Matsui Hiroko相关文献与解析，生知库 | 链接生命科学的每一步

Arthur, Timothy D; Nguyen, Jennifer P; D'Antonio-Chronowska, Agnieszka; Matsui, Hiroko; Silva, Nayara S; Joshua, Isaac N; Luchessi, André D; Greenwald, William W Young; D'Antonio, Matteo; Pera, Martin F; Frazer, Kelly A

信号转导

细胞生物学

发育与干细胞

干细胞

发表日期：2024

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Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease

精细绘制遗传变异与心脏性状和疾病相关的时空机制图谱

期刊:Nature Communications

影响因子:15.7

doi:10.1038/s41467-023-36638-2

D'Antonio, Matteo; Nguyen, Jennifer P; Arthur, Timothy D; Matsui, Hiroko; D'Antonio-Chronowska, Agnieszka; Frazer, Kelly A

发表日期：2023

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Analysis of regulatory network modules in hundreds of human stem cell lines reveals complex epigenetic and genetic factors contribute to pluripotency state differences between subpopulations

对数百种人类干细胞系调控网络模块的分析揭示了复杂的表观遗传和遗传因素导致亚群间多能性状态的差异。

期刊:

影响因子:

doi:10.1101/2023.05.20.541447

Arthur, Timothy D; Nguyen, Jennifer P; D'Antonio-Chronowska, Agnieszka; Matsui, Hiroko; Silva, Nayara S; Joshua, Isaac N; Luchessi, André D; Young Greenwald, William W; D'Antonio, Matteo; Pera, Martin F; Frazer, Kelly A

In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms

在心力衰竭中，RNA结合蛋白的重新激活与1523种胎儿特异性亚型的表达有关。

期刊:PLoS Computational Biology

影响因子:3.6

doi:10.1371/journal.pcbi.1009918

D'Antonio, Matteo; Nguyen, Jennifer P; Arthur, Timothy D; Matsui, Hiroko; Donovan, Margaret K R; D'Antonio-Chronowska, Agnieszka; Frazer, Kelly A

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

SARS-CoV-2 易感性和 COVID-19 疾病严重程度与影响多种组织中基因表达的遗传变异有关。

期刊:Cell Reports

影响因子:6.9

doi:10.1016/j.celrep.2021.110020

D'Antonio, Matteo; Nguyen, Jennifer P; Arthur, Timothy D; Matsui, Hiroko; D'Antonio-Chronowska, Agnieszka; Frazer, Kelly A

SARS-CoV-2

发表日期：2021

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Properties of structural variants and short tandem repeats associated with gene expression and complex traits

与基因表达和复杂性状相关的结构变异和短串联重复序列的特性

期刊:Nature Communications

影响因子:15.7

doi:10.1038/s41467-020-16482-4

Jakubosky, David; D'Antonio, Matteo; Bonder, Marc Jan; Smail, Craig; Donovan, Margaret K R; Young Greenwald, William W; Matsui, Hiroko; D'Antonio-Chronowska, Agnieszka; Stegle, Oliver; Smith, Erin N; Montgomery, Stephen B; DeBoever, Christopher; Frazer, Kelly A

发表日期：2020

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Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats

对一系列结构变异和短串联重复序列进行发现和质量分析

期刊:Nature Communications

影响因子:15.7

doi:10.1038/s41467-020-16481-5

Jakubosky, David; Smith, Erin N; D'Antonio, Matteo; Jan Bonder, Marc; Young Greenwald, William W; D'Antonio-Chronowska, Agnieszka; Matsui, Hiroko; Stegle, Oliver; Montgomery, Stephen B; DeBoever, Christopher; Frazer, Kelly A

发表日期：2020

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An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects.

从人类急性髓系白血病细胞系（HL-60-iPSC）衍生的 iPSC 系保留了白血病异常，并表现出髓系分化缺陷

期刊:Stem Cell Research

影响因子:0.7

doi:10.1016/j.scr.2020.102096

Yamasaki Amanda E, Warshaw Jane N, Kyalwazi Beverly L, Matsui Hiroko, Jepsen Kristen, Panopoulos Athanasia D

Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease

对MHC区域的系统性遗传分析揭示了HLA类型与疾病关联的机制基础

期刊:Elife

影响因子:6.4

doi:10.7554/eLife.48476

D'Antonio, Matteo; Reyna, Joaquin; Jakubosky, David; Donovan, Margaret Kr; Bonder, Marc-Jan; Matsui, Hiroko; Stegle, Oliver; Nariai, Naoki; D'Antonio-Chronowska, Agnieszka; Frazer, Kelly A

发表日期：2019

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Human iPSC-Derived Retinal Pigment Epithelium: A Model System for Prioritizing and Functionally Characterizing Causal Variants at AMD Risk Loci

人诱导多能干细胞衍生的视网膜色素上皮：用于优先筛选和功能表征AMD风险位点致病变异的模型系统

期刊:Stem Cell Reports

影响因子:5.1

doi:10.1016/j.stemcr.2019.04.012

Smith, Erin N; D'Antonio-Chronowska, Agnieszka; Greenwald, William W; Borja, Victor; Aguiar, Lana R; Pogue, Robert; Matsui, Hiroko; Benaglio, Paola; Borooah, Shyamanga; D'Antonio, Matteo; Ayyagari, Radha; Frazer, Kelly A

Complex regulatory networks influence pluripotent cell state transitions in human iPSCs

复杂的调控网络影响人类诱导多能干细胞的多能性状态转变

Fine mapping spatiotemporal mechanisms of genetic variants underlying cardiac traits and disease

精细绘制遗传变异与心脏性状和疾病相关的时空机制图谱

Analysis of regulatory network modules in hundreds of human stem cell lines reveals complex epigenetic and genetic factors contribute to pluripotency state differences between subpopulations

对数百种人类干细胞系调控网络模块的分析揭示了复杂的表观遗传和遗传因素导致亚群间多能性状态的差异。

In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms

在心力衰竭中，RNA结合蛋白的重新激活与1523种胎儿特异性亚型的表达有关。

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

SARS-CoV-2 易感性和 COVID-19 疾病严重程度与影响多种组织中基因表达的遗传变异有关。

Properties of structural variants and short tandem repeats associated with gene expression and complex traits

与基因表达和复杂性状相关的结构变异和短串联重复序列的特性

Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats

对一系列结构变异和短串联重复序列进行发现和质量分析

An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects.

从人类急性髓系白血病细胞系（HL-60-iPSC）衍生的 iPSC 系保留了白血病异常，并表现出髓系分化缺陷

Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease

对MHC区域的系统性遗传分析揭示了HLA类型与疾病关联的机制基础

Human iPSC-Derived Retinal Pigment Epithelium: A Model System for Prioritizing and Functionally Characterizing Causal Variants at AMD Risk Loci

人诱导多能干细胞衍生的视网膜色素上皮：用于优先筛选和功能表征AMD风险位点致病变异的模型系统