Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
Abstract Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary cerebrovascular disease caused by a NOTCH3 mutation. However, the underlying cellular and molecular mechanisms remain unidentified. Here, we generated non-integrative in...
| Published in: | Protein & Cell |
|---|---|
| Main Authors: | Chen Ling, Zunpeng Liu, Moshi Song, Weiqi Zhang, Si Wang, Xiaoqian Liu, Shuai Ma, Shuhui Sun, Lina Fu, Qun Chu, Juan Carlos Izpisua Belmonte, Zhaoxia Wang, Jing Qu, Yun Yuan, Guang-Hui Liu |
| Format: | Article |
| Language: | English |
| Published: |
Oxford University Press
2019-02-01
|
| Subjects: | |
| Online Access: | http://link.springer.com/article/10.1007/s13238-019-0608-1 |
Similar Items
Generation of a human iPSC line with Notch3 R133C mutation by CRISPR/Cas9: A tool for investigating CADASIL and therapeutic targets
by: Sema Aygar, et al.
Published: (2025-04-01)
by: Sema Aygar, et al.
Published: (2025-04-01)
NOTCH3 variants in patients with suspected CADASIL
by: Orhan Gorukmez, et al.
Published: (2023-01-01)
by: Orhan Gorukmez, et al.
Published: (2023-01-01)
Novel mutation of the NOTCH3 gene in Arabic family with CADASIL
by: Saeed Bohlega
Published: (2011-07-01)
by: Saeed Bohlega
Published: (2011-07-01)
Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review
by: Georgina Boston, et al.
Published: (2024-01-01)
by: Georgina Boston, et al.
Published: (2024-01-01)
CADASIL and A Family
by: Figen Varlıbaş, et al.
Published: (2008-04-01)
by: Figen Varlıbaş, et al.
Published: (2008-04-01)
A novel heterozygous mutation in the NOTCH 3 gene causing CADASIL
by: E Andreadou, et al.
Published: (2008-10-01)
by: E Andreadou, et al.
Published: (2008-10-01)
A Case of CADASIL with NOTCH3 Gene Mutation Presenting with Focal Epileptic Seizure: A Case of CADASIL Presenting with Focal Epileptic Seizure
by: Gülgün Uncu, et al.
Published: (2023-03-01)
by: Gülgün Uncu, et al.
Published: (2023-03-01)
Cadasil - genetic and ultrastructural diagnosis: case report
by: Julio Cesar Vasconcelos da Silva, et al.
by: Julio Cesar Vasconcelos da Silva, et al.
Study of the NOTCH3 Gene Reveals the First CADASIL Cases in Crete and a Novel Pathogenic Variant
by: Ioannis Zaganas, et al.
Published: (2025-09-01)
by: Ioannis Zaganas, et al.
Published: (2025-09-01)
CADASIL and cerebral microbleeds
by: Dilek Necioğlu Örken, et al.
Published: (2008-12-01)
by: Dilek Necioğlu Örken, et al.
Published: (2008-12-01)
CADASIL or NOTCH3 mutaion spectrum diseases? Interpretation of NOTCH3 mutations and clinical heterogeneity in CADASIL
by: Yuehui Wang, et al.
Published: (2025-09-01)
by: Yuehui Wang, et al.
Published: (2025-09-01)
Inflammatory-like presentation of CADASIL: a diagnostic challenge
by: Collongues Nicolas, et al.
Published: (2012-08-01)
by: Collongues Nicolas, et al.
Published: (2012-08-01)
Clinical and epidemiological profiles from a case series of 26 Brazilian CADASIL patients
by: Renata Nogueira, et al.
Published: (2023-05-01)
by: Renata Nogueira, et al.
Published: (2023-05-01)
De novo mutation in the NOTCH3 gene causing CADASIL
by: Dragan Stojanov, et al.
Published: (2014-05-01)
by: Dragan Stojanov, et al.
Published: (2014-05-01)
Investigating diagnostic sequencing techniques for CADASIL diagnosis
by: P. J. Dunn, et al.
Published: (2020-01-01)
by: P. J. Dunn, et al.
Published: (2020-01-01)
Headache and <i>NOTCH3</i> Gene Variants in Patients with CADASIL
by: Oliwia Szymanowicz, et al.
Published: (2023-10-01)
by: Oliwia Szymanowicz, et al.
Published: (2023-10-01)
CADASIL – obraz zmian morfologicznych i ich patomechanizm
by: Dorota Dziewulska
Published: (2011-12-01)
by: Dorota Dziewulska
Published: (2011-12-01)
A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL
by: Juyi Li, et al.
Published: (2022-11-01)
by: Juyi Li, et al.
Published: (2022-11-01)
Active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model
by: Daniel V Oliveira, et al.
Published: (2022-12-01)
by: Daniel V Oliveira, et al.
Published: (2022-12-01)
The pericyte: A critical cell in the pathogenesis of CADASIL
by: Marie-Magdeleine Ruchoux, et al.
Published: (2021-01-01)
by: Marie-Magdeleine Ruchoux, et al.
Published: (2021-01-01)
Corrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL
by: Juyi Li, et al.
Published: (2023-08-01)
by: Juyi Li, et al.
Published: (2023-08-01)
Novel Characteristics of Race-Specific Genetic Functions in Korean CADASIL
by: Yerim Kim, et al.
Published: (2019-08-01)
by: Yerim Kim, et al.
Published: (2019-08-01)
A temporal study on NF-κB-mediated autonomous inflammatory response in iPSC-CMs induced by microwave radiation
by: Chenjing Zhang, et al.
Published: (2025-09-01)
by: Chenjing Zhang, et al.
Published: (2025-09-01)
CADASIL: a propósito de um caso clínico
by: Ana Luísa Corte Real, et al.
Published: (2022-03-01)
by: Ana Luísa Corte Real, et al.
Published: (2022-03-01)
First report of a p.Cys484Tyr Notch3 mutation in a CADASIL patient with acute bilateral multiple subcortical infarcts—case report and brief review
by: Weili Liu, et al.
Published: (2024-02-01)
by: Weili Liu, et al.
Published: (2024-02-01)
Immune cells and RBCs derived from human induced pluripotent stem cells: method, progress, prospective challenges
by: Jin-he Jiang, et al.
Published: (2024-01-01)
by: Jin-he Jiang, et al.
Published: (2024-01-01)
Atypical clinical cases of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
by: Anna A. Moroz, et al.
Published: (2017-05-01)
by: Anna A. Moroz, et al.
Published: (2017-05-01)
CADASIL: pathogenesis, clinical and radiological findings and treatment CADASIL: patogênese, achados clínicos e radiológicos e tratamento
by: Charles André
Published: (2010-04-01)
by: Charles André
Published: (2010-04-01)
CADASIL
by: Swiss Medical Weekly
Published: (2007-06-01)
by: Swiss Medical Weekly
Published: (2007-06-01)
Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation
by: Jun Takei, et al.
Published: (2023-08-01)
by: Jun Takei, et al.
Published: (2023-08-01)
Patient with CADASIL – a diagnostic challenge
by: Julia Węgrzynek, et al.
Published: (2023-09-01)
by: Julia Węgrzynek, et al.
Published: (2023-09-01)
What factors determine phenotype of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)? Considerations in the context of a novel pathogenic R110C mutation in the NOTCH3 gene
by: Dorota Dziewulska, et al.
Published: (2017-12-01)
by: Dorota Dziewulska, et al.
Published: (2017-12-01)
CADASIL Syndrome Presenting as Adjustment Disorder
by: Sevda Bağ, et al.
Published: (2020-11-01)
by: Sevda Bağ, et al.
Published: (2020-11-01)
A clinical case of CADASIL syndrome in a patient after a new coronavirus infection COVID-19
by: Z. Sh. Dzhalilova, et al.
Published: (2023-08-01)
by: Z. Sh. Dzhalilova, et al.
Published: (2023-08-01)
CADASIL: A NOTCH3-associated cerebral small vessel disease
by: Lamei Yuan, et al.
Published: (2024-12-01)
by: Lamei Yuan, et al.
Published: (2024-12-01)
Case Report: Inflammatory CADASIL phenotype associated with a rare cysteine-sparing NOTCH3 variant
by: Abraham Madjidov, et al.
Published: (2025-05-01)
by: Abraham Madjidov, et al.
Published: (2025-05-01)
Depression in CADASIL patients
by: Lačković Maja, et al.
Published: (2014-01-01)
by: Lačković Maja, et al.
Published: (2014-01-01)
Autophagic control of cell ‘stemness’
by: Huize Pan, et al.
Published: (2013-03-01)
by: Huize Pan, et al.
Published: (2013-03-01)
Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene
by: Omer Hatim, et al.
Published: (2023-12-01)
by: Omer Hatim, et al.
Published: (2023-12-01)
Alzheimer’s in a dish – induced pluripotent stem cell-based disease modeling
by: Sherida de Leeuw, et al.
Published: (2019-07-01)
by: Sherida de Leeuw, et al.
Published: (2019-07-01)
Similar Items
-
Generation of a human iPSC line with Notch3 R133C mutation by CRISPR/Cas9: A tool for investigating CADASIL and therapeutic targets
by: Sema Aygar, et al.
Published: (2025-04-01) -
NOTCH3 variants in patients with suspected CADASIL
by: Orhan Gorukmez, et al.
Published: (2023-01-01) -
Novel mutation of the NOTCH3 gene in Arabic family with CADASIL
by: Saeed Bohlega
Published: (2011-07-01) -
Most common NOTCH3 mutations causing CADASIL or CADASIL-like cerebral small vessel disease: A systematic review
by: Georgina Boston, et al.
Published: (2024-01-01) -
CADASIL and A Family
by: Figen Varlıbaş, et al.
Published: (2008-04-01)
