pH Induced Conformational Transitions in the Transforming Growth Factor β-Induced Protein (TGFβIp) Associated Corneal Dystrophy Mutants (Q36748354)

16 August 2017

pH Induced Conformational Transitions in the Transforming Growth Factor β-Induced Protein (TGFβIp) Associated Corneal Dystrophy Mutants (English)

1 reference

16 August 2017

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4

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2 June 2020

Shyam S Chaurasia

10

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Lakshminarayanan Rajamani

2 June 2020

11

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2 June 2020

author name string

Elavazhagan Murugan

1

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2 June 2020

Anandalakshmi Venkatraman

2

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2 June 2020

Zhou Lei

3

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2 June 2020

Rayne Rui Yi Lim

5

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2 June 2020

Nandhakumar Muruganantham

6

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2 June 2020

Eunice Goh

7

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2 June 2020

Gary Swee Lim Peh

8

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2 June 2020

Roger W Beuerman

9

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2 June 2020

Jodhbir S Mehta

12

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2 June 2020

language of work or name

English

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publication date

31 March 2016

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16 August 2017

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2 June 2020

volume

6

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page(s)

23836

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Creative Commons Attribution 4.0 International

2 June 2020

copyright license

start time

31 March 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Corneal dystrophy-associated R124H mutation disrupts TGFBI interaction with Periostin and causes mislocalization to the lysosome

29 September 2017

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Soluble amyloid beta-oligomers affect dielectric membrane properties by bilayer insertion and domain formation: implications for cell toxicity

29 September 2017

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Congo red and thioflavin-T analogs detect Abeta oligomers

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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29 September 2017

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29 September 2017

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29 September 2017

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cDNA from human ocular ciliary epithelium homologous to beta ig-h3 is preferentially expressed as an extracellular protein in the corneal epithelium

29 September 2017

1 reference

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29 September 2017

1 reference

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29 September 2017

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A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy.

28 June 2018

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5 September 2018

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Real-time xCELLigence impedance analysis of the cytotoxicity of dental composite components on human gingival fibroblasts

5 September 2018

1 reference

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Identification of an amyloidogenic region on keratoepithelin via synthetic peptides

5 September 2018

1 reference

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A novel H572R mutation in the transforming growth factor-beta-induced gene in a Thai family with lattice corneal dystrophy type I.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

Monitoring protein aggregation during thermal unfolding in circular dichroism experiments.

5 September 2018

1 reference

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TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients

5 September 2018

1 reference

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Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

A model of FAS1 domain 4 of the corneal protein beta(ig)-h3 gives a clearer view on corneal dystrophies

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

A systematic investigation into the effect of protein destabilisation on beta 2-microglobulin amyloid formation

5 September 2018

1 reference

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BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

Transthyretin fibrillogenesis entails the assembly of monomers: a molecular model for in vitro assembled transthyretin amyloid-like fibrils

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

Vesicle permeabilization by protofibrillar alpha-synuclein is sensitive to Parkinson's disease-linked mutations and occurs by a pore-like mechanism.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

Expression, purification and characterization of fourth FAS1 domain of TGFβIp-associated corneal dystrophic mutants

5 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038/SREP23836

BIGH3 mutation spectrum in corneal dystrophies

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814907

Expression of fibrillins and other microfibril-associated proteins in human bone and osteoblast-like cells

20 October 2018

1 reference

12 December 2020

Cytochemical evidence for the leakage of acid phosphatase through ultrastructurally intact lysosomal membranes

1 reference

12 December 2020

BIGH3 gene analysis in the differential diagnosis of corneal dystrophies

1 reference

12 December 2020

Insulin Fibrillization at Acidic and Physiological pH Values is Controlled by Different Molecular Mechanisms

1 reference

12 December 2020

Heat-induced conversion of beta(2)-microglobulin and hen egg-white lysozyme into amyloid fibrils

1 reference

12 December 2020

Identifiers

DOI

10.1038/SREP23836

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27030015 AND SRC:MED&resulttype=core&format=json

2 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27030015 AND SRC:MED&resulttype=core&format=json

2 June 2020

PubMed publication ID

27030015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27030015 AND SRC:MED&resulttype=core&format=json