A citation-based method for searching scientific literature

Prasenjit Prasad Saha, S K Praveen Kumar, Shubhi Srivastava, Devanjan Sinha, Gautam Pareek, Patrick D'Silva. J Biol Chem 2014
Times Cited: 22



Angelica Olsson, Lisbet Lind, Lars-Eric Thornell, Monica Holmberg. Hum Mol Genet 2008
Times Cited: 94




List of shared articles



Times cited


Defective mitochondrial ISCs biogenesis switches on IRP1 to fine tune selective mitophagy.
Hao Wu, Huifang Wei, Di Zhang, Sheikh Arslan Sehgal, Dejiu Zhang, Xiaohui Wang, Yan Qin, Lei Liu, Quan Chen. Redox Biol 2020
7

Structure of the Human ACP-ISD11 Heterodimer.
María Georgina Herrera, Martín Ezequiel Noguera, Karl Ellioth Sewell, William Armando Agudelo Suárez, Luciana Capece, Sebastián Klinke, Javier Santos. Biochemistry 2019
6

The Power of Yeast in Modelling Human Nuclear Mutations Associated with Mitochondrial Diseases.
Camilla Ceccatelli Berti, Giulia di Punzio, Cristina Dallabona, Enrico Baruffini, Paola Goffrini, Tiziana Lodi, Claudia Donnini. Genes (Basel) 2021
8

Iron-Sulfur Protein Assembly in Human Cells.
Prasenjit Prasad Saha, Vinaya Vishwanathan, Kondalarao Bankapalli, Patrick D'Silva. Rev Physiol Biochem Pharmacol 2018
11

Mitochondrial Iron in Human Health and Disease.
Diane M Ward, Suzanne M Cloonan. Annu Rev Physiol 2019
50

Rescuing the Rescuer: On the Protein Complex between the Human Mitochondrial Acyl Carrier Protein and ISD11.
María Georgina Herrera, María Florencia Pignataro, Martín Ezequiel Noguera, Karen Magalí Cruz, Javier Santos. ACS Chem Biol 2018
12

A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy.
Andrea Legati, Aurelio Reyes, Camilla Ceccatelli Berti, Oliver Stehling, Silvia Marchet, Costanza Lamperti, Alberto Ferrari, Alan J Robinson, Ulrich Mühlenhoff, Roland Lill,[...]. J Med Genet 2017
22

FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis With Distinct Severity and Iron Regulation.
Sebastian Montealegre, Elise Lebigot, Hugo Debruge, Norma Romero, Bénédicte Héron, Pauline Gaignard, Antoine Legendre, Apolline Imbard, Stéphanie Gobin, Emmanuelle Lacène,[...]. Neurol Genet 2022
1