-
1
-
-
1642553650
-
Defective translational control facilitates vesicular stomatitis virus oncolysis
-
S. Balachandran, and G.N. Barber Defective translational control facilitates vesicular stomatitis virus oncolysis Cancer Cells 5 2004 51 65
-
(2004)
Cancer Cells
, vol.5
, pp. 51-65
-
-
Balachandran, S.1
Barber, G.N.2
-
2
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
M.M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding Anal. Biochem. 72 1976 248 254
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
3
-
-
16244373354
-
EIF2B5 mutations compromise GFAP(+) astrocyte generation in vanishing white matter leukodystrophy
-
J. Dietrich, M. Lacagnina, D. Gass, E. Richfield, M. Mayer-Proschel, M. Noble, C. Torres, and C. Proschel EIF2B5 mutations compromise GFAP(+) astrocyte generation in vanishing white matter leukodystrophy Nat. Med. 11 2005 277 283
-
(2005)
Nat. Med.
, vol.11
, pp. 277-283
-
-
Dietrich, J.1
Lacagnina, M.2
Gass, D.3
Richfield, E.4
Mayer-Proschel, M.5
Noble, M.6
Torres, C.7
Proschel, C.8
-
4
-
-
0011328943
-
Polycystische Umwandlung des Marklagers mit progredienten verlauf
-
W.-J. Eicke Polycystische Umwandlung des Marklagers mit progredienten verlauf Arch. Psychiatr. Nervenkr. 203 1962 599 609
-
(1962)
Arch. Psychiatr. Nervenkr.
, vol.203
, pp. 599-609
-
-
Eicke, W.-J.1
-
5
-
-
0036791923
-
Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus
-
A. Fogli, K. Wong, E. Eymard-Pierre, J. Wenger, J.P. Bouffard, E. Goldin, D.N. Black, O. Boespflug-Tanguy, and R. Schiffmann Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus Ann. Neurol. 52 2002 506 510
-
(2002)
Ann. Neurol.
, vol.52
, pp. 506-510
-
-
Fogli, A.1
Wong, K.2
Eymard-Pierre, E.3
Wenger, J.4
Bouffard, J.P.5
Goldin, E.6
Black, D.N.7
Boespflug-Tanguy, O.8
Schiffmann, R.9
-
6
-
-
2342657880
-
The effect of genotype on the natural history of eIF2B-related leukodystrophies
-
A. Fogli, R. Schiffmann, E. Bertini, S. Ughetto, P. Combes, E. Eymard-Pierre, C.R. Kaneski, M. Pineda, M. Troncoso, G. Uziel, R. Surtees, D. Pugin, M.P. Chaunu, D. Rodriguez, and O. Boespflug-Tanguy The effect of genotype on the natural history of eIF2B-related leukodystrophies Neurology 62 2004 1509 1517
-
(2004)
Neurology
, vol.62
, pp. 1509-1517
-
-
Fogli, A.1
Schiffmann, R.2
Bertini, E.3
Ughetto, S.4
Combes, P.5
Eymard-Pierre, E.6
Kaneski, C.R.7
Pineda, M.8
Troncoso, M.9
Uziel, G.10
Surtees, R.11
Pugin, D.12
Chaunu, M.P.13
Rodriguez, D.14
Boespflug-Tanguy, O.15
-
7
-
-
4043171216
-
Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients
-
A. Fogli, R. Schiffmann, L. Hugendubler, P. Combes, E. Bertini, D. Rodriguez, S.R. Kimball, and O. Boespflug-Tanguy Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients Eur. J. Hum. Genet. 12 2004 561 566
-
(2004)
Eur. J. Hum. Genet.
, vol.12
, pp. 561-566
-
-
Fogli, A.1
Schiffmann, R.2
Hugendubler, L.3
Combes, P.4
Bertini, E.5
Rodriguez, D.6
Kimball, S.R.7
Boespflug-Tanguy, O.8
-
8
-
-
0002470681
-
Mechanism and regulation of initiator methionyl-tRNA binding to ribosomes
-
N. Sonenberg J.W.B. Hershey M.B. Mathews Cold Spring Harbor Laboratory Press Cold Spring Harbor
-
A.G. Hinnebusch Mechanism and regulation of initiator methionyl-tRNA binding to ribosomes N. Sonenberg J.W.B. Hershey M.B. Mathews Translational Control of Gene Expression 2000 Cold Spring Harbor Laboratory Press Cold Spring Harbor 185 243
-
(2000)
Translational Control of Gene Expression
, pp. 185-243
-
-
Hinnebusch, A.G.1
-
9
-
-
0024582782
-
The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs
-
R.J. Kaufman, M.V. Davies, V.K. Pathak, and J.W. Hershey The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs Mol. Cell. Biol. 9 1989 946 958
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 946-958
-
-
Kaufman, R.J.1
Davies, M.V.2
Pathak, V.K.3
Hershey, J.W.4
-
11
-
-
0032489511
-
Nerve and epidermal growth factor induce protein synthesis and eIF2B activation in PC12 cells
-
M. Kleijn, G.I. Welsh, G.C. Scheper, H.O. Voorma, C.G. Proud, and A.A.M. Thomas Nerve and epidermal growth factor induce protein synthesis and eIF2B activation in PC12 cells J. Biol. Chem. 273 1998 5536 5541
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 5536-5541
-
-
Kleijn, M.1
Welsh, G.I.2
Scheper, G.C.3
Voorma, H.O.4
Proud, C.G.5
Thomas, A.A.M.6
-
12
-
-
0033361759
-
The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27
-
P.A. Leegwater, A.A. Konst, B. Kuyt, L.A. Sandkuijl, S. Naidu, C.B. Oudejans, R.B. Schutgens, J.C. Pronk, and M.S. van der Knaap The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27 Am. J. Hum. Genet. 65 1999 728 734
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 728-734
-
-
Leegwater, P.A.1
Konst, A.A.2
Kuyt, B.3
Sandkuijl, L.A.4
Naidu, S.5
Oudejans, C.B.6
Schutgens, R.B.7
Pronk, J.C.8
Van Der Knaap, M.S.9
-
13
-
-
18344386777
-
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter
-
P.A. Leegwater, G. Vermeulen, A.A. Konst, S. Naidu, J. Mulders, A. Visser, P. Kersbergen, D. Mobach, D. Fonds, C.G. van Berkel, R.J. Lemmers, R.R. Frants, C.B. Oudejans, R.B. Schutgens, J.C. Pronk, and M.S. van der Knaap Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter Nat. Genet. 29 2001 383 388
-
(2001)
Nat. Genet.
, vol.29
, pp. 383-388
-
-
Leegwater, P.A.1
Vermeulen, G.2
Konst, A.A.3
Naidu, S.4
Mulders, J.5
Visser, A.6
Kersbergen, P.7
Mobach, D.8
Fonds, D.9
Van Berkel, C.G.10
Lemmers, R.J.11
Frants, R.R.12
Oudejans, C.B.13
Schutgens, R.B.14
Pronk, J.C.15
Van Der Knaap, M.S.16
-
14
-
-
1842453031
-
Mutations linked to leukoencephalopathy with vanishing white matter impair the function of the eukaryotic initiation factor 2B complex in diverse ways
-
W. Li, X. Wang, M.S. van der Knaap, and C.G. Proud Mutations linked to leukoencephalopathy with vanishing white matter impair the function of the eukaryotic initiation factor 2B complex in diverse ways Mol. Cell. Biol. 24 2004 3295 3306
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 3295-3306
-
-
Li, W.1
Wang, X.2
Van Der Knaap, M.S.3
Proud, C.G.4
-
15
-
-
0025656869
-
Control of translation in adenovirus-infected cells
-
M.B. Mathews Control of translation in adenovirus-infected cells Enzyme 44 1990 250 264
-
(1990)
Enzyme
, vol.44
, pp. 250-264
-
-
Mathews, M.B.1
-
16
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
T. Mosmann Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
-
17
-
-
0028203337
-
Use of monoclonal antibodies to study the structure and function of eukaryotic protein synthesis initiation factor eIF-2B
-
S. Oldfield, B.L. Jones, D. Tanton, and C.G. Proud Use of monoclonal antibodies to study the structure and function of eukaryotic protein synthesis initiation factor eIF-2B Eur. J. Biochem. 221 1994 399 410
-
(1994)
Eur. J. Biochem.
, vol.221
, pp. 399-410
-
-
Oldfield, S.1
Jones, B.L.2
Tanton, D.3
Proud, C.G.4
-
18
-
-
0028588049
-
Translational control during heat shock
-
R. Panniers Translational control during heat shock Biochimie 76 1994 737 747
-
(1994)
Biochimie
, vol.76
, pp. 737-747
-
-
Panniers, R.1
-
19
-
-
0035231980
-
Regulation of eukaryotic initiation factor eIF2B
-
C.G. Proud Regulation of eukaryotic initiation factor eIF2B Prog. Mol. Subcell. Biol. 26 2001 95 114
-
(2001)
Prog. Mol. Subcell. Biol.
, vol.26
, pp. 95-114
-
-
Proud, C.G.1
-
20
-
-
1542344340
-
Mutations causing childhood ataxia with central nervous system hypomyelination reduce eukaryotic initiation factor 2B complex formation and activity
-
J.P. Richardson, S.S. Mohammad, and G.D. Pavitt Mutations causing childhood ataxia with central nervous system hypomyelination reduce eukaryotic initiation factor 2B complex formation and activity Mol. Cell. Biol. 24 2004 2352 2363
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 2352-2363
-
-
Richardson, J.P.1
Mohammad, S.S.2
Pavitt, G.D.3
-
21
-
-
0030870906
-
Inactivation of eIF2B and phosphorylation of PHAS-I in heat-shocked rat hepatoma cells
-
G.C. Scheper, J. Mulder, M. Kleijn, H.O. Voorma, A.A.M. Thomas, and R. van Wijk Inactivation of eIF2B and phosphorylation of PHAS-I in heat-shocked rat hepatoma cells J. Biol. Chem. 272 1997 26850 26856
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 26850-26856
-
-
Scheper, G.C.1
Mulder, J.2
Kleijn, M.3
Voorma, H.O.4
Thomas, A.A.M.5
Van Wijk, R.6
-
22
-
-
0032169947
-
Inactivation of eukaryotic initiation factor 2B in vitro by heat shock
-
G.C. Scheper, A.A.M. Thomas, and R. van Wijk Inactivation of eukaryotic initiation factor 2B in vitro by heat shock Biochem. J. 334 1998 463 467
-
(1998)
Biochem. J.
, vol.334
, pp. 463-467
-
-
Scheper, G.C.1
Thomas, A.A.M.2
Van Wijk, R.3
-
23
-
-
0028351908
-
Childhood ataxia with diffuse central nervous system hypomyelination
-
R. Schiffmann, J.R. Moller, B.D. Trapp, H.H. Shih, R.G. Farrer, D.A. Katz, J.R. Alger, C.C. Parker, P.E. Hauer, C.R. Kaneski, J.D. Heiss, E.M. Heiss, E.M. Kaye, R.H. Quarles, R.O. Brady, and N.W. Barton Childhood ataxia with diffuse central nervous system hypomyelination Ann. Neurol. 35 1994 331 340
-
(1994)
Ann. Neurol.
, vol.35
, pp. 331-340
-
-
Schiffmann, R.1
Moller, J.R.2
Trapp, B.D.3
Shih, H.H.4
Farrer, R.G.5
Katz, D.A.6
Alger, J.R.7
Parker, C.C.8
Hauer, P.E.9
Kaneski, C.R.10
Heiss, J.D.11
Heiss, E.M.12
Kaye, E.M.13
Quarles, R.H.14
Brady, R.O.15
Barton, N.W.16
-
24
-
-
0030975392
-
A new leukoencephalopathy with vanishing white matter
-
M.S. van der Knaap, P.G. Barth, F.J. Gabreels, E. Franzoni, J.H. Begeer, H. Stroink, J.J. Rotteveel, and J. Valk A new leukoencephalopathy with vanishing white matter Neurology 48 1997 845 855
-
(1997)
Neurology
, vol.48
, pp. 845-855
-
-
Van Der Knaap, M.S.1
Barth, P.G.2
Gabreels, F.J.3
Franzoni, E.4
Begeer, J.H.5
Stroink, H.6
Rotteveel, J.J.7
Valk, J.8
-
25
-
-
0031721955
-
Phenotypic variation in leukoencephalopathy with vanishing white matter
-
M.S. van der Knaap, W. Kamphorst, P.G. Barth, C.L. Kraaijeveld, E. Gut, and J. Valk Phenotypic variation in leukoencephalopathy with vanishing white matter Neurology 51 1998 540 547
-
(1998)
Neurology
, vol.51
, pp. 540-547
-
-
Van Der Knaap, M.S.1
Kamphorst, W.2
Barth, P.G.3
Kraaijeveld, C.L.4
Gut, E.5
Valk, J.6
-
26
-
-
0032886533
-
Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach
-
M.S. van der Knaap, S.N. Breiter, S. Naidu, A.A. Hart, and J. Valk Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach Radiology 213 1999 121 133
-
(1999)
Radiology
, vol.213
, pp. 121-133
-
-
Van Der Knaap, M.S.1
Breiter, S.N.2
Naidu, S.3
Hart, A.A.4
Valk, J.5
-
27
-
-
0036156978
-
Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter
-
M.S. van der Knaap, P.A. Leegwater, A.A. Konst, A. Visser, S. Naidu, C.B. Oudejans, R.B. Schutgens, and J.C. Pronk Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter Ann. Neurol. 51 2002 264 270
-
(2002)
Ann. Neurol.
, vol.51
, pp. 264-270
-
-
Van Der Knaap, M.S.1
Leegwater, P.A.2
Konst, A.A.3
Visser, A.4
Naidu, S.5
Oudejans, C.B.6
Schutgens, R.B.7
Pronk, J.C.8
-
28
-
-
0242522401
-
EIF2B-related disorders: Antenatal onset and involvement of multiple organs
-
M.S. van der Knaap, C.G. van Berkel, J. Herms, R. van Coster, M. Baethmann, S. Naidu, E. Boltshauser, M.A. Willemsen, B. Plecko, G.F. Hoffmann, C.G. Proud, G.C. Scheper, and J.C. Pronk eIF2B-related disorders: antenatal onset and involvement of multiple organs Am. J. Hum. Genet. 73 2003 1199 1207
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1199-1207
-
-
Van Der Knaap, M.S.1
Van Berkel, C.G.2
Herms, J.3
Van Coster, R.4
Baethmann, M.5
Naidu, S.6
Boltshauser, E.7
Willemsen, M.A.8
Plecko, B.9
Hoffmann, G.F.10
Proud, C.G.11
Scheper, G.C.12
Pronk, J.C.13
-
29
-
-
2342551021
-
3His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults
-
3His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults Neurology 62 2004 1598 1600
-
(2004)
Neurology
, vol.62
, pp. 1598-1600
-
-
Van Der Knaap, M.S.1
Leegwater, P.A.2
Van Berkel, C.G.3
Brenner, C.4
Storey, E.5
Di Rocco, M.6
Salvi, F.7
Pronk, J.C.8
-
30
-
-
2942568003
-
The life and death of oligodendrocytes in vanishing white matter disease
-
K. Van Haren, J.P. van der Voorn, D.R. Peterson, M.S. van der Knaap, and J.M. Powers The life and death of oligodendrocytes in vanishing white matter disease J. Neuropathol. Exp. Neurol. 63 2004 618 630
-
(2004)
J. Neuropathol. Exp. Neurol.
, vol.63
, pp. 618-630
-
-
Van Haren, K.1
Van Der Voorn, J.P.2
Peterson, D.R.3
Van Der Knaap, M.S.4
Powers, J.M.5
-
31
-
-
0037109062
-
Evidence that the dephosphorylation of Ser(535) in the epsilon-subunit of eukaryotic initiation factor (eIF) 2B is insufficient for the activation of eIF2B by insulin
-
X. Wang, M. Janmaat, A. Beugnet, F.E. Paulin, and C.G. Proud Evidence that the dephosphorylation of Ser(535) in the epsilon-subunit of eukaryotic initiation factor (eIF) 2B is insufficient for the activation of eIF2B by insulin Biochem. J. 367 2002 475 481
-
(2002)
Biochem. J.
, vol.367
, pp. 475-481
-
-
Wang, X.1
Janmaat, M.2
Beugnet, A.3
Paulin, F.E.4
Proud, C.G.5
-
33
-
-
0033770347
-
Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome
-
K. Wong, R.C. Armstrong, K.A. Gyure, A.L. Morrison, D. Rodriguez, R. Matalon, A.B. Johnson, R. Wollmann, E. Gilbert, T.Q. Le, C.A. Bradley, K. Crutchfield, and R. Schiffmann Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome Acta Neuropathol. (Berlin) 100 2000 635 646
-
(2000)
Acta Neuropathol. (Berlin)
, vol.100
, pp. 635-646
-
-
Wong, K.1
Armstrong, R.C.2
Gyure, K.A.3
Morrison, A.L.4
Rodriguez, D.5
Matalon, R.6
Johnson, A.B.7
Wollmann, R.8
Gilbert, E.9
Le, T.Q.10
Bradley, C.A.11
Crutchfield, K.12
Schiffmann, R.13
|