About: Gene therapy of primary T cell immunodeficiencies

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scientific article published on 10 April 2013

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articol științific (ro) articolo scientifico (it) artigo científico (gl) artigo científico (pt) artigo científico (pt-br) artikull shkencor (sq) artículo científico (es) bilimsel makale (tr) scienca artikolo (eo) vedecký článok (sk) vetenskaplig artikel (sv) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научная статья (ru) научни чланак (sr) מאמר מדעי (he) artikel ilmiah (id) article scientifique (fr) বৈজ্ঞানিক নিবন্ধ (bn) artículu científicu espublizáu en 2013 (ast) наукова стаття, опублікована у квітні 2013 (uk) 2013 թվականի ապրիլի 10-ին հրատարակված գիտական հոդված (hy) scientific article published on 10 April 2013 (en) scientific article published on 10 April 2013 (en-ca) scientific article published on 10 April 2013 (en-gb) مقالة علمية نشرت في 10 أبريل 2013 (ar) 2013 ഏപ്രില്‍ 10 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം (ml)
publication date	wds:Q38098818-5E42FED8-343F-4684-A2CE-D00DA0CE5154
publication date	2013-04-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q38098818-A5164346-27FA-4D36-95BD-AA37BA2C55F6
language of work or name	English
rdfs:label	Gene therapy of primary T cell immunodeficiencies (en) Gene therapy of primary T cell immunodeficiencies (nl) Gene therapy of primary T cell immunodeficiencies (ast)
skos:prefLabel	Gene therapy of primary T cell immunodeficiencies (en) Gene therapy of primary T cell immunodeficiencies (nl) Gene therapy of primary T cell immunodeficiencies (ast)
name	Gene therapy of primary T cell immunodeficiencies (en) Gene therapy of primary T cell immunodeficiencies (nl) Gene therapy of primary T cell immunodeficiencies (ast)
author	wds:Q38098818-2F2BD751-80D6-4C4B-8CB3-334E140AE7B8 wds:Q38098818-6EA3873B-299C-478A-9D63-A2794A18F847 wds:Q38098818-DFCFD523-06AC-4D91-82D6-5612E191ECD1
author	Alain Fischer Marina Cavazzana Salima Hacein-Bey-Abina
title	wds:Q38098818-18452E22-9886-46EA-9EB0-385CBF66125A
title	Gene therapy of primary T cell immunodeficiencies (en)
page(s)	wds:Q38098818-39F6625A-72EC-4A84-BBFC-6CB498F90210
page(s)	170-173
instance of	wds:Q38098818-871F9B85-E9FF-4973-BBE5-292338EC9F74
instance of	scholarly article
main subject	wds:Q38098818-42DB10B7-E17F-47FA-97AD-F4DE788322A0
main subject	gene therapy
PubMed ID	wds:Q38098818-166A8E62-DAD0-4AF3-B4D8-55A1C00771EF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23583799
PubMed ID	23583799
published in	wds:Q38098818-80AAFB1E-5BB7-4CEC-B927-7C9836862D01
published in	Gene
issue	wds:Q38098818-8CA9A1C4-549A-4F61-884B-8BFE5A17D89A
volume	wds:Q38098818-96F101FB-C51D-4BCC-9F1C-8DFF3AC6990D
issue	2
volume	525
DOI	wds:Q38098818-BF1926E7-E284-4CDA-A099-0DCD9A62090C
DOI	http://dx.doi.org/10.1016/J.GENE.2013.03.092
DOI	10.1016/J.GENE.2013.03.092
ResearchGate publication ID	wds:Q38098818-70F2CA70-D216-45CA-A410-BCF0CA3D7BCD
ResearchGate publication ID	236180512
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q38098818
is cites work of	Altering murine leukemia virus integration through disruption of the integrase and BET protein family interaction Recent advances in RNAi-based strategies for therapy and prevention of HIV-1/AIDS. Intravenous injection of a foamy virus vector to correct canine SCID-X1. Gene therapy on the move Wiskott-Aldrich syndrome: diagnosis, current management, and emerging treatments Gene therapy: charting a future course--summary of a National Institutes of Health Workshop, April 12, 2013. Preparation for a first-in-man lentivirus trial in patients with cystic fibrosis. Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States Retargeted Foamy Virus Vectors Integrate Less Frequently Near Proto-oncogenes Human artificial chromosome-based gene delivery vectors for biomedicine and biotechnology "Model t" cells: a time-tested vehicle for gene therapy Primary immunodeficiency diseases: a 30-year patient registry from the referral center for primary immunodeficiencies in Greece Genome editing: a tool for research and therapy: targeted genome editing hits the clinic Modern management of primary T-cell immunodeficiencies. Moonlighting adenosine deaminase: a target protein for drug development A unified pathogenesis for kidney diseases, including genetic diseases and cancers, by the protein-homeostasis-system hypothesis Beyond cystic fibrosis transmembrane conductance regulator therapy: a perspective on gene therapy and small molecule treatment for cystic fibrosis Multiparametric Whole Blood Dissection: A one-shot comprehensive picture of the human hematopoietic system. Human artificial chromosomes for pluripotent stem cell-based tissue replacement therapy Serial number tagging reveals a prominent sequence preference of retrotransposon integration The gene mutation analysis of a Wiskott-Aldrich syndrome family with normal mean platelet volume Impacts of leukocyte filtration and irradiation on coagulation factors in fresh frozen plasma Clinical potential of gene therapy: towards meeting the demand Rare Genetic Blood Disease Modeling in Zebrafish
is cites work of	wds:Q27682160-D796EA81-D4FE-4AD5-8AA7-73B77260CB6D

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