Literature DB >> 10790544

Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase.

T B Bartnikas1, D J Waggoner, R L Casareno, R Gaedigk, R A White, J D Gitlin.   

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Year:  2000        PMID： 10790544     DOI： 10.1007/s003350010078

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  4 in total

Review 1.  Exploring the Extended Biological Functions of the Human Copper Chaperone of Superoxide Dismutase 1.

Authors:  Yan Ge; Lu Wang; Duanhua Li; Chen Zhao; Jinjun Li; Tao Liu
Journal:  Protein J       Date:  2019-08       Impact factor: 2.371

2.  The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.

Authors:  H Patel; P E Hart; T T Warner; R S Houlston; M A Patton; S Jeffery; A H Crosby
Journal:  Am J Hum Genet       Date:  2001-05-25       Impact factor: 11.025

3.  Copper influx transporter 1 is required for FGF, PDGF and EGF-induced MAPK signaling.

Authors:  Cheng-Yu Tsai; J Cameron Finley; Sameh S Ali; Hemal H Patel; Stephen B Howell
Journal:  Biochem Pharmacol       Date:  2012-07-25       Impact factor: 5.858

4.  Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS).

Authors:  Asli N Silahtaroglu; Karen Brondum-Nielsen; Ole Gredal; Lene Werdelin; Marios Panas; Michael B Petersen; Niels Tommerup; Zeynep Tümer
Journal:  BMC Genet       Date:  2002-04-19       Impact factor: 2.797
  4 in total

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