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「"Kagami M "[Author]」の検索結果

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IGF2 Mutations: Report of Five Cases, Review of the Literature, and Comparison with H19/IGF2:IG-DMR Epimutations.

The potential of zooplankton in constraining chytrid epidemics in phytoplankton hosts.

Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool.

DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations.

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.

Photonic technologies for autonomous cars: feature introduction.

Fungi in aquatic ecosystems.

Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.

Fungi in the Marine Environment: Open Questions and Unsolved Problems.

Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.

Taming chlorophylls by early eukaryotes underpinned algal interactions and the diversification of the eukaryotes on the oxygenated Earth.

Association of four imprinting disorders and ART.

Severe in utero under-virilization in a 46,XY patient with Silver-Russell syndrome with 11p15 loss of methylation.

(Epi)genetic defects of are rare in Asian patients with central precocious puberty.

Temple syndrome diagnosed in an adult patient with clinical autism spectrum disorder.

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.

Introducing ribosomal tandem repeat barcoding for fungi.

Anaphylaxis to xylitol diagnosed by skin prick test and basophil activation test.

Influence of parasitic chytrids on the quantity and quality of algal dissolved organic matter (AOM).

Uniparental disomy as a cause of pediatric endocrine disorders.

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