-
1
-
-
85041516484
-
-
Bosman, F. T., Carneiro, F., Hruban, R. H. & Theise, N. D. WHO Classification of Tumours of the Digestive System 4th edn (International Agency for Research on Cancer, 2010).
-
-
-
-
2
-
-
77956354202
-
MEN1 in pancreatic endocrine tumors: Analysis of gene and protein status in 169 sporadic neoplasms reveals alterations in the vast majority of cases
-
Corbo, V. et al. MEN1 in pancreatic endocrine tumors: Analysis of gene and protein status in 169 sporadic neoplasms reveals alterations in the vast majority of cases. Endocr. Relat. Cancer 17, 771-783 (2010).
-
(2010)
Endocr. Relat. Cancer
, vol.17
, pp. 771-783
-
-
Corbo, V.1
-
3
-
-
79952279828
-
DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors
-
Jiao, Y. et al. DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors. Science 331, 1199-1203 (2011).
-
(2011)
Science
, vol.331
, pp. 1199-1203
-
-
Jiao, Y.1
-
4
-
-
74949122343
-
Pancreatic endocrine tumors: Expression profiling evidences a role for AKT-mTOR pathway
-
Missiaglia, E. et al. Pancreatic endocrine tumors: expression profiling evidences a role for AKT-mTOR pathway. J. Clin. Oncol. 28, 245-255 (2010).
-
(2010)
J. Clin. Oncol.
, vol.28
, pp. 245-255
-
-
Missiaglia, E.1
-
5
-
-
84930209646
-
Mutation-targeted therapy with sunitinib or everolimus in patients with advanced low-grade or intermediate-grade neuroendocrine tumours of the gastrointestinal tract and pancreas with or without cytoreductive surgery: Protocol for a phase II clinical trial
-
Neychev, V. et al. Mutation-targeted therapy with sunitinib or everolimus in patients with advanced low-grade or intermediate-grade neuroendocrine tumours of the gastrointestinal tract and pancreas with or without cytoreductive surgery: protocol for a phase II clinical trial. BMJ Open 5, e008248 (2015).
-
(2015)
BMJ Open
, vol.5
, pp. e008248
-
-
Neychev, V.1
-
6
-
-
79952254109
-
Cancer. New epigenetic drivers of cancers
-
Elsässer, S. J., Allis, C. D. & Lewis, P. W. Cancer. New epigenetic drivers of cancers. Science 331, 1145-1146 (2011).
-
(2011)
Science
, vol.331
, pp. 1145-1146
-
-
Elsässer, S.J.1
Allis, C.D.2
Lewis, P.W.3
-
7
-
-
79960700556
-
Altered telomeres in tumors with ATRX and DAXX mutations
-
Heaphy, C. M. et al. Altered telomeres in tumors with ATRX and DAXX mutations. Science 333, 425 (2011).
-
(2011)
Science
, vol.333
, pp. 425
-
-
Heaphy, C.M.1
-
8
-
-
84892717244
-
Loss of DAXX and ATRX are associated with chromosome instability and reduced survival of patients with pancreatic neuroendocrine tumors
-
Marinoni, I. et al. Loss of DAXX and ATRX are associated with chromosome instability and reduced survival of patients with pancreatic neuroendocrine tumors. Gastroenterology 146, 453-460 (2014).
-
(2014)
Gastroenterology
, vol.146
, pp. 453-460
-
-
Marinoni, I.1
-
9
-
-
84866700697
-
Qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profiles
-
Song, S. et al. qpure: A tool to estimate tumor cellularity from genome-wide single-nucleotide polymorphism profiles. PLoS One 7, e45835 (2012).
-
(2012)
PLoS One
, vol.7
, pp. e45835
-
-
Song, S.1
-
10
-
-
84923538176
-
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis
-
Nones, K. et al. Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis. Nat. Commun. 5, 5224 (2014).
-
(2014)
Nat. Commun.
, vol.5
, pp. 5224
-
-
Nones, K.1
-
11
-
-
84924056345
-
Whole genomes redefine the mutational landscape of pancreatic cancer
-
Waddell, N. et al. Whole genomes redefine the mutational landscape of pancreatic cancer. Nature 518, 495-501 (2015).
-
(2015)
Nature
, vol.518
, pp. 495-501
-
-
Waddell, N.1
-
12
-
-
76249097734
-
Genome Alteration Print (GAP): A tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays
-
Popova, T. et al. Genome Alteration Print (GAP): A tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays. Genome Biol. 10, R128 (2009).
-
(2009)
Genome Biol.
, vol.10
, pp. R128
-
-
Popova, T.1
-
13
-
-
79955166265
-
GISTIC2. 0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
-
Mermel, C. H. et al. GISTIC2. 0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers. Genome Biol. 12, R41 (2011).
-
(2011)
Genome Biol.
, vol.12
, pp. R41
-
-
Mermel, C.H.1
-
14
-
-
84882837534
-
Signatures of mutational processes in human cancer
-
Alexandrov, L. B. et al. Signatures of mutational processes in human cancer. Nature 500, 415-421 (2013).
-
(2013)
Nature
, vol.500
, pp. 415-421
-
-
Alexandrov, L.B.1
-
15
-
-
84861541343
-
Mutational processes molding the genomes of 21 breast cancers
-
Nik-Zainal, S. et al. Mutational processes molding the genomes of 21 breast cancers. Cell 149, 979-993 (2012).
-
(2012)
Cell
, vol.149
, pp. 979-993
-
-
Nik-Zainal, S.1
-
16
-
-
84973594792
-
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
-
Nik-Zainal, S. et al. Landscape of somatic mutations in 560 breast cancer whole-genome sequences. Nature 534, 47-54 (2016).
-
(2016)
Nature
, vol.534
, pp. 47-54
-
-
Nik-Zainal, S.1
-
17
-
-
84930638395
-
Whole-genome characterization of chemoresistant ovarian cancer
-
Patch, A. M. et al. Whole-genome characterization of chemoresistant ovarian cancer. Nature 521, 489-494 (2015).
-
(2015)
Nature
, vol.521
, pp. 489-494
-
-
Patch, A.M.1
-
18
-
-
0036478899
-
Inherited variants of MYH associated with somatic G:C-< T:A mutations in colorectal tumors
-
Al-Tassan, N. et al. Inherited variants of MYH associated with somatic G:C-< T:A mutations in colorectal tumors. Nat. Genet. 30, 227-232 (2002).
-
(2002)
Nat. Genet.
, vol.30
, pp. 227-232
-
-
Al-Tassan, N.1
-
19
-
-
84902303614
-
MUTYH-associated polyposis (MAP): Evidence for the origin of the common European mutations p. Tyr179Cys and p. Gly396Asp by founder events
-
Aretz, S. et al. MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p. Tyr179Cys and p. Gly396Asp by founder events. Eur. J. Hum. Genet. 22, 923-929 (2014).
-
(2014)
Eur. J. Hum. Genet.
, vol.22
, pp. 923-929
-
-
Aretz, S.1
-
20
-
-
70649083240
-
Expanded extracolonic tumor spectrum in MUTYH-associated polyposis
-
Vogt, S. et al. Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. Gastroenterology 137, 1976-1985 (2009).
-
(2009)
Gastroenterology
, vol.137
, pp. 1976-1985
-
-
Vogt, S.1
-
21
-
-
78650959663
-
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
-
Stephens, P. J. et al. Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell 144, 27-40 (2011).
-
(2011)
Cell
, vol.144
, pp. 27-40
-
-
Stephens, P.J.1
-
22
-
-
84862907577
-
Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations
-
Rausch, T. et al. Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. Cell 148, 59-71 (2012).
-
(2012)
Cell
, vol.148
, pp. 59-71
-
-
Rausch, T.1
-
23
-
-
34447560185
-
Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia
-
Georgitsi, M. et al. Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia. J. Clin. Endocrinol. Metab. 92, 3321-3325 (2007).
-
(2007)
J. Clin. Endocrinol. Metab.
, vol.92
, pp. 3321-3325
-
-
Georgitsi, M.1
-
24
-
-
84888369188
-
Somatic mutation of CDKN1B in small intestine neuroendocrine tumors
-
Francis, J. M. et al. Somatic mutation of CDKN1B in small intestine neuroendocrine tumors. Nat. Genet. 45, 1483-1486 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 1483-1486
-
-
Francis, J.M.1
-
25
-
-
0031872093
-
Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: Histopathological and molecular genetic analysis
-
Lubensky, I. A. et al. Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysis. Am. J. Pathol. 153, 223-231 (1998).
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 223-231
-
-
Lubensky, I.A.1
-
26
-
-
0037320555
-
Mutations in CHEK2 associated with prostate cancer risk
-
Dong, X. et al. Mutations in CHEK2 associated with prostate cancer risk. Am. J. Hum. Genet. 72, 270-280 (2003).
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 270-280
-
-
Dong, X.1
-
27
-
-
84887032986
-
IntOGen-mutations identifies cancer drivers across tumor types
-
Gonzalez-Perez, A. et al. IntOGen-mutations identifies cancer drivers across tumor types. Nat. Methods 10, 1081-1082 (2013).
-
(2013)
Nat. Methods
, vol.10
, pp. 1081-1082
-
-
Gonzalez-Perez, A.1
-
28
-
-
84863393080
-
Intratumor heterogeneity and branched evolution revealed by multiregion sequencing
-
Gerlinger, M. et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N. Engl. J. Med. 366, 883-892 (2012).
-
(2012)
N. Engl. J. Med.
, vol.366
, pp. 883-892
-
-
Gerlinger, M.1
-
29
-
-
84887599883
-
Distinct pathways regulated by menin and by MLL1 in hematopoietic stem cells and developing B cells
-
Li, B. E. et al. Distinct pathways regulated by menin and by MLL1 in hematopoietic stem cells and developing B cells. Blood 122, 2039-2046 (2013).
-
(2013)
Blood
, vol.122
, pp. 2039-2046
-
-
Li, B.E.1
-
30
-
-
84884584249
-
The malignant brain tumor (MBT) domain protein SFMBT1 is an integral histone reader subunit of the LSD1 demethylase complex for chromatin association and epithelial-to-mesenchymal transition
-
Tang, M. et al. The malignant brain tumor (MBT) domain protein SFMBT1 is an integral histone reader subunit of the LSD1 demethylase complex for chromatin association and epithelial-to-mesenchymal transition. J. Biol. Chem. 288, 27680-27691 (2013).
-
(2013)
J. Biol. Chem.
, vol.288
, pp. 27680-27691
-
-
Tang, M.1
-
31
-
-
84922259664
-
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas
-
Asai, A. et al. High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas. Gene 558, 220-226 (2015).
-
(2015)
Gene
, vol.558
, pp. 220-226
-
-
Asai, A.1
-
32
-
-
84937024265
-
Persephin: A potential key component in human oral cancer progression through the RET receptor tyrosine kinase-mitogen-activated protein kinase signaling pathway
-
Baba, T. et al. Persephin: A potential key component in human oral cancer progression through the RET receptor tyrosine kinase-mitogen-activated protein kinase signaling pathway. Mol. Carcinog. 54, 608-617 (2015).
-
(2015)
Mol. Carcinog.
, vol.54
, pp. 608-617
-
-
Baba, T.1
-
33
-
-
0035937727
-
Human glial cell line-derived neurotrophic factor receptor alpha 4 is the receptor for persephin and is predominantly expressed in normal and malignant thyroid medullary cells
-
Lindahl, M. et al. Human glial cell line-derived neurotrophic factor receptor alpha 4 is the receptor for persephin and is predominantly expressed in normal and malignant thyroid medullary cells. J. Biol. Chem. 276, 9344-9351 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 9344-9351
-
-
Lindahl, M.1
-
34
-
-
84856800302
-
Role of AMPK-mTOR-Ulk1/2 in the regulation of autophagy: Cross talk, shortcuts, and feedbacks
-
Alers, S., Löffler, A. S., Wesselborg, S. & Stork, B. Role of AMPK-mTOR-Ulk1/2 in the regulation of autophagy: cross talk, shortcuts, and feedbacks. Mol. Cell. Biol. 32, 2-11 (2012).
-
(2012)
Mol. Cell. Biol.
, vol.32
, pp. 2-11
-
-
Alers, S.1
Löffler, A.S.2
Wesselborg, S.3
Stork, B.4
-
35
-
-
84959433571
-
New brain tumor entities emerge from molecular classification of CNS-PNETs
-
Sturm, D. et al. New brain tumor entities emerge from molecular classification of CNS-PNETs. Cell 164, 1060-1072 (2016).
-
(2016)
Cell
, vol.164
, pp. 1060-1072
-
-
Sturm, D.1
-
36
-
-
0026686674
-
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
-
Delattre, O. et al. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours. Nature 359, 162-165 (1992).
-
(1992)
Nature
, vol.359
, pp. 162-165
-
-
Delattre, O.1
-
37
-
-
0027230568
-
Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation
-
May, W. A. et al. Ewing sarcoma 11;22 translocation produces a chimeric transcription factor that requires the DNA-binding domain encoded by FLI1 for transformation. Proc. Natl Acad. Sci. USA 90, 5752-5756 (1993).
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 5752-5756
-
-
May, W.A.1
-
38
-
-
80054782854
-
Promiscuous partnerships in Ewing's sarcoma
-
Sankar, S. & Lessnick, S. L. Promiscuous partnerships in Ewing's sarcoma. Cancer Genet. 204, 351-365 (2011).
-
(2011)
Cancer Genet.
, vol.204
, pp. 351-365
-
-
Sankar, S.1
Lessnick, S.L.2
-
39
-
-
84862076370
-
Malignant gastrointestinal neuroectodermal tumor: Clinicopathologic, immunohistochemical, ultrastructural, and molecular analysis of 16 cases with a reappraisal of clear cell sarcoma-like tumors of the gastrointestinal tract
-
Stockman, D. L. et al. Malignant gastrointestinal neuroectodermal tumor: clinicopathologic, immunohistochemical, ultrastructural, and molecular analysis of 16 cases with a reappraisal of clear cell sarcoma-like tumors of the gastrointestinal tract. Am. J. Surg. Pathol. 36, 857-868 (2012).
-
(2012)
Am. J. Surg. Pathol.
, vol.36
, pp. 857-868
-
-
Stockman, D.L.1
-
40
-
-
84905457348
-
The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation
-
Brohl, A. S. et al. The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. PLoS Genet. 10, e1004475 (2014).
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004475
-
-
Brohl, A.S.1
-
41
-
-
84908447818
-
The genomic landscape of pediatric Ewing sarcoma
-
Crompton, B. D. et al. The genomic landscape of pediatric Ewing sarcoma. Cancer Discov. 4, 1326-1341 (2014).
-
(2014)
Cancer Discov.
, vol.4
, pp. 1326-1341
-
-
Crompton, B.D.1
-
42
-
-
84908397914
-
Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations
-
Tirode, F. et al. Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. Cancer Discov. 4, 1342-1353 (2014).
-
(2014)
Cancer Discov.
, vol.4
, pp. 1342-1353
-
-
Tirode, F.1
-
43
-
-
84864619205
-
Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway
-
Lovejoy, C. A. et al. Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway. PLoS Genet. 8, e1002772 (2012).
-
(2012)
PLoS Genet.
, vol.8
, pp. e1002772
-
-
Lovejoy, C.A.1
-
44
-
-
84960109620
-
A cross-species analysis in pancreatic neuroendocrine tumors reveals molecular subtypes with distinctive clinical, metastatic, developmental, and metabolic characteristics
-
Sadanandam, A. et al. A cross-species analysis in pancreatic neuroendocrine tumors reveals molecular subtypes with distinctive clinical, metastatic, developmental, and metabolic characteristics. Cancer Discov. 5, 1296-1313 (2015).
-
(2015)
Cancer Discov
, vol.5
, pp. 1296-1313
-
-
Sadanandam, A.1
-
45
-
-
0037821661
-
Multiple tumor suppressor pathways negatively regulate telomerase
-
Lin, S. Y. & Elledge, S. J. Multiple tumor suppressor pathways negatively regulate telomerase. Cell 113, 881-889 (2003).
-
(2003)
Cell
, vol.113
, pp. 881-889
-
-
Lin, S.Y.1
Elledge, S.J.2
-
46
-
-
84878357685
-
A Tumor suppressor complex with GAP activity for the Rag GTPases that signal amino acid sufficiency to mTORC1
-
Bar-Peled, L. et al. A Tumor suppressor complex with GAP activity for the Rag GTPases that signal amino acid sufficiency to mTORC1. Science 340, 1100-1106 (2013).
-
(2013)
Science
, vol.340
, pp. 1100-1106
-
-
Bar-Peled, L.1
-
47
-
-
84880684921
-
MEN1 is a melanoma tumor suppressor that preserves genomic integrity by stimulating transcription of genes that promote homologous recombination-directed DNA repair
-
Fang, M. et al. MEN1 is a melanoma tumor suppressor that preserves genomic integrity by stimulating transcription of genes that promote homologous recombination-directed DNA repair. Mol. Cell. Biol. 33, 2635-2647 (2013).
-
(2013)
Mol. Cell. Biol.
, vol.33
, pp. 2635-2647
-
-
Fang, M.1
-
48
-
-
78751554804
-
The tumor suppressor protein menin inhibits AKT activation by regulating its cellular localization
-
Wang, Y. et al. The tumor suppressor protein menin inhibits AKT activation by regulating its cellular localization. Cancer Res. 71, 371-382 (2011).
-
(2011)
Cancer Res.
, vol.71
, pp. 371-382
-
-
Wang, Y.1
-
49
-
-
84880721384
-
Menin: A scaffold protein that controls gene expression and cell signaling
-
Matkar, S., Thiel, A. & Hua, X. Menin: A scaffold protein that controls gene expression and cell signaling. Trends Biochem. Sci. 38, 394-402 (2013).
-
(2013)
Trends Biochem. Sci.
, vol.38
, pp. 394-402
-
-
Matkar, S.1
Thiel, A.2
Hua, X.3
-
50
-
-
84976904305
-
ClinVar: Public archive of interpretations of clinically relevant variants
-
Landrum M. J. et al. ClinVar: public archive of interpretations of clinically relevant variants. Nucleic Acids Res. 44, D862-D868 (2016).
-
(2016)
Nucleic Acids Res.
, vol.44
, pp. D862-D868
-
-
Landrum, M.J.1
-
51
-
-
84869091997
-
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes
-
Biankin, A. V. et al. Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes. Nature 491, 399-405 (2012).
-
(2012)
Nature
, vol.491
, pp. 399-405
-
-
Biankin, A.V.1
-
52
-
-
84892833777
-
Discovery and saturation analysis of cancer genes across 21 tumour types
-
Lawrence, M. S. et al. Discovery and saturation analysis of cancer genes across 21 tumour types. Nature 505, 495-501 (2014).
-
(2014)
Nature
, vol.505
, pp. 495-501
-
-
Lawrence, M.S.1
-
53
-
-
11144355687
-
Role of inherited defects of MYH in the development of sporadic colorectal cancer
-
Kambara, T. et al. Role of inherited defects of MYH in the development of sporadic colorectal cancer. Genes Chromosom. Cancer 40, 1-9 (2004).
-
(2004)
Genes Chromosom. Cancer
, vol.40
, pp. 1-9
-
-
Kambara, T.1
-
54
-
-
79960825030
-
A quantitative PCR method for measuring absolute telomere length
-
O'Callaghan, N. J. & Fenech, M. A quantitative PCR method for measuring absolute telomere length. Biol. Proced. Online 13, 3 (2011).
-
(2011)
Biol. Proced. Online
, vol.13
, pp. 3
-
-
O'Callaghan, N.J.1
Fenech, M.2
-
55
-
-
84960194345
-
Genomic analyses identify molecular subtypes of pancreatic cancer
-
Bailey, P. et al. Genomic analyses identify molecular subtypes of pancreatic cancer. Nature 531, 47-52 (2016).
-
(2016)
Nature
, vol.531
, pp. 47-52
-
-
Bailey, P.1
-
56
-
-
77954182362
-
ConsensusClusterPlus: A class discovery tool with confidence assessments and item tracking
-
Wilkerson, M. D. & Hayes, D. N. ConsensusClusterPlus: A class discovery tool with confidence assessments and item tracking. Bioinformatics 26, 1572-1573 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 1572-1573
-
-
Wilkerson, M.D.1
Hayes, D.N.2
-
57
-
-
84896735766
-
Voom: Precision weights unlock linear model analysis tools for RNA-seq read counts
-
Law, C. W., Chen, Y., Shi, W. & Smyth, G. K. voom: Precision weights unlock linear model analysis tools for RNA-seq read counts. Genome Biol. 15, R29 (2014).
-
(2014)
Genome Biol.
, vol.15
, pp. R29
-
-
Law, C.W.1
Chen, Y.2
Shi, W.3
Smyth, G.K.4
-
58
-
-
84908327053
-
The 'dnet' approach promotes emerging research on cancer patient survival
-
Fang, H. & Gough, J. The 'dnet' approach promotes emerging research on cancer patient survival. Genome Med. 6, 64 (2014).
-
(2014)
Genome Med.
, vol.6
, pp. 64
-
-
Fang, H.1
Gough, J.2
-
59
-
-
33847399257
-
Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues
-
Lewis, T. B., Coffin, C. M. & Bernard, P. S. Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues. Mod. Pathol. 20, 397-404 (2007).
-
(2007)
Mod. Pathol.
, vol.20
, pp. 397-404
-
-
Lewis, T.B.1
Coffin, C.M.2
Bernard, P.S.3
-
60
-
-
37549038654
-
EWSR1-CREB1 and EWSR1-ATF1 fusion genes in angiomatoid fibrous histiocytoma
-
Rossi, S. et al. EWSR1-CREB1 and EWSR1-ATF1 fusion genes in angiomatoid fibrous histiocytoma. Clin. Cancer Res. 13, 7322-7328 (2007).
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 7322-7328
-
-
Rossi, S.1
-
61
-
-
70349180626
-
Structure and activation mechanism of the CHK2 DNA damage checkpoint kinase
-
Cai, Z., Chehab, N. H. & Pavletich, N. P. Structure and activation mechanism of the CHK2 DNA damage checkpoint kinase. Mol. Cell 35, 818-829 (2009).
-
(2009)
Mol. Cell
, vol.35
, pp. 818-829
-
-
Cai, Z.1
Chehab, N.H.2
Pavletich, N.P.3
-
62
-
-
0037093644
-
Increasing the precision of comparative models with YASARA NOVA-A self-parameterizing force field
-
Krieger, E., Koraimann, G. & Vriend, G. Increasing the precision of comparative models with YASARA NOVA-a self-parameterizing force field. Proteins 47, 393-402 (2002).
-
(2002)
Proteins
, vol.47
, pp. 393-402
-
-
Krieger, E.1
Koraimann, G.2
Vriend, G.3
-
63
-
-
36248979794
-
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts
-
Bell, D. W. et al. Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts. Int. J. Cancer 121, 2661-2667 (2007).
-
(2007)
Int. J. Cancer
, vol.121
, pp. 2661-2667
-
-
Bell, D.W.1
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