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

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

白细胞中人类 E3 泛素连接酶 CBL 的体细胞缺陷会损害 B 细胞的发育和功能,但不会影响 T 细胞的发育和功能。

Vatovec Taja, Neehus Anna-Lena, Jackson Katherine J L, Avery Danielle T, Bagarić Ivan, Erazo Lucia, Arango-Franco Carlos A, Ogishi Masato, Ahmed Syed F, Cederholm Axel, Russell Amanda J, Della Mina Erika, Al-Rifai Dena, Bull Rowena, Buetow Lori, Sobrino Steicy, Zhang Allison, Wahlster Lara, Michelet Marine, Parvaneh Nima, Peel Jessica, Barzaghi Federica, Leardini Davide, Philippot Quentin, Saettini Francesco, Dutrieux Jacques, de Muylder Benedicte, Vendemini Francesca, Baccelli Francesco, Catala Albert, Gambineri Eleonora, Veltroni Marinella, Pandiarajan Vignesh, Aguilar Yurena, Haerynck Filomeen, Elliott Michael, Turville Stuart, Brillot Fabienne, Khan Taushif, Consonni Filippo, Berteloot Laureline, Sewell William A, Rao Geetha, Largeaud Laetitia, Conti Francesca, Roullion Cecile, Masson Cécile, Pegoraro Francesco, Ye Tianyi, Joubran Samantha, Villalpando Emily, Bessot Boris, Seeleuthner Yoann, Le Voyer Tom, Rosain Jérémie, Li Hailun, Janda Zarah, Muratore Edoardo, Soudée Camille, Delabesse Eric, Goulvestre Claire, Shahrooei Mohammad, Puel Anne, André Isabelle, Bole-Feysot Christine, Abel Laurent, Erlacher Miriam, Béziat Vivien, Lagresle-Peyrou Chantal, Cheynier Remi, Six Emmanuelle, Marr Nico, Pasquet Marlène, Alsina Laia, Goodnow Christopher C, Landegren Nils, Aiuti Alessandro, Zhang Peng, Masetti Riccardo, Huang Danny T, Ma Cindy S, Casanova Jean-Laurent, Sankaran Vijay G, Bustamante Jacinta, Tangye Stuart G, Bohlen Jonathan

An inflammatory and quiescent HSC subpopulation expands with age in humans.

在人类中,炎症性和静止性造血干细胞亚群会随着年龄的增长而扩增。

Safina Ksenia R, Salik Basit, Kotliar Dylan, Curtis Michelle, Good Jonathan D, Weng Chen, David Shawn, Raychaudhuri Soumya, Kreso Antonia, Trowbridge Jennifer J, Sankaran Vijay G, van Galen Peter

Charting clonal evolution and behavior with GoT-Multi

利用 GoT-Multi 绘制克隆演化和行为图

Gudera, Jonas A; Sankaran, Vijay G

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

整合天然和人工基因变异,以解码对血液性状的调控影响。

Tardaguila Manuel, Von Schiller Dominique, Colombo Michela, Gori Ilaria, Coomber Eve L, Vanderstichele Thomas, Benaglio Paola, Chiereghin Chiara, Gerety Sebastian, Vuckovic Dragana, Landini Arianna, Clerici Giuditta, Casiraghi Aurora, Albers Patrick, Ray-Jones Helen, Burnham Katie L, Tokolyi Alex, Persyn Elodie, Spivakov Mikhail, Sankaran Vijay G, Walter Klaudia, Kundu Kousik, Pirastu Nicola, Inouye Michael, Paul Dirk S, Davenport Emma E, Sahlén Pelin, Watt Stephen, Soranzo Nicole

Detailed assessment of rare and common TERT variation in a family with a telomere biology disorder

对患有端粒生物学疾病的家族中罕见和常见的TERT变异进行详细评估

Zeigler, Logan P; Florez-Vargas, Oscar; Altintas, Burak; Niewisch, Marena R; Zhou, Weiyin; Giri, Neelam; Rafati, Maryam; Poeschla, Michael; Sankaran, Vijay G; Lai, Tsung-Po; Aviv, Abraham; Jones, Kristine; Luo, Wen; Liu, Jia; McReynolds, Lisa J; Zhao, Tianna; Prokunina-Olsson, Ludmila; Savage, Sharon A

Modeling mitochondrial inheritance enables high-precision single-cell lineage tracing in humans

线粒体遗传建模能够实现人类单细胞谱系的高精度追踪。

Gao, Teng; Weng, Chen; Johnson, Isaac; Poeschla, Michael; Gudera, Jonas; King, Emily; Rouya, Christopher; Donovan, Adriana; Bourke, Lauren; Shao, Ying; Marquez, Eladio; Tyagi, Rahul; Zon, Leonard I; Weissman, Jonathan S; Sankaran, Vijay G

Epigenome editing of human hematopoietic stem cells enables sustained and reversible thrombosis prevention

对人类造血干细胞进行表观基因组编辑可实现持续且可逆的血栓预防。

Ye, Tianyi; Xu, Wanying; Barrachina, Maria N; Lyu, Peng; Antoszewski, Mateusz; Volpe, Lucrezia Della; Guo, Chun-Jie; Lee, Andrew J; Theardy, Madelaine S; Shelton, Spencer D; Wahlster, Lara; Caulier, Alexis; Messa, Luana; Poeschla, Michael; Agarwal, Gaurav; Mitra, Ronodeep; Schmaier, Alec A; Weissman, Jonathan S; Machlus, Kellie R; Sankaran, Vijay G

Transcription factor networks disproportionately enrich for heritability of blood cell phenotypes

转录因子网络不成比例地富集了血细胞表型的遗传性

Martin-Rufino, Jorge Diego; Caulier, Alexis; Lee, Seayoung; Castano, Nicole; King, Emily; Joubran, Samantha; Jones, Marcus; Goldman, Seth R; Arora, Uma P; Wahlster, Lara; Lander, Eric S; Sankaran, Vijay G

Coupling CRISPR scanning with targeted chromatin accessibility profiling using a double-stranded DNA deaminase.

将 CRISPR 扫描与使用双链 DNA 脱氨酶的靶向染色质可及性分析相结合。

Roh Heejin, Shen Simon P, Hu Yan, Kwok Hui Si, Siegenfeld Allison P, Lee Ceejay, Zepeda Marcanthony U, Guo Chun-Jie, Roseman Shelby A, Comenho Caroline, Sankaran Vijay G, Buenrostro Jason D, Liau Brian B

CEBPA repression by MECOM blocks differentiation to drive aggressive leukemias

MECOM对CEBPA的抑制作用会阻断分化,从而驱动侵袭性白血病的发生。

Fleming, Travis J; Antoszewski, Mateusz; Lambo, Sander; Gundry, Michael C; Piussi, Riccardo; Wahlster, Lara; Shah, Sanjana; Reed, Fiona E; Dong, Kevin D; Paulo, Joao A; Gygi, Steven P; Mimoso, Claudia; Goldman, Seth R; Adelman, Karen; Perry, Jennifer A; Pikman, Yana; Stegmaier, Kimberly; Barrachina, Maria N; Machlus, Kellie R; Hovestadt, Volker; Arruda, Andrea; Minden, Mark D; Voit, Richard A; Sankaran, Vijay G