A citation-based method for searching scientific literature

Teresa Duda, Alexander Pertzev, Rameshwar K Sharma. Mol Cell Biochem 2018
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Integrative Signaling Networks of Membrane Guanylate Cyclases: Biochemistry and Physiology.
Rameshwar K Sharma, Teresa Duda, Clint L Makino. Front Mol Neurosci 2016
11
100

The dimerization domain in outer segment guanylate cyclase is a Ca²⁺-sensitive control switch module.
Patrick Zägel, Daniele Dell'Orco, Karl-Wilhelm Koch. Biochemistry 2013
32
66

Membrane Guanylate Cyclase catalytic Subdomain: Structure and Linkage with Calcium Sensors and Bicarbonate.
Sarangan Ravichandran, Teresa Duda, Alexandre Pertzev, Rameshwar K Sharma. Front Mol Neurosci 2017
7
66


A calcium-relay mechanism in vertebrate phototransduction.
Karl-Wilhelm Koch, Daniele Dell'orco. ACS Chem Neurosci 2013
57
33

Pigment epithelium-derived factor hinders photoreceptor cell death by reducing intracellular calcium in the degenerating retina.
Antonella Comitato, Preeti Subramanian, Giandomenico Turchiano, Monica Montanari, S Patricia Becerra, Valeria Marigo. Cell Death Dis 2018
27
33

Calcium dynamics change in degenerating cone photoreceptors.
Manoj Kulkarni, Dragana Trifunović, Timm Schubert, Thomas Euler, François Paquet-Durand. Hum Mol Genet 2016
16
33

Regulatory modes of rod outer segment membrane guanylate cyclase differ in catalytic efficiency and Ca(2+)-sensitivity.
Ji-Young Hwang, Christian Lange, Andreas Helten, Doris Höppner-Heitmann, Teresa Duda, Rameshwar K Sharma, Karl-Wilhelm Koch. Eur J Biochem 2003
95
33

CaF2 nanoparticles as surface carriers of GCAP1, a calcium sensor protein involved in retinal dystrophies.
Valerio Marino, Alberto Borsatto, Farina Vocke, Karl-Wilhelm Koch, Daniele Dell'Orco. Nanoscale 2017
11
33



Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.
Michel Michaelides, Alison J Hardcastle, David M Hunt, Anthony T Moore. Surv Ophthalmol 2006
155
33

The Y99C mutation in guanylyl cyclase-activating protein 1 increases intracellular Ca2+ and causes photoreceptor degeneration in transgenic mice.
Elena V Olshevskaya, Peter D Calvert, Michael L Woodruff, Igor V Peshenko, Andrey B Savchenko, Clint L Makino, Ye-Shih Ho, Gordon L Fain, Alexander M Dizhoor. J Neurosci 2004
86
33

Cone rod dystrophies.
Christian P Hamel. Orphanet J Rare Dis 2007
267
33



Network and atomistic simulations unveil the structural determinants of mutations linked to retinal diseases.
Simona Mariani, Daniele Dell'Orco, Angelo Felline, Francesco Raimondi, Francesca Fanelli. PLoS Comput Biol 2013
18
33


ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
802
33


Impact of cone dystrophy-related mutations in GCAP1 on a kinetic model of phototransduction.
Daniele Dell'Orco, Stefan Sulmann, Patrick Zägel, Valerio Marino, Karl-Wilhelm Koch. Cell Mol Life Sci 2014
15
33

Bicarbonate and Ca(2+) Sensing Modulators Activate Photoreceptor ROS-GC1 Synergistically.
Teresa Duda, Alexandre Pertzev, Clint L Makino, Rameshwar K Sharma. Front Mol Neurosci 2016
6
33

Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1.
Farina Vocke, Nicole Weisschuh, Valerio Marino, Silvia Malfatti, Samuel G Jacobson, Charlotte M Reiff, Daniele Dell'Orco, Karl-Wilhelm Koch. Hum Mol Genet 2017
22
33

Structural effects of Mg²⁺ on the regulatory states of three neuronal calcium sensors operating in vertebrate phototransduction.
Valerio Marino, Stefan Sulmann, Karl-Wilhelm Koch, Daniele Dell'Orco. Biochim Biophys Acta 2015
35
33

Stabilizing function for myristoyl group revealed by the crystal structure of a neuronal calcium sensor, guanylate cyclase-activating protein 1.
Ricardo Stephen, Grzegorz Bereta, Marcin Golczak, Krzysztof Palczewski, Marcelo Carlos Sousa. Structure 2007
94
33




Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration.
Blanca Arango-Gonzalez, Dragana Trifunović, Ayse Sahaboglu, Katharina Kranz, Stylianos Michalakis, Pietro Farinelli, Susanne Koch, Fred Koch, Sandra Cottet, Ulrike Janssen-Bienhold,[...]. PLoS One 2014
111
33

A mutation in guanylate cyclase activator 1A (GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1.
A M Payne, S M Downes, D A Bessant, R Taylor, G E Holder, M J Warren, A C Bird, S S Bhattacharya. Hum Mol Genet 1998
186
33

A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degeneration.
Koji M Nishiguchi, Izabela Sokal, Lili Yang, Nirmalya Roychowdhury, Krzysztof Palczewski, Eliot L Berson, Thaddeus P Dryja, Wolfgang Baehr. Invest Ophthalmol Vis Sci 2004
63
33

Calcium binding, structural stability and guanylate cyclase activation in GCAP1 variants associated with human cone dystrophy.
Daniele Dell'Orco, Petra Behnen, Sara Linse, Karl-Wilhelm Koch. Cell Mol Life Sci 2010
52
33

Protein and Signaling Networks in Vertebrate Photoreceptor Cells.
Karl-Wilhelm Koch, Daniele Dell'Orco. Front Mol Neurosci 2015
61
33


A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy.
Li Jiang, Dianna Wheaton, Grzegorz Bereta, Kang Zhang, Krzysztof Palczewski, David G Birch, Wolfgang Baehr. Vision Res 2008
32
33


Causes and consequences of inherited cone disorders.
Susanne Roosing, Alberta A H J Thiadens, Carel B Hoyng, Caroline C W Klaver, Anneke I den Hollander, Frans P M Cremers. Prog Retin Eye Res 2014
89
33

Novel GUCA1A mutations suggesting possible mechanisms of pathogenesis in cone, cone-rod, and macular dystrophy patients.
Kunka Kamenarova, Marta Corton, Blanca García-Sandoval, Patricia Fernández-San Jose, Valentin Panchev, Almudena Avila-Fernández, Maria Isabel López-Molina, Christina Chakarova, Carmen Ayuso, Shomi S Bhattacharya. Biomed Res Int 2013
22
33


A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD).
Izabela Sokal, William J Dupps, Michael A Grassi, Jeremiah Brown, Louisa M Affatigato, Nirmalya Roychowdhury, Lili Yang, Slawomir Filipek, Krzysztof Palczewski, Edwin M Stone,[...]. Invest Ophthalmol Vis Sci 2005
52
33

Ca(2+)-modulated vision-linked ROS-GC guanylate cyclase transduction machinery.
Karl-W Koch, Teresa Duda, Rameshwar K Sharma. Mol Cell Biochem 2010
40
33

GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy.
I Sokal, N Li, I Surgucheva, M J Warren, A M Payne, S S Bhattacharya, W Baehr, K Palczewski. Mol Cell 1998
119
33

GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity.
Xue Chen, Xunlun Sheng, Wenjuan Zhuang, Xiantao Sun, Guohua Liu, Xun Shi, Guofu Huang, Yan Mei, Yingjie Li, Xinyuan Pan,[...]. Genet Med 2017
15
33



Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase.
Veronique B D Kitiratschky, Petra Behnen, Ulrich Kellner, John R Heckenlively, Eberhart Zrenner, Herbert Jägle, Susanne Kohl, Bernd Wissinger, Karl-Wilhelm Koch. Hum Mutat 2009
61
33

Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A).
Li Jiang, Bradley J Katz, Zhenglin Yang, Yu Zhao, Nathan Faulkner, Jianbin Hu, Jennifer Baird, Wolfgang Baehr, Donnell J Creel, Kang Zhang. Mol Vis 2005
35
33

Retinal guanylyl cyclase activating protein 1 forms a functional dimer.
Sunghyuk Lim, Graham Roseman, Igor Peshenko, Grace Manchala, Diana Cudia, Alexander M Dizhoor, Glenn Millhauser, James B Ames. PLoS One 2018
17
33

Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.
Gaël Manes, Sonia Mamouni, Emilie Hérald, Anne-Claire Richard, Audrey Sénéchal, Karim Aouad, Béatrice Bocquet, Isabelle Meunier, Christian P Hamel. Mol Vis 2017
18
33

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
S E Wilkie, Y Li, E C Deery, R J Newbold, D Garibaldi, J B Bateman, H Zhang, W Lin, D J Zack, S S Bhattacharya,[...]. Am J Hum Genet 2001
83
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.