Rob Ofman相关文献与解析，生知库 | 链接生命科学的每一步

Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect

自噬抑制剂无法恢复最常见的过氧化物酶体生物合成缺陷细胞中的过氧化物酶体功能

期刊:Frontiers in Cell and Developmental Biology

doi:10.3389/fcell.2021.661298

Femke C C Klouwer, Kim D Falkenberg, Rob Ofman, Janet Koster, Démi van Gent, Sacha Ferdinandusse, Ronald J A Wanders, Hans R Waterham

Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophy

X连锁肾上腺脑白质营养不良症中的脂质诱导内质网应激

期刊:Biochimica et Biophysica Acta-Molecular Basis of Disease

影响因子:4.2

doi:10.1016/j.bbadis.2017.06.003

Malu-Clair van de Beek, Rob Ofman, Inge Dijkstra, Frits Wijburg, Marc Engelen, Ronald Wanders, Stephan Kemp

A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

ERAL1 基因发生纯合错义突变，该基因编码线粒体 rRNA 分子伴侣，可导致佩罗综合征

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddx152

Iliana A Chatzispyrou, Marielle Alders, Sergio Guerrero-Castillo, Ruben Zapata Perez, Martin A Haagmans, Laurent Mouchiroud, Janet Koster, Rob Ofman, Frank Baas, Hans R Waterham, Johannes N Spelbrink, Johan Auwerx, Marcel M Mannens, Riekelt H Houtkooper, Astrid S Plomp

信号转导

发表日期：2017

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Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing

HSD10 疾病中的线粒体能量衰竭是由于 mtDNA 转录处理缺陷造成的

期刊:Mitochondrion

影响因子:3.9

doi:10.1016/j.mito.2014.12.005

Kathryn C Chatfield, Curtis R Coughlin 2nd, Marisa W Friederich, Renata C Gallagher, Jay R Hesselberth, Mark A Lovell, Rob Ofman, Michael A Swanson, Janet A Thomas, Ronald J A Wanders, Eric P Wartchow, Johan L K Van Hove

信号转导

发表日期：2015

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Identification and characterization of Eci3, a murine kidney-specific Δ3,Δ2-enoyl-CoA isomerase

小鼠肾脏特异性 Δ3,Δ2-烯酰辅酶 A 异构酶 Eci3 的鉴定和表征

期刊:FASEB Journal

影响因子:4.4

doi:10.1096/fj.13-240416

Michel van Weeghel, Rob Ofman, Carmen A Argmann, Jos P N Ruiter, Nike Claessen, Saskia V Oussoren, Ronald J A Wanders, Jan Aten, Sander M Houten

信号转导

发表日期：2014

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Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation

线粒体蛋白质乙酰化是由脂肪酸氧化产生的乙酰辅酶 A 驱动的

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddu059

Olga Pougovkina, Heleen te Brinke, Rob Ofman, Arno G van Cruchten, Wim Kulik, Ronald J A Wanders, Sander M Houten, Vincent C J de Boer

表观遗传

发表日期：2014

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The proteome of human liver peroxisomes: identification of five new peroxisomal constituents by a label-free quantitative proteomics survey

人类肝脏过氧化物酶体的蛋白质组：通过无标记定量蛋白质组学调查鉴定五种新的过氧化物酶体成分

期刊:PLoS One

影响因子:2.9

doi:10.1371/journal.pone.0057395

Thomas Gronemeyer, Sebastian Wiese, Rob Ofman, Christian Bunse, Magdalena Pawlas, Heiko Hayen, Martin Eisenacher, Christian Stephan, Helmut E Meyer, Hans R Waterham, Ralf Erdmann, Ronald J Wanders, Bettina Warscheid

发表日期：2013

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Mevalonate kinase-deficient THP-1 cells show a disease-characteristic pro-inflammatory phenotype

缺乏甲羟戊酸激酶的 THP-1 细胞表现出疾病特征性的促炎表型

Identification of FDA-approved drugs that increase mevalonate kinase in hyper IgD syndrome

鉴定 FDA 批准的可增加高 IgD 综合征中甲羟戊酸激酶的药物

The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesis

醚脂/缩醛磷脂从头合成所需的长链脂肪酸的来源

Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis Defect

自噬抑制剂无法恢复最常见的过氧化物酶体生物合成缺陷细胞中的过氧化物酶体功能

Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophy

X连锁肾上腺脑白质营养不良症中的脂质诱导内质网应激

A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

ERAL1 基因发生纯合错义突变，该基因编码线粒体 rRNA 分子伴侣，可导致佩罗综合征

Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing

HSD10 疾病中的线粒体能量衰竭是由于 mtDNA 转录处理缺陷造成的

Identification and characterization of Eci3, a murine kidney-specific Δ3,Δ2-enoyl-CoA isomerase

小鼠肾脏特异性 Δ3,Δ2-烯酰辅酶 A 异构酶 Eci3 的鉴定和表征

Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation

线粒体蛋白质乙酰化是由脂肪酸氧化产生的乙酰辅酶 A 驱动的

The proteome of human liver peroxisomes: identification of five new peroxisomal constituents by a label-free quantitative proteomics survey

人类肝脏过氧化物酶体的蛋白质组：通过无标记定量蛋白质组学调查鉴定五种新的过氧化物酶体成分