(Q34572566)

English

Molecular basis for congenital deficiency of alpha 2-plasmin inhibitor. A frameshift mutation leading to elongation of the deduced amino acid sequence

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Molecular basis for congenital deficiency of alpha 2-plasmin inhibitor. A frameshift mutation leading to elongation of the deduced amino acid sequence (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

congenital disorder

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author name string

Miura O

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Hirosawa S

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Kato A

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Aoki N

4

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Europe PubMed Central

PubMed publication ID

3 August 2017

language of work or name

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publication date

1 May 1989

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Journal of Clinical Investigation

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Europe PubMed Central

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3 August 2017

83

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Europe PubMed Central

PubMed publication ID

3 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

1598-1604

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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1 reference

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Lambda replacement vectors carrying polylinker sequences

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

1 reference

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Structure of the carboxyl-terminal half of human alpha 2-plasmin inhibitor deduced from that of cDNA.

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Dideoxy sequencing method using denatured plasmid templates

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Organization of the human alpha 2-plasmin inhibitor gene

1 reference

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1 reference

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Structure of human alpha 2-plasmin inhibitor deduced from the cDNA sequence

1 reference

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Hemostasis associated with abnormalities of fibrinolysis

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alpha 2-Antiplasmin Enschede: dysfunctional alpha 2-antiplasmin molecule associated with an autosomal recessive hemorrhagic disorder

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Primary structure of human alpha 2-antiplasmin, a serine protease inhibitor (serpin)

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1 reference

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1 reference

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Fibrinolytic states in a patient with congenital deficiency of alpha 2-plasmin inhibitor

1 reference

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12 December 2020

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A reliable method for the recovery of DNA fragments from agarose and acrylamide gels

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DNA analysis in the diagnosis of hemoglobin disorders

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1 reference

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1 reference

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1 reference

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based on heuristic

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1 reference

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alpha 1-Antitrypsin nullGranite Falls, a nonexpressing alpha 1-antitrypsin gene associated with a frameshift to stop mutation in a coding exon

1 reference

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1 reference

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI114057

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

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