All papers authored by David Wiest
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2023
Yuanyuan Gao,
Yan Wang,
Daniel Chauss,
Alejandro V. Villarino,
Verena M. Link,
Hiroyuki Nagashima,
Camille A. Spinner,
Vishal N. Koparde 
,
Nicolas Bouladoux ,
Michael S. Abers,
Timothy J. Break ,
Laura B. Chopp ,
Jung-Hyun Park ,
Jinfang Zhu,
David L. Wiest
and 6 other authors
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,
Nicolas Bouladoux ,
Michael S. Abers,
Timothy J. Break ,
Laura B. Chopp ,
Jung-Hyun Park ,
Jinfang Zhu,
David L. Wiest
and 6 other authors
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2022
Jeremy J. Ratiu ,
William E. Barclay,
Elliot Lin ,
Qun Wang,
Sebastian Wellford ,
Naren Mehta ,
Melissa J. Harnois ,
Devon DiPalma ,
Sumedha Roy,
Alejandra V. Contreras,
Mari L. Shinohara ,
David Wiest ,
Yuan Zhuang
,
William E. Barclay,
Elliot Lin ,
Qun Wang,
Sebastian Wellford ,
Naren Mehta ,
Melissa J. Harnois ,
Devon DiPalma ,
Sumedha Roy,
Alejandra V. Contreras,
Mari L. Shinohara ,
David Wiest ,
Yuan Zhuang
Loss of Zfp335 triggers cGAS/STING-dependent apoptosis of post-β selection thymocytes
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Yong Zhang,
Billy Truong ,
Shawn P. Fahl ,
Esteban Martinez ,
Kathy Cai ,
Essel Dulaimi,
Yulan Gong,
Dan A. Liebermann,
Jonathan Soboloff,
Roland Dunbrack ,
Ross L. Levine ,
Steven Fletcher,
Dietmar J. Kappes,
Stephen Sykes ,
Paul Shapiro
and 1 other authors
,
Shawn P. Fahl ,
Esteban Martinez ,
Kathy Cai ,
Essel Dulaimi,
Yulan Gong,
Dan A. Liebermann,
Jonathan Soboloff,
Roland Dunbrack ,
Ross L. Levine ,
Steven Fletcher,
Dietmar J. Kappes,
Stephen Sykes ,
Paul Shapiro
and 1 other authors
The ERK2 DBP domain opposes pathogenesis of a JAK2V617F-driven myeloproliferative neoplasm
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2020
Alejandra V. Contreras ,
David L. Wiest
,
David L. Wiest
Recent advances in understanding the development and function of γδ T cells
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2019
Shuyun Rao,
Suraj Peri,
Jens Hoffmann ,
Kathy Q. Cai,
Bryan Harris,
Michele Rhodes,
Denise C. Connolly,
Joseph R. Testa,
David L. Wiest
,
Kathy Q. Cai,
Bryan Harris,
Michele Rhodes,
Denise C. Connolly,
Joseph R. Testa,
David L. Wiest
RPL22L1 induction in colorectal cancer is associated with poor prognosis and 5-FU resistance
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2016
Amos J. Simon,
Atar Lev,
Yong Zhang,
Batia Weiss,
Anna Rylova,
Eran Eyal,
Nitzan Kol,
Ortal Barel ,
Keren Cesarkas,
Michalle Soudack ,
Noa Greenberg-Kushnir ,
Michele Rhodes,
David L. Wiest ,
Ginette Schiby,
Iris Barshack
and 18 other authors
,
Keren Cesarkas,
Michalle Soudack ,
Noa Greenberg-Kushnir ,
Michele Rhodes,
David L. Wiest ,
Ginette Schiby,
Iris Barshack
and 18 other authors
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects
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