Published in Genomics on May 01, 1991
Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proc Natl Acad Sci U S A (1991) 2.83
novH: differential expression in developing kidney and Wilm's tumors. Am J Pathol (1998) 1.90
The Denys-Drash syndrome. J Med Genet (1994) 1.13
Molecular genetic analysis of chromosome 11p in familial Wilms tumour. Br J Cancer (1994) 1.01
Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor. Proc Natl Acad Sci U S A (1993) 0.98
Expression of the 11p13 Wilms' tumor gene, WT1, correlates with histologic category of Wilms' tumor. Am J Pathol (1992) 0.98
Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors. Mol Cytogenet (2016) 0.80
Genomic changes in the WT-gene (WT1) in Wilms' tumors and their correlation with histology. Am J Pathol (1992) 0.80
Loss of heterozygosity at 11p13 in Wilms' tumours does not necessarily involve mutations in the WT1 gene. Br J Cancer (1993) 0.77
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science (1990) 16.68
p53-dependent apoptosis modulates the cytotoxicity of anticancer agents. Cell (1993) 12.02
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature (1983) 11.57
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet (1997) 10.71
Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours. Nature (1996) 10.14
Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization. Chromosoma (1981) 9.30
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature (1992) 8.85
Phase II evaluation of clinical coding schemes: completeness, taxonomy, mapping, definitions, and clarity. CPRI Work Group on Codes and Structures. J Am Med Inform Assoc (1997) 7.18
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene. Cell (1988) 7.10
Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila. Nature (2001) 6.76
p53 status and the efficacy of cancer therapy in vivo. Science (1994) 6.72
Mouse small eye results from mutations in a paired-like homeobox-containing gene. Nature (1992) 6.32
Targeted integration of adeno-associated virus (AAV) into human chromosome 19. EMBO J (1991) 6.13
A family of cAMP-binding proteins that directly activate Rap1. Science (1998) 6.12
Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 alleles. Cell (1992) 6.03
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region. Cell (1991) 5.84
Self-reported antiretroviral therapy in injection drug users. JAMA (1998) 4.75
Bipolar affective disorders linked to DNA markers on chromosome 11. Nature (1987) 4.64
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
Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor. Science (1987) 4.32
Bone sarcomas linked to radiotherapy and chemotherapy in children. N Engl J Med (1987) 4.12
Persistence of viremia and the importance of long-term follow-up after acute hepatitis C infection. Hepatology (1999) 4.11
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription. Proc Natl Acad Sci U S A (2000) 4.01
Correlates of hepatitis C virus infections among injection drug users. Medicine (Baltimore) (1995) 3.85
Isolation and expression of a complementary DNA that confers multidrug resistance. Nature (1986) 3.84
Mutation and cancer: a model for Wilms' tumor of the kidney. J Natl Cancer Inst (1972) 3.78
A New Influence on Chemically Induced Sarcomata. Science (1948) 3.54
Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. Proc Natl Acad Sci U S A (1991) 3.43
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics (1992) 3.42
THE LIQUEFACTION OF SPONTANEOUS TUMORS OF THE MAMMARY GLAND IN MICE BY HEPTYL ALDEHYDE. Science (1938) 3.34
Isolation of human mdr DNA sequences amplified in multidrug-resistant KB carcinoma cells. Proc Natl Acad Sci U S A (1986) 3.19
Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts. Proc Natl Acad Sci U S A (1997) 3.18
Localization of the human insulin gene to the distal end of the short arm of chromosome 11. Proc Natl Acad Sci U S A (1981) 3.17
Changes in T-lymphocyte subsets in intravenous drug users with HIV-1 infection. JAMA (1992) 3.07
The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9. Nat Genet (1996) 3.05
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p. N Engl J Med (1989) 3.03
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell (1990) 3.02
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet (1998) 3.00
Mutation and cancer: neuroblastoma and pheochromocytoma. Am J Hum Genet (1972) 2.99
Base composition of deoxyribonucleic acid of sulfate-reducing bacteria deduced from buoyant density measurements in cesium chloride. J Bacteriol (1964) 2.89
Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proc Natl Acad Sci U S A (1991) 2.83
Pleuropulmonary blastoma: a marker for familial disease. J Pediatr (1996) 2.83
Genetic disease in offspring of long-term survivors of childhood and adolescent cancer. Am J Hum Genet (1998) 2.74
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nat Genet (1993) 2.69
Direct haplotyping of kilobase-size DNA using carbon nanotube probes. Nat Biotechnol (2000) 2.61
Genome instability in a region of human DNA enriched in Alu repeat sequences. Nature (1982) 2.60
THE TREATMENT OF SPONTANEOUS TUMORS IN DOGS BY THE INJECTION OF HEPTYL ALDEHYDE. Science (1938) 2.57
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. J Clin Oncol (1998) 2.55
Development of retrovirus vectors useful for expressing genes in cultured murine embryonal cells and hematopoietic cells in vivo. J Virol (1988) 2.55
Incidence and risk factors for hepatitis C among injection drug users in Baltimore, Maryland. J Clin Microbiol (1997) 2.55
A Rap guanine nucleotide exchange factor enriched highly in the basal ganglia. Proc Natl Acad Sci U S A (1998) 2.47
Determinants that contribute to cytoplasmic stability of human c-fos and beta-globin mRNAs are located at several sites in each mRNA. Mol Cell Biol (1988) 2.46
Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proc Natl Acad Sci U S A (1998) 2.46
Characterization of a thermophilic bacteriophage for Bacillus stearothermophilus. J Bacteriol (1966) 2.43
Amplification of specific DNA sequences correlates with multi-drug resistance in Chinese hamster cells. Nature (1984) 2.39
Abrogation of oncogene-associated apoptosis allows transformation of p53-deficient cells. Proc Natl Acad Sci U S A (1994) 2.37
Reductions in high-risk drug use behaviors among participants in the Baltimore needle exchange program. J Acquir Immune Defic Syndr Hum Retrovirol (1997) 2.36
The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues. Mol Cell Biol (1989) 2.35
Human erythroid burst-forming unit: T-cell requirement for proliferation in vitro. J Exp Med (1978) 2.33
Induction of Tumors by 3:4:5:6-Dibenzcarbazole in Male Mice of the CBA Strain, which Develops Spontaneous Hepatoma. Yale J Biol Med (1938) 2.26
Vitamin A deficiency and wasting as predictors of mortality in human immunodeficiency virus-infected injection drug users. J Infect Dis (1995) 2.25
Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proc Natl Acad Sci U S A (1989) 2.25
Isolation and characterization of DNA sequences amplified in multidrug-resistant hamster cells. Proc Natl Acad Sci U S A (1986) 2.19
A pilot study of isotretinoin in the treatment of juvenile chronic myelogenous leukemia. N Engl J Med (1994) 2.11
Temporal trends of incident human immunodeficiency virus infection in a cohort of injecting drug users in Baltimore, Md. Arch Intern Med (1995) 2.08
Spontaneous abnormalities in normal fibroblasts from patients with Li-Fraumeni cancer syndrome: aneuploidy and immortalization. Cancer Res (1990) 2.07
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. Am J Hum Genet (1987) 2.06
Isolation and characterization of human cDNA clones encoding a high mobility group box protein that recognizes structural distortions to DNA caused by binding of the anticancer agent cisplatin. Proc Natl Acad Sci U S A (1992) 2.04
Preparation of pancreatic mRNA: cell-free translation of an insulin-immunoreactive polypeptide. Nucleic Acids Res (1976) 1.99
The complex pathology of trinucleotide repeats. Curr Opin Cell Biol (1997) 1.98
Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Hum Mol Genet (2000) 1.94
A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I. Am J Hum Genet (1988) 1.92
Heredity and cancer in man. Prog Med Genet (1973) 1.91
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8. Am J Hum Genet (1995) 1.82
Frequent association of beta-catenin and WT1 mutations in Wilms tumors. Cancer Res (2000) 1.82
Certificates of confidentiality: a valuable tool for protecting genetic data. Am J Hum Genet (1995) 1.82
Mouse beta-globin DNA-binding protein B1 is identical to a proto-oncogene, the transcription factor Spi-1/PU.1, and is restricted in expression to hematopoietic cells and the testis. Mol Cell Biol (1993) 1.80
Ribonucleic acid and ribosomes of Bacillus stearothermophilus. J Bacteriol (1966) 1.80
Antibody to hepatitis C virus among cardiac surgery patients, homosexual men, and intravenous drug users in Baltimore, Maryland. Am J Epidemiol (1991) 1.76
Presence of messenger specifying sequences in the DNA of chromatin subunits. Proc Natl Acad Sci U S A (1976) 1.75
Bio-Electric Correlates of Methylcolanthrene-Induced Tumors in Mice. Yale J Biol Med (1938) 1.75
WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature (1991) 1.75
Syphilis serology in human immunodeficiency virus infection: evidence for false-negative fluorescent treponemal testing. J Infect Dis (1997) 1.74
Double-helical regions in nuclear precursor of mRNA (pre-mRNA). Biochim Biophys Acta (1973) 1.73
The use of RNA labeled in vitro with iodine-125 in molecular hybridization experiments. Biochim Biophys Acta (1972) 1.72
Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet (1993) 1.71
Familial retinoblastoma and chromosome 13 deletion transmitted via an insertional translocation. Science (1981) 1.70
Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics (1991) 1.69
Site-specific cleavage of human chromosome 4 mediated by triple-helix formation. Science (1991) 1.67
Presence of a highly repetitive and widely dispersed DNA sequence in the human genome. Proc Natl Acad Sci U S A (1981) 1.67
The organization of a nuclear DNA sequence from a higher plant: molecular cloning and characterization of soybean ribosomal DNA. Gene (1979) 1.67
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature (1988) 1.67
Risk factors for shooting gallery use and cessation among intravenous drug users. Am J Public Health (1991) 1.66
Seroepidemiology of hepatitis B virus in a population of injecting drug users. Association with drug injection patterns. Am J Epidemiol (1995) 1.65
Association of drug injection patterns with antibody to human immunodeficiency virus type 1 among intravenous drug users in Baltimore, Maryland. Am J Epidemiol (1990) 1.65