Artículos de revistas sobre el tema "MtDNA segregation"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "MtDNA segregation".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Takeda, Kumiko, Seiya Takahashi, Akira Onishi, Hirofumi Hanada y Hiroshi Imai. "Replicative Advantage and Tissue-Specific Segregation of RR Mitochondrial DNA Between C57BL/6 and RR Heteroplasmic Mice". Genetics 155, n.º 2 (1 de junio de 2000): 777–83. http://dx.doi.org/10.1093/genetics/155.2.777.
Texto completoLechuga-Vieco, Ana Victoria, Ana Latorre-Pellicer, Iain G. Johnston, Gennaro Prota, Uzi Gileadi, Raquel Justo-Méndez, Rebeca Acín-Pérez et al. "Cell identity and nucleo-mitochondrial genetic context modulate OXPHOS performance and determine somatic heteroplasmy dynamics". Science Advances 6, n.º 31 (julio de 2020): eaba5345. http://dx.doi.org/10.1126/sciadv.aba5345.
Texto completoRøyrvik, Ellen C. y Iain G. Johnston. "MtDNA sequence features associated with ‘selfish genomes’ predict tissue-specific segregation and reversion". Nucleic Acids Research 48, n.º 15 (27 de julio de 2020): 8290–301. http://dx.doi.org/10.1093/nar/gkaa622.
Texto completoTsang, William Y. y Bernard D. Lemire. "Stable heteroplasmy but differential inheritance of a large mitochondrial DNA deletion in nematodes". Biochemistry and Cell Biology 80, n.º 5 (1 de octubre de 2002): 645–54. http://dx.doi.org/10.1139/o02-135.
Texto completoLing, Feng, Rong Niu, Hideyuki Hatakeyama, Yu-ichi Goto, Takehiko Shibata y Minoru Yoshida. "Reactive oxygen species stimulate mitochondrial allele segregation toward homoplasmy in human cells". Molecular Biology of the Cell 27, n.º 10 (15 de mayo de 2016): 1684–93. http://dx.doi.org/10.1091/mbc.e15-10-0690.
Texto completoZelenaya-Troitskaya, Olga, Scott M. Newman, Koji Okamoto, Philip S. Perlman y Ronald A. Butow. "Functions of the High Mobility Group Protein, Abf2p, in Mitochondrial DNA Segregation, Recombination and Copy Number in Saccharomyces cerevisiae". Genetics 148, n.º 4 (1 de abril de 1998): 1763–76. http://dx.doi.org/10.1093/genetics/148.4.1763.
Texto completoOkamoto, Koji, Philip S. Perlman y Ronald A. Butow. "The Sorting of Mitochondrial DNA and Mitochondrial Proteins in Zygotes: Preferential Transmission of Mitochondrial DNA to the Medial Bud". Journal of Cell Biology 142, n.º 3 (10 de agosto de 1998): 613–23. http://dx.doi.org/10.1083/jcb.142.3.613.
Texto completoMeirelles, Flávio V. y Lawrence C. Smith. "Mitochondrial Genotype Segregation in a Mouse Heteroplasmic Lineage Produced by Embryonic Karyoplast Transplantation". Genetics 145, n.º 2 (1 de febrero de 1997): 445–51. http://dx.doi.org/10.1093/genetics/145.2.445.
Texto completoClark, A. G. y E. M. Lyckegaard. "Natural selection with nuclear and cytoplasmic transmission. III. Joint analysis of segregation and mtDNA in Drosophila melanogaster." Genetics 118, n.º 3 (1 de marzo de 1988): 471–81. http://dx.doi.org/10.1093/genetics/118.3.471.
Texto completoSmith, Lawrence C., Jacob Thundathil y France Filion. "Role of the mitochondrial genome in preimplantation development and assisted reproductive technologies". Reproduction, Fertility and Development 17, n.º 2 (2005): 15. http://dx.doi.org/10.1071/rd04084.
Texto completoMeeusen, Shelly, Quinton Tieu, Edith Wong, Eric Weiss, David Schieltz, John R. Yates y Jodi Nunnari. "Mgm101p Is a Novel Component of the Mitochondrial Nucleoid That Binds DNA and Is Required for the Repair of Oxidatively Damaged Mitochondrial DNA". Journal of Cell Biology 145, n.º 2 (19 de abril de 1999): 291–304. http://dx.doi.org/10.1083/jcb.145.2.291.
Texto completoLing, Feng y Takehiko Shibata. "Mhr1p-dependent Concatemeric Mitochondrial DNA Formation for Generating Yeast Mitochondrial Homoplasmic Cells". Molecular Biology of the Cell 15, n.º 1 (enero de 2004): 310–22. http://dx.doi.org/10.1091/mbc.e03-07-0508.
Texto completoGoffart, Steffi, Anu Hangas y Jaakko L. O. Pohjoismäki. "Twist and Turn—Topoisomerase Functions in Mitochondrial DNA Maintenance". International Journal of Molecular Sciences 20, n.º 8 (25 de abril de 2019): 2041. http://dx.doi.org/10.3390/ijms20082041.
Texto completoLuo, Shiyu, C. Alexander Valencia, Jinglan Zhang, Ni-Chung Lee, Jesse Slone, Baoheng Gui, Xinjian Wang et al. "Biparental Inheritance of Mitochondrial DNA in Humans". Proceedings of the National Academy of Sciences 115, n.º 51 (26 de noviembre de 2018): 13039–44. http://dx.doi.org/10.1073/pnas.1810946115.
Texto completoCao, Liqin, Ellen Kenchington y Eleftherios Zouros. "Differential Segregation Patterns of Sperm Mitochondria in Embryos of the Blue Mussel (Mytilus edulis)". Genetics 166, n.º 2 (1 de febrero de 2004): 883–94. http://dx.doi.org/10.1093/genetics/166.2.883.
Texto completoMoreira, Jesse D., Deepa M. Gopal, Darrell N. Kotton y Jessica L. Fetterman. "Gaining Insight into Mitochondrial Genetic Variation and Downstream Pathophysiology: What Can i(PSCs) Do?" Genes 12, n.º 11 (22 de octubre de 2021): 1668. http://dx.doi.org/10.3390/genes12111668.
Texto completoChomyn, A., G. Meola, N. Bresolin, S. T. Lai, G. Scarlato y G. Attardi. "In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria". Molecular and Cellular Biology 11, n.º 4 (abril de 1991): 2236–44. http://dx.doi.org/10.1128/mcb.11.4.2236-2244.1991.
Texto completoChomyn, A., G. Meola, N. Bresolin, S. T. Lai, G. Scarlato y G. Attardi. "In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria." Molecular and Cellular Biology 11, n.º 4 (abril de 1991): 2236–44. http://dx.doi.org/10.1128/mcb.11.4.2236.
Texto completoVachin, Pauline, Elodie Adda-Herzog, Gihad Chalouhi, Caroline Elie, Marlène Rio, Sophie Rondeau, Nadine Gigarel et al. "Segregation of mitochondrial DNA mutations in the human placenta: implication for prenatal diagnosis of mtDNA disorders". Journal of Medical Genetics 55, n.º 2 (28 de julio de 2017): 131–36. http://dx.doi.org/10.1136/jmedgenet-2017-104615.
Texto completoShitara, Hiroshi, Jun-Ichi Hayashi, Sumiyo Takahama, Hideki Kaneda y Hiromichi Yonekawa. "Maternal Inheritance of Mouse mtDNA in Interspecific Hybrids: Segregation of the Leaked Paternal mtDNA Followed by the Prevention of Subsequent Paternal Leakage". Genetics 148, n.º 2 (1 de febrero de 1998): 851–57. http://dx.doi.org/10.1093/genetics/148.2.851.
Texto completoYamada, Mitsutoshi, Kazuhiro Akashi, Reina Ooka, Kenji Miyado y Hidenori Akutsu. "Mitochondrial Genetic Drift after Nuclear Transfer in Oocytes". International Journal of Molecular Sciences 21, n.º 16 (16 de agosto de 2020): 5880. http://dx.doi.org/10.3390/ijms21165880.
Texto completoCupini, L. M., R. Massa, R. Floris, G. Manenti, B. Martini, A. Tessa, G. Nappi, G. Bernardi y F. M. Santorelli. "Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation". Neurology 60, n.º 4 (25 de febrero de 2003): 717–19. http://dx.doi.org/10.1212/01.wnl.0000048662.77572.fb.
Texto completoPickrell, Alicia M. y Richard J. Youle. "Mitochondrial Disease: mtDNA and Protein Segregation Mysteries in iPSCs". Current Biology 23, n.º 23 (diciembre de 2013): R1052—R1054. http://dx.doi.org/10.1016/j.cub.2013.10.048.
Texto completoBoldogh, Istvan R., Dan W. Nowakowski, Hyeong-Cheol Yang, Haesung Chung, Sharon Karmon, Patrina Royes y Liza A. Pon. "A Protein Complex Containing Mdm10p, Mdm12p, and Mmm1p Links Mitochondrial Membranes and DNA to the Cytoskeleton-based Segregation Machinery". Molecular Biology of the Cell 14, n.º 11 (noviembre de 2003): 4618–27. http://dx.doi.org/10.1091/mbc.e03-04-0225.
Texto completoBastiaans, E., D. K. Aanen, A. J. M. Debets, R. F. Hoekstra, B. Lestrade y M. F. P. M. Maas. "Regular bottlenecks and restrictions to somatic fusion prevent the accumulation of mitochondrial defects in Neurospora". Philosophical Transactions of the Royal Society B: Biological Sciences 369, n.º 1646 (5 de julio de 2014): 20130448. http://dx.doi.org/10.1098/rstb.2013.0448.
Texto completoLehtinen, Sanna K., Nicole Hance, Abdellatif El Meziane, M. Katariina Juhola, K. Martti I. Juhola, Ritva Karhu, Johannes N. Spelbrink, Ian J. Holt y Howard T. Jacobs. "Genotypic Stability, Segregation and Selection in Heteroplasmic Human Cell Lines Containing np 3243 Mutant mtDNA". Genetics 154, n.º 1 (1 de enero de 2000): 363–80. http://dx.doi.org/10.1093/genetics/154.1.363.
Texto completoVozáriková, Veronika, Nina Kunová, Jacob A. Bauer, Ján Frankovský, Veronika Kotrasová, Katarína Procházková, Vladimíra Džugasová et al. "Mitochondrial HMG-Box Containing Proteins: From Biochemical Properties to the Roles in Human Diseases". Biomolecules 10, n.º 8 (16 de agosto de 2020): 1193. http://dx.doi.org/10.3390/biom10081193.
Texto completoLing, Feng, Akiko Hori y Takehiko Shibata. "DNA Recombination-Initiation Plays a Role in the Extremely Biased Inheritance of Yeast [rho−] Mitochondrial DNA That Contains the Replication Origin ori5". Molecular and Cellular Biology 27, n.º 3 (20 de noviembre de 2006): 1133–45. http://dx.doi.org/10.1128/mcb.00770-06.
Texto completoSatta, Yoko, Nobue Toyohara, Chiaki Ohtaka, Yumi Tatsuno, Takao K. Watanabe, Etsuko T. Matsuura, Sadao I. Chigusa y Naoyuki Takahata. "Dubious maternal inheritance of mitochondrial DNA in D. simulans and evolution of D. mauritiana". Genetical Research 52, n.º 1 (agosto de 1988): 1–6. http://dx.doi.org/10.1017/s0016672300027245.
Texto completoKauppila, Timo E. S., Ana Bratic, Martin Borch Jensen, Francesca Baggio, Linda Partridge, Heinrich Jasper, Sebastian Grönke y Nils-Göran Larsson. "Mutations of mitochondrial DNA are not major contributors to aging of fruit flies". Proceedings of the National Academy of Sciences 115, n.º 41 (24 de septiembre de 2018): E9620—E9629. http://dx.doi.org/10.1073/pnas.1721683115.
Texto completoKaufman, Brett A., Nela Durisic, Jeffrey M. Mativetsky, Santiago Costantino, Mark A. Hancock, Peter Grutter y Eric A. Shoubridge. "The Mitochondrial Transcription Factor TFAM Coordinates the Assembly of Multiple DNA Molecules into Nucleoid-like Structures". Molecular Biology of the Cell 18, n.º 9 (septiembre de 2007): 3225–36. http://dx.doi.org/10.1091/mbc.e07-05-0404.
Texto completoViramontes, F., F. Filion y L. C. Smith. "5 NEUTRAL SEGREGATION OF DONOR CELL MITOCHONDRIA IN FETAL AND ADULT TISSUES OF SOMATIC CELL CLONES IN CATTLE". Reproduction, Fertility and Development 17, n.º 2 (2005): 153. http://dx.doi.org/10.1071/rdv17n2ab5.
Texto completoBattersby, Brendan J. y Eric A. Shoubridge. "Reactive oxygen species and the segregation of mtDNA sequence variants". Nature Genetics 39, n.º 5 (mayo de 2007): 571–72. http://dx.doi.org/10.1038/ng0507-571.
Texto completoKurtz, Andreas, Maria Lueth, Lan Kluwe, Tingguo Zhang, Rosemary Foster, Victor-Felix Mautner, Melanie Hartmann et al. "Somatic Mitochondrial DNA Mutations in Neurofibromatosis Type 1-Associated Tumors". Molecular Cancer Research 2, n.º 8 (1 de agosto de 2004): 433–41. http://dx.doi.org/10.1158/1541-7786.433.2.8.
Texto completoCieslak, Jakub, Lukasz Wodas, Alicja Borowska, Ernest G. Cothran, Anas M. Khanshour y Mariusz Mackowski. "Characterization of the Polish Primitive Horse (Konik) maternal lines using mitochondrial D-loop sequence variation". PeerJ 5 (24 de agosto de 2017): e3714. http://dx.doi.org/10.7717/peerj.3714.
Texto completoDiMauro, Salvatore. "A Brief History of Mitochondrial Pathologies". International Journal of Molecular Sciences 20, n.º 22 (12 de noviembre de 2019): 5643. http://dx.doi.org/10.3390/ijms20225643.
Texto completoAdel Hussein, Marwa, Ruaa Hameed Abdulridha, Ibtisam Jasim Sodan, Mais Adnan Al-Ward, May Ridha Jaafar, Hala Khalid Ibrahim Al-Sammarrie, Shahad Emad Neamah, Asmaa A. Jawad y Nadhum Hussen Safir. "Mitochondrial DNA and Disease: A review". Al-Nahrain Journal of Science 27, n.º 2 (1 de junio de 2024): 81–90. http://dx.doi.org/10.22401/anjs.27.2.08.
Texto completoPoulton, J. "Segregation of mitochondrial DNA (mtDNA) in human oocytes and in animal models of mtDNA disease: clinical implications". Reproduction 123, n.º 6 (1 de junio de 2002): 751–55. http://dx.doi.org/10.1530/reprod/123.6.751.
Texto completoYin, Tao, Jikun Wang, Hai Xiang, Carl A. Pinkert, Qiuyan Li y Xingbo Zhao. "Dynamic characteristics of the mitochondrial genome in SCNT pigs". Biological Chemistry 400, n.º 5 (27 de mayo de 2019): 613–23. http://dx.doi.org/10.1515/hsz-2018-0273.
Texto completoNunnari, J., W. F. Marshall, A. Straight, A. Murray, J. W. Sedat y P. Walter. "Mitochondrial transmission during mating in Saccharomyces cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mitochondrial DNA." Molecular Biology of the Cell 8, n.º 7 (julio de 1997): 1233–42. http://dx.doi.org/10.1091/mbc.8.7.1233.
Texto completoSaavedra, Carlos, Donald T. Stewart, Rebecca R. Stanwood y Eleftherios Zouros. "Species-Specific Segregation of Gender-Associated Mitochondrial DNA Types in an Area Where Two Mussel Species (Mytilus edulis and M. trossulus) Hybridize". Genetics 143, n.º 3 (1 de julio de 1996): 1359–67. http://dx.doi.org/10.1093/genetics/143.3.1359.
Texto completoNicholls, Thomas J., Cristina A. Nadalutti, Elisa Motori, Ewen W. Sommerville, Gráinne S. Gorman, Swaraj Basu, Emily Hoberg et al. "Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA". Molecular Cell 69, n.º 1 (enero de 2018): 9–23. http://dx.doi.org/10.1016/j.molcel.2017.11.033.
Texto completoJokinen⁎, Riikka, Paula Marttinen, Katarin Sandell, Tuula Manninen, Heli Teerenhovi, Timothy Wai, Daniella Teoli, J. C. Loredo-Osti, Eric A. Shoubridge y Brendan J. Battersby. "Cloning a novel mitochondrial protein which regulates tissue-specific mtDNA segregation". Mitochondrion 11, n.º 4 (julio de 2011): 641–42. http://dx.doi.org/10.1016/j.mito.2011.03.023.
Texto completoHowell, Neil, Soumitra S. Ghosh, Eoin Fahy y Laurence A. Bindoff. "Longitudinal analysis of the segregation of mtDNA mutations in heteroplasmic individuals". Journal of the Neurological Sciences 172, n.º 1 (enero de 2000): 1–6. http://dx.doi.org/10.1016/s0022-510x(99)00207-5.
Texto completoTesarova, M., H. Hansikova, J. Kytnarova, H. Houstkova, M. Bohm, L. Cerna, J. Zeman y J. Houstek. "Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G". Toxicology Mechanisms and Methods 14, n.º 1-2 (enero de 2004): 79–84. http://dx.doi.org/10.1080/15376520490257527.
Texto completoAretz, Ina, Christopher Jakubke y Christof Osman. "Power to the daughters – mitochondrial and mtDNA transmission during cell division". Biological Chemistry 401, n.º 5 (28 de abril de 2020): 533–46. http://dx.doi.org/10.1515/hsz-2019-0337.
Texto completoKustova, Maria E., Vasilina A. Sokolova, Oksana V. Kidgotko, Mikhail G. Bass, Faina M. Zakharova y Vadim B. Vasilyev. "Distribution of introduced human mitochondrial DNA in early stage mouse embryos". Medical academic journal 20, n.º 2 (2 de septiembre de 2020): 69–78. http://dx.doi.org/10.17816/maj34657.
Texto completoBlok, Rozanne B., Debra A. Gook, David R. Thorburn y Hans-Henrik M. Dahl. "Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes". American Journal of Human Genetics 60, n.º 6 (junio de 1997): 1495–501. http://dx.doi.org/10.1086/515453.
Texto completoCavelier, Lucia, Elena Jazin, Paula Jalonen y Ulf Gyllensten. "MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions". Human Genetics 107, n.º 1 (julio de 2000): 45–50. http://dx.doi.org/10.1007/s004390000305.
Texto completoCavelier, Lucia, Elena Jazin, Paula Jalonen y Ulf Gyllensten. "MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions". Human Genetics 107, n.º 1 (28 de julio de 2000): 45–50. http://dx.doi.org/10.1007/s004390050009.
Texto completo