A citation-based method for searching scientific literature

Cátia D Pereira, Filipa Martins, Mariana Santos, Thorsten Müeller, Odete A B da Cruz E Silva, Sandra Rebelo. Cells 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Lipid and protein dynamics that shape nuclear envelope identity.
Shirin Bahmanyar, Christian Schlieker. Mol Biol Cell 2020
7
66

Lamin B1 duplications cause autosomal dominant leukodystrophy.
Quasar S Padiath, Kazumasa Saigoh, Raphael Schiffmann, Hideaki Asahara, Takeshi Yamada, Anulf Koeppen, Kirk Hogan, Louis J Ptácek, Ying-Hui Fu. Nat Genet 2006
261
66


mTOR complex 1 regulates lipin 1 localization to control the SREBP pathway.
Timothy R Peterson, Shomit S Sengupta, Thurl E Harris, Anne E Carmack, Seong A Kang, Eric Balderas, David A Guertin, Katherine L Madden, Anne E Carpenter, Brian N Finck,[...]. Cell 2011
655
33


Structures of TorsinA and its disease-mutant complexed with an activator reveal the molecular basis for primary dystonia.
F Esra Demircioglu, Brian A Sosa, Jessica Ingram, Hidde L Ploegh, Thomas U Schwartz. Elife 2016
37
33


Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice.
Ji-Yeon Shin, Caroline Le Dour, Fusako Sera, Shinichi Iwata, Shunichi Homma, Leroy C Joseph, John P Morrow, William T Dauer, Howard J Worman. Nucleus 2014
10
33

The nuclear envelope protein, LAP1B, is a novel protein phosphatase 1 substrate.
Mariana Santos, Sandra Rebelo, Paula J M Van Kleeff, Connie E Kim, William T Dauer, Margarida Fardilha, Odete A da Cruz E Silva, Edgar F da Cruz E Silva. PLoS One 2013
21
33

Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation.
Jason C Choi, Antoine Muchir, Wei Wu, Shinichi Iwata, Shunichi Homma, John P Morrow, Howard J Worman. Sci Transl Med 2012
133
33

The Role of Torsin AAA+ Proteins in Preserving Nuclear Envelope Integrity and Safeguarding Against Disease.
Anthony J Rampello, Sarah M Prophet, Christian Schlieker. Biomolecules 2020
4
33


Inactivation of Tm6sf2, a Gene Defective in Fatty Liver Disease, Impairs Lipidation but Not Secretion of Very Low Density Lipoproteins.
Eriks Smagris, Shenise Gilyard, Soumik BasuRay, Jonathan C Cohen, Helen H Hobbs. J Biol Chem 2016
96
33

Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis.
Zobair M Younossi, Rohit Loomba, Mary E Rinella, Elisabetta Bugianesi, Giulio Marchesini, Brent A Neuschwander-Tetri, Lawrence Serfaty, Francesco Negro, Stephen H Caldwell, Vlad Ratziu,[...]. Hepatology 2018
145
33


Epigenetics in non-alcoholic fatty liver disease.
Jooho Lee, Yuri Kim, Simonetta Friso, Sang-Woon Choi. Mol Aspects Med 2017
50
33

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).
Katrin Hoffmann, Christine K Dreger, Ada L Olins, Donald E Olins, Leonard D Shultz, Barbara Lucke, Hartmut Karl, Reinhard Kaps, Dietmar Müller, Amparo Vayá,[...]. Nat Genet 2002
220
33

Genome-wide DNA methylation profiles in hepatocellular carcinoma.
Jing Shen, Shuang Wang, Yu-Jing Zhang, Maya Kappil, Hui-Chen Wu, Muhammad G Kibriya, Qiao Wang, Farzana Jasmine, Habib Ahsan, Po-Huang Lee,[...]. Hepatology 2012
134
33

Nuclear lipid droplets: a novel nuclear domain.
J P Layerenza, P González, M M García de Bravo, M P Polo, M S Sisti, A Ves-Losada. Biochim Biophys Acta 2013
56
33

Accumulation of PNPLA3 on lipid droplets is the basis of associated hepatic steatosis.
Soumik BasuRay, Yang Wang, Eriks Smagris, Jonathan C Cohen, Helen H Hobbs. Proc Natl Acad Sci U S A 2019
73
33

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein.
Peter Clayton, Björn Fischer, Anuska Mann, Sahar Mansour, Eva Rossier, Markus Veen, Christine Lang, Sevjidmaa Baasanjav, Moritz Kieslich, Katja Brossuleit,[...]. Nucleus 2010
28
33


Neutralization of Oxidized Phospholipids Ameliorates Non-alcoholic Steatohepatitis.
Xiaoli Sun, Jason S Seidman, Peng Zhao, Ty D Troutman, Nathanael J Spann, Xuchu Que, Fangli Zhou, Zhongji Liao, Martina Pasillas, Xiaohong Yang,[...]. Cell Metab 2020
30
33

Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.
Bruce Nmezi, Elisa Giorgio, Raili Raininko, Anna Lehman, Malte Spielmann, Mary Kay Koenig, Rahmat Adejumo, Melissa Knight, Ralitza Gavrilova, Murad Alturkustani,[...]. Neurol Genet 2019
8
33

Nuclear membrane diversity: underlying tissue-specific pathologies in disease?
Howard J Worman, Eric C Schirmer. Curr Opin Cell Biol 2015
64
33

Identification of protein disulfide isomerase 1 as a key isomerase for disulfide bond formation in apolipoprotein B100.
Shiyu Wang, Shuin Park, Vamsi K Kodali, Jaeseok Han, Theresa Yip, Zhouji Chen, Nicholas O Davidson, Randal J Kaufman. Mol Biol Cell 2015
17
33

Nuclear envelope-related lipodystrophies.
A C Guénantin, N Briand, G Bidault, P Afonso, V Béréziat, C Vatier, O Lascols, M Caron-Debarle, J Capeau, C Vigouroux. Semin Cell Dev Biol 2014
44
33

The ins and outs of endoplasmic reticulum-controlled lipid biosynthesis.
Julie Jacquemyn, Ana Cascalho, Rose E Goodchild. EMBO Rep 2017
61
33

Genome-nuclear lamina interactions and gene regulation.
Jop Kind, Bas van Steensel. Curr Opin Cell Biol 2010
128
33

Nuclear envelope-localized torsinA-LAP1 complex regulates hepatic VLDL secretion and steatosis.
Ji-Yeon Shin, Antonio Hernandez-Ono, Tatyana Fedotova, Cecilia Östlund, Michael J Lee, Sarah B Gibeley, Chun-Chi Liang, William T Dauer, Henry N Ginsberg, Howard J Worman. J Clin Invest 2019
18
33

Mislocalization to the nuclear envelope: an effect of the dystonia-causing torsinA mutation.
Rose E Goodchild, William T Dauer. Proc Natl Acad Sci U S A 2004
192
33

Lipins, lipids and nuclear envelope structure.
Symeon Siniossoglou. Traffic 2009
49
33

Pathogenic mutations in genes encoding nuclear envelope proteins and defective nucleocytoplasmic connections.
Cecilia Östlund, Wakam Chang, Gregg G Gundersen, Howard J Worman. Exp Biol Med (Maywood) 2019
3
33

The role of hepatic lipids in hepatic insulin resistance and type 2 diabetes.
Rachel J Perry, Varman T Samuel, Kitt F Petersen, Gerald I Shulman. Nature 2014
590
33

Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene.
Hans R Waterham, Janet Koster, Petra Mooyer, Gerard van Noort Gv, Richard I Kelley, William R Wilcox, Ronald J A Wanders, Raoul C M Hennekam, Jan C Oosterwijk. Am J Hum Genet 2003
142
33


Mechanism of hepatic insulin resistance in non-alcoholic fatty liver disease.
Varman T Samuel, Zhen-Xiang Liu, Xianqin Qu, Benjamin D Elder, Stefan Bilz, Douglas Befroy, Anthony J Romanelli, Gerald I Shulman. J Biol Chem 2004
881
33

Pathogenesis of Nonalcoholic Steatohepatitis and Hormone-Based Therapeutic Approaches.
Kook Hwan Kim, Myung-Shik Lee. Front Endocrinol (Lausanne) 2018
27
33

Mechanisms of NAFLD development and therapeutic strategies.
Scott L Friedman, Brent A Neuschwander-Tetri, Mary Rinella, Arun J Sanyal. Nat Med 2018
698
33

Pharmacokinetics, Safety, and CCR2/CCR5 Antagonist Activity of Cenicriviroc in Participants With Mild or Moderate Hepatic Impairment.
E Lefebvre, M Gottwald, K Lasseter, W Chang, M Willett, P F Smith, A Somasunderam, N S Utay. Clin Transl Sci 2016
35
33

Lipid droplets go nuclear.
Robert V Farese, Tobias C Walther. J Cell Biol 2016
19
33


PML isoform II plays a critical role in nuclear lipid droplet formation.
Yuki Ohsaki, Takeshi Kawai, Yukichika Yoshikawa, Jinglei Cheng, Eija Jokitalo, Toyoshi Fujimoto. J Cell Biol 2016
85
33



NASH: a mitochondrial disease.
Dominique Pessayre, Bernard Fromenty. J Hepatol 2005
271
33

Dissociation of hepatic steatosis and insulin resistance in mice overexpressing DGAT in the liver.
Mara Monetti, Malin C Levin, Matthew J Watt, Mini P Sajan, Stephen Marmor, Brian K Hubbard, Robert D Stevens, James R Bain, Christopher B Newgard, Robert V Farese,[...]. Cell Metab 2007
367
33

Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.
Imen Dorboz, Marie Coutelier, Anne T Bertrand, Jean-Hubert Caberg, Monique Elmaleh-Bergès, Jeanne Lainé, Giovanni Stevanin, Gisèle Bonne, Odile Boespflug-Tanguy, Laurent Servais. Orphanet J Rare Dis 2014
28
33

Human fatty liver disease: old questions and new insights.
Jonathan C Cohen, Jay D Horton, Helen H Hobbs. Science 2011
33

Hepatic ceramides dissociate steatosis and insulin resistance in patients with non-alcoholic fatty liver disease.
Panu K Luukkonen, You Zhou, Sanja Sädevirta, Marja Leivonen, Johanna Arola, Matej Orešič, Tuulia Hyötyläinen, Hannele Yki-Järvinen. J Hepatol 2016
195
33


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.