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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-199 Sentence denotes Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
T1 0-199 Sentence denotes Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
TextSentencer_T2 200-527 Sentence denotes The mutation pattern of mitochondrial DNA (mtDNA) in mainland Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) has been rarely reported, though previous data suggested that the mutation pattern of MELAS could be different among geographically localized populations.
T2 200-527 Sentence denotes The mutation pattern of mitochondrial DNA (mtDNA) in mainland Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) has been rarely reported, though previous data suggested that the mutation pattern of MELAS could be different among geographically localized populations.
TextSentencer_T3 528-716 Sentence denotes We presented the results of comprehensive mtDNA mutation analysis in 92 unrelated Chinese patients with MELAS (85 with classic MELAS and 7 with MELAS/Leigh syndrome (LS) overlap syndrome).
T3 528-716 Sentence denotes We presented the results of comprehensive mtDNA mutation analysis in 92 unrelated Chinese patients with MELAS (85 with classic MELAS and 7 with MELAS/Leigh syndrome (LS) overlap syndrome).
TextSentencer_T4 717-819 Sentence denotes The mtDNA A3243G mutation was the most common causal genotype in this patient group (79/92 and 85.9%).
T4 717-819 Sentence denotes The mtDNA A3243G mutation was the most common causal genotype in this patient group (79/92 and 85.9%).
TextSentencer_T5 820-880 Sentence denotes The second common gene mutation was G13513A (7/92 and 7.6%).
T5 820-880 Sentence denotes The second common gene mutation was G13513A (7/92 and 7.6%).
TextSentencer_T6 881-945 Sentence denotes Additionally, we identified T10191C (p.S45P) in ND3, A11470C (p.
T6 881-945 Sentence denotes Additionally, we identified T10191C (p.S45P) in ND3, A11470C (p.
TextSentencer_T7 946-1111 Sentence denotes K237N) in ND4, T13046C (p.M237T) in ND5 and a large-scale deletion (13025-13033:14417-14425) involving partial ND5 and ND6 subunits of complex I in one patient each.
T7 946-1111 Sentence denotes K237N) in ND4, T13046C (p.M237T) in ND5 and a large-scale deletion (13025-13033:14417-14425) involving partial ND5 and ND6 subunits of complex I in one patient each.
TextSentencer_T8 1112-1186 Sentence denotes Among them, A11470C, T13046C and the single deletion were novel mutations.
T8 1112-1186 Sentence denotes Among them, A11470C, T13046C and the single deletion were novel mutations.
TextSentencer_T9 1187-1310 Sentence denotes In summary, patients with mutations affecting mitochondrially encoded complex I (MTND) reached 12.0% (11/92) in this group.
T9 1187-1310 Sentence denotes In summary, patients with mutations affecting mitochondrially encoded complex I (MTND) reached 12.0% (11/92) in this group.
TextSentencer_T10 1311-1419 Sentence denotes It is noteworthy that all seven patients with MELAS/LS overlap syndrome were associated with MTND mutations.
T10 1311-1419 Sentence denotes It is noteworthy that all seven patients with MELAS/LS overlap syndrome were associated with MTND mutations.
TextSentencer_T11 1420-1544 Sentence denotes Our data emphasize the important role of MTND mutations in the pathogenicity of MELAS, especially MELAS/LS overlap syndrome.
T11 1420-1544 Sentence denotes Our data emphasize the important role of MTND mutations in the pathogenicity of MELAS, especially MELAS/LS overlap syndrome.