Published in Somatic Cell Genet on November 01, 1981
Thymidine-kinase activity of cultured cells from individuals with inherited galactokinase deficiency. Am J Hum Genet (1984) 0.91
Assignment of genes encoding metallothioneins I and II to Chinese hamster chromosome 3: evidence for the role of chromosome rearrangement in gene amplification. Mol Cell Biol (1984) 0.85
Construction and analysis of DNA sequence libraries from flow-sorted chromosomes: practical and theoretical considerations. Nucleic Acids Res (1984) 0.79
Genetic effects of chromosomal rearrangements in Chinese hamster ovary cells: expression and chromosomal assignment of TK, GALK, ACP1, ADA, and ITPA loci. Mol Cell Biol (1983) 0.78
Linkage of the MBG locus to another functionally hemizygous gene locus (IDH2) on chromosome Z3 in Chinese hamster ovary cells. Mol Cell Biol (1985) 0.77
MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells. Oncogene (2007) 6.55
Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia. Science (1993) 3.88
XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages. Mol Cell (1998) 3.73
Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair. Am J Hum Genet (1988) 3.41
The tal gene undergoes chromosome translocation in T cell leukemia and potentially encodes a helix-loop-helix protein. EMBO J (1990) 3.21
Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene. Proc Natl Acad Sci U S A (1995) 2.48
Site-specific recombination of the tal-1 gene is a common occurrence in human T cell leukemia. EMBO J (1990) 2.38
A refined physical map of the long arm of human chromosome 16. Genomics (1991) 2.15
Spontaneous abnormalities in normal fibroblasts from patients with Li-Fraumeni cancer syndrome: aneuploidy and immortalization. Cancer Res (1990) 2.07
Efficient pooling designs for library screening. Genomics (1995) 1.97
A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes. Am J Hum Genet (1990) 1.94
Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells. Somat Cell Mol Genet (1985) 1.91
Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. Genomics (1995) 1.74
Molecular cloning, expression, and chromosome 19 localization of a human Ro/SS-A autoantigen. J Clin Invest (1990) 1.64
Premutation allele pool in myotonic dystrophy type 2. Neurology (2008) 1.61
TAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemia. Proc Natl Acad Sci U S A (1991) 1.53
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus. Am J Hum Genet (1990) 1.39
Assignment of a human DNA-repair gene associated with sister-chromatid exchange to chromosome 19. Mutat Res (1986) 1.34
Primary structure of human lumican (keratan sulfate proteoglycan) and localization of the gene (LUM) to chromosome 12q21.3-q22. Genomics (1995) 1.32
Hypermutable myotonic dystrophy CTG repeats in transgenic mice. Nat Genet (1997) 1.29
Nucleotide excision repair genes as determinants of cellular sensitivity to cyclophosphamide analogs. Cancer Chemother Pharmacol (1996) 1.29
Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population. Am J Hum Genet (1994) 1.28
Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability. Hum Mol Genet (2000) 1.25
MicroRNAs 10a and 10b are potent inducers of neuroblastoma cell differentiation through targeting of nuclear receptor corepressor 2. Cell Death Differ (2011) 1.24
Coordinate amplification of metallothionein I and II genes in cadmium-resistant Chinese hamster cells: implications for mechanisms regulating metallothionein gene expression. Mol Cell Biol (1985) 1.23
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics (1989) 1.22
Isolation of human transcribed sequences from human-rodent somatic cell hybrids. Science (1989) 1.21
Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids. Somat Cell Mol Genet (1987) 1.19
Cloning and characterization of a mouse 3-methyladenine/7-methyl-guanine/3-methylguanine DNA glycosylase cDNA whose gene maps to chromosome 11. Carcinogenesis (1993) 1.17
Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci. Genomics (1993) 1.16
Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene. Genomics (1998) 1.14
Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia. Blood (1994) 1.12
Dual Alu polymerase chain reaction primers and conditions for isolation of human chromosome painting probes from hybrid cells. Cancer Genet Cytogenet (1993) 1.11
Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization. Cancer Genet Cytogenet (2000) 1.11
Cloning and characterization of 5E6(Ly-49C), a receptor molecule expressed on a subset of murine natural killer cells. J Exp Med (1995) 1.11
MicroRNA-204 increases sensitivity of neuroblastoma cells to cisplatin and is associated with a favourable clinical outcome. Br J Cancer (2012) 1.11
Characterization of a cell line (SW756) derived from a human squamous carcinoma of the uterine cervix. In Vitro (1982) 1.10
Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q. Carcinogenesis (2004) 1.09
High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells. Proc Natl Acad Sci U S A (1983) 1.09
Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma. Oncogene (2011) 1.08
The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia. Leukemia (1987) 1.07
Cloning of the human SIX1 gene and its assignment to chromosome 14. Genomics (1996) 1.05
Electrophoretic shift mutants in Chinese hamster ovary cells: evidence for genetic diploidy. Proc Natl Acad Sci U S A (1978) 1.05
Expression of human adenosine deaminase after fusion of adenosine deaminase-deficient cells with mouse fibroblasts. Proc Natl Acad Sci U S A (1978) 1.05
KBM-7, a human myeloid leukemia cell line with double Philadelphia chromosomes lacking normal c-ABL and BCR transcripts. Leukemia (1995) 1.05
Modulation of neuroblastoma disease pathogenesis by an extensive network of epigenetically regulated microRNAs. Oncogene (2012) 1.05
HEN1 and HEN2: a subgroup of basic helix-loop-helix genes that are coexpressed in a human neuroblastoma. Proc Natl Acad Sci U S A (1992) 1.04
Three linked enzyme loci in fishes: implications in the evolution of vertebrate chromosomes. Genetics (1977) 1.04
Characterization of the DiFi rectal carcinoma cell line derived from a familial adenomatous polyposis patient. In Vitro Cell Dev Biol (1993) 1.02
Regional assignment of a human DNA repair gene (XRCC5) to 2q35 by X-ray hybrid mapping. Genomics (1994) 1.01
High-resolution cytogenetic-based physical map of human chromosome 16. Genomics (1992) 1.01
De novo myotonic dystrophy mutation in a Nigerian kindred. Am J Hum Genet (1995) 1.00
Polymorphisms, linkage and mapping of four enzyme loci in the fish genus Xiphophorus (Poeciliidae). Genetics (1979) 0.99
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes. Genomics (2000) 0.98
Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28. Genomics (1996) 0.98
Identification of new DNA markers close to the myotonic dystrophy locus. J Med Genet (1991) 0.98
Human 3'-phosphoadenosine 5'-phosphosulfate synthetase 1 (PAPSS1) and PAPSS2: gene cloning, characterization and chromosomal localization. Biochem Biophys Res Commun (2000) 0.97
Frequency of minisatellite repeat number changes at the MS205 locus in human sperm before and after cancer chemotherapy. Environ Mol Mutagen (2000) 0.96
Molecular cloning of the human nucleotide-excision-repair gene ERCC4. Proc Natl Acad Sci U S A (1994) 0.96
Selective overproduction of adenosine deaminase in cultured mouse cells. J Biol Chem (1983) 0.94
Insertional inactivation of the downless gene in a family of transgenic mice. Mol Biol Med (1989) 0.93
Cloning and genetic characterization of the human kinesin light-chain (KLC) gene. DNA Cell Biol (1993) 0.93
Extrachromosomal amplification of the epidermal growth factor receptor gene in a human colon carcinoma cell line. Genes Chromosomes Cancer (1991) 0.92
Mapping of the phenol sulfotransferase gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7. Genomics (1993) 0.92
Necessity for two human chromosomes for human chorionic gonadotropin production in human-mouse hybrids. Somatic Cell Genet (1979) 0.90
An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivo. Oncogene (1996) 0.90
Direct mapping of seven genes encoding human type 2 cystatins to a single site located at 20p11.2. Genomics (1994) 0.89
Provisional assignment of TPI, GPI, and PEPD to Chinese hamster autosomes 8 and 9: a cytogenetic basis for functional haploidy of an autosomal linkage group in CHO cells. Cytogenet Cell Genet (1983) 0.89
Type I keratinocyte transglutaminase: expression in human skin and psoriasis. J Invest Dermatol (1992) 0.89
An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q. Am J Hum Genet (1993) 0.88
Chromosome 5 aberrations and genetic predisposition to lung cancer. Int J Cancer (1998) 0.88
Human sulfotransferases SULT1C1 and SULT1C2: cDNA characterization, gene cloning, and chromosomal localization. Genomics (2000) 0.88
Regional assignment of ADA and ITPA to mouse chromosome 2 (C1----ter). A demonstration of the conserved linkage of enzyme and proto-oncogene loci. J Hered (1984) 0.87
Genetic polymorphisms and gene expression variations at enzyme loci in chinese hamster cell lines. Somatic Cell Genet (1981) 0.87
Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesis. Blood (1995) 0.87
A human breast adenocarcinoma with chromosome and isoenzyme markers similar to those of the HeLa line. J Natl Cancer Inst (1979) 0.87
Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2. Genomics (1992) 0.86
Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16. Genomics (1993) 0.86
Assignment of the XRCC2 human DNA repair gene to chromosome 7q36 by complementation analysis. Genomics (1995) 0.86
Structural and functional hemi- and dizygous Chinese hamster chromosome 2 gene loci in CHO cells. Somatic Cell Genet (1982) 0.86
Chromosomal assignment of amplified genes in hydroxyurea-resistant hamster cells. Cytogenet Cell Genet (1987) 0.86
Ro/SS-A and the pathogenic significance of its antibodies. J Autoimmun (1989) 0.85
Assignment of genes encoding metallothioneins I and II to Chinese hamster chromosome 3: evidence for the role of chromosome rearrangement in gene amplification. Mol Cell Biol (1984) 0.85
Mutually exclusive genetic signatures of human breast tumor cell lines with a common chromosomal marker. Cancer Res (1979) 0.85
Linkage group V of platyfishes and Swordtails of the genus Xiphophorus (Poeciliidae): linkage of loci for malate dehydrogenase-2 and esterase-1 and esterase-4 with a gene controlling the severity of hybrid melanomas. J Natl Cancer Inst (1983) 0.85
Oncogenes and linkage groups: conservation during mammalian chromosome evolution. Chromosoma (1985) 0.85
Human indolethylamine N-methyltransferase: cDNA cloning and expression, gene cloning, and chromosomal localization. Genomics (1999) 0.85
Gene mapping and linkage analysis in Chinese hamster: assignment of the genes for APRT, LDHA, IDH2, and GAA to chromosome 3. Somatic Cell Genet (1983) 0.84
Increased expression of one of two adenosine deaminase alleles in a human choriocarcinoma cell line following selection with adenine nucleosides. J Biol Chem (1983) 0.84
Tumorigenic transformation of spontaneously immortalized fibroblasts from patients with a familial cancer syndrome. Oncogene (1991) 0.84
UV mutagenesis, cytotoxicity and split-dose recovery in a human-CHO cell hybrid having intermediate (6-4) photoproduct repair. Mutat Res (1989) 0.84