(Q41022147)

English

Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency

scientific article published on December 1, 1992

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scholarly article

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Europe PubMed Central

PMC publication ID

25 September 2017

Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

author name string

K. Yamamoto

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

M. Tanimoto

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

N. Emi

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

T. Matsushita

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

J. Takamatsu

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

H. Saito

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

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publication date

1 December 1992

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

full work available at URL

https://europepmc.org/articles/PMC443400

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Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

https://europepmc.org/articles/PMC443400?pdf=render

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content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1469096

29 September 2022

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

90

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

6

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

2439-2446

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

Characterization of a cDNA coding for human protein C

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Efficient infection of monkey cells with DNA of simian virus 40

1 reference

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26 September 2017

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Absence of thrombosis in subjects with heterozygous protein C deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Evolution and organization of the human protein C gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Biosynthetic protein transport and sorting by the endoplasmic reticulum and Golgi

1 reference

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26 September 2017

Molecular basis of alpha-1-antitrypsin deficiency

1 reference

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26 September 2017

Transport of secretory and membrane glycoproteins from the rough endoplasmic reticulum to the Golgi. A rate-limiting step in protein maturation and secretion.

1 reference

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26 September 2017

The rapid generation of oligonucleotide-directed mutations at high frequency using phosphorothioate-modified DNA.

1 reference

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26 September 2017

The nucleotide sequence of the gene for human protein C

1 reference

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26 September 2017

The structure and evolution of a 461 amino acid human protein C precursor and its messenger RNA, based upon the DNA sequence of cloned human liver cDNAs

1 reference

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26 September 2017

A novel trypsin-like serine protease (hepsin) with a putative transmembrane domain expressed by human liver and hepatoma cells

1 reference

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26 September 2017

Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD.

1 reference

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26 September 2017

Modification of enzymatically amplified DNA for the detection of point mutations.

1 reference

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26 September 2017

Protein C London 1: recurrent mutation at Arg 169 (CGG----TGG) in the protein C gene causing thrombosis

1 reference

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26 September 2017

Polypeptide chain binding proteins: catalysts of protein folding and related processes in cells

1 reference

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26 September 2017

Molecular aspects of heavy-chain class switching

1 reference

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26 September 2017

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

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26 September 2017

Hereditary thrombophilia: identification of nonsense and missense mutations in the protein C gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Mutations and a polymorphism in the factor VIII gene discovered by denaturing gradient gel electrophoresis

1 reference

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26 September 2017

Molecular cloning and expression of two distinct cDNA-encoding heparan sulfate proteoglycan core proteins from a rat endothelial cell line

1 reference

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26 September 2017

A new vitamin K-dependent protein. Purification from bovine plasma and preliminary characterization

1 reference

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26 September 2017

Anticoagulant properties of bovine plasma protein C following activation by thrombin

1 reference

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26 September 2017

Human plasma protein C: isolation, characterization, and mechanism of activation by alpha-thrombin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

26 September 2017

Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus

1 reference

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14 June 2018

Fast functional protein C assay using Protac, a novel protein C activator.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=443400

14 June 2018

Heavy-chain binding protein recognizes aberrant polypeptides translocated in vitro

1 reference

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14 June 2018

Possible absence of common polymorphisms in coagulation factor IX gene in Japanese subjects

1 reference

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14 June 2018

Hereditary alpha 2-plasmin inhibitor deficiency caused by a transport-deficient mutation (alpha 2-PI-Okinawa). Deletion of Glu137 by a trinucleotide deletion blocks intracellular transport.

1 reference

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14 June 2018

The clinical spectrum of heterozygous protein C deficiency in a large New England kindred

1 reference

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14 June 2018

Glycosylation of human protein C affects its secretion, processing, functional activities, and activation by thrombin

1 reference

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14 June 2018

Activated factor IX-antithrombin III complexes in human blood: quantification by an enzyme-linked differential antibody immunoassay and determination of the in vivo half-life

1 reference

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14 June 2018

The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects

1 reference

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14 June 2018

A new hereditary abnormal protein C (protein C Yonago) with a dysfunctional Gla-domain

1 reference

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The mutational specificity of DNA polymerases-alpha and -gamma during in vitro DNA synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype establishments for protein C deficiency by use of a DNA polymorphism in the gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single base-pair deletion in the protein C gene causing recurrent thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of a functional and immunologic assay for plasma protein C in the study of the heterogeneity of congenital protein C deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital protein C deficiency and venous thromboembolism. A study of three Dutch families

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteolytic formation and properties of a fragment of protein C containing the gamma-carboxyglutamic acid rich domain and the EGF-like region

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biosynthesis and secretion of functional protein S by a human megakaryoblastic cell line (MEG-01)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A thrombotic state due to an abnormal protein C

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Propeptide of human protein C is necessary for .gamma.-carboxylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activated protein C decreases plasminogen activator-inhibitor activity in endothelial cell-conditioned medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of crystalline alpha-chymotrypsin. 3. Crystallographic studies of substrates and inhibitors bound to the active site of alpha-chymotrypsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of action of human activated protein C, a thrombin-dependent anticoagulant enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/1469096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI116135

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

25 September 2017

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