Molecular and structural characterization of a TEAD mutation at the origin of Sveinsson's chorioretinal atrophy-Reference-Cited by-同舟云学术

Molecular and structural characterization of a TEAD mutation at the origin of Sveinsson's chorioretinal atrophy

Published:2019-04-11 Issue:12 Volume:286 Page:2381-2398
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:FEBS J

Author:

Bokhovchuk Fedir¹,Mesrouze Yannick¹,Izaac Aude²,Meyerhofer Marco¹,Zimmermann Catherine¹,Fontana Patrizia¹,Schmelzle Tobias¹,Erdmann Dirk¹,Furet Pascal³,Kallen Joerg²,Chène Patrick¹

Affiliation:

1. Disease Area Oncology Novartis Institutes for Biomedical Research Basel Switzerland

2. Chemical Biology & Therapeutics Novartis Institutes for Biomedical Research Basel Switzerland

3. Global Discovery Chemistry Novartis Institutes for Biomedical Research Basel Switzerland

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.14817

Reference44 articles.

1. Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer

2. The Hippo pathway in cellular reprogramming and regeneration of different organs

3. Mechanisms of Hippo pathway regulation

4. The TEAD Family and Its Oncogenic Role in Promoting Tumorigenesis

5. Quit your YAPing: a new target for cancer therapy: Figure 1.

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