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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
Download Full-text
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References
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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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
Download Full-text
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
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Chronic Granulomatous Disease
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Induced Pluripotent Stem Cells
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Pluripotent Stem Cells
◽
Granulomatous Disease
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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
Download Full-text
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
Download Full-text
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
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Patient Specific
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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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