A citation-based method for searching scientific literature

Stress and interferon signalling-mediated apoptosis contributes to pleiotropic anticancer responses induced by targeting NGLY1.
Ashwini Zolekar, Victor J T Lin, Nigam M Mishra, Yin Ying Ho, Hamed S Hayatshahi, Abhishek Parab, Rohit Sampat, Xiaoyan Liao, Peter Hoffmann, Jin Liu, Kyle A Emmitte, Yu-Chieh Wang. Br J Cancer 2018
Times Cited: 9






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List of co-cited articles
67 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Inhibition of NGLY1 Inactivates the Transcription Factor Nrf1 and Potentiates Proteasome Inhibitor Cytotoxicity.
Frederick M Tomlin, Ulla I M Gerling-Driessen, Yi-Chang Liu, Ryan A Flynn, Janakiram R Vangala, Christian S Lentz, Sandra Clauder-Muenster, Petra Jakob, William F Mueller, Diana Ordoñez-Rueda,[...]. ACS Cent Sci 2017
80
6
66

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.
Gregory M Enns, Vandana Shashi, Matthew Bainbridge, Michael J Gambello, Farah R Zahir, Thomas Bast, Rebecca Crimian, Kelly Schoch, Julia Platt, Rachel Cox,[...]. Genet Med 2014
127
6
66

Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation.
Christina Lam, Carlos Ferreira, Donna Krasnewich, Camilo Toro, Lea Latham, Wadih M Zein, Tanya Lehky, Carmen Brewer, Eva H Baker, Audrey Thurm,[...]. Genet Med 2017
72
6
66

Lethality of mice bearing a knockout of the Ngly1-gene is partially rescued by the additional deletion of the Engase gene.
Haruhiko Fujihira, Yuki Masahara-Negishi, Masaru Tamura, Chengcheng Huang, Yoichiro Harada, Shigeharu Wakana, Daisuke Takakura, Nana Kawasaki, Naoyuki Taniguchi, Gen Kondoh,[...]. PLoS Genet 2017
43
6
66

Drug screens of NGLY1 deficiency in worm and fly models reveal catecholamine, NRF2 and anti-inflammatory-pathway activation as potential clinical approaches.
Sangeetha Iyer, Joshua D Mast, Hillary Tsang, Tamy P Rodriguez, Nina DiPrimio, Madeleine Prangley, Feba S Sam, Zachary Parton, Ethan O Perlstein. Dis Model Mech 2019
9
5
55

Proteasome dysfunction triggers activation of SKN-1A/Nrf1 by the aspartic protease DDI-1.
Nicolas J Lehrbach, Gary Ruvkun. Elife 2016
110
5
55

Endo-β-N-acetylglucosaminidase forms N-GlcNAc protein aggregates during ER-associated degradation in Ngly1-defective cells.
Chengcheng Huang, Yoichiro Harada, Akira Hosomi, Yuki Masahara-Negishi, Junichi Seino, Haruhiko Fujihira, Yoko Funakoshi, Takehiro Suzuki, Naoshi Dohmae, Tadashi Suzuki. Proc Natl Acad Sci U S A 2015
67
5
55

Clinical application of exome sequencing in undiagnosed genetic conditions.
Anna C Need, Vandana Shashi, Yuki Hitomi, Kelly Schoch, Kevin V Shianna, Marie T McDonald, Miriam H Meisler, David B Goldstein. J Med Genet 2012
287
5
55

Transcriptome and functional analysis in a Drosophila model of NGLY1 deficiency provides insight into therapeutic approaches.
Katie G Owings, Joshua B Lowry, Yiling Bi, Matthew Might, Clement Y Chow. Hum Mol Genet 2018
34
5
55

N-glycanase NGLY1 regulates mitochondrial homeostasis and inflammation through NRF1.
Kun Yang, Ryan Huang, Haruhiko Fujihira, Tadashi Suzuki, Nan Yan. J Exp Med 2018
55
4
44

NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy.
Ahmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, Yesim Parman, Hande Kaymakçalan, Gozde Tugce Akgumus, Caner Caglar, Duygu Dolen, Emine Zeynep Erson-Omay, Akdes Serin Harmanci,[...]. Eur J Med Genet 2015
53
4
44

Protein Sequence Editing of SKN-1A/Nrf1 by Peptide:N-Glycanase Controls Proteasome Gene Expression.
Nicolas J Lehrbach, Peter C Breen, Gary Ruvkun. Cell 2019
47
4
44

The cytoplasmic peptide:N-glycanase (NGLY1) - Structure, expression and cellular functions.
Tadashi Suzuki, Chengcheng Huang, Haruhiko Fujihira. Gene 2016
60
4
44

Regulation of BMP4/Dpp retrotranslocation and signaling by deglycosylation.
Antonio Galeone, Joshua M Adams, Shinya Matsuda, Maximiliano F Presa, Ashutosh Pandey, Seung Yeop Han, Yuriko Tachida, Hiroto Hirayama, Thomas Vaccari, Tadashi Suzuki,[...]. Elife 2020
14
4
44

Ngly1 -/- rats develop neurodegenerative phenotypes and pathological abnormalities in their peripheral and central nervous systems.
Makoto Asahina, Reiko Fujinawa, Sayuri Nakamura, Kotaro Yokoyama, Ryuichi Tozawa, Tadashi Suzuki. Hum Mol Genet 2020
16
4
44

Tissue-specific regulation of BMP signaling by Drosophila N-glycanase 1.
Antonio Galeone, Seung Yeop Han, Chengcheng Huang, Akira Hosomi, Tadashi Suzuki, Hamed Jafar-Nejad. Elife 2017
23
4
44

Unexplained death in patients with NGLY1 mutations may be explained by adrenal insufficiency.
Britt J van Keulen, Joost Rotteveel, Martijn J J Finken. Physiol Rep 2019
16
3
33

Transcription factor Nrf1 mediates the proteasome recovery pathway after proteasome inhibition in mammalian cells.
Senthil K Radhakrishnan, Candy S Lee, Patrick Young, Anne Beskow, Jefferson Y Chan, Raymond J Deshaies. Mol Cell 2010
323
3
33

Multi-systemic involvement in NGLY1-related disorder caused by two novel mutations.
Jennifer Heeley, Marwan Shinawi. Am J Med Genet A 2015
35
3
33

Mitochondrial function requires NGLY1.
Jianping Kong, Min Peng, Julian Ostrovsky, Young Joon Kwon, Olga Oretsky, Elizabeth M McCormick, Miao He, Yair Argon, Marni J Falk. Mitochondrion 2018
29
3
33

N-Glycanase 1 Transcriptionally Regulates Aquaporins Independent of Its Enzymatic Activity.
Mitali A Tambe, Bobby G Ng, Hudson H Freeze. Cell Rep 2019
18
3
33

Cytosolic N-GlcNAc proteins are formed by the action of endo-β-N-acetylglucosaminidase.
Jason C Maynard, Haruhiko Fujihira, Gabby E Dolgonos, Tadashi Suzuki, Alma L Burlingame. Biochem Biophys Res Commun 2020
12
3
33

Identification of PNGase-dependent ERAD substrates in Saccharomyces cerevisiae.
Akira Hosomi, Mika Fujita, Azusa Tomioka, Hiroyuki Kaji, Tadashi Suzuki. Biochem J 2016
10
3
33

Repurposing of Proton Pump Inhibitors as first identified small molecule inhibitors of endo-β-N-acetylglucosaminidase (ENGase) for the treatment of NGLY1 deficiency, a rare genetic disease.
Yiling Bi, Matthew Might, Hariprasad Vankayalapati, Balagurunathan Kuberan. Bioorg Med Chem Lett 2017
23
3
33

Evidence for an essential deglycosylation-independent activity of PNGase in Drosophila melanogaster.
Yoko Funakoshi, Yuki Negishi, J Peter Gergen, Junichi Seino, Kumiko Ishii, William J Lennarz, Ichiro Matsuo, Yukishige Ito, Naoyuki Taniguchi, Tadashi Suzuki. PLoS One 2010
30
3
33

Defects in the Neuroendocrine Axis Contribute to Global Development Delay in a Drosophila Model of NGLY1 Deficiency.
Tamy Portillo Rodriguez, Joshua D Mast, Tom Hartl, Tom Lee, Peter Sand, Ethan O Perlstein. G3 (Bethesda) 2018
16
3
33

A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
7202
2
22

Deglycosylation-dependent fluorescent proteins provide unique tools for the study of ER-associated degradation.
Jeff E Grotzke, Qiao Lu, Peter Cresswell. Proc Natl Acad Sci U S A 2013
35
2
22

Antioxidants enhance mammalian proteasome expression through the Keap1-Nrf2 signaling pathway.
Mi-Kyoung Kwak, Nobunao Wakabayashi, Jennifer L Greenlaw, Masayuki Yamamoto, Thomas W Kensler. Mol Cell Biol 2003
354
2
22

The aspartyl protease DDI2 activates Nrf1 to compensate for proteasome dysfunction.
Shun Koizumi, Taro Irie, Shoshiro Hirayama, Yasuyuki Sakurai, Hideki Yashiroda, Isao Naguro, Hidenori Ichijo, Jun Hamazaki, Shigeo Murata. Elife 2016
91
2
22

The Png1-Rad23 complex regulates glycoprotein turnover.
Ikjin Kim, Jungmi Ahn, Chang Liu, Kaori Tanabe, Jennifer Apodaca, Tadashi Suzuki, Hai Rao. J Cell Biol 2006
101
2
22

Loss of nuclear factor E2-related factor 1 in the brain leads to dysregulation of proteasome gene expression and neurodegeneration.
Candy S Lee, Chiashan Lee, Terry Hu, Janice M Nguyen, Jiasheng Zhang, Maureen V Martin, Marquis P Vawter, Eric J Huang, Jefferson Y Chan. Proc Natl Acad Sci U S A 2011
102
2
22

N-linked glycosylation does not impair proteasomal degradation but affects class I major histocompatibility complex presentation.
Edith Kario, Boaz Tirosh, Hidde L Ploegh, Ami Navon. J Biol Chem 2008
35
2
22

Using a small molecule inhibitor of peptide: N-glycanase to probe its role in glycoprotein turnover.
Shahram Misaghi, Michael E Pacold, Daniël Blom, Hidde L Ploegh, Gregory Alan Korbel. Chem Biol 2004
94
2
22

A role for N-glycanase in the cytosolic turnover of glycoproteins.
Christian Hirsch, Daniël Blom, Hidde L Ploegh. EMBO J 2003
161
2
22

A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts.
Ping He, Jeff E Grotzke, Bobby G Ng, Murat Gunel, Hamed Jafar-Nejad, Peter Cresswell, Gregory M Enns, Hudson H Freeze. Glycobiology 2015
25
2
22

The retrotranslocation protein Derlin-1 binds peptide:N-glycanase to the endoplasmic reticulum.
Samiksha Katiyar, Shivanjali Joshi, William J Lennarz. Mol Biol Cell 2005
48
2
22

Central nervous system-specific deletion of transcription factor Nrf1 causes progressive motor neuronal dysfunction.
Akira Kobayashi, Takako Tsukide, Tomohiro Miyasaka, Tomoko Morita, Tatsuya Mizoroki, Yoshiro Saito, Yasuo Ihara, Akihiko Takashima, Noriko Noguchi, Akiyoshi Fukamizu,[...]. Genes Cells 2011
62
2
22

Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency.
Patricia L Hall, Christina Lam, John J Alexander, Ghazia Asif, Gerard T Berry, Carlos Ferreira, Hudson H Freeze, William A Gahl, Kim K Nickander, Jon D Sharer,[...]. Mol Genet Metab 2018
16
2
22

Potent ectopic bone-inducing activity of bone morphogenetic protein-4/7 heterodimer.
A Aono, M Hazama, K Notoya, S Taketomi, H Yamasaki, R Tsukuda, S Sasaki, Y Fujisawa. Biochem Biophys Res Commun 1995
204
2
22

Bone morphogenetic proteins: a critical review.
Beth Bragdon, Oleksandra Moseychuk, Sven Saldanha, Daniel King, Joanne Julian, Anja Nohe. Cell Signal 2011
419
2
22

Stress-activated cap'n'collar transcription factors in aging and human disease.
Gerasimos P Sykiotis, Dirk Bohmann. Sci Signal 2010
526
2
22

Type I receptor binding of bone morphogenetic protein 6 is dependent on N-glycosylation of the ligand.
Stefan Saremba, Joachim Nickel, Axel Seher, Alexander Kotzsch, Walter Sebald, Thomas D Mueller. FEBS J 2008
71
2
22

A conserved role for AMP-activated protein kinase in NGLY1 deficiency.
Seung Yeop Han, Ashutosh Pandey, Tereza Moore, Antonio Galeone, Lita Duraine, Tina M Cowan, Hamed Jafar-Nejad. PLoS Genet 2020
11
2
22

A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency.
Dana M Talsness, Katie G Owings, Emily Coelho, Gaelle Mercenne, John M Pleinis, Raghavendran Partha, Kevin A Hope, Aamir R Zuberi, Nathan L Clark, Cathleen M Lutz,[...]. Elife 2020
10
2
22

A Drosophila growth factor homolog, decapentaplegic, regulates homeotic gene expression within and across germ layers during midgut morphogenesis.
G E Panganiban, R Reuter, M P Scott, F M Hoffmann. Development 1990
225
2
22

JF1/B6F1 Ngly1-/- mouse as an isogenic animal model of NGLY1 deficiency.
Makoto Asahina, Reiko Fujinawa, Haruhiko Fujihira, Yuki Masahara-Negishi, Tomohiro Andou, Ryuichi Tozawa, Tadashi Suzuki. Proc Jpn Acad Ser B Phys Biol Sci 2021
8
2
25

Bone Morphogenetic Protein (BMP) signaling in development and human diseases.
Richard N Wang, Jordan Green, Zhongliang Wang, Youlin Deng, Min Qiao, Michael Peabody, Qian Zhang, Jixing Ye, Zhengjian Yan, Sahitya Denduluri,[...]. Genes Dis 2014
503
2
22

Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry.
Eli M Cahan, Steven L Frick. Orphanet J Rare Dis 2019
14
2
22

The Na-K-Cl cotransporter of secretory epithelia.
M Haas, B Forbush. Annu Rev Physiol 2000
303
2
22


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.

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