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MHHi016-B
Registration Summary
:
A
P
E
C
PCD-P1_CCNO clone 21
The cell line is
not submitted
yet.
(only basic data is shown)
General
Cell Line
hPSCreg name
MHHi016-B
Cite as:
When citing this cell line, please use the hPSCreg name (see
Naming Tool
) and the corresponding Research Resource ID (RRID).
MHHi016-B (RRID:CVCL_ZJ21)
Alternative name(s)
PCD-P1_CCNO clone 21
Cell line type
Human induced pluripotent stem cell (hiPSC)
Similar lines
No similar lines found.
Last update
18th November 2019
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Provider
Generator
Hannover Medical School (MHH)
External Databases
Cellosaurus
CVCL_ZJ21
Wikidata
Q98127236
General Information
Publications
Dahlmann J et al. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene. Stem cell research. 2020 Jul;46:101850.
Duong Phu M et al. Limitations and opportunities in the pharmacotherapy of ciliopathies. Pharmacology & therapeutics. 2021 Sep;225:107841.
Zhang YY et al. CCNO mutation as a cause of primary ciliary dyskinesia: A case report. World journal of clinical cases. 2022 Sep 6;10(25):9148-9155.
von Schledorn L et al. Primary Ciliary Dyskinesia Patient-Specific hiPSC-Derived Airway Epithelium in Air-Liquid Interface Culture Recapitulates Disease Specific Phenotypes In Vitro. Cells. 2023 May 24;12(11).
hIPSC Derivation
General
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