Gene Correction of iPSCs from a Wiskott-Aldrich Syndrome Patient Normalizes the Lymphoid Developmental and Functional Defects.
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OP9 Feeder Cells Are Superior to M2-10B4 Cells for the Generation of Mature and Functional Natural Killer Cells from Umbilical Cord Hematopoietic Progenitors.Cytokine-free directed differentiation of human pluripotent stem cells efficiently produces hemogenic endothelium with lymphoid potential.Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.Targeted genome editing restores T cell differentiation in a humanized X-SCID pluripotent stem cell disease model.Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome.A New Chapter on Targeted Gene Insertion for X-CGD: Do Not Skip the Intro(n).
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Gene Correction of iPSCs from a Wiskott-Aldrich Syndrome Patient Normalizes the Lymphoid Developmental and Functional Defects.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 06 July 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Gene Correction of iPSCs from ...... mental and Functional Defects.
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Gene Correction of iPSCs from ...... mental and Functional Defects.
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type
label
Gene Correction of iPSCs from ...... mental and Functional Defects.
@en
Gene Correction of iPSCs from ...... mental and Functional Defects.
@nl
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Gene Correction of iPSCs from ...... mental and Functional Defects.
@en
Gene Correction of iPSCs from ...... mental and Functional Defects.
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Gene Correction of iPSCs from ...... pmental and Functional Defects
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Ana M Crane
Brian R Davis
David E Paschon
Edward J Rebar
Jose Carlos Segovia
Manuel Gonzalez-Garay
Michael C Holmes
Rasoul Pourebrahim
Tamara J Laskowski
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P304
P356
10.1016/J.STEMCR.2016.06.003
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2016-07-07T00:00:00Z