Disulfide bond requirements for active Wnt ligands (Q34073894)

24841207

30 July 2017

title

Disulfide bond requirements for active Wnt ligands (English)

1 reference

30 July 2017

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

author name string

Bryan T MacDonald

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Annie Hien

2

1 reference

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4 June 2020

Xinjun Zhang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Oladoyin Iranloye

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Marian L Waterman

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Xi He

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

language of work or name

English

0 references

publication date

19 May 2014

1 reference

24841207

30 July 2017

number of pages

15

1 reference

Journal of Biological Chemistry

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

volume

289

1 reference

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4 June 2020

issue

26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

page(s)

18122-18136

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

4 June 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4140276/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Stearoyl CoA desaturase is required to produce active, lipid-modified Wnt proteins

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Use of a molecular genetic platform technology to produce human Wnt proteins reveals distinct local and distal signaling abilities

5 July 2018

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5 July 2018

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Structural architecture and functional evolution of Wnts

5 July 2018

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A uniform human Wnt expression library reveals a shared secretory pathway and unique signaling activities

5 July 2018

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Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation

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Structural basis of Wnt recognition by Frizzled

5 July 2018

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Mutations in WNT10A are present in more than half of isolated hypodontia cases.

5 July 2018

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Structural and Functional Studies of LRP6 Ectodomain Reveal a Platform for Wnt Signaling

5 July 2018

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Wnt antagonists bind through a short peptide to the first β-propeller domain of LRP5/6

5 July 2018

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WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Wnt signal amplification via activity, cooperativity, and regulation of multiple intracellular PPPSP motifs in the Wnt co-receptor LRP6.

5 July 2018

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Glycosylation and palmitoylation of Wnt-3a are coupled to produce an active form of Wnt-3a

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

5 July 2018

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5 July 2018

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WntD is a feedback inhibitor of Dorsal/NF-kappaB in Drosophila development and immunity

5 July 2018

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5 July 2018

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Unexpected complexity of the Wnt gene family in a sea anemone

5 July 2018

1 reference

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Wnt signals across the plasma membrane to activate the beta-catenin pathway by forming oligomers containing its receptors, Frizzled and LRP.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Wnt proteins are lipid-modified and can act as stem cell growth factors

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Cytoskeletal reorganization by soluble Wnt-3a protein signalling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Functional analysis of Wingless reveals a link between intercellular ligand transport and dorsal-cell-specific signaling

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

The segment polarity gene porcupine encodes a putative multitransmembrane protein involved in Wingless processing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Mutations in the segment polarity genes wingless and porcupine impair secretion of the wingless protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

The dishevelled protein is modified by wingless signaling in Drosophila

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

A newly recognized dwarfing syndrome.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Ectopic expression of the proto-oncogene int-1 in Xenopus embryos leads to duplication of the embryonic axis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Mutational analysis of mouse Wnt-1 identifies two temperature-sensitive alleles and attributes of Wnt-1 protein essential for transformation of a mammary cell line

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4140276

Single-cell imaging of Wnt palmitoylation by the acyltransferase porcupine.

5 July 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Drosophila WntD is a target and an inhibitor of the Dorsal/Twist/Snail network in the gastrulating embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Ligand receptor interactions in the Wnt signaling pathway in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

WNT10A variants are associated with non-syndromic tooth agenesis in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.575027

Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24841207

12 December 2020

inferred from PubMed ID database lookup

Mutations in WNT1 are a cause of osteogenesis imperfecta

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24841207

12 December 2020

inferred from PubMed ID database lookup

De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24841207

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1074/JBC.M114.575027

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

24841207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24841207%20AND%20SRC:MED&resulttype=core&format=json