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

Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease

LAG3基因起始密码子变异与LAG-3表达降低和自身免疫性甲状腺疾病风险增加相关。

Saedis Saevarsdottir ,Kristbjörg Bjarnadottir ,Thorsteinn Markusson ,Jonas Berglund ,Thorunn A Olafsdottir ,Gisli H Halldorsson ,Gudrun Rutsdottir ,Kristbjorg Gunnarsdottir ,Asgeir Orn Arnthorsson ,Sigrun H Lund ,Lilja Stefansdottir ,Julius Gudmundsson ,Ari J Johannesson ,Arni Sturluson ,Asmundur Oddsson ,Bjarni Halldorsson ,Björn R Ludviksson ,Egil Ferkingstad ,Erna V Ivarsdottir ,Gardar Sveinbjornsson ,Gerdur Grondal ,Gisli Masson ,Grimur Hjorleifsson Eldjarn ,Gudmundur A Thorisson ,Katla Kristjansdottir ,Kirk U Knowlton ,Kristjan H S Moore ,Sigurjon A Gudjonsson ,Solvi Rognvaldsson ,Stacey Knight ,Lincoln D Nadauld ,Hilma Holm ,Olafur T Magnusson ,Patrick Sulem ,Daniel F Gudbjartsson ,Thorunn Rafnar ,Gudmar Thorleifsson ,Pall Melsted ,Gudmundur L Norddahl ,Ingileif Jonsdottir ,Kari Stefansson

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

TCL1A的异常激活促进克隆性造血中的干细胞扩增

Joshua S Weinstock #,Jayakrishnan Gopakumar #,Bala Bharathi Burugula,Md Mesbah Uddin,Nikolaus Jahn,Julia A Belk,Hind Bouzid,Bence Daniel,Zhuang Miao,Nghi Ly,Taralynn M Mack,Sofia E Luna,Katherine P Prothro,Shaneice R Mitchell,Cecelia A Laurie,Lisa R Yanek,Lewis C Becker,Sharon L R Kardia,Patricia A Peyser,Jiang He,Michiel Rienstra,Pim Van der Harst,Robert Kaplan,Susan R Heckbert,Nicholas L Smith,Kerri L Wiggins,Donna K Arnett,Marguerite R Irvin,Hemant Tiwari,Michael J Cutler,Stacey Knight,J Brent Muhlestein,Adolfo Correa,Laura M Raffield,Yan Gao,Mariza de Andrade,Jerome I Rotter,Stephen S Rich,Russell P Tracy,Barbara A Konkle,Jill M Johnsen,Marsha M Wheeler,J Gustav Smith,Olle Melander,Peter M Nilsson,Brian S Custer,Ravindranath Duggirala,Joanne E Curran,John Blangero,Stephen McGarvey,L Keoki Williams,Shujie Xiao,Mao Yang,C Charles Gu,Yii-Der Ida Chen,Gregory M Marcus,John P Kane,Clive R Pullinger,M Benjamin Shoemaker,Dawood Darbar,Dan M Roden,Christine Albert,Charles Kooperberg,Ying Zhou,JoAnn E Manson,Pinkal Desai,Andrew D Johnson,Rasika A Mathias,Albert V Smith,Hyun M Kang,Ansuman T Satpathy,Pradeep Natarajan,Jacob O Kitzman,Eric A Whitsel,Alexander P Reiner,Alexander G Bick,Siddhartha Jaiswal

Analysis of the cartilage proteome from three different mouse models of genetic skeletal diseases reveals common and discrete disease signatures

对三种不同遗传性骨骼疾病小鼠模型的软骨蛋白质组进行分析,揭示了共同的和独特的疾病特征。

Bell, Peter A; Wagener, Raimund; Zaucke, Frank; Koch, Manuel; Selley, Julian; Warwood, Stacey; Knight, David; Boot-Handford, Raymond P; Thornton, David J; Briggs, Michael D