On the public citation graph

RAB6C Is a Retrogene that Encodes a Centrosomal Protein Involved in Cell Cycle Progression

https://doi.org/10.1016/j.jmb.2010.01.009
0 signed · 149 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/elps.1150150165openalex-snapshot
Several small GTP‐binding proteins are strongly down‐regulated in simian virus 40 (SV40) transformed human keratinocytes and may be required for the maintenance of the normal phenotype
inferredcites →https://doi.org/10.1002/j.1460-2075.1989.tb08581.xopenalex-snapshot
p34cdc2 is located in both nucleus and cytoplasm; part is centrosomally associated at G2/M and enters vesicles at anaphase.
inferredcites →https://doi.org/10.1006/abio.1993.1170openalex-snapshot
Solubilization and Purification of Enzymatically Active Glutathione S-Transferase (pGEX) Fusion Proteins
inferredcites →https://doi.org/10.1006/jmbi.2001.5072openalex-snapshot
Evolution of the rab family of small GTP-binding proteins
inferredcites →https://doi.org/10.1007/s00018-005-4486-8openalex-snapshot
The structural and mechanistic basis for recycling of Rab proteins between membrane compartments
inferredcites →https://doi.org/10.1016/j.canlet.2008.05.033openalex-snapshot
Does this band make sense? Limits to expression based cancer studies
inferredcites →https://doi.org/10.1016/j.cell.2007.11.048openalex-snapshot
Rab and Arl GTPase Family Members Cooperate in the Localization of the Golgin GCC185
inferredcites →https://doi.org/10.1016/j.cell.2008.08.007openalex-snapshot
A Tale of Too Many Centrosomes
inferredcites →https://doi.org/10.1016/j.cub.2005.04.055openalex-snapshot
mRNA Surveillance of Expressed Pseudogenes in C. elegans
inferredcites →https://doi.org/10.1016/j.devcel.2007.06.010openalex-snapshot
Rab6 Regulates Transport and Targeting of Exocytotic Carriers
inferredcites →https://doi.org/10.1016/j.devcel.2007.07.002openalex-snapshot
Plk4-Induced Centriole Biogenesis in Human Cells
inferredcites →https://doi.org/10.1016/j.gene.2006.11.007openalex-snapshot
Frequent emergence and functional resurrection of processed pseudogenes in the human and mouse genomes
inferredcites →https://doi.org/10.1016/j.yexcr.2005.01.022openalex-snapshot
Characterization of the human GARP (Golgi associated retrograde protein) complex
inferredcites →https://doi.org/10.1016/s0021-9258(18)31779-4openalex-snapshot
Rab proteins form in vivo complexes with two isoforms of the GDP-dissociation inhibitor protein (GDI).
inferredcites →https://doi.org/10.1016/s0021-9258(19)69848-0openalex-snapshot
Phase separation of integral membrane proteins in Triton X-114 solution.
inferredcites →https://doi.org/10.1016/s0167-4889(02)00164-7openalex-snapshot
WTH3, a new member of the Rab6 gene family, and multidrug resistance
inferredcites →https://doi.org/10.1016/s0378-1119(00)00395-4openalex-snapshot
Rab6c, a new member of the Rab gene family, is involved in drug resistance in MCF7/AdrR cells
inferredcites →https://doi.org/10.1016/s0960-9822(02)01221-6openalex-snapshot
The Rab6 GTPase Regulates Recruitment of the Dynactin Complex to Golgi Membranes
inferredcites →https://doi.org/10.1016/s0960-9822(99)80167-5openalex-snapshot
A novel Rab6-interacting domain defines a family of Golgi-targeted coiled-coil proteins
inferredcites →https://doi.org/10.1034/j.1600-0854.2002.030406.xopenalex-snapshot
Characterization of Novel Rab6‐Interacting Proteins Involved in Endosome‐to‐TGN Transport
inferredcites →https://doi.org/10.1038/15658openalex-snapshot
Evidence for a COP-I-independent transport route from the Golgi complex to the endoplasmic reticulum
inferredcites →https://doi.org/10.1038/345553a0openalex-snapshot
Small GTP-binding protein associated with Golgi cisternae
inferredcites →https://doi.org/10.1038/74184openalex-snapshot
Human LINE retrotransposons generate processed pseudogenes
inferredcites →https://doi.org/10.1038/mp.a001995.01openalex-snapshot
Rab6a
inferredcites →https://doi.org/10.1038/nature03798openalex-snapshot
Structural basis of family-wide Rab GTPase recognition by rabenosyn-5
inferredcites →https://doi.org/10.1038/nature06904openalex-snapshot
Pseudogene-derived small interfering RNAs regulate gene expression in mouse oocytes
inferredcites →https://doi.org/10.1038/ncb1474openalex-snapshot
The Plk1 target Kizuna stabilizes mitotic centrosomes to ensure spindle bipolarity
inferredcites →https://doi.org/10.1038/ncb1529openalex-snapshot
Loss of centrosome integrity induces p38—p53—p21-dependent G1—S arrest
inferredcites →https://doi.org/10.1038/ncb891openalex-snapshot
Bicaudal-D regulates COPI-independent Golgi–ER transport by recruiting the dynein–dynactin motor complex
inferredcites →https://doi.org/10.1038/nrm1788openalex-snapshot
Function and regulation of Rnd proteins
inferredcites →https://doi.org/10.1038/sj.bjc.6603724openalex-snapshot
WTH3 is a direct target of the p53 protein
inferredcites →https://doi.org/10.1038/sj.emboj.7600929openalex-snapshot
A role for the Rab6A′ GTPase in the inactivation of the Mad2‐spindle checkpoint
inferredcites →https://doi.org/10.1073/pnas.0511307103openalex-snapshot
Evolutionary fate of retroposed gene copies in the human genome
inferredcites →https://doi.org/10.1073/pnas.0602216103openalex-snapshot
The putatively functional Mkrn1-p1 pseudogene is neither expressed nor imprinted, nor does it regulate its source gene in trans
inferredcites →https://doi.org/10.1073/pnas.152205299openalex-snapshot
Multiple centrosomes arise from tetraploidy checkpoint failure and mitotic centrosome clusters in p53 and RB pocket protein-compromised cells
inferredcites →https://doi.org/10.1073/pnas.94.5.1828openalex-snapshot
GTP-bound forms of rab6 induce the redistribution of Golgi proteins into the endoplasmic reticulum
inferredcites →https://doi.org/10.1074/jbc.m209120200openalex-snapshot
Biochemical and Genetic Evidence for the Involvement of Yeast Ypt6-GTPase in Protein Retrieval to Different Golgi Compartments
inferredcites →https://doi.org/10.1074/jbc.m604363200openalex-snapshot
Biochemical and Structural Characterization of the Gem GTPase
inferredcites →https://doi.org/10.1074/mcp.m700569-mcp200openalex-snapshot
Large Scale Screening for Novel Rab Effectors Reveals Unexpected Broad Rab Binding Specificity
inferredcites →https://doi.org/10.1083/jcb.122.4.775openalex-snapshot
A cytosolic complex of p62 and rab6 associates with TGN38/41 and is involved in budding of exocytic vesicles from the trans-Golgi network
inferredcites →https://doi.org/10.1083/jcb.143.7.1883openalex-snapshot
Aggresomes: A Cellular Response to Misfolded Proteins
inferredcites →https://doi.org/10.1083/jcb.145.1.83openalex-snapshot
GMAP-210, A Cis-Golgi Network-associated Protein, Is a Minus End Microtubule-binding Protein
inferredcites →https://doi.org/10.1083/jcb.147.4.743openalex-snapshot
Rab6 Coordinates a Novel Golgi to ER Retrograde Transport Pathway in Live Cells
inferredcites →https://doi.org/10.1083/jcb.149.2.317openalex-snapshot
The Respective Contributions of the Mother and Daughter Centrioles to Centrosome Activity and Behavior in Vertebrate Cells
inferredcites →https://doi.org/10.1083/jcb.200110081openalex-snapshot
Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform
inferredcites →https://doi.org/10.1089/10665270050081478openalex-snapshot
A Greedy Algorithm for Aligning DNA Sequences
inferredcites →https://doi.org/10.1091/mbc.11.11.3819openalex-snapshot
Alternative Splicing of the HumanRab6AGene Generates Two Close but Functionally Different Isoforms
inferredcites →https://doi.org/10.1091/mbc.e02-08-0510openalex-snapshot
Centrosomes Split in the Presence of Impaired DNA Integrity during Mitosis
inferredcites →https://doi.org/10.1091/mbc.e04-03-0260openalex-snapshot
Regulation of Microtubule-dependent Recycling at theTrans-Golgi Network by Rab6A and Rab6A'
inferredcites →https://doi.org/10.1093/embo-reports/kvd058openalex-snapshot
Systematic subcellular localization of novel proteins identified by large‐scale cDNA sequencing
inferredcites →https://doi.org/10.1093/emboj/18.7.1772openalex-snapshot
Characterization of GAPCenA, a GTPase activating protein for Rab6, part of which associates with the centrosome
inferredcites →https://doi.org/10.1093/emboj/21.4.483openalex-snapshot
Aurora‐A overexpression reveals tetraploidization as a major route to centrosome amplification in p53−/− cells
inferredcites →https://doi.org/10.1093/molbev/msg050openalex-snapshot
Estimation of Divergence Times for Major Lineages of Primate Species
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/gkj144openalex-snapshot
The UCSC Genome Browser Database: update 2006
inferredcites →https://doi.org/10.1093/nar/gkq963openalex-snapshot
The UCSC Genome Browser database: update 2011
inferredcites →https://doi.org/10.1093/nar/gni103openalex-snapshot
A novel high-throughput (HTP) cloning strategy for site-directed designed chimeragenesis and mutation using the Gateway cloning system
inferredcites →https://doi.org/10.1101/gr.1429003openalex-snapshot
Millions of Years of Evolution Preserved: A Comprehensive Catalog of the Processed Pseudogenes in the Human Genome
inferredcites →https://doi.org/10.1101/gr.1455503openalex-snapshot
A Genome-Wide Survey of Human Pseudogenes
inferredcites →https://doi.org/10.1101/gr.2658304openalex-snapshot
High-Content Screening Microscopy Identifies Novel Proteins With a Putative Role in Secretory Membrane Traffic
inferredcites →https://doi.org/10.1101/gr.6252107openalex-snapshot
A novel testis ubiquitin-binding protein gene arose by exon shuffling in hominoids
inferredcites →https://doi.org/10.1107/s0907444904019158openalex-snapshot
Coot : model-building tools for molecular graphics
inferredcites →https://doi.org/10.1111/j.1365-2818.2007.01723.xopenalex-snapshot
Visualization and quantification of vesicle trafficking on a three‐dimensional cytoskeleton network in living cells
inferredcites →https://doi.org/10.1111/j.1600-0854.2006.00395.xopenalex-snapshot
Rab6A and Rab6A′ GTPases Play Non‐overlapping Roles in Membrane Trafficking
inferredcites →https://doi.org/10.1111/j.1600-0854.2006.00418.xopenalex-snapshot
Transport of Ricin from Endosomes to the Golgi Apparatus is Regulated by Rab6A and Rab6A′
inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00612.xopenalex-snapshot
Rab6‐interacting Protein 1 Links Rab6 and Rab11 Function
inferredcites →https://doi.org/10.1126/science.1166745openalex-snapshot
Orc1 Controls Centriole and Centrosome Copy Number in Human Cells
inferredcites →https://doi.org/10.1126/science.279.5350.580openalex-snapshot
Interaction of a Golgi-Associated Kinesin-Like Protein with Rab6
inferredcites →https://doi.org/10.1158/0008-5472.can-05-0658openalex-snapshot
WTH3, which Encodes a Small G Protein, Is Differentially Regulated in Multidrug-Resistant and Sensitive MCF7 Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1944openalex-snapshot
Epigenetic Regulation of WTH3 in Primary and Cultured Drug-Resistant Breast Cancer Cells
inferredcites →https://doi.org/10.1167/iovs.08-2755openalex-snapshot
Single choroideremia Gene in Nonmammalian Vertebrates Explains Early Embryonic Lethality of the Zebrafish Model of Choroideremia
inferredcites →https://doi.org/10.1186/1471-2164-9-466openalex-snapshot
Retrocopy contributions to the evolution of the human genome
inferredcites →https://doi.org/10.1186/1471-2407-8-327openalex-snapshot
Methylation of WTH3, a possible drug resistant gene, inhibits p53 regulated expression
inferredcites →https://doi.org/10.1242/jcs.02302openalex-snapshot
Microtubule nucleation and anchoring at the centrosome are independent processes linked by ninein function
inferredcites →https://doi.org/10.1242/jcs.103.3.785openalex-snapshot
The small gtp-binding protein rab6p is distributed from medial golgi to the Trans-golgi network as determined by a confocal microscopic approach
inferredcites →https://doi.org/10.1242/jcs.113.15.2725openalex-snapshot
The small GTPase Rab6B, a novel Rab6 subfamily member, is cell-type specifically expressed and localised to the Golgi apparatus
inferredcites →https://doi.org/10.1242/jcs.115.8.1663openalex-snapshot
Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo
inferredcites →https://doi.org/10.1371/journal.pbio.0060080openalex-snapshot
Chromosomal Gene Movements Reflect the Recent Origin and Biology of Therian Sex Chromosomes
inferredcites →https://doi.org/10.1371/journal.pbio.0060140openalex-snapshot
Birth and Rapid Subcellular Adaptation of a Hominoid-Specific CDC14 Protein
inferredcites →https://doi.org/10.1515/bc.2005.078openalex-snapshot
Rab6 interacts with the mint3 adaptor protein

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4653172openalex-extracted
The α 2A-Adrenergic Receptor ( ADRA2A) Modulates Susceptibility to Raynaud's Syndrome
inferred← citeshttps://doi.org/10.1002/ctm2.692openalex-snapshot
Multi‐omic landscaping of human midbrains identifies disease‐relevant molecular targets and pathways in advanced‐stage Parkinson's disease
inferred← citeshttps://doi.org/10.1002/jex2.141openalex-snapshot
RAB31 drives extracellular vesicle fusion and cancer‐associated fibroblast formation leading to oxaliplatin resistance in colorectal cancer
inferred← citeshttps://doi.org/10.1002/mc.22765openalex-snapshot
MiR‐5100 increases the cisplatin resistance of the lung cancer stem cells by inhibiting the Rab6
inferred← citeshttps://doi.org/10.1007/978-1-0716-1346-7_18openalex-snapshot
Generating Rab6 Conditional Knockout Mice
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_6openalex-snapshot
Multiple Roles of Rab GTPases at the Golgi
inferred← citeshttps://doi.org/10.1007/s00018-012-1021-6openalex-snapshot
Are Rab proteins the link between Golgi organization and membrane trafficking?
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2014.12.002openalex-snapshot
How Rab Proteins Determine Golgi Structure
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.05.005openalex-snapshot
Reconstitution of the targeting of Rab6A to the Golgi apparatus in semi-intact HeLa cells: A role of BICD2 in stabilizing Rab6A on Golgi membranes and a concerted role of Rab6A/BICD2 interactions in Golgi-to-ER retrograde transport
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107712openalex-snapshot
ELKS1 Captures Rab6-Marked Vesicular Cargo in Presynaptic Nerve Terminals
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.12.046openalex-snapshot
Interpopulation differences of retroduplication variations (RDVs) in rice retrogenes and their phenotypic correlations
inferred← citeshttps://doi.org/10.1016/j.cub.2022.02.018openalex-snapshot
Recurrent evolution of an inhibitor of ESCRT-dependent virus budding and LINE-1 retrotransposition in primates
inferred← citeshttps://doi.org/10.1016/j.gene.2018.08.033openalex-snapshot
Transcriptional activation of a chimeric retrogene PIPSL in a hominoid ancestor
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104808openalex-snapshot
Structural basis of ELKS/Rab6B interaction and its role in vesicle capturing enhanced by liquid-liquid phase separation
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2017.03.007openalex-snapshot
Golgi trafficking defects in postnatal microcephaly: The evidence for “Golgipathies”
inferred← citeshttps://doi.org/10.1016/j.xgen.2024.100630openalex-snapshot
Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity
inferred← citeshttps://doi.org/10.1021/acs.biochem.8b00987openalex-snapshot
A Quantitative Model for BicD2/Cargo Interactions
inferred← citeshttps://doi.org/10.1038/nrm3641openalex-snapshot
Protein adaptation: mitotic functions for membrane trafficking proteins
inferred← citeshttps://doi.org/10.1038/srep23560openalex-snapshot
Involvement of Rab6a in organelle rearrangement and cytoskeletal organization during mouse oocyte maturation
inferred← citeshttps://doi.org/10.1042/bst20120199openalex-snapshot
Novel functions for Rab GTPases in multiple aspects of tumour progression
inferred← citeshttps://doi.org/10.1042/bst20140178openalex-snapshot
The trials and tubule-ations of Rab6 involvement in Golgi-to-ER retrograde transport
inferred← citeshttps://doi.org/10.1073/pnas.2000102117openalex-snapshot
Novel genetic features of human and mouse Purkinje cell differentiation defined by comparative transcriptomics
inferred← citeshttps://doi.org/10.1080/1061186x.2017.1358725openalex-snapshot
Green fluorescent protein (GFP): is seeing believing and is that enough?
inferred← citeshttps://doi.org/10.1080/21541248.2017.1384087openalex-snapshot
Rab proteins as major determinants of the Golgi complex structure
inferred← citeshttps://doi.org/10.1080/21541248.2017.1397833openalex-snapshot
Consequences of Rab GTPase dysfunction in genetic or acquired human diseases
inferred← citeshttps://doi.org/10.1080/21541248.2023.2238330openalex-snapshot
Rab6-mediated retrograde trafficking from the Golgi: the trouble with tubules
inferred← citeshttps://doi.org/10.1089/dna.2015.2938openalex-snapshot
Mobile DNA Elements: The Seeds of Organic Complexity on Earth
inferred← citeshttps://doi.org/10.1101/2021.04.27.441704openalex-snapshot
Recurrent Emergence of an Antiviral Defense through Repeated Retrotransposition and Truncation of CHMP3
inferred← citeshttps://doi.org/10.1101/2023.10.04.23296526openalex-snapshot
The α 2A -adrenergic receptor ( ADRA2A ) modulates susceptibility to Raynaud’s syndrome
inferred← citeshttps://doi.org/10.1111/boc.201400083openalex-snapshot
Phenotypic characterisation of RAB6A knockout mouse embryonic fibroblasts
inferred← citeshttps://doi.org/10.1111/imcb.12503openalex-snapshot
Rab6b localizes to the Golgi complex in murine macrophages and promotes tumor necrosis factor release in response to mycobacterial infection
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2010.00503.xopenalex-snapshot
Marked Amplification and Diversification of Products of ras Genes from Rat Brain, Rab GTPases, in the Ciliates Tetrahymena thermophila and Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2011.01184.xopenalex-snapshot
Mitotic Moonlighting Functions for Membrane Trafficking Proteins
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2012.01343.xopenalex-snapshot
Electron T omography R eveals R ab6 I s E ssential to the T rafficking of trans‐ G olgi C lathrin and COPI ‐ C oated V esicles and the M aintenance of G olgi C isternal N umber
inferred← citeshttps://doi.org/10.1111/tra.12134openalex-snapshot
Rab6 Dependent Post‐Golgi Trafficking of HSV1 Envelope Proteins to Sites of Virus Envelopment
inferred← citeshttps://doi.org/10.1111/tra.70047openalex-snapshot
The Secret (Mitotic) Life of Clathrin
inferred← citeshttps://doi.org/10.1128/jvi.02605-10openalex-snapshot
A Role for the Small GTPase Rab6 in Assembly of Human Cytomegalovirus
inferred← citeshttps://doi.org/10.1142/s0219720018500063openalex-snapshot
Integrative analysis of gene expression and DNA methylation using unsupervised feature extraction for detecting candidate cancer biomarkers
inferred← citeshttps://doi.org/10.11588/heidok.00016264openalex-snapshot
Analysis of miR-30b as a Regulator of tsO45-G Anterograde Trafficking
inferred← citeshttps://doi.org/10.1159/000497035openalex-snapshot
Golgipathies in Neurodevelopment: A New View of Old Defects
inferred← citeshttps://doi.org/10.11606/d.5.2011.tde-18022011-153643openalex-snapshot
Determinação do perfil de expressão de microRNAs em câncer de mama em mulheres jovens
inferred← citeshttps://doi.org/10.1186/1741-7007-10-71openalex-snapshot
Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
inferred← citeshttps://doi.org/10.1242/dev.203038openalex-snapshot
The GTPase RAB6 is required for stem cell maintenance and cell migration in the gut epithelium
inferred← citeshttps://doi.org/10.1242/jcs.185702openalex-snapshot
Bidirectional traffic between the Golgi and the endosomes – machineries and regulation
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1002217openalex-snapshot
Thousands of Rab GTPases for the Cell Biologist
inferred← citeshttps://doi.org/10.1371/journal.pone.0035637openalex-snapshot
Mapping the Interactions between a RUN Domain from DENND5/Rab6IP1 and Sorting Nexin 1
inferred← citeshttps://doi.org/10.1371/journal.pone.0057034openalex-snapshot
Rab6a/a’ Are Important Golgi Regulators of Pro-Inflammatory TNF Secretion in Macrophages
inferred← citeshttps://doi.org/10.1371/journal.pone.0064149openalex-snapshot
A New Mint1 Isoform, but Not the Conventional Mint1, Interacts with the Small GTPase Rab6
inferred← citeshttps://doi.org/10.1371/journal.pone.0071886openalex-snapshot
Rab41 Is a Novel Regulator of Golgi Apparatus Organization That Is Needed for ER-To-Golgi Trafficking and Cell Growth
inferred← citeshttps://doi.org/10.1371/journal.pone.0080228openalex-snapshot
RABL6A, a Novel RAB-Like Protein, Controls Centrosome Amplification and Chromosome Instability in Primary Fibroblasts
inferred← citeshttps://doi.org/10.1371/journal.pone.0149314openalex-snapshot
RAB-6.1 and RAB-6.2 Promote Retrograde Transport in C. elegans
inferred← citeshttps://doi.org/10.1534/g3.112.004366openalex-snapshot
NANOGP8: Evolution of a Human-Specific Retro-Oncogene
inferred← citeshttps://doi.org/10.25560/78821openalex-snapshot
Intracellular trafficking of cancer-implicated proteins in women’s cancers
inferred← citeshttps://doi.org/10.3384/diss.diva-145398openalex-snapshot
Long-term prognostic and predictive factors in hormone receptor positive breast cancer
inferred← citeshttps://doi.org/10.3389/fcell.2016.00013openalex-snapshot
Identification of Rab41/6d Effectors Provides an Explanation for the Differential Effects of Rab41/6d and Rab6a/a' on Golgi Organization
inferred← citeshttps://doi.org/10.3389/fgene.2021.756784openalex-snapshot
Agent Repurposing for the Treatment of Advanced Stage Diffuse Large B-Cell Lymphoma Based on Gene Expression and Network Perturbation Analysis
inferred← citeshttps://doi.org/10.3390/books978-3-03842-541-0openalex-snapshot
Recent Progress in Understanding the Mechanism and Consequences of Retrotransposon Movement
inferred← citeshttps://doi.org/10.3390/cells10010072openalex-snapshot
Rab6A as a Pan-Astrocytic Marker in Mouse and Human Brain, and Comparison with Other Glial Markers (GFAP, GS, Aldh1L1, SOX9)
inferred← citeshttps://doi.org/10.3390/genes11050542openalex-snapshot
Complex Analysis of Retroposed Genes’ Contribution to Human Genome, Proteome and Transcriptome
inferred← citeshttps://doi.org/10.3390/ijms26062569openalex-snapshot
Correlation of Anti-TULP1 Autoantibodies with Breast Cancer and Autoimmune Retinopathy
inferred← citeshttps://doi.org/10.3390/v9040080openalex-snapshot
Protein-Coding Genes’ Retrocopies and Their Functions
inferred← citeshttps://doi.org/10.3892/mco.2020.2014openalex-snapshot
Low RAB6C expression is a predictor of tamoxifen benefit in estrogen receptor‑positive/progesterone receptor‑negative breast cancer
inferred← citeshttps://doi.org/10.3892/mmr.2021.12432openalex-snapshot
Rab6c is a new target of miR‑218 that can promote the progression of bladder cancer
inferred← citeshttps://doi.org/10.3892/ol.2019.11109openalex-snapshot
RAB6C is an independent prognostic factor of estrogen receptor‑positive/progesterone receptor‑negative breast cancer
inferred← citeshttps://doi.org/10.4161/sgtp.23707openalex-snapshot
The RhoD to centrosomal duplication
inferred← citeshttps://doi.org/10.6083/m48p5z7topenalex-snapshot
The Role of Rab6 in Presenting Mycobacterium Tuberculosis Antigens to CD8+ T Cells from Infected Epithelial Cells
inferred← citeshttps://doi.org/10.70675/3b69adddzddf6z407fz8873z266c1709027fopenalex-snapshot
The Golgi associated RAB6 GTPase as a general regulator of post-Golgi secretion
inferred← citeshttps://doi.org/10.70675/7d739ff8z5856z4e86zb4a6z4d85761d0a3dopenalex-snapshot
Membrane binding properties of RAB GTPases
inferred← citeshttps://doi.org/10.70675/808785c1z1979z4f05z95e9z14f86804be78openalex-snapshot
Rôle de la GTPase golgienne RAB6 dans la fonction du lignage sécrétoire mammaire
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.