A citation-based method for searching scientific literature

Charles K Abrams, Alejandro Peinado, Rola Mahmoud, Matan Bocarsly, Han Zhang, Paul Chang, Wesley M Botello-Smith, Mona M Freidin, Yun Luo. Am J Physiol Cell Physiol 2018
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine.
Noah A Levit, Caterina Sellitto, Hong-Zhan Wang, Leping Li, Miduturu Srinivas, Peter R Brink, Thomas W White. J Invest Dermatol 2015
19
100

The connexin 46 mutant (V44M) impairs gap junction function causing congenital cataract.
Lijuan Chen, Dongmei Su, Sijia Li, Lina Guan, Cuige Shi, Dianjun Li, Shanshan Hu, Xu Ma. J Genet 2017
2
100

A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death.
Jennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, Gladys H M R Brouns, Jos L V Broers, Barry J Coull, Vincent Oji, Michel van Geel, Maurice A M van Steensel, Patricia E Martin. Exp Dermatol 2019
7
100

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
William A Paznekas, Barbara Karczeski, Sascha Vermeer, R Brian Lowry, Martin Delatycki, Faivre Laurence, Pasi A Koivisto, Lionel Van Maldergem, Simeon A Boyadjiev, Joann N Bodurtha,[...]. Hum Mutat 2009
190
100

Targeted Proteomics-Based Quantitative Protein Atlas of Pannexin and Connexin Subtypes in Mouse and Human Tissues and Cancer Cell Lines.
Masanori Tachikawa, Yosuke Kaneko, Sumio Ohtsuki, Yasuo Uchida, Michitoshi Watanabe, Hideo Ohtsuka, Tetsuya Terasaki. J Pharm Sci 2020
5
100

Cat-Map: putting cataract on the map.
Alan Shiels, Thomas M Bennett, J Fielding Hejtmancik. Mol Vis 2010
188
100

Connexin-caused genetic diseases and corresponding mouse models.
Radoslaw Dobrowolski, Klaus Willecke. Antioxid Redox Signal 2009
95
100

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Ann M Flenniken, Lucy R Osborne, Nicole Anderson, Nadia Ciliberti, Craig Fleming, Joanne E I Gittens, Xiang-Qun Gong, Lois B Kelsey, Crystal Lounsbury, Luisa Moreno,[...]. Development 2005
187
100


Chemical chaperone treatment improves levels and distributions of connexins in Cx50D47A mouse lenses.
Oscar Jara, Peter J Minogue, Viviana M Berthoud, Eric C Beyer. Exp Eye Res 2018
5
100

The connexin 43 C-terminus: A tail of many tales.
Edward Leithe, Marc Mesnil, Trond Aasen. Biochim Biophys Acta Biomembr 2018
91
100

Focus on lens connexins.
Viviana M Berthoud, Anaclet Ngezahayo. BMC Cell Biol 2017
33
100

Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease.
Ruo-Gu Li, Ying-Jia Xu, Willy G Ye, Yan-Jie Li, Honghong Chen, Xing-Biao Qiu, Yi-Qing Yang, Donglin Bai. Heart Rhythm 2021
3
100

Connexin channels in congenital skin disorders.
Evelyn Lilly, Caterina Sellitto, Leonard M Milstone, Thomas W White. Semin Cell Dev Biol 2016
39
100

From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.
Isaac E García, Felicitas Bosen, Paula Mujica, Amaury Pupo, Carolina Flores-Muñoz, Oscar Jara, Carlos González, Klaus Willecke, Agustín D Martínez. J Invest Dermatol 2016
31
100


Phosphorylation regulates connexin43/ZO-1 binding and release, an important step in gap junction turnover.
Anastasia F Thévenin, Rachel A Margraf, Charles G Fisher, Rachael M Kells-Andrews, Matthias M Falk. Mol Biol Cell 2017
25
100

Gap junction remodeling in skin repair following wounding and disease.
Jared M Churko, Dale W Laird. Physiology (Bethesda) 2013
42
100


Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.
Akiko Seki, Taisuke Ishikawa, Xavier Daumy, Hiroyuki Mishima, Julien Barc, Ryo Sasaki, Kiyomasa Nishii, Kayoko Saito, Mari Urano, Seiko Ohno,[...]. J Am Coll Cardiol 2017
14
100

Dynamic UTR Usage Regulates Alternative Translation to Modulate Gap Junction Formation during Stress and Aging.
Michael J Zeitz, Patrick J Calhoun, Carissa C James, Thomas Taetzsch, Kijana K George, Stefanie Robel, Gregorio Valdez, James W Smyth. Cell Rep 2019
9
100

Atrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel function.
Yiguo Sun, Matthew D Hills, Willy G Ye, Xiaoling Tong, Donglin Bai. PLoS One 2014
19
100

Systematic review of CMTX1 patients with episodic neurological dysfunction.
Dandan Tian, Yating Zhao, Ruixia Zhu, Qu Li, Xu Liu. Ann Clin Transl Neurol 2021
2
100

The Cataract-linked Mutant Connexin50D47A Causes Endoplasmic Reticulum Stress in Mouse Lenses.
Viviana M Berthoud, Peter J Minogue, Paul A Lambert, Joseph I Snabb, Eric C Beyer. J Biol Chem 2016
18
100

Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia.
Nellie Kalcheva, Jiaxiang Qu, Nefthi Sandeep, Luis Garcia, Jie Zhang, Zhiyong Wang, Paul D Lampe, Sylvia O Suadicani, David C Spray, Glenn I Fishman. Proc Natl Acad Sci U S A 2007
96
100

Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.
Junko Shibayama, William Paznekas, Akiko Seki, Steven Taffet, Ethylin Wang Jabs, Mario Delmar, Hassan Musa. Circ Res 2005
87
100


Intracellular trafficking pathways of Cx43 gap junction channels.
Irina Epifantseva, Robin M Shaw. Biochim Biophys Acta Biomembr 2018
49
100

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation.
Michael H Gollob, Douglas L Jones, Andrew D Krahn, Lynne Danis, Xiang-Qun Gong, Qing Shao, Xiaoqin Liu, John P Veinot, Anthony S L Tang, Alexandre F R Stewart,[...]. N Engl J Med 2006
358
100

Mice harbouring an oculodentodigital dysplasia-linked Cx43 G60S mutation have severe hearing loss.
Julia M Abitbol, John J Kelly, Kevin J Barr, Brian L Allman, Dale W Laird. J Cell Sci 2018
7
100

Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel Properties.
Zunaira Shuja, Leping Li, Shashank Gupta, Gülistan Meşe, Thomas W White. J Invest Dermatol 2016
35
100

Mechanisms linking connexin mutations to human diseases.
John J Kelly, Jamie Simek, Dale W Laird. Cell Tissue Res 2015
57
100


Cataract-associated connexin 46 mutation alters its interaction with calmodulin and function of hemichannels.
Zhengping Hu, Manuel A Riquelme, Bin Wang, Vladislav Bugay, Robert Brenner, Sumin Gu, Jean X Jiang. J Biol Chem 2018
11
100

Electrical coupling and its channels.
Andrew L Harris. J Gen Physiol 2018
9
100

The severity of mammary gland developmental defects is linked to the overall functional status of Cx43 as revealed by genetically modified mice.
Michael K G Stewart, Xiang-Qun Gong, Kevin J Barr, Donglin Bai, Glenn I Fishman, Dale W Laird. Biochem J 2013
34
100

Spatio-temporal regulation of connexin43 phosphorylation and gap junction dynamics.
Joell L Solan, Paul D Lampe. Biochim Biophys Acta Biomembr 2018
64
100

Diseases of connexins expressed in myelinating glia.
Charles K Abrams. Neurosci Lett 2019
8
100


Active cochlear amplification is dependent on supporting cell gap junctions.
Yan Zhu, Chun Liang, Jin Chen, Liang Zong, Guang-Di Chen, Hong-Bo Zhao. Nat Commun 2013
47
100

Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1).
Francis B Panosyan, Matilde Laura, Alexander M Rossor, Chiara Pisciotta, Giuseppe Piscosquito, Joshua Burns, Jun Li, Sabrina W Yum, Richard A Lewis, John Day,[...]. Neurology 2017
23
100

Myogenic bladder defects in mouse models of human oculodentodigital dysplasia.
Tao Huang, Qing Shao, Kevin Barr, Jamie Simek, Glenn I Fishman, Dale W Laird. Biochem J 2014
11
100

Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease.
Andrea Carrer, Alessandro Leparulo, Giulia Crispino, Catalin Dacian Ciubotaru, Oriano Marin, Francesco Zonta, Mario Bortolozzi. Hum Mol Genet 2018
13
100

Connexins in Cardiovascular and Neurovascular Health and Disease: Pharmacological Implications.
Luc Leybaert, Paul D Lampe, Stefan Dhein, Brenda R Kwak, Peter Ferdinandy, Eric C Beyer, Dale W Laird, Christian C Naus, Colin R Green, Rainer Schulz. Pharmacol Rev 2017
124
100

Connexin43 mutations linked to skin disease have augmented hemichannel activity.
Miduturu Srinivas, Thomas F Jannace, Anthony G Cocozzelli, Leping Li, Nefeli Slavi, Caterina Sellitto, Thomas W White. Sci Rep 2019
19
100

Role of Connexin-Based Gap Junction Channels in Communication of Myelin Sheath in Schwann Cells.
Bruno A Cisterna, Pablo Arroyo, Carlos Puebla. Front Cell Neurosci 2019
8
100

Gap junctions and cancer: communicating for 50 years.
Trond Aasen, Marc Mesnil, Christian C Naus, Paul D Lampe, Dale W Laird. Nat Rev Cancer 2017
26
100

GJC2 missense mutations cause human lymphedema.
Robert E Ferrell, Catherine J Baty, Mark A Kimak, Jenny M Karlsson, Elizabeth C Lawrence, Marlise Franke-Snyder, Stephen D Meriney, Eleanor Feingold, David N Finegold. Am J Hum Genet 2010
93
100

Connexin 43 and Mitochondria in Cardiovascular Health and Disease.
Kerstin Boengler, Rainer Schulz. Adv Exp Med Biol 2017
46
100

Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants.
Mahmoud Noureldin, Honghong Chen, Donglin Bai. Int J Mol Sci 2018
10
100


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.