Published in Nature on April 16, 1981
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Secondary structure model for 23S ribosomal RNA. Nucleic Acids Res (1981) 7.12
Antibiotic resistance mutations in 16S and 23S ribosomal RNA genes of Escherichia coli. Nucleic Acids Res (1984) 3.94
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Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines. Nucleic Acids Res (1981) 1.72
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Primary sequence and partial secondary structure of the 12S kinetoplast (mitochondrial) ribosomal RNA from Leishmania tarentolae: conservation of peptidyl-transferase structural elements. Nucleic Acids Res (1985) 1.39
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Genetics of the mammalian oxidative phosphorylation system: characterization of a new oligomycin-resistant Chinese hamster ovary cell line. Mol Cell Biol (1982) 0.75
Identification of defined sequences in domain V of E. coli 23S rRNA in the 50S subunit accessible for hybridization with complementary oligodeoxyribonucleotides. Nucleic Acids Res (1988) 0.75
A common molecular basis for three inherited kidney stone diseases. Nature (1996) 4.26
MAOA, maltreatment, and gene-environment interaction predicting children's mental health: new evidence and a meta-analysis. Mol Psychiatry (2006) 4.16
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Characterization of fission yeast cohesin: essential anaphase proteolysis of Rad21 phosphorylated in the S phase. Genes Dev (2000) 2.94
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Localization of the X inactivation centre on the human X chromosome in Xq13. Nature (1991) 2.48
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. J Mol Biol (1985) 2.39
G1-phase and B-type cyclins exclude the DNA-replication factor Mcm4 from the nucleus. Nat Cell Biol (1999) 2.39
Fission yeast cdc21+ belongs to a family of proteins involved in an early step of chromosome replication. Nucleic Acids Res (1992) 2.27
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy. Nat Genet (1993) 2.23
Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays. Genes Brain Behav (2008) 2.08
Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: implications for Norrie disease. Genomics (1989) 1.93
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Dinucleotide repeat polymorphism at the MAOA locus. Nucleic Acids Res (1991) 1.77
Chromotin binding, nuclear localization and phosphorylation of Xenopus cdc21 are cell-cycle dependent and associated with the control of initiation of DNA replication. EMBO J (1996) 1.75
Fission yeast cdc21, a member of the MCM protein family, is required for onset of S phase and is located in the nucleus throughout the cell cycle. EMBO J (1996) 1.70
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Mol Psychiatry (2007) 1.68
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A human nuclear protein with sequence homology to a family of early S phase proteins is required for entry into S phase and for cell division. J Cell Sci (1994) 1.56
rar mutations which increase artificial chromosome stability in Saccharomyces cerevisiae identify transcription and recombination proteins. Nucleic Acids Res (1991) 1.50
Characterization of the genomic organization of human carcinoembryonic antigen (CEA): comparison with other family members and sequence analysis of 5' controlling region. Genomics (1990) 1.47
Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms. Mol Psychiatry (2005) 1.46
Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34. Cytogenet Cell Genet (1988) 1.44
Reversion of autonomously replicating sequence mutations in Saccharomyces cerevisiae: creation of a eucaryotic replication origin within procaryotic vector DNA. Mol Cell Biol (1990) 1.44
Assignment of the human tyrosine hydroxylase gene to chromosome 11. FEBS Lett (1984) 1.39
Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]. Nucleic Acids Res (1987) 1.36
Genomic organization of human centromeric alpha satellite DNA: characterization of a chromosome 17 alpha satellite sequence. DNA (1987) 1.33
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Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders. Hum Mol Genet (1997) 1.27
Isolation and characterization of a candidate gene for Norrie disease. Nat Genet (1992) 1.27
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). Hum Mol Genet (1994) 1.27
A fission yeast general translation factor reveals links between protein synthesis and cell cycle controls. J Cell Sci (2000) 1.22
Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies. Mol Psychiatry (2009) 1.21
Homologous expressed genes in the human sex chromosome pairing region. Nature (1985) 1.21
Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. Nature (1979) 1.19
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. Hum Mol Genet (1994) 1.18
Report of the committee on the genetic constitution of chromosomes 12 and 13. Cytogenet Cell Genet (1989) 1.18
Association between monoamine oxidase A activity in human male skin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat. Hum Genet (1999) 1.14
Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. Pharmacogenomics J (2010) 1.14
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp. Hum Genet (1989) 1.13
Language-impaired children: No sign of the FOXP2 mutation. Neuroreport (2002) 1.11
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome. Ann Hum Genet (1984) 1.10
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). Genomics (1995) 1.09
A direct light effect on maintaining photosynthetic activity of Nitella chloroplasts. J Cell Biol (1970) 1.08
The replication capacity of intact mammalian nuclei in Xenopus egg extracts declines with quiescence, but the residual DNA synthesis is independent of Xenopus MCM proteins. J Cell Sci (2000) 1.07
Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb. Hum Mol Genet (2000) 1.07
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Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact. Eur J Immunol (1990) 1.05
C-phycocyanin and allophycocyanin in two species of blue-green algae. Biochem J (1968) 1.05
Genome-wide association analysis of copy number variation in recurrent depressive disorder. Mol Psychiatry (2011) 1.05
Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism. Genes Brain Behav (2008) 1.05
Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2. Hum Genet (1992) 1.04
The current state of play on the molecular genetics of depression. Psychol Med (2012) 1.03
Estimating the heritability of reporting stressful life events captured by common genetic variants. Psychol Med (2012) 1.01
Depressive disorder moderates the effect of the FTO gene on body mass index. Mol Psychiatry (2011) 0.98
No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: results of the depression case control (DeCC) study and a meta-analysis. Am J Med Genet B Neuropsychiatr Genet (2008) 0.97
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome. Genomics (1992) 0.97
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome. Hum Genet (1990) 0.96
Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case. Cytogenet Cell Genet (1995) 0.95
A dinucleotide repeat polymorphism at the DMD locus. Nucleic Acids Res (1991) 0.95
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3. Genomics (1991) 0.94
Physical mapping of genes and sequences at the end of the human X chromosome short arm. Ann Hum Genet (1987) 0.93
Localisation of Y chromosome sequences in normal and 'XX' males. J Med Genet (1987) 0.92
Mutations in the Norrie disease gene. Hum Mutat (1995) 0.92
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Organization of the human monoamine oxidase genes and long-range physical mapping around them. Genomics (1992) 0.92
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene. Hum Mol Genet (1992) 0.91
Interspecific variation in products of animal mitochondrial protein synthesis. Nature (1976) 0.89
Isolation and detailed characterization of human cell lines resistant to D-threo-chloramphenicol. Exp Cell Res (1976) 0.89
A novel expression based approach for assessing the inactivation status of human X-linked genes. Eur J Hum Genet (2000) 0.89
Assignment to chromosome 16 of a gene necessary for the expression of human mitochondrial glutamate oxaloacetate transaminase (aspartate aminotransferase) (E.C. 2.6.1.1.). Biochem Genet (1980) 0.88
Norrie disease gene: characterization of deletions and possible function. Genomics (1993) 0.87
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp. Genomics (1997) 0.87
Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation. Eye (Lond) (1995) 0.87
Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27 beta (DXS255). Hum Genet (1989) 0.87
A model incorporating potential skewed X-inactivation in MZ girls suggests that X-linked QTLs exist for several social behaviours including autism spectrum disorder. Ann Hum Genet (2008) 0.86
Biochemical and immunological studies of the monoamine-oxidizing activities of cultured human cells. Biochem Soc Trans (1977) 0.86
TFIIS and strand-transfer proteins. Nature (1991) 0.86
Localization of human tryptophan hydroxylase (TPH) to chromosome 11p15.3----p14 by in situ hybridization. Cytogenet Cell Genet (1991) 0.86
Localisation of neurone-specific enolase (ENO2) to 12p13. Cytogenet Cell Genet (1990) 0.85
Characterization of a mutation within the NDP gene in a family with a manifesting female carrier. Hum Mol Genet (1993) 0.85
Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis. Genomics (1988) 0.85
Molecular weight differences between human platelet and placental monoamine oxidase. Biochem Pharmacol (1980) 0.85
Chromosome replication in early Xenopus embryos. Cold Spring Harb Symp Quant Biol (1985) 0.84
Cloning of mouse mitochondrial DNA in E. coli affects bacterial viability. Gene (1980) 0.84
Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus. Nucleic Acids Res (1992) 0.84
Ribosomes from the blue-green alga Anabeana variabilis. Arch Mikrobiol (1968) 0.84
DNA analysis and recombination in X-linked retinitis pigmentosa. Eye (Lond) (1990) 0.83
The yeast co-activator GAL11 positively influences transcription of the phosphoglycerate kinase gene, but only when RAP1 is bound to its upstream activation sequence. Mol Gen Genet (1994) 0.83
Long-range physical mapping around the human steroid sulfatase locus. Genomics (1990) 0.83
Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene. Hum Genet (1992) 0.82
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3. Hum Mol Genet (1992) 0.81
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif. Genomics (1992) 0.81
The isolation of an antimycin A-resistant human cell line. Exp Cell Res (1983) 0.81
Analysis of expression of hybrid yeast genes containing ARS elements. Mol Gen Genet (1989) 0.81