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Similar articles for PubMed (Select 24708131)

1.

Screening of common point-mutations and discovery of new T14727C change in mitochondrial genome of Vietnamese encephalomyopathy patients.

Truong HT, Nguyen VA, Nguyen LV, Pham VA, Phan TN.

Mitochondrial DNA. 2014 Apr 8. [Epub ahead of print]

PMID:
24708131
2.

Mitochonic Acid 5 (MA-5), a Derivative of the Plant Hormone Indole-3-Acetic Acid, Improves Survival of Fibroblasts from Patients with Mitochondrial Diseases.

Suzuki T, Yamaguchi H, Kikusato M, Matsuhashi T, Matsuo A, Sato T, Oba Y, Watanabe S, Minaki D, Saigusa D, Shimbo H, Mori N, Mishima E, Shima H, Akiyama Y, Takeuchi Y, Yuri A, Kikuchi K, Toyohara T, Suzuki C, Kohzuki M, Anzai J, Mano N, Kure S, Yanagisawa T, Tomioka Y, Toyomizu M, Ito S, Osaka H, Hayashi K, Abe T.

Tohoku J Exp Med. 2015;236(3):225-32. doi: 10.1620/tjem.236.225.

3.

Oxidative stress in inherited mitochondrial diseases.

Hayashi G, Cortopassi G.

Free Radic Biol Med. 2015 Jun 11. pii: S0891-5849(15)00262-2. doi: 10.1016/j.freeradbiomed.2015.05.039. [Epub ahead of print] Review.

PMID:
26073122
4.

Screening of mitochondrial mutations and insertion-deletion polymorphism in gestational diabetes mellitus in the Asian Indian population.

Khan IA, Shaik NA, Pasupuleti N, Chava S, Jahan P, Hasan Q, Rao P.

Saudi J Biol Sci. 2015 May;22(3):243-8. doi: 10.1016/j.sjbs.2014.11.001. Epub 2014 Nov 12.

5.

[Diabetes and hearing impairment due to mitochondrial mutation.]

Lauterlein JJ, Olsen I, Yderstræde K, Nielsen MF.

Ugeskr Laeger. 2014 Sep 15;176(38). pii: V05130313. Danish.

PMID:
25294200
6.

Striking pathology in Leigh syndrome associated with the MTATP6 T8993G mutation.

Sinko G, Garzuly F, Kalman B.

Pediatr Neurol. 2014 Oct;51(4):585-6. doi: 10.1016/j.pediatrneurol.2014.07.015. Epub 2014 Jul 19. No abstract available.

PMID:
25152966
7.

Homoplasmy of a mitochondrial 3697G>A mutation causes Leigh syndrome.

Negishi Y, Hattori A, Takeshita E, Sakai C, Ando N, Ito T, Goto Y, Saitoh S.

J Hum Genet. 2014 Jul;59(7):405-7. doi: 10.1038/jhg.2014.41. Epub 2014 May 15.

PMID:
24830958
8.

The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.

Leng Y, Liu Y, Fang X, Li Y, Yu L, Yuan Y, Wang Z.

Mitochondrial DNA. 2015 Apr;26(2):208-12. doi: 10.3109/19401736.2014.905860. Epub 2014 Apr 8.

PMID:
24708134
9.

[Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].

Liu XL, Bao XH, Ma YN, Chang XZ, Qin J, Wu XR.

Zhonghua Er Ke Za Zhi. 2013 Feb;51(2):130-5. Chinese.

PMID:
23527980
10.

Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA.

Nakaso K, Adachi Y, Fusayasu E, Doi K, Imamura K, Yasui K, Nakashima K.

J Clin Neurol. 2012 Sep;8(3):230-4. doi: 10.3988/jcn.2012.8.3.230. Epub 2012 Sep 27.

11.

[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].

Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX.

Yi Chuan. 2012 Aug;34(8):1031-42. Chinese.

PMID:
22917908
12.

A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.

Vastagh I, Gál A, Reményi V, Semjén J, Lukács T, Valikovics A, Molnár MJ.

Ideggyogy Sz. 2011 Nov 30;64(11-12):399-403.

PMID:
22611618
13.

Mitochondrial gene therapy improves respiration, biogenesis, and transcription in G11778A Leber's hereditary optic neuropathy and T8993G Leigh's syndrome cells.

Iyer S, Bergquist K, Young K, Gnaiger E, Rao RR, Bennett JP Jr.

Hum Gene Ther. 2012 Jun;23(6):647-57. doi: 10.1089/hum.2011.177. Epub 2012 Apr 17.

14.

Analysis of common mitochondrial DNA mutations by allele-specific oligonucleotide and Southern blot hybridization.

Tang S, Halberg MC, Floyd KC, Wang J.

Methods Mol Biol. 2012;837:259-79. doi: 10.1007/978-1-61779-504-6_18.

PMID:
22215554
15.

Hypersensitivity of A8344G MERRF mutated cybrid cells to staurosporine-induced cell death is mediated by calcium-dependent activation of calpains.

Rommelaere G, Michel S, Malaisse J, Charlier S, Arnould T, Renard P.

Int J Biochem Cell Biol. 2012 Jan;44(1):139-49. doi: 10.1016/j.biocel.2011.10.009. Epub 2011 Oct 22.

PMID:
22037425
16.

[The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].

Zhang Y, Zhang JJ, Ji YC, Zhang ML, Tong Y, Zhao FX, Qu J, Zhou XT, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):501-6. doi: 10.3760/cma.j.issn.1003-9406.2011.05.006. Chinese.

PMID:
21983721
17.

[Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies].

Xu JB, Ma YN, Pan H, Zheng XF, Zhang Y, Wang ST, Bu DF, Qi Y.

Zhonghua Yi Xue Za Zhi. 2011 Apr 12;91(14):969-72. Chinese.

PMID:
21609548
18.

Detection of heteroplasmic mitochondrial DNA in single mitochondria.

Reiner JE, Kishore RB, Levin BC, Albanetti T, Boire N, Knipe A, Helmerson K, Deckman KH.

PLoS One. 2010 Dec 16;5(12):e14359. doi: 10.1371/journal.pone.0014359.

19.

Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.

Maciel-Guerra AT, Zanchetta LM, Amaral Fernandes MS, Andrade PB, do Amor Divino Miranda PM, Sartorato EL.

Ophthalmic Genet. 2010 Sep;31(3):126-8. doi: 10.3109/13816810.2010.483721.

PMID:
20565249
20.

Parkin overexpression selects against a deleterious mtDNA mutation in heteroplasmic cybrid cells.

Suen DF, Narendra DP, Tanaka A, Manfredi G, Youle RJ.

Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):11835-40. doi: 10.1073/pnas.0914569107. Epub 2010 Jun 14.

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