Literature DB >> 21044052

Mutational analysis of ABCC2 gene in two siblings with neonatal-onset Dubin Johnson syndrome.

L Pacifico, C Carducci, E Poggiogalle, F Caravona, I Antonozzi, C Chiesa, G Maggiore.   

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Year:  2010        PMID： 21044052     DOI： 10.1111/j.1399-0004.2010.01497.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

Review 1.  Beyond Competitive Inhibition: Regulation of ABC Transporters by Kinases and Protein-Protein Interactions as Potential Mechanisms of Drug-Drug Interactions.

Authors:  Rebecca R Crawford; Praveen K Potukuchi; Erin G Schuetz; John D Schuetz
Journal:  Drug Metab Dispos       Date:  2018-03-07       Impact factor: 3.922

2.  Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis.

Authors:  Victoria M Pratt; Brittany N Beyer; Daniel L Koller; Todd C Skaar; David A Flockhart; Kenneth D Levy; Gail H Vance
Journal:  J Mol Diagn       Date:  2014-12-29       Impact factor: 5.568

3.  Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin-Johnson syndrome in a Chinese gril: A case report.

Authors:  Yuan Li; Yang Li; Yang Yang; Wen-Rui Yang; Jian-Ping Li; Guang-Xin Peng; Lin Song; Hui-Hui Fan; Lei Ye; You-Zhen Xiong; Zhi-Jie Wu; Kang Zhou; Xin Zhao; Li-Ping Jing; Feng-Kui Zhang; Li Zhang
Journal:  World J Clin Cases       Date:  2019-10-26       Impact factor: 1.337
  3 in total

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