-
1
-
-
70349773389
-
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy
-
Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, et al (2009) An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Dis Model Mech 2: 359-373
-
(2009)
Dis Model Mech
, vol.2
, pp. 359-373
-
-
Achilli, F.1
Bros-Facer, V.2
Williams, H.P.3
Banks, G.T.4
AlQatari, M.5
Chia, R.6
Tucci, V.7
Groves, M.8
Nickols, C.D.9
Seburn, K.L.10
-
2
-
-
0038067742
-
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
-
Antonellis A, Ellsworth RE, Sambuughin N, Puls I, Abel A, Lee-Lin SQ, Jordanova A, Kremensky I, Christodoulou K, Middleton LT, et al (2003) Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet 72: 1293-1299
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1293-1299
-
-
Antonellis, A.1
Ellsworth, R.E.2
Sambuughin, N.3
Puls, I.4
Abel, A.5
Lee-Lin, S.Q.6
Jordanova, A.7
Kremensky, I.8
Christodoulou, K.9
Middleton, L.T.10
-
3
-
-
52949118056
-
The role of aminoacyl-tRNA synthetases in genetic diseases
-
Antonellis A, Green ED (2008) The role of aminoacyl-tRNA synthetases in genetic diseases. Annu Rev Genomics Hum Genet 9: 87-107
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 87-107
-
-
Antonellis, A.1
Green, E.D.2
-
4
-
-
67651095905
-
Two-site phosphorylation of EPRS coordinates multimodal regulation of noncanonical translational control activity
-
Arif A, Jia J, Mukhopadhyay R, Willard B, Kinter M, Fox PL (2009) Two-site phosphorylation of EPRS coordinates multimodal regulation of noncanonical translational control activity. Mol Cell 35: 164-180
-
(2009)
Mol Cell
, vol.35
, pp. 164-180
-
-
Arif, A.1
Jia, J.2
Mukhopadhyay, R.3
Willard, B.4
Kinter, M.5
Fox, P.L.6
-
5
-
-
33746701345
-
Discovery of a new boron-containing antifungal agent, 5-fluoro-1,3-dihydro-1-hydroxy-2,1- benzoxaborole (AN2690), for the potential treatment of onychomycosis
-
Baker SJ, Zhang YK, Akama T, Lau A, Zhou H, Hernandez V, Mao W, Alley MR, Sanders V, Plattner JJ (2006) Discovery of a new boron-containing antifungal agent, 5-fluoro-1, 3-dihydro-1-hydroxy-2, 1- benzoxaborole (AN2690), for the potential treatment of onychomycosis. J Med Chem 49: 4447-4450
-
(2006)
J Med Chem
, vol.49
, pp. 4447-4450
-
-
Baker, S.J.1
Zhang, Y.K.2
Akama, T.3
Lau, A.4
Zhou, H.5
Hernandez, V.6
Mao, W.7
Alley, M.R.8
Sanders, V.9
Plattner, J.J.10
-
6
-
-
67650677056
-
Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice
-
Banks GT, Bros-Facer V, Williams HP, Chia R, Achilli F, Bryson JB, Greensmith L, Fisher EM (2009) Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice. PLoS ONE 4: e6218
-
(2009)
PLoS ONE
, vol.4
-
-
Banks, G.T.1
Bros-Facer, V.2
Williams, H.P.3
Chia, R.4
Achilli, F.5
Bryson, J.B.6
Greensmith, L.7
Fisher, E.M.8
-
7
-
-
84858985882
-
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans
-
Bayat V, Thiffault I, Jaiswal M, Tetreault M, Donti T, Sasarman F, Bernard G, Demers-Lamarche J, Dicaire MJ, Mathieu J, et al (2012) Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. PLoS Biol 10: e1001288
-
(2012)
PLoS Biol
, vol.10
-
-
Bayat, V.1
Thiffault, I.2
Jaiswal, M.3
Tetreault, M.4
Donti, T.5
Sasarman, F.6
Bernard, G.7
Demers-Lamarche, J.8
Dicaire, M.J.9
Mathieu, J.10
-
8
-
-
79851508857
-
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome
-
Belostotsky R, Ben-Shalom E, Rinat C, Becker-Cohen R, Feinstein S, Zeligson S, Segel R, Elpeleg O, Nassar S, Frishberg Y (2011) Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome. Am J Hum Genet 88: 193-200
-
(2011)
Am J Hum Genet
, vol.88
, pp. 193-200
-
-
Belostotsky, R.1
Ben-Shalom, E.2
Rinat, C.3
Becker-Cohen, R.4
Feinstein, S.5
Zeligson, S.6
Segel, R.7
Elpeleg, O.8
Nassar, S.9
Frishberg, Y.10
-
9
-
-
84859704385
-
Leucyl-tRNA synthetase controls TORC1 via the EGO complex
-
Bonfils G, Jaquenoud M, Bontron S, Ostrowicz C, Ungermann C, De Virgilio C (2012) Leucyl-tRNA synthetase controls TORC1 via the EGO complex. Mol Cell 46: 105-110
-
(2012)
Mol Cell
, vol.46
, pp. 105-110
-
-
Bonfils, G.1
Jaquenoud, M.2
Bontron, S.3
Ostrowicz, C.4
Ungermann, C.5
De Virgilio, C.6
-
10
-
-
0037178780
-
Axonal protein synthesis provides a mechanism for localized regulation at an intermediate target
-
Brittis PA, Lu Q, Flanagan JG (2002) Axonal protein synthesis provides a mechanism for localized regulation at an intermediate target. Cell 110: 223-235
-
(2002)
Cell
, vol.110
, pp. 223-235
-
-
Brittis, P.A.1
Lu, Q.2
Flanagan, J.G.3
-
11
-
-
84872609485
-
Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients
-
Cassandrini D, Cilio MR, Bianchi M, Doimo M, Balestri M, Tessa A, Rizza T, Sartori G, Meschini MC, Nesti C, et al (2013) Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients. J Inherit Metab Dis 36: 43-53
-
(2013)
J Inherit Metab Dis
, vol.36
, pp. 43-53
-
-
Cassandrini, D.1
Cilio, M.R.2
Bianchi, M.3
Doimo, M.4
Balestri, M.5
Tessa, A.6
Rizza, T.7
Sartori, G.8
Meschini, M.C.9
Nesti, C.10
-
12
-
-
35348983348
-
Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia
-
Edvardson S, Shaag A, Kolesnikova O, Gomori JM, Tarassov I, Einbinder T, Saada A, Elpeleg O (2007) Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia. Am J Hum Genet 81: 857-862
-
(2007)
Am J Hum Genet
, vol.81
, pp. 857-862
-
-
Edvardson, S.1
Shaag, A.2
Kolesnikova, O.3
Gomori, J.M.4
Tarassov, I.5
Einbinder, T.6
Saada, A.7
Elpeleg, O.8
-
13
-
-
84867131148
-
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy
-
Elo JM, Yadavalli SS, Euro L, Isohanni P, Gotz A, Carroll CJ, Valanne L, Alkuraya FS, Uusimaa J, Paetau A, et al (2012) Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy. Hum Mol Genet 21: 4521-4529
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4521-4529
-
-
Elo, J.M.1
Yadavalli, S.S.2
Euro, L.3
Isohanni, P.4
Gotz, A.5
Carroll, C.J.6
Valanne, L.7
Alkuraya, F.S.8
Uusimaa, J.9
Paetau, A.10
-
14
-
-
80051754461
-
Dominant Intermediate Charcot-Marie-Tooth disorder is not due to a catalytic defect in tyrosyl-tRNA synthetase
-
Froelich CA, First EA (2011) Dominant Intermediate Charcot-Marie-Tooth disorder is not due to a catalytic defect in tyrosyl-tRNA synthetase. Biochemistry 50: 7132-7145
-
(2011)
Biochemistry
, vol.50
, pp. 7132-7145
-
-
Froelich, C.A.1
First, E.A.2
-
15
-
-
67649891971
-
Noncanonical activity of seryl-tRNA synthetase is involved in vascular development
-
Fukui H, Hanaoka R, Kawahara A (2009) Noncanonical activity of seryl-tRNA synthetase is involved in vascular development. Circ Res 104: 1253-1259
-
(2009)
Circ Res
, vol.104
, pp. 1253-1259
-
-
Fukui, H.1
Hanaoka, R.2
Kawahara, A.3
-
16
-
-
79955797332
-
Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy
-
Gotz A, Tyynismaa H, Euro L, Ellonen P, Hyotylainen T, Ojala T, Hamalainen RH, Tommiska J, Raivio T, Oresic M, et al (2011) Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy. Am J Hum Genet 88: 635-642
-
(2011)
Am J Hum Genet
, vol.88
, pp. 635-642
-
-
Gotz, A.1
Tyynismaa, H.2
Euro, L.3
Ellonen, P.4
Hyotylainen, T.5
Ojala, T.6
Hamalainen, R.H.7
Tommiska, J.8
Raivio, T.9
Oresic, M.10
-
17
-
-
77956095201
-
New functions of aminoacyl-tRNA synthetases beyond translation
-
Guo M, Yang XL, Schimmel P (2010) New functions of aminoacyl-tRNA synthetases beyond translation. Nat Rev Mol Cell Biol 11: 668-674
-
(2010)
Nat Rev Mol Cell Biol
, vol.11
, pp. 668-674
-
-
Guo, M.1
Yang, X.L.2
Schimmel, P.3
-
18
-
-
77954382835
-
Charcot-Marie-Tooth disease type 2D with a novel glycyl-tRNA synthetase gene (GARS) mutation
-
Hamaguchi A, Ishida C, Iwasa K, Abe A, Yamada M (2010) Charcot-Marie-Tooth disease type 2D with a novel glycyl-tRNA synthetase gene (GARS) mutation. J Neurol 257: 1202-1204
-
(2010)
J Neurol
, vol.257
, pp. 1202-1204
-
-
Hamaguchi, A.1
Ishida, C.2
Iwasa, K.3
Abe, A.4
Yamada, M.5
-
19
-
-
84862777407
-
Leucyl-tRNA synthetase is an intracellular leucine sensor for the mTORC1-signaling pathway
-
Han JM, Jeong SJ, Park MC, Kim G, Kwon NH, Kim HK, Ha SH, Ryu SH, Kim S (2012) Leucyl-tRNA synthetase is an intracellular leucine sensor for the mTORC1-signaling pathway. Cell 149: 410-424
-
(2012)
Cell
, vol.149
, pp. 410-424
-
-
Han, J.M.1
Jeong, S.J.2
Park, M.C.3
Kim, G.4
Kwon, N.H.5
Kim, H.K.6
Ha, S.H.7
Ryu, S.H.8
Kim, S.9
-
20
-
-
79961094170
-
Dispersed disease-causing neomorphic mutations on a single protein promote the same localized conformational opening
-
He W, Zhang HM, Chong YE, Guo M, Marshall AG, Yang XL (2011) Dispersed disease-causing neomorphic mutations on a single protein promote the same localized conformational opening. Proc Natl Acad Sci USA 108: 12307-12312
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 12307-12312
-
-
He, W.1
Zhang, H.M.2
Chong, Y.E.3
Guo, M.4
Marshall, A.G.5
Yang, X.L.6
-
21
-
-
67649882602
-
Genetic evidence for a noncanonical function of seryl-tRNA synthetase in vascular development
-
Herzog W, Muller K, Huisken J, Stainier DY (2009) Genetic evidence for a noncanonical function of seryl-tRNA synthetase in vascular development. Circ Res 104: 1260-1266
-
(2009)
Circ Res
, vol.104
, pp. 1260-1266
-
-
Herzog, W.1
Muller, K.2
Huisken, J.3
Stainier, D.Y.4
-
22
-
-
0033782994
-
Aminoacyl-tRNA synthesis
-
Ibba M, Soll D (2000) Aminoacyl-tRNA synthesis. Annu Rev Biochem 69: 617-650
-
(2000)
Annu Rev Biochem
, vol.69
, pp. 617-650
-
-
Ibba, M.1
Soll, D.2
-
23
-
-
33751001764
-
Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene
-
James PA, Cader MZ, Muntoni F, Childs AM, Crow YJ, Talbot K (2006) Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene. Neurology 67: 1710-1712
-
(2006)
Neurology
, vol.67
, pp. 1710-1712
-
-
James, P.A.1
Cader, M.Z.2
Muntoni, F.3
Childs, A.M.4
Crow, Y.J.5
Talbot, K.6
-
24
-
-
84865361604
-
Protection of extraribosomal RPL13a by GAPDH and dysregulation by S-nitrosylation
-
Jia J, Arif A, Willard B, Smith JD, Stuehr DJ, Hazen SL, Fox PL (2012) Protection of extraribosomal RPL13a by GAPDH and dysregulation by S-nitrosylation. Mol Cell 47: 656-663
-
(2012)
Mol Cell
, vol.47
, pp. 656-663
-
-
Jia, J.1
Arif, A.2
Willard, B.3
Smith, J.D.4
Stuehr, D.J.5
Hazen, S.L.6
Fox, P.L.7
-
25
-
-
31744448271
-
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy
-
Jordanova A, Irobi J, Thomas FP, Van Dijck P, Meerschaert K, Dewil M, Dierick I, Jacobs A, De Vriendt E, Guergueltcheva V, et al (2006) Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy. Nat Genet 38: 197-202
-
(2006)
Nat Genet
, vol.38
, pp. 197-202
-
-
Jordanova, A.1
Irobi, J.2
Thomas, F.P.3
Van Dijck, P.4
Meerschaert, K.5
Dewil, M.6
Dierick, I.7
Jacobs, A.8
De Vriendt, E.9
Guergueltcheva, V.10
-
26
-
-
84867263450
-
AIMP3/p18 controls translational initiation by mediating the delivery of charged initiator tRNA to initiation complex
-
Kang T, Kwon NH, Lee JY, Park MC, Kang E, Kim HH, Kang TJ, Kim S (2012) AIMP3/p18 controls translational initiation by mediating the delivery of charged initiator tRNA to initiation complex. J Mol Biol 423: 475-481
-
(2012)
J Mol Biol
, vol.423
, pp. 475-481
-
-
Kang, T.1
Kwon, N.H.2
Lee, J.Y.3
Park, M.C.4
Kang, E.5
Kim, H.H.6
Kang, T.J.7
Kim, S.8
-
27
-
-
84862776804
-
Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase
-
Keller TL, Zocco D, Sundrud MS, Hendrick M, Edenius M, Yum J, Kim YJ, Lee HK, Cortese JF, Wirth DF, et al (2012) Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase. Nat Chem Biol 8: 311-317
-
(2012)
Nat Chem Biol
, vol.8
, pp. 311-317
-
-
Keller, T.L.1
Zocco, D.2
Sundrud, M.S.3
Hendrick, M.4
Edenius, M.5
Yum, J.6
Kim, Y.J.7
Lee, H.K.8
Cortese, J.F.9
Wirth, D.F.10
-
28
-
-
84868110113
-
Interaction of two translational components, lysyl-tRNA synthetase and p40/37LRP, in plasma membrane promotes laminin-dependent cell migration
-
Kim DG, Choi JW, Lee JY, Kim H, Oh YS, Lee JW, Tak YK, Song JM, Razin E, Yun SH, et al (2012a) Interaction of two translational components, lysyl-tRNA synthetase and p40/37LRP, in plasma membrane promotes laminin-dependent cell migration. FASEB J 26: 4142-4159
-
(2012)
FASEB J
, vol.26
, pp. 4142-4159
-
-
Kim, D.G.1
Choi, J.W.2
Lee, J.Y.3
Kim, H.4
Oh, Y.S.5
Lee, J.W.6
Tak, Y.K.7
Song, J.M.8
Razin, E.9
Yun, S.H.10
-
29
-
-
80053152058
-
Aminoacyl-tRNA synthetases and tumorigenesis: more than housekeeping
-
Kim S, You S, Hwang D (2011) Aminoacyl-tRNA synthetases and tumorigenesis: more than housekeeping. Nat Rev Cancer 11: 708-718
-
(2011)
Nat Rev Cancer
, vol.11
, pp. 708-718
-
-
Kim, S.1
You, S.2
Hwang, D.3
-
30
-
-
84865623601
-
Cancer association study of aminoacyl-tRNA synthetase signaling network in glioblastoma
-
Kim YW, Kwon C, Liu JL, Kim SH, Kim S (2012b) Cancer association study of aminoacyl-tRNA synthetase signaling network in glioblastoma. PLoS ONE 7: e40960
-
(2012)
PLoS ONE
, vol.7
-
-
Kim, Y.W.1
Kwon, C.2
Liu, J.L.3
Kim, S.H.4
Kim, S.5
-
31
-
-
83755207354
-
Dual role of methionyl-tRNA synthetase in the regulation of translation and tumor suppressor activity of aminoacyl-tRNA synthetase-interacting multifunctional protein-3
-
Kwon NH, Kang T, Lee JY, Kim HH, Kim HR, Hong J, Oh YS, Han JM, Ku MJ, Lee SY, et al (2011) Dual role of methionyl-tRNA synthetase in the regulation of translation and tumor suppressor activity of aminoacyl-tRNA synthetase-interacting multifunctional protein-3. Proc Natl Acad Sci USA 108: 19635-19640
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 19635-19640
-
-
Kwon, N.H.1
Kang, T.2
Lee, J.Y.3
Kim, H.H.4
Kim, H.R.5
Hong, J.6
Oh, Y.S.7
Han, J.M.8
Ku, M.J.9
Lee, S.Y.10
-
32
-
-
79953787680
-
Clinically asymptomatic adult patient with extensive LBSL MRI pattern and DARS2 mutations
-
Labauge P, Dorboz I, Eymard-Pierre E, Dereeper O, Boespflug-Tanguy O (2011) Clinically asymptomatic adult patient with extensive LBSL MRI pattern and DARS2 mutations. J Neurol 258: 335-337
-
(2011)
J Neurol
, vol.258
, pp. 335-337
-
-
Labauge, P.1
Dorboz, I.2
Eymard-Pierre, E.3
Dereeper, O.4
Boespflug-Tanguy, O.5
-
33
-
-
73349114324
-
A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charco-Marie-Tooth disease
-
Latour P, Thauvin-Robinet C, Baudelet-Mery C, Soichot P, Cusin V, Faivre L, Locatelli MC, Mayencon M, Sarcey A, Broussolle E, et al (2010) A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charco-Marie-Tooth disease. Am J Hum Genet 86: 77-82
-
(2010)
Am J Hum Genet
, vol.86
, pp. 77-82
-
-
Latour, P.1
Thauvin-Robinet, C.2
Baudelet-Mery, C.3
Soichot, P.4
Cusin, V.5
Faivre, L.6
Locatelli, M.C.7
Mayencon, M.8
Sarcey, A.9
Broussolle, E.10
-
34
-
-
33748432548
-
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration
-
Lee JW, Beebe K, Nangle LA, Jang J, Longo-Guess CM, Cook SA, Davisson MT, Sundberg JP, Schimmel P, Ackerman SL (2006) Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration. Nature 443: 50-55
-
(2006)
Nature
, vol.443
, pp. 50-55
-
-
Lee, J.W.1
Beebe, K.2
Nangle, L.A.3
Jang, J.4
Longo-Guess, C.M.5
Cook, S.A.6
Davisson, M.T.7
Sundberg, J.P.8
Schimmel, P.9
Ackerman, S.L.10
-
35
-
-
77950653171
-
Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes
-
Li R, Guan MX (2010) Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes. Mol Cell Biol 30: 2147-2154
-
(2010)
Mol Cell Biol
, vol.30
, pp. 2147-2154
-
-
Li, R.1
Guan, M.X.2
-
36
-
-
78650210763
-
Leukoencephalopathy with brainstem and spinal cord involvement and normal lactate: a new mutation in the DARS2 gene
-
Lin J, Chiconelli Faria E, Da Rocha AJ, Rodrigues Masruha M, Pereira Vilanova LC, Scheper GC, Van der Knaap MS (2010) Leukoencephalopathy with brainstem and spinal cord involvement and normal lactate: a new mutation in the DARS2 gene. J Child Neurol 25: 1425-1428
-
(2010)
J Child Neurol
, vol.25
, pp. 1425-1428
-
-
Lin, J.1
Chiconelli Faria, E.2
Da Rocha, A.J.3
Rodrigues Masruha, M.4
Pereira Vilanova, L.C.5
Scheper, G.C.6
Van der Knaap, M.S.7
-
37
-
-
83655212414
-
The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan
-
Lin KP, Soong BW, Yang CC, Huang LW, Chang MH, Lee IH, Antonellis A, Lee YC (2011) The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan. PLoS ONE 6: e29393
-
(2011)
PLoS ONE
, vol.6
-
-
Lin, K.P.1
Soong, B.W.2
Yang, C.C.3
Huang, L.W.4
Chang, M.H.5
Lee, I.H.6
Antonellis, A.7
Lee, Y.C.8
-
38
-
-
80755143679
-
Local RNA translation at the synapse and in disease
-
Liu-Yesucevitz L, Bassell GJ, Gitler AD, Hart AC, Klann E, Richter JD, Warren ST, Wolozin B (2011) Local RNA translation at the synapse and in disease. J Neurosci 31: 16086-16093
-
(2011)
J Neurosci
, vol.31
, pp. 16086-16093
-
-
Liu-Yesucevitz, L.1
Bassell, G.J.2
Gitler, A.D.3
Hart, A.C.4
Klann, E.5
Richter, J.D.6
Warren, S.T.7
Wolozin, B.8
-
39
-
-
84862695017
-
Th17 cells: biology, pathogenesis of autoimmune and inflammatory diseases, and therapeutic strategies
-
Maddur MS, Miossec P, Kaveri SV, Bayry J (2012) Th17 cells: biology, pathogenesis of autoimmune and inflammatory diseases, and therapeutic strategies. Am J Pathol 181: 8-18
-
(2012)
Am J Pathol
, vol.181
, pp. 8-18
-
-
Maddur, M.S.1
Miossec, P.2
Kaveri, S.V.3
Bayry, J.4
-
40
-
-
84857685584
-
A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N)
-
McLaughlin HM, Sakaguchi R, Giblin W, Wilson TE, Biesecker L, Lupski JR, Talbot K, Vance JM, Zuchner S, Lee YC, et al (2012) A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N). Hum Mutat 33: 244-253
-
(2012)
Hum Mutat
, vol.33
, pp. 244-253
-
-
McLaughlin, H.M.1
Sakaguchi, R.2
Giblin, W.3
Wilson, T.E.4
Biesecker, L.5
Lupski, J.R.6
Talbot, K.7
Vance, J.M.8
Zuchner, S.9
Lee, Y.C.10
-
41
-
-
77957724879
-
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy
-
McLaughlin HM, Sakaguchi R, Liu C, Igarashi T, Pehlivan D, Chu K, Iyer R, Cruz P, Cherukuri PF, Hansen NF, et al (2010) Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy. Am J Hum Genet 87: 560-566
-
(2010)
Am J Hum Genet
, vol.87
, pp. 560-566
-
-
McLaughlin, H.M.1
Sakaguchi, R.2
Liu, C.3
Igarashi, T.4
Pehlivan, D.5
Chu, K.6
Iyer, R.7
Cruz, P.8
Cherukuri, P.F.9
Hansen, N.F.10
-
42
-
-
78751529272
-
A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria
-
Messmer M, Florentz C, Schwenzer H, Scheper GC, van der Knaap MS, Marechal-Drouard L, Sissler M (2011) A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria. Biochem J 433: 441-446
-
(2011)
Biochem J
, vol.433
, pp. 441-446
-
-
Messmer, M.1
Florentz, C.2
Schwenzer, H.3
Scheper, G.C.4
van der Knaap, M.S.5
Marechal-Drouard, L.6
Sissler, M.7
-
43
-
-
84855289563
-
Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels
-
Motley WW, Seburn KL, Nawaz MH, Miers KE, Cheng J, Antonellis A, Green ED, Talbot K, Yang XL, Fischbeck KH, et al (2011) Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels. PLoS Genet 7: e1002399
-
(2011)
PLoS Genet
, vol.7
-
-
Motley, W.W.1
Seburn, K.L.2
Nawaz, M.H.3
Miers, K.E.4
Cheng, J.5
Antonellis, A.6
Green, E.D.7
Talbot, K.8
Yang, X.L.9
Fischbeck, K.H.10
-
45
-
-
55049140658
-
DAPK-ZIPK-L13a axis constitutes a negative-feedback module regulating inflammatory gene expression
-
Mukhopadhyay R, Ray PS, Arif A, Brady AK, Kinter M, Fox PL (2008) DAPK-ZIPK-L13a axis constitutes a negative-feedback module regulating inflammatory gene expression. Mol Cell 32: 371-382
-
(2008)
Mol Cell
, vol.32
, pp. 371-382
-
-
Mukhopadhyay, R.1
Ray, P.S.2
Arif, A.3
Brady, A.K.4
Kinter, M.5
Fox, P.L.6
-
46
-
-
0035861676
-
Structural basis for the recognition of isoleucyl-adenylate and an antibiotic, mupirocin, by isoleucyl-tRNA synthetase
-
Nakama T, Nureki O, Yokoyama S (2001) Structural basis for the recognition of isoleucyl-adenylate and an antibiotic, mupirocin, by isoleucyl-tRNA synthetase. J Biol Chem 276: 47387-47393
-
(2001)
J Biol Chem
, vol.276
, pp. 47387-47393
-
-
Nakama, T.1
Nureki, O.2
Yokoyama, S.3
-
47
-
-
19944431746
-
The haploinsufficient tumor suppressor p18 upregulates p53 via interactions with ATM/ATR
-
Park BJ, Kang JW, Lee SW, Choi SJ, Shin YK, Ahn YH, Choi YH, Choi D, Lee KS, Kim S (2005a) The haploinsufficient tumor suppressor p18 upregulates p53 via interactions with ATM/ATR. Cell 120: 209-221
-
(2005)
Cell
, vol.120
, pp. 209-221
-
-
Park, B.J.1
Kang, J.W.2
Lee, S.W.3
Choi, S.J.4
Shin, Y.K.5
Ahn, Y.H.6
Choi, Y.H.7
Choi, D.8
Lee, K.S.9
Kim, S.10
-
48
-
-
84863251058
-
Secreted human glycyl-tRNA synthetase implicated in defense against ERK-activated tumorigenesis
-
Park MC, Kang T, Jin D, Han JM, Kim SB, Park YJ, Cho K, Park YW, Guo M, He W, et al (2012) Secreted human glycyl-tRNA synthetase implicated in defense against ERK-activated tumorigenesis. Proc Natl Acad Sci USA 109: E640- E647
-
(2012)
Proc Natl Acad Sci USA
, vol.109
-
-
Park, M.C.1
Kang, T.2
Jin, D.3
Han, J.M.4
Kim, S.B.5
Park, Y.J.6
Cho, K.7
Park, Y.W.8
Guo, M.9
He, W.10
-
49
-
-
77951139250
-
Aminoacyl-tRNA synthetase-interacting multifunctional proteins (AIMPs): a triad for cellular homeostasis
-
Park SG, Choi EC, Kim S (2010) Aminoacyl-tRNA synthetase-interacting multifunctional proteins (AIMPs): a triad for cellular homeostasis. IUBMB Life 62: 296-302
-
(2010)
IUBMB Life
, vol.62
, pp. 296-302
-
-
Park, S.G.1
Choi, E.C.2
Kim, S.3
-
50
-
-
25144489447
-
Functional expansion of aminoacyl-tRNA synthetases and their interacting factors: new perspectives on housekeepers
-
Park SG, Ewalt KL, Kim S (2005b) Functional expansion of aminoacyl-tRNA synthetases and their interacting factors: new perspectives on housekeepers. Trends Biochem Sci 30: 569-574
-
(2005)
Trends Biochem Sci
, vol.30
, pp. 569-574
-
-
Park, S.G.1
Ewalt, K.L.2
Kim, S.3
-
51
-
-
18144400079
-
Human lysyl-tRNA synthetase is secreted to trigger proinflammatory response
-
Park SG, Kim HJ, Min YH, Choi EC, Shin YK, Park BJ, Lee SW, Kim S (2005c) Human lysyl-tRNA synthetase is secreted to trigger proinflammatory response. Proc Natl Acad Sci USA 102: 6356-6361
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 6356-6361
-
-
Park, S.G.1
Kim, H.J.2
Min, Y.H.3
Choi, E.C.4
Shin, Y.K.5
Park, B.J.6
Lee, S.W.7
Kim, S.8
-
52
-
-
49649110170
-
Aminoacyl tRNA synthetases and their connections to disease
-
Park SG, Schimmel P, Kim S (2008) Aminoacyl tRNA synthetases and their connections to disease. Proc Natl Acad Sci USA 105: 11043-11049
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 11043-11049
-
-
Park, S.G.1
Schimmel, P.2
Kim, S.3
-
53
-
-
79955634426
-
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome
-
Pierce SB, Chisholm KM, Lynch ED, Lee MK, Walsh T, Opitz JM, Li W, Klevit RE, King MC (2011) Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci USA 108: 6543-6548
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 6543-6548
-
-
Pierce, S.B.1
Chisholm, K.M.2
Lynch, E.D.3
Lee, M.K.4
Walsh, T.5
Opitz, J.M.6
Li, W.7
Klevit, R.E.8
King, M.C.9
-
54
-
-
60149091561
-
A stress-responsive RNA switch regulates VEGFA expression
-
Ray PS, Jia J, Yao P, Majumder M, Hatzoglou M, Fox PL (2009) A stress-responsive RNA switch regulates VEGFA expression. Nature 457: 915-919
-
(2009)
Nature
, vol.457
, pp. 915-919
-
-
Ray, P.S.1
Jia, J.2
Yao, P.3
Majumder, M.4
Hatzoglou, M.5
Fox, P.L.6
-
55
-
-
77955061839
-
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia-MLASA syndrome
-
Riley LG, Cooper S, Hickey P, Rudinger-Thirion J, McKenzie M, Compton A, Lim SC, Thorburn D, Ryan MT, Giege R, et al (2010) Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia-MLASA syndrome. Am J Hum Genet 87: 52-59
-
(2010)
Am J Hum Genet
, vol.87
, pp. 52-59
-
-
Riley, L.G.1
Cooper, S.2
Hickey, P.3
Rudinger-Thirion, J.4
McKenzie, M.5
Compton, A.6
Lim, S.C.7
Thorburn, D.8
Ryan, M.T.9
Giege, R.10
-
56
-
-
34250799619
-
An antifungal agent inhibits an aminoacyl-tRNA synthetase by trapping tRNA in the editing site
-
Rock FL, Mao W, Yaremchuk A, Tukalo M, Crepin T, Zhou H, Zhang YK, Hernandez V, Akama T, Baker SJ, et al (2007) An antifungal agent inhibits an aminoacyl-tRNA synthetase by trapping tRNA in the editing site. Science 316: 1759-1761
-
(2007)
Science
, vol.316
, pp. 1759-1761
-
-
Rock, F.L.1
Mao, W.2
Yaremchuk, A.3
Tukalo, M.4
Crepin, T.5
Zhou, H.6
Zhang, Y.K.7
Hernandez, V.8
Akama, T.9
Baker, S.J.10
-
57
-
-
84861337799
-
Trp-tRNA synthetase bridges DNA-PKcs to PARP-1 to link IFN-gamma and p53 signaling
-
Sajish M, Zhou Q, Kishi S, Valdez DM, Jr, Kapoor M, Guo M, Lee S, Kim S, Yang XL, Schimmel P (2012) Trp-tRNA synthetase bridges DNA-PKcs to PARP-1 to link IFN-gamma and p53 signaling. Nat Chem Biol 8: 547-554
-
(2012)
Nat Chem Biol
, vol.8
, pp. 547-554
-
-
Sajish, M.1
Zhou, Q.2
Kishi, S.3
Valdez Jr., D.M.4
Kapoor, M.5
Guo, M.6
Lee, S.7
Kim, S.8
Yang, X.L.9
Schimmel, P.10
-
58
-
-
5444271940
-
Noncanonical function of glutamyl-prolyl-tRNA synthetase: gene-specific silencing of translation
-
Sampath P, Mazumder B, Seshadri V, Gerber CA, Chavatte L, Kinter M, Ting SM, Dignam JD, Kim S, Driscoll DM, et al (2004) Noncanonical function of glutamyl-prolyl-tRNA synthetase: gene-specific silencing of translation. Cell 119: 195-208
-
(2004)
Cell
, vol.119
, pp. 195-208
-
-
Sampath, P.1
Mazumder, B.2
Seshadri, V.3
Gerber, C.A.4
Chavatte, L.5
Kinter, M.6
Ting, S.M.7
Dignam, J.D.8
Kim, S.9
Driscoll, D.M.10
-
59
-
-
84863880664
-
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia
-
Sasarman F, Nishimura T, Thiffault I, Shoubridge EA (2012) A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia. Hum Mutat 33: 1201-1206
-
(2012)
Hum Mutat
, vol.33
, pp. 1201-1206
-
-
Sasarman, F.1
Nishimura, T.2
Thiffault, I.3
Shoubridge, E.A.4
-
60
-
-
34047109743
-
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
-
Scheper GC, van der Klok T, van Andel RJ, van Berkel CG, Sissler M, Smet J, Muravina TI, Serkov SV, Uziel G, Bugiani M, et al (2007) Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation. Nat Genet 39: 534-539
-
(2007)
Nat Genet
, vol.39
, pp. 534-539
-
-
Scheper, G.C.1
van der Klok, T.2
van Andel, R.J.3
van Berkel, C.G.4
Sissler, M.5
Smet, J.6
Muravina, T.I.7
Serkov, S.V.8
Uziel, G.9
Bugiani, M.10
-
61
-
-
0023061339
-
Aminoacyl tRNA synthetases: general scheme of structure-function relationships in the polypeptides and recognition of transfer RNAs
-
Schimmel P (1987) Aminoacyl tRNA synthetases: general scheme of structure-function relationships in the polypeptides and recognition of transfer RNAs. Annu Rev Biochem 56: 125-158
-
(1987)
Annu Rev Biochem
, vol.56
, pp. 125-158
-
-
Schimmel, P.1
-
62
-
-
52949154680
-
Development of tRNA synthetases and connection to genetic code and disease
-
Schimmel P (2008) Development of tRNA synthetases and connection to genetic code and disease. Protein Sci 17: 1643-1652
-
(2008)
Protein Sci
, vol.17
, pp. 1643-1652
-
-
Schimmel, P.1
-
63
-
-
33748545328
-
An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model
-
Seburn KL, Nangle LA, Cox GA, Schimmel P, Burgess RW (2006) An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model. Neuron 51: 715-726
-
(2006)
Neuron
, vol.51
, pp. 715-726
-
-
Seburn, K.L.1
Nangle, L.A.2
Cox, G.A.3
Schimmel, P.4
Burgess, R.W.5
-
64
-
-
44349149820
-
Implication of leucyl-tRNA synthetase 1 (LARS1) over-expression in growth and migration of lung cancer cells detected by siRNA targeted knock-down analysis
-
Shin SH, Kim HS, Jung SH, Xu HD, Jeong YB, Chung YJ (2008) Implication of leucyl-tRNA synthetase 1 (LARS1) over-expression in growth and migration of lung cancer cells detected by siRNA targeted knock-down analysis. Exp Mol Med 40: 229-236
-
(2008)
Exp Mol Med
, vol.40
, pp. 229-236
-
-
Shin, S.H.1
Kim, H.S.2
Jung, S.H.3
Xu, H.D.4
Jeong, Y.B.5
Chung, Y.J.6
-
65
-
-
0033551859
-
Insights into editing from an ile-tRNA synthetase structure with tRNAile and mupirocin
-
Silvian LF, Wang J, Steitz TA (1999) Insights into editing from an ile-tRNA synthetase structure with tRNAile and mupirocin. Science 285: 1074-1077
-
(1999)
Science
, vol.285
, pp. 1074-1077
-
-
Silvian, L.F.1
Wang, J.2
Steitz, T.A.3
-
66
-
-
84860615998
-
Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations
-
Steenweg ME, Ghezzi D, Haack T, Abbink TE, Martinelli D, van Berkel CG, Bley A, Diogo L, Grillo E, Te Water Naude J, et al (2012) Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations. Brain 135: 1387-1394
-
(2012)
Brain
, vol.135
, pp. 1387-1394
-
-
Steenweg, M.E.1
Ghezzi, D.2
Haack, T.3
Abbink, T.E.4
Martinelli, D.5
van Berkel, C.G.6
Bley, A.7
Diogo, L.8
Grillo, E.9
Te Water Naude, J.10
-
67
-
-
67650882733
-
Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy
-
Storkebaum E, Leitao-Goncalves R, Godenschwege T, Nangle L, Mejia M, Bosmans I, Ooms T, Jacobs A, Van Dijck P, Yang XL, et al (2009) Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy. Proc Natl Acad Sci USA 106: 11782-11787
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 11782-11787
-
-
Storkebaum, E.1
Leitao-Goncalves, R.2
Godenschwege, T.3
Nangle, L.4
Mejia, M.5
Bosmans, I.6
Ooms, T.7
Jacobs, A.8
Van Dijck, P.9
Yang, X.L.10
-
68
-
-
78751702871
-
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations
-
Stum M, McLaughlin HM, Kleinbrink EL, Miers KE, Ackerman SL, Seburn KL, Antonellis A, Burgess RW (2011) An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations. Mol Cell Neurosci 46: 432-443
-
(2011)
Mol Cell Neurosci
, vol.46
, pp. 432-443
-
-
Stum, M.1
McLaughlin, H.M.2
Kleinbrink, E.L.3
Miers, K.E.4
Ackerman, S.L.5
Seburn, K.L.6
Antonellis, A.7
Burgess, R.W.8
-
69
-
-
58249110558
-
Genome-wide polysome profiling reveals an inflammation-responsive posttranscriptional operon in gamma interferon-activated monocytes
-
Vyas K, Chaudhuri S, Leaman DW, Komar AA, Musiyenko A, Barik S, Mazumder B (2009) Genome-wide polysome profiling reveals an inflammation-responsive posttranscriptional operon in gamma interferon-activated monocytes. Mol Cell Biol 29: 458-470
-
(2009)
Mol Cell Biol
, vol.29
, pp. 458-470
-
-
Vyas, K.1
Chaudhuri, S.2
Leaman, D.W.3
Komar, A.A.4
Musiyenko, A.5
Barik, S.6
Mazumder, B.7
-
70
-
-
34547745843
-
RNA transport and localized protein synthesis in neurological disorders and neural repair
-
Wang W, van Niekerk E, Willis DE, Twiss JL (2007) RNA transport and localized protein synthesis in neurological disorders and neural repair. Dev Neurobiol 67: 1166-1182
-
(2007)
Dev Neurobiol
, vol.67
, pp. 1166-1182
-
-
Wang, W.1
van Niekerk, E.2
Willis, D.E.3
Twiss, J.L.4
-
71
-
-
80051637832
-
mTORC1 signaling: what we still don't know
-
Wang X, Proud CG (2011) mTORC1 signaling: what we still don't know. J Mol Cell Biol 3: 206-220
-
(2011)
J Mol Cell Biol
, vol.3
, pp. 206-220
-
-
Wang, X.1
Proud, C.G.2
-
72
-
-
84863230283
-
Unique domain appended to vertebrate tRNA synthetase is essential for vascular development
-
Xu X, Shi Y, Zhang HM, Swindell EC, Marshall AG, Guo M, Kishi S, Yang XL (2012) Unique domain appended to vertebrate tRNA synthetase is essential for vascular development. Nat Commun 3: 681
-
(2012)
Nat Commun
, vol.3
, pp. 681
-
-
Xu, X.1
Shi, Y.2
Zhang, H.M.3
Swindell, E.C.4
Marshall, A.G.5
Guo, M.6
Kishi, S.7
Yang, X.L.8
-
73
-
-
84875512580
-
Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2
-
Yamashita S, Miyake N, Matsumoto N, Osaka H, Iai M, Aida N, Tanaka Y (2012) Neuropathology of leukoencephalopathy with brainstem and spinal cord involvement and high lactate caused by a homozygous mutation of DARS2. Brain Dev in press
-
(2012)
Brain Dev
-
-
Yamashita, S.1
Miyake, N.2
Matsumoto, N.3
Osaka, H.4
Iai, M.5
Aida, N.6
Tanaka, Y.7
-
74
-
-
66449115592
-
LysRS serves as a key signaling molecule in the immune response by regulating gene expression
-
Yannay-Cohen N, Carmi-Levy I, Kay G, Yang CM, Han JM, Kemeny DM, Kim S, Nechushtan H, Razin E (2009) LysRS serves as a key signaling molecule in the immune response by regulating gene expression. Mol Cell 34: 603-611
-
(2009)
Mol Cell
, vol.34
, pp. 603-611
-
-
Yannay-Cohen, N.1
Carmi-Levy, I.2
Kay, G.3
Yang, C.M.4
Han, J.M.5
Kemeny, D.M.6
Kim, S.7
Nechushtan, H.8
Razin, E.9
-
75
-
-
84862777633
-
Coding region polyadenylation generates a truncated tRNA synthetase that counters translation repression
-
Yao P, Potdar AA, Arif A, Ray PS, Mukhopadhyay R, Willard B, Xu Y, Yan J, Saidel GM, Fox PL (2012) Coding region polyadenylation generates a truncated tRNA synthetase that counters translation repression. Cell 149: 88-100
-
(2012)
Cell
, vol.149
, pp. 88-100
-
-
Yao, P.1
Potdar, A.A.2
Arif, A.3
Ray, P.S.4
Mukhopadhyay, R.5
Willard, B.6
Xu, Y.7
Yan, J.8
Saidel, G.M.9
Fox, P.L.10
-
76
-
-
53049108811
-
Unique residues crucial for optimal editing in yeast cytoplasmic leucyl-tRNA synthetase are revealed by using a novel knockout yeast strain
-
Yao P, Zhou XL, He R, Xue MQ, Zheng YG, Wang YF, Wang ED (2008) Unique residues crucial for optimal editing in yeast cytoplasmic leucyl-tRNA synthetase are revealed by using a novel knockout yeast strain. J Biol Chem 283: 22591-22600
-
(2008)
J Biol Chem
, vol.283
, pp. 22591-22600
-
-
Yao, P.1
Zhou, X.L.2
He, R.3
Xue, M.Q.4
Zheng, Y.G.5
Wang, Y.F.6
Wang, E.D.7
-
77
-
-
80054689158
-
Mitochondrial tRNA mutations and disease
-
Yarham JW, Elson JL, Blakely EL, McFarland R, Taylor RW (2010) Mitochondrial tRNA mutations and disease. Wiley Interdiscip Rev RNA 1: 304-324
-
(2010)
Wiley Interdiscip Rev RNA
, vol.1
, pp. 304-324
-
-
Yarham, J.W.1
Elson, J.L.2
Blakely, E.L.3
McFarland, R.4
Taylor, R.W.5
-
78
-
-
84863615583
-
Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy
-
Zhao Z, Hashiguchi A, Hu J, Sakiyama Y, Okamoto Y, Tokunaga S, Zhu L, Shen H, Takashima H (2012) Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy. Neurology 78: 1644-1649
-
(2012)
Neurology
, vol.78
, pp. 1644-1649
-
-
Zhao, Z.1
Hashiguchi, A.2
Hu, J.3
Sakiyama, Y.4
Okamoto, Y.5
Tokunaga, S.6
Zhu, L.7
Shen, H.8
Takashima, H.9
|