Preparation and screening of an arrayed human genomic library generated with the P1 cloning system. - Wikidata - wikimedia - TriplyDB

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.

http://www.wikidata.org/entity/Q35126048

about

Functionally distinct double-stranded RNA-binding domains associated with alternative splice site variants of the interferon-inducible double-stranded RNA-specific adenosine deaminase Molecular cloning of human GDP-mannose 4,6-dehydratase and reconstitution of GDP-fucose biosynthesis in vitro Isolation and characterization of human casein kinase I epsilon (CKI), a novel member of the CKI gene family Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.The human DNA polymerase beta gene structure. Evidence of alternative splicing in gene expression An arrayed human genomic library constructed in the PAC shuttle vector pJCPAC-Mam2 for genome-wide association studies and gene therapy Human RNA-specific adenosine deaminase ADAR1 transcripts possess alternative exon 1 structures that initiate from different promoters, one constitutively active and the other interferon inducible Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3 Structure of the human oxytocinase/insulin-regulated aminopeptidase gene and localization to chromosome 5q21 Identification and characterization of the multiple endocrine neoplasia type 1 (MEN1) gene High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays High-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISH Human homologs of the Xenopus oocyte cortical granule lectin XL35.Construction of bacteriophage P1 libraries with large inserts.Rational design of landmark probes for quantitative DNA fiber mapping (QDFM).A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23 Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.GATA-1 and Oct-1 are required for expression of the human alpha-hemoglobin-stabilizing protein gene.Systematic screening of an arrayed cDNA library by PCR Mapping ESTs by fiber-FISH Modification of bacterial artificial chromosome clones using Cre recombinase: introduction of selectable markers for expression in eukaryotic cells 'Chromosomal Rainbows' Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors.Frequent genetic alterations in simple urothelial hyperplasias of the bladder in patients with papillary urothelial carcinoma.Bioinformatic Tools Identify Chromosome-Specific DNA Probes and Facilitate Risk Assessment by Detecting Aneusomies in Extra-embryonic Tissues.A humanized mouse model for the reduced folate carrier.An arrayed bacteriophage P1 genomic library of Pneumocystis carinii.Isolating large nested deletions in bacterial and P1 artificial chromosomes by in vivo P1 packaging of products of Cre-catalysed recombination between the endogenous and a transposed loxP site.Validation of DNA probes for molecular cytogenetics by mapping onto immobilized circular DNA.A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.Transfer of P1 inserts into a yeast-bacteria shuttle vector by co-transformation mediated homologous recombination.Chromosome 18q paracentric inversion in a family with mental retardation and hearing loss.Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.Hypermethylation of the spleen tyrosine kinase promoter in T-lineage acute lymphoblastic leukemia.Analysis of a 69-kb contiguous genomic sequence at a putative tumor suppressor gene locus on human chromosome 6q27.Identification of transcription factor binding sites important in the regulation of the human interleukin-5 gene.Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: Localization to Chromosome 7q32 and identification of a pseudogene on 11pl5

P2860

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P2860

Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.

http://www.wikidata.org/entity/Q35126048

description

1994 nî lūn-bûn

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1994 թուականի Մարտին հրատարակուած գիտական յօդուած

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1994 թվականի մարտին հրատարակված գիտական հոդված

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1994年の論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年论文

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Proceedings of the National Academy of Sciences of the United States of America

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Preparation and screening of a ...... ed with the P1 cloning system.

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Ackerman SL

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Balkenhol TC

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Coulby JN

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Pfrogner BD

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Sauer RH

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Sternberg N

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P2860

Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector

A rapid alkaline extraction procedure for screening recombinant plasmid DNA

Using bacteriophage P1 system to clone high molecular weight genomic DNA.

A mouse genomic library in the bacteriophage P1 cloning system: organization and characterization.

A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: improved cloning efficacy.

The human Y chromosome: overlapping DNA clones spanning the euchromatic region.

Producing a P1 bacteriophage library from pine: isolation and cloning of very high molecular weight DNA.

Characterization of bacteriophage P1 library containing inserts of Drosophila DNA of 75-100 kilobase pairs.

Generation of a 50,000-member human DNA library with an average DNA insert size of 75-100 kbp in a bacteriophage P1 cloning vector.

Tandem arrangement of the albumin and alpha-fetoprotein genes in the human genome.

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2629-2633

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10.1073/PNAS.91.7.2629

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7

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