Federica Rachele Danti, Federica Invernizzi, Isabella Moroni, Barbara Garavaglia, Nardo Nardocci, Giovanna Zorzi. Front Neurol 2021
Times Cited: 1
Times Cited: 1
List of co-cited articles
articles co-cited >1
Times Cited
Times Co-cited
Similarity
MICU1 motifs define mitochondrial calcium uniporter binding and activity.
Nicholas E Hoffman, Harish C Chandramoorthy, Santhanam Shamugapriya, Xueqian Zhang, Sudarsan Rajan, Karthik Mallilankaraman, Rajesh Kumar Gandhirajan, Ronald J Vagnozzi, Lukas M Ferrer, Krishnalatha Sreekrishnanilayam,[...]. Cell Rep 2013
Nicholas E Hoffman, Harish C Chandramoorthy, Santhanam Shamugapriya, Xueqian Zhang, Sudarsan Rajan, Karthik Mallilankaraman, Rajesh Kumar Gandhirajan, Ronald J Vagnozzi, Lukas M Ferrer, Krishnalatha Sreekrishnanilayam,[...]. Cell Rep 2013
100
Developmental brain abnormalities and acute encephalopathy in a patient with myopathy with extrapyramidal signs secondary to pathogenic variants in MICU1.
Katelynn M Wilton, Joel A Morales-Rosado, Duygu Selcen, Karthik Muthusamy, Sarah Ewing, Katherine Agre, Katherine Nickels, Eric W Klee, Mai-Lan Ho, Eva Morava. JIMD Rep 2020
Katelynn M Wilton, Joel A Morales-Rosado, Duygu Selcen, Karthik Muthusamy, Sarah Ewing, Katherine Agre, Katherine Nickels, Eric W Klee, Mai-Lan Ho, Eva Morava. JIMD Rep 2020
100
MCUR1 is an essential component of mitochondrial Ca2+ uptake that regulates cellular metabolism.
Karthik Mallilankaraman, César Cárdenas, Patrick J Doonan, Harish C Chandramoorthy, Krishna M Irrinki, Tünde Golenár, György Csordás, Priyanka Madireddi, Jun Yang, Marioly Müller,[...]. Nat Cell Biol 2012
Karthik Mallilankaraman, César Cárdenas, Patrick J Doonan, Harish C Chandramoorthy, Krishna M Irrinki, Tünde Golenár, György Csordás, Priyanka Madireddi, Jun Yang, Marioly Müller,[...]. Nat Cell Biol 2012
100
A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter.
Diego De Stefani, Anna Raffaello, Enrico Teardo, Ildikò Szabò, Rosario Rizzuto. Nature 2011
Diego De Stefani, Anna Raffaello, Enrico Teardo, Ildikò Szabò, Rosario Rizzuto. Nature 2011
100
Alternating hemiplegia and paroxysmal torticollis caused by SCN4A mutation: A new phenotype?
Bi Chun Duan, Lee-Chin Wong, Wang-Tso Lee. Neurology 2019
Bi Chun Duan, Lee-Chin Wong, Wang-Tso Lee. Neurology 2019
100
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned.
Roula Ghaoui, Sandra T Cooper, Monkol Lek, Kristi Jones, Alastair Corbett, Stephen W Reddel, Merrilee Needham, Christina Liang, Leigh B Waddell, Garth Nicholson,[...]. JAMA Neurol 2015
Roula Ghaoui, Sandra T Cooper, Monkol Lek, Kristi Jones, Alastair Corbett, Stephen W Reddel, Merrilee Needham, Christina Liang, Leigh B Waddell, Garth Nicholson,[...]. JAMA Neurol 2015
100
Characterization and temporal development of cores in a mouse model of malignant hyperthermia.
Simona Boncompagni, Ann E Rossi, Massimo Micaroni, Susan L Hamilton, Robert T Dirksen, Clara Franzini-Armstrong, Feliciano Protasi. Proc Natl Acad Sci U S A 2009
Simona Boncompagni, Ann E Rossi, Massimo Micaroni, Susan L Hamilton, Robert T Dirksen, Clara Franzini-Armstrong, Feliciano Protasi. Proc Natl Acad Sci U S A 2009
100
Prediction whether a human cDNA sequence contains initiation codon by combining statistical information and similarity with protein sequences.
T Nishikawa, T Ota, T Isogai. Bioinformatics 2000
T Nishikawa, T Ota, T Isogai. Bioinformatics 2000
100
Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report.
Marzieh Mojbafan, Somayeh Takrim Nojehdeh, Faezeh Rahiminejad, Yalda Nilipour, Seyed Hasan Tonekaboni, Sirous Zeinali. BMC Med Genet 2020
Marzieh Mojbafan, Somayeh Takrim Nojehdeh, Faezeh Rahiminejad, Yalda Nilipour, Seyed Hasan Tonekaboni, Sirous Zeinali. BMC Med Genet 2020
100
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood.
David Lewis-Smith, Kimberli J Kamer, Helen Griffin, Anne-Marie Childs, Karen Pysden, Denis Titov, Jennifer Duff, Angela Pyle, Robert W Taylor, Patrick Yu-Wai-Man,[...]. Neurol Genet 2016
David Lewis-Smith, Kimberli J Kamer, Helen Griffin, Anne-Marie Childs, Karen Pysden, Denis Titov, Jennifer Duff, Angela Pyle, Robert W Taylor, Patrick Yu-Wai-Man,[...]. Neurol Genet 2016
100
MICU1 encodes a mitochondrial EF hand protein required for Ca(2+) uptake.
Fabiana Perocchi, Vishal M Gohil, Hany S Girgis, X Robert Bao, Janet E McCombs, Amy E Palmer, Vamsi K Mootha. Nature 2010
Fabiana Perocchi, Vishal M Gohil, Hany S Girgis, X Robert Bao, Janet E McCombs, Amy E Palmer, Vamsi K Mootha. Nature 2010
100
MICU1 is an essential gatekeeper for MCU-mediated mitochondrial Ca(2+) uptake that regulates cell survival.
Karthik Mallilankaraman, Patrick Doonan, César Cárdenas, Harish C Chandramoorthy, Marioly Müller, Russell Miller, Nicholas E Hoffman, Rajesh Kumar Gandhirajan, Jordi Molgó, Morris J Birnbaum,[...]. Cell 2012
Karthik Mallilankaraman, Patrick Doonan, César Cárdenas, Harish C Chandramoorthy, Marioly Müller, Russell Miller, Nicholas E Hoffman, Rajesh Kumar Gandhirajan, Jordi Molgó, Morris J Birnbaum,[...]. Cell 2012
100
A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients.
Sara Musa, Wafaa Eyaid, Kimberli Kamer, Rehab Ali, Mariam Al-Mureikhi, Noora Shahbeck, Fatma Al Mesaifri, Nawal Makhseed, Zakkiriah Mohamed, Wafaa Ali AlShehhi,[...]. JIMD Rep 2019
Sara Musa, Wafaa Eyaid, Kimberli Kamer, Rehab Ali, Mariam Al-Mureikhi, Noora Shahbeck, Fatma Al Mesaifri, Nawal Makhseed, Zakkiriah Mohamed, Wafaa Ali AlShehhi,[...]. JIMD Rep 2019
100
The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population.
Weiyi Mu, Nicoline Schiess, Jennifer L Orthmann-Murphy, Ayman W El-Hattab. J Neurogenet 2019
Weiyi Mu, Nicoline Schiess, Jennifer L Orthmann-Murphy, Ayman W El-Hattab. J Neurogenet 2019
100
Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family.
Fatemeh Bitarafan, Mehrnoosh Khodaeian, Elham Amjadi Sardehaei, Fatemeh Zahra Darvishi, Navid Almadani, Yalda Nilipour, Masoud Garshasbi. Mol Cell Pediatr 2021
Fatemeh Bitarafan, Mehrnoosh Khodaeian, Elham Amjadi Sardehaei, Fatemeh Zahra Darvishi, Navid Almadani, Yalda Nilipour, Masoud Garshasbi. Mol Cell Pediatr 2021
100
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling.
Clare V Logan, György Szabadkai, Jenny A Sharpe, David A Parry, Silvia Torelli, Anne-Marie Childs, Marjolein Kriek, Rahul Phadke, Colin A Johnson, Nicola Y Roberts,[...]. Nat Genet 2014
Clare V Logan, György Szabadkai, Jenny A Sharpe, David A Parry, Silvia Torelli, Anne-Marie Childs, Marjolein Kriek, Rahul Phadke, Colin A Johnson, Nicola Y Roberts,[...]. Nat Genet 2014
100
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency.
William A Irwin, Natascha Bergamin, Patrizia Sabatelli, Carlo Reggiani, Aram Megighian, Luciano Merlini, Paola Braghetta, Marta Columbaro, Dino Volpin, Giorgio M Bressan,[...]. Nat Genet 2003
William A Irwin, Natascha Bergamin, Patrizia Sabatelli, Carlo Reggiani, Aram Megighian, Luciano Merlini, Paola Braghetta, Marta Columbaro, Dino Volpin, Giorgio M Bressan,[...]. Nat Genet 2003
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.