(Q33770305)

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A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression

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scholarly article

1 reference

Europe PubMed Central

29 July 2017

A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression (English)

1 reference

Europe PubMed Central

29 July 2017

Marfan syndrome

1 reference

based on heuristic

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Gustavo Ribeiro Fernandes

object named as

Gustavo R Fernandes

3

0 references

Lygia Veiga Pereira

object named as

Lygia V Pereira

11

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author name string

Bruno L Lima

1

1 reference

Europe PubMed Central

29 July 2017

Enrico J C Santos

2

1 reference

Europe PubMed Central

29 July 2017

Christian Merkel

4

1 reference

Europe PubMed Central

29 July 2017

Marco R B Mello

5

1 reference

Europe PubMed Central

29 July 2017

Juliana P A Gomes

6

1 reference

Europe PubMed Central

29 July 2017

Marina Soukoyan

7

1 reference

Europe PubMed Central

29 July 2017

Alexandre Kerkis

8

1 reference

Europe PubMed Central

29 July 2017

Silvia M G Massironi

9

1 reference

Europe PubMed Central

29 July 2017

José A Visintin

10

1 reference

Europe PubMed Central

29 July 2017

language of work or name

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publication date

30 November 2010

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

5

1 reference

Europe PubMed Central

29 July 2017

11

1 reference

Europe PubMed Central

29 July 2017

e14136

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Europe PubMed Central

29 July 2017

copyright license

Creative Commons Attribution 4.0 International

30 November 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

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describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2994728/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Quantitative methods in the study of pulmonary pathology

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Fundamental of medical image processing with personal computer system--development of Plugins by ImageJ

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Identification of a cardiac disease modifier gene using forward genetics in the mouse

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Isolation of genomic DNA from mouse tails

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Therapy of Marfan syndrome

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TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome

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Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome

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Defective secretion of recombinant fragments of fibrillin-1: implications of protein misfolding for the pathogenesis of Marfan syndrome and related disorders

1 reference

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Dysregulation of TGF-beta activation contributes to pathogenesis in Marfan syndrome

1 reference

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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New insights into the assembly of extracellular microfibrils from the analysis of the fibrillin 1 mutation in the tight skin mouse

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Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1

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Fibrillin-1: organization in microfibrils and structural properties

1 reference

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Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

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Ascertainment and severity of Marfan syndrome in a Scottish population

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Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly

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Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene

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Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

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Osteopoietic engraftment after bone marrow transplantation: effect of inbred strain of mice

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Influence of genetic background and gender on hypertension and renal failure in COX-2-deficient mice

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Differential effect of FBN1 mutations on in vitro proteolysis of recombinant fibrillin-1 fragments.

1 reference

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Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.

1 reference

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Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival

1 reference

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Efficient removal of loxP-flanked DNA sequences in a gene-targeted locus by transient expression of Cre recombinase in fertilized eggs

1 reference

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12 December 2020

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inferred from PubMed ID database lookup

Marfan gene discovered

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Basic Defects in the Marfan Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The FBN1 (R2726W) mutation is not fully penetrant

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical variability in the Marfan syndrome(s)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/21152435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0014136

1 reference

Europe PubMed Central

29 July 2017

2010PLoSO...514136L

0 references

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

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