(Q39963571)

15 September 2017

title

Deficiency of Adenosine Deaminase 2 Causes Antibody Deficiency (English)

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15 September 2017

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9

Bodo Grimbacher

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15 September 2017

Johanna Schepp

1

1 reference

15 September 2017

Alla Bulashevska

2

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15 September 2017

Wilma Mannhardt-Laakmann

3

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15 September 2017

Hongzhi Cao

4

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15 September 2017

Fang Yang

5

1 reference

15 September 2017

Maximilian Seidl

6

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15 September 2017

Susan Kelly

7

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15 September 2017

Michael Hershfield

8

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15 September 2017

publication date

27 February 2016

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Journal of Clinical Immunology

15 September 2017

published in

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15 September 2017

volume

36

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15 September 2017

issue

3

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15 September 2017

page(s)

179-186

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https://scigraph.springernature.com/pub.10.1007/s10875-016-0245-x

15 September 2017

exact match

0 references

cites work

Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.

1 reference

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Early-onset stroke and vasculopathy associated with mutations in ADA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Mutations in CECR1 associated with a neutrophil signature in peripheral blood

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Human adenosine deaminase 2 induces differentiation of monocytes into macrophages and stimulates proliferation of T helper cells and macrophages.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Fast gapped-read alignment with Bowtie 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

The variant call format and VCFtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

A method and server for predicting damaging missense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Mutant ADA2 in vasculopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Unexplained early-onset lacunar stroke and inflammatory skin lesions: Consider ADA2 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-016-0245-X

Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26922074

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10875-016-0245-X

1 reference

15 September 2017

1 reference