Chromosomal localization of human satellites 2 and 3 by a FISH method using oligonucleotides as probes

No abstract is available for this paper.

• Publication year

  1994

• Venue

  Human Genetics

• Publication date

  1994-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF00201662PMID 8168808
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15

  2005cited by this paper
• The chromosomal localisation of human satellite DNA I

  2004influential reference
• Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis

  2004cited by this paper
• Localisation of satellite DNA sequences on human metaphase chromosomes using bromodeoxyuridine-labelled probes

  2004cited by this paper
• Molecular Cloning: A Laboratory Manual

  2001cited by this paper
• Assignment of human satellite 1 DNA as revealed by fluorescent in situ hybridization with oligonucleotides

  1994cited by this paper
• Characterisation of a boundary between satellite III and alphoid sequences on human chromosome 10.

  1992cited by this paper
• A satellite III sequence shared by human chromosomes 13, 14, and 21 that is contiguous with alpha satellite DNA.

  1992cited by this paper
• A chromosome 14-specific human satellite III DNA subfamily that shows variable presence on different chromosomes 14.

  1992cited by this paper
• A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescent in situ hybridization.

  1991cited by this paper
• Non-isotopic detection of chromosome 1 in human meiosis and demonstration of disomic sperm nuclei

  1991cited by this paper
• Evolution of alpha satellite.

  1991cited by this paper
• A survey of the genomic distribution of alpha satellite DNA on all the human chromosomes, and derivation of a new consensus sequence.

  1991cited by this paper
• A SURVEY OF THE GENOMIC DISTRIBUTION OF ALPHA SATELLITE DNA ON ALL THE HUMAN CHROMOSOMES, AND DERIVATION OF A NEW CONSENSUS SEQUENCE

  1991cited by this paper
• A homologous subfamily of satellite III DNA on human chromosomes 14 and 22.

  1990cited by this paper
• Human Satellite III DNA: Genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences

  1989cited by this paper
• Human satellite-III DNA: an example of a “macrosatellite” polymorphism

  1988cited by this paper
• Satellite II DNA of human lymphocytes: tandem repeats of a simple sequenceelement

  1988cited by this paper
• Satellite DNA

  1986cited by this paper
• Molecular hybridization to meiotic chromosomes in man reveals sequence arrangement on the no. 9 chromosome and provides clues to the nature of "parameres".

  1986cited by this paper
• Sequence relationships of three human satellite DNAs.

  1986influential reference
• A direct demonstration of somatically paired heterochromatin of human chromosomes.

  1983cited by this paper
• Simple repeated sequences in human satellite DNA.

  1982influential reference
• Highly repeated sequences in mammalian genomes.

  1982cited by this paper
• Satellite DNA sequences in the human acrocentric chromosomes: information from translocations and heteromorphisms.

  1981cited by this paper
• Cloning of human satellite III DNA: different components are on different chromosomes.

  1979influential reference
• A study of sequence homologies in four satellite DNAs of man.

  1979influential reference
• Specific arrangements of human satellite III DNA sequences in human chromosomes

  1979cited by this paper
• Satellite DNA's

  1977cited by this paper
• Reverse fluorescent chromosome banding with chromomycin and DAPI

  1976cited by this paper
• The location of four human satellite DNAs on human chromosomes.

  1975influential reference
• Location of human satellite DNAs on the Y chromosome

  1974cited by this paper
• 5-Methylcytosine localised in mammalian constitutive heterochromatin

  1974cited by this paper
• Satellite DNA.

  1973cited by this paper
• The chromosomal location of human satellite DNA III

  1973cited by this paper
• Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

  1972cited by this paper
• Location of satellite and homogeneous DNA sequences on human chromosomes.

  1971cited by this paper

• DUX4-induced HSATII RNA accumulation drives protein aggregation, impacting RNA processing pathways.

  2026cites this paper
• HSATII RNA-dependent triplex formation in early human embryogenesis as a potential mechanism for Y chromosome loss in Turner syndrome

  2025cites this paper
• Epigenetic Modeling of Jumping Translocations of 1q Heterochromatin in Acute Myeloid Leukemia After 5'‐Azacytidine Treatment

  2024cites this paper
• DUX4-induced HSATII RNA accumulation drives protein aggregation impacting RNA processing pathways

  2024cites this paper
• DUX4-induced HSATII transcription causes KDM2A/B–PRC1 nuclear foci and impairs DNA damage response

  2024cites this paper
• Sharpening new scissors: Designing a CRISPR-Cas9 construct for inducible and interchangeable HSATII expression in Tig-1 fibroblasts

  2023cites this paper
• The Structure of Simple Satellite Variation in the Human Genome and Its Correlation With Centromere Ancestry

  2023cites this paper
• A classical revival: Human satellite DNAs enter the genomics era.

  2022cites this paper
• The Dynamic Structure and Rapid Evolution of Human Centromeric Satellite DNA

  2022cites this paper
• Genomic Tackling of Human Satellite DNA: Breaking Barriers through Time

  2021influential citation
• Evidence for divergence of DNA methylation maintenance and a conserved inhibitory mechanism from DNA demethylation in chickens and mammals

  2021cites this paper
• Differential enrichment of H3K9me3 at annotated satellite DNA repeats in human cell lines and during fetal development in mouse

  2021cites this paper
• Complete genomic and epigenetic maps of human centromeres

  2021cites this paper
• Sequence, Chromatin and Evolution of Satellite DNA

  2021cites this paper
• White spot syndrome viral protein VP9 alters the cellular higher‐order chromatin structure

  2020cites this paper
• Probing the function of long noncoding RNAs in the nucleus

  2020cites this paper
• Ectopic expression of pericentric HSATII RNA results in nuclear RNA accumulation, MeCP2 recruitment, and cell division defects

  2020influential citation
• Repeat RNAs associate with replication forks and post-replicative DNA

  2020cites this paper
• Human pericentromeric tandemly repeated DNA is transcribed at the end of oocyte maturation and is associated with membraneless mitochondria-associated structures

  2020cites this paper
• Satellite 2 repeat DNA in blood plasma as a candidate biomarker for the detection of cancer.

  2020cites this paper
• Chromosomal rearrangements at hypomethylated Satellite 2 sequences are associated with impaired replication efficiency and increased fork stalling

  2019influential citation
• DNA methylation in satellite repeats disorders.

  2019cites this paper
• High Satellite Repeat Turnover in Great Apes Studied with Short- and Long-Read Technologies

  2019cites this paper
• Centromeric Satellite DNAs: Hidden Sequence Variation in the Human Population

  2019cites this paper
• High inter- and intraspecific turnover of satellite repeats in great apes

  2018cites this paper
• Loss of Tumor Suppressor STAG2 Promotes Telomere Recombination and Extends the Replicative Lifespan of Normal Human Cells.

  2017cites this paper
• 1 Genetics of Down Syndrome

  2017cites this paper
• Elucidate the Mechanism of Telomere Maintenance in STAG2 Mutated Tumor Cells

  2017cites this paper
• Illuminating the structure and dynamics of chromatin by fluorescence labeling

  2017cites this paper
• Demethylating and anti‐hepatocarcinogenic potential of hesperidin, a natural polyphenol of Citrus juices

  2017cites this paper
• The Promises and Challenges of Genomic Studies of Human Centromeres.

  2017cites this paper
• Quantitation of circulating satellite RNAs in pancreatic cancer patients.

  2016cites this paper
• Satellite RNAs promote pancreatic oncogenic processes via the dysfunction of YBX1

  2016cites this paper
• The use of DAPI fluorescence lifetime imaging for investigating chromatin condensation in human chromosomes

  2016cites this paper
• Genomic Characterization of Large Heterochromatic Gaps in the Human Genome Assembly

  2014cites this paper
• The Epithelial-to-Mesenchymal Transition (EMT), a Particular Case

  2014cites this paper
• Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications

  2014cites this paper
• Genetic and functional analysis of ZBTB24, which is mutated in type 2 ICF syndrome

  2014cites this paper
• Sequence-specific microscopic visualization of DNA methylation status at satellite repeats in individual cell nuclei and chromosomes

  2013cites this paper
• Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients

  2013cites this paper
• Regulation and dymanic behavior of the heat shock transcription factor HSF-1 in C. elegans

  2013cites this paper
• Detection of characteristic heterochromatin distribution, highly amplified rRNA genes and presence of the human satellite III DNA motif in the scleractinian coral Echinophyllia aspera Ellis and Solander 1788

  2013cites this paper
• Comprehensive FISH Probe Design Tool Applied to Imaging Human Immunoglobulin Class Switch Recombination

  2012cites this paper
• Satellite 2 demethylation induced by 5-azacytidine is associated with missegregation of chromosomes 1 and 16 in human somatic cells.

  2012cites this paper
• Transcription in the maintenance of centromere chromatin identity

  2012cites this paper
• Chromosome-wide regulation of euchromatin-specific 5mC to 5hmC conversion in mouse ES cells and female human somatic cells

  2012cites this paper
• Role of DNMT3B in the regulation of early neural and neural crest specifiers

  2012cites this paper
• Tandemly repeated DNA families in the mouse genome

  2011cites this paper
• Heterochromatic Variations and Pregnancy Losses in Humans

  2011cites this paper
• Genetics of Down Syndrome

  2011cites this paper
• Effects of Folic Acid Supplementation on Human Leukocyte DNA Methylation and Gene Expression

  2011cites this paper
• Application of Padlock Probe Based Nucleic Acid Analysis In Situ

  2010cites this paper
• Heat shock factor 1 binds to and transcribes satellite II and III sequences at several pericentromeric regions in heat-shocked cells.

  2010cites this paper
• DNA methylation at imprinted and non-imprinted genes in the sperm of men affected by severe male factor infertility

  2010cites this paper
• Comparative Study of Extracellular DNA by FISH

  2010cites this paper
• Concerted evolution of members of the multisequence family chAB4 located on various nonhomologous chromosomes

  2009cites this paper
• The organization of classical satellite DNAs in human chromosomes: an approach using AluI and TaqI restriction endonucleases.

  2009cites this paper
• ASPECTS EPIGENETIQUES DES CANCERS BRONCHO-PULMONAIRES & IMPLICATION DE L'HISTONE ACETYLTRANSFERASE Tip60

  2009cites this paper
• ROLE PATHOLOGIQUE DES ANOMALIES DE L'HETEROCHROMATINE PERICENTROMERIQUE DU CHROMOSOME 1 DANS LES LYMPHOMES B MALINS NON-HODGKINIENS

  2009influential citation
• Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia

  2009cites this paper
• A transcriptomic analysis of human centromeric and pericentric sequences in normal and tumor cells

  2009cites this paper
• Circulating Nucleic Acids in Plasma and Serum

  2008cites this paper
• Cancer-Linked DNA Hypermethylation and Hypomethylation: Chromosome Position Effects

  2008cites this paper
• Constitutive heterochromatin DNA fragments are demethylated and decondensed in senescent primary fibroblasts MRC5 and malignant A431 cell line

  2007cites this paper
• Tiling resolution array CGH, expression, and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3

  2007cites this paper
• Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3.

  2007cites this paper
• The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution.

  2006cites this paper
• Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes.

  2006cites this paper
• Human Population Cytogenetics: A Review*

  2005cites this paper
• A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO‐1 and UBC9

  2005cites this paper
• Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).

  2005cites this paper
• DNA methylation and cancer-associated genetic instability.

  2005cites this paper
• DNA hypomethylation on pericentromeric satellite regions significantly correlates with loss of heterozygosity on chromosome 9 in urothelial carcinomas.

  2005cites this paper
• DNA methylation and cancer therapy.

  2005cites this paper
• A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO‐1 and UBC9 (Am J Med Genet 136A: 31–37, 2005)

  2005cites this paper
• Association of pKi-67 with satellite DNA of the human genome in early G1 cells

  2004cites this paper
• The Efficiency of In-situ Hybridization on Human Chromosomes with Alphoid DNAs is Enhanced by Previous Digestion with AluI and TaqI

  2004cites this paper
• Ionizing radiation-induced instant pairing of heterochromatin of homologous chromosomes in human cells

  2004cites this paper
• Satellite III sequences on 14p and their relevance to Robertsonian translocation formation

  2004cites this paper
• Chromatin architecture of the human genome: gene-rich domains are enriched in open chromatin fibers.

  2004cites this paper
• Identification and characterization of satellite III subfamilies to the acrocentric chromosomes

  2004cites this paper
• FISHing with locked nucleic acids (LNA): evaluation of different LNA/DNA mixmers.

  2003cites this paper
• Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10).

  2003cites this paper
• The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease.

  2003cites this paper
• Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations

  2003cites this paper
• Methylation matters: modeling a manageable genome.

  2002cites this paper
• Demethylation of classical satellite 2 and 3 DNA with chromosomal instability in senescent human fibroblasts.

  2002cites this paper
• Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis

  2002cites this paper
• Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells.

  2002cites this paper
• DNA methylation and chromatin – unraveling the tangled web

  2002cites this paper
• The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p

  2001cites this paper
• 5-Bromodeoxyuridine suppresses position effect variegation of transgenes in HeLa cells.

  2001cites this paper
• Oncology nurse training in cancer genetics.

  2001cites this paper
• Functional characterisation of mitochondrial tRNA(Tyr) mutation (5877-->GA) associated with familial chronic progressive external ophthalmoplegia.

  2001cites this paper
• DNA methyltransferase expression and DNA methylation of CPG islands and peri‐centromeric satellite regions in human colorectal and stomach cancers

  2001cites this paper
• Expression of mRNA for DNA methyltransferases and methyl‐CpG–binding proteins and DNA methylation status on CpG islands and pericentromeric satellite regions during human hepatocarcinogenesis

  2001cites this paper
• Oncology nurse training in cancer genetics

  2001cites this paper
• DNA methylation, methyltransferases, and cancer

  2001cites this paper
• DNA methylation in health and disease

  2000cites this paper
• Genetic and physical analyses of the centromeric and pericentromeric regions of human chromosome 5: recombination across 5cen.

  1999cites this paper