Generation of heterozygous fibrillin-1 mutant cloned pigs from genome-edited foetal fibroblasts (Q28604300)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27074716%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

title

Generation of heterozygous fibrillin-1 mutant cloned pigs from genome-edited foetal fibroblasts (English)

1 reference

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1 April 2020

1 reference

4

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1 April 2020

Oltea Sampetrean

10

1 reference

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1 April 2020

Hideyuki Saya

13

1 reference

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1 April 2020

5

Kazuaki Nakano

1 reference

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1 April 2020

author name string

Kazuhiro Umeyama

1

1 reference

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1 April 2020

Kota Watanabe

2

1 reference

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1 April 2020

Masahito Watanabe

3

1 reference

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1 April 2020

Masateru Kitashiro

6

1 reference

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1 April 2020

Hitomi Matsunari

7

1 reference

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1 April 2020

Tokuhiro Kimura

8

1 reference

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1 April 2020

Yoshimi Arima

9

1 reference

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1 April 2020

Masaki Nagaya

11

1 reference

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1 April 2020

Masahiro Saito

12

1 reference

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1 April 2020

Kenjiro Kosaki

14

1 reference

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1 April 2020

Hiroshi Nagashima

15

1 reference

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1 April 2020

Morio Matsumoto

16

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1 April 2020

language of work or name

English

0 references

publication date

14 April 2016

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1 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27074716%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

volume

6

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1 April 2020

page(s)

24413

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Creative Commons Attribution 4.0 International

1 April 2020

copyright license

start time

1 April 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils

17 March 2017

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17 March 2017

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6 April 2017

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7 April 2017

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Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype

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Engraftment of human iPS cells and allogeneic porcine cells into pigs with inactivated RAG2 and accompanying severe combined immunodeficiency

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Generation of interleukin-2 receptor gamma gene knockout pigs from somatic cells genetically modified by zinc finger nuclease-encoding mRNA

29 September 2017

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Efficient nonmeiotic allele introgression in livestock using custom endonucleases

29 September 2017

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Molecular mechanisms of thoracic aortic dissection

29 September 2017

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The c.7409G>A (p.Cys2470Tyr) Variant of FBN1: Phenotypic Variability across Three Generations

29 September 2017

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Double knockout pigs deficient in N-glycolylneuraminic acid and galactose α-1,3-galactose reduce the humoral barrier to xenotransplantation

29 September 2017

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Efficient TALEN-mediated gene knockout in livestock

29 September 2017

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Generation of Fbn1 conditional null mice implicates the extracellular microfibrils in osteoprogenitor recruitment

29 September 2017

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Experimental animal models in scoliosis research: a review of the literature

29 September 2017

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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

29 September 2017

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Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe Marfan syndrome

29 September 2017

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In vivo studies of mutant fibrillin-1 microfibrils

29 September 2017

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Microfibril structure masks fibrillin-2 in postnatal tissues

29 September 2017

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Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27074716

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27074716

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fibrillin controls TGF-beta activation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27074716

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SREP24413

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27074716%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

1 April 2020

1018342557

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27074716%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27074716%20AND%20SRC:MED&resulttype=core&format=json