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「火球」の隕石を発見「すごい音がして怖かった」隕石の起源は (NHK)

先月、広い範囲で目撃された「火球」が燃え尽きずに、隕石(いんせき)として落ちているのを発見した千葉県の女性が取材に応じ、当時の状況について「すごい大きな音がして...

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  3. 東京 武蔵村山市の病原体扱う施設 移転先...
  4. 研究環境基盤部会 共同利用・共同研究拠点...

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「"Straniero L "[Author]」の検索結果

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SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy.

Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders.

Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.

First Replication of the Involvement of in Intellectual Disability Syndrome With Seizures and Dysmorphic Features.

A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest.

The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1.

The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p.

DNAJC12 and dopa-responsive non-progressive Parkinsonism.

2,6-Difluorobenzamide inhibitors of the bacterial cell division protein FtsZ: design, synthesis and Structure Activity Relationship study.

Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis.

Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites.

Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay.

Functional Characterization of Two Novel Splicing Mutations in the OCA2 Gene Associated with Oculocutaneous Albinism Type II.

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