Published in J Cell Sci on October 25, 2005
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Direct Exposure to Ethanol Disrupts Junctional Cell-Cell Contact and Hippo-YAP Signaling in HL-1 Murine Atrial Cardiomyocytes. PLoS One (2015) 0.75
Association of the Hermansky-Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects. BMC Psychiatry (2013) 0.75
Role of Endolysosomes in Skeletal Muscle Pathology Observed in a Cholesterol-Fed Rabbit Model of Alzheimer's Disease. Front Aging Neurosci (2016) 0.75
Taking a lipidation-dependent path toward endolysosomes. Commun Integr Biol (2015) 0.75
BECN1/Beclin 1 sorts cell-surface APP/amyloid β precursor protein for lysosomal degradation. Autophagy (2016) 0.75
Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1. J Biol Chem (2017) 0.75
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Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet (2012) 3.21
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1). Nat Genet (2003) 2.78
Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1). J Biol Chem (2004) 2.62
Recurrent CNVs disrupt three candidate genes in schizophrenia patients. Am J Hum Genet (2008) 2.61
BLOC-1 interacts with BLOC-2 and the AP-3 complex to facilitate protein trafficking on endosomes. Mol Biol Cell (2006) 2.37
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The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology. Nat Genet (2004) 2.16
BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles. Mol Biol Cell (2006) 2.11
Tag SNPs chosen from HapMap perform well in several population isolates. Genet Epidemiol (2007) 2.10
An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis. Nucleic Acids Res (2002) 2.06
Transcriptome-based determination of multiple transcription regulator activities in Escherichia coli by using network component analysis. Proc Natl Acad Sci U S A (2003) 2.03
Inferring protein domain interactions from databases of interacting proteins. Genome Biol (2005) 1.97
Reversing melanoma cross-resistance to BRAF and MEK inhibitors by co-targeting the AKT/mTOR pathway. PLoS One (2011) 1.89
BLOC-1, a novel complex containing the pallidin and muted proteins involved in the biogenesis of melanosomes and platelet-dense granules. J Biol Chem (2002) 1.86
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Hum Mol Genet (2006) 1.84
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome. Nat Genet (2012) 1.61
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Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4. Proc Natl Acad Sci U S A (2003) 1.41
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Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding protein. Biochem J (2006) 1.27
Characterization of BLOC-2, a complex containing the Hermansky-Pudlak syndrome proteins HPS3, HPS5 and HPS6. Traffic (2004) 1.26
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
Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients. Biol Psychiatry (2011) 1.18
A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cells. Mol Cancer Ther (2011) 1.13
The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2). J Biol Chem (2004) 1.13
Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks. Dev Biol (2003) 1.10
Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function. Mol Biol Cell (2008) 1.07
Clinical features and associated syndromes of mal de debarquement. J Neurol (2008) 1.02
Bad signals jam organelle traffic. Nat Med (2007) 1.02
RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. Ann Appl Stat (2010) 1.01
Genetic modifiers of abnormal organelle biogenesis in a Drosophila model of BLOC-1 deficiency. Hum Mol Genet (2009) 1.00
Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34. Hum Mol Genet (2006) 0.98
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Dysbindin-containing complexes and their proposed functions in brain: from zero to (too) many in a decade. ASN Neuro (2011) 0.97
A novel mutation in KCNA1 causes episodic ataxia without myokymia. Hum Mutat (2004) 0.95
The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome. Semin Cell Dev Biol (2002) 0.95
Early origin of genes encoding subunits of biogenesis of lysosome-related organelles complex-1, -2 and -3. Traffic (2010) 0.94
A generalized framework for network component analysis. IEEE/ACM Trans Comput Biol Bioinform (2006) 0.94
An immunoblotting assay to facilitate the molecular diagnosis of Hermansky-Pudlak syndrome. Mol Genet Metab (2007) 0.94
The Drosophila pigmentation gene pink (p) encodes a homologue of human Hermansky-Pudlak syndrome 5 (HPS5). Traffic (2006) 0.94
Linkage disequilibrium and haplotype homozygosity in population samples genotyped at a high marker density. Hum Hered (2006) 0.92
Volume measures for linkage disequilibrium. BMC Genet (2006) 0.90
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry (2014) 0.90
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Hum Mol Genet (2005) 0.88
Increased paternal age and the influence on burden of genomic copy number variation in the general population. Hum Genet (2013) 0.88
Reconstructing ancestral haplotypes with a dictionary model. J Comput Biol (2006) 0.87
Phenotype mining in CNV carriers from a population cohort. Hum Mol Genet (2011) 0.87
Tumor necrosis factor modulates transcription of myelin basic protein gene through nuclear factor kappa B in a human oligodendroglioma cell line. Int J Dev Neurosci (2002) 0.86
A dictionary model for haplotyping, genotype calling, and association testing. Genet Epidemiol (2007) 0.86
Normal lytic granule secretion by cytotoxic T lymphocytes deficient in BLOC-1, -2 and -3 and myosins Va, VIIa and XV. Traffic (2005) 0.85
Reconstructing DNA copy number by joint segmentation of multiple sequences. BMC Bioinformatics (2012) 0.84
Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder. Am J Med Genet B Neuropsychiatr Genet (2006) 0.83
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Markov Models for inferring copy number variations from genotype data on Illumina platforms. Hum Hered (2009) 0.83
The pallidin (Pldn) gene and the role of SNARE proteins in melanosome biogenesis. Pigment Cell Res (2002) 0.81
Epigenetic regulation of melanoma tumor suppressor miRNA-124a. Epigenomics (2013) 0.80
Role of miR-18b/MDM2/p53 circuitry in melanoma progression. Epigenomics (2013) 0.78
TFPI2 methylation can serve as an epigenetic biomarker of metastatic melanoma. Epigenomics (2013) 0.75
Empirical bayes estimation of a sparse vector of gene expression changes. Stat Appl Genet Mol Biol (2005) 0.75