「大脳型副腎白質ジストロフィーの病態機序の解明」の関連論文
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心臓組織マクロファージの機械的ストレス応答機構の解析
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無巨核球性血小板減少症を伴う橈尺骨癒合症のモデルマウス作製と病態解析
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ZMYM4 のマウス胎児・胎盤発生における役割
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Understanding the functional role of selected bioactive compounds and altered genes on gastric carcinogenesis of the differentiated subtype using A4gnt-deficient mice model
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遺伝性痙性対麻痺28型のモデルとしてのDdhd1ノックアウトマウスの解析
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Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs
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Oligodendrogenesis and myelin formation in the forebrain require platelet-derived growth factor receptor-alpha
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Bioinformatics analysis of autophagy-lysosomal degradation in cardiac aging
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四肢の骨格形態・形成に関与するZMAT2遺伝子の機能解析
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Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice
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母体免疫活性化モデルマウスにおける胎仔の自律神経障害と心拍変動に関する研究
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筋組織におけるジストロフィンの新たな生物学的意義に関する研究
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Physiological role of mitochondrial tRNA f5C modification by Alkbh1
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Importance of methodology in the evaluation of renal mononuclear phagocytes and analysis of a model of experimental nephritis with Shpl conditional knockout mice.
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Generation of knockout rabbits with X-linked severe combined immunodeficiency (X-SCID) using CRISPR/Cas9
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高齢MRP4欠損マウス網膜における遺伝子発現プロファイリングと表現型の変化
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mTOR新規相互作用分子 Flightless-Iの神経系における機能解析
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眼皮膚白皮症6型:日本人症例における新規遺伝子バリアントとモデルマウスによる原因遺伝子の機能解析
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移植後拒絶反応におけるOGG1の役割
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Roles of transcription factor AP-2β in sleep regulation in mice
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Meclozine ameliorates skeletal muscle pathology and increases muscle forces in mdx mice
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Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect
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血管性認知障害におけるグリア細胞の病態生理学的役割の解明
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Role of endogenous myosin phosphatase inhibitory protein, CPI-17 in vascular smooth muscle
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X連鎖性好中球減少症(XLN)の病態に関する研究
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血中タンパク質 Mac-2bp の新規生理的機能解析
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インフルエンザ易罹患性に関わる遺伝子の解析
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Studies on physiological functions and regulatory mechanisms of a newly identified murine testis-specific long noncoding RNA, Start [an abstract of entire text]
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KEAP1の抑制によるNRF2経路の活性化がもたらす加齢性難聴の予防効果の検討
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A mouse model of Timothy syndrome exhibits altered social competitive dominance and inhibitory neuron development
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インスリン受容体基質2の欠損が脳内のアミロイドβ動態に及ぼす影響の解析
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The role of CaMKII-Tiam1 complex on learning and memory
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Pathogenesis of EVI-1 Overexpressing Acute Myeloid Leukemia
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PDGF receptor signal mediates the contribution of Nestin-positive cell lineage to subcutaneous fat development.
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日本人侵襲性歯周炎の疾患関連遺伝子 Lipase-Aのヒト歯根膜細胞における機能解析
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Direct reprogramming of adult adipose-derived regenerative cells toward cardiomyocytes using six transcriptional factors
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Identification of the new gene causing cerebellar ataxia and investigation of pathogenic mechanism
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Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility
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Generation and characterization of a novel mouse model that allows spatiotemporal quantification of pancreatic β-cell proliferation
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疾患特異的ヒトiPS細胞を用いた新規ADPKD病態モデルの作製
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DNA修復機構欠損マウスにおけるUVB照射により形成された皮膚腫瘍の網羅的遺伝子変異解析
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PRKN遺伝子変異患者における分子遺伝学的多様性および神経病理学的特徴
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Transcriptome-wide Analysis of Intracranial Artery in Patients with Moyamoya Disease Showing Up-regulation of Immune Response, and Down-regulation of Oxidative Phosphorylation and DNA Repair
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Characterization of Dclk1 isoforms in the developing mouse brain
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Investigation of therapeutic target of DNMT3A-mutant acute myeloid leukemia
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Cereblon依存的なユビキチン・プロテアソーム経路はサリドマイドの催眠作用に関与しているか
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内在性SIK3を介した睡眠要求および概日リズムを制御する神経細胞集団の同定
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Evaluation of recombinant vaccinia viruses for oncolytic virotherapy
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The Molecular Cell Biology of KIF4 in the Brain : Analysis of KIF4 Mutation Mouse
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Pristane/Hypoxia (PriHx) Mouse as a Novel Model of Pulmonary Hypertension Reflecting Inflammation and Fibrosis