A citation-based method for searching scientific literature

Mahsa Motavaf, Xianhua Piao. Front Cell Neurosci 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity



Cerebral Spinal Fluid levels of Cytokines are elevated in Patients with Metachromatic Leukodystrophy.
Kathryn A Thibert, Gerald V Raymond, Jakub Tolar, Weston P Miller, Paul J Orchard, Troy C Lund. Sci Rep 2016
14
100

Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (ZO-1) in mouse brain.
X Li, A V Ionescu, B D Lynn, S Lu, N Kamasawa, M Morita, K G V Davidson, T Yasumura, J E Rash, J I Nagy. Neuroscience 2004
85
100

Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene.
Swee-Hee Wong, Wen-Hung Wang, Pin-Hua Chen, Shuan-Yow Li, Jiann-Jou Yang. Int J Med Sci 2017
3
100


Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43.
Wendi Roscoe, Gregory I L Veitch, Xiang-Qun Gong, Emily Pellegrino, Donglin Bai, Elizabeth McLachlan, Qing Shao, Gerald M Kidder, Dale W Laird. J Biol Chem 2005
96
100

Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.
Charles K Abrams, Mikhail Goman, Sarah Wong, Steven S Scherer, Kleopas A Kleopa, Alejandro Peinado, Mona M Freidin. Sci Rep 2017
14
100

Oligodendrocyte Development and Regenerative Therapeutics in Multiple Sclerosis.
Nadjet Gacem, Brahim Nait-Oumesmar. Life (Basel) 2021
2
100

Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.
Hung-Li Wang, Wen-Teng Chang, Tu-Hsueh Yeh, Tony Wu, Mei-Shin Chen, Ching-Yi Wu. Neurobiol Dis 2004
36
100



Systemic inflammation disrupts oligodendrocyte gap junctions and induces ER stress in a model of CNS manifestations of X-linked Charcot-Marie-Tooth disease.
Margarita Olympiou, Irene Sargiannidou, Kyriaki Markoullis, Christos Karaiskos, Alexia Kagiava, Styliana Kyriakoudi, Charles K Abrams, Kleopas A Kleopa. Acta Neuropathol Commun 2016
18
100


Myelination defects and neuronal hyperexcitability in the neocortex of connexin 32-deficient mice.
B Sutor, C Schmolke, B Teubner, C Schirmer, K Willecke. Cereb Cortex 2000
76
100


The molecular pathogenesis of Pelizaeus-Merzbacher disease.
J Garbern, F Cambi, M Shy, J Kamholz. Arch Neurol 1999
93
100

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease.
Jennifer L Orthmann-Murphy, Alan D Enriquez, Charles K Abrams, Steven S Scherer. Mol Cell Neurosci 2007
81
100

Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects.
Irene Sargiannidou, Natalie Vavlitou, Sophia Aristodemou, Andreas Hadjisavvas, Kyriacos Kyriacou, Steven S Scherer, Kleopas A Kleopa. J Neurosci 2009
86
100

Central nervous system involvement in a novel connexin 32 mutation affecting identical twins.
W Marques, J G Sweeney, N W Wood, S J Wroe, W Marques. J Neurol Neurosurg Psychiatry 1999
28
100


Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant connexin 32 (GJB1).
W Matsuyama, M Nakagawa, T Moritoyo, H Takashima, F Umehara, K Hirata, M Suehara, M Osame. J Hum Genet 2001
28
100

Molecular mechanisms of inherited demyelinating neuropathies.
Steven S Scherer, Lawrence Wrabetz. Glia 2008
120
100

Four classes of intercellular channels between glial cells in the CNS.
Bruce M Altevogt, David L Paul. J Neurosci 2004
130
100

Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects.
Marie E Egan, Marilyn Pearson, Scott A Weiner, Vanathy Rajendran, Daniel Rubin, Judith Glöckner-Pagel, Susan Canny, Kai Du, Gergely L Lukacs, Michael J Caplan. Science 2004
394
100

Analysis of gap junction assembly using mutated connexins detected in Charcot-Marie-Tooth X-linked disease.
P E Martin, E T Mambetisaeva, D A Archer, C H George, W H Evans. J Neurochem 2000
57
100

Endoplasmic reticulum stress: cell life and death decisions.
Chunyan Xu, Beatrice Bailly-Maitre, John C Reed. J Clin Invest 2005
100


Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.
Mehrdad Khajavi, Kensuke Shiga, Wojciech Wiszniewski, Feng He, Chad A Shaw, Jiong Yan, Theodore G Wensel, G Jackson Snipes, James R Lupski. Am J Hum Genet 2007
100
100


Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes.
Kleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, David L Paul, Steven S Scherer. Glia 2004
91
100

Influence of the scaffolding protein Zonula Occludens (ZOs) on membrane channels.
Jean-Claude Hervé, Mickaël Derangeon, Denis Sarrouilhe, Nicolas Bourmeyster. Biochim Biophys Acta 2014
31
100


Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.
Oliver Tress, Marta Maglione, Armin Zlomuzica, Dennis May, Nikolai Dicke, Joachim Degen, Ekrem Dere, Helmut Kettenmann, Dieter Hartmann, Klaus Willecke. PLoS Genet 2011
54
100

Epithelial cell adhesion and the regulation of gene expression.
Maria S Balda, Karl Matter. Trends Cell Biol 2003
115
100

Recommendations from the INHAND Apoptosis/Necrosis Working Group.
Susan A Elmore, Darlene Dixon, James R Hailey, Takanori Harada, Ronald A Herbert, Robert R Maronpot, Thomas Nolte, Jerold E Rehg, Susanne Rittinghausen, Thomas J Rosol,[...]. Toxicol Pathol 2016
73
100

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
Jennifer L Orthmann-Murphy, Ettore Salsano, Charles K Abrams, Alberto Bizzi, Graziella Uziel, Mona M Freidin, Eleonora Lamantea, Massimo Zeviani, Steven S Scherer, Davide Pareyson. Brain 2009
91
100


Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct.
Meejin Ahn, Jonathan Lee, Andreas Gustafsson, Alan Enriquez, Eric Lancaster, Jai-Yoon Sul, Philip G Haydon, David L Paul, Yan Huang, Charles K Abrams,[...]. J Neurosci Res 2008
61
100

The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease.
Cherie M Southwood, James Garbern, Wei Jiang, Alexander Gow. Neuron 2002
210
100

Changes in object recognition and anxiety-like behaviour in mice expressing a Cx47 mutation that causes Pelizaeus-Merzbacher-like disease.
Armin Zlomuzica, Oliver Tress, Sonja Binder, Catherine Rovira, Klaus Willecke, Ekrem Dere. Dev Neurosci 2012
11
100

Dystroglycan promotes filopodial formation and process branching in differentiating oligodendroglia.
Christopher Eyermann, Kevin Czaplinski, Holly Colognato. J Neurochem 2012
35
100

Connections between cells of the developing squid as revealed by electrophysiological methods.
D D Potter, E J Furshpan, E S Lennox. Proc Natl Acad Sci U S A 1966
252
100

Neuronal connexin36 association with zonula occludens-1 protein (ZO-1) in mouse brain and interaction with the first PDZ domain of ZO-1.
Xinbo Li, Carl Olson, Shijun Lu, Naomi Kamasawa, Thomas Yasumura, John E Rash, James I Nagy. Eur J Neurosci 2004
111
100

LM and EM immunolocalization of the gap junctional protein connexin 43 in rat brain.
T Yamamoto, A Ochalski, E L Hertzberg, J I Nagy. Brain Res 1990
182
100

The ZO-1-associated Y-box factor ZONAB regulates epithelial cell proliferation and cell density.
Maria S Balda, Michelle D Garrett, Karl Matter. J Cell Biol 2003
282
100




Rapid and Specific Immunomagnetic Isolation of Mouse Primary Oligodendrocytes.
Rafael E Flores-Obando, Mona M Freidin, Charles K Abrams. J Vis Exp 2018
7
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.