Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28592631)
Watch
English
Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
title
Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin
(English)
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
main subject
Signal sequence receptor, alpha
1 reference
stated in
GOA release 2020-03-11
Lectin, mannose-binding, 1
1 reference
stated in
GOA release 2020-03-11
author
Randy Schekman
series ordinal
8
object named as
Randy Schekman
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Jinoh Kim
object named as
Jinoh Kim
series ordinal
7
0 references
David Ginsburg
object named as
David Ginsburg
series ordinal
10
0 references
author name string
Bin Zhang
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Chunlei Zheng
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Min Zhu
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Jiayi Tao
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Matthew P. Vasievich
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Andrea Baines
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
Randal J. Kaufman
series ordinal
9
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
language of work or name
English
0 references
publication date
22 September 2011
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
published in
Blood
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
volume
118
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
issue
12
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
page(s)
3384–3391
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
cites work
Structural basis for the cooperative interplay between the two causative gene products of combined factor V and factor VIII deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Sequential steps and checkpoints in the early exocytic compartment during secretory IgM biogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
LMAN1 and MCFD2 form a cargo receptor complex and interact with coagulation factor VIII in the early secretory pathway
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
The murine platelet and plasma factor V pools are biosynthetically distinct and sufficient for minimal hemostasis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Biosynthetic origin and functional significance of murine platelet factor V
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Liver injury in alpha1-antitrypsin deficiency: an aggregated protein induces mitochondrial injury
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
The structure and function of murine factor V and its inactivation by protein C
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
The recycling of ERGIC-53 in the early secretory pathway. ERGIC-53 carries a cytosolic endoplasmic reticulum-exit determinant interacting with COPII
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
ERGIC-53 is a functional mannose-selective and calcium-dependent human homologue of leguminous lectins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
A putative novel class of animal lectins in the secretory pathway homologous to leguminous lectins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
ERGIC-53, a membrane protein of the endoplasmic reticulum-Golgi intermediate compartment, is identical to MR60, an intracellular mannose-specific lectin of myelomonocytic cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
17 March 2017
Spontaneous Irs1 passenger mutation linked to a gene-targeted SerpinB2 allele
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Molecular basis of LMAN1 in coordinating LMAN1-MCFD2 cargo receptor formation and ER-to-Golgi transport of FV/FVIII
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Protein sorting receptors in the early secretory pathway
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
ERp44 and ERGIC-53 synergize in coupling efficiency and fidelity of IgM polymerization and secretion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
EF-hand domains of MCFD2 mediate interactions with both LMAN1 and coagulation factor V or VIII.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Genotype-phenotype correlation in combined deficiency of factor V and factor VIII.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Identification of ERGIC-53 as an intracellular transport receptor of alpha1-antitrypsin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Receptor-mediated protein transport in the early secretory pathway
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Cargo selectivity of the ERGIC-53/MCFD2 transport receptor complex
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
ER storage diseases: a role for ERGIC-53 in controlling the formation and shape of Russell bodies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Carbohydrate- and conformation-dependent cargo capture for ER-exit
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
The lectin ERGIC-53 is a cargo transport receptor for glycoproteins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Mistargeting of the lectin ERGIC-53 to the endoplasmic reticulum of HeLa cells impairs the secretion of a lysosomal enzyme
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
29 September 2017
Further characterization of factor VIII-deficient mice created by gene targeting: RNA and protein studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
3 June 2018
Ligands "activate" integrin alpha IIb beta 3 (platelet GPIIb-IIIa).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
3 June 2018
A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
Uncoupled packaging of amyloid precursor protein and presenilin 1 into coat protein complex II vesicles
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
ER export of ERGIC-53 is controlled by cooperation of targeting determinants in all three of its domains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
Human recombinant pro-dipeptidyl peptidase I (cathepsin C) can be activated by cathepsins L and S but not by autocatalytic processing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
Expression of factor VIII by murine liver sinusoidal endothelial cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3179404
retrieved
27 November 2018
A tail vein bleeding time model and delayed bleeding in hemophiliac mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21795745
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Expression and characterization of recombinant murine factor VIII
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21795745
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Secretable human platelet-derived factor V originates from the plasma pool
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21795745
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Megakaryocytes endocytose and subsequently modify human factor V in vivo to form the entire pool of a unique platelet-derived cofactor
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21795745
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
That which does not kill me makes me stronger: adapting to chronic ER stress
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21795745
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1182/BLOOD-2011-05-352815
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
PMCID
3179404
0 references
PubMed ID
21795745
1 reference
stated in
PubMed
PubMed ID
21795745
retrieved
31 January 2017
ResearchGate publication ID
51527295
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
