ISCU (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "ISCU" in English language version.

Last modified: 02:39:05, 19 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

5121nih.gov

5^th place

2110doi.org

2^nd place

62ensembl.org

630^th place

326^th place

51uniprot.org

2,402^nd place

2,501^st place

51creativecommons.org

580^th place

287^th place

51omim.org

3,900^th place

3,720^th place

11adsabs.harvard.edu

14^th place

9^th place

11semanticscholar.org

15^th place

8^th place

11books.google.com

3^rd place

11socialstyrelsen.se

low place

11ebi.ac.uk

4,422^nd place

7,719^th place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Hwang DM, Dempsey A, Tan KT, Liew CC (November 1996). "A modular domain of NifU, a nitrogen fixation cluster protein, is highly conserved in evolution". Journal of Molecular Evolution. 43 (5): 536–540. Bibcode:1996JMolE..43..536H. doi:10.1007/BF02337525. PMID 8875867. S2CID 21873104.

books.google.com (Global: 3^rd place; English: 3^rd place)

Saltin B (2000). Exercise and Circulation in Health and Disease. Human Kinetics. ISBN 978-0-88011-632-9.

creativecommons.org (Global: 580^th place; English: 287^th place)

"ISCU - Iron-sulfur cluster assembly enzyme ISCU, mitochondrial precursor - Homo sapiens (Human) - ISCU gene & protein". UniProt. Retrieved 2018-09-04. This article incorporates text available under the CC BY 4.0 license.

doi.org (Global: 2^nd place; English: 2^nd place)

Hwang DM, Dempsey A, Tan KT, Liew CC (November 1996). "A modular domain of NifU, a nitrogen fixation cluster protein, is highly conserved in evolution". Journal of Molecular Evolution. 43 (5): 536–540. Bibcode:1996JMolE..43..536H. doi:10.1007/BF02337525. PMID 8875867. S2CID 21873104.
Tong WH, Rouault T (November 2000). "Distinct iron-sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells". The EMBO Journal. 19 (21): 5692–5700. doi:10.1093/emboj/19.21.5692. PMC 305809. PMID 11060020.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Larsson LE, Linderholm H, Mueller R, Ringqvist T, Soernaes R (October 1964). "Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1". Journal of Neurology, Neurosurgery, and Psychiatry. 27 (5): 361–380. doi:10.1136/jnnp.27.5.361. PMC 495765. PMID 14213465.
Mochel F, Knight MA, Tong WH, Hernandez D, Ayyad K, Taivassalo T, et al. (March 2008). "Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance". American Journal of Human Genetics. 82 (3): 652–660. doi:10.1016/j.ajhg.2007.12.012. PMC 2427212. PMID 18304497.
Crooks DR, Natarajan TG, Jeong SY, Chen C, Park SY, Huang H, et al. (January 2014). "Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron-sulfur cluster depletion in human skeletal muscle". Human Molecular Genetics. 23 (1): 24–39. doi:10.1093/hmg/ddt393. PMC 3857942. PMID 23943793.
Legati A, Reyes A, Ceccatelli Berti C, Stehling O, Marchet S, Lamperti C, et al. (December 2017). "A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy". Journal of Medical Genetics. 54 (12): 815–824. doi:10.1136/jmedgenet-2017-104822. PMC 5740555. PMID 29079705.
Kollberg G, Melberg A, Holme E, Oldfors A (February 2011). "Transient restoration of succinate dehydrogenase activity after rhabdomyolysis in iron-sulphur cluster deficiency myopathy". Neuromuscular Disorders. 21 (2): 115–120. doi:10.1016/j.nmd.2010.11.010. PMID 21196119.
Sanaker PS, Toompuu M, Hogan VE, He L, Tzoulis C, Chrzanowska-Lightowlers ZM, et al. (June 2010). "Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802 (6): 539–544. doi:10.1016/j.bbadis.2010.02.010. PMID 20206689.
Kollberg G, Tulinius M, Melberg A, Darin N, Andersen O, Holmgren D, et al. (August 2009). "Clinical manifestation and a new ISCU mutation in iron-sulphur cluster deficiency myopathy". Brain. 132 (Pt 8): 2170–2179. doi:10.1093/brain/awp152. PMID 19567699.

ebi.ac.uk (Global: 4,422^nd place; English: 7,719^th place)

"235 binary interactions found for search term ISCU". IntAct Molecular Interaction Database. EMBL-EBI. Retrieved 2018-09-05.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000136003 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000025825 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Hwang DM, Dempsey A, Tan KT, Liew CC (November 1996). "A modular domain of NifU, a nitrogen fixation cluster protein, is highly conserved in evolution". Journal of Molecular Evolution. 43 (5): 536–540. Bibcode:1996JMolE..43..536H. doi:10.1007/BF02337525. PMID 8875867. S2CID 21873104.
Tong WH, Rouault T (November 2000). "Distinct iron-sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells". The EMBO Journal. 19 (21): 5692–5700. doi:10.1093/emboj/19.21.5692. PMC 305809. PMID 11060020.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Mochel F, Haller RG (2009-03-31). "Myopathy with Deficiency of ISCU – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". Myopathy with Deficiency of ISCU. GeneReviews. PMID 20301757. Updated 2011 Sep 1 This article incorporates text from this source, which is in the public domain.
Larsson LE, Linderholm H, Mueller R, Ringqvist T, Soernaes R (October 1964). "Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1". Journal of Neurology, Neurosurgery, and Psychiatry. 27 (5): 361–380. doi:10.1136/jnnp.27.5.361. PMC 495765. PMID 14213465.
Mochel F, Knight MA, Tong WH, Hernandez D, Ayyad K, Taivassalo T, et al. (March 2008). "Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance". American Journal of Human Genetics. 82 (3): 652–660. doi:10.1016/j.ajhg.2007.12.012. PMC 2427212. PMID 18304497.
Crooks DR, Natarajan TG, Jeong SY, Chen C, Park SY, Huang H, et al. (January 2014). "Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron-sulfur cluster depletion in human skeletal muscle". Human Molecular Genetics. 23 (1): 24–39. doi:10.1093/hmg/ddt393. PMC 3857942. PMID 23943793.
Legati A, Reyes A, Ceccatelli Berti C, Stehling O, Marchet S, Lamperti C, et al. (December 2017). "A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy". Journal of Medical Genetics. 54 (12): 815–824. doi:10.1136/jmedgenet-2017-104822. PMC 5740555. PMID 29079705.
Kollberg G, Melberg A, Holme E, Oldfors A (February 2011). "Transient restoration of succinate dehydrogenase activity after rhabdomyolysis in iron-sulphur cluster deficiency myopathy". Neuromuscular Disorders. 21 (2): 115–120. doi:10.1016/j.nmd.2010.11.010. PMID 21196119.
Sanaker PS, Toompuu M, Hogan VE, He L, Tzoulis C, Chrzanowska-Lightowlers ZM, et al. (June 2010). "Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802 (6): 539–544. doi:10.1016/j.bbadis.2010.02.010. PMID 20206689.
Kollberg G, Tulinius M, Melberg A, Darin N, Andersen O, Holmgren D, et al. (August 2009). "Clinical manifestation and a new ISCU mutation in iron-sulphur cluster deficiency myopathy". Brain. 132 (Pt 8): 2170–2179. doi:10.1093/brain/awp152. PMID 19567699.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Tong WH, Rouault T (November 2000). "Distinct iron-sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells". The EMBO Journal. 19 (21): 5692–5700. doi:10.1093/emboj/19.21.5692. PMC 305809. PMID 11060020.
"Entrez Gene: ISCU iron-sulfur cluster scaffold homolog (E. coli)". This article incorporates text from this source, which is in the public domain.
"UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
Mochel F, Haller RG (2009-03-31). "Myopathy with Deficiency of ISCU – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". Myopathy with Deficiency of ISCU. GeneReviews. PMID 20301757. Updated 2011 Sep 1 This article incorporates text from this source, which is in the public domain.
Larsson LE, Linderholm H, Mueller R, Ringqvist T, Soernaes R (October 1964). "Hereditary metabolic myopathy with paroxysmal myoglobinuria due to abnormal glycolysis1". Journal of Neurology, Neurosurgery, and Psychiatry. 27 (5): 361–380. doi:10.1136/jnnp.27.5.361. PMC 495765. PMID 14213465.
Mochel F, Knight MA, Tong WH, Hernandez D, Ayyad K, Taivassalo T, et al. (March 2008). "Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance". American Journal of Human Genetics. 82 (3): 652–660. doi:10.1016/j.ajhg.2007.12.012. PMC 2427212. PMID 18304497.
Crooks DR, Natarajan TG, Jeong SY, Chen C, Park SY, Huang H, et al. (January 2014). "Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron-sulfur cluster depletion in human skeletal muscle". Human Molecular Genetics. 23 (1): 24–39. doi:10.1093/hmg/ddt393. PMC 3857942. PMID 23943793.
Legati A, Reyes A, Ceccatelli Berti C, Stehling O, Marchet S, Lamperti C, et al. (December 2017). "A novel de novo dominant mutation in ISCU associated with mitochondrial myopathy". Journal of Medical Genetics. 54 (12): 815–824. doi:10.1136/jmedgenet-2017-104822. PMC 5740555. PMID 29079705.

omim.org (Global: 3,900^th place; English: 3,720^th place)

"Entry - #255125 - Myopathy WITH Lactic Acidosis, Hereditary; HML - OMIM". www.omim.org. Retrieved 2024-04-05.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Hwang DM, Dempsey A, Tan KT, Liew CC (November 1996). "A modular domain of NifU, a nitrogen fixation cluster protein, is highly conserved in evolution". Journal of Molecular Evolution. 43 (5): 536–540. Bibcode:1996JMolE..43..536H. doi:10.1007/BF02337525. PMID 8875867. S2CID 21873104.

socialstyrelsen.se (Global: low place; English: low place)

"Linderholms myopati". Socialstyrelsen (in Swedish). 2019-05-30. Retrieved 2024-04-05.

uniprot.org (Global: 2,402^nd place; English: 2,501^st place)

"ISCU - Iron-sulfur cluster assembly enzyme ISCU, mitochondrial precursor - Homo sapiens (Human) - ISCU gene & protein". UniProt. Retrieved 2018-09-04. This article incorporates text available under the CC BY 4.0 license.

ISCU (English Wikipedia)

adsabs.harvard.edu (Global: 14th place; English: 9th place)

ui.adsabs.harvard.edu

books.google.com (Global: 3rd place; English: 3rd place)

creativecommons.org (Global: 580th place; English: 287th place)

doi.org (Global: 2nd place; English: 2nd place)

ebi.ac.uk (Global: 4,422nd place; English: 7,719th place)

ensembl.org (Global: 630th place; English: 326th place)