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Retro2 binds directly to Sec16A a Scheme of bioorthogonal click

Phosphorylationcoupled autoregulation of TANGO1 and Sec16A maintains

Subcellular SEC16A The Human Protein Atlas

The ER marker SEC61BGFP does not colocalize with perinuclear SEC16A or

Relocalized Sec16A colocalizes with the ER marker proteins ac

Phosphorylationcoupled autoregulation of TANGO1 and Sec16A maintains

LRRK2 colocalizes with Sec16A proteins at the dERES of cultured

Sec16A drives Sec body formation in INS1 cells A PCR of Sec16A and

SEC16A forms a complex with PI31 and TBK1 A Immunoblot analysis

The organization of perinuclear RAB10 and SEC16A with GLUT4 has

Sec16A silencing inhibits unconventional ΔF508-CFTR trafficking to the ...

Sec16A silencing inhibits unconventional F508CFTR trafficking to the

Sec16A and Sec31A immunoelectron microscopy AC Localisation of

A GFPSec16B shows a high degree of overlap with endogenous Sec16A

SEC16A is a RAB10 effector A Representative images of in situ PLA

ULKMediated Phosphorylation of SEC16A at S846 Is Required for Assembly

SEC16A and Intracellular Trafficking Abnormalities in Axial

Interaction of Sec16A CCD and Sec13 A Triplicate spots of yeast

SEC16A is a RAB10 effector required for insulinstimulated GLUT4

Sec16A and Sec31A immunoelectron microscopy AC Localisation of

A GFPSec16B shows a high degree of overlap with endogenous Sec16A

Increase in Sec16A detected by indirect immunofluorescence early in PV

Private rare deletions in SEC16A and MAMDC4 may represent novel

SEC16A is not required for maintenance of reticular ER morphology

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STED Imaging Shows Close Juxtaposition of Sec16A and ERGIC53 Remains

SEC16A is required for GLUT4 translocation A Quantification of PM to

Sec16A is critical for both conventional and unconventional secretion

Phosphorylationcoupled autoregulation of TANGO1 and Sec16A maintains

A GFPSec16B shows a high degree of overlap with endogenous Sec16A

Leucinerich repeat kinase 2 regulates Sec16A at ER exit sites to allow

SEC16A KD does not affect insulin signal transduction or TR

$Increases in Sec16A levels in membrane and cytosolic fractions early in ...$

Increases in Sec16A levels in membrane and cytosolic fractions early in

Construction of pathogenic Sec16a mutation mouse model using CRISPR

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Relocalization of Sec16A in GRASPmediated unconventional secretion of

Construction of pathogenic Sec16a mutation mouse model using CRISPR

Anti SEC16A pAb Catalog No ATLHPA005684

SEC16A and RAB10 are required for GLUT4 vesicle mobilization from a

Construction of pathogenic Sec16a mutation mouse model using CRISPR

Sec16A colocalizes and interacts with GRASP55 ad The cellular

RAB10 colocalizes with HAGLUT4GFP and SEC16A at the perinuclear

SEC16A independently regulates ERtoGolgi and GLUT4 trafficking A

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Subcellular SEC16A The Human Protein Atlas

Downregulation of Syn5 and Sec16A expression impair hRSV replication

Private rare deletions in SEC16A and MAMDC4 may represent novel

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Requirement of Sec16A and p115 for optimal type I IFN innate immune

Construction of pathogenic Sec16a mutation mouse model using CRISPR

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Subcellular SEC16A The Human Protein Atlas

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Alteration of Sec16A subcellular distribution in dendrites of Lrrk2

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Depletion of Sec16A phenocopies Retro2 effects a HeLa cells

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Structural comparison of Sec16 and Sec31 A Domain organization of

Schematic of the role of RAB10SEC16A in insulinregulated GLUT4

Sec16A a key protein in COPII vesicle formation regulates the

Sec16Apositive structures in stressed INS1 cells are Sec bodies A

Multimodal regulation of the ERES scaffolding protein Sec16 A

DYRK3 enables secretory trafficking by maintaining the liquidlike

Requirements for the localisation of GFPSec16A in HeLa cells The top

Sec16A a key protein in COPII vesicle formation regulates the

Sec16Apositive structures in stressed INS1 cells are Sec bodies A

Figure 1 from Regulation of Sec16 levels and dynamics links

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Sec16A a key protein in COPII vesicle formation regulates the

Sec16Apositive structures in stressed INS1 cells are Sec bodies A

Sec16A a key protein in COPII vesicle formation regulates the

DYRK3 enables secretory trafficking by maintaining the liquidlike

Localization of GFPSec16A COPII subunits and ERGIC components AB

SEC16ASEC16 ab70722 Abcam

Multimodal regulation of the ERES scaffolding protein Sec16 A

MAG5SEC16A Fusion Proteins Colocalize with YFPSEC24A and SEC13AGFP

Comparison of the Dynamics of MAG5SEC16A with That of SEC24 at ERESs

MAG5SEC16A Interacts with SEC13 and SEC31 A and B Immunoblots A

DYRK3 enables secretory trafficking by maintaining the liquidlike

A Deficiency of MAG5SEC16A Does Not Affect the Association of COPII

Images and plots of sideaveraged Golgi proteins A ERES protein

MAG5SEC16A Fusion Proteins Colocalize with YFPSEC24A and SEC13AGFP

An alternative splicing signature defines the basallike phenotype and

AntiSEC16A Human Protein Atlas Antibody

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Sec16A but not core COPII components is required for unconventional

AntiSEC16ASEC16 antibody ab70722 Abcam

DYRK3 enables secretory trafficking by maintaining the liquidlike

Loss of hepatic VMP1 trapped VLDL in the bilayer of endoplasmic

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Figure 1 from Regulation of Sec16 levels and dynamics links

Sec16B is involved in the endoplasmic reticulum export of the

SEC16A

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MAG5SEC16A Fusion Proteins Colocalize with YFPSEC24A and SEC13AGFP

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Knockdown of Sec16B induces elongation of peroxisomes HeLa cells were

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COPIIASO colocalization does not require de novo COPII assembly at

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