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  1. Pubblicazioni

GENOMICS

Rivista
Codice:
E069825
ISSN:
0888-7543
  • Dati Generali

Dati Generali

Pubblicazioni (98)

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  • decrescente
1.5-Mb YAC contig in Xq28 formatted with sequence-tagged sites and including a region unstable in the clones
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A 2.4-MEGABASE PHYSICAL MAP SPANNING THE CYP2C GENE-CLUSTER ON CHROMOSOME 10Q24
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A 9.1-kb Gap in the Genome Reference Map Is Shown to Be a Stable Deletion/Insertion Polymorphism of Ancestral Origin.
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A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes.
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A low-copy repeat in Xq26 represents a novel putatively prenylated protein gene (CXX1) and its pseudogenes (DXS9914, DXS9915, and DXS9916)
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A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome
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A study of the impact of DNA helical rise on protein-DNA interaction
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ALU AND L1 SEQUENCE DISTRIBUTIONS IN XQ24-Q28 AND THEIR COMPARATIVE UTILITY IN YAC CONTIG ASSEMBLY AND VERIFICATION
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ALU and L1 sequence distribution in Xq24-q28 and its utility in YAC contig assembly and verification.
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Actin-binding protein (ABP-280) filamin gene maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28
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An integrated physical and genetic map spanning chromosome band 10q24
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Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) gene.
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Assembly of the Antifreeze Glycoprotein/ Trypsinogen-Like Protease Genomic Locus in the Antarctic fish Dissostichus mawsoni (Norman)
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CBFA2T1, a gene rearranged in human leukemia, is a member of a multigene family
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CHROMOSOME LOCATIONS OF HUMAN EMX AND OTX GENES
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CLUSTERED ORGANIZATION OF KRUPPEL ZINC-FINGER GENES AT XP11.23, FLANKING A TRANSLOCATION BREAKPOINT AT OATL1 - A PHYSICAL MAP WITH LOCUS ASSIGNMENTS FOR ZNF21, ZNF41, ZNF81, AND ELK1
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Characterization and fine localization of two new genes in Xq28 using the genomic sequence EST database screening approach
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Chemogenomic profiling of the cellular effects associated with histone H3 acetylation impairment by a quinoline-derived compound
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Classification of selectively constrained DNA elements using feature vectors and rule-based classifiers
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Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32.
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Cloning of GPR37, a Gene Located on Chromosome 7 Encoding a Putative G-Protein-Coupled Peptide Receptor, from a Human Frontal Brain EST Library
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Cloning of PC3B, a novel member of the PC3/BTG/TOB family of growth inhibitory genes, highly expressed in the olfactory epithelium
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Cloning of PC3B, a novel member of the PC3/BTG/TOB family of growth inhibitory genes, highly expressed in the olfactory epithelium.
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Cloning of the human interferon-related developmental regulator (IFRD1) gene coding for the PC4 protein, a member of a novel family of developmentally regulated genes.
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Computer gene mapping by EagI-based STSs
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Construction of a 5-Mb YAC contig from the putative 10q25 tumor-suppressor region for glioblastomas
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Construction of a YAC contig covering human chromosome 6p22
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DISTRIBUTION OF MODERATELY REPETITIVE SEQUENCES PTR5 AND LF1 IN XQ24-Q28 HUMAN DNA AND THEIR USE IN ASSEMBLING YAC CONTIGS
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Detailed physical analysis of a 1.5-megabase YAC contig containing the MXI1 and ADRA2A genes
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EVX2, A HUMAN HOMEOBOX GENE HOMOLOGOUS TO THE EVEN-SKIPPED SEGMENTATION GENE, IS LOCALIZED AT THE 5' END OF HOX4 LOCUS ON CHROMOSOME-2
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Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E
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Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region
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Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region
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Exon-intron organization of the human dystrophin gene
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Expression analysis of twenty-one transcripts physically anchored within the chromosomal region 10q24
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FOXL2 inactivation by a translocation 171 kb away: Analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences
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FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences.
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Folate-sensitive fragile site FRA10A is due to and expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein
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G6PD haplotypes spanning Xq28 from F8C to Red/Green Colour vision
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GENETIC-MAPPING OF A GENE ENCODING AN ATYPICAL PROTEIN-KINASE-C, PROTEIN-KINASE-C-LAMBDA, TO THE PROXIMAL REGION OF MOUSE CHROMOSOME-3
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GENOMIC ORGANIZATION OF THE HUMAN DYSTROPHIN GENE ACROSS THE MAJOR DELETION HOT-SPOT AND THE 3'-REGION
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GENOMIC ORGANIZATION OF THE HUMAN VP16 ACCESSORY PROTEIN, A HOUSEKEEPING GENE (HCFC1) MAPPING TO XQ28
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Gene expression profiles in apoptotic neurons
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Gene expression profiles of apoptotic neurons
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Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22.
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Genomic organization of the human VP16 accessory protein (HCF), a housekeeping gene mapping to Xq28.
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Genomic profiling of cortical neurons following exposure to beta-amyloid
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Genomic profiling of cortical neurons following exposure to beta-amyloid
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Guinea pig p53 mRNA: identification of new elements in coding and untranslated regions and their functional and evolutionary implications
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HUMAN PROTEIN-KINASE-C LOTA GENE (PRKCI) IS CLOSELY LINKED TO THE BTK GENE IN XQ21.3
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Human CD40L gene, gp39, maps to 2 megabases telomeric to HPRT.
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Human glucose-6-phosphate dehydrogenase gene carried on a yeast artificial chromosome encodes active enzyme in monkey cells
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Human glucose-6-phosphate dehydrogenase gene carried on a yeast artificial chromosome encodes active enzyme in monkey cells.
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Identification and Characterization of a Novel RING-Finger Gene (RNF4) Mapping at 4p16.3
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Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes
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Identification and chromosomal mapping of a third mouse runt-like locus
Articolo
Identification and purification of overlapping cosmid clones of the region Xq24-qter of human X chromosome using HPLC
Articolo
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene,
Articolo
Instability of interstitial telomeric sequences in the human genome
Articolo
Investigating the mechanism of chromosomal deletion: Characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene
Articolo
Is this the real time for genomics?
Articolo
Is this the real time for genomics?
Articolo
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome
Articolo
Isolation of a pancreas specfic gene located on human chromosome 14q31:expression analysis in human pancreatic ductal carcinomas
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Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26
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KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs
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KIF3C, a novel member of the kinesin superfamily: Sequence, expression, and mapping to human chromosome 2 at 2p23
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Laser microdissection of the fragile X region:identification of cosmid clones and of conserved sequences in this region
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Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts
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Molecular cloning and chromosomal localization of the mouse Gpr37 gene encoding an orphan G-protein-coupled peptide receptor expressed in brain and testis
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Monomorphism of human cytochrome c.
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Nucleotide distance influences co-methylation between nearby CpG sites
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Origin, duplication and reshuffling of plasmid genes: Insights from Burkholderia vietnamiensis G4 genome
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PARTIAL DIGESTION WITH RESTRICTION ENZYMES OF UV-IRRADIATED HUMAN GENOMIC DNA A METHOD FOR IDENTIFYING RESTRICTION SITE POLYMORPHISMS
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Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28
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Physical and transcript map of the hereditary prostate cancer region at Xq27
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Polyphenol oxidase genes as integral part of the evolutionary history of domesticated tetraploid wheat
Articolo
Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome
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Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp
Articolo
Somatic instability of the expanded GAA triplet-repeat sequence in Friedreich ataxia progresses throughout life.
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Surf-5: a gene in the tightly clustered mouse Surfeit Locus is highly conserved and transcribed divergently from the rpL7a (Surf3) gene.
Articolo
THE EXON-INTRON ORGANIZATION OF THE HUMAN X-LINKED GENE (FLN1) ENCODING ACTIN-BINDING PROTEIN-280
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The ZNF75 zinc finger gene subfamily: Isolation and mapping of the four members in humans and great apes
Articolo
The chromosome localization and the HCF repeats of the human host cell factor gene (HCFC1) are conserved in the mouse homologue
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The complete sequence of the Host Cell Factor 1 (HCFC1) gene and its promoter: A role for YY1 transcription factor in the regulation of its expression
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The gene for the muscle-specific enolase is on the short arm of human chromosome 17.
Articolo
The human L35a ribosomal protein (rpL35a) gene is located at chromosome band 3q29-qter.
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The iduronate sulfatase gene: isolation of a 1.2 Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome.
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The nucleotide sequence of a CpG island demonstrates the presence of the first exon of the gene encoding the human lysosomal membrane protein h-lamp2, and assigns the gene to Xq24
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Transcription map of Xq27: Candidates for several X-linked diseases
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Transcriptome analysis of human primary endothelial cells (HUVEC) from umbilical cords of gestational diabetic mothers reveals candidate sites for an epigenetic modulation of specific gene expression
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X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes
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YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28
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YAC contig organization and CpG island analysis in Xq28
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YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter
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Yeast artificial chromosome-based genome mapping: Some lessons from Xq24-q28
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Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28
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ZNF75 - ISOLATION OF A CDNA CLONE OF THE KRAB ZINC-FINGER GENE SUBFAMILY MAPPED IN YACS 1 MB TELOMERIC OF HPRT
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