Therapeutic effects of proteoliposomes on X-linked chronic granulomatous disease: proof of concept using macrophages differentiated from patient-specific induced pluripotent stem cells

International Journal of Nanomedicine ◽

10.2147/ijn.s128611 ◽

2017 ◽

Vol Volume 12 ◽

pp. 2161-2177 ◽

Cited By ~ 10

Author(s):

Julie Brault ◽

Guillaume Vaganay ◽

Aline Le Roy ◽

Jean-Luc Lenormand ◽

Sandra Cortes ◽

...

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Patient Specific ◽

Therapeutic Effects ◽

Granulomatous Disease ◽

Proof Of Concept ◽

Induced Pluripotent

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Optimization of X-linked chronic granulomatous disease modelization by using patient-specific induced pluripotent stem cells

Experimental Hematology ◽

10.1016/j.exphem.2013.05.112 ◽

2013 ◽

Vol 41 (8) ◽

pp. S28

Author(s):

Julie Brault ◽

Erwan Goutagny ◽

Tomo Saric ◽

Karl-Heinz Krause ◽

Marie-José Stasia ◽

...

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Patient Specific ◽

Granulomatous Disease ◽

Induced Pluripotent

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220. Modeling X-Linked Chronic Granulomatous Disease Using Neutrophils Differentiated from Patient-Derived Induced Pluripotent Stem Cells

Molecular Therapy ◽

10.1016/s1525-0016(16)37661-4 ◽

2010 ◽

Vol 18 ◽

pp. S84

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Granulomatous Disease ◽

Induced Pluripotent

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TALEN-mediated functional correction of X-linked chronic granulomatous disease in patient-derived induced pluripotent stem cells

Biomaterials ◽

10.1016/j.biomaterials.2015.07.057 ◽

2015 ◽

Vol 69 ◽

pp. 191-200 ◽

Cited By ~ 47

Author(s):

Anne-Kathrin Dreyer ◽

Dirk Hoffmann ◽

Nico Lachmann ◽

Mania Ackermann ◽

Doris Steinemann ◽

...

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Granulomatous Disease ◽

Functional Correction ◽

Induced Pluripotent

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Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells

Stem Cells ◽

10.1002/stem.3006 ◽

2019 ◽

Vol 37 (7) ◽

pp. 876-887 ◽

Cited By ~ 1

Author(s):

Alessandra Castelli ◽

Lucia Susani ◽

Ciro Menale ◽

Sharon Muggeo ◽

Elena Caldana ◽

...

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Granulomatous Disease ◽

Induced Pluripotent

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Faculty Opinions recommendation of TALEN-mediated functional correction of X-linked chronic granulomatous disease in patient-derived induced pluripotent stem cells.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.725732722.793535142 ◽

2017 ◽

Author(s):

Andrew Gennery

Keyword(s):

Stem Cells ◽

Chronic Granulomatous Disease ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Granulomatous Disease ◽

Functional Correction ◽

Induced Pluripotent

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Derivation and Functional Analysis of Patient-Specific Induced Pluripotent Stem Cells as an In Vitro Model of Chronic Granulomatous Disease

Stem Cells ◽

10.1002/stem.1053 ◽

2012 ◽

Vol 30 (4) ◽

pp. 599-611 ◽

Cited By ~ 52

Author(s):

Yan Jiang ◽

Sally A. Cowley ◽

Ulrich Siler ◽

Dario Melguizo ◽

Katarzyna Tilgner ◽

...

Keyword(s):

Stem Cells ◽

Functional Analysis ◽

Chronic Granulomatous Disease ◽

Pluripotent Stem Cells ◽

In Vitro Model ◽

Patient Specific ◽

Granulomatous Disease ◽

Vitro Model ◽

Induced Pluripotent

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279. Derivation and Functional Analysis of Patient Specific Induced Pluripotent Stem Cells as an In Vitro Model of Chronic Granulomatous Disease

Molecular Therapy ◽

10.1016/s1525-0016(16)36083-x ◽

2012 ◽

Vol 20 ◽

pp. S110

Keyword(s):

Stem Cells ◽

Functional Analysis ◽

Chronic Granulomatous Disease ◽

Pluripotent Stem Cells ◽

In Vitro Model ◽

Patient Specific ◽

Granulomatous Disease ◽

Vitro Model ◽

Induced Pluripotent

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Faculty Opinions recommendation of Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.717970938.793473728 ◽

2013 ◽

Author(s):

Thomas Hund

Keyword(s):

Stem Cells ◽

Hypertrophic Cardiomyopathy ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Familial Hypertrophic Cardiomyopathy ◽

Calcium Handling ◽

Patient Specific ◽

Induced Pluripotent

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Faculty Opinions recommendation of Targeted correction of RUNX1 mutation in FPD patient-specific induced pluripotent stem cells rescues megakaryopoietic defects.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.718528132.793500091 ◽

2014 ◽

Author(s):

A Koneti Rao ◽

Natthapol Songdej

Keyword(s):

Stem Cells ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Patient Specific ◽

Induced Pluripotent ◽

Runx1 Mutation

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Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader–Willi syndrome retain maternal uniparental disomy (UPD)

Stem Cell Research ◽

10.1016/j.scr.2019.101647 ◽

2019 ◽

Vol 41 ◽

pp. 101647

Author(s):

Bo-Young Kim ◽

Jin-Sung Lee ◽

Yong-Ou Kim ◽

Mi-Hyun Park ◽

Soo Kyung Koo

Keyword(s):

Stem Cells ◽

Induced Pluripotent Stem Cells ◽

Pluripotent Stem Cells ◽

Uniparental Disomy ◽

Patient Specific ◽

Prader Willi Syndrome ◽

Maternal Uniparental Disomy ◽

Induced Pluripotent

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