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RLTPR gene

Known as: RLTPR, leucine rich repeat containing 16C, RGD-, LEUCINE-RICH REPEAT-, TROPOMODULIN DOMAIN-, AND PROLINE-RICH DOMAIN-CONTAINING PROTEIN 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Peripheral eosinophilia in primary immunodeficiencies of actin dysregulation: A case series of Wiskott-Aldrich syndrome, CARMIL2 and DOCK8 deficiency and review of the literature.
2018
2018
A CASE OF RECURRENT ASPIRATION PNEUMONIA AND PERSISTENT EOSINOPHILIA
2017
2017
"Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis (Linhares et al., 2014)" turns out to be EBV+ leiomyomatosis caused by CARMIL2 mutations.
Highly Cited
2016
Highly Cited
2016
The scaffolding function of the RLTPR protein explains its essential role for CD28 co-stimulation in mouse and human T cells
In two complementary papers, Casanova, Malissen, and collaborators report the discovery of human RLTPR deficiency, the first… 
2015
2015
Title: CARMIL2 is a Novel Molecular Connection between Vimentin and Actin Essential for Cell Migration and Invadopodia Formation Running Head: CARMIL2 Links Vimentin and Actin
Cancer-cell migration requires the regulation of actin networks at protrusions associated with invadopodia and other leading… 
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