「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」の関連論文
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Expansion of human iPSC-derived ureteric bud organoids with repeated branching potential
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慢性腎臓病の分子病態の解明に向けた腎エリスロポエチン産生細胞由来細胞株の樹立と解析
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全胞状奇胎由来幹細胞株の樹立と分子細胞学的検討
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Newly established patient-derived organoid model of intracranial meningioma
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The CD44/COL17A1 pathway promotes the formation of multilayered, transformed epithelia
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超低頻度な体細胞点突然変異定量法の新規開発とがん化学療法による正常血液細胞への変異蓄積の証明
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男児外性器皮膚線維芽細胞におけるアンドロゲン標的候補遺伝子の探索
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アデノ随伴ウイルスベクターを用いた成熟プルキンエ細胞におけるRAR関連オーファン受容体αのノックダウンは脊髄小脳失調症の小脳異常表現型を再現する および アデノ随伴ウイルスベクターとCRISPR-dSaCas9システムを用いた脊髄小脳失調症1型ノックインマウスの新規治療戦略
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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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A novel patient-derived pancreatic acinar cell carcinoma cell line shows high sensitivity to bortezomib
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A Patient-derived iPSC Model Revealed the Involvement of Oxidative Stress in Molecular Pathogenesis of Facio-scapulo-humeral Muscular Dystrophy(FSHD)
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Microenvironmental Impact on Tumour Cell Phenotype and Genotype in Adult and Paediatric Tumours
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PLD1 promotes tumor invasion by regulation of MMP-13 expression via NF-κB signaling in bladder cancer
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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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Novel transgenic enteroid to establish platform for investigating mechanisms of intestinal epithelial cell function [an abstract of entire text]
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Establishment and characterization of cell lines from human endometrial epithelial and mesenchymal cells from patients with endometriosis
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Differentiation of human induced pluripotent stem cells into hypothalamic vasopressin neurons with minimal exogenous signals and partial conversion to the naive state
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Direct reprogramming of adult adipose-derived regenerative cells toward cardiomyocytes using six transcriptional factors
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Transplantation of human iPSC-derived muscle stem cells in the diaphragm of Duchenne muscular dystrophy model mice
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Study on the Dome-like Structures with Altered Microenvironment Induced by Basal Extrusion of RasV12-transformed Cells [an abstract of entire text]
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腎同所性移植モデルを応用した腎がん悪性形質制御機構の解析
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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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マウスラクナ梗塞に対するヒト骨髄由来多能性幹細胞(Muse細胞)経静脈投与による神経修復
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X連鎖性鉄芽球性貧血におけるフェロトーシス関連遺伝子の転写制御
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マルチリージョンシークエンスを用いた腫瘍内不均一性と腫瘍進化の過程の解析
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癌患者ゲノミクスデータ解析を基盤とした乳癌幹細胞性維持機構の解明
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口腔白板症におけるp62発現と臨床病理的因子の解析
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The regenerative effect of portal vein injection of liver organoids by retrorsine/partial hepatectomy in rats
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Drug library screening identifies histone deacetylase inhibition as a novel therapeutic strategy for choriocarcinoma
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RNAスプライシングに関連する遺伝子の変異を有する骨髄異形成症候群に関する検討
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Studies on the epithelial injury-related molecules inducing the urinary system disorders in animals [an abstract of entire text]
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乳がん患者由来オルガノイドの腫瘍内不均一性の検討と,その背後にある分子生物学的特徴の探索
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Analysis of neural development using human iPS cells carrying genetic mutations related to neuropsychiatric disorders
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Isolation and characterisation of peripheral blood-derived feline mesenchymal stem cells
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慢性心筋梗塞に対する自家iPS細胞を用いた心筋再生療法の開発
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Development of a method for large scale production of pancreatic islet progenitors derived from human iPS cells
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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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新規カニクイザル栄養膜幹細胞株の樹立とその分化能解析
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淡明細胞型腎癌における線維芽細胞増殖因子受容体タイプ4の発現と機能の解析
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Primate-specific POTE-actin gene could play a role in human folliculogenesis by controlling the proliferation of granulosa cells
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鶏卵漿尿膜培養が、肺腺癌での血管新生におけるTIPARP (2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible poly (ADP-ribose) polymerase) の役割を解明した。
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Identification and Functional Analysis of Genes Critical to Tumorigenesis
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膵癌間質における酸化ストレス応答機構の解析
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大腸癌におけるERK阻害薬感受性とMAPK経路遺伝子変異の関連性
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がん幹細胞性の維持に寄与する因子の解析
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慢性腎臓病モデルマウスを用いた腎間質線維芽細胞の役割に関する研究
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Development of an in vitro human liver model by using iPS cells
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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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Improved methods for the differentiation of hypothalamic vasopressin neurons using mouse induced pluripotent stem cells
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Identification of the new gene causing cerebellar ataxia and investigation of pathogenic mechanism