A citation-based method for searching scientific literature

Laura V Young, William Morrison, Craig Campbell, Emma C Moore, Michel G Arsenault, Athan G Dial, Sean Ng, Catherine A Bellissimo, Christopher G R Perry, Vladimir Ljubicic, Adam P Johnston. Am J Physiol Cell Physiol 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.
Joe N Kornegay, Janet R Bogan, Daniel J Bogan, Martin K Childers, Juan Li, Peter Nghiem, David A Detwiler, C Aaron Larsen, Robert W Grange, Ratna K Bhavaraju-Sanka,[...]. Mamm Genome 2012
94
100

Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy.
Jerry R Mendell, Nathalie Goemans, Linda P Lowes, Lindsay N Alfano, Katherine Berry, James Shao, Edward M Kaye, Eugenio Mercuri. Ann Neurol 2016
269
100

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice.
Ahlke Heydemann, Ermelinda Ceco, Jackie E Lim, Michele Hadhazy, Pearl Ryder, Jennifer L Moran, David R Beier, Abraham A Palmer, Elizabeth M McNally. J Clin Invest 2009
117
100


Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies.
Daniela Piga, Sabrina Salani, Francesca Magri, Roberta Brusa, Eleonora Mauri, Giacomo P Comi, Nereo Bresolin, Stefania Corti. Ther Adv Neurol Disord 2019
17
100

Generation of muscular dystrophy model rats with a CRISPR/Cas system.
Katsuyuki Nakamura, Wataru Fujii, Masaya Tsuboi, Jun Tanihata, Naomi Teramoto, Shiho Takeuchi, Kunihiko Naito, Keitaro Yamanouchi, Masugi Nishihara. Sci Rep 2014
80
100

CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene.
Tatiana V Egorova, Evgenia D Zotova, Denis A Reshetov, Anna V Polikarpova, Svetlana G Vassilieva, Dmitry V Vlodavets, Alexey A Gavrilov, Sergey V Ulianov, Vladimir L Buchman, Alexei V Deykin. Dis Model Mech 2019
14
100

Contractile properties of diaphragm muscle segments from old mdx and old transgenic mdx mice.
G S Lynch, J A Rafael, R T Hinkle, N M Cole, J S Chamberlain, J A Faulkner. Am J Physiol 1997
80
100

Differential expression of dystrophin isoforms in strains of mdx mice with different mutations.
W B Im, S F Phelps, E H Copen, E G Adams, J L Slightom, J S Chamberlain. Hum Mol Genet 1996
157
100

Mechanics of dystrophin deficient skeletal muscles in very young mice and effects of age.
Michael A Lopez, Sherina Bontiff, Mary Adeyeye, Aziz I Shaibani, Matthew S Alexander, Shari Wynd, Aladin M Boriek. Am J Physiol Cell Physiol 2021
1
100

New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.
G A Cox, S F Phelps, V M Chapman, J S Chamberlain. Nat Genet 1993
168
100

Mechanisms inducing low bone density in Duchenne muscular dystrophy in mice and humans.
Anna Rufo, Andrea Del Fattore, Mattia Capulli, Francesco Carvello, Loredana De Pasquale, Serge Ferrari, Dominique Pierroz, Lucia Morandi, Michele De Simone, Nadia Rucci,[...]. J Bone Miner Res 2011
92
100

Cellular senescence-mediated exacerbation of Duchenne muscular dystrophy.
Hidetoshi Sugihara, Naomi Teramoto, Katsuyuki Nakamura, Takanori Shiga, Taku Shirakawa, Masafumi Matsuo, Masashi Ogasawara, Ichizo Nishino, Takashi Matsuwaki, Masugi Nishihara,[...]. Sci Rep 2020
5
100

Hsp72 preserves muscle function and slows progression of severe muscular dystrophy.
Stefan M Gehrig, Chris van der Poel, Timothy A Sayer, Jonathan D Schertzer, Darren C Henstridge, Jarrod E Church, Severine Lamon, Aaron P Russell, Kay E Davies, Mark A Febbraio,[...]. Nature 2012
170
100

Using CRISPR/Cas9 System to Knock out Exon 48 in DMD Gene.
Mahintaj Dara, Vahid Razban, Mahdieh Talebzadeh, Sepideh Moradi, Mehdi Dianatpour. Avicenna J Med Biotechnol 2021
1
100

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.
V M Chapman, D R Miller, D Armstrong, C T Caskey. Proc Natl Acad Sci U S A 1989
172
100

Natural disease history of the D2-mdx mouse model for Duchenne muscular dystrophy.
Maaike van Putten, Kayleigh Putker, Maurice Overzier, W A Adamzek, Svetlana Pasteuning-Vuhman, Jaap J Plomp, Annemieke Aartsma-Rus. FASEB J 2019
31
100

Spatiotemporal Mapping Reveals Regional Gastrointestinal Dysfunction in mdx Dystrophic Mice Ameliorated by Oral L-arginine Supplementation.
Kristy Swiderski, Rebecka Bindon, Jennifer Trieu, Timur Naim, Shana Schokman, Mathusi Swaminathan, Anita J L Leembruggen, Elisa L Hill-Yardin, René Koopman, Joel C Bornstein,[...]. J Neurogastroenterol Motil 2020
2
100

Metabolic remodeling of dystrophic skeletal muscle reveals biological roles for dystrophin and utrophin in adaptation and plasticity.
Justin P Hardee, Karen J B Martins, Paula M Miotto, James G Ryall, Stefan M Gehrig, Boris Reljic, Timur Naim, Jin D Chung, Jen Trieu, Kristy Swiderski,[...]. Mol Metab 2021
3
100

The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy.
David W Hammers, Cora C Hart, Michael K Matheny, Lillian A Wright, Megan Armellini, Elisabeth R Barton, H Lee Sweeney. Sci Rep 2020
3
100

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy.
A E Deconinck, J A Rafael, J A Skinner, S C Brown, A C Potter, L Metzinger, D J Watt, J G Dickson, J M Tinsley, K E Davies. Cell 1997
552
100

Antibody against the C-terminal portion of dystrophin crossreacts with the 400 kDa protein in the pia mater of dystrophin-deficient mdx mouse brain.
S Ishiura, K Arahata, T Tsukahara, R Koga, H Anraku, M Yamaguchi, T Kikuchi, I Nonaka, H Sugita. J Biochem 1990
42
100

TGF-β-driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model.
Davi Ag Mázala, James S Novak, Marshall W Hogarth, Marie Nearing, Prabhat Adusumalli, Christopher B Tully, Nayab F Habib, Heather Gordish-Dressman, Yi-Wen Chen, Jyoti K Jaiswal,[...]. JCI Insight 2020
19
100

Eteplirsen in the treatment of Duchenne muscular dystrophy.
Kenji Rowel Q Lim, Rika Maruyama, Toshifumi Yokota. Drug Des Devel Ther 2017
171
100

Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy.
Joe W McGreevy, Chady H Hakim, Mark A McIntosh, Dongsheng Duan. Dis Model Mech 2015
217
100

Effect of genetic background on the dystrophic phenotype in mdx mice.
William D Coley, Laurent Bogdanik, Maria Candida Vila, Qing Yu, Jack H Van Der Meulen, Sree Rayavarapu, James S Novak, Marie Nearing, James L Quinn, Allison Saunders,[...]. Hum Mol Genet 2016
87
100

Mammalian animal models for Duchenne muscular dystrophy.
Raffaella Willmann, Stefanie Possekel, Judith Dubach-Powell, Thomas Meier, Markus A Ruegg. Neuromuscul Disord 2009
136
100

Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.
Joachim Berger, Silke Berger, Thomas E Hall, Graham J Lieschke, Peter D Currie. Neuromuscul Disord 2010
54
100

Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy.
Thibaut Larcher, Aude Lafoux, Laurent Tesson, Séverine Remy, Virginie Thepenier, Virginie François, Caroline Le Guiner, Helicia Goubin, Maéva Dutilleul, Lydie Guigand,[...]. PLoS One 2014
85
100

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.
E Araki, K Nakamura, K Nakao, S Kameya, O Kobayashi, I Nonaka, T Kobayashi, M Katsuki. Biochem Biophys Res Commun 1997
79
100

Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old.
G S Lynch, R T Hinkle, J S Chamberlain, S V Brooks, J A Faulkner. J Physiol 2001
231
100

In-frame dystrophin following exon 51-skipping improves muscle pathology and function in the exon 52-deficient mdx mouse.
Yoshitsugu Aoki, Akinori Nakamura, Toshifumi Yokota, Takashi Saito, Hitoshi Okazawa, Tetsuya Nagata, Shin'ichi Takeda. Mol Ther 2010
85
100

X chromosome-linked muscular dystrophy (mdx) in the mouse.
G Bulfield, W G Siller, P A Wight, K J Moore. Proc Natl Acad Sci U S A 1984
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.