Literature DB >> 10712425

CADASIL: Notch signaling defect or protein accumulation problem?

N B Spinner1.   

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Year:  2000        PMID： 10712425      PMCID： PMC292459          DOI： 10.1172/JCI9511

Source DB:  PubMed          Journal:  J Clin Invest        ISSN： 0021-9738            Impact factor:   14.808


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  18 in total

1.  Mutations in the human Jagged1 gene are responsible for Alagille syndrome.

Authors:  T Oda; A G Elkahloun; B L Pike; K Okajima; I D Krantz; A Genin; D A Piccoli; P S Meltzer; N B Spinner; F S Collins; S C Chandrasekharappa
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

2.  Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.

Authors:  L Li; I D Krantz; Y Deng; A Genin; A B Banta; C C Collins; M Qi; B J Trask; W L Kuo; J Cochran; T Costa; M E Pierpont; E B Rand; D A Piccoli; L Hood; N B Spinner
Journal:  Nat Genet       Date:  1997-07       Impact factor: 38.330

3.  Requirement for dynamin during Notch signaling in Drosophila neurogenesis.

Authors:  L Seugnet; P Simpson; M Haenlin
Journal:  Dev Biol       Date:  1997-12-15       Impact factor: 3.582

4.  Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.

Authors:  A Joutel; K Vahedi; C Corpechot; A Troesch; H Chabriat; C Vayssière; C Cruaud; J Maciazek; J Weissenbach; M G Bousser; J F Bach; E Tournier-Lasserve
Journal:  Lancet       Date:  1997-11-22       Impact factor: 79.321

5.  alpha-Synuclein--a link between Parkinson and Alzheimer diseases?

Authors:  N Heintz; H Zoghbi
Journal:  Nat Genet       Date:  1997-08       Impact factor: 38.330

6.  Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Authors:  A Joutel; C Corpechot; A Ducros; K Vahedi; H Chabriat; P Mouton; S Alamowitch; V Domenga; M Cécillion; E Marechal; J Maciazek; C Vayssiere; C Cruaud; E A Cabanis; M M Ruchoux; J Weissenbach; J F Bach; M G Bousser; E Tournier-Lasserve
Journal:  Nature       Date:  1996-10-24       Impact factor: 49.962

7.  Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

Authors:  M H Polymeropoulos; C Lavedan; E Leroy; S E Ide; A Dehejia; A Dutra; B Pike; H Root; J Rubenstein; R Boyer; E S Stenroos; S Chandrasekharappa; A Athanassiadou; T Papapetropoulos; W G Johnson; A M Lazzarini; R C Duvoisin; G Di Iorio; L I Golbe; R L Nussbaum
Journal:  Science       Date:  1997-06-27       Impact factor: 47.728

8.  Alzheimer's disease: initial report of the purification and characterization of a novel cerebrovascular amyloid protein.

Authors:  G G Glenner; C W Wong
Journal:  Biochem Biophys Res Commun       Date:  1984-05-16       Impact factor: 3.575

9.  The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.

Authors:  A Joutel; F Andreux; S Gaulis; V Domenga; M Cecillon; N Battail; N Piga; F Chapon; C Godfrain; E Tournier-Lasserve
Journal:  J Clin Invest       Date:  2000-03       Impact factor: 14.808

10.  TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms.

Authors:  L W Ellisen; J Bird; D C West; A L Soreng; T C Reynolds; S D Smith; J Sklar
Journal:  Cell       Date:  1991-08-23       Impact factor: 41.582
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  9 in total

Review 1.  Notch and disease: a growing field.

Authors:  Angeliki Louvi; Spyros Artavanis-Tsakonas
Journal:  Semin Cell Dev Biol       Date:  2012-02-20       Impact factor: 7.727

2.  A CADASIL-mutated Notch 3 receptor exhibits impaired intracellular trafficking and maturation but normal ligand-induced signaling.

Authors:  Helena Karlström; Paul Beatus; Karin Dannaeus; Gavin Chapman; Urban Lendahl; Johan Lundkvist
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-13       Impact factor: 11.205

Review 3.  An overview of notch signaling in adult tissue renewal and maintenance.

Authors:  Chihiro Sato; Guojun Zhao; Ma Xenia G Ilagan
Journal:  Curr Alzheimer Res       Date:  2012-02       Impact factor: 3.498

4.  Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway.

Authors:  Anne Joutel; Marie Monet; Valérie Domenga; Florence Riant; Elisabeth Tournier-Lasserve
Journal:  Am J Hum Genet       Date:  2004-01-08       Impact factor: 11.025

5.  Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  Marie Magdeleine Ruchoux; Valérie Domenga; Peggy Brulin; Jacqueline Maciazek; Sylvie Limol; Elisabeth Tournier-Lasserve; Anne Joutel
Journal:  Am J Pathol       Date:  2003-01       Impact factor: 4.307

Review 6.  CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches.

Authors:  Arianna Manini; Leonardo Pantoni
Journal:  Mol Neurobiol       Date:  2021-01-19       Impact factor: 5.590

Review 7.  Targeting Notch3 in Hepatocellular Carcinoma: Molecular Mechanisms and Therapeutic Perspectives.

Authors:  Catia Giovannini; Luigi Bolondi; Laura Gramantieri
Journal:  Int J Mol Sci       Date:  2016-12-28       Impact factor: 5.923

Review 8.  A Notch updated.

Authors:  An-Chi Tien; Akhila Rajan; Hugo J Bellen
Journal:  J Cell Biol       Date:  2009-03-02       Impact factor: 10.539

9.  Increased expression of Notch1 in temporal lobe epilepsy: animal models and clinical evidence.

Authors:  Xijin Liu; Zhiyong Yang; Yaping Yin; Xuejun Deng
Journal:  Neural Regen Res       Date:  2014-03-01       Impact factor: 5.135
  9 in total

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