Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes. (Q37395852)

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scientific article published on January 2009

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English	Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes.	scientific article published on January 2009

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

Europe PubMed Central

Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

based on heuristic

inferred from title

stem cell transplantation

1 reference

based on heuristic

inferred from title

ectodermal dysplasia

1 reference

based on heuristic

inferred from title

Jason L. Hornick

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Perdita Permaul

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

Anupama Narla

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

Sung-Yun Pai

4

1 reference

Europe PubMed Central

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21 January 2020

publication date

1 January 2009

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

Immunologic Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

44

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Europe PubMed Central

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21 January 2020

1-3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

89-98

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations

1 reference

https://api.crossref.org/works/10.1007/S12026-008-8085-2

21 January 2018

The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intractable diarrhea of infancy with epithelial and basement membrane abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Signals from within: the DNA-damage-induced NF-kappaB response

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kappaB activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of cell adhesion molecules in infants with intestinal epithelial dysplasia (tufting enteropathy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor necrosis factor alpha negatively regulates the expression of the carcinoma-associated antigen epithelial cell adhesion molecule

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autocrine laminin-5 ligates alpha6beta4 integrin and activates RAC and NFkappaB to mediate anchorage-independent survival of mammary tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation: early recognition and diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of EpCAM as the gene for congenital tufting enteropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha2beta1 integrin signalling enhances cyclooxygenase-2 expression in intestinal epithelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intestinal epithelial dysplasia (tufting enteropathy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human nuclear factor kappa B essential modulator mutation can result in immunodeficiency without ectodermal dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NEMO, NFkappaB signaling and incontinentia pigmenti

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted deletion of the integrin beta4 signaling domain suppresses laminin-5-dependent nuclear entry of mitogen-activated protein kinases and NF-kappaB, causing defects in epidermal growth and migration

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of inducible chemoresistance: enhanced anti-tumor therapy through increased apoptosis by inhibition of NF-kappaB

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited disorders of NF-kappaB-mediated immunity in man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19225723

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12026-008-8085-2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

release_vvxla3aambcoteyc2qdbxdnmby

1 reference

https://api.fatcat.wiki/v0/release/vvxla3aambcoteyc2qdbxdnmby

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19225723 AND SRC:MED&resulttype=core&format=json

21 January 2020

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