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Cell Biology
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Incorporating Mouse Genome
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Mammalian Genome
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Mammalian Genome
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http://hub.abes.fr/springer/periodical/335/m/web
http://hub.abes.fr/springer/periodical/335/m/print
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335
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http://hub.abes.fr/springer/periodical/335/1991/volume_1
http://hub.abes.fr/springer/periodical/335/1991/volume_2
http://hub.abes.fr/springer/periodical/335/1992/volume_2
http://hub.abes.fr/springer/periodical/335/1992/volume_3
http://hub.abes.fr/springer/periodical/335/1993/volume_4
http://hub.abes.fr/springer/periodical/335/1994/volume_5
http://hub.abes.fr/springer/periodical/335/1995/volume_6
http://hub.abes.fr/springer/periodical/335/1996/volume_7
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An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
The International Mammalian Genome Society
DNA variants with telomere probe enable genetic mapping of ends of mouse chromosomes
Comparison of interspecific to intersubspecific backcrosses demonstrates species and sex differences in recombination frequency on mouse Chromosome 16
B2-like repetitive sequence from the X Chromosome of the American mink (Mustela vison)
List of cloned mouse genes with unique expression patterns during spermatogenesis
The recombinant congenic strains—a novel genetic tool applied to the study of colon tumor development in the mouse
A mouse Y Chromosome pseudogene is related to human ubiquitin activating enzyme E1
Localization of the pig gene ESD to Chromosome 13 by in situ hybridization
Mouse X Chromosome
Localization of the human Chromosome 5q genes Gabra-1, Gabrg-2, Il-4, Il-5, and Irf-1 on mouse Chromosome 11
The gene coding for the immunoglobulin heavy chain binding protein BiP (Hsce-70) maps to mouse Chromosome 2
Strain distribution pattern of 25 simple sequence length polymorohisms in the AXB and BXA recombinant inbred strains
A human Chromosome 7-specific genomic DNA library in yeast artificial chromosomes
Localization of murine HLH gene NSCL to Chromosome 1 by use of recombinant inbred strains
Cross-species conservation of a polymorphic dinucleotide repeat in the dystrophin gene
Estimation of microsatellite mutation rates in recombinant inbred strains of mouse
The same genomic region is disrupted in two transgene-induced limb deformity alleles
Assignment of 22 loci in the rat by somatic hybrid and linkage analysis
Detailed physical and genetic mapping in the region of plasminogen, D17Rp17e, and quaking
Incorporation of copy-number control elements into yeast artificial chromosomes by targeted homologous recombination
GART, SON, IFNAR, and CRF2-4 genes cluster on human Chromosome 21 and mouse Chromosome 16
Striking conservation of the brain-specific region of the dystrophin gene
Genetic linkage of the erythroid-specific δ-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X Chromosome
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse
High-resolution genetic map and YAC contig around the mouse neurological locus reeler
Mammalian genome, volume 5, number 7, 1994, pp 416-423
cDNA sequence of Aldgh, the mouse homolog of the X-linked adrenoleukodystrophy gene
Molecular analysis of four lactate dehydrogenase-A mutants in the mouse
Genetic mapping of DNA topoisomerase I-related sequences to mouse Chromosomes 2 and 14
Pulsed field gel electrophoretic analysis of the rat major histocompatibility complex class III region shows extensive inter-species conservation
YAC clones targeting gene-rich regions of human Chromosome 3
Mapping vector-adjacent DNA from a 7q human telomeric YAC using RARE
A small-insert bovine genomic library highly enriched for microsatellite repeat sequences
The mh gene causing double-muscling in cattle maps to bovine Chromosome 2
Mapping of body weight loci on mouse Chromosome X
Assignment of the gene coding for HPRT enzyme to Syrian hamster X Chromosome by microcell fusion
The rat athymic nude (rnu) locus is closely linked to the inducible nitric oxide synthase gene (Nos2)
Mouse cyclin F maps to a conserved linkage group on mouse Chromosome 17
Genetic mapping near the myd locus on mouse Chromosome 8
The gonadotrophin-releasing hormone receptor maps to sheep Chromosome 6 outside of the region of the FecB locus
A novel partial t haplotype with a Brachyury-independent effect on tail phenotype
Localization of the mouse mammary tumor provirus, Mtv44, on Chromosome 11
Gtl2lacZ, an insertional mutation on mouse Chromosome 12 with parental origin-dependent phenotype
Location of the DBP transcription factor gene in human and mouse
Mapping the ovine genes encoding IL3, IIA, IL5, and CSF2 to sheep Chromosome 5ql3-ql5 by FISH
Genetic mapping of the Brca1 gene on mouse Chromosome 11
Isolation of the canine α-L-fucosidase cDNA and definition of the fucosidosis mutation in English Springer Spaniels
Assignment ofc-KIT gene to swine Chromosome 8pl2-p21 by fluorescence in situ hybridization
The gene encoding tripeptidyl peptidase II maps to Chromosome 1 in the mouse
Microsatellites at a common site in the second ORF of L1 elements in mammalian genomes
Potential CpG-rich islands clustering around single-minded gene in Down syndrome chromosomal region
Smcx lies distal to DXHX674 and DXHX679 on the mouse X Chromosome
Syntenic assignment of human serotonin receptor subtype 2 (HTR2), esterase D (ESD), and fms-related tyrosine kinase (FLT) homologs to bovine Chromosome 12
The ets-related mouse Pea3 gene maps to distal Chromosome 11
Effect of the mouse scid mutation on meiotic recombination
A precise localization of a mouse gene encoding increased phosphoglycerate mutase activity (Pgamlel) on Chromosome 19
Comparative mapping on the mouse X Chromosome defines a myotubular myopathy equivalent region
PCR-analyzed microsatellites for the inbred mouse strain 129/Sv, the strain most commonly used in gene knockout technology
Structure and localization of the thrombin receptor gene on mouse Chromosome 13
Genetic mapping of farnesyltransferase alpha(Fnta) to mouse Chromosome 8
Physical mapping of connexin 32 (GJB1) and 43 (GJA1) genes to bovine Chromosomes Xq22 and 9q15/16 by fluorescence in situ hybridization
Isolation and chromosomal location of mE4, a novel murine gene of the immunoglobulin superfamily
The mouse homolog of the Drosophila discs large tumor suppressor gene maps to Chromosome 16
Microsatellite instability in IVS3 of murine c-fes gene: Tumor-associated rearrangement and mammalian divergence
Close linkage of three neuronal genes on distal mouse Chromosome 15
Mouse chromosome 8
Mouse chromosome 14
Characterization of N-myc amplification in a human neuroblastoma cell line by clones isolated following the phenol emulsion reassociation technique and by hexagonal field gel electrophoresis
Localization of growth arrest-specific genes on mouse Chromosomes 1, 7, 8, 11, 13, and 16
Localization of genes and anonymous DNA probes on the short arm of Chromosome 7
Mouse Chromosome 8
Linkage among esterase-6 (Es-6), neural cell adhesion molecule (NCAM), and apolipoprotein C-III (apoc-3) genes on rat Chromosome 8
Methylation status of ribosomal RNA gene clusters in the flow-sorted human acrocentric chromosomes
The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito
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