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

Diagnostic relevance of SH2B3 mutations in suspected myeloid malignancies and acute leukemia: insights from a large-scale NGS-based screening study

SH2B3突变在疑似髓系恶性肿瘤和急性白血病诊断中的意义:一项基于大规模NGS筛查研究的启示

Ben Dhia, Leïla; Wemeau, Mathieu; Fenwarth, Laurène; Marceau-Renaut, Alice; Fournier, Elise; Ducourneau, Benoît; Tricot, Sabine; Deschildt, Manon; Huchette, Pascal; Darre, Stéphane; Benhalima, Ilyes; Margat, Emilie; Bories, Claire; Dufossé, Maxime; Boyer, Thomas; Paubelle, Etienne; Charbonnier, Amandine; Lebon, Delphine; Hieulle, Julia; Dennetiere, Sophie; Malbranque, Zoé; Daniel, Adrien; Bruges, Judith; Pascal, Laurent; Brijs, Jan; Carpentier, Benjamin; Willaume, Alexandre; Coiteux, Valérie; Goursaud, Laure; Preudhomme, Claude; Nibourel, Olivier; Duployez, Nicolas

Reduced Function of the Adaptor SH2B3 Promotes T1D via Altered Cytokine-Regulated, T-Cell-Intrinsic Immune Tolerance

衔接蛋白SH2B3功能降低通过改变细胞因子调节的T细胞固有免疫耐受性促进1型糖尿病的发生

Watson, Taylor K; Rosen, Aaron B I; Drow, Travis; Medjo, Jacob A; MacQuivey, Matthew A; Ge, Yan; Liggitt, H Denny; Grosvenor, Dane A; Dill-McFarland, Kimberly A; Altman, Matthew C; Concannon, Patrick J; Buckner, Jane H; Rawlings, David J; Allenspach, Eric J

Biallelic SH2B3 germline variants are associated with a neonatal myeloproliferative disease and multisystemic involvement

SH2B3基因双等位基因变异与新生儿骨髓增生性疾病和多系统受累相关。

Leardini, Davide; Flex, Elisabetta; Stieglitz, Elliot; Cerasi, Sara; Bertuccio, Salvatore Nicola; Baccelli, Francesco; Kállay, Krisztián; Kjollerstrom, Paula; Batalha, Sara; Carpentieri, Giovanna; Pedace, Lucia; Ciolfi, Andrea; Hammad, Mahmoud; Miranda, Maria; Rojas, Marta; Rao, Anupama; Innes, Andrew J; Rudelius, Martina; Santini, Valeria; Raddi, Marco; Teh, Kok-Hoi; De Vito, Rita; Yoshimi, Ayami; Tartaglia, Marco; Locatelli, Franco; Niemeyer, Charlotte M; Masetti, Riccardo

KAT2A-H3K79succ-Mediated SH2B3 Upregulation Promotes TNBC Metastasis Through Diminishing the Ubiquitin-Dependent Degradation of Vimentin

KAT2A-H3K79succ介导的SH2B3上调通过减少波形蛋白的泛素依赖性降解促进三阴性乳腺癌转移

Shi, Xiaohui; Hao, Ran; Yang, Zhan; Wang, Xiaoran; Lu, Yiwei; Wang, Xiaohan; Ji, Huanqi; Ma, Shen; Liu, Xuehua; Hu, Jie; Qi, Yixin

LNK/SH2B3 loss of function increases susceptibility to murine and human atrial fibrillation

LNK/SH2B3功能丧失会增加小鼠和人类患心房颤动的易感性

Murphy, Matthew B; Yang, Zhenjiang; Subati, Tuerdi; Farber-Eger, Eric; Kim, Kyungsoo; Blackwell, Daniel J; Fleming, Matthew R; Stark, Joshua M; Van Amburg, Joseph C; Woodall, Kaylen K; Van Beusecum, Justin P; Agrawal, Vineet; Smart, Charles D; Pitzer, Ashley; Atkinson, James B; Fogo, Agnes B; Bastarache, Julie A; Kirabo, Annet; Wells, Quinn S; Madhur, Meena S; Barnett, Joey V; Murray, Katherine T

Rare SH2B3 coding variants in lupus patients impair B cell tolerance and predispose to autoimmunity

狼疮患者中罕见的SH2B3编码变异会损害B细胞耐受性并易导致自身免疫性疾病。

Yaoyuan Zhang ,Rhiannon Morris # ,Grant J Brown # ,Ayla May D Lorenzo ,Xiangpeng Meng ,Nadia J Kershaw ,Pamudika Kiridena ,Gaétan Burgio ,Simon Gross ,Jean Y Cappello ,Qian Shen ,Hao Wang ,Cynthia Turnbull ,Tom Lea-Henry ,Maurice Stanley ,Zhijia Yu ,Fiona D Ballard ,Aaron Chuah ,James C Lee ,Ann-Maree Hatch ,Anselm Enders ,Seth L Masters ,Alexander P Headley ,Peter Trnka ,Dominic Mallon ,Jeffery T Fletcher ,Giles D Walters ,Mario Šestan ,Marija Jelušić ,Matthew C Cook ,Vicki Athanasopoulos ,David A Fulcher ,Jeffrey J Babon ,Carola G Vinuesa # ,Julia I Ellyard #

Germline bi-allelic SH2B3/LNK alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder

生殖系双等位基因SH2B3/LNK改变易导致新生儿幼年型骨髓单核细胞白血病样疾病

Arfeuille, Chloé; Vial, Yoann; Cadenet, Margaux; Caye-Eude, Aurélie; Fenneteau, Odile; Neven, Quentin; Bonnard, Adeline A; Pizzi, Simone; Carpentieri, Giovanna; Capri, Yline; Girardi, Katia; Pedace, Lucia; Macchiaiolo, Marina; Boudhar, Kamel; Khaled, Monia Ben; Chahla, Wadih Abou; Lutun, Anne; Fahd, Mony; Drunat, Séverine; Flex, Elisabetta; Dalle, Jean-Hugues; Strullu, Marion; Locatelli, Franco; Tartaglia, Marco; Cavé, Hélène

LNK/SH2B3 as a novel driver in juvenile myelomonocytic leukemia

LNK/SH2B3作为幼年型骨髓单核细胞白血病的新型驱动基因

Wintering, Astrid; Hecht, Anna; Meyer, Julia; Wong, Eric B; Hübner, Juwita; Abelson, Sydney; Feldman, Kira; Kennedy, Vanessa E; Peretz, Cheryl A C; French, Deborah L; Maguire, Jean Ann; Jobaliya, Chintan; Vasquez, Marta Rojas; Desai, Sunil; Dulman, Robin; Nemecek, Eneida; Haines, Hilary; Hammad, Mahmoud; El Haddad, Alaa; Kogan, Scott C; Abdullaev, Zied; Chehab, Farid F; Tasian, Sarah K; Smith, Catherine C; Loh, Mignon L; Stieglitz, Elliot

SH2B3 alterations in a novel genetic condition, juvenile myelomonocytic leukemia, and myeloproliferative neoplasia

SH2B3 改变与一种新的遗传疾病、幼年型骨髓单核细胞白血病和骨髓增生性肿瘤有关

Niemeyer, Charlotte M; Erlacher, Miriam

CTLA4, SH2B3, and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of Type 1 diabetes patients

CTLA4、SH2B3 和 CLEC16A 对 1 型糖尿病患者亲属早期胰岛自身免疫的进展具有不同的影响

Vandewalle, Julie; Desouter, Aster K; Van der Auwera, Bart J; Tenoutasse, Sylvie; Gillard, Pieter; De Block, Christophe; Keymeulen, Bart; Gorus, Frans K; Van de Casteele, Mark