Volume 19(5); March 11, 1991 Fine structural features of the chloroplast genome: comparison of the sequenced chloroplast genomes. PMCID: PMC333770 Detection of homologous recombination between yeast artificial chromosomes with overlapping inserts. PMCID: PMC333771 Isolation and nucleotide sequence of the Aspergillus restrictus gene coding for the ribonucleolytic toxin restrictocin and its expression in Aspergillus nidulans: the leader sequence protects producing strains from suicide. PMCID: PMC333772 Cloning and characterization of the MboII restriction-modification system. PMCID: PMC333773 A sequence dimorphism in a conserved domain of human 28S rRNA. Uneven distribution of variant genes among individuals. Differential expression in HeLa cells. PMCID: PMC333774 Computer simulations and experimental studies of gel mobility patterns for weak and strong non-cooperative protein binding to two targets on the same DNA: application to binding of tet repressor variants to multiple and single tet operator sites. PMCID: PMC333775 An avian 40 KDa nucleoprotein binds preferentially to a promoter sequence containing one single pair of methylated CpG. PMCID: PMC333776 The human ubiquitin-52 amino acid fusion protein gene shares several structural features with mammalian ribosomal protein genes. PMCID: PMC333777 Structure of oxidatively damaged nucleic acid adducts. 3. Tautomerism, ionization and protonation of 8-hydroxyadenosine studied by 15N NMR spectroscopy. PMCID: PMC333778 Stepwise cloning and molecular characterization of the HgiDI restriction-modification system from Herpetosiphon giganteus Hpa2. PMCID: PMC333779 Preparation of europium-labelled DNA probes and their properties. PMCID: PMC333780 Identification and sequence determination of the host factor gene for bacteriophage Q beta. PMCID: PMC333781 Specific inhibition of human DNA ligase adenylation by a distamycin derivative possessing antitumor activity. PMCID: PMC333782 Cloning, expression and characterization of the human transcription elongation factor, TFIIS. PMCID: PMC333783 PCR with 5-methyl-dCTP replacing dCTP. PMCID: PMC333784 Isolation of cDNA clones encoding an enzyme from bovine cells that repairs oxidative DNA damage in vitro: homology with bacterial repair enzymes. PMCID: PMC333785 The U1 snRNA gene repeat from the sea urchin (Strongylocentrotus purpuratus): the 70 kilobase tandem repeat ends directly 3' to a U1 gene. PMCID: PMC333786 Identification of a gene encoding the predicted ribosomal protein L7b divergently transcribed from POL1 in fission yeast Schizosaccharomyces pombe. PMCID: PMC333787 Genomic organization of the human thyroid hormone receptor alpha (c-erbA-1) gene. PMCID: PMC333788 Inhibition of translation initiation by antisense oligonucleotides via an RNase-H independent mechanism. PMCID: PMC333789 Cloning and sequence analysis of TFE, a helix-loop-helix transcription factor able to recognize the thyroglobulin gene promoter in vitro. PMCID: PMC333790 A segment of a plasmid gene required for conjugal transfer encodes a site-specific, single-strand DNA endonuclease and ligase. PMCID: PMC333791 The transcription factor LF-A1 interacts with a bipartite recognition sequence in the promoter regions of several liver-specific genes. PMCID: PMC333792 A pseudogene for a novel ubiquitin C-terminal hydrolase of S. cerevisiae. PMCID: PMC333793 Human MyoD: cDNA and deduced amino acid sequence. PMCID: PMC333794 Complete nucleotide sequence of a 16S ribosomal RNA gene from Streptomyces griseus subsp. griseus. PMCID: PMC333795 Budding yeast CAN1 gene as a selection marker in fission yeast. PMCID: PMC333796 PCR based diagnosis in the presence of 8% (v/v) blood. PMCID: PMC333797 BfaI, a new MaeI isoschizomer from Bacteroides fragilis, recognizes the sequence 5' C decreases TAG 3'. PMCID: PMC333798 Linear amplification DNA sequencing directly from single phage plaques and bacterial colonies. PMCID: PMC333799 Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. PMCID: PMC333800 Direct PCR from CVS and blood lysates for detection of cystic fibrosis and Duchenne muscular dystrophy deletions. PMCID: PMC333801 A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors. PMCID: PMC333802 A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119) PMCID: PMC333803 A frequent HincII polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118) PMCID: PMC333804 RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3 PMCID: PMC333805 An SstI RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3 PMCID: PMC333806 An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3 PMCID: PMC333807 A dinucleotide repeat polymorphism at the DMD locus PMCID: PMC333808 TaqI polymorphism at D5S205, located within 5q11.2–13.3 PMCID: PMC333809 Dinucleotide repeat polymorphism at the human c-fms proto-oncogene for the CFS-1 receptor (CFS1R) PMCID: PMC333810 PCR-based detection of polymorphic DdeI and KpnI sites in intron 5 of the adenylate kinase (AK1) gene PMCID: PMC333811 Dinucleotide repeat polymorphism at the DXS538 locus PMCID: PMC333812 NcoI RFLP in the pseudogene (CYP2D8P) of the human debrisoquine 4-hydroxylase locus PMCID: PMC333813 FnuD II RFLP at the human dopamine-β-hydroxylase (DβH) locus PMCID: PMC333814 Dinucleotide repeat polymorphism in the human glucagon gene (GCG) PMCID: PMC333815 A new polymorphic probe on chromosome 3p: λLIB41–51 (D3S632) PMCID: PMC333816 Dinucleotide repeat polymorphism at the human cysteine-proteinase inhibitor pseudogene (CSTP1) PMCID: PMC333817 HinfI polymorphism within the 3′ untranslated region of the candidate Wilms tumour gene PMCID: PMC333818 Isoleucine397 is changed to threonine in two females with hemophilia B PMCID: PMC333819 PCR detection of existing and new polymorphism at the TIMP locus PMCID: PMC333820 PCR detection of a BclI RFLP in the human ALPL gene PMCID: PMC333821 RFLP for BgIII at the human skeletal muscle sodium channel locus PMCID: PMC333822 The cDNA of the human neuromedin B gene (NMB) mapped to 15q11-qter recognizes an XbaI RFLP PMCID: PMC333823 A BgIII RFLP at the human prolactin gene locus on chromosome 6 (PRL) PMCID: PMC333824 A highly polymorphic VNTR locus on the long arm of chromosome 4 PMCID: PMC333825 Dinucleotide repeat polymorphism at the D1S117 locus PMCID: PMC333826 A dinucleotide repeat polymorphism at the D1S116 locus PMCID: PMC333827 Dinucleotide repeat polymorphism at the D21S172 locus PMCID: PMC333828 A TaqI RFLP detected by the probe TN157 (D7S145) at the human chromosome region 7p13–14.2 PMCID: PMC333829 A new polymorphic probe on chromosome 3p: λLIB46-100 (D3S641) PMCID: PMC333830 Dinucleotide repeat polymorphism at the D14S42 locus PMCID: PMC333831 Dinucleotide repeat polymorphism at the D6S109 locus PMCID: PMC333832 Splice junction mutations in factor IX gene resulting in severe hemophilia B PMCID: PMC333833 Synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid-5-ene dehydrogenase (HSD) PMCID: PMC333834 New nucleotide sequence data on the EMBL File Server PMCID: PMC333835 Journal Matter Original table of contents page Administrative content — journal masthead, notices, indexes, etc. Advertisements | ||