Evidence map›Paper›PMID 30065114›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo.

Rami Khoriaty, Geoffrey G Hesketh, Amélie Bernard, Angela C Weyand, Dattatreya Mellacheruvu, Guojing Zhu, Mark J Hoenerhoff, Beth McGee, Lesley Everett, Elizabeth J Adams and 7 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Hereditary disorders of ineffective erythropoiesis.Blood cells, molecules & diseases · 2025
    Review
  9. Article
  10. Genetics of hemostasis: from bedside to bench and back again.The Journal of clinical investigation · 2024
    Article
  11. Functional overlap between the mammalianProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Functional overlap between the mammalianbioRxiv : the preprint server for biology · 2024
    Article
  14. New Cases and Mutations inInternational journal of molecular sciences · 2023
    Article
  15. IncreasedCancers · 2023
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Rami KhoriatyDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI 48109; ramikhor@umich.edu ginsburg@umich.edu.
Geoffrey G HeskethLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, M5G 1X5 ON, Canada.
Amélie BernardLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Angela C WeyandDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI 48109.
Dattatreya MellacheruvuDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Guojing ZhuLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Mark J HoenerhoffIn Vivo Animal Core, Unit for Laboratory Animal Medicine, University of Michigan, Ann Arbor, MI 48109.
Beth McGeeLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Lesley EverettLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Elizabeth J AdamsLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Bin ZhangGenomic Medicine Institute, Cleveland Clinic Lerner Research Institute, Cleveland, OH 44106.
Thomas L SaundersTransgenic Animal Model Core, University of Michigan, Ann Arbor, MI 48109.
Alexey I NesvizhskiiDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Daniel J KlionskyLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Jordan A ShavitProgram in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109.
Anne-Claude GingrasLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, M5G 1X5 ON, Canada.
David GinsburgDepartment of Internal Medicine, University of Michigan, Ann Arbor, MI 48109; ramikhor@umich.edu ginsburg@umich.edu.ORCID 0000-0002-6436-8942

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
TRANSGENIC MODELS FOR THE STUDY OF FACTOR V FUNCTIONP01HL057346 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GORDON, DAVID · 1997 to 2013
$19.9M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
ALTERNATIVE VACUOLAR TARGETING MECHANISMS IN YEASTR01GM053396 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KLIONSKY, DANIEL J. · 1995 to 2018
$12.1M
Training Program in Molecular HematologyT32HL007622 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SUNG WON CHOI, Jordan A. Shavit · 1986 to 2026
$9.2M
COMPUTATIONAL TOOLS FOR MASS SPECTROMETRY-BASED INTERACTOME DATAR01GM094231 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 2010 to 2026
$5.4M
ER-to-Golgi transport of coagulation factors V and VIIIR01HL094505 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI ZHANG, BIN · 2009 to 2022
$5.1M
The Molecular Genetics of HemostasisR35HL135793 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GINSBURG, DAVID · 2017 to 2023
$4.1M
Molecular Genetic Study of von Willebrand FactorR01HL039693 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GINSBURG, DAVID · 1989 to 2016
$2.4M
Dissecting the Genetics of Human Hemostatic Disorders Using ZebrafishR01HL124232 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAVIT, JORDAN A · 2015 to 2019
$1.9M
The Evolution of the Mammalian SEC23 Paralogs and the Molecular Pathogenesis of Congenital Dyserythropoietic Anemia type IIK08HL128794 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHORIATY, RAMI · 2015 to 2019
$812k
CIHR FDN 143301Howard Hughes Medical InstituteNCI NIH HHS P30 CA046592NHLBI NIH HHS K08 HL128794NHLBI NIH HHS P01 HL057346NHLBI NIH HHS R01 HL039693NHLBI NIH HHS R01 HL094505NHLBI NIH HHS R01 HL124232NHLBI NIH HHS R35 HL135793NHLBI NIH HHS T32 HL007622NIGMS NIH HHS R01 GM053396NIGMS NIH HHS R01 GM094231NIGMS NIH HHS T32 GM007315
6 · The paper itself

Abstract

Approximately one-third of the mammalian proteome is transported from the endoplasmic reticulum-to-Golgi via COPII-coated vesicles. SEC23, a core component of coat protein-complex II (COPII), is encoded by two paralogous genes in vertebrates (

Indexed as

Anemia, Dyserythropoietic, CongenitalBone MarrowCOP-Coated VesiclesErythrocytesGene Expression RegulationHEK293 CellsHumansMultiprotein ComplexesSpecies SpecificityVesicular Transport ProteinsMultiprotein ComplexesSEC23A protein, humanSec23a protein, mouseSEC23B protein, humanSEC23B protein, mouseVesicular Transport Proteinsendoplasmic reticulummiceSEC23transgenicvesicular transport proteins

Identifiers

PMID30065114
PMCPMC6099849

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.