Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Correction: Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancerPloS one, 2017-05, Vol.12 (5), p.e0178275-e0178275 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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2 |
Material Type: Artigo
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Correction: A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in JapanYoshida, Yoko ; Miyata, Toshiyuki ; Matsumoto, Masanori ; Shirotani-Ikejima, Hiroko ; Uchida, Yumiko ; Ohyama, Yoshifumi ; Kokubo, Tetsuro ; Fujimura, YoshihiroPloS one, 2017-05, Vol.12 (5), p.e0178015-e0178015 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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3 |
Material Type: Artigo
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Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital CataractZhu, Yanan ; Yu, Hao ; Wang, Wei ; Gong, Xiaohua ; Yao, KePloS one, 2015-05, Vol.10 (5), p.e0125949-e0125949 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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4 |
Material Type: Artigo
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Correction: Species-Specific Codon Context Rules Unveil Non-Neutrality Effects of Synonymous MutationsMoura, Gabriela R ; Pinheiro, Miguel ; Freitas, Adelaide ; Oliveira, José L ; Frommlet, Jörg C ; Carreto, Laura ; Soares, Ana R ; Bezerra, Ana R ; Santos, Manuel A SPloS one, 2015-12, Vol.10 (12), p.e0145593-e0145593 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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5 |
Material Type: Artigo
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Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese FamilyGao, Xue ; Wang, Guo-Jian ; Yuan, Yong-Yi ; Xin, Feng ; Han, Ming-Yu ; Lu, Jing-Qiao ; Zhao, Hui ; Yu, Fei ; Xu, Jin-Cao ; Zhang, Mei-Guang ; Dong, Jiang ; Lin, Xi ; Dai, PuPloS one, 2015-10, Vol.10 (10), p.e0137883-e0137883 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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6 |
Material Type: Artigo
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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulationSasani, Thomas A ; Pedersen, Brent S ; Gao, Ziyue ; Baird, Lisa ; Przeworski, Molly ; Jorde, Lynn B ; Quinlan, Aaron ReLife, 2019-09, Vol.8 [Periódico revisado por pares]England: eLife Sciences Publications LtdTexto completo disponível |
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7 |
Material Type: Artigo
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Genome-wide DNA mutations in Arabidopsis plants after multigenerational exposure to high temperaturesLu, Zhaogeng ; Cui, Jiawen ; Wang, Li ; Teng, Nianjun ; Zhang, Shoudong ; Lam, Hon-Ming ; Zhu, Yingfang ; Xiao, Siwei ; Ke, Wensi ; Lin, Jinxing ; Xu, Chenwu ; Jin, BiaoGenome Biology, 2021-05, Vol.22 (1), p.160-160, Article 160 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Correction: Mutation rules and the evolution of sparseness and modularity in biological systemsPloS one, 2015-03, Vol.10 (3), p.e0118129-e0118129 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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9 |
Material Type: Artigo
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Correction: Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutationLee, Jung Seok ; Kang, Chul-hoo ; Park, Sukh Que ; Choi, H Alex ; Sim, Ki-BumPloS one, 2015-04, Vol.10 (4), p.e0125297-e0125297 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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10 |
Material Type: Artigo
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Correction: PDCD10 gene mutations in multiple cerebral cavernous malformationsPloS one, 2015-04, Vol.10 (4), p.e0123486-e0123486 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |