Published in Exp Cell Res on February 01, 1977
Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture. Am J Hum Genet (1979) 5.18
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics. Am J Hum Genet (1979) 4.10
Chromosomal mosaicism in amniotic fluid cell cultures. Am J Hum Genet (1979) 0.92
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells. Proc Natl Acad Sci U S A (1997) 5.24
[A new technic of analysis of the human karyotype]. C R Acad Sci Hebd Seances Acad Sci D (1971) 2.62
The need for more reliable information on the incidence and prevalence of occupationally related problems. Occup Med (Lond) (1994) 2.54
[Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1]. Exp Cell Res (1976) 2.07
High resolution R- and G-banding on the same preparation. Hum Genet (1981) 1.94
[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]. C R Acad Sci Hebd Seances Acad Sci D (1973) 1.89
NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. Genomics (2001) 1.85
Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum Genet (1979) 1.75
A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes. Cytogenet Cell Genet (1992) 1.64
Systematic analysis of 95 reciprocal translocations of autosomes. Hum Genet (1978) 1.59
Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy. Proc Natl Acad Sci U S A (1989) 1.59
Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations. Clin Genet (1976) 1.53
[Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)]. Ann Genet (1972) 1.50
Mutations in OGG1, a gene involved in the repair of oxidative DNA damage, are found in human lung and kidney tumours. Oncogene (1998) 1.49
Human gene mapping using an X/autosome translocation. Somatic Cell Genet (1976) 1.44
[The Dr phenotype: a study of threee cases with a ring D chromosome]. Ann Genet (1968) 1.41
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)]. Cytogenet Cell Genet (1973) 1.40
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. Hum Mol Genet (1997) 1.40
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8). Nucleic Acids Res (1987) 1.38
Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet (1992) 1.38
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38
Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma (1976) 1.36
[The mechanism of chromosome segmentation induced by BUDR (5-bromodeoxyuridine)]. Ann Genet (1974) 1.35
Sensitivity to CPT-11 of xenografted human colorectal cancers as a function of microsatellite instability and p53 status. Br J Cancer (2000) 1.32
Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique. Genes Chromosomes Cancer (1994) 1.30
Physical mapping of human loci homologous to the chicken nov proto-oncogene. Oncogene (1992) 1.26
Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions. Genes Chromosomes Cancer (1995) 1.24
SOD2: a new type of tumor-suppressor gene? Int J Cancer (1992) 1.24
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. Humangenetik (1973) 1.23
[New system of chromosome banding: the T bands (author's transl)]. Chromosoma (1973) 1.23
[Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet (1977) 1.22
Genes occupy a fixed and symmetrical position on sister chromatids. Cell (1991) 1.20
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness. Cell (1987) 1.20
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia. Hum Genet (1988) 1.18
Establishment and characterisation of a new tumorigenic cell line with a normal karyotype derived from a human breast adenocarcinoma. Br J Cancer (1990) 1.17
[Four new cases of X-autosome translocation in man (author's transl)]. Humangenetik (1975) 1.17
High glycolysis in gliomas despite low hexokinase transcription and activity correlated to chromosome 10 loss. Br J Cancer (1996) 1.17
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet (1979) 1.17
The cell cycle of lymphocytes in Fanconi anemia. Hum Genet (1982) 1.16
[Study of progeny of individuals bearing a t(DqDq) translocation]. Ann Genet (1970) 1.15
Increased p53 protein content of colorectal tumours correlates with poor survival. Br J Cancer (1992) 1.13
[Partial trisomy 21 (21q21 - 21q22.2)]. Ann Genet (1976) 1.12
A familial Y-autosome translocation in man. Clin Genet (1971) 1.12
Cytogenetic study of breast cancer: clinicopathologic significance of homogeneously staining regions in 84 patients. Hum Pathol (1992) 1.12
Proto-oncogene amplification and homogeneously staining regions in human breast carcinomas. Genes Chromosomes Cancer (1990) 1.11
DNA hypomethylation in breast cancer: an independent parameter of tumor progression? Cancer Genet Cytogenet (1997) 1.11
Gliomas are driven by glycolysis: putative roles of hexokinase, oxidative phosphorylation and mitochondrial ultrastructure. Anticancer Res (1997) 1.10
Deletion of band 13q21 is compatible with normal phenotype. Hum Genet (1985) 1.09
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. Int J Cancer (1988) 1.08
Cytogenetics of colorectal adenocarcinomas. Cancer Genet Cytogenet (1990) 1.08
[Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. Ann Genet (1973) 1.08
An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. Ann Genet (1973) 1.07
Simultaneous monitoring of P53 protein and DNA content of colorectal adenocarcinomas by flow cytometry. Int J Cancer (1990) 1.07
Comparison of RBG-banded karyotypes of cattle, sheep, and goats. Cytogenet Cell Genet (1991) 1.06
Highly recurrent der(1;16)(q10;p10) and other 16q arm alterations in lobular breast cancer. Genes Chromosomes Cancer (1998) 1.06
Amplification of DNA sequences from chromosome 19q13.1 in human pancreatic cell lines. Genomics (1998) 1.06
Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. Cytogenet Cell Genet (1993) 1.05
Alterations of DNA methylation patterns in germ cells and Sertoli cells from developing mouse testis. Cytogenet Cell Genet (1999) 1.05
[Ring 15 chromosome: r(15). Identification by controlled denaturation]. Ann Genet (1972) 1.03
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization. Hum Genet (1989) 1.03
Reconstruction of the ancestral karyotype of eutherian mammals. Chromosome Res (2003) 1.02
Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females. Proc Natl Acad Sci U S A (1989) 1.02
Intracellular pH governs the subcellular distribution of hexokinase in a glioma cell line. Biochem J (1996) 1.02
[Segregation of a balanced translocation t(5p-;Gp+)]. Ann Genet (1968) 1.01
Osteosarcoma following retinoblastoma: age at onset and latency period. Ophthalmic Genet (2001) 1.01
Z-DNA immunoreactivity in fixed metaphase chromosomes of primates. Proc Natl Acad Sci U S A (1983) 1.01
Variations of chromosome radiation sensitivity in fetal and adult mice during gestation. Mutat Res (1991) 1.01
Characterization of SRp46, a novel human SR splicing factor encoded by a PR264/SC35 retropseudogene. Mol Cell Biol (1998) 1.01
Consistent deficiencies of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinism. Ann Genet (1985) 1.00
Common methylation characteristics of sex chromosomes in somatic and germ cells from mouse, lemur and human. Chromosome Res (2000) 1.00
[Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)]. Ann Genet (1976) 1.00
Dihydrofolate reductase gene amplification-associated shift of differentiation in methotrexate-adapted HT-29 cells. J Cell Biol (1991) 0.99
Identification of a human guanine nucleotide-releasing factor (H-GRF55) specific for Ras proteins. Oncogene (1993) 0.99
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines. Hum Genet (1993) 0.99
Segmentation of human chromosomes induced by 5-ACR (5-azacytidine). Hum Genet (1976) 0.99
Fine mapping of human HOX gene clusters. Cytogenet Cell Genet (1996) 0.99
[Application of the controlled denaturation method: denaturation of previously stained preparations]. Ann Genet (1972) 0.98
Improvement in the morphology of Ti-based surfaces: a new process to increase in vitro human osteoblast response. Biomaterials (2002) 0.98
[Mitotic and meiotic analysis of an Y-autosome translocation(author's transl)]. Humangenetik (1975) 0.98
Oncogene amplification in human gliomas: a molecular cytogenetic analysis. Oncogene (1994) 0.97
The peripheral benzodiazepine receptors: a review. J Neurooncol (2000) 0.97
Chromosomal assignment of two human B-raf(Rmil) proto-oncogene loci: B-raf-1 encoding the p94Braf/Rmil and B-raf-2, a processed pseudogene. Oncogene (1992) 0.97
Predominance of normal karyotype in colorectal tumors from hereditary non-polyposis colorectal cancer patients. Genes Chromosomes Cancer (1995) 0.97
[A second example of telomeric fusion 2 X chromosomes]. Ann Genet (1975) 0.97
[Effect of the ionic medium on controlled heat denaturation of human chromosomes]. Ann Genet (1972) 0.96
Sex chromosome rearrangements in Polyphaga beetles. Sex Dev (2009) 0.96
Distinct chromosomal alterations associated with TP53 status of LoVo cells under PALA selective pressure: a parallel with cytogenetic pathways of colorectal cancers. Oncogene (1999) 0.96
Clinical and experimental progression of a new model of human prostate cancer and therapeutic approach. Am J Pathol (2001) 0.95
Recurrent cytogenetic alterations of prostate carcinoma and amplification of c-myc or epidermal growth factor receptor in subclones of immortalized PNT1 human prostate epithelial cell line. Int J Cancer (1995) 0.95
Genetic evolution of breast cancers. III: Age-dependent variations in the correlations between biological indicators of prognosis. Breast Cancer Res Treat (1995) 0.95
The ancestral karyotype of platyrrhine monkeys. Cytogenet Cell Genet (1981) 0.95
Characterization of chromosome changes in two human prostatic carcinoma cell lines (PC-3 and DU145) using chromosome painting and comparative genomic hybridization. Cancer Genet Cytogenet (1997) 0.95
Preservation of chromosome and DNA characteristics of human colorectal adenocarcinomas after passage in nude mice. Int J Cancer (1989) 0.95
Analysis of distribution in the human, pig, and rat genomes points toward a general subtelomeric origin of minisatellite structures. Genomics (1998) 0.95
Existence of two distinct processes of chromosomal evolution in near-diploid colorectal tumors. Cancer Genet Cytogenet (1988) 0.94
Effect of grooved titanium substratum on human osteoblastic cell growth. J Biomed Mater Res (2002) 0.94
[Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]. Ann Genet (1975) 0.94
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe. Hum Hered (1988) 0.94
[Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)]. Humangenetik (1975) 0.94
[Monosomy for the centromeric regions of chromosome 21]. Exp Cell Res (1972) 0.94