Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema (Q35881940)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8755917%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

title

Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema (English)

1 reference

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18 October 2019

1 reference

Verpy E

1

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18 October 2019

Biasotto M

2

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18 October 2019

Brai M

3

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18 October 2019

Misiano G

4

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18 October 2019

Meo T

5

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18 October 2019

Tosi M

6

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18 October 2019

language of work or name

English

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publication date

1 August 1996

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American Journal of Human Genetics

18 October 2019

published in

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18 October 2019

volume

59

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18 October 2019

issue

2

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18 October 2019

page(s)

308-319

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8755917%20AND%20SRC:MED&resulttype=core&format=json

HEREDITARY ANGIONEUROTIC EDEMA: TWO GENETIC VARIANTS.

18 October 2019

cites work

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11 July 2018

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11 July 2018

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The rapid detection of unknown mutations in nucleic acids.

11 July 2018

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Transcriptional regulation of the C1 inhibitor gene by gamma-interferon.

11 July 2018

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Efficient detection of point mutations on color-coded strands of target DNA.

11 July 2018

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Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.

11 July 2018

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

11 July 2018

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COOH-terminal substitutions in the serpin C1 inhibitor that cause loop overinsertion and subsequent multimerization

11 July 2018

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Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

11 July 2018

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Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function

11 July 2018

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What do dysfunctional serpins tell us about molecular mobility and disease?

11 July 2018

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Current methods of mutation detection

11 July 2018

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Human C1 inhibitor: primary structure, cDNA cloning, and chromosomal localization

11 July 2018

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An IgG autoantibody which inactivates C1-inhibitor

11 July 2018

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C1 inhibitor and hereditary angioneurotic edema

11 July 2018

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Chemical reactivity of matched cytosine and thymine bases near mismatched and unmatched bases in a heteroduplex between DNA strands with multiple differences

11 July 2018

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Ribonucleoprotein and protein factors bind to an H-DNA-forming c-myc DNA element: possible regulators of the c-myc gene.

11 July 2018

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Increased Sp1 binding mediates erythroid-specific overexpression of a mutated (HPFH) gamma-globulin promoter

11 July 2018

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Scanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavage

11 July 2018

1 reference

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

11 July 2018

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Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

11 July 2018

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Complete nucleotide sequence of the gene for human C1 inhibitor with an unusually high density of Alu elements

11 July 2018

1 reference

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Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele

11 July 2018

1 reference

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Nonsense mutations affect C1 inhibitor messenger RNA levels in patients with type I hereditary angioneurotic edema

11 July 2018

1 reference

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A naturally occurring gamma globin gene mutation enhances SP1 binding activity

11 July 2018

1 reference

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An RNA splice site mutation in the C1-inhibitor gene causes type I hereditary angio-oedema

11 July 2018

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Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus

11 July 2018

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Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients

11 July 2018

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Recovery from Hemophilia B Leyden: An Androgen-Responsive Element in the Factor IX Promoter

11 July 2018

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Pleiotropic effects of antithrombin strand 1C substitution mutations

11 July 2018

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C1 inhibitor hinge region mutations produce dysfunction by different mechanisms

11 July 2018

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A single base deletion from the C1-inhibitor gene causes type I hereditary angio-oedema

11 July 2018

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Efficient, automatic detection of heterozygous bases during large-scale DNA sequence screening.

11 July 2018

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Mutation detection by fluorescent chemical cleavage: application to hemophilia B.

24 September 2018

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Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene

24 September 2018

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Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products

24 September 2018

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Functional analysis of the serpin domain of C1 inhibitor

14 November 2018

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12 December 2020

Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases

1 reference

12 December 2020

Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis

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12 December 2020

[Hereditary angioedema. Genealogic studies and clinical considerations on 2 genetic forms in a case study of 10 patients]

1 reference

12 December 2020

Altered C1 inhibitor genes in type I hereditary angioedema

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12 December 2020

Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys)

1 reference

12 December 2020

A point mutation in the C1-inhibitor gene causes type I hereditary angiooedema

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8755917%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

PubMed publication ID

8755917

1 reference