Cargando…

Detection of Vascular Notch3 Deposits in Unfixed Frozen Skin Biopsy Sample in CADASIL

This study aimed to evaluate the utility of immunohistochemical staining of vascular Notch3 deposits in biopsied unfixed frozen skin samples from patients with suspected cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). We analyzed vascular Notch3...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ueda, Akihiko, Nakajima, Makoto, Misumi, Yohei, Nakahara, Keiichi, Shinriki, Satoru, Tasaki, Masayoshi, Matsui, Hirotaka, Ueda, Mitsuharu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2022
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239429/ https://www.ncbi.nlm.nih.gov/pubmed/35775048 http://dx.doi.org/10.3389/fneur.2022.881528

Ejemplares similares

Plasma growth differentiation factor 15: a novel tool to detect early changes of hereditary transthyretin amyloidosis
por: Okada, Masamitsu, et al.
Publicado: (2020)

New simple and quick method to analyze serum variant transthyretins: direct MALDI method for the screening of hereditary transthyretin amyloidosis
por: Nomura, Toshiya, et al.
Publicado: (2019)

Using Unfixed, Frozen Tissues to Study Natural Mucin Distribution
por: Cohen, Miriam, et al.
Publicado: (2012)

Involvement of Macrophages in the Pathogenesis of Familial Amyloid Polyneuropathy and Efficacy of Human iPS Cell-Derived Macrophages in Its Treatment
por: Suenaga, Genki, et al.
Publicado: (2016)

A novel protocol to detect green fluorescent protein in unfixed, snap-frozen tissue
por: Scandella, Valentina, et al.
Publicado: (2020)

Transient optic neuritis and perineuritis associated with anti-MOG antibody after SARS-CoV-2 mRNA vaccination
por: Singu, Takaomi, et al.
Publicado: (2022)

Unique role of DDX41, a DEAD-box type RNA helicase, in hematopoiesis and leukemogenesis
por: Shinriki, Satoru, et al.
Publicado: (2022)

DDX41 coordinates RNA splicing and transcriptional elongation to prevent DNA replication stress in hematopoietic cells
por: Shinriki, Satoru, et al.
Publicado: (2022)

Active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model
por: Oliveira, Daniel V, et al.
Publicado: (2022)

Inflammatory state exists in familial amyloid polyneuropathy that may be triggered by mutated transthyretin
por: Suenaga, Genki, et al.
Publicado: (2017)

NOTCH3 Variants in Patients with Suspected CADASIL
por: Gorukmez, Orhan, et al.
Publicado: (2023)

Broadening the Genetic Horizons of CADASIL: New Variants of the NOTCH3 Gene Revealed and their Association with CADASIL
por: Mishra, Biswamohan, et al.
Publicado: (2023)

Sequestration of latent TGF-β binding protein 1 into CADASIL-related Notch3-ECD deposits
por: Kast, Jessica, et al.
Publicado: (2014)

Current Management and Therapeutic Strategies for Cerebral Amyloid Angiopathy
por: Inoue, Yasuteru, et al.
Publicado: (2021)

Headache and NOTCH3 Gene Variants in Patients with CADASIL
por: Szymanowicz, Oliwia, et al.
Publicado: (2023)

Teaching percutaneous renal biopsy using unfixed human cadavers
por: Oliver, Scott W., et al.
Publicado: (2015)

Novel mutation of the notch3 gene in arabic family with CADASIL
por: Bohlega, Saeed
Publicado: (2011)

Biochemical Characterization and Cellular Effects of CADASIL Mutants of NOTCH3
por: Meng, He, et al.
Publicado: (2012)

NOTCH3 and CADASIL syndrome: a genetic and structural overview
por: Papakonstantinou, Eleni, et al.
Publicado: (2019)

Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance
por: Takeuchi, Yosuke, et al.
Publicado: (2022)

A CADASIL-Like Case with a Novel Noncysteine Mutation of the NOTCH3 Gene and Granular Deposits in the Renal Arterioles
por: Nakamura, Kuniyuki, et al.
Publicado: (2015)

Unfixed Endogenous Retroviral Insertions in the Human Population
por: Marchi, Emanuele, et al.
Publicado: (2014)

Fluorescent detection of PARP activity in unfixed tissue
por: Belhadj, Soumaya, et al.
Publicado: (2021)

Step‐by‐step typing for the accurate diagnosis of concurrent light chain and transthyretin cardiac amyloidosis
por: Moriyama, Hidenori, et al.
Publicado: (2022)

Hypoxia suppresses cylindromatosis (CYLD) expression to promote inflammation in glioblastoma: possible link to acquired resistance to anti-VEGF therapy
por: Guo, Jianying, et al.
Publicado: (2014)

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients
por: Tikka, Saara, et al.
Publicado: (2009)

Identification of a Known Mutation in Notch 3 in Familiar CADASIL in China
por: Tan, Zhen-Xuan, et al.
Publicado: (2012)

Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL
por: Rutten, Julie W., et al.
Publicado: (2016)

Notch3 and its CADASIL mutants differentially regulate cellular phenotypes
por: Lin, Chunjing, et al.
Publicado: (2021)

NOTCH3 Variants and Genotype-Phenotype Features in Chinese CADASIL Patients
por: Hu, Yacen, et al.
Publicado: (2021)

A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL
por: Li, Juyi, et al.
Publicado: (2022)

Miller Fisher Syndrome Following Vaccination against SARS-CoV-2
por: Yamakawa, Makoto, et al.
Publicado: (2022)

Histopathological Features of Gerhardt Syndrome in a Patient With Multiple System Atrophy: An Autopsy Case Report
por: Nakahara, Keiichi, et al.
Publicado: (2022)

Reversible Periventricular Hyperintensity Lesions in Cerebral Amyloid Angiopathy: A Case Mimicking Cerebral Amyloid Angiopathy-related Inflammation
por: Inoue, Yasuteru, et al.
Publicado: (2022)

Molecular Chaperone BRICHOS Inhibits CADASIL-Mutated NOTCH3 Aggregation In Vitro
por: Oliveira, Daniel V., et al.
Publicado: (2022)

Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations
por: Ni, Wang, et al.
Publicado: (2022)

Corrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL
por: Li, Juyi, et al.
Publicado: (2023)

Combined deficiency of Notch1 and Notch3 causes pericyte dysfunction, models CADASIL, and results in arteriovenous malformations
por: Kofler, Natalie M., et al.
Publicado: (2015)

DEMONSTRATION OF MYELIN FIGURES IN UNFIXED, FREEZE-ETCHED FUNGUS SPORES
por: Cole, Garry T., et al.
Publicado: (1971)

Urinary Transthyretin as a Biomarker in ATTRv Val50Met Amyloidosis
por: Matsushita, Hiroaki, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_bg9diec80du7b4ifo72kdcboio