-
1
-
-
84861451481
-
Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy
-
Ackermann EJ, Guo S, Booten S, Alvarado L, Benson M, Hughes S, Monia BP. 2012. Clinical development of an antisense therapy for the treatment of transthyretin-associated polyneuropathy. Amyloid 19 (Suppl 1):43–44. doi: 10.3109/13506129.2012.673140, PMID: 22494066
-
(2012)
Amyloid
, vol.19
, pp. 43-44
-
-
Ackermann, E.J.1
Guo, S.2
Booten, S.3
Alvarado, L.4
Benson, M.5
Hughes, S.6
Monia, B.P.7
-
2
-
-
84865148154
-
New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy
-
Alonso-Montes C, Naves-Diaz M, Fernandez-Martin JL, Rodriguez-Reguero J, Moris C, Coto E, Cannata-Andia JB, Rodriguez I. 2012. New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy. Molecular Biology Reports 39:8777–8785. doi: 10.1007/s11033-012-1740-7, PMID: 22718505
-
(2012)
Molecular Biology Reports
, vol.39
, pp. 8777-8785
-
-
Alonso-Montes, C.1
Naves-Diaz, M.2
Fernandez-Martin, J.L.3
Rodriguez-Reguero, J.4
Moris, C.5
Coto, E.6
Cannata-Andia, J.B.7
Rodriguez, I.8
-
3
-
-
1942453894
-
HRC is a direct transcriptional target of MEF2 during cardiac, skeletal, and arterial smooth muscle development in vivo
-
Anderson JP, Dodou E, Heidt AB, De Val SJ, Jaehnig EJ, Greene SB, Olson EN, Black BL. 2004. HRC is a direct transcriptional target of MEF2 during cardiac, skeletal, and arterial smooth muscle development in vivo. Molecular and Cellular Biology 24:3757–3768. doi: 10.1128/MCB.24.9.3757-3768.2004, PMID: 15082771
-
(2004)
Molecular and Cellular Biology
, vol.24
, pp. 3757-3768
-
-
Anderson, J.P.1
Dodou, E.2
Heidt, A.B.3
De Val, S.J.4
Jaehnig, E.J.5
Greene, S.B.6
Olson, E.N.7
Black, B.L.8
-
4
-
-
27944495710
-
RNAi-mediated suppression of the mitochondrial iron chaperone, frataxin
-
Drosophila
-
Anderson PR, Kirby K, Hilliker AJ, Phillips JP. 2005. RNAi-mediated suppression of the mitochondrial iron chaperone, frataxin, in Drosophila. Human Molecular Genetics 14:3397–3405. doi: 10.1093/hmg/ddi367, PMID: 16203742
-
(2005)
Human Molecular Genetics
, vol.14
, pp. 3397-3405
-
-
Anderson, P.R.1
Kirby, K.2
Hilliker, A.J.3
Phillips, J.P.4
-
5
-
-
84901917562
-
Lipid peroxidation: Production, metabolism, and signaling mechanisms of Malondialdehyde and 4-hydroxy-2-nonenal
-
Ayala A, Muñoz MF, Argüelles S. 2014. Lipid peroxidation: production, metabolism, and signaling mechanisms of Malondialdehyde and 4-hydroxy-2-nonenal. Oxidative Medicine and Cellular Longevity 2014:1–31. doi: 10.1155/2014/360438
-
(2014)
Oxidative Medicine and Cellular Longevity
, vol.2014
, pp. 1-31
-
-
Ayala, A.1
Muñoz, M.F.2
Argüelles, S.3
-
6
-
-
77950858020
-
High AAV vector purity results in serotype- and tissue-independent enhancement of transduction efficiency
-
Ayuso E, Mingozzi F, Montane J, Leon X, Anguela XM, Haurigot V, Edmonson SA, Africa L, Zhou S, High KA, Bosch F, Wright JF. 2010. High AAV vector purity results in serotype- and tissue-independent enhancement of transduction efficiency. Gene Therapy 17:503–510. doi: 10.1038/gt.2009.157, PMID: 19956269
-
(2010)
Gene Therapy
, vol.17
, pp. 503-510
-
-
Ayuso, E.1
Mingozzi, F.2
Montane, J.3
Leon, X.4
Anguela, X.M.5
Haurigot, V.6
Edmonson, S.A.7
Africa, L.8
Zhou, S.9
High, K.A.10
Bosch, F.11
Wright, J.F.12
-
7
-
-
0030846021
-
1997. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin
-
Babcock M, de Silva D, Oaks R, Davis-Kaplan S, Jiralerspong S, Montermini L, Pandolfo M, Kaplan J. 1997. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin. Science 276:1709–1712. doi: 10.1126/science.276.5319.1709, PMID: 9180083
-
Science
, vol.276
, pp. 1709-1712
-
-
Babcock, M.1
De Silva, D.2
Oaks, R.3
Davis-Kaplan, S.4
Jiralerspong, S.5
Montermini, L.6
Pandolfo, M.7
Kaplan, J.8
-
8
-
-
80053628321
-
Friedreich’s ataxia: The vicious circle hypothesis revisited
-
Bayot A, Santos R, Camadro JM, Rustin P. 2011. Friedreich’s ataxia: the vicious circle hypothesis revisited. BMC Medicine 9:112. doi: 10.1186/1741-7015-9-112, PMID: 21985033
-
(2011)
BMC Medicine
, vol.9
, pp. 112
-
-
Bayot, A.1
Santos, R.2
Camadro, J.M.3
Rustin, P.4
-
9
-
-
34347370842
-
Selective iron chelation in Friedreich ataxia: Biologic and clinical implications
-
Boddaert N, Le Quan Sang KH, Rötig A, Leroy-Willig A, Gallet S, Brunelle F, Sidi D, Thalabard JC, Munnich A, Cabantchik ZI. 2007. Selective iron chelation in Friedreich ataxia: biologic and clinical implications. Blood 110: 401–408. doi: 10.1182/blood-2006-12-065433, PMID: 17379741
-
(2007)
Blood
, vol.110
, pp. 401-408
-
-
Boddaert, N.1
Le Quan Sang, K.H.2
Rötig, A.3
Leroy-Willig, A.4
Gallet, S.5
Brunelle, F.6
Sidi, D.7
Thalabard, J.C.8
Munnich, A.9
Cabantchik, Z.I.10
-
10
-
-
0033957174
-
Clinical, biochemical and molecular genetic correlations in Friedreich’s ataxia
-
Bradley JL, Blake JC, Chamberlain S, Thomas PK, Cooper JM, Schapira AH. 2000. Clinical, biochemical and molecular genetic correlations in Friedreich’s ataxia. Human Molecular Genetics 9:275–282. doi: 10.1093/hmg/9.2.275, PMID: 10607838
-
(2000)
Human Molecular Genetics
, vol.9
, pp. 275-282
-
-
Bradley, J.L.1
Blake, J.C.2
Chamberlain, S.3
Thomas, P.K.4
Cooper, J.M.5
Schapira, A.H.6
-
11
-
-
13344270899
-
Friedreich’s ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, et al. 1996. Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271:1423–1427. doi: 10.1126/science.271.5254.1423, PMID: 8596916
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
Montermini, L.2
Moltò, M.D.3
Pianese, L.4
Cossée, M.5
Cavalcanti, F.6
Monros, E.7
Rodius, F.8
Duclos, F.9
Monticelli, A.10
Zara, F.11
Cañizares, J.12
Koutnikova, H.13
Bidichandani, S.I.14
Gellera, C.15
Brice, A.16
Trouillas, P.17
De Michele, G.18
Filla, A.19
De Frutos, R.20
more..
-
12
-
-
0033199841
-
Phosphorylation of Ser-241 is essential for the activity of 3- phosphoinositide-dependent protein kinase-1: Identification of five sites of phosphorylation in vivo
-
Casamayor A, Morrice NA, Alessi DR. 1999. Phosphorylation of Ser-241 is essential for the activity of 3- phosphoinositide-dependent protein kinase-1: identification of five sites of phosphorylation in vivo. Biochemical Journal 342:287–292. doi: 10.1042/bj3420287, PMID: 10455013
-
(1999)
Biochemical Journal
, vol.342
, pp. 287-292
-
-
Casamayor, A.1
Morrice, N.A.2
Alessi, D.R.3
-
13
-
-
84979698328
-
Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration
-
Chen K, Lin G, Haelterman NA, Ho TS, Li T, Li Z, Duraine L, Graham BH, Jaiswal M, Yamamoto S, Rasband MN, Bellen HJ. 2016. Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration. eLife 5:e16043. doi: 10.7554/eLife.16043, PMID: 27343351
-
(2016)
Elife
, vol.5
-
-
Chen, K.1
Lin, G.2
Haelterman, N.A.3
Ho, T.S.4
Li, T.5
Li, Z.6
Duraine, L.7
Graham, B.H.8
Jaiswal, M.9
Yamamoto, S.10
Rasband, M.N.11
Bellen, H.J.12
-
14
-
-
80051933968
-
The Mef2A transcription factor coordinately regulates a costamere gene program in cardiac muscle
-
Ewen EP, Snyder CM, Wilson M, Desjardins D, Naya FJ. 2011. The Mef2A transcription factor coordinately regulates a costamere gene program in cardiac muscle. Journal of Biological Chemistry 286:29644–29653. doi: 10.1074/jbc.M111.268094, PMID: 21724844
-
(2011)
Journal of Biological Chemistry
, vol.286
, pp. 29644-29653
-
-
Ewen, E.P.1
Snyder, C.M.2
Wilson, M.3
Desjardins, D.4
Naya, F.J.5
-
15
-
-
44949131860
-
In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses
-
Grimm D, Lee JS, Wang L, Desai T, Akache B, Storm TA, Kay MA. 2008. In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses. Journal of Virology 82: 5887–5911. doi: 10.1128/JVI.00254-08, PMID: 18400866
-
(2008)
Journal of Virology
, vol.82
, pp. 5887-5911
-
-
Grimm, D.1
Lee, J.S.2
Wang, L.3
Desai, T.4
Akache, B.5
Storm, T.A.6
Kay, M.A.7
-
16
-
-
84926154812
-
A hierarchy of ankyrin-spectrin complexes clusters sodium channels at nodes of Ranvier
-
Ho TS, Zollinger DR, Chang KJ, Xu M, Cooper EC, Stankewich MC, Bennett V, Rasband MN. 2014. A hierarchy of ankyrin-spectrin complexes clusters sodium channels at nodes of Ranvier. Nature Neuroscience 17:1664–1672. doi: 10.1038/nn.3859, PMID: 25362473
-
(2014)
Nature Neuroscience
, vol.17
, pp. 1664-1672
-
-
Ho, T.S.1
Zollinger, D.R.2
Chang, K.J.3
Xu, M.4
Cooper, E.C.5
Stankewich, M.C.6
Bennett, V.7
Rasband, M.N.8
-
17
-
-
71449093193
-
The dorsal root ganglion in Friedreich’s ataxia
-
Koeppen AH, Morral JA, Davis AN, Qian J, Petrocine SV, Knutson MD, Gibson WM, Cusack MJ, Li D. 2009. The dorsal root ganglion in Friedreich’s ataxia. Acta Neuropathologica 118:763–776. doi: 10.1007/s00401-009-0589-x, PMID: 19727777
-
(2009)
Acta Neuropathologica
, vol.118
, pp. 763-776
-
-
Koeppen, A.H.1
Morral, J.A.2
Davis, A.N.3
Qian, J.4
Petrocine, S.V.5
Knutson, M.D.6
Gibson, W.M.7
Cusack, M.J.8
Li, D.9
-
18
-
-
79952814526
-
Friedreich’s ataxia: Pathology, pathogenesis, and molecular genetics
-
Koeppen AH. 2011. Friedreich’s ataxia: pathology, pathogenesis, and molecular genetics. Journal of the Neurological Sciences 303:1–12. doi: 10.1016/j.jns.2011.01.010, PMID: 21315377
-
(2011)
Journal of the Neurological Sciences
, vol.303
, pp. 1-12
-
-
Koeppen, A.H.1
-
19
-
-
84863522393
-
Sphingolipid signaling mediates iron toxicity
-
Lee YJ, Huang X, Kropat J, Henras A, Merchant SS, Dickson RC, Chanfreau GF. 2012. Sphingolipid signaling mediates iron toxicity. Cell Metabolism 16:90–96. doi: 10.1016/j.cmet.2012.06.004, PMID: 22768841
-
(2012)
Cell Metabolism
, vol.16
, pp. 90-96
-
-
Lee, Y.J.1
Huang, X.2
Kropat, J.3
Henras, A.4
Merchant, S.S.5
Dickson, R.C.6
Chanfreau, G.F.7
-
20
-
-
84855389519
-
CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy
-
Ljungberg MC, Ali YO, Zhu J, Wu CS, Oka K, Zhai RG, Lu HC. 2012. CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy. Human Molecular Genetics 21:251–267. doi: 10.1093/hmg/ddr492, PMID: 22027 994
-
(2012)
Human Molecular Genetics
, vol.21
, pp. 251-267
-
-
Ljungberg, M.C.1
Ali, Y.O.2
Zhu, J.3
Wu, C.S.4
Oka, K.5
Zhai, R.G.6
Lu, H.C.7
-
21
-
-
33846794302
-
Causative role of oxidative stress in a Drosophila model of Friedreich ataxia
-
Llorens JV, Navarro JA, Martínez-Sebastián MJ, Baylies MK, Schneuwly S, Botella JA, Moltó MD. 2007. Causative role of oxidative stress in a Drosophila model of Friedreich ataxia. The FASEB Journal 21:333–344. doi: 10.1096/fj.05-5709com, PMID: 17167074
-
(2007)
The FASEB Journal
, vol.21
, pp. 333-344
-
-
Llorens, J.V.1
Navarro, J.A.2
Martínez-Sebastián, M.J.3
Baylies, M.K.4
Schneuwly, S.5
Botella, J.A.6
Moltó, M.D.7
-
22
-
-
0031437930
-
Oxidative stress does not appear to be involved in the aetiology of Friedreich’s ataxia
-
Macevilly CJ, Muller DP. 1997. Oxidative stress does not appear to be involved in the aetiology of Friedreich’s ataxia. Restorative Neurology and Neuroscience 11:131–137. doi: 10.3233/RNN-1997-11303, PMID: 21551537
-
(1997)
Restorative Neurology and Neuroscience
, vol.11
, pp. 131-137
-
-
Macevilly, C.J.1
Muller, D.P.2
-
23
-
-
84904734583
-
Dysregulation of cellular iron metabolism in Friedreich ataxia: From primary iron-sulfur cluster deficit to mitochondrial iron accumulation
-
Martelli A, Puccio H. 2014. Dysregulation of cellular iron metabolism in Friedreich ataxia: from primary iron-sulfur cluster deficit to mitochondrial iron accumulation. Frontiers in Pharmacology 5:130. doi: 10.3389/fphar.2014.00130, PMID: 24917819
-
(2014)
Frontiers in Pharmacology
, vol.5
, pp. 130
-
-
Martelli, A.1
Puccio, H.2
-
24
-
-
0037101845
-
The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins
-
Mühlenhoff U, Richhardt N, Ristow M, Kispal G, Lill R. 2002. The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins. Human Molecular Genetics 11:2025–2036. doi: 10.1093/hmg/11.17.2025, PMID: 12165564
-
(2002)
Human Molecular Genetics
, vol.11
, pp. 2025-2036
-
-
Mühlenhoff, U.1
Richhardt, N.2
Ristow, M.3
Kispal, G.4
Lill, R.5
-
25
-
-
0037083893
-
Selective determination of mitochondrial chelatable iron in viable cells with a new fluorescent sensor
-
Petrat F, Weisheit D, Lensen M, de Groot H, Sustmann R, Rauen U. 2002. Selective determination of mitochondrial chelatable iron in viable cells with a new fluorescent sensor. Biochemical Journal 362:137–147. doi: 10.1042/bj3620137, PMID: 11829750
-
(2002)
Biochemical Journal
, vol.362
, pp. 137-147
-
-
Petrat, F.1
Weisheit, D.2
Lensen, M.3
De Groot, H.4
Sustmann, R.5
Rauen, U.6
-
26
-
-
84912101598
-
CRISPR-Cas9 knockin mice for genome editing and cancer modeling
-
Platt RJ, Chen S, Zhou Y, Yim MJ, Swiech L, Kempton HR, Dahlman JE, Parnas O, Eisenhaure TM, Jovanovic M, Graham DB, Jhunjhunwala S, Heidenreich M, Xavier RJ, Langer R, Anderson DG, Hacohen N, Regev A, Feng G, Sharp PA, et al. 2014. CRISPR-Cas9 knockin mice for genome editing and cancer modeling. Cell 159:440–455. doi: 10.1016/j.cell.2014.09.014, PMID: 25263330
-
(2014)
Cell
, vol.159
, pp. 440-455
-
-
Platt, R.J.1
Chen, S.2
Zhou, Y.3
Yim, M.J.4
Swiech, L.5
Kempton, H.R.6
Dahlman, J.E.7
Parnas, O.8
Eisenhaure, T.M.9
Jovanovic, M.10
Graham, D.B.11
Jhunjhunwala, S.12
Heidenreich, M.13
Xavier, R.J.14
Langer, R.15
Erson, D.G.16
Hacohen, N.17
Regev, A.18
Feng, G.19
Sharp, P.A.20
more..
-
27
-
-
36849039931
-
Regulation of skeletal muscle sarcomere integrity and postnatal muscle function by Mef2c
-
Potthoff MJ, Arnold MA, McAnally J, Richardson JA, Bassel-Duby R, Olson EN. 2007. Regulation of skeletal muscle sarcomere integrity and postnatal muscle function by Mef2c. Molecular and Cellular Biology 27:8143–8151. doi: 10.1128/MCB.01187-07, PMID: 17875930
-
(2007)
Molecular and Cellular Biology
, vol.27
, pp. 8143-8151
-
-
Potthoff, M.J.1
Arnold, M.A.2
McAnally, J.3
Richardson, J.A.4
Bassel-Duby, R.5
Olson, E.N.6
-
28
-
-
0035138072
-
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
-
Puccio H, Simon D, Cossée M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin P, Koenig M. 2001. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits. Nature Genetics 27:181–186. doi: 10.1038/84818, PMID: 11175786
-
(2001)
Nature Genetics
, vol.27
, pp. 181-186
-
-
Puccio, H.1
Simon, D.2
Cossée, M.3
Criqui-Filipe, P.4
Tiziano, F.5
Melki, J.6
Hindelang, C.7
Matyas, R.8
Rustin, P.9
Koenig, M.10
-
29
-
-
0031253821
-
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia
-
Rötig A, de Lonlay P, Chretien D, Foury F, Koenig M, Sidi D, Munnich A, Rustin P. 1997. Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia. Nature Genetics 17:215–217. doi: 10.1038/ng1097-215, PMID: 9326946
-
(1997)
Nature Genetics
, vol.17
, pp. 215-217
-
-
Rötig, A.1
De Lonlay, P.2
Chretien, D.3
Foury, F.4
Koenig, M.5
Sidi, D.6
Munnich, A.7
Rustin, P.8
-
31
-
-
77954930779
-
Friedreich ataxia: Molecular mechanisms, redox considerations, and therapeutic opportunities
-
Santos R, Lefevre S, Sliwa D, Seguin A, Camadro JM, Lesuisse E. 2010. Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities. Antioxidants & Redox Signaling 13:651–690. doi: 10.1089/ars.2009.3015, PMID: 20156111
-
(2010)
Antioxidants & Redox Signaling
, vol.13
, pp. 651-690
-
-
Santos, R.1
Lefevre, S.2
Sliwa, D.3
Seguin, A.4
Camadro, J.M.5
Lesuisse, E.6
-
32
-
-
14044273058
-
Friedreich ataxia: The oxidative stress paradox
-
Seznec H, Simon D, Bouton C, Reutenauer L, Hertzog A, Golik P, Procaccio V, Patel M, Drapier JC, Koenig M, Puccio H. 2005. Friedreich ataxia: the oxidative stress paradox. Human Molecular Genetics 14:463–474. doi: 10.1093/hmg/ddi042, PMID: 15615771
-
(2005)
Human Molecular Genetics
, vol.14
, pp. 463-474
-
-
Seznec, H.1
Simon, D.2
Bouton, C.3
Reutenauer, L.4
Hertzog, A.5
Golik, P.6
Procaccio, V.7
Patel, M.8
Drapier, J.C.9
Koenig, M.10
Puccio, H.11
-
33
-
-
77956100048
-
Defects in mitochondrial axonal transport and membrane potential without increased reactive oxygen species production in a Drosophila model of Friedreich ataxia
-
Shidara Y, Hollenbeck PJ. 2010. Defects in mitochondrial axonal transport and membrane potential without increased reactive oxygen species production in a Drosophila model of Friedreich ataxia. Journal of Neuroscience 30:11369–11378. doi: 10.1523/JNEUROSCI.0529-10.2010, PMID: 20739558
-
(2010)
Journal of Neuroscience
, vol.30
, pp. 11369-11378
-
-
Shidara, Y.1
Hollenbeck, P.J.2
-
34
-
-
1442324707
-
Friedreich ataxia mouse models with progressive cerebellar and sensory ataxia reveal autophagic neurodegeneration in dorsal root ganglia
-
Simon D, Seznec H, Gansmuller A, Carelle N, Weber P, Metzger D, Rustin P, Koenig M, Puccio H. 2004. Friedreich ataxia mouse models with progressive cerebellar and sensory ataxia reveal autophagic neurodegeneration in dorsal root ganglia. Journal of Neuroscience 24:1987–1995. doi: 10.1523/JNEUROSCI.4549-03.2004, PMID: 14985441
-
(2004)
Journal of Neuroscience
, vol.24
, pp. 1987-1995
-
-
Simon, D.1
Seznec, H.2
Gansmuller, A.3
Carelle, N.4
Weber, P.5
Metzger, D.6
Rustin, P.7
Koenig, M.8
Puccio, H.9
-
35
-
-
84907303923
-
Cerebellar pathology in Friedreich’s ataxia: Atrophied dentate nuclei with normal iron content
-
Solbach K, Kraff O, Minnerop M, Beck A, Schöls L, Gizewski ER, Ladd ME, Timmann D. 2014. Cerebellar pathology in Friedreich’s ataxia: atrophied dentate nuclei with normal iron content. NeuroImage: Clinical 6:93–99. doi: 10.1016/j.nicl.2014.08.018, PMID: 25379420
-
(2014)
Neuroimage: Clinical
, vol.6
, pp. 93-99
-
-
Solbach, K.1
Kraff, O.2
Minnerop, M.3
Beck, A.4
Schöls, L.5
Gizewski, E.R.6
Ladd, M.E.7
Timmann, D.8
-
36
-
-
84926061715
-
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9
-
Swiech L, Heidenreich M, Banerjee A, Habib N, Li Y, Trombetta J, Sur M, Zhang F. 2015. In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9. Nature Biotechnology 33:102–106. doi: 10.1038/nbt.3055, PMID: 25326897
-
(2015)
Nature Biotechnology
, vol.33
, pp. 102-106
-
-
Swiech, L.1
Heidenreich, M.2
Banerjee, A.3
Habib, N.4
Li, Y.5
Trombetta, J.6
Sur, M.7
Zhang, F.8
-
37
-
-
79955745733
-
Maintenance of neuronal polarity
-
Szu-Yu Ho T, Rasband MN. 2011. Maintenance of neuronal polarity. Developmental Neurobiology 71:474–482. doi: 10.1002/dneu.20843, PMID: 21557501
-
(2011)
Developmental Neurobiology
, vol.71
, pp. 474-482
-
-
Szu-Yu Ho, T.1
Rasband, M.N.2
-
38
-
-
0033956898
-
Activating transcription factor 3 (ATF3) induction by axotomy in sensory and motoneurons: A novel neuronal marker of nerve injury
-
Tsujino H, Kondo E, Fukuoka T, Dai Y, Tokunaga A, Miki K, Yonenobu K, Ochi T, Noguchi K. 2000. Activating transcription factor 3 (ATF3) induction by axotomy in sensory and motoneurons: A novel neuronal marker of nerve injury. Molecular and Cellular Neuroscience 15:170–182. doi: 10.1006/mcne.1999.0814, PMID: 10673325
-
(2000)
Molecular and Cellular Neuroscience
, vol.15
, pp. 170-182
-
-
Tsujino, H.1
Kondo, E.2
Fukuoka, T.3
Dai, Y.4
Tokunaga, A.5
Miki, K.6
Yonenobu, K.7
Ochi, T.8
Noguchi, K.9
-
39
-
-
0028842908
-
Regulation of the Nur77 orphan steroid receptor in activation-induced apoptosis
-
Woronicz JD, Lina A, Calnan BJ, Szychowski S, Cheng L, Winoto A. 1995. Regulation of the Nur77 orphan steroid receptor in activation-induced apoptosis. Molecular and Cellular Biology 15:6364–6376. doi: 10.1128/MCB.15.11.6364, PMID: 7565789
-
(1995)
Molecular and Cellular Biology
, vol.15
, pp. 6364-6376
-
-
Woronicz, J.D.1
Lina, A.2
Calnan, B.J.3
Szychowski, S.4
Cheng, L.5
Winoto, A.6
-
40
-
-
33646942503
-
Myocyte enhancer factors 2A and 2C induce dilated cardiomyopathy in transgenic mice
-
Xu J, Gong NL, Bodi I, Aronow BJ, Backx PH, Molkentin JD. 2006. Myocyte enhancer factors 2A and 2C induce dilated cardiomyopathy in transgenic mice. Journal of Biological Chemistry 281:9152–9162. doi: 10.1074/jbc.M510217200, PMID: 16469744
-
(2006)
Journal of Biological Chemistry
, vol.281
, pp. 9152-9162
-
-
Xu, J.1
Gong, N.L.2
Bodi, I.3
Aronow, B.J.4
Backx, P.H.5
Molkentin, J.D.6
-
41
-
-
84890223214
-
Membrane domain organization of myelinated axons requires bII spectrin
-
Zhang C, Susuki K, Zollinger DR, Dupree JL, Rasband MN. 2013. Membrane domain organization of myelinated axons requires bII spectrin. Journal of Cell Biology 203:437–443. doi: 10.1083/jcb.201308116, PMID: 24217619
-
(2013)
Journal of Cell Biology
, vol.203
, pp. 437-443
-
-
Zhang, C.1
Susuki, K.2
Zollinger, D.R.3
Dupree, J.L.4
Rasband, M.N.5
-
42
-
-
0033022953
-
Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield
-
Zolotukhin S, Byrne BJ, Mason E, Zolotukhin I, Potter M, Chesnut K, Summerford C, Samulski RJ, Muzyczka N. 1999. Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Therapy 6:973–985. doi: 10.1038/sj.gt.3300938, PMID: 10455399
-
(1999)
Gene Therapy
, vol.6
, pp. 973-985
-
-
Zolotukhin, S.1
Byrne, B.J.2
Mason, E.3
Zolotukhin, I.4
Potter, M.5
Chesnut, K.6
Summerford, C.7
Samulski, R.J.8
Muzyczka, N.9
|