(Q40704590)

English

Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris.

scientific article published on 23 July 2015

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scholarly article

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20 February 2020

Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris (English)

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20 February 2020

Generalized pustular psoriasis

1 reference

based on heuristic

inferred from title

8

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20 February 2020

Richard C Trembath

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20 February 2020

Christopher Griffiths

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20 February 2020

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20 February 2020

Catherine H Smith

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20 February 2020

Francesca Capon

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20 February 2020

Jonathan N. Barker

20

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20 February 2020

Alexander Navarini

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Alexander A Navarini

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20 February 2020

Satveer K Mahil

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Satveer K Mahil

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20 February 2020

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A David Burden

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20 February 2020

9

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Annamari Ranki

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20 February 2020

Dorottya M Berki

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Dorottya M Berki

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20 February 2020

author name string

Lu Liu

2

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20 February 2020

Eugene S Tan

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20 February 2020

Takeshi Ogo

10

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20 February 2020

Gabriela Petrof

11

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20 February 2020

Michael Duckworth

13

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20 February 2020

Michael H Allen

14

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20 February 2020

Pasquale Vito

15

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20 February 2020

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publication date

23 July 2015

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20 February 2020

Journal of Investigative Dermatology

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20 February 2020

135

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20 February 2020

12

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20 February 2020

2964-2970

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20 February 2020

https://scigraph.springernature.com/pub.10.1038/jid.2015.288

0 references

Familial pityriasis rubra pilaris is caused by mutations in CARD14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oncogenic CARD11 mutations in human diffuse large B cell lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of IL36RN function does not confer susceptibility to psoriasis vulgaris.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AP1S3 mutations are associated with pustular psoriasis and impaired Toll-like receptor 3 trafficking

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting functional effect of human missense mutations using PolyPhen-2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oncogenic CARD11 mutations induce hyperactive signaling by disrupting autoinhibition by the PKC-responsive inhibitory domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative splicing of CARMA2/CARD14 transcripts generates protein variants with differential effect on NF-κB activation and endoplasmic reticulum stress-induced cell death

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NIH Image to ImageJ: 25 years of image analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PSORS2 is due to mutations in CARD14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting the functional effect of amino acid substitutions and indels

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARD14 expression in dermal endothelial cells in psoriasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare pathogenic variants in IL36RN underlie a spectrum of psoriasis-associated pustular phenotypes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variant analysis of CARD14 in a Chinese Han population with psoriasis vulgaris and generalized pustular psoriasis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A general framework for estimating the relative pathogenicity of human genetic variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SROOGLE: webserver for integrative, user-friendly visualization of splicing signals

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARD14 c.526G>C (p.Asp176His) is a significant risk factor for generalized pustular psoriasis with psoriasis vulgaris in the Japanese cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting coiled coils from protein sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/26203641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/JID.2015.288

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26203641%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26203641%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

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