The ERK1/2-Hepatocyte Nuclear Factor 4α Axis Regulates Human ABCC6 Gene Expression in Hepatocytes-Reference-Cited by-同舟云学术

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The ERK1/2-Hepatocyte Nuclear Factor 4α Axis Regulates Human ABCC6 Gene Expression in Hepatocytes

Published:2010-07 Issue:30 Volume:285 Page:22800-22808
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

de Boussac Hugues,Ratajewski Marcin,Sachrajda Iwona,Köblös Gabriella,Tordai Attila,Pulaski Lukasz,Buday László,Váradi András,Arányi Tamás

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference48 articles.

1. Pseudoxanthoma elasticum: clinical phenotypes, molecular genetics and putative pathomechanisms

2. Mutations in ABCC6 cause pseudoxanthoma elasticum

3. Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum

4. Pseudoxanthoma elasticum: Mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter

5. Pseudoxanthoma elasticum: genetic diagnostic markers

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bone Marrow–Derived ABCC6 Is an Essential Regulator of Ectopic Calcification In Pseudoxanthoma Elasticum;Journal of Investigative Dermatology;2024-08

2. Deubiquitinase OTUD5 promotes hepatitis B virus replication by removing K48-linked ubiquitination of HBV core/precore and upregulates HNF4ɑ expressions by inhibiting the ERK1/2/mitogen-activated protein kinase pathway;Cellular and Molecular Life Sciences;2023-10-28

3. ABC Transporters in Intestinal and Liver Efflux;Oral Bioavailability and Drug Delivery;2023-10-10

4. Plasma Level of Pyrophosphate Is Low in Pseudoxanthoma Elasticum Owing to Mutations in the ABCC6 Gene, but It Does Not Correlate with ABCC6 Genotype;Journal of Clinical Medicine;2023-01-29

5. The pathogenic c.1171A>G (p.Arg391Gly) and c.2359G>A (p.Val787Ile) ABCC6 variants display incomplete penetrance causing pseudoxanthoma elasticum in a subset of individuals;Human Mutation;2022-11-15

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