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Kagistia H Utami
31  Ergebnisse:
Personensuche X
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1

Unbiased Profiling of Isogenic Huntington Disease hPSC-Deri..:

Ooi, Jolene ; Langley, Sarah R. ; Xu, Xiaohong...
Cell Reports.  26 (2019)  9 - p. 2494-2508.e7 , 2019
Link: https://doi.org/10.1016/..
 
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2

Personalized genome sequencing coupled with iPSC technology..:

Aksoy, Irene ; Utami, Kagistia H. ; Winata, Cecilia L....
Human Molecular Genetics.  26 (2016)  2 - p. 367-382 , 2016
Link: https://doi.org/10.1093/..
 
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3

Detection of Chromosomal Breakpoints in Patients with Devel..:

Utami, Kagistia H. ; Hillmer, Axel M. ; Aksoy, Irene...
PLoS ONE.  9 (2014)  3 - p. e90852 , 2014
Link: https://doi.org/10.1371/..
 
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4

Combined deletion of two Condensin II system genes (NCAPG2 ..:

Perche, Olivier ; Menuet, Arnaud ; Marcos, Mélanie...
European Journal of Medical Genetics.  56 (2013)  11 - p. 635-641 , 2013
Link: https://doi.org/10.1016/..
 
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5

Detection of chromosomal breakpoints in patients with devel..:

Kagistia H Utami ; Axel M Hillmer ; Irene Aksoy...
http://europepmc.org/articles/PMC3946304?pdf=render.  , 2014
Link: https://doi.org/10.1371/..
 
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6

Unbiased profiling of isogenic huntington disease hPSC-deri..:

Ooi, Jolene ; Langley, Sarah Raye ; Xu, Xiaohong...
Cell Reports.  , 2019
Link: http://hdl.handle.net/10..
 
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7

Unbiased profiling of isogenic huntington disease hPSC-deri..:

Ziaei, Amin ; Zeng, Ruizhu ; Low, Donovan...
Cell Reports.  , 2019
Link: https://hdl.handle.net/1..
 
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8

Integrative Analysis Identifies Key Molecular Signatures Un..:

Utami, Kagistia Hana ; Skotte, Niels H. ; Colaço, Ana R....
Biological Psychiatry.  88 (2020)  6 - p. 500-511 , 2020
Link: https://doi.org/10.1016/..
 
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9

Neurodevelopmental deficits in human isogenic Fragile X Syn..:

Utami, Kagistia Hana ; Skotte, Niels H. ; Colaco, Ana R....
IBRO Reports.  6 (2019)  - p. S507 , 2019
Link: https://doi.org/10.1016/..
 
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10

A homozygous loss-of-function CAMK2A mutation causes growth..:

Chia, Poh Hui ; Zhong, Franklin Lei ; Niwa, Shinsuke...
eLife.  7 (2018)  - p. , 2018
Link: https://doi.org/10.7554/..
 
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11

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase c..:

Holger Hengel ; Célia Bosso-Lefèvre ; George Grady...
https://doi.org/10.1038/s41467-020-14360-7.  , 2020
Link: https://doi.org/10.1038/..
 
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12

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase c..:

Hengel, H. (Holger) ; Bosso-Lefèvre, C. (Célia) ; Grady, G. (George)...
http://repub.eur.nl/pub/124422.  , 2020
Link: http://repub.eur.nl/pub/..
 
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13

A homozygous loss-of-function CAMK2A mutation causes growth..:

Poh Hui Chia ; Franklin Lei Zhong ; Shinsuke Niwa...
https://elifesciences.org/articles/32451.  , 2018
Link: https://doi.org/10.7554/..
 
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14

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase c..:

Hengel, Holger ; Bosso-Lefèvre, Célia ; Grady, George...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992768/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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15

Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase c..:

Hengel, Holger ; Bosso-Lefèvre, Célia ; Grady, George...
qt5f80k46t.  , 2020
Link: https://escholarship.org..
 
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