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

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

High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome

高通量剪接分析鉴定肾病综合征中已知的和新的WT1外显子9变异体

Smith, Cathy; Burugula, Bala Bharathi; Dunn, Ian; Aradhya, Swaroop; Kitzman, Jacob O; Yee, Jennifer Lai

GCAF(TMEM251) regulates lysosome biogenesis by activating the mannose-6-phosphate pathway

GCAF(TMEM251)通过激活甘露糖-6-磷酸途径调控溶酶体生物合成。

Weichao Zhang # ,Xi Yang # ,Yingxiang Li ,Linchen Yu ,Bokai Zhang ,Jianchao Zhang ,Woo Jung Cho ,Varsha Venkatarangan ,Liang Chen ,Bala Bharathi Burugula ,Sarah Bui ,Yanzhuang Wang ,Cunming Duan ,Jacob O Kitzman ,Ming Li

Longitudinal profiling of clonal hematopoiesis provides insight into clonal dynamics

对克隆性造血的纵向分析有助于深入了解克隆动态

Uddin, Md Mesbah; Zhou, Ying; Bick, Alexander G; Burugula, Bala Bharathi; Jaiswal, Siddhartha; Desai, Pinkal; Honigberg, Michael C; Love, Shelly-Ann; Barac, Ana; Hayden, Kathleen M; Manson, JoAnn E; Whitsel, Eric A; Kooperberg, Charles; Natarajan, Pradeep; Reiner, Alexander P; Kitzman, Jacob O

Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk

对赋予林奇综合征风险的MSH2错义变异进行大规模并行功能测试

Jia, Xiaoyan; Burugula, Bala Bharathi; Chen, Victor; Lemons, Rosemary M; Jayakody, Sajini; Maksutova, Mariam; Kitzman, Jacob O

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

97,691个全基因组中克隆性造血的遗传病因

Bick, Alexander G; Weinstock, Joshua S; Nandakumar, Satish K; Fulco, Charles P; Bao, Erik L; Zekavat, Seyedeh M; Szeto, Mindy D; Liao, Xiaotian; Leventhal, Matthew J; Nasser, Joseph; Chang, Kyle; Laurie, Cecelia; Burugula, Bala Bharathi; Gibson, Christopher J; Lin, Amy E; Taub, Margaret A; Aguet, Francois; Ardlie, Kristin; Mitchell, Braxton D; Barnes, Kathleen C; Moscati, Arden; Fornage, Myriam; Redline, Susan; Psaty, Bruce M; Silverman, Edwin K; Weiss, Scott T; Palmer, Nicholette D; Vasan, Ramachandran S; Burchard, Esteban G; Kardia, Sharon L R; He, Jiang; Kaplan, Robert C; Smith, Nicholas L; Arnett, Donna K; Schwartz, David A; Correa, Adolfo; de Andrade, Mariza; Guo, Xiuqing; Konkle, Barbara A; Custer, Brian; Peralta, Juan M; Gui, Hongsheng; Meyers, Deborah A; McGarvey, Stephen T; Chen, Ida Yii-Der; Shoemaker, M Benjamin; Peyser, Patricia A; Broome, Jai G; Gogarten, Stephanie M; Wang, Fei Fei; Wong, Quenna; Montasser, May E; Daya, Michelle; Kenny, Eimear E; North, Kari E; Launer, Lenore J; Cade, Brian E; Bis, Joshua C; Cho, Michael H; Lasky-Su, Jessica; Bowden, Donald W; Cupples, L Adrienne; Mak, Angel C Y; Becker, Lewis C; Smith, Jennifer A; Kelly, Tanika N; Aslibekyan, Stella; Heckbert, Susan R; Tiwari, Hemant K; Yang, Ivana V; Heit, John A; Lubitz, Steven A; Johnsen, Jill M; Curran, Joanne E; Wenzel, Sally E; Weeks, Daniel E; Rao, Dabeeru C; Darbar, Dawood; Moon, Jee-Young; Tracy, Russell P; Buth, Erin J; Rafaels, Nicholas; Loos, Ruth J F; Durda, Peter; Liu, Yongmei; Hou, Lifang; Lee, Jiwon; Kachroo, Priyadarshini; Freedman, Barry I; Levy, Daniel; Bielak, Lawrence F; Hixson, James E; Floyd, James S; Whitsel, Eric A; Ellinor, Patrick T; Irvin, Marguerite R; Fingerlin, Tasha E; Raffield, Laura M; Armasu, Sebastian M; Wheeler, Marsha M; Sabino, Ester C; Blangero, John; Williams, L Keoki; Levy, Bruce D; Sheu, Wayne Huey-Herng; Roden, Dan M; Boerwinkle, Eric; Manson, JoAnn E; Mathias, Rasika A; Desai, Pinkal; Taylor, Kent D; Johnson, Andrew D; Auer, Paul L; Kooperberg, Charles; Laurie, Cathy C; Blackwell, Thomas W; Smith, Albert V; Zhao, Hongyu; Lange, Ethan; Lange, Leslie; Rich, Stephen S; Rotter, Jerome I; Wilson, James G; Scheet, Paul; Kitzman, Jacob O; Lander, Eric S; Engreitz, Jesse M; Ebert, Benjamin L; Reiner, Alexander P; Jaiswal, Siddhartha; Abecasis, Gonçalo; Sankaran, Vijay G; Kathiresan, Sekar; Natarajan, Pradeep

Loss of Neurokinin-1 Receptor Alters Ocular Surface Homeostasis and Promotes an Early Development of Herpes Stromal Keratitis

神经激肽-1受体的缺失会改变眼表稳态并促进疱疹性基质角膜炎的早期发展

Subhash Gaddipati, Pushpa Rao, Andrew David Jerome, Bala Bharathi Burugula, Norma P Gerard, Susmit Suvas

Histone deacetylases and phosphorylated polymerase II C-terminal domain recruit Spt6 for cotranscriptional histone reassembly

组蛋白去乙酰化酶和磷酸化聚合酶 II C 端结构域募集 Spt6 进行共转录组蛋白重组

Bala Bharathi Burugula, Célia Jeronimo, Rakesh Pathak, Jeffery W Jones, François Robert, Chhabi K Govind