Leucine‐rich repeat kinase 2‐sensitive Na + /Ca 2+ exchanger activity in dendritic cells-Reference-Cited by-同舟云学术

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Leucine‐rich repeat kinase 2‐sensitive Na + /Ca 2+ exchanger activity in dendritic cells

Published:2015-01-21 Issue:5 Volume:29 Page:1701-1710
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Yan Jing¹,Ahnilaji Ahmad¹,Schmid Evi¹²,Elvira Bernat¹,Shimshek Derya R.³,Putten Herman³⁴,Wagner Carsten A.⁵,Shumilina Ekaterina¹,Lang Florian¹

Affiliation:

1. Department of PhysiologyUniversity of TübingenTübingenGermany

2. Department of Pediatric Surgery and Pediatric UrologyUniversity Children's Hospital TübingenTübingenGermany

3. Department of NeuroscienceNovartis Institutes for BioMedical ResearchBaselSwitzerland

4. National Contest for Life FoundationHamburgGermany

5. Institute of Physiology, University of ZurichZürichSwitzerland

Funder

Deutsche Forschungsgemeinschaft

Michael J. Fox Foundation for Parkinson's Research

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.14-264028

Reference54 articles.

1. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

2. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

3. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

4. Genomewide Association Study of Leprosy

5. The leucine rich repeat kinase 2 (LRRK2) G2019S substitution mutation

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1. Dendritic cells in Parkinson's disease: Regulatory role and therapeutic potential;European Journal of Pharmacology;2024-08

2. Regulation of K+-Dependent Na+/Ca2+-Exchangers (NCKX);International Journal of Molecular Sciences;2022-12-29

3. High ORAI3 expression correlates with good prognosis in human muscle-invasive bladder cancer;Gene;2022-01

4. LRRK2 Biology from structure to dysfunction: research progresses, but the themes remain the same;Molecular Neurodegeneration;2019-12

5. Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease;PLOS Genetics;2019-06-06

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