コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ey have focused on the frequency of a single mitochondrial DNA deletion.
2 ect repeats flank two-thirds of the reported mitochondrial DNA deletions.
3 nal ophthalmoplegia associated with multiple mitochondrial DNA deletions.
4 Seventy-eight patients (67%) had a single mitochondrial DNA deletion, 12 (10%) had a point mutatio
5 ignificantly lower in patients with a single mitochondrial DNA deletion (2%) as compared to those wit
6 confounded by any age-dependent increases in mitochondrial DNA deletions also detected by the long po
7 the respiratory chain defects, secondary to mitochondrial DNA deletion and depletion, are likely to
8 complexes I and IV due to clonally-expanded mitochondrial DNA deletions and a significant reduction
10 nuclear DNA defects and single, large-scale mitochondrial DNA deletions and is less frequently assoc
11 d an additional, progressive accumulation of mitochondrial DNA deletions and point mutations accompan
13 sma thiobarbituric acid-reactive substances, mitochondrial DNA deletions, and renal expression of fib
15 ALAS2) gene cause microcytic anemia, whereas mitochondrial DNA deletions are responsible for Pearsons
16 pathway may play a role in the generation of mitochondrial DNA deletions associated with a number of
18 hy is a rare finding in patients with single mitochondrial DNA deletions but that it is highly predic
19 tochrome-c oxidase-deficient fibers revealed mitochondrial DNA deletions, consistent with damage from
20 spiration-deficient cells (rho(-)) harboring mitochondrial DNA deletion exhibit dependency on glycoly
22 source in vitro can induce the formation of mitochondrial DNA deletions in a PCR detection assay.
23 sent the third most common cause of multiple mitochondrial DNA deletions in adults, following POLG [p
24 ther POLG, C10orf2 or RRM2B, or had multiple mitochondrial DNA deletions in muscle without an identif
27 ve addressed the question of the spectrum of mitochondrial DNA deletions in skin and whether this can
28 rome c oxidase-deficient fibres and multiple mitochondrial DNA deletions in the majority of patients
29 hrome c oxidase-negative fibres and multiple mitochondrial DNA deletions in the muscle of patients wi
30 h increased mitochondrial protein carbonyls, mitochondrial DNA deletions, increased autophagy and sig
31 eurons show increased mitochondrial defects, mitochondrial DNA deletion levels, and susceptibility to
32 mental mitochondrial abnormalities contained mitochondrial DNA deletion mutations as revealed by lase
35 G), which leads to the formation of multiple mitochondrial DNA deletions over time, similar to aging
36 is, glomerular basement membrane thickening, mitochondrial DNA deletions, reduction of nerve conducti
37 se chain reaction technique to determine the mitochondrial DNA deletion spectrum of almost the entire
38 Nonchromosomal stripe (NCS) mutants carry mitochondrial DNA deletions that affect subunits of resp
39 hort of 87 patients with single, large-scale mitochondrial DNA deletions we demonstrate that a variet
42 nal ophthalmoplegia associated with multiple mitochondrial DNA deletions, whereas recessive SLC25A4 m
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。