Discovery of selective activators of PRC2 mutant EED-I363M

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Discovery of selective activators of PRC2 mutant EED-I363M ; volume:9 ; number:1 ; day:25 ; month:4 ; year:2019 ; pages:1-10 ; date:12.2019
Scientific reports ; 9, Heft 1 (25.4.2019), 1-10, 12.2019

Classification: Naturwissenschaften

Creator: Suh, Junghyun L.
Barnash, Kimberly D.
Abramyan, Tigran M.
Li, Fengling
The, Juliana
Engelberg, Isabelle A.
Vedadi, Masoud
Brown, Peter J.
Kireev, Dmitri B.
Arrowsmith, Cheryl H.
James, Lindsey I.
Frye, Stephen V.

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-019-43005-z

URN: urn:nbn:de:101:1-2019051611340973104508

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:53 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Suh, Junghyun L.
Barnash, Kimberly D.
Abramyan, Tigran M.
Li, Fengling
The, Juliana
Engelberg, Isabelle A.
Vedadi, Masoud
Brown, Peter J.
Kireev, Dmitri B.
Arrowsmith, Cheryl H.
James, Lindsey I.
Frye, Stephen V.
SpringerLink (Online service)

Other Objects (12)

Hochschulschrift

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Hochschulschrift

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Hochschulschrift

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Discovery of selective activators of PRC2 mutant EED-I363M

Object Details

References and Relationships

Classification and Topics

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Small molecule discovery for signaling research - NLRP3 inflammasome activators

Quantitative Comparison of HSF1 Activators

Discovery of novel cardiac troponin activators using fluorescence polarization-based high throughput screening assays

Establishing a yeast-based screening system for discovery of human GLUT5 inhibitors and activators

Discovery of the bacterial HslV protease activators as lead molecules with novel mode of action

Mutant-selective topologic conversion facilitates selective degradation of a pathogenic prion isoform

Machine Learning‐Driven Discovery of Structurally Related Natural Products as Activators of the Cardiac Calcium Pump SERCA2a

Structure optimization of new tumor-selective Passerini α-acyloxy carboxamides as Caspase-3/7 activators

Formation and Structure of Hydrolytic Methylaluminoxane Activators

The esogetic crystal activators

Are Methylaluminoxane Activators Sheets?

Discovery and molecular basis of subtype-selective cyclophilin inhibitors

Related objects

Reset password