「Oct motif variants in Beckwith-Wiedemann syndrome patients disrupt maintenance of the hypomethylated state of the H19/IGF2 imprinting control region」の関連論文
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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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microRNA-875-5pは歯の発生において上皮―間葉相互作用における間葉細胞の凝集に重要な役割を果たす
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20番染色体母性片親性ダイソミーの臨床像および内分泌的特徴の解明
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Studies on the relationship of mitochondrial RNA processing to cell division control underlying early development of lateral roots in Arabidopsis
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Studies on the pathophysiology and current treatment status of ion channel-related muscle diseases
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Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients
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Circadian rhythm affects the magnitude of contact hypersensitivity response in 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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Density and Maturity of Peritumoral Tertiary Lymphoid Structures in Oesophageal Squamous Cell Carcinoma Predicts Patient Survival and Response to Immune Checkpoint Inhibitors
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浸潤性膵管癌におけるCD109の造腫瘍性に関する研究
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卵巣癌における糖転移酵素C2GnT1発現と機能の解析
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Tracing location by applying Emerald luciferase in an early phase of murine endometriotic lesion formation
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Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
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Investigation of the subcellular localization-dependent anti- or pro-tumor functions of maspin in human lung adenocarcinoma cell line
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ヒストンH3K36me2およびH3K36me3はマウス卵子におけるDNMT3A依存的DNAメチル化に必須なクロマチンプラットフォームを形成する
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忘れられない一枚の心電図 : カルモジュリン病
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CRISPR/Cas9システムを用いた逆遺伝学的アプローチによる精子形成メカニズムの解明
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悪性リンパ腫における血中循環細胞外遊離DNAを用いたゲノム解析に関する研究
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Ependymoma-like tumors with mesenchymal differentiation harboring C11orf95-NCOA1/2 or -RELA fusion: a hitherto unclassified tumor related to ependymoma
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IκBα is required for full transcriptional induction of some NFκB-regulated genes in response to TNF in MCF-7 cells
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新規「胎生システム」を獲得した可能性が高い昆虫の極めて特殊な発生に関する研究
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Proteomic analysis of exosome-enriched fractions derived from cerebrospinal fluid of amyotrophic lateral sclerosis patients
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Clinical features of isolated proximal‐type immunoglobulin G4‐related sclerosing cholangitis
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Osteocytes as main responders to Low Intensity Pulsed Ultrasound for the treatment of fracture healing [an abstract of entire text]
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A single-institution study on predictors of short-term progression from mild cognitive impairment in Parkinson's disease to Parkinson's disease with dementia
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大腸癌の抗EGFR抗体薬感受性に関与するDNAメチル化異常と遺伝子発現の関連性
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生体肝移植グラフト質的評価マーカーとしてのLRRN2発現上昇
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Studies on the formation and elongation of the delimiting membrane in Bipolaris maydis
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卵巣癌におけるクロマチンリモデリング 因子CHD4の機能に関する研究
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miR-1260bは小胞体ストレス制御関連のATF6βを介して歯周炎の骨吸収を抑制する
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Structural abnormalities in nucleus accumbens in patients with panic disorder
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Identification of Biomarkers for Non–small-cell Lung Cancer Patients Treated With an Immune Checkpoint Inhibitor
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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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小児脳腫瘍特異的細胞傷害性T細胞にキメラ抗原受容体を応用した新規治療戦略の確立
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Point mutation in the stop codon MAV_RS14660 increases the growth rate of Mycobacterium avium subspecies hominissuis
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軟骨細胞におけるSox9遺伝子の発現制御機構の解明
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マウス胃オルガノイドを用いたWnt阻害因子Dickkopf 3のエピジェネティックな変化による転写因子T-box3を介した加齢に伴う胃発癌機序の解明
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ゲノム構造変化による感音難聴の発症メカニズムの解明に関する研究
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The role of the RIP family of Rho effectors in the regulation of cell division orientation in Arabidopsis thaliana leaves
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IMAGE-I症候群における新規POLE遺伝子変異の同定とその病態解析
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哺乳動物細胞株による高活性シトクロムP450発現系の構築と遺伝子多型バリアント酵素機能解析への応用
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Gene expression profiling using targeted RNA-sequencing to elucidate the progression from histologically normal lung tissues to non-invasive lesions in invasive lung adenocarcinoma
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Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
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Mitochondrial pyruvate carrier 1 expression controls cancer epithelial-mesenchymal transition and radioresistance
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In vitro胆汁鬱滞肝毒性評価系の構築
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ロングリードシーケンサーMinIONを用いたゲノム編集マウス遺伝型解析プラットフォームの開発
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呼吸機能と関連があるヒトRAGE一塩基多型ノックインマウスの作製とその機能解析
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Molecular mechanism underlying inter-organelle translocation of piRNA precursor
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複数の遺伝子変異が関与する遺伝性難聴症例の解析
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メチオニンアデノシルトランスフェラーゼ2aを介したB細胞活性化抑制機構と全身性エリテマトーデス治療への応用