Pesquisas alternativas:
combs » comes (Expandir a Pesquisa)
nucl » null (Expandir a Pesquisa)
nino » nine (Expandir a Pesquisa), ning (Expandir a Pesquisa), nina (Expandir a Pesquisa)
nara » nar (Expandir a Pesquisa), nada (Expandir a Pesquisa), naa (Expandir a Pesquisa)
combs » comes (Expandir a Pesquisa)
nucl » null (Expandir a Pesquisa)
nino » nine (Expandir a Pesquisa), ning (Expandir a Pesquisa), nina (Expandir a Pesquisa)
nara » nar (Expandir a Pesquisa), nada (Expandir a Pesquisa), naa (Expandir a Pesquisa)
81
Por Blok, M J, Spruijt, L, de Coo, I F M, Schoonderwoerd, K, Hendrickx, A, Smeets, H J
Publicado em 2007
“... in 15 patients, 5 of which were present in the ND5 gene. One sequence variant was new and three were...”Publicado em 2007
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82
Por Franco, Tathyana Mar Amorim, Favrot, Lorenza, Vergnolle, Olivia, Blanchard, John S.
Publicado no ACS Chem Biol (2017)
“...-PMP complex can be fit to a single exponential, the formation of the MtIlvE L-cycloserine-PMP complex...”Publicado no ACS Chem Biol (2017)
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83
“..., L-tryptophan, to form an active repressor complex. The side chain of residue valine 58 of Trp...”
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84
“... by the m5C MT, while simultaneously inducing methylation by the m2G MT. A purified complex containing...”
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85
Por Papanikolaou, Amalia, Keliris, Georgios A., Papageorgiou, T. Dorina, Schiefer, Ulrich, Logothetis, Nikos K., Smirnakis, Stelios M.
Publicado no Neuroimage (2018)
“... temporal area complex (V5/MT+). However, it remains unknown whether the organization of hV5/MT+ changes...”Publicado no Neuroimage (2018)
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86
Por Patowary, Ashok, Nesbitt, Ryan, Archer, Marilyn, Bernier, Raphael, Brkanac, Zoran
Publicado no Autism Res (2017)
“...Autism is a complex genetic disorder where both de‐novo and inherited genetics factors play a role...”Publicado no Autism Res (2017)
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87
Por Coskun, Pinar, Wyrembak, Joanne, Schriner, Sam, Chen, Hsiao-Wen, Marciniack, Christine, LaFerla, Frank, Wallace, Douglas C.
Publicado em 2011
“..., and mitochondrial DNA (mtDNA) integrity. mtDNA lineages, haplogroups, such haplogroup H5a which harbors the mt...”Publicado em 2011
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88
“... in immune complexes (B.S. Schaffhausen and T.L. Benjamin, J. Virol. 40:184-196, 1981). Here we report...”
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89
“.... RESULTS: We show here that MtN5 is a NF-responsive gene expressed at a very early phase of symbiosis...”
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90
“... mtDNA mutations have the capacity to cause a variety of aging phenotypes in mammals, and they do so...”
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91
“... genome, except that the mutant genome contains a fused nad4-nad7 gene and is deleted for the small fourth...”
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92
Por Kumar, Manoj, Kaur, Punit, Kumar, Manoj, Saxena, Rohit, Sharma, Pradeep, Dada, Rima
Publicado em 2012
“...), followed by complex III (19.14%; 9/47), then complex IV (19.14%; 9/47), then complex V (8.5%; 4/47...”Publicado em 2012
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93
“...Mitochondrial DNA (mtDNA) is inherited as a protein–DNA complex (the nucleoid). We show...”
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94
Por Saenz, Melissa, Lewis, Lindsay B., Huth, Alexander G., Fine, Ione, Koch, Christof
Publicado em 2008
“...Using functional magnetic resonance imaging, we found that cortical visual motion area MT+/V5...”Publicado em 2008
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95
Por Karnaouri, Anthi, Matsakas, Leonidas, Topakas, Evangelos, Rova, Ulrika, Christakopoulos, Paul
Publicado no Front Microbiol (2016)
“... widely proven. In this study, four core cellulases (MtCBH7, MtCBH6, MtEG5, and MtEG7), in the presence...”Publicado no Front Microbiol (2016)
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96
Por Wong, L‐J C, Yim, D, Bai, R‐K, Kwon, H, Vacek, M M, Zane, J, Hoppel, C L, Kerr, D S
Publicado em 2006
“..., which were then identified by direct DNA sequencing. RESULTS: A novel heteroplasmic mtDNA mutation, G...”Publicado em 2006
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97
Por Metodiev, Metodi D., Thompson, Kyle, Alston, Charlotte L., Morris, Andrew A.M., He, Langping, Assouline, Zarah, Rio, Marlène, Bahi-Buisson, Nadia, Pyle, Angela, Griffin, Helen, Siira, Stefan, Filipovska, Aleksandra, Munnich, Arnold, Chinnery, Patrick F., McFarland, Robert, Rötig, Agnès, Taylor, Robert W.
Publicado no Am J Hum Genet (2016)
“...2 and MRPP3, form the mitochondrial ribonuclease P (mt-RNase P) complex that cleaves the 5′ ends...”Publicado no Am J Hum Genet (2016)
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98
Por Fujimoto, Shigeyuki, Itsumura, Naoya, Tsuji, Tokuji, Anan, Yasumi, Tsuji, Natsuko, Ogra, Yasumitsu, Kimura, Tomoki, Miyamae, Yusaku, Masuda, Seiji, Nagao, Masaya, Kambe, Taiho
Publicado em 2013
“...-loading by the zinc transporter 5 (ZnT5)-ZnT6 hetero-complex and ZnT7 homo-complex (zinc transport...”Publicado em 2013
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99
“... doubled in MT+/+ mice and increased by a significant 15% in MT-/- mice. There was no increase in hepatic...”
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100
Por Piotrowska-Nowak, Agnieszka, Elson, Joanna L., Sobczyk-Kopciol, Agnieszka, Piwonska, Aleksandra, Puch-Walczak, Aleksandra, Drygas, Wojciech, Ploski, Rafal, Bartnik, Ewa, Tonska, Katarzyna
Publicado no Front Genet (2019)
“..., and environmental factors. A role for mitochondrial dysfunction and mitochondrial DNA (mtDNA) variation has been...”Publicado no Front Genet (2019)
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Artigo