(Q38290368)

English

Two Mutations in the Promoter Region of the Human Protein C Gene Both Cause Type I Protein C Deficiency by Disruption of Two HNF-3 Binding Sites

scientific article published on October 13, 1995

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

Two mutations in the promoter region of the human protein C gene both cause type I protein C deficiency by disruption of two HNF-3 binding sites (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

Two Mutations in the Promoter Region of the Human Protein C Gene Both Cause Type I Protein C Deficiency by Disruption of Two HNF-3 Binding Sites (English)

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

protein C deficiency

1 reference

based on heuristic

inferred from title

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%3A7592627

31 May 2024

1

object named as

C. A. Spek

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7592627

31 May 2024

author name string

J. S. Greengard

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%3A7592627

31 May 2024

J. H. Griffin

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%3A7592627

31 May 2024

R. M. Bertina

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7592627

31 May 2024

P. H. Reitsma

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%3A7592627

31 May 2024

language of work or name

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publication date

1 October 1995

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

13 October 1995

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7592627

31 May 2024

number of pages

6

1 reference

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inferred from page(s)

full work available at URL

http://www.jbc.org/article/S0021925818575141/pdf

Portable Document Format

online access status

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%3A7592627

31 May 2024

https://api.elsevier.com/content/article/PII:S0021925818575141?httpAccept=text/xml

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

https://api.elsevier.com/content/article/PII:S0021925818575141?httpAccept=text/plain

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

https://syndication.highwire.org/content/doi/10.1074/jbc.270.41.24216

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

270

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

41

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

24216-24221

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

Deficiency of protein C in congenital thrombotic disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Sublocalization of the human protein C gene on chromosome 2q13-q14.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The nucleotide sequence of the gene for human protein C

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Evolution and organization of the human protein C gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The basics of basal transcription by RNA polymerase II.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The complexities of eukaryotic transcription initiation: regulation of preinitiation complex assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The liver-specific transcription factor LF-B1 contains a highly diverged homeobox DNA binding domain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Hepatocyte nuclear factor 3 alpha belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene fork head

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Liver-enriched transcription factor HNF-4 is a novel member of the steroid hormone receptor superfamily

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

DBP, a liver-enriched transcriptional activator, is expressed late in ontogeny and its tissue specificity is determined posttranscriptionally

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

LAP, a novel member of the C/EBP gene family, encodes a liver-enriched transcriptional activator protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Disruption of a C/EBP binding site in the factor IX promoter is associated with haemophilia B.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia

1 reference

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21 January 2018

Two distinct enhancers with different cell specificities coexist in the regulatory region of polyoma.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Cell-specific expression of the rat insulin gene: evidence for role of two distinct 5' flanking elements

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The DNA-binding specificity of the hepatocyte nuclear factor 3/forkhead domain is influenced by amino-acid residues adjacent to the recognition helix

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Multiple hepatocyte-enriched nuclear factors function in the regulation of transthyretin and alpha 1-antitrypsin genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

An RNA-protein contact determined by 5-bromouridine substitution, photocrosslinking and sequencing

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Hierarchy and positive/negative interplays of the hepatocyte nuclear factors HNF-1, -3 and -4 in the liver-specific enhancer for the human alpha-1-microglobulin/bikunin precursor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Cell-type specific activity of two glucocorticoid responsive units of rat tyrosine aminotransferase gene is associated with multiple binding sites for C/EBP and a novel liver-specific nuclear factor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Hepatic nuclear factor 3- and hormone-regulated expression of the phosphoenolpyruvate carboxykinase and insulin-like growth factor-binding protein 1 genes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Decreased expression of hepatocyte nuclear factor 3 alpha during the acute-phase response influences transthyretin gene transcription

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Expression of hepatic transcription factors during liver development and oval cell differentiation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Modulation of liver-specific transcription by interactions between hepatocyte nuclear factor 3 and nuclear factor 1 binding DNA in close apposition

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

The mechanism by which the human apolipoprotein B gene reducer operates involves blocking of transcriptional activation by hepatocyte nuclear factor 3.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Protein C prevents the coagulopathic and lethal effects of Escherichia coli infusion in the baboon

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Crystal structure of TFIID TATA-box binding protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

A simple phase-extraction assay for chloramphenicol acyltransferase activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

CCAAT/enhancer binding protein activates the promoter of the serum albumin gene in cultured hepatoma cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Duality of TBP, the universal transcription factor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.270.41.24216

21 January 2018

Protein S and C4b-Binding Protein: Components Involved in the Regulation of the Protein C Anticoagulant System

1

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

Regulation of blood coagulation by the protein C system

2

1 reference

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31 May 2024

The protein C anticoagulant pathway

3

1 reference

10.1074/JBC.270.41.24216

https://api.crossref.org/works/10.1074/JBC.270.41.24216

31 May 2024

Identifiers

10.1074/JBC.270.41.24216

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 September 2017

ResearchGate publication ID

0 references

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