| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An integration-free iPSC line ZZUNEUi029-A derived from peripheral blood mononuclear cells of a patient with familial hypercholesterolemia carrying a mutation in LDLR gene
|
Zhu, Kui
|
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71 |
C |
p.
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artikel
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| 2 |
Combining a tetracycline (Tet)-inducible gRNA system and CRISPRa for titratable and timely controlled enhancement of endogenous SHISA3 activation in human induced pluripotent stem cells (hiPSC)
|
Priesmeier, Laura
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|
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71 |
C |
p.
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artikel
|
| 3 |
Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects
|
Alonzo, Matthew
|
|
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71 |
C |
p.
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artikel
|
| 4 |
CRISPR-Cas9-mediated disruption of B2M and CIITA genes eliminates HLA class I and II expression in human induced pluripotent stem cells (MUSIi001-A-2)
|
Thongsin, Nontaphat
|
|
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71 |
C |
p.
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artikel
|
| 5 |
CRISPR/Cas9-mediated generation of human embryonic stem cell sub-lines with HPRT1 gene knockout to model Lesch Nyhan disease
|
Boissart, Claire
|
|
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71 |
C |
p.
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artikel
|
| 6 |
Derivation of induced pluripotent stem cell SJTUi003-A from a 69-year-old Chinese Han Sporadic Alzheimer’s disease patient with APOEε3/ε4 genetic background
|
Li, Hui
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71 |
C |
p.
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artikel
|
| 7 |
Establishment of a controlled induced pluripotent stem cell line SDPHi004-A from a healthy male donor
|
Feng, Ziwen
|
|
|
71 |
C |
p.
|
artikel
|
| 8 |
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
|
Li, Benchang
|
|
|
71 |
C |
p.
|
artikel
|
| 9 |
Establishment of a TNFRSF11B knock-out human induced pluripotent stem cell line (KSCBi002-B-2) via CRISPR/Cas9 system
|
Jeong, Jujin
|
|
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71 |
C |
p.
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artikel
|
| 10 |
Establishment of induced pluripotent stem cell line SDPHi003-A from a healthy male donor
|
Xi, Yue
|
|
|
71 |
C |
p.
|
artikel
|
| 11 |
Generation and characterization of a human induced pluripotent stem cell line (SDQLCHi052-A) from peripheral blood mononuclear cells derived from a healthy Chinese donor
|
Wan, Zirui
|
|
|
71 |
C |
p.
|
artikel
|
| 12 |
Generation and characterization of induced pluripotent stem cell line IITGi001-A derived from adult human primary dermal fibroblasts
|
Raina, Khyati
|
|
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71 |
C |
p.
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artikel
|
| 13 |
Generation of a FLNA knockout hESC line (WAe009-A-P) to model cardiac valvular dysplasia using CRISPR/Cas9
|
Lu, Fengyuan
|
|
|
71 |
C |
p.
|
artikel
|
| 14 |
Generation of a homozygous CRYAB p.Arg120Gly mutant (UKEi001-A-1) from a human iPSC line
|
Pietsch, Niels
|
|
|
71 |
C |
p.
|
artikel
|
| 15 |
Generation of a homozygous RANGRF knockout hiPSC line by CRISPR/Cas9 system
|
Jiang, Meiling
|
|
|
71 |
C |
p.
|
artikel
|
| 16 |
Generation of a human induced pluripotent stem cell line from a patient with dent disease
|
Fang, Xianying
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|
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71 |
C |
p.
|
artikel
|
| 17 |
Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22)
|
Ozgoren, Oguz K.
|
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71 |
C |
p.
|
artikel
|
| 18 |
Generation of a human induced pluripotent stem cell line harboring the infant leukemia-associated fusion gene, KMT2A-AFF1 (IMSUTi002-A-2)
|
Takahashi, Masayuki
|
|
|
71 |
C |
p.
|
artikel
|
| 19 |
Generation of a human iPSC line (ZJSHDPi001-A) from peripheral blood mononuclear cells of a patient with Developmental epileptic encephalopathy-47 carrying FGF12 gene mutation (c.334G > A)
|
Gao, Liuyan
|
|
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71 |
C |
p.
|
artikel
|
| 20 |
Generation of a human Tropomyosin 1 knockout iPSC line
|
Wilken, Madison B.
|
|
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71 |
C |
p.
|
artikel
|
| 21 |
Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9
|
Schuurmans, Imke M.E.
|
|
|
71 |
C |
p.
|
artikel
|
| 22 |
Generation of an induced pluripotent stem cell line (ESi107-A) from a transthyretin amyloid cardiomyopathy (ATTR-CM) patient carrying a p.Ser43Asn mutation in the TTR gene
|
Montero-Calle, Pilar
|
|
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71 |
C |
p.
|
artikel
|
| 23 |
Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant
|
Li, Serena
|
|
|
71 |
C |
p.
|
artikel
|
| 24 |
Generation of an induced pluripotent stem cell line (NCHi010-A) from a 6-year-old female with Down syndrome and without congenital heart disease
|
Yu, Yang
|
|
|
71 |
C |
p.
|
artikel
|
| 25 |
Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD)
|
Heseding, Hannah
|
|
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71 |
C |
p.
|
artikel
|
| 26 |
Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Nav1.2 protein encoded by the SCN2A gene
|
Ovchinnikov, D.A.
|
|
|
71 |
C |
p.
|
artikel
|
| 27 |
Generation of an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome due to STK11 mutation
|
Wang, Teng
|
|
|
71 |
C |
p.
|
artikel
|
| 28 |
Generation of a transgene-free iPS cell line (SDQLCHi053-A) from a young girl carrying a heterozygous mutation (c.427C > T) in SYNGAP1 gene
|
Wang, Yanxin
|
|
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71 |
C |
p.
|
artikel
|
| 29 |
Generation of a transgenic mouse embryonic stem cell line overexpressing DNMT1
|
Choudhury, Sumana
|
|
|
71 |
C |
p.
|
artikel
|
| 30 |
Generation of CHOPe003-A ESC line to study an ACTG2 variant affecting smooth muscle development and function
|
Hashmi, Sohaib K.
|
|
|
71 |
C |
p.
|
artikel
|
| 31 |
Generation of CHOPi012-A iPSC line from a patient with visceral myopathy-related chronic intestinal pseudo-obstruction
|
Hashmi, Sohaib K.
|
|
|
71 |
C |
p.
|
artikel
|
| 32 |
Generation of control iPSC lines CBRCULi008-A and CBRCULi009-A derived from lymphoblastoid cell lines
|
Chapotte-Baldacci, Charles-Albert
|
|
|
71 |
C |
p.
|
artikel
|
| 33 |
Generation of eight hiPSCs lines from two pathogenic variants in CACNA1A using the CRISPR-Cas9 gene editing technology
|
Rivera-Sánchez, Paula
|
|
|
71 |
C |
p.
|
artikel
|
| 34 |
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A)
|
Kobayashi, Gerson S.
|
|
|
71 |
C |
p.
|
artikel
|
| 35 |
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9
|
Ben yacoub, Tasnim
|
|
|
71 |
C |
p.
|
artikel
|
| 36 |
Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation
|
Cattelan, Giada
|
|
|
71 |
C |
p.
|
artikel
|
| 37 |
Generation of induced pluripotent stem cell lines from three individuals with autism spectrum disorder
|
Pugsley, Kealan
|
|
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71 |
C |
p.
|
artikel
|
| 38 |
Generation of induced pluripotent stem cell line (XWHNi002-A) from a female with APP gene mutation
|
Sun, Wenxian
|
|
|
71 |
C |
p.
|
artikel
|
| 39 |
Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinson's disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456*
|
Jonsgaard Larsen, Lasse
|
|
|
71 |
C |
p.
|
artikel
|
| 40 |
Generation of iPSC line NCHi012-A from a patient with Alagille syndrome and heterozygous pathogenic variant in the JAG1 gene
|
Cunningham, David
|
|
|
71 |
C |
p.
|
artikel
|
| 41 |
Generation of iPSC lines from three Stargardt patients carrying bi-allelic ABCA4 variants
|
Karjosukarso, Dyah W.
|
|
|
71 |
C |
p.
|
artikel
|
| 42 |
Generation of myoglobin (MB)-knockout human embryonic stem cell (hESC) line (KAIMRCe002-A-1S) using CRISPR/Cas9 technology
|
Alowaysi, Maryam
|
|
|
71 |
C |
p.
|
artikel
|
| 43 |
Generation of the human iPSC lines AKOSi011-A carrying the mutation p.Pro65Ser/p.Asp35T and AKOSi012-A, carrying the mutation p.Tyr231His, derived from FAHN patient fibroblasts
|
Efendic, Fatima
|
|
|
71 |
C |
p.
|
artikel
|
| 44 |
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C)
|
Stewart, Rachel
|
|
|
71 |
C |
p.
|
artikel
|
| 45 |
Generation of three induced pluripotent stem cell lines (RAUi001-A, RAUi001-B and RAUi001-C) from peripheral blood mononuclear cells of a healthy Armenian individual
|
Grigor’eva, Elena V.
|
|
|
71 |
C |
p.
|
artikel
|
| 46 |
Generation of three isogenic control lines from patient-derived iPSCs carrying bi-allelic ABCA4 variants underlying Stargardt disease
|
Karjosukarso, Dyah W.
|
|
|
71 |
C |
p.
|
artikel
|
| 47 |
Generation of two Alpha-I antitrypsin deficiency patient-derived induced pluripotent stem cell lines ISRM-AATD-iPSC-1 (HHUUKDi011-A) and ISRM-AATD-iPSC-2 (HHUUKDi012-A)
|
Ncube, Audrey
|
|
|
71 |
C |
p.
|
artikel
|
| 48 |
Generation of two edited iPSCs lines by CRISPR/Cas9 with point mutations in PKP2 gene for arrhythmogenic cardiomyopathy in vitro modeling
|
Amin, Guadalupe
|
|
|
71 |
C |
p.
|
artikel
|
| 49 |
Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson’s disease
|
Devito, Liani G.
|
|
|
71 |
C |
p.
|
artikel
|
| 50 |
Generation of two human induced pluripotent stem cell lines from a patient with Neurofibromatosis type 1 (NF1) and pathogenic NF1 gene variant c.1466 A>G BCRTi011-A as well as a first-degree healthy relative (BCRTi010-A)
|
Batool, Lilas
|
|
|
71 |
C |
p.
|
artikel
|
| 51 |
Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors
|
Piechota, Marta
|
|
|
71 |
C |
p.
|
artikel
|
| 52 |
Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson’s disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
|
Chemla, Axel
|
|
|
71 |
C |
p.
|
artikel
|
| 53 |
Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12
|
Panchuk, I.O.
|
|
|
71 |
C |
p.
|
artikel
|
| 54 |
Genetic repair of a human induced pluripotent cell line from patient with Dutch-type cerebral amyloid angiopathy
|
Nahon, Dennis M.
|
|
|
71 |
C |
p.
|
artikel
|
| 55 |
Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c.236G>A (p.R79H)
|
Chen, Weijie
|
|
|
71 |
C |
p.
|
artikel
|
| 56 |
Induced pluripotent stem cell line generated from a patient with differences in sex development (DSD) and multiple genetic variants including a large deletion in NR5A1
|
Siebert, Aisha L.
|
|
|
71 |
C |
p.
|
artikel
|
| 57 |
Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A)
|
Chahine, Mohamed
|
|
|
71 |
C |
p.
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artikel
|
| 58 |
Modelling Duchenne muscular dystrophy in vitro with newly generated, blood cell-derived induced pluripotent stem cell line ORIONi003-A
|
Hajduchova, Dominika
|
|
|
71 |
C |
p.
|
artikel
|
| 59 |
Three induced pluripotent stem cell lines (TRNDi033-A, TRNDi034-A, TRNDi035-A) generated from lymphoblasts of three apparently healthy individuals
|
Owusu-Ansah, Kofi
|
|
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71 |
C |
p.
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artikel
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