Published in J Biol Chem on February 05, 2015
Development of Functional Fluorescent Molecular Probes for the Detection of Biological Substances. Biosensors (Basel) (2015) 0.90
Zinc transporters and dysregulated channels in cancers. Front Biosci (Landmark Ed) (2017) 0.75
ZnT2-Mediated Zinc Import Into Paneth Cell Granules Is Necessary for Coordinated Secretion and Paneth Cell Function in Mice. Cell Mol Gastroenterol Hepatol (2016) 0.75
Molecular Basis of Transient Neonatal Zinc Deficiency: NOVEL ZnT2 MUTATIONS DISRUPTING ZINC BINDING AND PERMEATION. J Biol Chem (2016) 0.75
The mucolipin-1 (TRPML1) ion channel, transmembrane-163 (TMEM163) protein, and lysosomal zinc handling. Front Biosci (Landmark Ed) (2017) 0.75
Visualization of interactions among bZIP and Rel family proteins in living cells using bimolecular fluorescence complementation. Mol Cell (2002) 10.81
Zinc transporters and the cellular trafficking of zinc. Biochim Biophys Acta (2006) 3.40
The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress. Methods (2005) 3.40
Design and implementation of bimolecular fluorescence complementation (BiFC) assays for the visualization of protein interactions in living cells. Nat Protoc (2006) 3.22
Structure of the zinc transporter YiiP. Science (2007) 2.95
Efflux and compartmentalization of zinc by members of the SLC30 family of solute carriers. Pflugers Arch (2003) 2.17
Cognitive loss in zinc transporter-3 knock-out mice: a phenocopy for the synaptic and memory deficits of Alzheimer's disease? J Neurosci (2010) 1.74
Visualization of molecular interactions using bimolecular fluorescence complementation analysis: characteristics of protein fragment complementation. Chem Soc Rev (2009) 1.74
Estimating the global prevalence of zinc deficiency: results based on zinc availability in national food supplies and the prevalence of stunting. PLoS One (2012) 1.73
Current understanding of ZIP and ZnT zinc transporters in human health and diseases. Cell Mol Life Sci (2014) 1.58
Identification of a mutation in SLC30A2 (ZnT-2) in women with low milk zinc concentration that results in transient neonatal zinc deficiency. J Biol Chem (2006) 1.52
Structural basis for autoregulation of the zinc transporter YiiP. Nat Struct Mol Biol (2009) 1.43
The SLC39 family of zinc transporters. Mol Aspects Med (2013) 1.41
The SLC30 family of zinc transporters - a review of current understanding of their biological and pathophysiological roles. Mol Aspects Med (2013) 1.32
Zinc transporter 2 (SLC30A2) can suppress the vesicular zinc defect of adaptor protein 3-depleted fibroblasts by promoting zinc accumulation in lysosomes. Exp Cell Res (2007) 1.20
Demonstration and characterization of the heterodimerization of ZnT5 and ZnT6 in the early secretory pathway. J Biol Chem (2009) 1.20
Zinc transporter-2 (ZnT2) variants are localized to distinct subcellular compartments and functionally transport zinc. Biochem J (2009) 1.12
The EVER proteins as a natural barrier against papillomaviruses: a new insight into the pathogenesis of human papillomavirus infections. Microbiol Mol Biol Rev (2009) 1.09
Compound heterozygous mutations in SLC30A2/ZnT2 results in low milk zinc concentrations: a novel mechanism for zinc deficiency in a breast-fed infant. PLoS One (2013) 1.07
Constitutive expression of hZnT4 zinc transporter in human breast epithelial cells. Biochem J (2002) 1.04
Discovery of human zinc deficiency: 50 years later. J Trace Elem Med Biol (2012) 1.04
SLC30A8 (ZnT8) Polymorphism is Associated with Young Age at Type 1 Diabetes Onset. Rev Diabet Stud (2008) 1.02
Prolactin regulates ZNT2 expression through the JAK2/STAT5 signaling pathway in mammary cells. Am J Physiol Cell Physiol (2009) 1.01
Inward-facing conformation of the zinc transporter YiiP revealed by cryoelectron microscopy. Proc Natl Acad Sci U S A (2013) 0.99
Functional analysis of two single nucleotide polymorphisms in SLC30A2 (ZnT2): implications for mammary gland function and breast disease in women. Physiol Genomics (2010) 0.97
Nuclear GPCRs in cardiomyocytes: an insider's view of β-adrenergic receptor signaling. Am J Physiol Heart Circ Physiol (2011) 0.97
A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency. J Biol Chem (2012) 0.94
Intracellular zinc homeostasis in leukocyte subsets is regulated by different expression of zinc exporters ZnT-1 to ZnT-9. J Leukoc Biol (2007) 0.92
SLC30A3 (ZnT3) oligomerization by dityrosine bonds regulates its subcellular localization and metal transport capacity. PLoS One (2009) 0.91
ZnT-1 expression in astroglial cells protects against zinc toxicity and slows the accumulation of intracellular zinc. Glia (2004) 0.89
Zn2+ efflux through lysosomal exocytosis prevents Zn2+-induced toxicity. J Cell Sci (2014) 0.88
Three-dimensional structure of beta-cell-specific zinc transporter, ZnT-8, predicted from the type 2 diabetes-associated gene variant SLC30A8 R325W. Diabetol Metab Syndr (2010) 0.87
A histidine-rich motif mediates mitochondrial localization of ZnT2 to modulate mitochondrial function. Am J Physiol Cell Physiol (2011) 0.87
ZnT3 mRNA levels are reduced in Alzheimer's disease post-mortem brain. Mol Neurodegener (2009) 0.86
Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn (2+) for Normal Growth and Development. Int J Endocrinol (2013) 0.86
Dissecting the pharmacology of G protein-coupled receptor signaling complexes using bimolecular fluorescence complementation. Methods Mol Biol (2012) 0.84
In situ dimerization of multiple wild type and mutant zinc transporters in live cells using bimolecular fluorescence complementation. J Biol Chem (2014) 0.84
Dimerization of ABCG2 analysed by bimolecular fluorescence complementation. PLoS One (2011) 0.84
Visualization by BiFC of different C/EBPβ dimers and their interaction with HP1α reveals a differential subnuclear distribution of complexes in living cells. Exp Cell Res (2010) 0.82
Transient neonatal zinc deficiency due to a new autosomal dominant mutation in gene SLC30A2 (ZnT-2). Pediatr Dermatol (2014) 0.81
Gap junctions contribute to astrocytic resistance against zinc toxicity. Brain Res Bull (2011) 0.81
Transient neonatal zinc deficiency. Am J Clin Nutr (1986) 0.80