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「"Kagami M "[Author]」の検索結果

193件中 81件~100件表示    検索結果をPubMedで見る PubMedで見る

Psychological adjustment and psychosocial stress among Japanese couples with a history of recurrent pregnancy loss.

Community structure of planktonic fungi and the impact of parasitic chytrids on phytoplankton in Lake Inba, Japan.

Radiological evaluation of dysmorphic thorax of paternal uniparental disomy 14.

Changes in the pharmacokinetics of digoxin in polyuria in streptozotocin-induced diabetic mice and lithium carbonate-treated mice.

Increases in the expression levels of aquaporin-2 and aquaporin-3 in the renal collecting tubules alleviate dehydration associated with polyuria in diabetes mellitus.

Byakkokaninjinto prevents body water loss by increasing the expression of kidney aquaporin-2 and skin aquaporin-3 in KKAy mice.

Prenatal findings of paternal uniparental disomy 14: Delineation of further patient.

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.

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