-
1
-
-
0003611323
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Adams, A., D. E. Gottschling, C. A. Kaiser, and T. Stearns, 1997 Methods in Yeast Genetics. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1997)
Methods in Yeast Genetics
-
-
Adams, A.1
Gottschling, D.E.2
Kaiser, C.A.3
Stearns, T.4
-
2
-
-
77957731889
-
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy
-
Agamy, O., B. Ben Zeev, D. Lev, B. Marcus, D. Fine et al., 2010 Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy. Am. J. Hum. Genet. 87: 538-544.
-
(2010)
Am. J. Hum. Genet
, vol.87
, pp. 538-544
-
-
Agamy, O.1
Ben Zeev, B.2
Lev, D.3
Marcus, B.4
Fine, D.5
-
3
-
-
84881193117
-
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder
-
Akizu, N., V. Cantagrel, J. Schroth, N. Cai, K. Vaux et al., 2013 AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder. Cell 154: 505-517.
-
(2013)
Cell
, vol.154
, pp. 505-517
-
-
Akizu, N.1
Cantagrel, V.2
Schroth, J.3
Cai, N.4
Vaux, K.5
-
4
-
-
0033567131
-
The yeast exosome and human PM-Scl are related complexes of 39/59 exonucleases
-
Allmang, C., E. Petfalski, A. Podtelejnikov, M. Mann, D. Tollervey et al., 1999 The yeast exosome and human PM-Scl are related complexes of 39/59 exonucleases. Genes Dev. 13: 2148-2158.
-
(1999)
Genes Dev
, vol.13
, pp. 2148-2158
-
-
Allmang, C.1
Petfalski, E.2
Podtelejnikov, A.3
Mann, M.4
Tollervey, D.5
-
5
-
-
33748377124
-
Quantification of protein half-lives in the budding yeast proteome
-
Belle, A., A. Tanay, L. Bitincka, R. Shamir, and E. K. O’Shea, 2006 Quantification of protein half-lives in the budding yeast proteome. Proc. Natl. Acad. Sci. USA 103: 13004-13009.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 13004-13009
-
-
Belle, A.1
Tanay, A.2
Bitincka, L.3
Shamir, R.4
O’Shea, E.K.5
-
6
-
-
84880314374
-
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement
-
Biancheri, R., D. Cassandrini, F. Pinto, R. Trovato, M. Di Rocco et al., 2013 EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. J. Neurol. 260: 1866-1870.
-
(2013)
J. Neurol
, vol.260
, pp. 1866-1870
-
-
Biancheri, R.1
Cassandrini, D.2
Pinto, F.3
Trovato, R.4
Di Rocco, M.5
-
7
-
-
84903975963
-
EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia
-
Boczonadi, V., J. S. Muller, A. Pyle, J. Munkley, T. Dor et al., 2014 EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia. Nat. Commun. 5: 4287.
-
(2014)
Nat. Commun
, vol.5
, pp. 4287
-
-
Boczonadi, V.1
Muller, J.S.2
Pyle, A.3
Munkley, J.4
Dor, T.5
-
8
-
-
70350336247
-
The yeast exosome functions as a macromolecular cage to channel RNA substrates for degradation
-
Bonneau, F., J. Basquin, J. Ebert, E. Lorentzen, and E. Conti, 2009 The yeast exosome functions as a macromolecular cage to channel RNA substrates for degradation. Cell 139: 547-559.
-
(2009)
Cell
, vol.139
, pp. 547-559
-
-
Bonneau, F.1
Basquin, J.2
Ebert, J.3
Lorentzen, E.4
Conti, E.5
-
9
-
-
0035794216
-
Three novel components of the human exosome
-
Brouwer, R., C. Allmang, R. Raijmakers, Y. van Aarssen, W. V. Egberts et al., 2001 Three novel components of the human exosome. J. Biol. Chem. 276: 6177-6184.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 6177-6184
-
-
Brouwer, R.1
Allmang, C.2
Raijmakers, R.3
Van Aarssen, Y.4
Egberts, W.V.5
-
10
-
-
0034118002
-
The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo
-
Brown, J. T., X. Bai, and A. W. Johnson, 2000 The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo. RNA 6: 449-457.
-
(2000)
RNA
, vol.6
, pp. 449-457
-
-
Brown, J.T.1
Bai, X.2
Johnson, A.W.3
-
11
-
-
50449096432
-
TRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
-
Budde, B. S., Y. Namavar, P. G. Barth, B. T. Poll-The, G. Nurnberg et al., 2008 tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nat. Genet. 40: 1113-1118.
-
(2008)
Nat. Genet
, vol.40
, pp. 1113-1118
-
-
Budde, B.S.1
Namavar, Y.2
Barth, P.G.3
Poll-The, B.T.4
Nurnberg, G.5
-
12
-
-
79960681216
-
Rrp6, Rrp47 and cofactors of the nuclear exosome
-
Butler, J. S., and P. Mitchell, 2010 Rrp6, Rrp47 and cofactors of the nuclear exosome. Adv. Exp. Med. Biol. 702: 91-104.
-
(2010)
Adv. Exp. Med. Biol
, vol.702
, pp. 91-104
-
-
Butler, J.S.1
Mitchell, P.2
-
13
-
-
27644435644
-
Structural framework for the mechanism of archaeal exosomes in RNA processing
-
Buttner, K., K. Wenig, and K. P. Hopfner, 2005 Structural framework for the mechanism of archaeal exosomes in RNA processing. Mol. Cell 20: 461-471.
-
(2005)
Mol. Cell
, vol.20
, pp. 461-471
-
-
Buttner, K.1
Wenig, K.2
Hopfner, K.P.3
-
14
-
-
79951494668
-
Initial genome sequencing and analysis of multiple myeloma
-
Chapman, M. A., M. S. Lawrence, J. J. Keats, K. Cibulskis, C. Sougnez et al., 2011 Initial genome sequencing and analysis of multiple myeloma. Nature 471: 467-472.
-
(2011)
Nature
, vol.471
, pp. 467-472
-
-
Chapman, M.A.1
Lawrence, M.S.2
Keats, J.J.3
Cibulskis, K.4
Sougnez, C.5
-
15
-
-
0030595329
-
Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly
-
Chen, P., and M. Hochstrasser, 1996 Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly. Cell 86: 961-972.
-
(1996)
Cell
, vol.86
, pp. 961-972
-
-
Chen, P.1
Hochstrasser, M.2
-
16
-
-
84958073326
-
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt
-
Di Donato, N., T. Neuhann, A. K. Kahlert, B. Klink, K. Hackmann et al., 2016 Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt. J. Med. Genet. 53: 419-425.
-
(2016)
J. Med. Genet
, vol.53
, pp. 419-425
-
-
Di Donato, N.1
Neuhann, T.2
Kahlert, A.K.3
Klink, B.4
Hackmann, K.5
-
17
-
-
33846068920
-
A single subunit, Dis3, is essentially responsible for yeast exosome core activity
-
Dziembowski, A., E. Lorentzen, E. Conti, and B. Seraphin, 2007 A single subunit, Dis3, is essentially responsible for yeast exosome core activity. Nat. Struct. Mol. Biol. 14: 15-22.
-
(2007)
Nat. Struct. Mol. Biol
, vol.14
, pp. 15-22
-
-
Dziembowski, A.1
Lorentzen, E.2
Conti, E.3
Seraphin, B.4
-
18
-
-
35348983348
-
Deleterious mutation in the mitochondrial arginyltransfer RNA synthetase gene is associated with pontocerebellar hypoplasia
-
Edvardson, S., A. Shaag, O. Kolesnikova, J. M. Gomori, I. Tarassov et al., 2007 Deleterious mutation in the mitochondrial arginyltransfer 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
-
19
-
-
84894504906
-
EXOSC3 mutations in pontocerebellar hypoplasia type 1: Novel mutations and genotype-phenotype correlations
-
Eggens, V. R., P. G. Barth, J. M. Niermeijer, J. N. Berg, N. Darin et al., 2014 EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations. Orphanet J. Rare Dis. 9: 23.
-
(2014)
Orphanet J. Rare Dis
, vol.9
, pp. 23
-
-
Eggens, V.R.1
Barth, P.G.2
Niermeijer, J.M.3
Berg, J.N.4
Darin, N.5
-
20
-
-
0035898660
-
The exosome of Trypanosoma brucei
-
Estevez, A. M., T. Kempf, and C. Clayton, 2001 The exosome of Trypanosoma brucei. EMBO J. 20: 3831-3839.
-
(2001)
EMBO J
, vol.20
, pp. 3831-3839
-
-
Estevez, A.M.1
Kempf, T.2
Clayton, C.3
-
21
-
-
0042317221
-
The roles of intersubunit interactions in exosome stability
-
Estevez, A. M., B. Lehner, C. M. Sanderson, T. Ruppert, and C. Clayton, 2003 The roles of intersubunit interactions in exosome stability. J. Biol. Chem. 278: 34943-34951.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 34943-34951
-
-
Estevez, A.M.1
Lehner, B.2
Sanderson, C.M.3
Ruppert, T.4
Clayton, C.5
-
22
-
-
84859487192
-
SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome
-
Fabre, A., B. Charroux, C. Martinez-Vinson, B. Roquelaure, E. Odul et al., 2012 SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome. Am. J. Hum. Genet. 90: 689-692.
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 689-692
-
-
Fabre, A.1
Charroux, B.2
Martinez-Vinson, C.3
Roquelaure, B.4
Odul, E.5
-
23
-
-
84890553188
-
Syndromic (Phenotypic) diarrhoea of infancy/trichohepato-enteric syndrome
-
Fabre, A., A. Breton, M. E. Coste, V. Colomb, B. Dubern et al., 2013 Syndromic (phenotypic) diarrhoea of infancy/trichohepato-enteric syndrome. Arch. Dis. Child. 99: 35-38
-
(2013)
Arch. Dis. Child
, vol.99
, pp. 35-38
-
-
Fabre, A.1
Breton, A.2
Coste, M.E.3
Colomb, V.4
Dubern, B.5
-
24
-
-
10044286102
-
5-fluorouracil enhances exosome-dependent accumulation of polyadenylated rRNAs
-
Fang, F., J. Hoskins, and J. S. Butler, 2004 5-fluorouracil enhances exosome-dependent accumulation of polyadenylated rRNAs. Mol. Cell. Biol. 24: 10766-10776.
-
(2004)
Mol. Cell. Biol
, vol.24
, pp. 10766-10776
-
-
Fang, F.1
Hoskins, J.2
Butler, J.S.3
-
25
-
-
84991736463
-
The RNA exosome channeling and direct access conformations have distinct in vivo functions
-
Han, J., and A. van Hoof, 2016 The RNA exosome channeling and direct access conformations have distinct in vivo functions. Cell Reports 16: 3348-3358.
-
(2016)
Cell Reports
, vol.16
, pp. 3348-3358
-
-
Han, J.1
Van Hoof, A.2
-
26
-
-
84875623194
-
CLP1 links tRNA metabolism to progressive motor-neuron loss
-
Hanada, T., S. Weitzer, B. Mair, C. Bernreuther, B. J. Wainger et al., 2013 CLP1 links tRNA metabolism to progressive motor-neuron loss. Nature 495: 474-480.
-
(2013)
Nature
, vol.495
, pp. 474-480
-
-
Hanada, T.1
Weitzer, S.2
Mair, B.3
Bernreuther, C.4
Wainger, B.J.5
-
27
-
-
77952855204
-
Mutations in TTC37 cause trichohepatoenteric syndrome (Phenotypic diarrhea of infancy)
-
Hartley, J. L., N. C. Zachos, B. Dawood, M. Donowitz, J. Forman et al., 2010 Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy). Gastroenterology 138: 2388-2398.
-
(2010)
Gastroenterology 138
, vol.138
, pp. 2388-2398
-
-
Hartley, J.L.1
Zachos, N.C.2
Dawood, B.3
Donowitz, M.4
Forman, J.5
-
28
-
-
0000577868
-
The 39 to 59 degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 39 to 59 exonucleases of the exosome complex
-
Jacobs Anderson, J. S., and R. Parker, 1998 The 39 to 59 degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 39 to 59 exonucleases of the exosome complex. EMBO J. 17: 1497-1506.
-
(1998)
EMBO J
, vol.17
, pp. 1497-1506
-
-
Jacobs Anderson, J.S.1
Parker, R.2
-
29
-
-
2642574393
-
Nuclear surveillance and degradation of hypomodified initiator tRNAMet in S. Cerevisiae
-
Kadaba, S., A. Krueger, T. Trice, A. M. Krecic, A. G. Hinnebusch et al., 2004 Nuclear surveillance and degradation of hypomodified initiator tRNAMet in S. cerevisiae. Genes Dev. 18: 1227-1240.
-
(2004)
Genes Dev
, vol.18
, pp. 1227-1240
-
-
Kadaba, S.1
Krueger, A.2
Trice, T.3
Krecic, A.M.4
Hinnebusch, A.G.5
-
30
-
-
0002064084
-
Neuroblastoma: Cell culture analysis of a differentiating stem cell system
-
Klebe, R. J., and F. H. Ruddle, 1969 Neuroblastoma: cell culture analysis of a differentiating stem cell system. J. Cell Biol. 43: 69a.
-
(1969)
J. Cell Biol
, vol.43
-
-
Klebe, R.J.1
Ruddle, F.H.2
-
31
-
-
84992358935
-
Structure of a cytoplasmic 11-subunit RNA exosome complex
-
Kowalinski, E., A. Kogel, J. Ebert, P. Reichelt, E. Stegmann et al., 2016 Structure of a cytoplasmic 11-subunit RNA exosome complex. Mol. Cell 63: 125-134.
-
(2016)
Mol. Cell
, vol.63
, pp. 125-134
-
-
Kowalinski, E.1
Kogel, A.2
Ebert, J.3
Reichelt, P.4
Stegmann, E.5
-
32
-
-
20444368818
-
RNA degradation by the exosome is promoted by a nuclear polyadenylation complex
-
LaCava, J., J. Houseley, C. Saveanu, E. Petfalski, E. Thompson et al., 2005 RNA degradation by the exosome is promoted by a nuclear polyadenylation complex. Cell 121: 713-724.
-
(2005)
Cell
, vol.121
, pp. 713-724
-
-
Lacava, J.1
Houseley, J.2
Saveanu, C.3
Petfalski, E.4
Thompson, E.5
-
33
-
-
57749189164
-
Endonucleolytic RNA cleavage by a eukaryotic exosome
-
Lebreton, A., R. Tomecki, A. Dziembowski, and B. Seraphin, 2008 Endonucleolytic RNA cleavage by a eukaryotic exosome. Nature 456: 993-996.
-
(2008)
Nature
, vol.456
, pp. 993-996
-
-
Lebreton, A.1
Tomecki, R.2
Dziembowski, A.3
Seraphin, B.4
-
34
-
-
34247617365
-
Beta-subunit appendages promote 20S proteasome assembly by overcoming an Ump1-dependent checkpoint
-
Li, X., A. R. Kusmierczyk, P. Wong, A. Emili, and M. Hochstrasser, 2007 Beta-subunit appendages promote 20S proteasome assembly by overcoming an Ump1-dependent checkpoint. EMBO J. 26: 2339-2349.
-
(2007)
EMBO J
, vol.26
, pp. 2339-2349
-
-
Li, X.1
Kusmierczyk, A.R.2
Wong, P.3
Emili, A.4
Hochstrasser, M.5
-
35
-
-
84893752136
-
Visualization of distinct substrate-recruitment pathways in the yeast exosome by EM
-
Liu, J. J., M. A. Bratkowski, X. Liu, C. Y. Niu, A. Ke et al., 2014 Visualization of distinct substrate-recruitment pathways in the yeast exosome by EM. Nat. Struct. Mol. Biol. 21: 95-102.
-
(2014)
Nat. Struct. Mol. Biol
, vol.21
, pp. 95-102
-
-
Liu, J.J.1
Bratkowski, M.A.2
Liu, X.3
Niu, C.Y.4
Ke, A.5
-
36
-
-
33845407784
-
Reconstitution, activities, and structure of the eukaryotic RNA exosome
-
Liu, Q., J. C. Greimann, and C. D. Lima, 2006 Reconstitution, activities, and structure of the eukaryotic RNA exosome. Cell 127: 1223-1237.
-
(2006)
Cell
, vol.127
, pp. 1223-1237
-
-
Liu, Q.1
Greimann, J.C.2
Lima, C.D.3
-
37
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta C(T))
-
Livak, K. J., and T. D. Schmittgen, 2001 Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta C(T)). Method. Methods 25: 402-408.
-
(2001)
Method. Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
38
-
-
34247844604
-
RNA channelling by the archaeal exosome
-
Lorentzen, E., A. Dziembowski, D. Lindner, B. Seraphin, and E. Conti, 2007 RNA channelling by the archaeal exosome. EMBO Rep. 8: 470-476.
-
(2007)
EMBO Rep
, vol.8
, pp. 470-476
-
-
Lorentzen, E.1
Dziembowski, A.2
Lindner, D.3
Seraphin, B.4
Conti, E.5
-
39
-
-
80051730960
-
Interaction profiling identifies the human nuclear exosome targeting complex
-
Lubas, M., M. S. Christensen, M. S. Kristiansen, M. Domanski, L. G. Falkenby et al., 2011 Interaction profiling identifies the human nuclear exosome targeting complex. Mol. Cell 43: 624-637.
-
(2011)
Mol. Cell
, vol.43
, pp. 624-637
-
-
Lubas, M.1
Christensen, M.S.2
Kristiansen, M.S.3
Domanski, M.4
Falkenby, L.G.5
-
40
-
-
84920950118
-
The human nuclear exosome targeting complex is loaded onto newly synthesized RNA to direct early ribonucleolysis
-
Lubas, M., P. R. Andersen, A. Schein, A. Dziembowski, G. Kudla et al., 2015 The human nuclear exosome targeting complex is loaded onto newly synthesized RNA to direct early ribonucleolysis. Cell Reports 10: 178-192.
-
(2015)
Cell Reports
, vol.10
, pp. 178-192
-
-
Lubas, M.1
Andersen, P.R.2
Schein, A.3
Dziembowski, A.4
Kudla, G.5
-
41
-
-
10744225364
-
Discovering modes of action for therapeutic compounds using a genome-wide screen of yeast heterozygotes
-
Lum, P. Y., C. D. Armour, S. B. Stepaniants, G. Cavet, M. K. Wolf et al., 2004 Discovering modes of action for therapeutic compounds using a genome-wide screen of yeast heterozygotes. Cell 116: 121-137.
-
(2004)
Cell
, vol.116
, pp. 121-137
-
-
Lum, P.Y.1
Armour, C.D.2
Stepaniants, S.B.3
Cavet, G.4
Wolf, M.K.5
-
42
-
-
84874742223
-
Crystal structure of an RNA-bound 11-subunit eukaryotic exosome complex
-
Makino, D. L., M. Baumgartner, and E. Conti, 2013 Crystal structure of an RNA-bound 11-subunit eukaryotic exosome complex. Nature 495: 70-75.
-
(2013)
Nature
, vol.495
, pp. 70-75
-
-
Makino, D.L.1
Baumgartner, M.2
Conti, E.3
-
43
-
-
78649469070
-
RNA channelling by the eukaryotic exosome
-
Malet, H., M. Topf, D. K. Clare, J. Ebert, F. Bonneau et al., 2010 RNA channelling by the eukaryotic exosome. EMBO Rep. 11: 936-942.
-
(2010)
EMBO Rep
, vol.11
, pp. 936-942
-
-
Malet, H.1
Topf, M.2
Clare, D.K.3
Ebert, J.4
Bonneau, F.5
-
44
-
-
0029939247
-
The 39 end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism
-
Mitchell, P., E. Petfalski, and D. Tollervey, 1996 The 39 end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism. Genes Dev. 10: 502-513.
-
(1996)
Genes Dev
, vol.10
, pp. 502-513
-
-
Mitchell, P.1
Petfalski, E.2
Tollervey, D.3
-
45
-
-
0030702085
-
The exosome: A conserved eukaryotic RNA processing complex containing multiple 39/59 exoribonucleases
-
Mitchell, P., E. Petfalski, A. Shevchenko, M. Mann, and D. Tollervey, 1997 The exosome: a conserved eukaryotic RNA processing complex containing multiple 39/59 exoribonucleases. Cell 91: 457-466.
-
(1997)
Cell
, vol.91
, pp. 457-466
-
-
Mitchell, P.1
Petfalski, E.2
Shevchenko, A.3
Mann, M.4
Tollervey, D.5
-
46
-
-
84868200452
-
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development
-
Mochida, G.H., V. S. Ganesh, M. I. deMichelena, H. Dias, K. D. Atabay et al., 2012 CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nat. Genet. 44: 1260-1264.
-
(2012)
Nat. Genet
, vol.44
, pp. 1260-1264
-
-
Mochida, G.H.1
Ganesh, V.S.2
Demichelena, M.I.3
Dias, H.4
Atabay, K.D.5
-
47
-
-
79956307284
-
TSEN54 mutations cause pontocerebellar hypoplasia type 5
-
Namavar, Y., D. Chitayat, P. G. Barth, F. van Ruissen, M. B. de Wissel et al., 2011 TSEN54 mutations cause pontocerebellar hypoplasia type 5. Eur. J. Hum. Genet. 19: 724-726.
-
(2011)
Eur. J. Hum. Genet
, vol.19
, pp. 724-726
-
-
Namavar, Y.1
Chitayat, D.2
Barth, P.G.3
Van Ruissen, F.4
De Wissel, M.B.5
-
48
-
-
68249087651
-
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene
-
Renbaum, P., E. Kellerman, R. Jaron, D. Geiger, R. Segel et al., 2009 Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene. Am. J. Hum. Genet. 85: 281-289.
-
(2009)
Am. J. Hum. Genet
, vol.85
, pp. 281-289
-
-
Renbaum, P.1
Kellerman, E.2
Jaron, R.3
Geiger, D.4
Segel, R.5
-
49
-
-
85012054078
-
The 39 to 59 exoribonuclease DIS3: From structure and mechanisms to biological functions and role in human disease
-
Robinson, S. R., A. W. Oliver, T. J. Chevassut, and S. F. Newbury, 2015 The 39 to 59 exoribonuclease DIS3: from structure and mechanisms to biological functions and role in human disease. Biomolecules 5: 1515-1539.
-
(2015)
Biomolecules
, vol.5
, pp. 1515-1539
-
-
Robinson, S.R.1
Oliver, A.W.2
Chevassut, T.J.3
Newbury, S.F.4
-
50
-
-
84873671848
-
Pontocerebellar hypoplasia type 1: Clinical spectrum and relevance of EXOSC3 mutations
-
Rudnik-Schoneborn, S., J. Senderek, J. C. Jen, G. Houge, P. Seeman et al., 2013 Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations. Neurology 80: 438-446.
-
(2013)
Neurology
, vol.80
, pp. 438-446
-
-
Rudnik-Schoneborn, S.1
Senderek, J.2
Jen, J.C.3
Houge, G.4
Seeman, P.5
-
51
-
-
0003903343
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., E. F. Fritsch, and T. Maniatis, 1989 Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
52
-
-
57749210245
-
Determining in vivo activity of the yeast cytoplasmic exosome
-
Schaeffer, D., S. Meaux, A. Clark, and A. van Hoof, 2008 Determining in vivo activity of the yeast cytoplasmic exosome. Methods Enzymol. 448: 227-239.
-
(2008)
Methods Enzymol
, vol.448
, pp. 227-239
-
-
Schaeffer, D.1
Meaux, S.2
Clark, A.3
Van Hoof, A.4
-
53
-
-
58149236691
-
The exosome contains domains with specific endoribonuclease, exoribonuclease and cytoplasmic mRNA decay activities
-
Schaeffer, D., B. Tsanova, A. Barbas, F. P. Reis, E. G. Dastidar et al., 2009 The exosome contains domains with specific endoribonuclease, exoribonuclease and cytoplasmic mRNA decay activities. Nat. Struct. Mol. Biol. 16: 56-62.
-
(2009)
Nat. Struct. Mol. Biol
, vol.16
, pp. 56-62
-
-
Schaeffer, D.1
Tsanova, B.2
Barbas, A.3
Reis, F.P.4
Dastidar, E.G.5
-
54
-
-
85008498310
-
Functions of the cytoplasmic exosome
-
edited by T. H. Jensen. Landes Bioscience, New York
-
Schaeffer, D., A. Clark, A. A. Klauer, B. Tsanova, and A. van Hoof, 2010 Functions of the cytoplasmic exosome, in RNA Exosome, edited by T. H. Jensen. Landes Bioscience, New York.
-
(2010)
RNA Exosome
-
-
Schaeffer, D.1
Clark, A.2
Klauer, A.A.3
Tsanova, B.4
Van Hoof, A.5
-
55
-
-
84899581919
-
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration
-
Schaffer, A. E., V. R. Eggens, A. O. Caglayan, M. S. Reuter, E. Scott et al., 2014 CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration. Cell 157: 651-663.
-
(2014)
Cell
, vol.157
, pp. 651-663
-
-
Schaffer, A.E.1
Eggens, V.R.2
Caglayan, A.O.3
Reuter, M.S.4
Scott, E.5
-
56
-
-
29244475356
-
MPP6 is an exosome-associated RNA-binding protein involved in 5.8S rRNA maturation
-
Schilders, G., R. Raijmakers, J. M. Raats, and G. J. Pruijn, 2005 MPP6 is an exosome-associated RNA-binding protein involved in 5.8S rRNA maturation. Nucleic Acids Res. 33: 6795-6804.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 6795-6804
-
-
Schilders, G.1
Raijmakers, R.2
Raats, J.M.3
Pruijn, G.J.4
-
57
-
-
34250339672
-
C1D and hMtr4p associate with the human exosome subunit PM/Scl-100 and are involved in pre-rRNA processing
-
Schilders, G., E. van Dijk, and G. J. Pruijn, 2007 C1D and hMtr4p associate with the human exosome subunit PM/Scl-100 and are involved in pre-rRNA processing. Nucleic Acids Res. 35: 2564-2572.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 2564-2572
-
-
Schilders, G.1
Van Dijk, E.2
Pruijn, G.J.3
-
58
-
-
84884592355
-
Threading the barrel of the RNA exosome
-
Schneider, C., and D. Tollervey, 2013 Threading the barrel of the RNA exosome. Trends Biochem. Sci. 38: 485-493.
-
(2013)
Trends Biochem. Sci
, vol.38
, pp. 485-493
-
-
Schneider, C.1
Tollervey, D.2
-
59
-
-
84889254442
-
Homozygous EXOSC3 mutation c.92G/C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma
-
Schwabova, J., D. S. Brozkova, B. Petrak, M. Mojzisova, K. Pavlickova et al., 2013 Homozygous EXOSC3 mutation c.92G/C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma. J. Neurogenet. 27: 163-169.
-
(2013)
J. Neurogenet
, vol.27
, pp. 163-169
-
-
Schwabova, J.1
Brozkova, D.S.2
Petrak, B.3
Mojzisova, M.4
Pavlickova, K.5
-
60
-
-
75949116417
-
Polyadenylation and degradation of incomplete RNA polymerase I transcripts in mammalian cells
-
Shcherbik, N., M. Wang, Y. R. Lapik, L. Srivastava, and D. G. Pestov, 2010 Polyadenylation and degradation of incomplete RNA polymerase I transcripts in mammalian cells. EMBO Rep. 11: 106-111.
-
(2010)
EMBO Rep
, vol.11
, pp. 106-111
-
-
Shcherbik, N.1
Wang, M.2
Lapik, Y.R.3
Srivastava, L.4
Pestov, D.G.5
-
61
-
-
0024669291
-
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae
-
Sikorski, R. S., and P. Hieter, 1989 A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics 122: 19-27.
-
(1989)
Genetics
, vol.122
, pp. 19-27
-
-
Sikorski, R.S.1
Hieter, P.2
-
62
-
-
84864383638
-
Comparison of the yeast and human nuclear exosome complexes
-
Sloan, K. E., C. Schneider, and N. J. Watkins, 2012 Comparison of the yeast and human nuclear exosome complexes. Biochem. Soc. Trans. 40: 850-855.
-
(2012)
Biochem. Soc. Trans
, vol.40
, pp. 850-855
-
-
Sloan, K.E.1
Schneider, C.2
Watkins, N.J.3
-
63
-
-
77954867631
-
Dis3-like 1: A novel exoribonuclease associated with the human exosome
-
Staals, R. H., A. W. Bronkhorst, G. Schilders, S. Slomovic, G. Schuster et al., 2010 Dis3-like 1: a novel exoribonuclease associated with the human exosome. EMBO J. 29: 2358-2367.
-
(2010)
EMBO J
, vol.29
, pp. 2358-2367
-
-
Staals, R.H.1
Bronkhorst, A.W.2
Schilders, G.3
Slomovic, S.4
Schuster, G.5
-
64
-
-
77954877566
-
The human core exosome interacts with differentially localized processive RNases: HDIS3 and hDIS3L
-
Tomecki, R., M. S. Kristiansen, S. Lykke-Andersen, A. Chlebowski, K. M. Larsen et al., 2010 The human core exosome interacts with differentially localized processive RNases: hDIS3 and hDIS3L. EMBO J. 29: 2342-2357.
-
(2010)
EMBO J
, vol.29
, pp. 2342-2357
-
-
Tomecki, R.1
Kristiansen, M.S.2
Lykke-Andersen, S.3
Chlebowski, A.4
Larsen, K.M.5
-
65
-
-
84893317824
-
Multiple myeloma-associated hDIS3 mutations cause perturbations in cellular RNA metabolism and suggest hDIS3 PIN domain as a potential drug target
-
Tomecki, R., K. Drazkowska, I. Kucinski, K. Stodus, R. J. Szczesny et al., 2013 Multiple myeloma-associated hDIS3 mutations cause perturbations in cellular RNA metabolism and suggest hDIS3 PIN domain as a potential drug target. Nucleic Acids Res. 42: 1270-1290.
-
(2013)
Nucleic Acids Res
, vol.42
, pp. 1270-1290
-
-
Tomecki, R.1
Drazkowska, K.2
Kucinski, I.3
Stodus, K.4
Szczesny, R.J.5
-
66
-
-
84878942836
-
Molecular architecture and assembly of the eukaryotic proteasome
-
Tomko, Jr., R. J., and M. Hochstrasser, 2013 Molecular architecture and assembly of the eukaryotic proteasome. Annu. Rev. Biochem. 82: 415-445.
-
(2013)
Annu. Rev. Biochem
, vol.82
, pp. 415-445
-
-
Tomko, R.J.1
Hochstrasser, M.2
-
67
-
-
0033777266
-
Function of the ski4p (Csl4p) and Ski7p proteins in 39-to-59 degradation of mRNA
-
Van Hoof, A., R. R. Staples, R. E. Baker, and R. Parker, 2000 Function of the ski4p (Csl4p) and Ski7p proteins in 39-to-59 degradation of mRNA. Mol. Cell. Biol. 20: 8230-8243.
-
(2000)
Mol. Cell. Biol
, vol.20
, pp. 8230-8243
-
-
Van Hoof, A.1
Staples, R.R.2
Baker, R.E.3
Parker, R.4
-
68
-
-
0037155584
-
Exosome-mediated recognition and degradation of mRNAs lacking a termination codon
-
Van Hoof, A., P. A. Frischmeyer, H. C. Dietz, and R. Parker, 2002 Exosome-mediated recognition and degradation of mRNAs lacking a termination codon. Science 295: 2262-2264.
-
(2002)
Science
, vol.295
, pp. 2262-2264
-
-
Van Hoof, A.1
Frischmeyer, P.A.2
Dietz, H.C.3
Parker, R.4
-
69
-
-
30744467674
-
Nrd1 interacts with the nuclear exosome for 39 processing of RNA polymerase II transcripts
-
Vasiljeva, L., and S. Buratowski, 2006 Nrd1 interacts with the nuclear exosome for 39 processing of RNA polymerase II transcripts. Mol. Cell 21: 239-248.
-
(2006)
Mol. Cell
, vol.21
, pp. 239-248
-
-
Vasiljeva, L.1
Buratowski, S.2
-
70
-
-
84861608931
-
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration
-
Wan, J., M. Yourshaw, H. Mamsa, S. Rudnik-Schoneborn, M. P. Menezes et al., 2012 Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration. Nat. Genet. 44: 704-708.
-
(2012)
Nat. Genet
, vol.44
, pp. 704-708
-
-
Wan, J.1
Yourshaw, M.2
Mamsa, H.3
Rudnik-Schoneborn, S.4
Menezes, M.P.5
-
71
-
-
84866927206
-
Structure and activities of the eukaryotic RNA exosome
-
Wasmuth, E. V., and C. D. Lima, 2012 Structure and activities of the eukaryotic RNA exosome. Enzymes 31: 53-75.
-
(2012)
Enzymes
, vol.31
, pp. 53-75
-
-
Wasmuth, E.V.1
Lima, C.D.2
-
72
-
-
84904821452
-
Structure of an Rrp6-RNA exosome complex bound to poly(A) RNA
-
Wasmuth, E. V., K. Januszyk, and C. D. Lima, 2014 Structure of an Rrp6-RNA exosome complex bound to poly(A) RNA. Nature 511: 435-439.
-
(2014)
Nature
, vol.511
, pp. 435-439
-
-
Wasmuth, E.V.1
Januszyk, K.2
Lima, C.D.3
-
73
-
-
84885701940
-
An interplay between transcription, processing, and degradation determines tRNA levels in yeast
-
Wichtowska, D., T. W. Turowski, and M. Boguta, 2013 An interplay between transcription, processing, and degradation determines tRNA levels in yeast. Wiley Interdiscip. Rev. RNA 4: 709-722.
-
(2013)
Wiley Interdiscip. Rev. RNA
, vol.4
, pp. 709-722
-
-
Wichtowska, D.1
Turowski, T.W.2
Boguta, M.3
|