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「"Kagami M "[Author]」の検索結果

186件中 81件~100件表示    検索結果をPubMedで見る PubMedで見る

Fabrication of large-core, high-Δ optical waveguides in polymers.

Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype.

The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers.

Variable-ratio tap for plastic optical fiber.

Development of a Real-Time PCR assay for quantitative assessment of uncultured freshwater zoosporic fungi.

Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.

Optical attenuator for plastic optical fiber with small dependencies on mode and wavelength.

The UDP-glucose receptor P2RY14 triggers innate mucosal immunity in the female reproductive tract by inducing IL-8.

Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2.

Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR.

Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.

Placentomegaly in paternal uniparental disomy for human chromosome 14.

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.

Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.

Pharmacological characterization and gene expression profiling of an L5/L6 spinal nerve ligation model for neuropathic pain in mice.

Adaptation of the fungal parasite Zygorhizidium planktonicum during 200 generations of growth on homogeneous and heterogeneous populations of its host, the diatom Asterionella formosa.

Simultaneous fabrication of optical channel waveguides and out-of-plane branching mirrors from a polymeric slab structure.

Placental hypoplasia in maternal uniparental disomy for chromosome 7.

Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta.

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

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