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《遗传学杂志》2005年第05期

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mutation rates, spectra and hotspots in mismatch repair-deficient caenorhabditis elegans
mutations of a redundant -tubulin gene affect caenorhabditis elegans early embryonic cleavage via mei-1/katanin-dependent and -independent pathways
high-resolution mapping of the drosophila fourth chromosome using site-directed terminal deficiencies
drosophila signal peptide peptidase is an essential protease for larval development
slit-roundabout signaling neutralizes netrin-frazzled-mediated attractant cue to specify the lateral positioning of longitudinal axon pathways
synthetic lethality of retinoblastoma mutant cells in the drosophila eye by mutation of a novel peptidyl prolyl isomerase gene
a genetic screen in drosophila for identifying novel components of the hedgehog signaling pathway
quantitative trait loci that control dengue-2 virus dissemination in the mosquito aedes aegypti
adaptive molecular evolution for 13,000 phage generations
characterization of active r2 retrotransposition in the rdna locus of drosophila simulans
origin and evolution of a chimeric fusion gene in drosophila subobscura, d. madeirensis and d. guanche
the ku protein complex is involved in length regulation of drosophila telomeres
a second-generation genetic linkage map of tilapia ( oreochromis spp.)
identification of zebrafish insertional mutants with defects in visual system development and function
the zebrafish pob gene encodes a novel protein required for survival of red cone photoreceptor cells
evolution of salamander life cycles
eae19, a new locus on rat chromosome 15 regulating experimental autoimmune encephalomyelitis
linkage disequilibrium grouping of single nucleotide polymorphisms (snps) reflecting haplotype phylogeny for efficient selection of tag snps
mutation rate variation at human dinucleotide microsatellites
lineage-specific loss of function of bitter taste receptor genes in humans and nonhuman primates
maternal transmission ratio distortion at the mouse om locus results from meiotic drive at the second meiotic division
mutations in the saccharomyces cerevisiae lsm1 gene that affect mrna decapping and 3‘ end protection
elephants and human color-blind deuteranopes have identical sets of visual pigments
a gene(s) for all- trans -retinoic acid-induced forelimb defects mapped and confirmed to murine chromosome 1
a role for dna mismatch repair protein msh2 in error-prone double-strand-break repair in mammalian chromosomes
using molecular sizes of simple sequence repeats vs. discrete binned data in assessing probability of ancestry
transmission ratio distortion in intraspecific hybrids of mimulus guttatus
natural allelic variation in the temperature-compensation mechanisms of the arabidopsis thaliana circadian clock
improving quantitative trait loci mapping resolution in experimental crosses by the use of genotypically selected samples
bayesian estimation of recent migration rates after a spatial expansion
stochastic models for horizontal gene transfer
the origin of subfunctions and modular gene regulation
quantitative trait locus study design from an information perspective
bayesian shrinkage estimation of quantitative trait loci parameters
-synuclein targets the plasma membrane via the secretory pathway and induces toxicity in yeast
intron size and exon evolution in drosophila
revisiting purine-histidine cross-pathway regulation in saccharomyces cerevisiae
evolution of human immunodeficiency virus under selection and weak recombination
isolation and characterization of novel xrs2 mutations in saccharomyces cerevisiae
evidence that spt10 and spt21 of saccharomyces cerevisiae play distinct roles in vivo and functionally interact with mcb-binding factor, scb-binding factor and snf
differential activation of m26 -containing meiotic recombination hot spots in schizosaccharomyces pombe
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