-
1
-
-
19944426444
-
Human cortical dysplasia and epilepsy: an ontogenetic hypothesis based on volumetric MRI and NeuN neuronal density and size measurements
-
PID: 1529736
-
Andres M, Andre VM, Nguyen S, Salamon N, Cepeda C, Levine MS, Leite JP, Neder L, Vinters HV, Mathern GW (2005) Human cortical dysplasia and epilepsy: an ontogenetic hypothesis based on volumetric MRI and NeuN neuronal density and size measurements. Cereb Cortex 15:194–210
-
(2005)
Cereb Cortex
, vol.15
, pp. 194-210
-
-
Andres, M.1
Andre, V.M.2
Nguyen, S.3
Salamon, N.4
Cepeda, C.5
Levine, M.S.6
Leite, J.P.7
Neder, L.8
Vinters, H.V.9
Mathern, G.W.10
-
2
-
-
0034431467
-
Analysis of gene-specific DNA damage and repair using quantitative polymerase chain reaction
-
COI: 1:CAS:528:DC%2BD3cXosVCrurc%3D, PID: 1102032
-
Ayala-Torres S, Chen Y, Svoboda T, Rosenblatt J, Van Houten B (2000) Analysis of gene-specific DNA damage and repair using quantitative polymerase chain reaction. Methods 22:135–147
-
(2000)
Methods
, vol.22
, pp. 135-147
-
-
Ayala-Torres, S.1
Chen, Y.2
Svoboda, T.3
Rosenblatt, J.4
Van Houten, B.5
-
3
-
-
34250355048
-
Mitochondrial genetic background modifies breast cancer risk
-
COI: 1:CAS:528:DC%2BD2sXltl2gsrg%3D, PID: 1751039
-
Bai RK, Leal SM, Covarrubias D, Liu A, Wong LJ (2007) Mitochondrial genetic background modifies breast cancer risk. Cancer Res 67:4687–4694
-
(2007)
Cancer Res
, vol.67
, pp. 4687-4694
-
-
Bai, R.K.1
Leal, S.M.2
Covarrubias, D.3
Liu, A.4
Wong, L.J.5
-
4
-
-
52649175410
-
Mitochondrial DNA variant interactions modify breast cancer risk
-
PID: 1870956
-
Bai R, Wong L, Leal SM (2008) Mitochondrial DNA variant interactions modify breast cancer risk. J Hum Genet 53:924–928
-
(2008)
J Hum Genet
, vol.53
, pp. 924-928
-
-
Bai, R.1
Wong, L.2
Leal, S.M.3
-
5
-
-
32144433872
-
A developmental and genetic classification for malformations of cortical development
-
COI: 1:STN:280:DC%2BD2Mnpt1GqsA%3D%3D, PID: 1619242
-
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB (2005) A developmental and genetic classification for malformations of cortical development. Neurology 65:1873–1887
-
(2005)
Neurology
, vol.65
, pp. 1873-1887
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Jackson, G.D.3
Guerrini, R.4
Dobyns, W.B.5
-
6
-
-
36749037338
-
Mitochondrial dysfunction in neurodegenerative disorders
-
COI: 1:CAS:528:DC%2BD2sXht1eru7nO, PID: 1795631
-
Baron M, Kudin A, Kunz W (2007) Mitochondrial dysfunction in neurodegenerative disorders. Biochem Soc Trans 35:1228–1231
-
(2007)
Biochem Soc Trans
, vol.35
, pp. 1228-1231
-
-
Baron, M.1
Kudin, A.2
Kunz, W.3
-
7
-
-
84865703692
-
Mitochondrial diseases and epilepsy
-
COI: 1:CAS:528:DC%2BC38XhsFOmsr%2FL, PID: 2294672
-
Bindoff LA, Engelsen BA (2012) Mitochondrial diseases and epilepsy. Epilepsia 53(suppl 4):92–97
-
(2012)
Epilepsia
, vol.53
, pp. 92-97
-
-
Bindoff, L.A.1
Engelsen, B.A.2
-
8
-
-
78149418393
-
Regionalized pathology correlates with augmentations of mtDNA copy numbers in patients with myoclonic epilepsy with ragged-red fibers (MERRF-Syndrome)
-
PID: 2097600
-
Brinckmann A, Weiss C, Wilbert F, von Moers A, Zwirner A, Stoltenburg-Didinger G, Wilichowski E, Schuelke M (2010) Regionalized pathology correlates with augmentations of mtDNA copy numbers in patients with myoclonic epilepsy with ragged-red fibers (MERRF-Syndrome). PLoS ONE 5:e13513
-
(2010)
PLoS ONE
, vol.5
, pp. e13513
-
-
Brinckmann, A.1
Weiss, C.2
Wilbert, F.3
von Moers, A.4
Zwirner, A.5
Stoltenburg-Didinger, G.6
Wilichowski, E.7
Schuelke, M.8
-
9
-
-
0035933047
-
Epileptic phenotypes associated with mitochondrial disorders
-
COI: 1:CAS:528:DC%2BD3MXktlCjsbk%3
-
Canafoglia L, Franceschetti S, Antozzi C, Carrara F, Farina L, Granata T, Lamantea E, Savoiardo M, Uziel G, Villani F, Zeviani M, Avanzini G (2001) Epileptic phenotypes associated with mitochondrial disorders. J Neurol 56:1340–1346
-
(2001)
J Neurol
, vol.56
, pp. 1340-1346
-
-
Canafoglia, L.1
Franceschetti, S.2
Antozzi, C.3
Carrara, F.4
Farina, L.5
Granata, T.6
Lamantea, E.7
Savoiardo, M.8
Uziel, G.9
Villani, F.10
Zeviani, M.11
Avanzini, G.12
-
10
-
-
0033112848
-
Studies on mitochondrial pathogenesis of Rett syndrome: ultrastructural data from skin and muscle biopsies and mutational analysis at mtDNA nucleotides 10463 and 2835
-
COI: 1:STN:280:DyaK1Mzos1SltA%3D%3D, PID: 1045761
-
Cardaioli E, Dotti MT, Hayek G, Zappella M, Federico A (1999) Studies on mitochondrial pathogenesis of Rett syndrome: ultrastructural data from skin and muscle biopsies and mutational analysis at mtDNA nucleotides 10463 and 2835. J Submicrosc Cytol Pathol 31:301–304
-
(1999)
J Submicrosc Cytol Pathol
, vol.31
, pp. 301-304
-
-
Cardaioli, E.1
Dotti, M.T.2
Hayek, G.3
Zappella, M.4
Federico, A.5
-
11
-
-
34249930833
-
Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington’s disease patients
-
COI: 1:CAS:528:DC%2BD2sXmtlaiu7s%3D, PID: 1754388
-
Chen C, Wu Y, Cheng M, Liu JL, Lee YM, Lee PW, Soong BW, Chiu DT (2007) Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington’s disease patients. Biochem Biophys Res Commun 359:335–340
-
(2007)
Biochem Biophys Res Commun
, vol.359
, pp. 335-340
-
-
Chen, C.1
Wu, Y.2
Cheng, M.3
Liu, J.L.4
Lee, Y.M.5
Lee, P.W.6
Soong, B.W.7
Chiu, D.T.8
-
12
-
-
84878888076
-
Mitochondrial genetics
-
COI: 1:CAS:528:DC%2BC3sXpsFChsL8%3D, PID: 2370409
-
Chinnery PF, Hudson G (2013) Mitochondrial genetics. Br Med Bull 106:135–159
-
(2013)
Br Med Bull
, vol.106
, pp. 135-159
-
-
Chinnery, P.F.1
Hudson, G.2
-
13
-
-
0035782926
-
Lessons from mitochondrial DNA mutations
-
DiMauro S (2001) Lessons from mitochondrial DNA mutations. Semin Cell Dev Biol 9:397–405
-
(2001)
Semin Cell Dev Biol
, vol.9
, pp. 397-405
-
-
DiMauro, S.1
-
14
-
-
77954477989
-
Epileptic phenotypes in children with respiratory chain disorders
-
PID: 2019677
-
El Sabbagh S, Lebre A-S, Bahi-Buisson N, Delonlay P, Soufflet C, Boddaert N, Rio M, Rçtig A, Dulac O, Munnich A, Desguerre I (2010) Epileptic phenotypes in children with respiratory chain disorders. Epilepsia 51:1225–1235
-
(2010)
Epilepsia
, vol.51
, pp. 1225-1235
-
-
El Sabbagh, S.1
Lebre, A.-S.2
Bahi-Buisson, N.3
Delonlay, P.4
Soufflet, C.5
Boddaert, N.6
Rio, M.7
Rçtig, A.8
Dulac, O.9
Munnich, A.10
Desguerre, I.11
-
15
-
-
13644254927
-
Estrogen, mitochondria, and growth of cancer and non-cancer cells
-
Felty Q, Roy D (2005) Estrogen, mitochondria, and growth of cancer and non-cancer cells. J Carcinog 4:e1
-
(2005)
J Carcinog
, vol.4
, pp. e1
-
-
Felty, Q.1
Roy, D.2
-
16
-
-
0036592842
-
Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome
-
Filiano JJ, Goldenthal MJ, Rhodes H, Marín-García J (2002) Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome. J Child Neurol 17:435–439
-
(2002)
J Child Neurol
, vol.17
, pp. 435-439
-
-
Filiano, J.J.1
Goldenthal, M.J.2
Rhodes, H.3
Marín-García, J.4
-
17
-
-
38749142509
-
The evaluation of oxidative DNA damage in children with brain damage using 8-hydroxyguanosine levels
-
PID: 1776607
-
Fukuda M, Yamauchi H, Yamamoto H, Aminakab M, Murakamia H, Kamiyamaa N, Miyamotoa Y, Koitabashia Y (2008) The evaluation of oxidative DNA damage in children with brain damage using 8-hydroxyguanosine levels. Brain Dev 30:131–136
-
(2008)
Brain Dev
, vol.30
, pp. 131-136
-
-
Fukuda, M.1
Yamauchi, H.2
Yamamoto, H.3
Aminakab, M.4
Murakamia, H.5
Kamiyamaa, N.6
Miyamotoa, Y.7
Koitabashia, Y.8
-
18
-
-
0021518209
-
Stochastic relaxation, Gibbs distributions and the Bayesian restoration of images
-
COI: 1:STN:280:DC%2BC38rks12gsQ%3D%3D, PID: 2249965
-
Geman S, Geman D (1984) Stochastic relaxation, Gibbs distributions and the Bayesian restoration of images. IEEE Trans Pattern Anal Mach Intell 6:721–742
-
(1984)
IEEE Trans Pattern Anal Mach Intell
, vol.6
, pp. 721-742
-
-
Geman, S.1
Geman, D.2
-
19
-
-
33646236099
-
Genetic basis of Alzheimer’s dementia: role of mtDNA mutations
-
COI: 1:CAS:528:DC%2BD28XnsFWhtb4%3D, PID: 1668180
-
Grazina M, Pratas J, Silva F, Oliveira S, Santana I, Oliveira C (2006) Genetic basis of Alzheimer’s dementia: role of mtDNA mutations. Genes Brain Behav 5(Suppl 2):92–107
-
(2006)
Genes Brain Behav
, vol.5
, pp. 92-107
-
-
Grazina, M.1
Pratas, J.2
Silva, F.3
Oliveira, S.4
Santana, I.5
Oliveira, C.6
-
20
-
-
0942279783
-
Cortical dysplastic lesions in children with intractable epilepsy: role of complete resection
-
PID: 1475893
-
Hader WJ, Mackay M, Otsubo H, Chitoku S, Weiss S, Becker L, Snead OC 3rd, Rutka JT (2004) Cortical dysplastic lesions in children with intractable epilepsy: role of complete resection. J Neurosurg 100:110–117
-
(2004)
J Neurosurg
, vol.100
, pp. 110-117
-
-
Hader, W.J.1
Mackay, M.2
Otsubo, H.3
Chitoku, S.4
Weiss, S.5
Becker, L.6
Snead, O.C.7
Rutka, J.T.8
-
21
-
-
0032231458
-
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA
-
COI: 1:CAS:528:DyaK1cXnvFakur8%3
-
Hanna M, Nelson P, Rahman S, Lane RJM, Land L, Heales S, Cooper MJ, Schapira AHV, Morgan-Hughes JA, Wood NW (1998) Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Am J Genet 63:29–36
-
(1998)
Am J Genet
, vol.63
, pp. 29-36
-
-
Hanna, M.1
Nelson, P.2
Rahman, S.3
Lane, R.J.M.4
Land, L.5
Heales, S.6
Cooper, M.J.7
Schapira, A.H.V.8
Morgan-Hughes, J.A.9
Wood, N.W.10
-
22
-
-
0037677723
-
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber Hereditary Optic Neuropathy
-
COI: 1:CAS:528:DC%2BD3sXktlyit7g%3
-
Howell N, Oostra R, Bolhuis P, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C (2003) Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber Hereditary Optic Neuropathy. Am J Genet 72:1460–1469
-
(2003)
Am J Genet
, vol.72
, pp. 1460-1469
-
-
Howell, N.1
Oostra, R.2
Bolhuis, P.3
Spruijt, L.4
Clarke, L.A.5
Mackey, D.A.6
Preston, G.7
Herrnstadt, C.8
-
23
-
-
0034926430
-
A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy
-
COI: 1:CAS:528:DC%2BD3MXlvVamtLo%3D, PID: 1145519
-
Hsieh RH, Li J-Y, Pang C-Y, Wei Y-H (2001) A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy. J Biomed Sci 8:328–335
-
(2001)
J Biomed Sci
, vol.8
, pp. 328-335
-
-
Hsieh, R.H.1
Li, J.-Y.2
Pang, C.-Y.3
Wei, Y.-H.4
-
24
-
-
0037904747
-
Single cell lineage analysis in human focal cortical dysplasia
-
PID: 1276404
-
Hua Y, Crino PB (2003) Single cell lineage analysis in human focal cortical dysplasia. Cereb Cortex 13:693–699
-
(2003)
Cereb Cortex
, vol.13
, pp. 693-699
-
-
Hua, Y.1
Crino, P.B.2
-
25
-
-
84914168203
-
-
MITOMAP: A Human Mitochondrial Genome Database (2009)
-
MITOMAP: A Human Mitochondrial Genome Database (2009) http://www.mitomap.org/MITOMAP.
-
-
-
-
26
-
-
84914168201
-
Surgical treatment of intractable epilepsy associated with focal cortical dysplasia
-
Jizong Z, Zhou F, Hongmin B (2011) Surgical treatment of intractable epilepsy associated with focal cortical dysplasia. In Humberto Foyaca-Sibat (Ed.) Novel treatment of epilepsy, ISBN: 978-953-307-667-6: http://www.intechopen.com/books/novel-treatment-of-epilepsy/surgicaltreatment-of-intractable-epilepsy-associated-with-focal-cortical-dysplasia
-
(2011)
Novel treatment of epilepsy
-
-
Jizong, Z.1
Zhou, F.2
Hongmin, B.3
-
27
-
-
84878517297
-
Reverse engineering of modified genes by Bayesian Network analysis defines molecular determinants critical to the development of glioblastoma
-
COI: 1:CAS:528:DC%2BC3sXpsFylur0%3D, PID: 2373797
-
Kunkle BW, Yoo C, Roy D (2013) Reverse engineering of modified genes by Bayesian Network analysis defines molecular determinants critical to the development of glioblastoma. PLoS ONE 8(5):e64140
-
(2013)
PLoS ONE
, vol.8
, Issue.5
, pp. e64140
-
-
Kunkle, B.W.1
Yoo, C.2
Roy, D.3
-
28
-
-
13444271923
-
Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress
-
COI: 1:CAS:528:DC%2BD2MXhtVKisbw%3D, PID: 1569484
-
Lee H, Wei Y (2005) Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. Int J Biochem Cell Biol 37:822–834
-
(2005)
Int J Biochem Cell Biol
, vol.37
, pp. 822-834
-
-
Lee, H.1
Wei, Y.2
-
29
-
-
0034214103
-
Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells
-
COI: 1:CAS:528:DC%2BD3cXksF2mtrk%3D, PID: 1081643
-
Lee H, Yin P, Lu C, Chi CW, Wei YH (2000) Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells. Biochem J 348:425–432
-
(2000)
Biochem J
, vol.348
, pp. 425-432
-
-
Lee, H.1
Yin, P.2
Lu, C.3
Chi, C.W.4
Wei, Y.H.5
-
30
-
-
77649191873
-
Mitochondrial DNA copy number in peripheral blood associated with cognitive function in apparently healthy elderly women
-
COI: 1:CAS:528:DC%2BC3cXitlSmt7Y%3D, PID: 2011404
-
Lee J, Park K, Im J, Kim MY, Lee DC (2010) Mitochondrial DNA copy number in peripheral blood associated with cognitive function in apparently healthy elderly women. Clin Chim Acta 411:592–596
-
(2010)
Clin Chim Acta
, vol.411
, pp. 592-596
-
-
Lee, J.1
Park, K.2
Im, J.3
Kim, M.Y.4
Lee, D.C.5
-
31
-
-
0043066954
-
Increased variation in mtDNA in patients with familial sensorineural hearing impairment
-
COI: 1:CAS:528:DC%2BD3sXlsFKnu7k%3D, PID: 1280267
-
Lehtonen MS, Moilanen JS, Majamaa K (2003) Increased variation in mtDNA in patients with familial sensorineural hearing impairment. Hum Genet 113:220–227
-
(2003)
Hum Genet
, vol.113
, pp. 220-227
-
-
Lehtonen, M.S.1
Moilanen, J.S.2
Majamaa, K.3
-
32
-
-
33747885370
-
Brain development in children and adolescents: insights from anatomical magnetic resonance imaging
-
PID: 1688718
-
Lenroot R, Giedd J (2006) Brain development in children and adolescents: insights from anatomical magnetic resonance imaging. Neurosci Biobehav Rev 30:718–729
-
(2006)
Neurosci Biobehav Rev
, vol.30
, pp. 718-729
-
-
Lenroot, R.1
Giedd, J.2
-
33
-
-
0032486118
-
Yield of mtDNA mutation analysis in 2,000 patients
-
COI: 1:STN:280:DyaK1c3ptl2mug%3D%3D, PID: 963216
-
Liang MH, Wong LJ (1998) Yield of mtDNA mutation analysis in 2,000 patients. Am J Med Genet 77:395–400
-
(1998)
Am J Med Genet
, vol.77
, pp. 395-400
-
-
Liang, M.H.1
Wong, L.J.2
-
34
-
-
57349183018
-
Low copy number and low oxidative damage of mitochondrial DNA are associated with tumor progression in lung cancer tissues after neoadjuvant chemotherapy
-
PID: 1868512
-
Lin C, Wang L, Tsai C, Wei YH (2008) Low copy number and low oxidative damage of mitochondrial DNA are associated with tumor progression in lung cancer tissues after neoadjuvant chemotherapy. Interact Cardiovasc Thorac Surg 7:954–958
-
(2008)
Interact Cardiovasc Thorac Surg
, vol.7
, pp. 954-958
-
-
Lin, C.1
Wang, L.2
Tsai, C.3
Wei, Y.H.4
-
35
-
-
33645533854
-
Alterations in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies
-
COI: 1:CAS:528:DC%2BD28Xkslensro%3D, PID: 1662977
-
Liu C, Cheng W, Lee C, Ma YS, Lin CY, Huang CC, Wei YH (2006) Alterations in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies. Acta Neurol Scand 113:334–341
-
(2006)
Acta Neurol Scand
, vol.113
, pp. 334-341
-
-
Liu, C.1
Cheng, W.2
Lee, C.3
Ma, Y.S.4
Lin, C.Y.5
Huang, C.C.6
Wei, Y.H.7
-
36
-
-
33847250334
-
Oxidative stress in surgically treated patients with refractory epilepsy
-
COI: 1:CAS:528:DC%2BD2sXisVWgtLg%3D, PID: 1729148
-
Lopez J, Gonzalez M, Lorigados L, Morales L, Riverón G, Bauzá JY (2007) Oxidative stress in surgically treated patients with refractory epilepsy. Clin Biochem 40:292–298
-
(2007)
Clin Biochem
, vol.40
, pp. 292-298
-
-
Lopez, J.1
Gonzalez, M.2
Lorigados, L.3
Morales, L.4
Riverón, G.5
Bauzá, J.Y.6
-
37
-
-
84914166514
-
Malformations of cortical development and epilepsy in children
-
Luna B, Bhatia B, Ragheb B, Miller I, Jayakar P, Felty Q, Roy D (2011) Malformations of cortical development and epilepsy in children. Encycl Environ Health Gene Environ Interact 2:595–602
-
(2011)
Encycl Environ Health Gene Environ Interact
, vol.2
, pp. 595-602
-
-
Luna, B.1
Bhatia, B.2
Ragheb, B.3
Miller, I.4
Jayakar, P.5
Felty, Q.6
Roy, D.7
-
38
-
-
31544454702
-
The increase in mitochondrial DNA copy number in the tissue of γ-irradiated mice
-
COI: 1:CAS:528:DC%2BD28XhtFahsL8%3D, PID: 1634128
-
Malakhova L, Bezlepkin V, Antipova V, Ushakova T, Fomenko L, Sirota N, Gaziev AI (2005) The increase in mitochondrial DNA copy number in the tissue of γ-irradiated mice. Cell Mol Biol Lett 10:721–732
-
(2005)
Cell Mol Biol Lett
, vol.10
, pp. 721-732
-
-
Malakhova, L.1
Bezlepkin, V.2
Antipova, V.3
Ushakova, T.4
Fomenko, L.5
Sirota, N.6
Gaziev, A.I.7
-
39
-
-
78650555076
-
Estrogen-induced ROS mediated redox signaling contributes in the development of breast cancer
-
COI: 1:CAS:528:DC%2BC3MXhtF2mtQ%3D%3D, PID: 2103620
-
Okoh V, Deoraj A, Roy D (2011) Estrogen-induced ROS mediated redox signaling contributes in the development of breast cancer. Biochem Biophys Acta 1815:115–133
-
(2011)
Biochem Biophys Acta
, vol.1815
, pp. 115-133
-
-
Okoh, V.1
Deoraj, A.2
Roy, D.3
-
40
-
-
84914104620
-
Free radical epilepsy and anti-oxidant: an overview
-
COI: 1:CAS:528:DC%2BC3MXjs1aiurw%3
-
Patil C, Ahire Y, Pathade P, Pathade VV, Mali PR (2011) Free radical epilepsy and anti-oxidant: an overview. Int Res J Pharm 2:64–71
-
(2011)
Int Res J Pharm
, vol.2
, pp. 64-71
-
-
Patil, C.1
Ahire, Y.2
Pathade, P.3
Pathade, V.V.4
Mali, P.R.5
-
41
-
-
34249671789
-
Mitochondrial dysfunction and molecular pathways of disease
-
COI: 1:CAS:528:DC%2BD2sXmtVOrt7c%3D, PID: 1723937
-
Pieczenik S, Neustadt J (2007) Mitochondrial dysfunction and molecular pathways of disease. Exp Mol Pathol 83:84–92
-
(2007)
Exp Mol Pathol
, vol.83
, pp. 84-92
-
-
Pieczenik, S.1
Neustadt, J.2
-
42
-
-
33746307556
-
Cortical dysplasia: neuropathological aspects
-
PID: 1676385
-
Rickert CH (2006) Cortical dysplasia: neuropathological aspects. Childs Nerv Syst 22:821–826
-
(2006)
Childs Nerv Syst
, vol.22
, pp. 821-826
-
-
Rickert, C.H.1
-
43
-
-
34249854298
-
Signature of mitochondria of steroidal hormones-dependent normal and cancer cells: potential molecular targets for cancer therapy
-
COI: 1:CAS:528:DC%2BD28Xht1WgsLzO, PID: 1712729
-
Roy D, Felty Q, Narayan S, Jayakar P (2007) Signature of mitochondria of steroidal hormones-dependent normal and cancer cells: potential molecular targets for cancer therapy. Front Biosci 12:154–173
-
(2007)
Front Biosci
, vol.12
, pp. 154-173
-
-
Roy, D.1
Felty, Q.2
Narayan, S.3
Jayakar, P.4
-
44
-
-
0030818636
-
Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation
-
COI: 1:STN:280:DyaK2szmsFeksg%3D%3D, PID: 922220
-
Santorelli FM, Tanji K, Shanske S, DiMauro S (1997) Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation. Neurology 49:270–273
-
(1997)
Neurology
, vol.49
, pp. 270-273
-
-
Santorelli, F.M.1
Tanji, K.2
Shanske, S.3
DiMauro, S.4
-
45
-
-
0033664091
-
Cortical malformations and epilepsy
-
COI: 1:STN:280:DC%2BD3M%2FnvVGjsQ%3D%3
-
Schwartzkroin PA, Walsh CA (2000) Cortical malformations and epilepsy. Ment Retard Dev Diagn 6:268–280
-
(2000)
Ment Retard Dev Diagn
, vol.6
, pp. 268-280
-
-
Schwartzkroin, P.A.1
Walsh, C.A.2
-
46
-
-
0036557977
-
Mitochondrial disorders: a potential under-recognized etiology of infantile spasms
-
PID: 1215058
-
Shah NS, Mitchell WG, Boles RG (2002) Mitochondrial disorders: a potential under-recognized etiology of infantile spasms. J Child Neurol 17:369–372
-
(2002)
J Child Neurol
, vol.17
, pp. 369-372
-
-
Shah, N.S.1
Mitchell, W.G.2
Boles, R.G.3
-
47
-
-
70450253281
-
Mitochondrial copy number and risk of breast cancer: a pilot study
-
COI: 1:CAS:528:DC%2BD1MXhsV2ks73E, PID: 1978893
-
Shen J, Platek M, Mahasneh A, Ambrosone CB, Zhao H (2010) Mitochondrial copy number and risk of breast cancer: a pilot study. Mitochondrion 10:62–68
-
(2010)
Mitochondrion
, vol.10
, pp. 62-68
-
-
Shen, J.1
Platek, M.2
Mahasneh, A.3
Ambrosone, C.B.4
Zhao, H.5
-
48
-
-
0027200741
-
Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
-
COI: 1:CAS:528:DyaK3sXmt1egt7o%3D, PID: 810486
-
Shoffner JM, Brown MD, Torroni A, Lott MT, Cabell MF, Mirra SS, Beal MF, Yang CC, Gearing M, Salvo R, Watts RL, Juncos JL, Hansen LA, Crain BJ, Fayad M, Reckord CL, Wallace DC (1993) Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 17:171–184
-
(1993)
Genomics
, vol.17
, pp. 171-184
-
-
Shoffner, J.M.1
Brown, M.D.2
Torroni, A.3
Lott, M.T.4
Cabell, M.F.5
Mirra, S.S.6
Beal, M.F.7
Yang, C.C.8
Gearing, M.9
Salvo, R.10
Watts, R.L.11
Juncos, J.L.12
Hansen, L.A.13
Crain, B.J.14
Fayad, M.15
Reckord, C.L.16
Wallace, D.C.17
-
49
-
-
77950420275
-
Mitochondrial DNA damage in spinal and bulbar muscular atrophy patients and carriers
-
COI: 1:CAS:528:DC%2BC3cXktVShs7c%3D, PID: 2003573
-
Su S, Jou S, Cheng W, Lin T, Li J, Huang C, Lee Y, Soong B, Liu C (2010) Mitochondrial DNA damage in spinal and bulbar muscular atrophy patients and carriers. Clin Chim Acta 411:626–630
-
(2010)
Clin Chim Acta
, vol.411
, pp. 626-630
-
-
Su, S.1
Jou, S.2
Cheng, W.3
Lin, T.4
Li, J.5
Huang, C.6
Lee, Y.7
Soong, B.8
Liu, C.9
-
50
-
-
0035258312
-
Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by multiplex molecular beacon based real-time fluorescence PCR
-
COI: 1:STN:280:DC%2BD3M3jsVGmtA%3D%3D, PID: 1116091
-
Szuhai KS, van den Ouweland JM, Dirks RW, Lemaître M, Truffert J, Janssen G, Tanke H, Holme E, Maassen J, Raap A (2001) Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by multiplex molecular beacon based real-time fluorescence PCR. Nucleic Acids Res 29:e13
-
(2001)
Nucleic Acids Res
, vol.29
, pp. e13
-
-
Szuhai, K.S.1
van den Ouweland, J.M.2
Dirks, R.W.3
Lemaître, M.4
Truffert, J.5
Janssen, G.6
Tanke, H.7
Holme, E.8
Maassen, J.9
Raap, A.10
-
51
-
-
0035462463
-
Modifications in mitochondrial DNA by stilbene estrogen and hepatocarcinogenicity
-
COI: 1:CAS:528:DC%2BD3MXms1Shtbk%3D, PID: 1149631
-
Thomas RD, Roy D (2001) Modifications in mitochondrial DNA by stilbene estrogen and hepatocarcinogenicity. Oncol Rep 8:1035–1038
-
(2001)
Oncol Rep
, vol.8
, pp. 1035-1038
-
-
Thomas, R.D.1
Roy, D.2
-
52
-
-
84878602088
-
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features
-
COI: 1:CAS:528:DC%2BC3sXhtVaks7bN, PID: 2344809
-
Uusimaa J, Gowda V, McShane A, Smith C, Evans J, Shrier A, Narasimhan M, O'Rourke A, Rajabally Y, Hedderly T, Cowan F, Fratter C, Poulton J (2013) Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features. Epilepsia 54:1002–1011
-
(2013)
Epilepsia
, vol.54
, pp. 1002-1011
-
-
Uusimaa, J.1
Gowda, V.2
McShane, A.3
Smith, C.4
Evans, J.5
Shrier, A.6
Narasimhan, M.7
O'Rourke, A.8
Rajabally, Y.9
Hedderly, T.10
Cowan, F.11
Fratter, C.12
Poulton, J.13
-
53
-
-
78751648925
-
Mitochondrial dysfunction and oxidative stress: a contributing link to acquired epilepsy
-
COI: 1:CAS:528:DC%2BC3cXhsF2jur7F, PID: 2113235
-
Waldbaum S, Patel M (2010a) Mitochondrial dysfunction and oxidative stress: a contributing link to acquired epilepsy. J Bioenerg Biomembr 42:449–455
-
(2010)
J Bioenerg Biomembr
, vol.42
, pp. 449-455
-
-
Waldbaum, S.1
Patel, M.2
-
54
-
-
72249087964
-
Mitochondria, oxidative stress, and temporal lobe epilepsy
-
COI: 1:CAS:528:DC%2BD1MXhs1Wjtr%2FJ, PID: 1985044
-
Waldbaum S, Patel M (2010b) Mitochondria, oxidative stress, and temporal lobe epilepsy. Epilepsy Res 88:23–45
-
(2010)
Epilepsy Res
, vol.88
, pp. 23-45
-
-
Waldbaum, S.1
Patel, M.2
-
55
-
-
34247164656
-
Mechanisms of epileptogenesis in tuberous sclerosis complex and related malformations of cortical development with abnormal glioneuronal proliferation
-
Wong M (2007) Mechanisms of epileptogenesis in tuberous sclerosis complex and related malformations of cortical development with abnormal glioneuronal proliferation. Epilepsia 48:617–630
-
(2007)
Epilepsia
, vol.48
, pp. 617-630
-
-
Wong, M.1
-
56
-
-
70349202340
-
Animal models of focal cortical dysplasia and tuberous sclerosis complex: recent progress towards clinical applications
-
COI: 1:CAS:528:DC%2BD1MXhtlCgs77K, PID: 1976145
-
Wong M (2009) Animal models of focal cortical dysplasia and tuberous sclerosis complex: recent progress towards clinical applications. Epilepsia 50(Suppl):34–44
-
(2009)
Epilepsia
, vol.50
, pp. 34-44
-
-
Wong, M.1
-
57
-
-
0036358442
-
Discovery of causal relationships in a gene-regulation pathway from a mixture of experimental and observational DNA microarray data
-
Yoo C, Thorsson V, Cooper GF (2002) Discovery of causal relationships in a gene-regulation pathway from a mixture of experimental and observational DNA microarray data. Pac Symp Biocomput 7:498–509
-
(2002)
Pac Symp Biocomput
, vol.7
, pp. 498-509
-
-
Yoo, C.1
Thorsson, V.2
Cooper, G.F.3
|