Jacques Drouin相关文献与解析，生知库 | 链接生命科学的每一步

HOX13-dependent chromatin accessibility underlies the transition towards the digit development program

HOX13 依赖的染色质可及性是数字发育程序转变的基础

Ines Desanlis #, Yacine Kherdjemil #, Alexandre Mayran #, Yasser Bouklouch, Claudia Gentile, Rushikesh Sheth, Rolf Zeller, Jacques Drouin, Marie Kmita

信号转导

发表日期：2020

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Human iPSC-derived Down syndrome astrocytes display genome-wide perturbations in gene expression, an altered adhesion profile, and increased cellular dynamics

人类 iPSC 衍生的唐氏综合征星形胶质细胞表现出基因表达的全基因组扰动、粘附特性的改变和细胞动力学的增强

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddaa003

Blandine Ponroy Bally, W Todd Farmer, Emma V Jones, Selin Jessa, J Benjamin Kacerovsky, Alexandre Mayran, Huashan Peng, Julie L Lefebvre, Jacques Drouin, Arnold Hayer, Carl Ernst, Keith K Murai

Pioneer and nonpioneer factor cooperation drives lineage specific chromatin opening

先驱因子和非先驱因子的合作推动谱系特异性染色质开放

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-019-11791-9

Alexandre Mayran, Kevin Sochodolsky, Konstantin Khetchoumian, Juliette Harris, Yves Gauthier, Amandine Bemmo, Aurelio Balsalobre, Jacques Drouin

信号转导

发表日期：2019

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Pituitary cell translation and secretory capacities are enhanced cell autonomously by the transcription factor Creb3l2

转录因子 Creb3l2 可自主增强垂体细胞的翻译和分泌能力

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-019-11894-3

Konstantin Khetchoumian, Aurélio Balsalobre, Alexandre Mayran, Helen Christian, Valérie Chénard, Julie St-Pierre, Jacques Drouin

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

CABLES1基因功能丧失突变是库欣病的一种新病因。

期刊:Endocrine-Related Cancer

影响因子:4.1

doi:10.1530/ERC-17-0131

Laura C Hernández-Ramírez ,Ryhem Gam ,Nuria Valdés ,Maya B Lodish ,Nathan Pankratz ,Aurelio Balsalobre ,Yves Gauthier ,Fabio R Faucz ,Giampaolo Trivellin ,Prashant Chittiboina ,John Lane ,Denise M Kay ,Aggeliki Dimopoulos ,Stephan Gaillard ,Mario Neou ,Jérôme Bertherat ,Guillaume Assié ,Chiara Villa ,James L Mills ,Jacques Drouin ,Constantine A Stratakis

发表日期：2017

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Distal Limb Patterning Requires Modulation of cis-Regulatory Activities by HOX13

远端肢体模式需要 HOX13 调节顺式调节活动

期刊:Cell Reports

影响因子:7.5

doi:10.1016/j.celrep.2016.11.039

Rushikesh Sheth, Iros Barozzi, David Langlais, Marco Osterwalder, Stephen Nemec, Hanqian L Carlson, H Scott Stadler, Axel Visel, Jacques Drouin, Marie Kmita

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发表日期：2016

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Rgs6 is required for adult maintenance of dopaminergic neurons in the ventral substantia nigra

Rgs6 是成年人维持腹侧黑质多巴胺能神经元所必需的

期刊:PLoS Genetics

影响因子:

doi:10.1371/journal.pgen.1004863

Panojot Bifsha, Jianqi Yang, Rory A Fisher, Jacques Drouin

Chromatin opening ability of pioneer factor Pax7 depends on unique isoform and C-terminal domain

先锋因子 Pax7 的染色质开放能力取决于独特的亚型和 C 端结构域

Pax7 pioneer factor action requires both paired and homeo DNA binding domains

Pax7 先锋因子的作用需要配对和同源 DNA 结合域

Control of mouse limb initiation and antero-posterior patterning by Meis transcription factors

梅斯转录因子对小鼠肢体起始和前后模式的控制

HOX13-dependent chromatin accessibility underlies the transition towards the digit development program

HOX13 依赖的染色质可及性是数字发育程序转变的基础

Human iPSC-derived Down syndrome astrocytes display genome-wide perturbations in gene expression, an altered adhesion profile, and increased cellular dynamics

人类 iPSC 衍生的唐氏综合征星形胶质细胞表现出基因表达的全基因组扰动、粘附特性的改变和细胞动力学的增强

Pioneer and nonpioneer factor cooperation drives lineage specific chromatin opening

先驱因子和非先驱因子的合作推动谱系特异性染色质开放

Pituitary cell translation and secretory capacities are enhanced cell autonomously by the transcription factor Creb3l2

转录因子 Creb3l2 可自主增强垂体细胞的翻译和分泌能力

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

CABLES1基因功能丧失突变是库欣病的一种新病因。

Distal Limb Patterning Requires Modulation of cis-Regulatory Activities by HOX13

远端肢体模式需要 HOX13 调节顺式调节活动

Rgs6 is required for adult maintenance of dopaminergic neurons in the ventral substantia nigra

Rgs6 是成年人维持腹侧黑质多巴胺能神经元所必需的