Published in Genomics on March 01, 1997
An abundance of bidirectional promoters in the human genome. Genome Res (2004) 5.90
A unified phylogeny-based nomenclature for histone variants. Epigenetics Chromatin (2012) 1.82
Coupling of DNA synthesis and histone synthesis in S phase independent of cyclin/cdk2 activity. Mol Cell Biol (2002) 1.49
Core histones and HIRIP3, a novel histone-binding protein, directly interact with WD repeat protein HIRA. Mol Cell Biol (1998) 1.41
Replication-dependent histone gene expression is related to Cajal body (CB) association but does not require sustained CB contact. Mol Biol Cell (2001) 1.38
H1 histones: current perspectives and challenges. Nucleic Acids Res (2013) 1.35
BAL1 and BBAP are regulated by a gamma interferon-responsive bidirectional promoter and are overexpressed in diffuse large B-cell lymphomas with a prominent inflammatory infiltrate. Mol Cell Biol (2006) 1.29
3' end processing of Drosophila melanogaster histone pre-mRNAs: requirement for phosphorylated Drosophila stem-loop binding protein and coevolution of the histone pre-mRNA processing system. Mol Cell Biol (2002) 1.10
Molecular evolutionary characterization of the mussel Mytilus histone multigene family: first record of a tandemly repeated unit of five histone genes containing an H1 subtype with "orphon" features. J Mol Evol (2004) 1.04
Liquid chromatography mass spectrometry profiling of histones. J Chromatogr B Analyt Technol Biomed Life Sci (2007) 1.00
H2B Tyr37 phosphorylation suppresses expression of replication-dependent core histone genes. Nat Struct Mol Biol (2012) 0.98
Early evolution of histone genes: prevalence of an 'orphon' H1 lineage in protostomes and birth-and-death process in the H2A family. J Mol Evol (2008) 0.89
Variants of core histones and their roles in cell fate decisions, development and cancer. Nat Rev Mol Cell Biol (2017) 0.84
Differential contributions of histone H3 and H4 residues to heterochromatin structure. Genetics (2011) 0.82
Human replication-dependent histone H3 genes are activated by a tandemly arranged pair of two CCAAT boxes. Biochem J (2004) 0.82
Pharmacological unmasking microarray approach-based discovery of novel DNA methylation markers for hepatocellular carcinoma. J Korean Med Sci (2012) 0.78
Role of H1 linker histones in mammalian development and stem cell differentiation. Biochim Biophys Acta (2015) 0.78
The HIST1 Locus Escapes Reprogramming in Cloned Bovine Embryos. G3 (Bethesda) (2016) 0.77
cAMP/phorbol ester response element is involved in transcriptional regulation of the human replacement histone gene H3.3B. Biochem J (1998) 0.77
Common evolutionary origin and birth-and-death process in the replication-independent histone H1 isoforms from vertebrate and invertebrate genomes. J Mol Evol (2005) 0.77
Progress in epigenetic histone modification analysis by mass spectrometry for clinical investigations. Expert Rev Proteomics (2015) 0.77
Transcriptional events during the recovery from MRSA lung infection: a mouse pneumonia model. PLoS One (2013) 0.76
Complex evolutionary history of the mammalian histone H1.1-H1.5 gene family. Mol Biol Evol (2017) 0.75
Rapid mapping of markers applying vectorette technology to YAC fragmentation allows easy assembly of a high-density STS bacterial clone contig spanning the markers D6S1260-D6S1918. Mamm Genome (1998) 0.75
Lambda replacement vectors carrying polylinker sequences. J Mol Biol (1983) 32.76
A physical map of the human genome. Nature (2001) 12.39
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nat Genet (1998) 6.82
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature (1990) 5.13
Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. EMBO Rep (2000) 5.06
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature (1993) 5.05
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nat Genet (1996) 4.36
Cloning of the T gene required in mesoderm formation in the mouse. Nature (1990) 4.20
Selective isolation of cosmid clones by homologous recombination in Escherichia coli. Proc Natl Acad Sci U S A (1984) 4.11
Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. Genome Res (2001) 3.97
A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast. Nat Genet (1996) 3.67
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium. Nature (2000) 3.61
Analysis of cosmids using linearization by phage lambda terminase. Gene (1985) 2.98
Construction and use of human chromosome jumping libraries from NotI-digested DNA. Nature (1987) 2.58
Sequence interpretation. Functional annotation of mouse genome sequences. Science (2001) 2.54
Dickkopf genes are co-ordinately expressed in mesodermal lineages. Mech Dev (1999) 2.36
Primer design for large scale sequencing. Nucleic Acids Res (1998) 2.31
The importin beta/importin 7 heterodimer is a functional nuclear import receptor for histone H1. EMBO J (1999) 2.31
Clustering of multiallele DNA markers near the Huntington's disease gene. J Clin Invest (1989) 2.25
Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array. Genome Res (2001) 2.25
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours. Nat Genet (1997) 2.18
Molecular approaches to mammalian genetics. Cold Spring Harb Symp Quant Biol (1986) 1.99
Fragile X syndrome without CCG amplification has an FMR1 deletion. Nat Genet (1992) 1.91
Processing and quality control of DNA array hybridization data. Bioinformatics (2000) 1.86
Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1. Br J Haematol (1999) 1.84
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene. Am J Hum Genet (1999) 1.80
Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome. J Pediatr (2000) 1.74
A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. Am J Hum Genet (1992) 1.73
A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. Hum Mol Genet (1999) 1.70
Cloning of gp-340, a putative opsonin receptor for lung surfactant protein D. Proc Natl Acad Sci U S A (1999) 1.69
Identifying splits with clear separation: a new class discovery method for gene expression data. Bioinformatics (2001) 1.67
The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: alternative biallelic variation in rhesus monkeys. Rapid communication. J Neural Transm (Vienna) (1997) 1.65
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. Nat Genet (1994) 1.62
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Mol Psychiatry (2003) 1.47
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15. Hum Mol Genet (2001) 1.44
A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene. Am J Hum Genet (1990) 1.41
Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation. Genomics (1990) 1.39
Nuclear envelope and chromatin compositional differences comparing undifferentiated and retinoic acid- and phorbol ester-treated HL-60 cells. Exp Cell Res (2001) 1.35
DMBT1 encodes a protein involved in the immune defense and in epithelial differentiation and is highly unstable in cancer. Cancer Res (2000) 1.32
Differential distribution of lysine and arginine residues in the closely related histones H1 and H5. Analysis of a human H1 gene. J Mol Biol (1986) 1.30
A strategy for the selection of transcribed sequences in the Xq28 region. Hum Mol Genet (1992) 1.28
The (6;9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34. Mol Cell Biol (1990) 1.27
Construction of a NotI linking library and isolation of new markers close to the Huntington's disease gene. Nucleic Acids Res (1988) 1.24
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions. Mamm Genome (2000) 1.23
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. Mol Psychiatry (2006) 1.23
Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet (1997) 1.21
Genomic organization of the adrenoleukodystrophy gene. Genomics (1994) 1.19
The human histone gene cluster at the D6S105 locus. Hum Genet (1997) 1.19
Histone H1 zero: a major player in cell differentiation? FASEB J (1994) 1.19
Dyskerin localizes to the nucleolus and its mislocalization is unlikely to play a role in the pathogenesis of dyskeratosis congenita. Hum Mol Genet (1999) 1.18
A family of cosmid vectors with the multi-copy R6K replication origin. Gene (1987) 1.16
Alternative splicing in the fragile X gene FMR1. Hum Mol Genet (1993) 1.16
The melanoma antigen gene (MAGE) family is clustered in the chromosomal band Xq28. Genomics (1995) 1.16
Comprehensive allelotype and genetic anaysis of 466 human nervous system tumors. J Neuropathol Exp Neurol (2000) 1.15
Early increase in histone H1(0) mRNA during differentiation of F9 cells to parietal endoderm. EMBO J (1988) 1.15
Comparative genome sequence analysis of the Bpa/Str region in mouse and Man. Genome Res (2000) 1.13
Acetylation of histones in nucleosomes. Mol Cell Biochem (1982) 1.11
Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q). Genes Chromosomes Cancer (1999) 1.10
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts. J Biol Chem (1998) 1.09
Molecular cloning and analysis of the fragile X region in man. Nucleic Acids Res (1991) 1.08
Normalization of array hybridization experiments in differential gene expression analysis. Nucleic Acids Res (1999) 1.08
Transcription and chromatin structure. Cold Spring Harb Symp Quant Biol (1974) 1.07
Spermatogenesis proceeds normally in mice without linker histone H1t. Histochem Cell Biol (2000) 1.06
New genes in the class II region of the human major histocompatibility complex. Genomics (1991) 1.05
Discrimination of direct and indirect interactions in a network of regulatory effects. J Comput Biol (2007) 1.05
Analysis of reelin as a candidate gene for autism. Mol Psychiatry (2003) 1.05
A gene in human chromosome band Xq28 (GABRE) defines a putative new subunit class of the GABAA neurotransmitter receptor. Genomics (1997) 1.05
Expression of the mouse testicular histone gene H1t during spermatogenesis. Histochem Cell Biol (1996) 1.04
Prognostic impacts of cytogenetic findings in clear cell renal cell carcinoma: gain of 5q31-qter predicts a distinct clinical phenotype with favorable prognosis. Cancer Res (2001) 1.04
Expression of mRNA and protein of nucleoproteins during human spermiogenesis. Mol Hum Reprod (1998) 1.04
Deleted in Malignant Brain Tumors 1 is a versatile mucin-like molecule likely to play a differential role in digestive tract cancer. Cancer Res (2001) 1.03
Loss of 9p leads to p16INK4A down-regulation and enables RB/E2F1-dependent cell cycle promotion in gastrointestinal stromal tumours (GISTs). J Pathol (2008) 1.03
Core histones and linker histones are imported into the nucleus by different pathways. Eur J Cell Biol (2001) 1.02
The human replacement histone H3.3B gene (H3F3B). Genomics (1995) 1.01
Testis-specific expression of a novel human H3 histone gene. Exp Cell Res (1996) 1.01
Isolation and characterization of two human H1 histone genes within clusters of core histone genes. Genomics (1991) 1.00
Molecular cloning of tissue-specific transcripts of a transketolase-related gene: implications for the evolution of new vertebrate genes. Genomics (1996) 1.00
Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad. Hum Mol Genet (1993) 1.00
Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport. Hum Mol Genet (1995) 1.00
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome. Hum Mol Genet (1992) 0.99
The genomic structure of the DMBT1 gene: evidence for a region with susceptibility to genomic instability. Oncogene (1999) 0.99
Genomic structure of a novel chloride channel gene, CLIC2, in Xq28. Genomics (1997) 0.99
Conserved dyad symmetry structures at the 3' end of H5 histone genes. Analysis of the duck H5 gene. J Mol Biol (1984) 0.99
Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1. Hum Mol Genet (1995) 0.98
Digestion of chromosomal proteins in formaldehyde treated chromatin. Hoppe Seylers Z Physiol Chem (1978) 0.98
Transcriptional organization of a 450-kb region of the human X chromosome in Xq28. Proc Natl Acad Sci U S A (1993) 0.98
Movement of histones in chromatin induced by shearing. Eur J Biochem (1976) 0.97
Varied expression patterns of human H1 histone genes in different cell lines. DNA Cell Biol (1997) 0.97
The human H2A and H2B histone gene complement. Biol Chem (1999) 0.96