日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Unraveling the role of TP53 mutations in myeloproliferative neoplasms: Molecular mechanisms of leukemic transformation

揭示TP53突变在骨髓增生性肿瘤中的作用:白血病转化的分子机制

da Silva-Benedito, Suzana; Bernardo, Paula Sabbo; Martin, Jean-Edouard; Marty, Caroline; Plo, Isabelle; Antony-Debré, Iléana; Monte-Mór, Bárbara da Costa Reis

Foxi1 regulates multipotent mucociliary progenitors and ionocyte specification through transcriptional and epigenetic mechanisms.

Foxi1 通过转录和表观遗传机制调节多能性粘液纤毛祖细胞和离子细胞的分化。

Bowden Sarah, Brislinger-Engelhardt Magdalena Maria, Hansen Mona, Andricek Aisha, Temporal-Plo Africa, Weber Damian, Hägele Sandra, Lorenz Fabian, Litwin Tim, Kreutz Clemens, Walentek Peter

Automated overview of complete endoscopies with unsupervised learned descriptors

利用无监督学习描述符自动概览完整的内镜检查结果

Barbed, O Leon; Azagra, Pablo; Plo, Juan; Murillo, Ana C

Nanoscale Band Gap Modulation and Dual Moiré Superlattices of Hexagonal Boron Nitride Weakly Coupled to Graphite

纳米尺度带隙调制和弱耦合石墨的六方氮化硼的双莫尔超晶格

J R Costa, Fábio; Arribas, Daniel; G L Brito, Thiago; Cheng, Tin S; Bradford, Jonathan; Thompson, Amelia; Saywell, Alex; Mellor, Christopher J; Beton, Peter H; Novikov, Sergei V; Plo, Juliette; Gil, Bernard; Cassabois, Guillaume; Zagonel, Luiz Fernando; Kuhnke, Klaus; Kern, Klaus; Rosławska, Anna

JAK2 inhibition mediates clonal selection of RAS pathway mutations in myeloproliferative neoplasms

JAK2抑制介导骨髓增生性肿瘤中RAS通路突变的克隆选择

Nabih Maslah # ,Nina Kaci # ,Blandine Roux # ,Gabriela Alexe ,Raphael Marie ,Hélène Pasquer ,Emmanuelle Verger ,Rafael Daltro De Oliveira ,Cécile Culeux ,Bochra Mlayah ,Nicolas Gauthier ,Fanny Gonzales ,Lin-Pierre Zhao ,Saravanan Ganesan ,Panhong Gou ,Frank Ling ,Juliette Soret-Dulphy ,Nathalie Parquet ,William Vainchenker ,Emmanuel Raffoux ,Rose Ann Padua ,Stéphane Giraudier ,Caroline Marty ,Isabelle Plo ,Camille Lobry ,Kimberly Stegmaier ,Alexandre Puissant ,Jean-Jacques Kiladjian ,Bruno Cassinat ,Lina Benajiba

Expanding the phenotypic and genetic landscape of congenital neutropenia through whole-exome and genome sequencing

通过全外显子组和全基因组测序扩展先天性中性粒细胞减少症的表型和遗传图谱

Marti, Séverine; Pellet, Philippe; Beaupain, Blandine; Durix, Léa; Buratti, Julien; Réguerre, Yves; Aladjidi, Nathalie; Azarnoush, Saba; Clauin, Severine; Chahla, Wahid Abou; Blaison, Gilles; Bertand, Jeremy; Bodet, Damien; Brethon, Benoit; Chane-Teng, Jessica; Delafoy, Manon; Dupraz, Chrystelle; Gandemer, Virginie; Denizeau, Philippe; Goldenberg, Alice; Hirsch, Pierre; l'Haridon, Anaïs; Marie-Cardine, Aude; Vera, Gabriella; Nelken, Brigitte; Nizery, Laure; Nolla, Marie; Pasquet, Marlène; Rosain, Jérémie; Terriou, Louis; Plo, Isabelle; Donadieu, Jean; Bellanné-Chantelot, Christine

Telomere occupancy by TRF2 is altered by KIT mutations and correlates with mastocytosis regression

KIT基因突变会改变TRF2对端粒的占据情况,并且这种改变与肥大细胞增生症的消退相关。

Bruneau, Julie; Georgin-Lavialle, Sophie; Ladraa, Sophia; Belaid, Zakia; Plo, Isabelle; Letard, Sébastien; Soucie, Erinn; Draskovic, Irena; Goudin, Nicolas; Bouillié, Marie; Lepelletier, Yves; Rossignol, Julien; Polivka, Laura; Frenzel, Laurent; Lortholary, Olivier; Fraitag, Sylvie; Bodemer, Christine; Revy, Patrick; Arock, Michel; Molina, Thierry-Jo; Londono-Vallejo, Arturo; Dubreuil, Patrice; Maouche-Chretien, Leila; Hermine, Olivier

Increased RhoA pathway activation downstream of αIIbβ3/SRC contributes to heterozygous Bernard Soulier syndrome

αIIbβ3/SRC下游RhoA通路激活增强是导致杂合子Bernard Soulier综合征的原因之一。

Lordier, Larissa; Di Buduo, Christian A; Kauskot, Alexandre; Balayn, Nathalie; Lavenu-Bombled, Cécile; Baschieri, Francesco; Proulle, Valérie; Oyarzun, Cecilia P Marin; Careddu, Francesca; Biunno, Ida; Manoliu, Tudor; Rameau, Philippe; Plo, Isabelle; Papadopoulos, Nicolas; Constantinescu, Stefan; Vainchenker, William; Nguyen, Guillaume Nam; Ballerini, Paola; Favier, Remi; Balduini, Alessandra; Raslova, Hana

New approaches to standard of care in early-phase myeloproliferative neoplasms: can interferon-α alter the natural history of the disease?

早期骨髓增生性肿瘤标准治疗的新方法:干扰素-α能否改变疾病的自然病程?

Pasquier, Florence; Pegliasco, Jean; Martin, Jean-Edouard; Marti, Severine; Plo, Isabelle

IFN-I-Mediated Transcriptional Reprogramming Drives Myeloid-skewed Hematopoiesis in Sickle Cell Anemia

IFN-I介导的转录重编程驱动镰状细胞贫血症中的髓系偏向造血

Serra, Marion; Aglave, Marine; Salma, Mohammad; Akkaya, Steven; Hermand, Patricia; Lefevre, Carine; Duval, Romain; Merrer, Jade; Leye, Fallou; Magne, Joelle; Plo, Isabelle; Blanc, Lionel; Soler, Eric; Azouzi, Slim; Koehl, Berengere