Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities (Q33594555)

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28 July 2017

title

Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities (English)

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28 July 2017

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1

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2 June 2020

Juan Pablo Abonia

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2 June 2020

author name string

Guangping Sun

2

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2 June 2020

Kelly D Stone

3

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2 June 2020

Celeste Nelson

4

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Laura Wisch

5

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2 June 2020

Michelle O'Brien

6

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Nina Jones

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Andrew Lindsley

8

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Hirsh D Komarow

9

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Yun Bai

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2 June 2020

Linda M Scott

11

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Daly Cantave

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Irina Maric

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Marc E Rothenberg

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Lawrence B Schwartz

16

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Joshua D Milner

17

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Todd M Wilson

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2 June 2020

language of work or name

English

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publication date

25 January 2014

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24472624

The Journal of Allergy and Clinical Immunology

28 July 2017

published in

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volume

133

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issue

5

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page(s)

1471-1474

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TGFβ receptor mutations impose a strong predisposition for human allergic disease

2 June 2020

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.

21 June 2018

1 reference

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Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

Definitions, criteria and global classification of mast cell disorders with special reference to mast cell activation syndromes: a consensus proposal

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

Inhibition of CD203c membrane up-regulation in human basophils by high dilutions of histamine: a controlled replication study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

STAT3 mutations in the hyper-IgE syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

A germline mutation in KIT in familial diffuse cutaneous mastocytosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4016972

Somatic D816V KIT mutation in a case of adult-onset familial mastocytosis.

21 June 2018

1 reference

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10.1016/J.JACI.2013.11.039

30 October 2018

Identifiers

DOI

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2 June 2020

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