Published in Leukemia on February 01, 2006
The p21Waf1 pathway is involved in blocking leukemogenesis by the t(8;21) fusion protein AML1-ETO. Blood (2007) 1.17
Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion. Oncol Rep (2013) 0.85
Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review. Exp Hematol Oncol (2014) 0.84
5'RUNX1-3'USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications. Mol Cytogenet (2014) 0.80
Deubiquitinases in cancer. Oncotarget (2015) 0.78
Cryptic chromosomal aberrations waiting to be discovered. Leukemia (2006) 0.75
RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report. Oncol Rep (2016) 0.75
Overexpression and Biological Function of Ubiquitin-Specific Protease 42 in Gastric Cancer. PLoS One (2016) 0.75
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet (1997) 12.94
Substantial genetic influence on cognitive abilities in twins 80 or more years old. Science (1997) 5.76
Percutaneous pyelolithotomy. A new extraction technique. Scand J Urol Nephrol (1976) 5.01
The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nat Genet (1996) 4.59
Rapid diagnosis of herpes simplex encephalitis by nested polymerase chain reaction assay of cerebrospinal fluid. Lancet (1991) 4.33
Control of resistance, exchange, and capacitance functions in the peripheral circulation. Pharmacol Rev (1968) 3.19
[Spinal manipulation is only a part of total care]. Lakartidningen (1992) 3.17
Cytogenetic evidence of clonality in cutaneous benign fibrous histiocytomas: a report of the CHAMP study group. Histopathology (2000) 3.05
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors. Proc Natl Acad Sci U S A (2001) 2.91
Fibril in senile systemic amyloidosis is derived from normal transthyretin. Proc Natl Acad Sci U S A (1990) 2.87
Relationship between Epstein-Barr virus (EBV) DNA and the EBV-determined nuclear antigen (EBNA) in Burkitt lymphoma biopsies and other lymphoproliferative malignancies. Int J Cancer (1974) 2.80
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc Natl Acad Sci U S A (2000) 2.61
Heritability for Alzheimer's disease: the study of dementia in Swedish twins. J Gerontol A Biol Sci Med Sci (1997) 2.59
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration. Leukemia (2006) 2.45
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group. Am J Pathol (1996) 2.42
Age-related change in peripheral blood T-lymphocyte subpopulations and cytomegalovirus infection in the very old: the Swedish longitudinal OCTO immune study. Mech Ageing Dev (2000) 2.37
Abolished tubuloglomerular feedback and increased plasma renin in adenosine A1 receptor-deficient mice. Am J Physiol Regul Integr Comp Physiol (2001) 2.29
HIV in pregnant women and their offspring: evidence for late transmission. Lancet (1991) 2.27
Onset of terminal decline in cognitive abilities in individuals without dementia. Neurology (2008) 2.24
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms. Cancer Res (1997) 2.14
Evidence that the amyloid fibril protein in senile systemic amyloidosis is derived from normal prealbumin. Biochem Biophys Res Commun (1988) 2.13
Changes in CD8 and CD4 lymphocyte subsets, T cell proliferation responses and non-survival in the very old: the Swedish longitudinal OCTO-immune study. Mech Ageing Dev (1998) 2.12
Epstein-Barr virus-associated complement-fixing and nuclear antigens in Burkitt lymphoma biopsies. Int J Cancer (1974) 2.10
Surface immunoglobulin-moieties on lymphoid cells. Exp Cell Res (1970) 2.09
Use of multiple PCR primer sets for optimal detection of human papillomavirus. J Clin Microbiol (1996) 2.03
Encephalitis in immunocompetent patients due to herpes simplex virus type 1 or 2 as determined by type-specific polymerase chain reaction and antibody assays of cerebrospinal fluid. J Med Virol (1993) 2.01
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11). Genes Chromosomes Cancer (1992) 1.99
Oligodendrocyte progenitor cells can act as cell of origin for experimental glioma. Oncogene (2009) 1.96
Full-length sequence of an ethiopian human immunodeficiency virus type 1 (HIV-1) isolate of genetic subtype C. AIDS Res Hum Retroviruses (1996) 1.92
Specific binding of proinsulin C-peptide to human cell membranes. Proc Natl Acad Sci U S A (1999) 1.91
Molybdenum at high pressure and temperature: melting from another solid phase. Phys Rev Lett (2008) 1.89
Whole-arm t(1;16) and i(1q) as sole anomalies identify gain of 1q as a primary chromosomal abnormality in breast cancer. Genes Chromosomes Cancer (1992) 1.86
Midlife overweight and obesity increase late-life dementia risk: a population-based twin study. Neurology (2011) 1.84
Myeloperoxidase-mediated iodination in granulocytes. Scand J Haematol (1972) 1.83
Cell surface localized IgM-kappa immunoglobulin reactivity in a case of chronic lymphocytic leukaemia. Clin Exp Immunol (1970) 1.80
Immune parameters in a longitudinal study of a very old population of Swedish people: a comparison between survivors and nonsurvivors. J Gerontol A Biol Sci Med Sci (1995) 1.78
Fusion of the EWS and CHOP genes in myxoid liposarcoma. Oncogene (1996) 1.77
Geographic heterogeneity of neoplasia-associated chromosome aberrations. Genes Chromosomes Cancer (1991) 1.72
Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. Cancer Res (1994) 1.70
Effects of arterial carbon dioxide tension and oxygen saturation on cerebral blood flow autoregulation in dogs. Acta Physiol Scand Suppl (1965) 1.70
Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participants. Leukemia (1998) 1.67
Isochromosomes in neoplasia. Genes Chromosomes Cancer (1994) 1.64
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS. Genomics (1996) 1.59
Impaired phytohaemagglutinin-induced cytotoxicity in vitro of lymphocytes from patients with Hodgkin's disease or chronic lymphatic leukaemia. Clin Exp Immunol (1967) 1.57
Epstein-Barr virus (EBV)-associated antibody patterns in malignant lymphoma and leukemia. I. Hodgkin's disease. Int J Cancer (1970) 1.57
Sympathetic control of rhythmically active vascular smooth muscle as studied by a nerve-muscle preparation of portal vein. Acta Physiol Scand (1968) 1.56
Altered density, metabolism and surface receptors of eosinophils in eosinophilia. Immunology (1982) 1.53
Prospective randomized multicentre study of laparoscopic versus open appendicectomy. Br J Surg (1999) 1.52
Cardiac puncture of fetus with Hurler's disease avoiding abortion of unaffected co-twin. Lancet (1978) 1.52
Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status. Leukemia (2007) 1.52
Pre-compiling medical logic modules into C++ in building medical decision support systems. Comput Methods Programs Biomed (1993) 1.49
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group). Am J Surg Pathol (1996) 1.48
Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin. Cancer Genet Cytogenet (1988) 1.48
Modifications of human and viral deoxyribonucleic acid by formaldehyde fixation. Lab Invest (1994) 1.48
Senile cardiac amyloidosis: evidence of two different amyloid substances in the ageing heart. Scand J Immunol (1979) 1.48
Recent improvement in outcome of unrelated donor transplantation for aplastic anemia. Bone Marrow Transplant (2007) 1.47
Occupational exposure to petroleum products in men with acute non-lymphocytic leukaemia. Br Med J (1978) 1.47
Clinical significance of cytogenetic findings in solid tumors. Cancer Genet Cytogenet (1997) 1.46
Disruption of the E1 and E2 reading frames of HPV 16 in cervical carcinoma is associated with poor prognosis. Int J Gynecol Pathol (1998) 1.44
Typing of human papillomavirus by pyrosequencing. Lab Invest (2001) 1.44
Clinical utility of immunoglobulin heavy chain gene rearrangement identification for tumour cell detection in multiple myeloma. Br J Haematol (1998) 1.42
The effect of hyperosmolarity on intacet and isolated vascular smooth muscle. Possible role in exercise hyperemia. Angiologica (1967) 1.42
Contractile properties of two varieties of twitch muscle fibres in Xenopus laevis. Acta Physiol Scand (1982) 1.42
Molecular dynamics study of melting and fcc-bcc transitions in Xe. Phys Rev Lett (2001) 1.41
Trisomy 7 in short-term cultures of colorectal adenocarcinomas. Genes Chromosomes Cancer (1991) 1.41
Plasma cytokine profiles in elderly humans. Mech Ageing Dev (2003) 1.40
Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha. Leukemia (1996) 1.39
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1991) 1.39
Adenosine-dopamine interactions in the brain. Neuroscience (1992) 1.39
[Occupational medical tests in the past]. Lakartidningen (1996) 1.39
Stimulation of high-affinity adenosine A2 receptors decreases the affinity of dopamine D2 receptors in rat striatal membranes. Proc Natl Acad Sci U S A (1991) 1.39
[Private health insurance can improve health care]. Lakartidningen (1995) 1.38
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro. J Virol (2000) 1.38
Comparative genomic hybridization reveals frequent gains of 20q, 8q, 11q, 12p, and 17q, and losses of 18q, 9p, and 15q in pancreatic cancer. Genes Chromosomes Cancer (1997) 1.37
The effect of acute arterial hypertension on the blood-brain barrier to protein tracers. Acta Neuropathol (1970) 1.37
The distribution of sodium, potassium and chloride in the smooth muscle of the rat portal vein. Acta Physiol Scand (1970) 1.36
Cytogenetic analysis of 363 consecutively ascertained diffuse large B-cell lymphomas. Genes Chromosomes Cancer (1999) 1.35
Report of the committee on structural chromosome changes in neoplasia. Cytogenet Cell Genet (1989) 1.32
Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer (1993) 1.32
Abrogation of experimental colitis correlates with increased apoptosis in mice deficient for CD44 variant exon 7 (CD44v7). J Exp Med (2000) 1.31
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum Genet (1999) 1.31
Genetic convergence and divergence in tumor progression. Cancer Res (1988) 1.31
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. Am J Surg Pathol (1997) 1.30
Physical state of HPV16 and chromosomal mapping of the integrated form in cervical carcinomas. Diagn Mol Pathol (2001) 1.30
Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas. Hum Genet (1988) 1.30
Clonal heterogeneity in breast cancer: karyotypic comparisons of multiple intra- and extra-tumorous samples from 3 patients. Int J Cancer (1995) 1.30