A citation-based method for searching scientific literature

Maria L Sapar, Chun Han. J Genet Genomics 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


SARM1 activation triggers axon degeneration locally via NAD⁺ destruction.
Josiah Gerdts, E J Brace, Yo Sasaki, Aaron DiAntonio, Jeffrey Milbrandt. Science 2015
290
50

The Highwire ubiquitin ligase promotes axonal degeneration by tuning levels of Nmnat protein.
Xin Xiong, Yan Hao, Kan Sun, Jiaxing Li, Xia Li, Bibhudatta Mishra, Pushpanjali Soppina, Chunlai Wu, Richard I Hume, Catherine A Collins. PLoS Biol 2012
129
50

dSarm/Sarm1 is required for activation of an injury-induced axon death pathway.
Jeannette M Osterloh, Jing Yang, Timothy M Rooney, A Nicole Fox, Robert Adalbert, Eric H Powell, Amy E Sheehan, Michelle A Avery, Rachel Hackett, Mary A Logan,[...]. Science 2012
376
50

Axon Self-Destruction: New Links among SARM1, MAPKs, and NAD+ Metabolism.
Josiah Gerdts, Daniel W Summers, Jeffrey Milbrandt, Aaron DiAntonio. Neuron 2016
199
50


Axon Death Pathways Converge on Axundead to Promote Functional and Structural Axon Disassembly.
Lukas J Neukomm, Thomas C Burdett, Andrew M Seeds, Stefanie Hampel, Jaeda C Coutinho-Budd, Jonathan E Farley, Jack Wong, Yonca B Karadeniz, Jeannette M Osterloh, Amy E Sheehan,[...]. Neuron 2017
53
50

Transcription factor Pebbled/RREB1 regulates injury-induced axon degeneration.
Jonathan E Farley, Thomas C Burdett, Romina Barria, Lukas J Neukomm, Kevin P Kenna, John E Landers, Marc R Freeman. Proc Natl Acad Sci U S A 2018
27
50

A local mechanism mediates NAD-dependent protection of axon degeneration.
Jing Wang, Qiwei Zhai, Ying Chen, Estelle Lin, Wei Gu, Michael W McBurney, Zhigang He. J Cell Biol 2005
298
50

Wallerian degeneration of injured axons and synapses is delayed by a Ube4b/Nmnat chimeric gene.
T G Mack, M Reiner, B Beirowski, W Mi, M Emanuelli, D Wagner, D Thomson, T Gillingwater, F Court, L Conforti,[...]. Nat Neurosci 2001
467
50

Absence of SARM1 rescues development and survival of NMNAT2-deficient axons.
Jonathan Gilley, Giuseppe Orsomando, Isabel Nascimento-Ferreira, Michael P Coleman. Cell Rep 2015
104
50

NMNAT1 inhibits axon degeneration via blockade of SARM1-mediated NAD+ depletion.
Yo Sasaki, Takashi Nakagawa, Xianrong Mao, Aaron DiAntonio, Jeffrey Milbrandt. Elife 2016
117
50

Rapid in vivo forward genetic approach for identifying axon death genes in Drosophila.
Lukas J Neukomm, Thomas C Burdett, Michael A Gonzalez, Stephan Züchner, Marc R Freeman. Proc Natl Acad Sci U S A 2014
37
50

Phosphatidylserine recognition and induction of apoptotic cell clearance by Drosophila engulfment receptor Draper.
Tran Thanh Tung, Kaz Nagaosa, Yu Fujita, Asana Kita, Hiroki Mori, Ryo Okada, Saori Nonaka, Yoshinobu Nakanishi. J Biochem 2013
41
50

Epidermal cells are the primary phagocytes in the fragmentation and clearance of degenerating dendrites in Drosophila.
Chun Han, Yuanquan Song, Hui Xiao, Denan Wang, Nathalie C Franc, Lily Yeh Jan, Yuh-Nung Jan. Neuron 2014
87
50

Phosphatidylserine Externalization Results from and Causes Neurite Degeneration in Drosophila.
Maria L Sapar, Hui Ji, Bei Wang, Amy R Poe, Kush Dubey, Xingjie Ren, Jian-Quan Ni, Chun Han. Cell Rep 2018
37
50

Unwrapping glial biology: Gcm target genes regulating glial development, diversification, and function.
Marc R Freeman, Jeffrey Delrow, Junhyong Kim, Eric Johnson, Chris Q Doe. Neuron 2003
282
50

The Drosophila cell corpse engulfment receptor Draper mediates glial clearance of severed axons.
Jennifer M MacDonald, Margaret G Beach, Ermelinda Porpiglia, Amy E Sheehan, Ryan J Watts, Marc R Freeman. Neuron 2006
328
50

Mitochondria as a central sensor for axonal degenerative stimuli.
Felipe A Court, Michael P Coleman. Trends Neurosci 2012
138
25

Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration.
Toshiyuki Araki, Yo Sasaki, Jeffrey Milbrandt. Science 2004
829
25

An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model.
Kevin L Seburn, Leslie A Nangle, Gregory A Cox, Paul Schimmel, Robert W Burgess. Neuron 2006
153
25

The Wlds mutation delays robust loss of motor and sensory axons in a genetic model for myelin-related axonopathy.
Mohtashem Samsam, Weiqian Mi, Carsten Wessig, Jürgen Zielasek, Klaus V Toyka, Michael P Coleman, Rudolf Martini. J Neurosci 2003
121
25

The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management.
J Chad Hoyle, Michael C Isfort, Jennifer Roggenbuck, W David Arnold. Appl Clin Genet 2015
38
25

Nicotinamide Riboside Opposes Type 2 Diabetes and Neuropathy in Mice.
Samuel A J Trammell, Benjamin J Weidemann, Ankita Chadda, Matthew S Yorek, Amey Holmes, Lawrence J Coppey, Alexander Obrosov, Randy H Kardon, Mark A Yorek, Charles Brenner. Sci Rep 2016
159
25

NAD+ Intermediates: The Biology and Therapeutic Potential of NMN and NR.
Jun Yoshino, Joseph A Baur, Shin-Ichiro Imai. Cell Metab 2018
331
25

Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response.
Nicole T Liberati, Katherine A Fitzgerald, Dennis H Kim, Rhonda Feinbaum, Douglas T Golenbock, Frederick M Ausubel. Proc Natl Acad Sci U S A 2004
152
25

The SARM1 Toll/Interleukin-1 Receptor Domain Possesses Intrinsic NAD+ Cleavage Activity that Promotes Pathological Axonal Degeneration.
Kow Essuman, Daniel W Summers, Yo Sasaki, Xianrong Mao, Aaron DiAntonio, Jeffrey Milbrandt. Neuron 2017
258
25

Clinical implications of genetic advances in Charcot-Marie-Tooth disease.
Alexander M Rossor, James M Polke, Henry Houlden, Mary M Reilly. Nat Rev Neurol 2013
212
25

CREB-activity and nmnat2 transcription are down-regulated prior to neurodegeneration, while NMNAT2 over-expression is neuroprotective, in a mouse model of human tauopathy.
M Cecilia Ljungberg, Yousuf O Ali, Jie Zhu, Chia-Shan Wu, Kazuhiro Oka, R Grace Zhai, Hui-Chen Lu. Hum Mol Genet 2012
83
25

c-Jun N-terminal kinase (JNK) signaling: recent advances and challenges.
Marie A Bogoyevitch, Kevin R W Ngoei, Teresa T Zhao, Yvonne Y C Yeap, Dominic C H Ng. Biochim Biophys Acta 2010
219
25

Antisense oligonucleotides in neurological disorders.
Claudia D Wurster, Albert C Ludolph. Ther Adv Neurol Disord 2018
70
25

A loss-of-function variant in the human histidyl-tRNA synthetase (HARS) gene is neurotoxic in vivo.
Aimée Vester, Gisselle Velez-Ruiz, Heather M McLaughlin, James R Lupski, Kevin Talbot, Jeffery M Vance, Stephan Züchner, Ricardo H Roda, Kenneth H Fischbeck, Leslie G Biesecker,[...]. Hum Mutat 2013
85
25



Assembly of CNS myelin in the absence of proteolipid protein.
M Klugmann, M H Schwab, A Pühlhofer, A Schneider, F Zimmermann, I R Griffiths, K A Nave. Neuron 1997
337
25

WldS mice are resistant to paclitaxel (taxol) neuropathy.
Min Sheng Wang, Albert A Davis, Deborah G Culver, Jonathan D Glass. Ann Neurol 2002
118
25

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.
Albena Jordanova, Joy Irobi, Florian P Thomas, Patrick Van Dijck, Kris Meerschaert, Maarten Dewil, Ines Dierick, An Jacobs, Els De Vriendt, Velina Guergueltcheva,[...]. Nat Genet 2006
270
25

A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.
Pei-Chien Tsai, Bing-Wen Soong, Inès Mademan, Yen-Hua Huang, Chia-Rung Liu, Cheng-Tsung Hsiao, Hung-Ta Wu, Tze-Tze Liu, Yo-Tsen Liu, Yen-Ting Tseng,[...]. Brain 2017
48
25

Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia.
Julia M Edgar, Mark McLaughlin, Donald Yool, Su-Chun Zhang, Jill H Fowler, Paul Montague, Jennifer A Barrie, Mailis C McCulloch, Ian D Duncan, James Garbern,[...]. J Cell Biol 2004
227
25

The human NAD metabolome: Functions, metabolism and compartmentalization.
Andrey Nikiforov, Veronika Kulikova, Mathias Ziegler. Crit Rev Biochem Mol Biol 2015
134
25

Nicotinamide riboside, a form of vitamin B3, protects against excitotoxicity-induced axonal degeneration.
Pauline Vaur, Bernard Brugg, Mathias Mericskay, Zhenlin Li, Mark S Schmidt, Denis Vivien, Cyrille Orset, Etienne Jacotot, Charles Brenner, Eric Duplus. FASEB J 2017
51
25

MAPK signaling promotes axonal degeneration by speeding the turnover of the axonal maintenance factor NMNAT2.
Lauren J Walker, Daniel W Summers, Yo Sasaki, E J Brace, Jeffrey Milbrandt, Aaron DiAntonio. Elife 2017
92
25

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation.
James Y Garbern, Donald A Yool, Gregory J Moore, Ian B Wilds, Michael W Faulk, Matthias Klugmann, Klaus-Amin Nave, Erik A Sistermans, Marjo S van der Knaap, Thomas D Bird,[...]. Brain 2002
198
25

Disease Modeling and Therapeutic Strategies in CMT2A: State of the Art.
Kordelia Barbullushi, Elena Abati, Federica Rizzo, Nereo Bresolin, Giacomo P Comi, Stefania Corti. Mol Neurobiol 2019
12
25

The Wlds transgene reduces axon loss in a Charcot-Marie-Tooth disease 1A rat model and nicotinamide delays post-traumatic axonal degeneration.
Gerd Meyer zu Horste, Timo A Miesbach, Johanna I Muller, Robert Fledrich, Ruth M Stassart, Bernd C Kieseier, Michael P Coleman, Michael W Sereda. Neurobiol Dis 2011
43
25

MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2.
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, J Michael Schröder, Joachim Weis, Chantal Ceuterick, Albena Jordanova, Eva Nelis, Els De Vriendt, Matthias Van Hul,[...]. Brain 2006
268
25

Bicyclic-Capped Histone Deacetylase 6 Inhibitors with Improved Activity in a Model of Axonal Charcot-Marie-Tooth Disease.
Sida Shen, Veronick Benoy, Joel A Bergman, Jay H Kalin, Mariana Frojuello, Giulio Vistoli, Wanda Haeck, Ludo Van Den Bosch, Alan P Kozikowski. ACS Chem Neurosci 2016
45
25

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
Francesca Achilli, Virginie Bros-Facer, Hazel P Williams, Gareth T Banks, Mona AlQatari, Ruth Chia, Valter Tucci, Michael Groves, Carole D Nickols, Kevin L Seburn,[...]. Dis Model Mech 2009
68
25


An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations.
Morgane Stum, Heather M McLaughlin, Erica L Kleinbrink, Kathy E Miers, Susan L Ackerman, Kevin L Seburn, Anthony Antonellis, Robert W Burgess. Mol Cell Neurosci 2011
57
25

The axon degeneration gene SARM1 is evolutionarily distinct from other TIR domain-containing proteins.
Harsha Malapati, Spencer M Millen, William J Buchser. Mol Genet Genomics 2017
11
25


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.