-
1
-
-
0016348695
-
Distinct hematological disorder with deletion of long arm of no. 5 chromosome
-
Van den Berghe, H. et al. Distinct hematological disorder with deletion of long arm of no.5 chromosome. Nature 251, 437-438 (1974).
-
(1974)
Nature
, vol.251
, pp. 437-438
-
-
Van Den Berghe, H.1
-
2
-
-
5444237608
-
The 5q-syndrome
-
Giagounidis, A.A., Germing, U., Wainscoat, J.S., Boultwood, J. & Aul, C. The 5q-syndrome. Hematology 9, 271-277 (2004).
-
(2004)
Hematology
, vol.9
, pp. 271-277
-
-
Giagounidis, A.A.1
Germing, U.2
Wainscoat, J.S.3
Boultwood, J.4
Aul, C.5
-
3
-
-
33749438404
-
Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion
-
List, A. et al. Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion. N. Engl. J. Med. 355, 1456-1465 (2006).
-
(2006)
N. Engl. J. Med.
, vol.355
, pp. 1456-1465
-
-
List, A.1
-
4
-
-
0036786901
-
The World Health Organization (WHO) classifcation of the myeloid neoplasms
-
Vardiman, J.W., Harris, N.L. & Brunning, R.D. The World Health Organization (WHO) classifcation of the myeloid neoplasms. Blood 100, 2292-2302 (2002).
-
(2002)
Blood
, vol.100
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
5
-
-
0028170959
-
The 5q-syndrome
-
Boultwood, J., Lewis, S. & Wainscoat, J.S. The 5q-syndrome. Blood 84, 3253-3260 (1994).
-
(1994)
Blood
, vol.84
, pp. 3253-3260
-
-
Boultwood, J.1
Lewis, S.2
Wainscoat, J.S.3
-
6
-
-
0027315865
-
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases
-
Le Beau, M.M. et al. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proc. Natl. Acad. Sci. USA 90, 5484-5488 (1993).
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 5484-5488
-
-
Le Beau, M.M.1
-
7
-
-
0028214564
-
Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: Delineation of the critical region on 5q and identifcation of a 5q-breakpoint
-
Boultwood, J. et al. Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q-syndrome: delineation of the critical region on 5q and identifcation of a 5q-breakpoint. Genomics 19, 425-432 (1994).
-
(1994)
Genomics
, vol.19
, pp. 425-432
-
-
Boultwood, J.1
-
8
-
-
0037097597
-
Narrowing and genomic annotation of the commonly deleted region of the 5q-syndrome
-
Boultwood, J. et al. Narrowing and genomic annotation of the commonly deleted region of the 5q-syndrome. Blood 99, 4638-4641 (2002).
-
(2002)
Blood
, vol.99
, pp. 4638-4641
-
-
Boultwood, J.1
-
9
-
-
0035862552
-
Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q)
-
Lai, F. et al. Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q). Genomics 71, 235-245 (2001).
-
(2001)
Genomics
, vol.71
, pp. 235-245
-
-
Lai, F.1
-
10
-
-
35748956094
-
+ cells in patients with the 5q-syndrome
-
Boultwood, J. et al. Gene expression profling of CD34+ cells in patients with the 5q-syndrome. Br. J. Haematol. 139, 578-589 (2007).
-
(2007)
Br. J. Haematol.
, vol.139
, pp. 578-589
-
-
Boultwood, J.1
-
11
-
-
0035843169
-
Inactivation of the apoptosis effector Apaf-1 in malignant melanoma
-
Soengas, M.S. et al. Inactivation of the apoptosis effector Apaf-1 in malignant melanoma. Nature 409, 207-211 (2001).
-
(2001)
Nature
, vol.409
, pp. 207-211
-
-
Soengas, M.S.1
-
12
-
-
0034066405
-
Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplifcation of MYCN
-
Teitz, T. et al. Caspase 8 is deleted or silenced preferentially in childhood neuroblastomas with amplifcation of MYCN. Nat. Med. 6, 529-535 (2000).
-
(2000)
Nat. Med.
, vol.6
, pp. 529-535
-
-
Teitz, T.1
-
13
-
-
0033741904
-
SPARC a matricellular protein: At the crossroads of cell-matrix
-
Brekken, R.A. & Sage, E.H. SPARC, a matricellular protein: at the crossroads of cell-matrix. Matrix Biol. 19, 569-580 (2000).
-
(2000)
Matrix Biol.
, vol.19
, pp. 569-580
-
-
Brekken, R.A.1
Sage, E.H.2
-
14
-
-
34548128327
-
Common deleted genes in the 5q-syndrome: Thrombocytopenia and reduced erythroid colony formation in SPARC null mice
-
Lehmann, S. et al. Common deleted genes in the 5q-syndrome: thrombocytopenia and reduced erythroid colony formation in SPARC null mice. Leukemia 21, 1931-1936 (2007).
-
(2007)
Leukemia
, vol.21
, pp. 1931-1936
-
-
Lehmann, S.1
-
15
-
-
38349088899
-
Identifcation of RPS14 as a 5q-syndrome gene by RNA interference screen
-
Ebert, B.L. et al. Identifcation of RPS14 as a 5q-syndrome gene by RNA interference screen. Nature 451, 335-339 (2008).
-
(2008)
Nature
, vol.451
, pp. 335-339
-
-
Ebert, B.L.1
-
16
-
-
0032907438
-
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anemia
-
Draptchinskaia, N. et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anemia. Nat. Genet. 21, 169-175 (1999).
-
(1999)
Nat. Genet.
, vol.21
, pp. 169-175
-
-
Draptchinskaia, N.1
-
17
-
-
33846703338
-
CHD5 is a tumor suppressor at human 1p36
-
Bagchi, A. et al. CHD5 is a tumor suppressor at human 1p36. Cell 128, 459-475 (2007).
-
(2007)
Cell
, vol.128
, pp. 459-475
-
-
Bagchi, A.1
-
18
-
-
0033950653
-
Genomic interval engineering of mice identifes a novel modulator of triglyceride production
-
Zhu, Y. et al. Genomic interval engineering of mice identifes a novel modulator of triglyceride production. Proc. Natl. Acad. Sci. USA 97, 1137-1142 (2000).
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 1137-1142
-
-
Zhu, Y.1
-
19
-
-
0034641705
-
Rapid generation of nested chromosomal deletions on mouse chromosome 2
-
LePage, D.F., Church, D.M., Millie, E., Hassold, T.J. & Conlon, R.A. Rapid generation of nested chromosomal deletions on mouse chromosome 2. Proc. Natl. Acad. Sci. USA 97, 10471-10476 (2000).
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 10471-10476
-
-
Lepage, D.F.1
Church, D.M.2
Millie, E.3
Hassold, T.J.4
Conlon, R.A.5
-
20
-
-
0034641134
-
Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder Treacher Collins syndrome
-
Dixon, J., Brakebusch, C., Fassler, R. & Dixon, M.J. Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome. Hum. Mol. Genet. 9, 1473-1480 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1473-1480
-
-
Dixon, J.1
Brakebusch, C.2
Fassler, R.3
Dixon, M.J.4
-
21
-
-
0345582392
-
Engineering de novo reciprocal chromosomal translocations associated with Mll to replicate primary events of human cancer
-
Forster, A. et al. Engineering de novo reciprocal chromosomal translocations associated with Mll to replicate primary events of human cancer. Cancer Cell 3, 449-458 (2003).
-
(2003)
Cancer Cell
, vol.3
, pp. 449-458
-
-
Forster, A.1
-
22
-
-
24944446028
-
Cerebral hypoplasia and craniofacial defects in mice lacking heparan sulfate Ndst1 gene function
-
Grobe, K. et al. Cerebral hypoplasia and craniofacial defects in mice lacking heparan sulfate Ndst1 gene function. Development 132, 3777-3786 (2005).
-
(2005)
Development
, vol.132
, pp. 3777-3786
-
-
Grobe, K.1
-
23
-
-
0027309316
-
+ T cell selection in mice lacking invariant chain expression
-
Bikoff, E.K. et al. Defective major histocompatibility complex class II assembly, transport, peptide acquisition and CD4+ T cell selection in mice lacking invariant chain expression. J. Exp. Med. 177, 1699-1712 (1993).
-
(1993)
J. Exp. Med.
, vol.177
, pp. 1699-1712
-
-
Bikoff, E.K.1
-
24
-
-
38949170601
-
Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function
-
Jones, N.C. et al. Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function. Nat. Med. 14, 125-133 (2008).
-
(2008)
Nat. Med.
, vol.14
, pp. 125-133
-
-
Jones, N.C.1
-
25
-
-
48249117726
-
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects
-
McGowan, K.A. et al. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. Nat. Genet. 40, 963-970 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 963-970
-
-
McGowan, K.A.1
-
26
-
-
33845196230
-
Ribosomal protein S6 gene haploinsuffciency is associated with activation of a p53-dependent checkpoint during gastrulation
-
Panic, L. et al. Ribosomal protein S6 gene haploinsuffciency is associated with activation of a p53-dependent checkpoint during gastrulation. Mol. Cell. Biol. 26, 8880-8891 (2006).
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 8880-8891
-
-
Panic, L.1
-
27
-
-
63649157049
-
How common are extraribosomal functions of ribosomal proteins?
-
Warner, J.R. & McIntosh, K.B. How common are extraribosomal functions of ribosomal proteins? Mol. Cell 34, 3-11 (2009).
-
(2009)
Mol Cell
, vol.34
, pp. 3-11
-
-
Warner, J.R.1
McIntosh, K.B.2
-
28
-
-
55549088527
-
P53 family in development
-
Danilova, N., Sakamoto, K.M. & Lin, S. p53 family in development. Mech. Dev. 125, 919-931 (2008).
-
(2008)
Mech. Dev.
, vol.125
, pp. 919-931
-
-
Danilova, N.1
Sakamoto, K.M.2
Lin, S.3
-
29
-
-
21244463426
-
SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells
-
Kiel, M.J. et al. SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells. Cell 121, 1109-1121 (2005).
-
(2005)
Cell
, vol.121
, pp. 1109-1121
-
-
Kiel, M.J.1
-
30
-
-
0035979247
-
Growth inhibition and DNA damage induced by Cre recombinase in mammalian cells
-
Loonstra, A. et al. Growth inhibition and DNA damage induced by Cre recombinase in mammalian cells. Proc. Natl. Acad. Sci. USA 98, 9209-9214 (2001).
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 9209-9214
-
-
Loonstra, A.1
-
31
-
-
44649092154
-
Haploinsuffciency of RPS14 in 5q-syndrome is associated with deregulation of ribosomal-and translation-related genes
-
Pellagatti, A. et al. Haploinsuffciency of RPS14 in 5q-syndrome is associated with deregulation of ribosomal-and translation-related genes. Br. J. Haematol. 142, 57-64 (2008).
-
(2008)
Br. J. Haematol.
, vol.142
, pp. 57-64
-
-
Pellagatti, A.1
-
32
-
-
26944450063
-
Roles of eukaryotic ribosomal proteins in maturation and transport of pre-18S rRNA and ribosome function
-
Ferreira-Cerca, S., Poll, G., Gleizes, P.E., Tschochner, H. & Milkereit, P. Roles of eukaryotic ribosomal proteins in maturation and transport of pre-18S rRNA and ribosome function. Mol. Cell 20, 263-275 (2005).
-
(2005)
Mol. Cell
, vol.20
, pp. 263-275
-
-
Ferreira-Cerca, S.1
Poll, G.2
Gleizes, P.E.3
Tschochner, H.4
Milkereit, P.5
-
33
-
-
2342631284
-
The carboxy-terminal extension of yeast ribosomal protein S14 is necessary for maturation of 43S preribosomes
-
Jakovljevic, J. et al. The carboxy-terminal extension of yeast ribosomal protein S14 is necessary for maturation of 43S preribosomes. Mol. Cell 14, 331-342 (2004).
-
(2004)
Mol. Cell
, vol.14
, pp. 331-342
-
-
Jakovljevic, J.1
-
34
-
-
41149087836
-
Inherited aplastic anemias/bone marrow failure syndromes
-
Dokal, I. & Vulliamy, T. Inherited aplastic anemias/bone marrow failure syndromes. Blood Rev. 22, 141-153 (2008).
-
(2008)
Blood Rev.
, vol.22
, pp. 141-153
-
-
Dokal, I.1
Vulliamy, T.2
-
35
-
-
33845303558
-
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia
-
Gazda, H.T. et al. Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia. Am. J. Hum. Genet. 79, 1110-1118 (2006).
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 1110-1118
-
-
Gazda, H.T.1
-
36
-
-
0029940791
-
Diamond-Blackfan anemia. Natural history and sequelae of treatment
-
Janov, A.J., Leong, T., Nathan, D.G. & Guinan, E.C. Diamond-Blackfan anemia. Natural history and sequelae of treatment. Medicine (Baltimore) 75, 77-78 (1996).
-
(1996)
Medicine (Baltimore)
, vol.75
, pp. 77-78
-
-
Janov, A.J.1
Leong, T.2
Nathan, D.G.3
Guinan, E.C.4
-
37
-
-
34047182008
-
The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast
-
Menne, T.F. et al. The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast. Nat. Genet. 39, 486-495 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 486-495
-
-
Menne, T.F.1
-
38
-
-
29144438951
-
Inactivation of S6 ribosomal protein gene in T lymphocytes activates a p53-dependent checkpoint response
-
Sulic, S. et al. Inactivation of S6 ribosomal protein gene in T lymphocytes activates a p53-dependent checkpoint response. Genes Dev. 19, 3070-3082 (2005).
-
(2005)
Genes Dev.
, vol.19
, pp. 3070-3082
-
-
Sulic, S.1
-
39
-
-
57649107153
-
Ribosomal protein S19 defciency in zebrafsh leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family
-
Danilova, N., Sakamoto, K.M. & Lin, S. Ribosomal protein S19 defciency in zebrafsh leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family. Blood 112, 5228-5237 (2008).
-
(2008)
Blood
, vol.112
, pp. 5228-5237
-
-
Danilova, N.1
Sakamoto, K.M.2
Lin, S.3
-
40
-
-
3242671307
-
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor
-
Valdez, B.C., Henning, D., So, R.B., Dixon, J. & Dixon, M.J. The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor. Proc. Natl. Acad. Sci. USA 101, 10709-10714 (2004).
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 10709-10714
-
-
Valdez, B.C.1
Henning, D.2
So, R.B.3
Dixon, J.4
Dixon, M.J.5
-
41
-
-
26444526314
-
The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation
-
Gonzales, B. et al. The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. Hum. Mol. Genet. 14, 2035-2043 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2035-2043
-
-
Gonzales, B.1
-
42
-
-
33748614339
-
Tcof1/Treacle is required for neural crest cell formation and proliferation defciencies that cause craniofacial abnormalities
-
Dixon, J. et al. Tcof1/Treacle is required for neural crest cell formation and proliferation defciencies that cause craniofacial abnormalities. Proc. Natl. Acad. Sci. USA 103, 13403-13408 (2006).
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 13403-13408
-
-
Dixon, J.1
-
43
-
-
64049107857
-
Absence of nucleolar disruption after impairment of 40S ribosome biogenesis reveals an rpL11-translation-dependent mechanism of p53 induction
-
Fumagalli, S. et al. Absence of nucleolar disruption after impairment of 40S ribosome biogenesis reveals an rpL11-translation-dependent mechanism of p53 induction. Nat. Cell Biol. 11, 501-508 (2009).
-
(2009)
Nat. Cell Biol.
, vol.11
, pp. 501-508
-
-
Fumagalli, S.1
-
44
-
-
28844485066
-
Differential roles of microtubule assembly and sliding in proplatelet formation by megakaryocytes
-
Patel, S.R. et al. Differential roles of microtubule assembly and sliding in proplatelet formation by megakaryocytes. Blood 106, 4076-4085 (2005).
-
(2005)
Blood
, vol.106
, pp. 4076-4085
-
-
Patel, S.R.1
-
45
-
-
33751197239
-
Nuclear translocation of the calcium-binding protein ALG-2 induced by the RNA-binding protein RBM22
-
Montaville, P. et al. Nuclear translocation of the calcium-binding protein ALG-2 induced by the RNA-binding protein RBM22. Biochim. Biophys. Acta 1763, 1335-1343 (2006).
-
(2006)
Biochim. Biophys. Acta
, vol.1763
, pp. 1335-1343
-
-
Montaville, P.1
-
46
-
-
7444220147
-
Aberrant and alternative splicing in cancer
-
Venables, J.P. Aberrant and alternative splicing in cancer. Cancer Res. 64, 7647-7654 (2004).
-
(2004)
Cancer Res.
, vol.64
, pp. 7647-7654
-
-
Venables, J.P.1
-
47
-
-
0041836238
-
Synaptopodin-defcient mice lack a spine apparatus and show defcits in synaptic plasticity
-
Deller, T. et al. Synaptopodin-defcient mice lack a spine apparatus and show defcits in synaptic plasticity. Proc. Natl. Acad. Sci. USA 100, 10494-10499 (2003).
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 10494-10499
-
-
Deller, T.1
-
48
-
-
0035871973
-
NID67, a small putative membrane protein, is preferentially induced by NGF in PC12 pheochromocytoma cells
-
Vician, L., Silver, A.L., Farias-Eisner, R. & Herschman, H.R. NID67, a small putative membrane protein, is preferentially induced by NGF in PC12 pheochromocytoma cells. J. Neurosci. Res. 64, 108-120 (2001).
-
(2001)
J. Neurosci. Res.
, vol.64
, pp. 108-120
-
-
Vician, L.1
Silver, A.L.2
Farias-Eisner, R.3
Herschman, H.R.4
-
49
-
-
0026561121
-
Mice defcient for p53 are developmentally normal but susceptible to spontaneous tumours
-
Donehower, L.A. et al. Mice defcient for p53 are developmentally normal but susceptible to spontaneous tumours. Nature 356, 215-221 (1992).
-
(1992)
Nature
, vol.356
, pp. 215-221
-
-
Donehower, L.A.1
|