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Expression and Clinical Significance of Genes Frequently Mutated in Small CellLung Cancers Defined by Whole Exome/RNA Sequencing
Carcinogenesis
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原著論文2
Masahio Gotoh,et al.
Comprehensive exploration of novel chimeric transcripts in clear cell renal cell carcinomas using whole transcriptome analysis
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原著論文3
Tsuneo Ikenoue,et al.
Attenuated Familial Adenomatous Polyposis with Desmoids by an APC Mutation
Human Genome Variation
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原著論文4
Eriko Nakano, et al.
Targeted Next-Generation Sequencing Effectively Analyzed the Cystic Fibrosis Transmembrane Conductance Regulator Gene in Pancreatitis.
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原著論文5
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Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.
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原著論文6
Yasuhiro Yamazaki,et al.
Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: Impaired production of IL-17A and IL-22, and the Presence of anti-IL-17F autoantibody
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原著論文7
Toshinao Kawai, et al.
Interstitial lung disease with multiple microgranulomas in chronic granulomatous disease.
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原著論文8
Masaaki Mori,et al.
Palivizumab use in Japanese infants and children with immunocompromised conditions
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原著論文9
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原著論文10
Michael Beck,et al
The natural history of MPS I: global perspectives from the MPS I Registry.
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原著論文11
Kaustuv Bhattachaya
Orphanet Overcoming the barriers to diagnosis of Morquio A syndrome.
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原著論文12
Haplotype defined by the MLH1-93G/A polymorphism is associated with MLH1
Miyakura Y, Tahara M, Lefor AT, Yasuda Y, Sugano K.
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