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市川海老蔵さん 團十郎襲名を延期 緊急事態宣言受け (NHK)

歌舞伎俳優の市川海老蔵さんは歌舞伎界の大名跡、市川團十郎をことし5月に襲名する予定でしたが「緊急事態宣言」を受けて襲名を延期することになりました。 市川團十郎は...

  1. [企業] ドイツのEvotec社がオース...
  2. 新型コロナ治療に期待「アヒガン」200万...
  3. [企業] Menlo社のNK1受容体遮断...
  4. アルムがCOVID-19患者のCT画像の...

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「"Millat G "[Author]」の検索結果

68件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes.

Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy.

Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy.

A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation.

Clinical management and viral genomic diversity analysis of a child's influenza A(H1N1)pdm09 infection in the context of a severe combined immunodeficiency.

Atrial Structural Remodeling Gene Variants in Patients with Atrial Fibrillation.

TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome.

First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy.

Cardiac voltage-gated sodium channel mutations associated with left atrial dysfunction and stroke in children.

Single, short in-del, and copy number variations detection in monogenic dyslipidemia using an NGS strategy.

A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband.

Early repolarization syndrome caused by de novo duplication of KCND3 detected by next-generation sequencing.

Nuclear envelopathies: a complex LINC between nuclear envelope and pathology.

Characterization of oseltamivir-resistant influenza virus populations in immunosuppressed patients using digital-droplet PCR: Comparison with qPCR and next generation sequencing analysis.

Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with Dilated Cardiomyopathy.

TRPM4 non-selective cation channel variants in long QT syndrome.

Remotely sensing the German Wadden Sea-a new approach to address national and international environmental legislation.

Homozygous PKP2 deletion associated with neonatal Left Ventricule Non Compaction.

A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death.

HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy.

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