Published in Chromosoma on June 23, 1977
Identification and high-density mapping of gene-rich regions in chromosome group 5 of wheat. Genetics (1996) 3.30
Chromosomal localization of human leukocyte, fibroblast, and immune interferon genes by means of in situ hybridization. Proc Natl Acad Sci U S A (1982) 2.08
The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase. Mol Cell Biol (1992) 1.66
Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype. Am J Hum Genet (1986) 1.59
Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24. Am J Hum Genet (1982) 1.57
Identification and physical localization of useful genes and markers to a major gene-rich region on wheat group 1S chromosomes. Genetics (2001) 1.39
Down syndrome: gene dosage at the transcriptional level in skin fibroblasts. Proc Natl Acad Sci U S A (1979) 1.09
Computer image analysis of variance between human chromosome replication sequences and G-bands. Am J Hum Genet (1982) 0.79
Amplified dihydrofolate reductase genes are located in chromosome regions containing DNA that replicates during the first half of S-phase. J Cell Biol (1982) 0.79
Role of androgen receptor in progression of LNCaP prostate cancer cells from G1 to S phase. PLoS One (2013) 0.79
The chromosomes of man--clinical and biologic significance. A review. Am J Pathol (1977) 0.75
Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization. Chromosoma (1981) 9.30
Mouse small eye results from mutations in a paired-like homeobox-containing gene. Nature (1992) 6.32
High resolution of human chromosomes. Science (1976) 5.56
The chromosomal basis of human neoplasia. Science (1983) 4.26
The origin of man: a chromosomal pictorial legacy. Science (1982) 4.02
Distinctive chromosomal abnormalities in histologic subtypes of non-Hodgkin's lymphoma. N Engl J Med (1982) 3.82
Constitutive fragile sites and cancer. Science (1984) 3.30
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
Retinoblastoma and subband deletion of chromosome 13. Am J Dis Child (1978) 3.11
Base composition of deoxyribonucleic acid of sulfate-reducing bacteria deduced from buoyant density measurements in cesium chloride. J Bacteriol (1964) 2.89
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science (1980) 2.72
Genome instability in a region of human DNA enriched in Alu repeat sequences. Nature (1982) 2.60
Characterization of a thermophilic bacteriophage for Bacillus stearothermophilus. J Bacteriol (1966) 2.43
DNA methylation: correlation with DNase I sensitivity of chicken ovalbumin and conalbumin chromatin. Nucleic Acids Res (1979) 2.31
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. Am J Hum Genet (1987) 2.06
Preparation of pancreatic mRNA: cell-free translation of an insulin-immunoreactive polypeptide. Nucleic Acids Res (1976) 1.99
Multiple recurrent genomic defects in follicular lymphoma. A possible model for cancer. N Engl J Med (1987) 1.94
Differential nuclease sensitivity of the ovalbumin and beta-globin chromatin regions in erythrocytes and oviduct cells of laying hen. Nucleic Acids Res (1980) 1.91
Arginine deprivation as a targeted therapy for cancer. Curr Pharm Des (2008) 1.82
New chromosome techniques in the study of human neoplasia. Hum Pathol (1981) 1.82
Ribonucleic acid and ribosomes of Bacillus stearothermophilus. J Bacteriol (1966) 1.80
The characterization of high-resolution G-banded chromosomes of man. Chromosoma (1978) 1.79
Mid-prophase human chromosomes. The attainment of 2000 bands. Hum Genet (1981) 1.79
Presence of messenger specifying sequences in the DNA of chromatin subunits. Proc Natl Acad Sci U S A (1976) 1.75
A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes. Cytogenet Cell Genet (1978) 1.75
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
A simple G-banding technique. Lancet (1973) 1.72
Presence of a highly repetitive and widely dispersed DNA sequence in the human genome. Proc Natl Acad Sci U S A (1981) 1.67
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature (1988) 1.67
Heterochromatin, satellite DNA, and cell function. Structural DNA of eucaryotes may support and protect genes and aid in speciation. Science (1971) 1.67
High-resolution chromosome analysis in clinical medicine. Prog Clin Pathol (1978) 1.64
Populations of repeated DNA sequences in the human genome. J Mol Biol (1972) 1.62
Expression of the Wilms' tumor gene (WT1) in human leukemias. Leukemia (1992) 1.60
Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24. Am J Hum Genet (1982) 1.57
Mammalian pancreatic preproglucagon contains three glucagon-related peptides. Proc Natl Acad Sci U S A (1983) 1.51
Regulation of the proto-oncogenes bcl-2 and c-myc by the Wilms' tumor suppressor gene WT1. Cancer Res (1995) 1.46
New chromosomal syndromes. Am J Dis Child (1975) 1.39
Familial renal cell carcinoma: hereditary or coincidental? J Urol (1990) 1.39
Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. Am J Hum Genet (1991) 1.39
Cloning, expression and localization of an RNA helicase gene from a human lymphoid cell line with chromosomal breakpoint 11q23.3. Nucleic Acids Res (1992) 1.38
Truncation mutations in the transactivation region of PAX6 result in dominant-negative mutants. J Biol Chem (1998) 1.35
Release of free bases from deoxyribonucleic acid after reaction with bleomycin. Mol Pharmacol (1972) 1.33
Satellite DNA in constitutive heterochromatin of the guinea pig. Science (1970) 1.32
mRNA in human cells contains sequences complementary to the Alu family of repeated DNA. Proc Natl Acad Sci U S A (1981) 1.32
Coordinated induction of MRP/GS-X pump and gamma-glutamylcysteine synthetase by heavy metals in human leukemia cells. J Biol Chem (1996) 1.31
All patients with acute nonlymphocytic leukemia may have a chromosomal defect. N Engl J Med (1981) 1.29
Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins. Am J Hum Genet (1994) 1.29
Chromosomal localization of the human alpha 1-antitrypsin gene (PI) to 14q31-32. Am J Hum Genet (1985) 1.26
Characterization of banding patterns of metaphase-prophase G-banded chromosomes and their use in gene mapping. Cytogenet Cell Genet (1978) 1.26
Distal deletion of chromosome Ip in ductal carcinoma of the breast. Am J Hum Genet (1989) 1.25
Recent amplification of an alpha satellite DNA in humans. Nucleic Acids Res (1985) 1.25
Mitosis-specific monoclonal antibody MPM-2 inhibits Xenopus oocyte maturation and depletes maturation-promoting activity. Proc Natl Acad Sci U S A (1989) 1.23
Properties of the deoxyribonucleic acid of the thermophilic bacteriophage TP-84. Biochemistry (1965) 1.23
Trisomy 9 mosaicism. Clin Genet (1977) 1.22
Partial trisomy 8 (8q24) and the trisomy-8 syndrome. Humangenetik (1974) 1.22
Localization of the human glucagon gene (GCG) to chromosome segment 2q36----37. Cytogenet Cell Genet (1984) 1.22
Arginine deprivation, autophagy, apoptosis (AAA) for the treatment of melanoma. Curr Mol Med (2010) 1.21
Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood (1986) 1.20
Localization of repetitive DNA in the chromosomes of Microtus agrestis by means of in situ hybridization. Chromosoma (1970) 1.19
Dissection of the transactivation function of the transcription factor encoded by the eye developmental gene PAX6. J Biol Chem (1998) 1.19
Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11. Cell (1988) 1.18
Congenital asymmetry associated with trisomy 18 mosaicism. Am J Dis Child (1965) 1.18
Two structurally different genes produce the same secreted human placental lactogen hormone. J Biol Chem (1983) 1.18
Structure of the human glucagon gene. Nucleic Acids Res (1986) 1.17
Properties of 5-fluorouracil-containing ribonucleic acid and ribosomes from Bacillus subtilis. J Bacteriol (1968) 1.16
Localization of mouse satellite DNA in constitutive heterochromatin. Exp Cell Res (1970) 1.15
A panel of restriction fragment length polymorphisms for chromosomal band 11p13. Hum Genet (1990) 1.15
Trisomy for the distal segment of chromosome 13: a new syndrome. Am J Dis Child (1974) 1.14
The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee. Science (1980) 1.14
Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13. Humangenetik (1974) 1.14
Salt-induced structural changes in nucleosomes. Nucleic Acids Res (1977) 1.14
Distribution of repetitious DNA in human chromosomes. Experientia (1971) 1.12
Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. Am J Hum Genet (1987) 1.10
Parental origin of de novo constitutional deletions of chromosomal band 11p13. Am J Hum Genet (1990) 1.10
Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1. J Pediatr (1980) 1.10
MRP class of human ATP binding cassette (ABC) transporters: historical background and new research directions. Xenobiotica (2008) 1.10
Compositional heterogeneity of human heterochromatin. Proc Natl Acad Sci U S A (1972) 1.07
Inverted repetitive sequences in the human genome. Biochemistry (1976) 1.07
Overexpression of the multidrug resistance gene mdr3 in spontaneous and chemically induced mouse hepatocellular carcinomas. Mol Cell Biol (1990) 1.07
Structure of the human gene encoding the invariant gamma-chain of class II histocompatibility antigens. Nucleic Acids Res (1985) 1.06
Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphoma. Cancer Genet Cytogenet (1984) 1.06
Negative argininosuccinate synthetase expression in melanoma tumours may predict clinical benefit from arginine-depleting therapy with pegylated arginine deiminase. Br J Cancer (2012) 1.06
Functional analysis of paired box missense mutations in the PAX6 gene. Hum Mol Genet (1997) 1.06
Preferential damage of active chromatin by bleomycin. Cancer Res (1981) 1.06
Alterations at the rel locus in human lymphoma. Oncogene (1991) 1.05
Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus. Genomics (1991) 1.05
Expression of multidrug resistance protein/GS-X pump and gamma-glutamylcysteine synthetase genes is regulated by oxidative stress. J Biol Chem (1998) 1.05
Inheritance of unequal numbers of the genes encoding the human neutrophil defensins HP-1 and HP-3. J Biol Chem (1995) 1.04
Transcriptional silencer of the Wilms' tumor gene WT1 contains an Alu repeat. J Biol Chem (1995) 1.04
Differential expression of the human thymosin-beta 4 gene in lymphocytes, macrophages, and granulocytes. J Immunol (1987) 1.04
Human immunodeficiency virus gp120 binding C'C" ridge of CD4 domain 1 is also involved in interaction with class II major histocompatibility complex molecules. Proc Natl Acad Sci U S A (1992) 1.04
The human sex-determining gene SRY is a direct target of WT1. J Biol Chem (2001) 1.04
The human placental lactogen genes: structure, function, evolution and transcriptional regulation. Endocr Rev (1991) 1.04
Mutation in the PAX6 gene in twenty patients with aniridia. Hum Mutat (2000) 1.03
Model for the formation of double minutes from prematurely condensed chromosomes of replicating micronuclei in drug-treated Chinese hamster ovary cells undergoing DNA amplification. Cancer Res (1989) 1.03
Inhibition of mTOR restores cisplatin sensitivity through down-regulation of growth and anti-apoptotic proteins. Eur J Pharmacol (2008) 1.03
NF-kappaB-mediated induction of mdr1b expression by insulin in rat hepatoma cells. J Biol Chem (1997) 1.02
Chromosomal rearrangements, genes, and fragile sites in cancer: clinical and biologic implications. Important Adv Oncol (1986) 1.02
Overexpression of gamma-glutamylcysteine synthetase suppresses tumor necrosis factor-induced apoptosis and activation of nuclear transcription factor-kappa B and activator protein-1. Oncogene (1999) 1.02