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Journal articles on the topic 'DNA variation'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Kučinskas, V. "Human mitochondrial DNA variation in Lithuania." Anthropologischer Anzeiger 52, no. 4 (1994): 289–95. http://dx.doi.org/10.1127/anthranz/52/1994/289.

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2

Collins, Francis S., Mark S. Guyer, and Aravinda Chakravarti. "Variations on a Theme: Cataloging Human DNA Sequence Variation." Science 278, no. 5343 (1997): 1580–81. http://dx.doi.org/10.1126/science.278.5343.1580.

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3

Baughman, Joshua M., and Vamsi K. Mootha. "Buffering mitochondrial DNA variation." Nature Genetics 38, no. 11 (2006): 1232–33. http://dx.doi.org/10.1038/ng1106-1232.

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4

Lalith Perera. "CHLOROPLAST DNA VARIATION IN COCONUT IS OPPOSITE TO ITS NUCLEAR DNA VARIATION." CORD 18, no. 02 (2002): 34. http://dx.doi.org/10.37833/cord.v18i02.359.

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The pattern of world distribution of two major fruit morphotypes of coconuts has led to development of theories on origin, domestication and dissemination of coconut. Results of recent nuclear DNA analyses are in agreement with these theories with several other new insights. Compared to the plant nuclear genome however, the plant organelle genomes, the chloroplast genome and the mitochondrial genome are highly conserved and are maternally inherited in most angiosperms. Therefore, most useful information have come from regions of DNA located in organelle genome for studying phylogeny in angiosp

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5

Kopinski, Piotr K., Larry N. Singh, Shiping Zhang, Marie T. Lott, and Douglas C. Wallace. "Mitochondrial DNA variation and cancer." Nature Reviews Cancer 21, no. 7 (2021): 431–45. http://dx.doi.org/10.1038/s41568-021-00358-w.

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6

Barbujani, Guido. "DNA Variation and Language Affinities." American Journal of Human Genetics 61, no. 5 (1997): 1011–14. http://dx.doi.org/10.1086/301620.

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7

Bernoco, D., and G. R. Byrns. "DNA fingerprint variation in horses." Animal Biotechnology 2, no. 2 (1991): 145–60. http://dx.doi.org/10.1080/10495399109525755.

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8

Srivastava, Sangeeta, and U. C. Lavania. "Evolutionary DNA variation in Papaver." Genome 34, no. 5 (1991): 763–68. http://dx.doi.org/10.1139/g91-118.

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In 23 species of Papaver L., 2C nuclear DNA amounts range from 4.64 pg in Papaver persicum (2n = 14) to 22.43 pg in Papaver orientale (2n = 42), revealing a fivefold variation within the genus. However, such variation is limited to only twofold among the species that have the same chromosome number (2n = 14). The distribution of DNA is discontinuously spread over six groups in the genus. A strong positive correlation exists between nuclear DNA content and metaphase chromosome length. Viewed in the context of evolutionary divergence, it is revealed that DNA reduction has taken place in conjunct

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9

TAYLOR, DAVID B., ALLEN L. SZALANSKI, and RICHARD D. PETERSON II. "Mitochondrial DNA variation in screwworm." Medical and Veterinary Entomology 10, no. 2 (1996): 161–69. http://dx.doi.org/10.1111/j.1365-2915.1996.tb00723.x.

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10

Ramachandran, C., and R. K. J. Narayan. "Chromosomal DNA variation in Cucumis." Theoretical and Applied Genetics 69-69, no. 5-6 (1985): 497–502. http://dx.doi.org/10.1007/bf00251092.

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11

Kidd, K. K., A. J. Pakstis, W. C. Speed, and J. R. Kidd. "Understanding Human DNA Sequence Variation." Journal of Heredity 95, no. 5 (2004): 406–20. http://dx.doi.org/10.1093/jhered/esh060.

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12

Joëlle, Cros, Gavalda Marie-Christine, Chabrillange Nathalie, and Hamon Serge. "Coffee nuclear DNA content variation." Biology of the Cell 76, no. 2 (1992): 276. http://dx.doi.org/10.1016/0248-4900(92)90398-k.

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13

Schaal, Barbara A., Stephen L. O'Kane, and Steven H. Rogstad. "DNA variation in plant populations." Trends in Ecology & Evolution 6, no. 10 (1991): 329–33. http://dx.doi.org/10.1016/0169-5347(91)90041-u.

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14

Raina, S. N., P. K. Srivastav, and S. Rama Rao. "Nuclear DNA variation in Tephrosia." Genetica 69, no. 1 (1986): 27–33. http://dx.doi.org/10.1007/bf00122931.

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15

Yang, Guo, Huitong Zhou, Jiang Hu, Yuzhu Luo, and Jon G. H. Hickford. "Variation in the Yak Dectin-1 Gene (CLEC7A)." DNA and Cell Biology 30, no. 12 (2011): 1069–71. http://dx.doi.org/10.1089/dna.2011.1276.

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16

Kajita, Tadashi, and Hiroyoshi Ohashi. "Chloroplast DNA variation inDesmodium subgenusPodocarpium (Leguminosae): Infrageneric phylogeny and infraspecific variations." Journal of Plant Research 107, no. 3 (1994): 349–54. http://dx.doi.org/10.1007/bf02344263.

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17

Laurent, Jon M., Sudarshan Pinglay, Leslie Mitchell, and Ran Brosh. "Probing the dark matter of the human genome with big DNA." Biochemist 41, no. 3 (2019): 46–48. http://dx.doi.org/10.1042/bio04103046.

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Less than 2% of our genome is protein-coding DNA. The vast expanses of non-coding DNA make up the genome's “dark matter”, where introns, repetitive and regulatory elements reside. Variation between individuals in non-coding regulatory DNA is emerging as a major factor in the genetics of numerous diseases and traits, yet very little is known about how such variations contribute to disease risk. Studying the genetics of regulatory variation is technically challenging as regulatory elements can affect genes located tens of thousands of base pairs away, and often, multiple distal regulatory variat

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18

Brower, A. V. Z., and T. M. Boyce. "Mitochondrial DNA Variation in Monarch Butterflies." Evolution 45, no. 5 (1991): 1281. http://dx.doi.org/10.2307/2409734.

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19

WILLIAMS, CHRISTEN LENNEY, BARBARA LUNDRIGAN, and OLIN E. RHODES. "MICROSATELLITE DNA VARIATION IN TULE ELK." Journal of Wildlife Management 68, no. 1 (2004): 109–19. http://dx.doi.org/10.2193/0022-541x(2004)068[0109:mdvite]2.0.co;2.

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20

Iezzoni, A. F., and A. M. Hancock. "CHLOROPLAST DNA VARIATION IN SOUR CHERRY." Acta Horticulturae, no. 410 (November 1996): 115–20. http://dx.doi.org/10.17660/actahortic.1996.410.17.

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21

Soltis, Douglas E., Pamela S. Soltis, John N. Thompson, and Olle Pellmyr. "Chloroplast DNA Variation in Lithophragma (Saxifragaceae)." Systematic Botany 17, no. 4 (1992): 607. http://dx.doi.org/10.2307/2419730.

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22

Antonova, Olga U., and Tatyana A. Gavrilenko. "Organelle DNA variation in potato species." Ecological genetics 4, no. 1 (2006): 3–10. http://dx.doi.org/10.17816/ecogen413-10.

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The genetic diversity of 34 species of the genus Solanum was studied using chloroplast (cp) DNA and mitochondrial (mt) DNA specific PCR primers. 11 cpDNA haplotypes and 16 mtDNA haplotypes were discovered. Traditional botanical taxonomy of potato species was not supported by cpDNA data. Cladistic relationships of 34 species support their geographical and genome differentiation. A derived clades contains E-, B- and A-genome species of the section Petota suggesting a coevolution of chloroplast and nuclear genomes.

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23

Palmer, Jeffrey D., Robert K. Jansen, Helen J. Michaels, Mark W. Chase, and James R. Manhart. "Chloroplast DNA Variation and Plant Phylogeny." Annals of the Missouri Botanical Garden 75, no. 4 (1988): 1180. http://dx.doi.org/10.2307/2399279.

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24

Price, H. James. "DNA Content Variation among Higher Plants." Annals of the Missouri Botanical Garden 75, no. 4 (1988): 1248. http://dx.doi.org/10.2307/2399283.

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25

Poggio, Lidia, and Juan H. Hunziker. "Nuclear DNA content variation in Bulnesia." Journal of Heredity 77, no. 1 (1986): 43–48. http://dx.doi.org/10.1093/oxfordjournals.jhered.a110165.

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26

Moriyama, E. N., and J. R. Powell. "Intraspecific nuclear DNA variation in Drosophila." Molecular Biology and Evolution 13, no. 1 (1996): 261–77. http://dx.doi.org/10.1093/oxfordjournals.molbev.a025563.

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27

Chen, W. K., J. D. Swartz, L. J. Rush, and C. E. Alvarez. "Mapping DNA structural variation in dogs." Genome Research 19, no. 3 (2008): 500–509. http://dx.doi.org/10.1101/gr.083741.108.

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28

BENTLEY, D. R. "DNA Sequence Variation of Homo sapiens." Cold Spring Harbor Symposia on Quantitative Biology 68 (January 1, 2003): 55–64. http://dx.doi.org/10.1101/sqb.2003.68.55.

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29

Ricaut, F. X., T. Thomas, C. Arganini, et al. "Mitochondrial DNA Variation in Karkar Islanders." Annals of Human Genetics 72, no. 3 (2008): 349–67. http://dx.doi.org/10.1111/j.1469-1809.2008.00430.x.

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30

Ravi Prasad, B. V., Chris E. Ricker, W. Scott Atkins, et al. "Mitochondrial DNA Variation in Nicobarese Islanders." Human Biology 73, no. 5 (2001): 715–25. http://dx.doi.org/10.1353/hub.2001.0072.

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31

Kouvatsi, Anastasia, Nikoletta Karaiskou, Apostolos Apostolidis, and George Kirmizidis. "Mitochondrial DNA Sequence Variation in Greeks." Human Biology 73, no. 6 (2001): 855–69. http://dx.doi.org/10.1353/hub.2001.0085.

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32

Mancuso, Michelangelo, Massimiliano Filosto, Daniele Orsucci, and Gabriele Siciliano. "Mitochondrial DNA sequence variation and neurodegeneration." Human Genomics 3, no. 1 (2008): 71. http://dx.doi.org/10.1186/1479-7364-3-1-71.

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33

Cullis, C. A., and W. Cleary. "DNA variation in flax tissue culture." Canadian Journal of Genetics and Cytology 28, no. 2 (1986): 247–51. http://dx.doi.org/10.1139/g86-034.

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The DNAs from leaves and callus from a series of flax genotrophs have been compared. The probes used for this comparison represent all of the highly repeated DNA sequence families in the flax genome. The abundance of most of the families could vary in culture, but the extent of variation was dependent on the genotroph. The extent of the variation observed between leaf DNA and callus DNA from a single genotroph was greater than that observed between the genotrophs in vivo. The DNAs from the progeny of a number of regenerated plants were also compared. They sometimes differed both from the callu

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34

Samuel, Rosabelle, J. B. Smith, and M. D. Bennett. "Nuclear DNA variation in Piper (Piperaceae)." Canadian Journal of Genetics and Cytology 28, no. 6 (1986): 1041–43. http://dx.doi.org/10.1139/g86-145.

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Significant interspecific variation in DNA amount was observed among nine species of Piper. The DNA amount of a wild octoploid accession of Piper nigrum was approximately double that of the cultivated tetraploid variety of the same species. However, three New World diploid species had higher nuclear DNA amounts than several New or Old World tetraploid species. The DNA content per basic genome was, on the whole, lower in cultivated than in wild species.Key words: Piperaceae, Piper, Piper nigrum (black pepper), polyploids, DNA amounts.

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35

Jianxun, Cui, Ren Xiuhai, and Yu Qixing. "Nuclear DNA Content Variation in Fishes." CYTOLOGIA 56, no. 3 (1991): 425–29. http://dx.doi.org/10.1508/cytologia.56.425.

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36

Underhill, Peter A. "Browsing DNA cipherspace for sequence variation." Trends in Genetics 13, no. 1 (1997): 9–10. http://dx.doi.org/10.1016/s0168-9525(96)30115-7.

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37

White, Matthew M. "Mitochondrial DNA Sequence Variation in Saugers." Transactions of the American Fisheries Society 141, no. 3 (2012): 795–801. http://dx.doi.org/10.1080/00028487.2012.675921.

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38

Maruszak, Aleksandra, Krzysztof Safranow, Katarzyna Gawęda-Walerych, et al. "Mitochondrial DNA variation in Alzheimer’s disease." Pharmacological Reports 63, no. 5 (2011): 1278. http://dx.doi.org/10.1016/s1734-1140(11)70662-4.

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39

Qamar, Raheel, Qasim Ayub, Aisha Mohyuddin, et al. "Y-Chromosomal DNA Variation in Pakistan." American Journal of Human Genetics 70, no. 5 (2002): 1107–24. http://dx.doi.org/10.1086/339929.

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40

Yamada, Kyoji, Teiichi Morita, Kyojiro Masuda, and Michizo Sugai. "Chloroplast DNA Variation in the genusSesamum." Journal of Plant Research 106, no. 1 (1993): 81–87. http://dx.doi.org/10.1007/bf02344377.

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41

Silva Jr., Wilson A., Sandro L. Bonatto, Adriano J. Holanda, et al. "Correction: Mitochondrial DNA Variation in Amerindians." American Journal of Human Genetics 72, no. 5 (2003): 1346–48. http://dx.doi.org/10.1086/375118.

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42

Brower, A. V. Z., and T. M. Boyce. "MITOCHONDRIAL DNA VARIATION IN MONARCH BUTTERFLIES." Evolution 45, no. 5 (1991): 1281–86. http://dx.doi.org/10.1111/j.1558-5646.1991.tb04393.x.

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43

Hovig, Eivind, Birgitte Smith-S??rensen, Andr?? G. Uitterlinden, and Anne-Lise B??rresen. "Detection of DNA variation in cancer." Pharmacogenetics 2, no. 6 (1992): 317–28. http://dx.doi.org/10.1097/00008571-199212000-00011.

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44

Boscaiu, Monica, Philippe Ellul, Pilar Soriano, and Oscar Vicente. "Nuclear DNA content variation inHalimiumandXolantha(Cistaceae)." Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology 142, no. 1 (2008): 17–23. http://dx.doi.org/10.1080/11263500701872143.

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45

Halldén, C., C. Lind, and T. Bryngelsson. "Minicircle variation in Beta mitochondrial DNA." Theoretical and Applied Genetics 77, no. 3 (1989): 337–42. http://dx.doi.org/10.1007/bf00305825.

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46

Ohgane, Jun, Teruhiko Wakayama, Yasushi Kogo, et al. "DNA methylation variation in cloned mice." genesis 30, no. 2 (2001): 45–50. http://dx.doi.org/10.1002/gene.1031.

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47

Moriyama, E.N., and J.R. Powell. "Intraspecific Nuclear DNA Variation in Drosophila." Molecular Biology and Evolution 13 (June 5, 1996): 261–77. https://doi.org/10.5281/zenodo.10759357.

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48

Liu, Chao, Mingbo Wang, Lingli Wang, Qigao Guo, and Guolu Liang. "Extensive genetic and DNA methylation variation contribute to heterosis in triploid loquat hybrids." Genome 61, no. 6 (2018): 437–47. http://dx.doi.org/10.1139/gen-2017-0232.

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We aim to overcome the unclear origin of the loquat and elucidate the heterosis mechanism of the triploid loquat. Here we investigated the genetic and epigenetic variations between the triploid plant and its parental lines using amplified fragment length polymorphism (AFLP) and methylation-sensitive amplified fragment length polymorphism (MSAP) analyses. We show that in addition to genetic variations, extensive DNA methylation variation occurred during the formation process of triploid loquat, with the triploid hybrid having increased DNA methylation compared to the parents. Furthermore, a cor

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49

Czerneková, V., T. Kott, and I. Majzlík. "Mitochondrial D-loop sequence variation among Hucul horse." Czech Journal of Animal Science 58, No. 10 (2013): 437–42. http://dx.doi.org/10.17221/6992-cjas.

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Genetic variation in the Czech Hucul horse population was analyzed using a sequence analysis of the D-loop region of mitochondrial DNA. One hundred and sixty-five Hucul horses were tested. Sequencing of the 700-base pairs fragment of the mitochondrial DNA D-loop region revealed 38 mutation sites representing 14 haplotypes, which were clustered into six haplogroups. The genetic information obtained from the mitochondrial DNA typing is of utmost importance for the future breed-conservation strategies. &nbsp;

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50

Palmer, Jeffrey D. "Chloroplast DNA Evolution and Biosystematic Uses of Chloroplast DNA Variation." American Naturalist 130 (July 1987): S6—S29. http://dx.doi.org/10.1086/284689.

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