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Mechanism of Ret dysfunction by Hirschsprung mutations affecting its extracellular domain
Toshihide Iwashita
, Hideki Murakarni
,
Naoya Asai
,
Masahide Takahashi
研究成果
:
ジャーナルへの寄稿
›
学術論文
›
査読
96
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被引用数 (Scopus)
概要
フィンガープリント
フィンガープリント
「Mechanism of Ret dysfunction by Hirschsprung mutations affecting its extracellular domain」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。
並べ替え順
重み付け
アルファベット順
Keyphrases
Hirschsprung Disease
100%
Extracellular Domain
100%
Missense mutation
50%
Plasma Membrane
33%
Surface Expression
33%
Disease Phenotype
33%
Disease-causing mutations
33%
Frameshift mutation
16%
Multiple Endocrine Neoplasia Type 2 (MEN2)
16%
Kinase Activity
16%
Gastrointestinal Tract
16%
Congenital Disorders
16%
Nonsense mutation
16%
Sporadic Cases
16%
RET Proto-oncogene
16%
Familial Cases
16%
Transforming Activity
16%
Tyrosine Kinase Domain
16%
Ganglion Cells
16%
Short Segment
16%
Neuroscience
Missense Mutation
100%
Cell Membrane
66%
Tyrosine Kinase
33%
Receptor Tyrosine Kinase
33%
Epileptic Absence
33%
Kinase
33%
Ganglion Cell
33%
Nonsense Mutation
33%
Frameshift Mutation
33%
Proto Oncogene
33%
Endocrine Neoplasia
33%
Congenital Disorder
33%
Protein Ret
33%
Biochemistry, Genetics and Molecular Biology
Missense Mutation
100%
Cell Membrane
66%
Surface Property
66%
Phosphotransferase
33%
Kinase
33%
Receptor Tyrosine Kinase
33%
Tyrosine Kinase
33%
Nonsense Mutation
33%
Frameshift Mutation
33%
Proto Oncogene
33%
Gastrointestinal Tract
33%
Medicine and Dentistry
Hirschsprung's Disease
100%
Missense Mutation
50%
Cell Surface
33%
Cell Membrane
33%
Epileptic Absence
16%
Phosphotransferase
16%
Frameshift Mutation
16%
Protein Tyrosine Kinase
16%
Gastrointestinal Tract
16%
Nonsense Mutation
16%
Proto Oncogene
16%
Congenital Disorder
16%
Ganglion
16%
Protein Ret
16%
Multiple Endocrine Neoplasia
16%