Nicolas Pilon相关文献与解析，生知库 | 链接生命科学的每一步

Maximilian Breuer, Maximilian Rummler, Jaskaran Singh, Sabrina Maher, Charlotte Zaouter, Priyanka Jamadagni, Nicolas Pilon, Bettina M Willie, Shunmoogum A Patten

信号转导

发表日期：2024

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Efficient enzyme-free method to assess the development and maturation of the innate and adaptive immune systems in the mouse colon

一种高效的无酶方法，用于评估小鼠结肠先天性和适应性免疫系统的发育和成熟

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-024-61834-5

Nejia Lassoued ，Alexis Yero ，Mohammad-Ali Jenabian ，Rodolphe Soret ，Nicolas Pilon

The CHARGE syndrome-associated protein FAM172A controls AGO2 nuclear import

CHARGE 综合征相关蛋白 FAM172A 控制 AGO2 核输入

期刊:Life Science Alliance

影响因子:3.3

doi:10.26508/lsa.202302133

Sephora Sallis, Félix-Antoine Bérubé-Simard, Benoit Grondin, Elizabeth Leduc, Fatiha Azouz, Catherine Bélanger, Nicolas Pilon

信号转导

发表日期：2023

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CHARGE syndrome-associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms

CHARGE 综合征相关蛋白 FAM172A 和 CHD7 通过转录和可变剪接机制影响男性性别决定和分化

期刊:FASEB Journal

影响因子:4.4

doi:10.1096/fj.202100837RR

Catherine Bélanger, Tatiana Cardinal, Elizabeth Leduc, Robert S Viger, Nicolas Pilon

NR2F1 regulates a Schwann cell precursor-vs-melanocyte cell fate switch in a mouse model of Waardenburg syndrome type IV

NR2F1 调节瓦登堡综合征 IV 型小鼠模型中的施万细胞前体细胞与黑素细胞的命运转换

期刊:Pigment Cell & Melanoma Research

影响因子:3.9

doi:10.1111/pcmr.13054

Grégoire Bonnamour, Baptiste Charrier, Sephora Sallis, Elizabeth Leduc, Nicolas Pilon

Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression

染色质重塑剂 CHD7 通过促进 PAQR3 表达，促进 GABA 能神经元的发育

期刊:EMBO Reports

影响因子:6.5

doi:10.15252/embr.202050958

Priyanka Jamadagni, Maximilian Breuer, Kathrin Schmeisser, Tatiana Cardinal, Betelhem Kassa, J Alex Parker, Nicolas Pilon, Eric Samarut, Shunmoogum A Patten

Genetic Background Influences Severity of Colonic Aganglionosis and Response to GDNF Enemas in the Holstein Mouse Model of Hirschsprung Disease

遗传背景影响先天性巨结肠荷斯坦小鼠模型中结肠神经节缺失症的严重程度和对 GDNF 灌肠剂的反应

期刊:International Journal of Molecular Sciences

影响因子:0.7

doi:10.3390/ijms222313140

Rodolphe Soret, Nejia Lassoued, Grégoire Bonnamour, Guillaume Bernas, Aurélie Barbe, Mélanie Pelletier, Manon Aichi, Nicolas Pilon

神经

发表日期：2021

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Male-biased aganglionic megacolon in the TashT mouse model of Hirschsprung disease involves upregulation of p53 protein activity and Ddx3y gene expression

先天性巨结肠 TashT 小鼠模型中，雄性偏向的无神经节巨结肠与 p53 蛋白活性和 Ddx3y 基因表达上调有关

期刊:PLoS Genetics

影响因子:

doi:10.1371/journal.pgen.1009008

Tatiana Cardinal, Karl-Frédérik Bergeron, Rodolphe Soret, Ouliana Souchkova, Christophe Faure, Amélina Guillon, Nicolas Pilon

Gut microbiota-mediated Gene-Environment interaction in the TashT mouse model of Hirschsprung disease

先天性巨结肠 TashT 小鼠模型中肠道菌群介导的基因-环境相互作用

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-018-36967-z

Aboubacrine Mahamane Touré, Mathieu Landry, Ouliana Souchkova, Steven W Kembel, Nicolas Pilon

Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4

小鼠神经嵴细胞中 Nr2f1-A830082K12Rik 基因对的上调导致类似于瓦登堡综合征 4 型的复杂表型

期刊:Disease Models & Mechanisms

影响因子:4

doi:10.1242/dmm.026773

Karl-F Bergeron, Chloé M A Nguyen, Tatiana Cardinal, Baptiste Charrier, David W Silversides, Nicolas Pilon

CHD7 regulates craniofacial cartilage development via controlling HTR2B expression

CHD7 通过控制 HTR2B 表达来调节颅面软骨发育

Efficient enzyme-free method to assess the development and maturation of the innate and adaptive immune systems in the mouse colon

一种高效的无酶方法，用于评估小鼠结肠先天性和适应性免疫系统的发育和成熟

The CHARGE syndrome-associated protein FAM172A controls AGO2 nuclear import

CHARGE 综合征相关蛋白 FAM172A 控制 AGO2 核输入

CHARGE syndrome-associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms

CHARGE 综合征相关蛋白 FAM172A 和 CHD7 通过转录和可变剪接机制影响男性性别决定和分化

NR2F1 regulates a Schwann cell precursor-vs-melanocyte cell fate switch in a mouse model of Waardenburg syndrome type IV

NR2F1 调节瓦登堡综合征 IV 型小鼠模型中的施万细胞前体细胞与黑素细胞的命运转换

Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression

染色质重塑剂 CHD7 通过促进 PAQR3 表达，促进 GABA 能神经元的发育

Genetic Background Influences Severity of Colonic Aganglionosis and Response to GDNF Enemas in the Holstein Mouse Model of Hirschsprung Disease

遗传背景影响先天性巨结肠荷斯坦小鼠模型中结肠神经节缺失症的严重程度和对 GDNF 灌肠剂的反应

Male-biased aganglionic megacolon in the TashT mouse model of Hirschsprung disease involves upregulation of p53 protein activity and Ddx3y gene expression

先天性巨结肠 TashT 小鼠模型中，雄性偏向的无神经节巨结肠与 p53 蛋白活性和 Ddx3y 基因表达上调有关

Gut microbiota-mediated Gene-Environment interaction in the TashT mouse model of Hirschsprung disease

先天性巨结肠 TashT 小鼠模型中肠道菌群介导的基因-环境相互作用

Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4

小鼠神经嵴细胞中 Nr2f1-A830082K12Rik 基因对的上调导致类似于瓦登堡综合征 4 型的复杂表型