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Amendments and Corrections | 15 February 2012
Correction: Corrigendum: Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors
- Alexander Adibekian
- , Brent R Martin
- , Chu Wang
- , Ku-Lung Hsu
- , Daniel A Bachovchin
- , Sherry Niessen
- , Heather Hoover
- & Benjamin F Cravatt
Nature Chemical Biology 8 , 318–318

Rights & permissionsfor article Correction: Corrigendum: Click-generated triazole ureas as ultrapotent <i>in vivo</i>–active serine hydrolase inhibitors . Opens in a new window.
Research | 18 September 2011
Metabolomics annotates ABHD3 as a physiologic regulator of medium-chain phospholipids
- Jonathan Z Long
- , Justin S Cisar
- , David Milliken
- , Sherry Niessen
- , Chu Wang
- , Sunia A Trauger
- , Gary Siuzdak
- & Benjamin F Cravatt
Nature Chemical Biology 7 , 763–765

Rights & permissionsfor article Metabolomics annotates ABHD3 as a physiologic regulator of medium-chain phospholipids . Opens in a new window.
Research | 23 August 2005
A streamlined platform for high-content functional proteomics of primary human specimens
- Nadim Jessani
- , Sherry Niessen
- , BinQing Q Wei
- , Monica Nicolau
- , Mark Humphrey
- , Youngran Ji
- , Wonshik Han
- , Dong-Young Noh
- , John R Yates III
- , Stefanie S Jeffrey
- & Benjamin F Cravatt
Nature Methods 2 , 691–697

Rights & permissionsfor article A streamlined platform for high-content functional proteomics of primary human specimens . Opens in a new window.
Research | 19 November 2006
Forward chemical genetic approach identifies new role for GAPDH in insulin signaling
- Jaeki Min
- , Yun Kyung Kim
- , Patricia G Cipriani
- , Mira Kang
- , Sonya M Khersonsky
- , Daniel P Walsh
- , Ji-Young Lee
- , Sherry Niessen
- , John R Yates III
- , Kristin Gunsalus
- , Fabio Piano
- & Young-Tae Chang
Nature Chemical Biology 3 , 55–59

Rights & permissionsfor article Forward chemical genetic approach identifies new role for GAPDH in insulin signaling . Opens in a new window.
Research | 11 October 2016 | Open
Chemoproteomic profiling reveals that cathepsin D off-target activity drives ocular toxicity of β-secretase inhibitors
- Andrea M. Zuhl
- , Charles E. Nolan
- , Michael A. Brodney
- , Sherry Niessen
- , Kevin Atchison
- , Christopher Houle
- , David A. Karanian
- , Claude Ambroise
- , Jeffrey W. Brulet
- , Elizabeth M. Beck
- , Shawn D. Doran
- , Brian T. O’Neill
- , Christopher W. am Ende
- , Cheng Chang
- , Kieran F. Geoghegan
- , Graham M. West
- , Joshua C. Judkins
- , Xinjun Hou
- , David R. Riddell
- & Douglas S. Johnson
Nature Communications 7 , 1–14

Rights & permissionsfor article Chemoproteomic profiling reveals that cathepsin D off-target activity drives ocular toxicity of β-secretase inhibitors . Opens in a new window.
Research | 22 December 2013
Integrated phenotypic and activity-based profiling links Ces3 to obesity and diabetes
- Eduardo Dominguez
- , Andrea Galmozzi
- , Jae Won Chang
- , Ku-Lung Hsu
- , Joanna Pawlak
- , Weiwei Li
- , Cristina Godio
- , Jason Thomas
- , David Partida
- , Sherry Niessen
- , Paul E O'Brien
- , Aaron P Russell
- , Matthew J Watt
- , Daniel K Nomura
- , Benjamin F Cravatt
- & Enrique Saez
Nature Chemical Biology 10 , 113–121

Rights & permissionsfor article Integrated phenotypic and activity-based profiling links Ces3 to obesity and diabetes . Opens in a new window.
Research | 13 July 2014
A road map to evaluate the proteome-wide selectivity of covalent kinase inhibitors
- Bryan R Lanning
- , Landon R Whitby
- , Melissa M Dix
- , John Douhan
- , Adam M Gilbert
- , Erik C Hett
- , Theodore O Johnson
- , Chris Joslyn
- , John C Kath
- , Sherry Niessen
- , Lee R Roberts
- , Mark E Schnute
- , Chu Wang
- , Jonathan J Hulce
- , Baoxian Wei
- , Laurence O Whiteley
- , Matthew M Hayward
- & Benjamin F Cravatt
Nature Chemical Biology 10 , 760–767

Rights & permissionsfor article A road map to evaluate the proteome-wide selectivity of covalent kinase inhibitors . Opens in a new window.
Research | 15 May 2011
Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors
- Alexander Adibekian
- , Brent R Martin
- , Chu Wang
- , Ku-Lung Hsu
- , Daniel A Bachovchin
- , Sherry Niessen
- , Heather Hoover
- & Benjamin F Cravatt
Nature Chemical Biology 7 , 469–478

Rights & permissionsfor article Click-generated triazole ureas as ultrapotent <i>in vivo</i>–active serine hydrolase inhibitors . Opens in a new window.
Research | 26 March 2006
Proteomic profiling of metalloprotease activities with cocktails of active-site probes
Nature Chemical Biology 2 , 274–281

Rights & permissionsfor article Proteomic profiling of metalloprotease activities with cocktails of active-site probes . Opens in a new window.

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Correction: Corrigendum: Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors

Metabolomics annotates ABHD3 as a physiologic regulator of medium-chain phospholipids

A streamlined platform for high-content functional proteomics of primary human specimens

Forward chemical genetic approach identifies new role for GAPDH in insulin signaling

Chemoproteomic profiling reveals that cathepsin D off-target activity drives ocular toxicity of β-secretase inhibitors

Integrated phenotypic and activity-based profiling links Ces3 to obesity and diabetes

A road map to evaluate the proteome-wide selectivity of covalent kinase inhibitors

Click-generated triazole ureas as ultrapotent in vivo–active serine hydrolase inhibitors

Proteomic profiling of metalloprotease activities with cocktails of active-site probes

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