-
1
-
-
67651181046
-
Paroxysmal nocturnal hemoglobinuria: Stem cells and clonality
-
Brodsky RA. Paroxysmal nocturnal hemoglobinuria: stem cells and clonality. Hematology Am Soc Hematol Educ Program. 2008;111-115.
-
(2008)
Hematology Am Soc Hematol Educ Program.
, pp. 111-115
-
-
Brodsky, R.A.1
-
2
-
-
0027310539
-
Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
-
Takeda J, et al. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 1993;73(4):703-711.
-
(1993)
Cell
, vol.73
, Issue.4
, pp. 703-711
-
-
Takeda, J.1
-
3
-
-
33750628439
-
Current concepts in the pathophysiology and treatment of aplastic anemia
-
Young NS, Calado RT, Scheinberg P. Current concepts in the pathophysiology and treatment of aplastic anemia. Blood. 2006;108(8):2509-2519.
-
(2006)
Blood
, vol.108
, Issue.8
, pp. 2509-2519
-
-
Young, N.S.1
Calado, R.T.2
Scheinberg, P.3
-
4
-
-
0031042052
-
Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria/aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone
-
Maciejewski JP, Sloand EM, Sato T, Anderson S, Young NS. Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria/aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone. Blood. 1997;89(4):1173-1181.
-
(1997)
Blood
, vol.89
, Issue.4
, pp. 1173-1181
-
-
Maciejewski, J.P.1
Sloand, E.M.2
Sato, T.3
Anderson, S.4
Young, N.S.5
-
5
-
-
0033609114
-
Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
-
Araten DJ, Nafa K, Pakdeesuwan K, Luzzatto L. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals. Proc Natl Acad Sci U S A. 1999;96(9):5209-5214.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, Issue.9
, pp. 5209-5214
-
-
Araten, D.J.1
Nafa, K.2
Pakdeesuwan, K.3
Luzzatto, L.4
-
6
-
-
33845494914
-
Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH)
-
Inoue N, et al. Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH). Blood. 2006;108(13):4232-4236.
-
(2006)
Blood
, vol.108
, Issue.13
, pp. 4232-4236
-
-
Inoue, N.1
-
7
-
-
79751533094
-
Deletions of Xp22.2 including PIG-A locus lead to paroxysmal nocturnal hemoglobinuria
-
O'Keefe CL, et al. Deletions of Xp22.2 including PIG-A locus lead to paroxysmal nocturnal hemoglobinuria. Leukemia. 2011;25(2):379-382.
-
(2011)
Leukemia.
, vol.25
, Issue.2
, pp. 379-382
-
-
O'Keefe, C.L.1
-
8
-
-
0034650953
-
N-RAS gene mutation in patients with aplastic anemia and aplastic anemia/paroxysmal nocturnal hemoglobinuria during evolution to clonal disease
-
Mortazavi Y, Tooze JA, Gordon-Smith EC, Rutherford TR. N-RAS gene mutation in patients with aplastic anemia and aplastic anemia/paroxysmal nocturnal hemoglobinuria during evolution to clonal disease. Blood. 2000;95(2):646-650.
-
(2000)
Blood
, vol.95
, Issue.2
, pp. 646-650
-
-
Mortazavi, Y.1
Tooze, J.A.2
Gordon-Smith, E.C.3
Rutherford, T.R.4
-
9
-
-
84864027326
-
Paroxysmal nocturnal hemoglobinuria and concurrent JAK2 (V617F) mutation
-
Sugimori C, et al. Paroxysmal nocturnal hemoglobinuria and concurrent JAK2 (V617F) mutation. Blood Cancer J. 2012;2(3):e63.
-
(2012)
Blood Cancer J.
, vol.2
, Issue.3
, pp. e63
-
-
Sugimori, C.1
-
10
-
-
84863337617
-
Clonal architecture of secondary acute myeloid leukemia
-
Walter MJ, et al. Clonal architecture of secondary acute myeloid leukemia. N Engl J Med. 2012;366(12):1090-1098.
-
(2012)
N Engl J Med.
, vol.366
, Issue.12
, pp. 1090-1098
-
-
Walter, M.J.1
-
11
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley TJ, et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature. 2008;456(7218):66-72.
-
(2008)
Nature
, vol.456
, Issue.7218
, pp. 66-72
-
-
Ley, T.J.1
-
12
-
-
0028299834
-
Omatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
-
Bessler M, Mason P, Hillmen P, Luzzatto L. omatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet. 1994;343(8903):951-953.
-
(1994)
Lancet
, vol.343
, Issue.8903
, pp. 951-953
-
-
Bessler, M.1
Mason, P.2
Hillmen, P.3
Luzzatto, L.4
-
13
-
-
4544283421
-
Netrin-1 controls colorectal tumorigenesis by regulating apoptosis
-
Mazelin L, et al. Netrin-1 controls colorectal tumorigenesis by regulating apoptosis. Nature. 2004;431(7004):80-84.
-
(2004)
Nature
, vol.431
, Issue.7004
, pp. 80-84
-
-
Mazelin, L.1
-
14
-
-
10344239412
-
Netrin-1 and its receptors in tumorigenesis
-
Arakawa H. Netrin-1 and its receptors in tumorigenesis. Nat Rev Cancer. 2004;4(12):978-987.
-
(2004)
Nat Rev Cancer.
, vol.4
, Issue.12
, pp. 978-987
-
-
Arakawa, H.1
-
15
-
-
84855928422
-
The neuroimmune guidance cue netrin-1 promotes atherosclerosis by inhibiting the emigration of macrophages from plaques
-
Van Gils JM, et al. The neuroimmune guidance cue netrin-1 promotes atherosclerosis by inhibiting the emigration of macrophages from plaques. Nat Immunol. 2012;13(2):136-143.
-
(2012)
Nat Immunol.
, vol.13
, Issue.2
, pp. 136-143
-
-
Van Gils, J.M.1
-
16
-
-
66849093831
-
Gene expression profiling provides insights into the pathways involved in solid pseudopapillary neoplasm of the pancreas
-
Cavard C, et al. Gene expression profiling provides insights into the pathways involved in solid pseudopapillary neoplasm of the pancreas. J Pathol. 2009;218(2):201-209.
-
(2009)
J Pathol.
, vol.218
, Issue.2
, pp. 201-209
-
-
Cavard, C.1
-
17
-
-
84884365015
-
The causes and consequences of genetic heterogeneity in cancer evolution
-
Burrell RA, McGranahan N, Bartek J, Swanton C. The causes and consequences of genetic heterogeneity in cancer evolution. Nature. 2013;501(7467):338-345.
-
(2013)
Nature
, vol.501
, Issue.7467
, pp. 338-345
-
-
Burrell, R.A.1
McGranahan, N.2
Bartek, J.3
Swanton, C.4
-
18
-
-
84884377472
-
Tumour heterogeneity and cancer cell plasticity
-
Meacham CE, Morrison SJ. Tumour heterogeneity and cancer cell plasticity. Nature. 2013;501(7467):328-337.
-
(2013)
Nature
, vol.501
, Issue.7467
, pp. 328-337
-
-
Meacham, C.E.1
Morrison, S.J.2
-
19
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
Cancer Genome Atlas Research Network. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature. 2008;455(7216):1061-1068.
-
(2008)
Nature
, vol.455
, Issue.7216
, pp. 1061-1068
-
-
Cancer Genome Atlas Research Network1
-
20
-
-
84878372012
-
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
-
Cancer Genome Atlas Research Network. Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med. 2013;368(22):2059-2074.
-
(2013)
N Engl J Med.
, vol.368
, Issue.22
, pp. 2059-2074
-
-
Cancer Genome Atlas Research Network1
-
21
-
-
80052158097
-
The mutational landscape of head and neck squamous cell carcinoma
-
Stransky N, et al. The mutational landscape of head and neck squamous cell carcinoma. Science. 2011;333(6046):1157-1160.
-
(2011)
Science
, vol.333
, Issue.6046
, pp. 1157-1160
-
-
Stransky, N.1
-
22
-
-
84555192302
-
Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes
-
Graubert TA, et al. Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes. Nat Genet. 2011;44(1):53-57.
-
(2011)
Nat Genet.
, vol.44
, Issue.1
, pp. 53-57
-
-
Graubert, T.A.1
-
23
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H, et al. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis. Blood. 2012;119(14):3203-3210.
-
(2012)
Blood
, vol.119
, Issue.14
, pp. 3203-3210
-
-
Makishima, H.1
-
24
-
-
78650175023
-
Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2
-
Ko M, et al. Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2. Nature. 2010;468(7325):839-843.
-
(2010)
Nature
, vol.468
, Issue.7325
, pp. 839-843
-
-
Ko, M.1
-
25
-
-
84862829019
-
Differential gene expression profiling of primary cutaneous melanoma and sentinel lymph node metastases
-
Koh SS, et al. Differential gene expression profiling of primary cutaneous melanoma and sentinel lymph node metastases. Mod Pathol. 2012;25(6):828-837.
-
(2012)
Mod Pathol.
, vol.25
, Issue.6
, pp. 828-837
-
-
Koh, S.S.1
-
26
-
-
84899095665
-
Bromodomain-PHD finger protein 1 is critical for leukemogenesis associated with MOZ-TIF2 fusion
-
Shima H, et al. Bromodomain-PHD finger protein 1 is critical for leukemogenesis associated with MOZ-TIF2 fusion. Int J Hematol. 2014;99(1):21-31.
-
(2014)
Int J Hematol.
, vol.99
, Issue.1
, pp. 21-31
-
-
Shima, H.1
-
27
-
-
84873847720
-
FoxQ1 promotes glioma cells proliferation and migration by regulating NRXN3 expression
-
Sun HT, Cheng SX, Tu Y, Li XH, Zhang S. FoxQ1 promotes glioma cells proliferation and migration by regulating NRXN3 expression. PLoS One. 2013;8(1):e55693.
-
(2013)
PLoS One.
, vol.8
, Issue.1
, pp. e55693
-
-
Sun, H.T.1
Cheng, S.X.2
Tu, Y.3
Li, X.H.4
Zhang, S.5
-
28
-
-
84864014101
-
KDM3B is the H3K9 demethylase involved in transcriptional activation of lmo2 in leukemia
-
Kim JY, et al. KDM3B is the H3K9 demethylase involved in transcriptional activation of lmo2 in leukemia. Mol Cell Biol. 2012;32(14):2917-2933.
-
(2012)
Mol Cell Biol.
, vol.32
, Issue.14
, pp. 2917-2933
-
-
Kim, J.Y.1
-
29
-
-
84876874946
-
Mice lacking the sodium-dependent phosphate import protein, PiT1 (SLC20A1), have a severe defect in terminal erythroid differentiation and early B cell development
-
Liu L, Sanchez-Bonilla M, Crouthamel M, Giachelli C, Keel S. Mice lacking the sodium-dependent phosphate import protein, PiT1 (SLC20A1), have a severe defect in terminal erythroid differentiation and early B cell development. Exp Hematol. 2013;41(5):432-443.
-
(2013)
Exp Hematol.
, vol.41
, Issue.5
, pp. 432-443
-
-
Liu, L.1
Sanchez-Bonilla, M.2
Crouthamel, M.3
Giachelli, C.4
Keel, S.5
-
30
-
-
1242337458
-
Mucins and mucin binding proteins in colorectal cancer
-
Byrd JC, Bresalier RS. Mucins and mucin binding proteins in colorectal cancer. Cancer Metastasis Rev. 2004;23(1-2):77-99.
-
(2004)
Cancer Metastasis Rev.
, vol.23
, Issue.1-2
, pp. 77-99
-
-
Byrd, J.C.1
Bresalier, R.S.2
-
31
-
-
77953526533
-
High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes
-
Cheung KJ, et al. High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes. Genes Chromosomes Cancer. 2010;49(8):669-681.
-
(2010)
Genes Chromosomes Cancer.
, vol.49
, Issue.8
, pp. 669-681
-
-
Cheung, K.J.1
-
32
-
-
70249147186
-
Experimental and bioinformatic characterisation of the promoter region of the Marfan syndrome gene, FBN1
-
Summers KM, et al. Experimental and bioinformatic characterisation of the promoter region of the Marfan syndrome gene, FBN1. Genomics. 2009;94(4):233-240.
-
(2009)
Genomics.
, vol.94
, Issue.4
, pp. 233-240
-
-
Summers, K.M.1
-
33
-
-
84904726416
-
SUZ12 is involved in progression of non-small cell lung cancer by promoting cell proliferation metastasis
-
Liu C, et al. SUZ12 is involved in progression of non-small cell lung cancer by promoting cell proliferation metastasis. Tumour Biol. 2014;35(6):6073-6082.
-
(2014)
Tumour Biol.
, vol.35
, Issue.6
, pp. 6073-6082
-
-
Liu, C.1
-
34
-
-
84873568880
-
The ASXL-BAP1 axis: New factors in myelopoiesis, cancer and epigenetics
-
Abdel-Wahab O, Dey A. The ASXL-BAP1 axis: new factors in myelopoiesis, cancer and epigenetics. Leukemia. 2013;27(1):10-15.
-
(2013)
Leukemia.
, vol.27
, Issue.1
, pp. 10-15
-
-
Abdel-Wahab, O.1
Dey, A.2
-
35
-
-
84877898479
-
Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22-translocation
-
Panagopoulos I, et al. Fusion of the ZC3H7B and BCOR genes in endometrial stromal sarcomas carrying an X;22-translocation. Genes Chromosomes Cancer. 2013;52(7):610-618.
-
(2013)
Genes Chromosomes Cancer.
, vol.52
, Issue.7
, pp. 610-618
-
-
Panagopoulos, I.1
-
36
-
-
76049108205
-
The helicase protein DHX29 promotes translation initiation, cell proliferation, and tumorigenesis
-
Parsyan A, et al. The helicase protein DHX29 promotes translation initiation, cell proliferation, and tumorigenesis. Proc Natl Acad Sci U S A. 2009;106(52):22217-22222.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, Issue.52
, pp. 22217-22222
-
-
Parsyan, A.1
-
37
-
-
84859944702
-
BCR-ABL1 tyrosine kinase sustained MECOM expression in chronic myeloid leukaemia
-
Roy S, et al. BCR-ABL1 tyrosine kinase sustained MECOM expression in chronic myeloid leukaemia. Br J Haematol. 2012;157(4):446-456.
-
(2012)
Br J Haematol.
, vol.157
, Issue.4
, pp. 446-456
-
-
Roy, S.1
-
38
-
-
84883744431
-
Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies
-
Gomez-Segui I, et al. Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies. Leukemia. 2013;27(9):1943-1946.
-
(2013)
Leukemia.
, vol.27
, Issue.9
, pp. 1943-1946
-
-
Gomez-Segui, I.1
-
39
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics R, et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med. 2005;352(17):1779-1790.
-
(2005)
N Engl J Med.
, vol.352
, Issue.17
, pp. 1779-1790
-
-
Kralovics, R.1
-
40
-
-
0030935631
-
Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene
-
Rollinson S, Richards S, Norfolk D, Bibi K, Morgan G, Hillmen P. Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene. Blood. 1997;89(8):3069-3071.
-
(1997)
Blood
, vol.89
, Issue.8
, pp. 3069-3071
-
-
Rollinson, S.1
Richards, S.2
Norfolk, D.3
Bibi, K.4
Morgan, G.5
Hillmen, P.6
-
41
-
-
84887172353
-
A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT
-
Krawitz PM, et al. A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT. Blood. 2013;122(7):1312-1315.
-
(2013)
Blood
, vol.122
, Issue.7
, pp. 1312-1315
-
-
Krawitz, P.M.1
-
42
-
-
28444483571
-
Diagnosis and management of paroxysmal nocturnal hemoglobinuria
-
Parker C, et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood. 2005;106(12):3699-3709.
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3699-3709
-
-
Parker, C.1
-
43
-
-
68949213291
-
Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies
-
Maciejewski JP, Tiu RV, O'Keefe C. Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies. Br J Haematol. 2009;146(5):479-488.
-
(2009)
Br J Haematol.
, vol.146
, Issue.5
, pp. 479-488
-
-
Maciejewski, J.P.1
Tiu, R.V.2
O'Keefe, C.3
-
44
-
-
38949123096
-
Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML
-
Gondek LP, et al. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. Blood. 2008;111(3):1534-1542.
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1534-1542
-
-
Gondek, L.P.1
-
45
-
-
70449715477
-
New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia
-
Tiu RV, et al. New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia. J Clin Oncol. 2009;27(31):5219-5226.
-
(2009)
J Clin Oncol.
, vol.27
, Issue.31
, pp. 5219-5226
-
-
Tiu, R.V.1
-
46
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K, et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature. 2011;478(7367):64-69.
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 64-69
-
-
Yoshida, K.1
-
47
-
-
78651271733
-
Integrative genomics viewer
-
Robinson JT, et al. Integrative genomics viewer. Nat Biotechnol. 2011;29(1):24-26.
-
(2011)
Nat Biotechnol.
, vol.29
, Issue.1
, pp. 24-26
-
-
Robinson, J.T.1
-
48
-
-
84880976662
-
Somatic SETBP1 mutations in myeloid malignancies
-
Makishima H, et al. Somatic SETBP1 mutations in myeloid malignancies. Nat Genet. 2013;45(8):942-946.
-
(2013)
Nat Genet.
, vol.45
, Issue.8
, pp. 942-946
-
-
Makishima, H.1
|