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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Osmotic stress‐induced phosphorylation by NLK at Ser128 activates YAP
Audrey W. Hong, Zhipeng Meng, Hai‐Xin Yuan, et al.
EMBO Reports (2016) Vol. 18, Iss. 1, pp. 72-86
Open Access | Times Cited: 139

Showing 1-25 of 139 citing articles:

The Hippo Pathway: Biology and Pathophysiology
Shenghong Ma, Zhipeng Meng, Rui Chen, et al.
Annual Review of Biochemistry (2018) Vol. 88, Iss. 1, pp. 577-604
Closed Access | Times Cited: 1042
Hippo–YAP/TAZ signalling in organ regeneration and regenerative medicine
Iván M. Moya, Georg Halder
Nature Reviews Molecular Cell Biology (2018) Vol. 20, Iss. 4, pp. 211-226
Closed Access | Times Cited: 758
The Hippo Signaling Pathway in Development and Disease
Yonggang Zheng, Duojia Pan
Developmental Cell (2019) Vol. 50, Iss. 3, pp. 264-282
Open Access | Times Cited: 720
Long noncoding RNA GAS5 inhibits progression of colorectal cancer by interacting with and triggering YAP phosphorylation and degradation and is negatively regulated by the m6A reader YTHDF3
Wen Ni, Su Yao, Yunxia Zhou, et al.
Molecular Cancer (2019) Vol. 18, Iss. 1
Open Access | Times Cited: 491
The Hippo Signaling Network and Its Biological Functions
Jyoti R. Misra, Kenneth D. Irvine
Annual Review of Genetics (2018) Vol. 52, Iss. 1, pp. 65-87
Open Access | Times Cited: 400
Interplay between YAP/TAZ and Metabolism
Ja Hyun Koo, Kun‐Liang Guan
Cell Metabolism (2018) Vol. 28, Iss. 2, pp. 196-206
Open Access | Times Cited: 352
The Hippo signalling pathway and its implications in human health and diseases
Minyang Fu, Yuan Hu, Tianxia Lan, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 332
Phase separation of YAP reorganizes genome topology for long-term YAP target gene expression
Danfeng Cai, Daniel Feliciano, Peng Dong, et al.
Nature Cell Biology (2019) Vol. 21, Iss. 12, pp. 1578-1589
Open Access | Times Cited: 325
Regulation of the Hippo Pathway Transcription Factor TEAD
Kimberly C. Lin, Hyun Woo Park, Kun‐Liang Guan
Trends in Biochemical Sciences (2017) Vol. 42, Iss. 11, pp. 862-872
Open Access | Times Cited: 274
Regulation of TEAD Transcription Factors in Cancer Biology
Hyunbin D. Huh, Dong Yeop Kim, Han-Sol Jeong, et al.
Cells (2019) Vol. 8, Iss. 6, pp. 600-600
Open Access | Times Cited: 215
The Hippo Pathway, YAP/TAZ, and the Plasma Membrane
Valentina Rausch, Carsten Gram Hansen
Trends in Cell Biology (2019) Vol. 30, Iss. 1, pp. 32-48
Open Access | Times Cited: 212
The Role of Hippo Pathway in Cancer Stem Cell Biology.
Jae Hyung Park, Ji Eun Shin, Hyun Woo Park
PubMed (2018) Vol. 41, Iss. 2, pp. 83-92
Closed Access | Times Cited: 192
Regulation of Hippo pathway transcription factor TEAD by p38 MAPK-induced cytoplasmic translocation
Kimberly C. Lin, Toshiro Moroishi, Zhipeng Meng, et al.
Nature Cell Biology (2017) Vol. 19, Iss. 8, pp. 996-1002
Open Access | Times Cited: 182
Hippo signalling in the liver: role in development, regeneration and disease
Jacquelyn O. Russell, Fernando D. Camargo
Nature Reviews Gastroenterology & Hepatology (2022) Vol. 19, Iss. 5, pp. 297-312
Open Access | Times Cited: 128
Insights into recent findings and clinical application of YAP and TAZ in cancer
James Franklin, ZhengMing Wu, Kun‐Liang Guan
Nature reviews. Cancer (2023) Vol. 23, Iss. 8, pp. 512-525
Closed Access | Times Cited: 110
The Hippo signaling pathway in development and regeneration
Zhenxing Zhong, Zhihan Jiao, Fa‐Xing Yu
Cell Reports (2024) Vol. 43, Iss. 3, pp. 113926-113926
Open Access | Times Cited: 53
When Phased without Water: Biophysics of Cellular Desiccation, from Biomolecules to Condensates
Paulette S. Romero-Pérez, Yanniv Dorone, Eduardo Flores, et al.
Chemical Reviews (2023) Vol. 123, Iss. 14, pp. 9010-9035
Open Access | Times Cited: 43
Phosphorylation by NLK inhibits YAP ‐14‐3‐3‐interactions and induces its nuclear localization
Sungho Moon, Wantae Kim, So Young Kim, et al.
EMBO Reports (2016) Vol. 18, Iss. 1, pp. 61-71
Open Access | Times Cited: 149
SET1A-Mediated Mono-Methylation at K342 Regulates YAP Activation by Blocking Its Nuclear Export and Promotes Tumorigenesis
Lan Fang, Hongqi Teng, Yilin Wang, et al.
Cancer Cell (2018) Vol. 34, Iss. 1, pp. 103-118.e9
Open Access | Times Cited: 146
A LATS biosensor screen identifies VEGFR as a regulator of the Hippo pathway in angiogenesis
Taha Azad, Helena J. Janse van Rensburg, Elizabeth D. Lightbody, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 141
Integration of Hippo-YAP Signaling with Metabolism
Consuelo Ibar, Kenneth D. Irvine
Developmental Cell (2020) Vol. 54, Iss. 2, pp. 256-267
Open Access | Times Cited: 120
Laminar flow inhibits the Hippo/YAP pathway via autophagy and SIRT1-mediated deacetylation against atherosclerosis
Ping Yuan, Hu Q, Xuemei He, et al.
Cell Death and Disease (2020) Vol. 11, Iss. 2
Open Access | Times Cited: 96
RASSF1A uncouples Wnt from Hippo signalling and promotes YAP mediated differentiation via p73
Angelos Papaspyropoulos, Leanne Bradley, Asmita Thapa, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 89
The Hippo Pathway in Prostate Cancer
Omar Salem, Carsten Gram Hansen
Cells (2019) Vol. 8, Iss. 4, pp. 370-370
Open Access | Times Cited: 86
GPCR-Hippo Signaling in Cancer
Jiaqian Luo, Fa‐Xing Yu
Cells (2019) Vol. 8, Iss. 5, pp. 426-426
Open Access | Times Cited: 83
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