(Q34181756)

English

Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

31 July 2017

Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide (English)

1 reference

Europe PubMed Central

31 July 2017

1 reference

based on heuristic

inferred from title

paroxysmal extreme pain disorder

1 reference

based on heuristic

inferred from title

prolidase deficiency

1 reference

based on heuristic

inferred from title

author name string

Tanoue A

1

1 reference

Europe PubMed Central

31 July 2017

Endo F

2

1 reference

Europe PubMed Central

31 July 2017

Akaboshi I

3

1 reference

Europe PubMed Central

31 July 2017

Oono T

4

1 reference

Europe PubMed Central

31 July 2017

Arata J

5

1 reference

Europe PubMed Central

31 July 2017

Matsuda I

6

1 reference

Europe PubMed Central

31 July 2017

language of work or name

0 references

publication date

1 April 1991

1 reference

Europe PubMed Central

31 July 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

31 July 2017

87

1 reference

Europe PubMed Central

31 July 2017

1171-1176

1 reference

Europe PubMed Central

31 July 2017

4

1 reference

Europe PubMed Central

31 July 2017

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

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=295128

5 July 2018

New host cell system for regulated simian virus 40 DNA replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Primary structure and gene localization of human prolidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Prolidase deficiency: biochemical classification of alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Expression vector system based on the chicken beta-actin promoter directs efficient production of interleukin-5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Structural organization of the gene for human prolidase (peptidase D) and demonstration of a partial gene deletion in a patient with prolidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Prolidase deficiency: its dermatological manifestations and some additional biochemical studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295128

28 October 2018

Immunochemical studies of human prolidase with monoclonal and polyclonal antibodies: absence of the subunit of prolidase in erythrocytes from a patient with prolidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunoaffinity purification of human erythrocyte prolidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peptidase D (prolidase) variants in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening method for prolidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the formation of spontaneous deletions: The importance of short sequence homologies in the generation of large deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression and regulation of Escherichia coli lacZ gene fusions in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage between the loci for myotonic dystrophy and peptidase D

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presence in human cells and tissues of two prolidases and their alteration in prolidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical studies on prolidase in sera from control, patients with prolidase deficiency and their mother

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI115115

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34181756&oldid=1512375402"