoriel et moteur chez les

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30

Hayes, Matthew. "Algorithms to Resolve Large Scale and Complex StructuralVariants in the Human Genome." Case Western Reserve University School of Graduate Studies / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=case1372864570.

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31

Borge, Thomas. "Genetics and the Origin of Two Flycatcher Species." Doctoral thesis, Uppsala University, Evolutionary Biology, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3919.

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<p>In this thesis, different genetic tools are used to investigate pre- and postzygotic barriers to gene exchange and their role in speciation in the pied flycatcher (<i>Ficedula hypoleuca</i>) and the collared flycatcher (<i>F. albicollis</i>). This species complex consists of four genetically distinct clades that apparently diverged in allopatry (I). Sequencing of introns from autosomal and Z-linked genes from the two species reveals signs of selection on the Z-chromosome. Sexual selection acting on Z-linked genes might explain this pattern (II). By using large-scale genotyping of single nuc

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32

Li, Mingyin. "Anatomische, cytologische und histologische Untersuchungen zur somatischen Variation in verschiedenen Teilklonen von Pelargonium zonale "Kleiner Liebling"." Doctoral thesis, Humboldt-Universität zu Berlin, Landwirtschaftlich-Gärtnerische Fakultät, 2005. http://dx.doi.org/10.18452/15226.

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Die vorliegende Arbeit befasst sich mit den morphologischen bzw. cytologischen Anomalien eines mutierten Klons 5/74/2 aus der haploiden Sorte `Kleiner Liebling` von Pelargonium zonale. An histologischen Schnitten wurden die Ploidiestufen verschiedener Zellschichten von Cytochimären durch Chromosomenzählung direkt bestimmt. Es wurde festgestellt, dass die Epidermis in den Blättern vom Klon 5/74/2 verschiedene Ploidiestufen aufweist. Solche Variabilität trat in den L2- und L3-bürtigen Zellschichten nicht auf. Somit wurde hier erstmals eine Periklinalcytochimäre mit verschiedenen Ploidie in der E

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33

Gillet-Markowska, Alexandre. "Etude quantitative des variations structurelles des chromosomes chez Saccharomyces cerevisiae." Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066233/document.

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L’accumulation de remaniements de la structure des chromosomes aussi appelés variations structurelles (SV) est un important contributeur à la transformation des cellules malignes et à la constitution d’une hétérogénéité intratumorale. Nous avons développé un outil bio-informatique qui permet désormais d’obtenir une image fine de ces SV qui se produisent dans le génome humain. Nous avons ainsi pu démontrer l’existence de SV présentes à de faibles fréquences dans différentes populations cellulaires supposées clonales montrant que les taux de formation des SV pourraient être grandement sous-estim

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34

Pandya, Arpita. "Human Y-chromosomal DNA variation." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298658.

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35

Hansson, Caisa Marie. "Analysis of Genetic Alterations in Patients Affected with Neurofibromatosis Type 2 and its Associated Tumors." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6511.

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36

Khuzwayo, Sabelo Lethukuthula. "Functional analysis of subtelomeric breakage motifs using yeast as a model organism." Thesis, Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/41119.

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Genome wide studies have uncovered the existence of large-scale copy number variation (CNV) in the human genome. The human genome of different individuals was initially estimated to be 99.9% similar, but population studies on CNV have revealed that it is 12-16% copy number variable. Abnormal genomic CNVs are frequently found in subtelomeres of patients with mental retardation (MR) and other neurological disorders. Rearrangements of chromosome subtelomeric regions represent a high proportion of cytogenetic abnormalities and account for approximately 30% of pathogenic CNVs. Although DNA double s

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37

Gillet-Markowska, Alexandre. "Etude quantitative des variations structurelles des chromosomes chez Saccharomyces cerevisiae." Electronic Thesis or Diss., Paris 6, 2015. http://www.theses.fr/2015PA066233.

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L’accumulation de remaniements de la structure des chromosomes aussi appelés variations structurelles (SV) est un important contributeur à la transformation des cellules malignes et à la constitution d’une hétérogénéité intratumorale. Nous avons développé un outil bio-informatique qui permet désormais d’obtenir une image fine de ces SV qui se produisent dans le génome humain. Nous avons ainsi pu démontrer l’existence de SV présentes à de faibles fréquences dans différentes populations cellulaires supposées clonales montrant que les taux de formation des SV pourraient être grandement sous-estim

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38

Buckley, Patrick. "Development and Application of Microarray-Based Comparative Genomic Hybridization : Analysis of Neurofibromatosis Type-2, Schwannomatosis and Related Tumors." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4786.

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39

Zerjal, Tatiana. "Human genetic variation from a Y-chromosomal perspective." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249177.

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40

Lloyd, Davina. "The induction, in vitro, of chromosomal variation in Rosa." Thesis, University of East London, 1986. http://roar.uel.ac.uk/3644/.

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The culture in vitro was investigated in 7 clones of roses representing a range of genotypes and ploidy levels. Particular attention was paid to a sterile hybrid, R. persica x xanthina , from which it was hoped to obtain tetraploid clones. It was anticipated that tetraploid clones might be fertile and that this would facilitate introgressive hybridization of R.persica genes into various classes of cultivated roses. Propagation medium was developed based on MS salts and vitamins supplemented with BAP and NAA. Doubling times of 2-4 weeks were obtained on optimum media. Transplantation to soil wa

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41

Pascoe, Philip Lionel. "Chromosomal variation in Nucella lapillus (L.) and other muricid gastropods." Thesis, University of Plymouth, 2002. http://hdl.handle.net/10026.1/2654.

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The Robertsonian polymorphism (numerical change in the chromosome complement by centric fusion or fission) in the dog-whelk (Nucella lapillus, Mollusca: Gastropoda) has been known and studied sporadically for almost 50 years. However, the possible causes, consequences and proposed correlations of this phenomenon remain enigmatic. Nucella lapillus (2n = 26 to 36), has undergone a marked reduction in chromosome number from its ancestral form; most other muricid species have a diploid chromosome number in the range 2n = 60- 70. Correlations have been proposed between chromosome number (or karyoty

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42

Elder, John Franklin. "Chromosomal complements and variation in some Venezuelan annual killifishes (cyprinodontidae)." Thesis, Virginia Tech, 1988. http://hdl.handle.net/10919/43853.

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<p>Karyotypes of nine species of Venezuelan annual killifishes were compared. Karyotypic differences were found between species and between some genera.</p><p> A chromosomal sexual dimorphism was found in <u>Pterolebias hoignei</u> (2N = 46). Males of this species possess a single large "Y" chromosome. No chromosomal divergence was detected among conspecific populations from different localities. <u>Pterolebias hoignei</u> and <u>Pterolebias zonatus</u> were found to differ both in diploid number (46 and 42 respectively) and in metacentric chromosome number (6 and 12 respectively).</p><p> All

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43

Mercer, Simon John. "Chromosomal variation of the common shrew Sorex araneus L. in Britain." Thesis, University of Oxford, 1991. http://ora.ox.ac.uk/objects/uuid:0d19aebd-9fa0-47a2-8b37-f016a0ba527a.

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Throughout the range of the common shrew (Sorex araneus Linnaeus 1767), repeated Robertsonian fusion mutations have led to a karyotypic polymorphism dividing the species into chromosome races. Studies of fertility were undertaken in the male, both of homozygotes and of heterozygotes forming meiotic multivalents of varying complexity. Observations made at pachytene, diakinesis/metaphase I and metaphase II did not provide evidence for fertility impairment in homozygotes or simple heterozygotes. Males forming a chain of seven chromosomes during meiotic prophase I were produced through a program o

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44

Beech, Robin Nicholas. "Insertion-deletion variation in the DNA of three natural populations of Drosophila melanogaster." Thesis, University of Edinburgh, 1987. http://hdl.handle.net/1842/10772.

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45

HuÌˆbner, Roland Karl Peter. "Chromosomal and biochemical variation in wild mice from Switzerland : relevance for models of chromosomal evolution in European house mice." Thesis, University of Oxford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316879.

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46

Karcanias, Alexandra. "Investigation of genomic DNA copy number variation on the human sex chromosomes associated with genetic pathologies." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612017.

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47

Rönn, Ann-Charlotte. "Analysis of Nucleotide Variations in Non-human Primates." Doctoral thesis, Uppsala University, Molecular Medicine, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7904.

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<p>Many of our closest relatives, the primates, are endangered and could be extinct in a near future. To increase the knowledge of non-human primate genomes, and at the same time acquire information on our own genomic evolution, studies using high-throughput technologies are applied, which raises the demand for large amounts of high quality DNA.</p><p>In study I and II, we evaluated the multiple displacement amplification (MDA) technique, a whole genome amplification method, on a wide range of DNA sources, such as blood, hair and semen, by comparing MDA products to genomic DNA as templates for

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GuÌˆnduÌˆz, Islam. "Evolutionary genetics of the house mouse (Mus musculus domesticus) with particular emphasis on chromosomal and mitochondrial DNA variation." Thesis, University of York, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369328.

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Wall, Wilson. "A study of variation in human chromosomes shown by photometry, G, C, replication banding and in situ hybridisation." Thesis, Open University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314792.

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Ghim, Shinje. "Etude de la topologie des sites et des variations antigéniques du virus respiratoire syncitial." Lyon 1, 1989. http://www.theses.fr/1989LYO10186.

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Les etudes de la topologie antigenique et fonctionnelle de la proteine de fusion du virus respiratoire syncitial (vrs) et des variations antigeniques du vrs ont ete realisees respectivement par le moyen de la competition en elisa sur cellules infectees avec quatorze anticorps monoclonaux (acmc) et par la technique d'immunofluorescence sur dix-sept souches avec vingt-et-un acmc ainsi que sur des prelevements nasopharynges. Les resultats montrent la presence d'au moins quatre sites antigeniques sur la proteine de fusion et une variation antigenique des souches analysees. Parmi ces quatre sites a

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