(Q41828458)

12 October 2017

Leukocyte adhesion deficiency syndrome: a controversy solved (English)

1 reference

leukocyte-adhesion deficiency syndrome

12 October 2017

0 references

author name string

Clare L Abram

series ordinal

1

1 reference

PMC publication ID

4464832

12 October 2017

Clifford A Lowell

series ordinal

2

1 reference

12 October 2017

5 May 2009

1 reference

Immunology & Cell Biology

12 October 2017

1 reference

12 October 2017

87

1 reference

12 October 2017

6

1 reference

12 October 2017

440-442

1 reference

The ins and outs of leukocyte integrin signaling

12 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Kindlin-3 is required for beta2 integrin-mediated leukocyte adhesion to endothelial cells

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Loss of Kindlin-1 causes skin atrophy and lethal neonatal intestinal epithelial dysfunction

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Kindlins: essential regulators of integrin signalling and cell-matrix adhesion

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Leukocyte adhesion deficiencies: molecular basis, clinical findings, and therapeutic options.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Kindlin-3: a new gene involved in the pathogenesis of LAD-III.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

A novel genetic leukocyte adhesion deficiency in subsecond triggering of integrin avidity by endothelial chemokines results in impaired leukocyte arrest on vascular endothelium under shear flow.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4464832

Natural history and early diagnosis of LAD-1/variant syndrome

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19417769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The clinical spectrum of leukocyte adhesion deficiency (LAD) III due to defective CalDAG-GEF1

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19417769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

LAD-1/variant syndrome is caused by mutations in FERMT3.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19417769

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/ICB.2009.32

1 reference

12 October 2017

1 reference

PMC publication ID

4464832

12 October 2017

PubMed publication ID

19417769

1 reference

PMC publication ID

4464832