Inheritance of glomus tumours.

PubWeight™: 0.77‹?›

🔗 View Article (PMID 1969034)

Published in Lancet on March 17, 1990

Authors

T J Hulsebos, R M Slater, A Westerveld

Articles by these authors

Nucleotide sequence of the filamentous bacteriophage M13 DNA genome: comparison with phage fd. Gene (1980) 10.77

Molecular cloning of a human DNA repair gene. Nature (1984) 3.50

Use of survivors' cardiorespiratory values as therapeutic goals in septic shock. Crit Care Med (1989) 3.33

Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. Cell (1986) 3.17

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nat Genet (1999) 2.75

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N Engl J Med (1996) 2.66

Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22. Cytogenet Cell Genet (1980) 1.88

Loss of human genetic markers in man--Chinese hamster somatic cell hybrids. Nat New Biol (1971) 1.88

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS. Hum Mol Genet (2001) 1.79

High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered. Genomics (1992) 1.74

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. J Clin Invest (1988) 1.68

Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions. Hum Genet (1987) 1.67

Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Mol Cell Biol (1990) 1.57

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28. Am J Hum Genet (1991) 1.56

Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification. Nat Genet (1993) 1.55

Mutational analysis of the human nucleotide excision repair gene ERCC1. Nucleic Acids Res (1996) 1.53

Effects of alfentanil and lidocaine on the hemodynamic responses to laryngoscopy and tracheal intubation. J Clin Anesth (1990) 1.49

Retinitis pigmentosa: defined from a molecular point of view. Surv Ophthalmol (1999) 1.47

Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification. Hum Mol Genet (1995) 1.45

The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. Mutat Res (1989) 1.42

Regional assignment of the gene locus for steroid sulfatase. Hum Genet (1980) 1.40

A complication of percutaneous tracheostomy whilst using the Combitube for airway control. Eur J Anaesthesiol (1997) 1.39

Adverse events following NPSA guidelines. Anaesthesia (2003) 1.39

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum Genet (1988) 1.36

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. Biochem Biophys Res Commun (1990) 1.36

Evolution and mutagenesis of the mammalian excision repair gene ERCC-1. Nucleic Acids Res (1988) 1.34

Differences between rodent and human cell lines in the amount of integrated DNA after transfection. Exp Cell Res (1987) 1.34

Molecular cloning of the human DNA excision repair gene ERCC-6. Mol Cell Biol (1990) 1.32

Human antigen and enzyme markers in man-Chinese hamster somatic cell hybrids: evidence for synteny between the HL-A, PGM3, ME1, and IPO-B loci. Proc Natl Acad Sci U S A (1974) 1.32

Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization. Exp Cell Res (1974) 1.32

Chromosomal assignment and regional localization of CS, ENO2, GAPDH, LDHB, PEPB, and TPI in man-rodent cell hybrids. Cytogenet Cell Genet (1978) 1.31

Genomic characterization of the human DNA excision repair gene ERCC-1. Nucleic Acids Res (1987) 1.31

Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids. Assignment of PGM3 to chromosome C6 and regional mapping of the PGD, PGM1 and pep-C genes on chromosome A1. Humangenetik (1973) 1.24

A simplified method of treating burns of the hands. Br J Plast Surg (1971) 1.23

Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies. Hum Genet (1983) 1.22

Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics (1989) 1.22

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci U S A (1995) 1.19

Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations. Hum Genet (1981) 1.18

Cloning, mapping, and expression analysis of a gene encoding a novel mammalian EGF-related protein (SCUBE1). Genomics (2000) 1.15

Lampbrush loop-specific protein of Drosophila hydei. Proc Natl Acad Sci U S A (1984) 1.14

Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification. Oncogene (1995) 1.13

Anaphylactoid reaction to oxytocin in pregnancy. Anaesthesia (1985) 1.13

X-linkage of human phosphoglycerate kinase confirmed in man-mouse and man-Chinese hamster somatic cell hybrids. Am J Hum Genet (1971) 1.13

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome. Am J Hum Genet (2000) 1.10

TEL/AML1 gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia. Blood (2000) 1.10

The chromosomal localization of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22. Hum Genet (1985) 1.10

Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders. Biochem Biophys Res Commun (1988) 1.08

Phenotypic heterogeneity within the first complementation group of UV-sensitive mutants of Chinese hamster cell lines. Mutat Res (1988) 1.07

Glioneuronal tumors and medically intractable epilepsy: a clinical study with long-term follow-up of seizure outcome after surgery. Epilepsy Res (2001) 1.06

Absence of oncogene amplifications and occasional activation of N-ras in lymphoblastic leukemia of childhood. Blood (1986) 1.06

Comparative genomic hybridization analysis of Wilms tumors. Cytogenet Cell Genet (1997) 1.05

1p36: every subband a suppressor? Eur J Cancer (1995) 1.05

Evidence for linkage of 3-phosphoglycerate kinase, hypoxanthine-guanine-phosphoribosyl transferase, and glucose 6-phosphate dehydrogenase loci in Chinese hamster cells studied by using a relationship between gene multiplicity and enzyme activity. Biochem Genet (1972) 1.04

Maintenance of vascular endothelial cell-specific properties after immortalization with an amphotrophic replication-deficient retrovirus containing human papilloma virus 16 E6/E7 DNA. Exp Cell Res (1995) 1.03

Transfection of the cloned human excision repair gene ERCC-1 to UV-sensitive CHO mutants only corrects the repair defect in complementation group-2 mutants. Mutat Res (1988) 1.03

Genetic sub-types of human malignant astrocytoma correlate with survival. Int J Cancer (1998) 1.02

Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line. Mutat Res (1987) 1.02

Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma. Genes Chromosomes Cancer (1996) 1.00

Assignment of the AK1:Np:ABO linkage group to human chromosome 9. Proc Natl Acad Sci U S A (1976) 1.00

Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts. Exp Cell Res (1990) 0.98

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. Hum Mol Genet (1997) 0.98

Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus. Hum Genet (1996) 0.97

X-linkage of human -galactosidase. Nat New Biol (1972) 0.97

In vitro drug-resistance profile in infant acute lymphoblastic leukemia in relation to age, MLL rearrangements and immunophenotype. Leukemia (2004) 0.97

Involvement of Y chromosomal loci in the synthesis of Drosophila hydei sperm proteins. Dev Biol (1983) 0.97

Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16). Leukemia (1997) 0.97

DNA repair monitored by an enzymatic assay in multinucleate xeroderma pigmentosum cells after fusion. Nature (1974) 0.96

Somatic cell genetics of human interferon production in human-rodent cell hybrids. J Gen Virol (1979) 0.95

Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13. Stroke (2004) 0.94

Molecular analysis of genetic changes in ependymomas. Genes Chromosomes Cancer (1995) 0.94

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. Genomics (1994) 0.93

Genetic relation between the Zellweger syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata. N Engl J Med (1986) 0.93

Analysis of mutations in the SCH gene in schwannomas. Genes Chromosomes Cancer (1994) 0.93

Assessment of chromosomal gains and losses in oral squamous cell carcinoma by comparative genomic hybridisation. Oral Oncol (1997) 0.92

Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Res (1990) 0.92

The role of type III collagen in spontaneous cervical arterial dissections. Ann Neurol (1998) 0.92

UV stimulation of DNA-mediated transformation of human cells. Mol Cell Biol (1985) 0.92

Report of the Committee on the Genetic Constitution of Chromosomes 18, 19, 20, 21, and 22. Cytogenet Cell Genet (1984) 0.92

Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood. Int J Cancer (1991) 0.92

The site of action of 2,4-dinitrophenol and salicylic acid upon the uncoupler-induced K+ efflux from non-metabolizing yeast. Biochim Biophys Acta (1980) 0.89

The genetic defect in the various types of human beta-galactosidase deficiency. Hum Genet (1980) 0.89

Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22. Eur J Hum Genet (2000) 0.88

Photoreactivation and excision repair of ultraviolet radiation-injured DNA in primary embryonic chick cells. Biophys J (1974) 0.88

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity. Am J Hum Genet (1994) 0.88

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3. Cytogenet Cell Genet (1995) 0.88

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family. Cytogenet Cell Genet (1989) 0.88

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Med Pediatr Oncol (1996) 0.88

Fine mapping of a region of common deletion on chromosome arm 10p in human glioma. Genes Chromosomes Cancer (1997) 0.88

Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation. Cytogenet Cell Genet (1975) 0.87

Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells. Exp Cell Res (1985) 0.87

Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization. Genes Chromosomes Cancer (2001) 0.86

Identification of DNA repair genes in the human genome. Cold Spring Harb Symp Quant Biol (1986) 0.86

CDKN2 deletions have no prognostic value in childhood precursor-B acute lymphoblastic leukaemia. Leukemia (2005) 0.86

MDR1 expression in poor-risk acute myeloid leukemia with partial or complete monosomy 7. Leukemia (2001) 0.86