90 related articles for article (PubMed ID: 10712425)
1. CADASIL: Notch signaling defect or protein accumulation problem?
Spinner NB
J Clin Invest; 2000 Mar; 105(5):561-2. PubMed ID: 10712425
[No Abstract] [Full Text] [Related]
2. [Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation].
Ishibashi K; Murata T; Miki Y; Hara M; Mori H
No To Shinkei; 2005 May; 57(5):415-8. PubMed ID: 15981641
[TBL] [Abstract][Full Text] [Related]
3. Distribution pattern of Notch3 mutations suggests a gain-of-function mechanism for CADASIL.
Donahue CP; Kosik KS
Genomics; 2004 Jan; 83(1):59-65. PubMed ID: 14667809
[TBL] [Abstract][Full Text] [Related]
4. [A case of CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lekoencephalopathy) with Notch 3 (Arg169Cys) mutation and typical granular osmiophilic materials in peripheral small arteries].
Kotani N; Hara H; Fujimura H; Miyashita T; Miyaguchi K; Tabira T
Rinsho Shinkeigaku; 2004; 44(4-5):274-9. PubMed ID: 15287509
[TBL] [Abstract][Full Text] [Related]
5. A CADASIL-mutated Notch 3 receptor exhibits impaired intracellular trafficking and maturation but normal ligand-induced signaling.
Karlström H; Beatus P; Dannaeus K; Chapman G; Lendahl U; Lundkvist J
Proc Natl Acad Sci U S A; 2002 Dec; 99(26):17119-24. PubMed ID: 12482954
[TBL] [Abstract][Full Text] [Related]
6. Expression patterns of Notch1, Notch2, and Notch3 suggest multiple functional roles for the Notch-DSL signaling system during brain development.
Irvin DK; Zurcher SD; Nguyen T; Weinmaster G; Kornblum HI
J Comp Neurol; 2001 Jul; 436(2):167-81. PubMed ID: 11438922
[TBL] [Abstract][Full Text] [Related]
7. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
Otori T; Katayama Y
Nihon Rinsho; 2004 Jan; 62 Suppl():331-4. PubMed ID: 15011378
[No Abstract] [Full Text] [Related]
8. Gene symbol: NOTCH3. Disease: CADASIL.
Rojas-Marcos I; Encarnacion M; Martinez-Yelamos S; Ferrer I; Arbizu T; Gil-Peralta A; Garcia-Lozano JR
Hum Genet; 2004 Jul; 115(2):175. PubMed ID: 15300988
[No Abstract] [Full Text] [Related]
9. Skin biopsy findings in CADASIL.
Smith BW; Henneberry J; Connolly T
Neurology; 2002 Sep; 59(6):961. PubMed ID: 12297597
[No Abstract] [Full Text] [Related]
10. [A case of CADASIL in early stage].
Kotorii S; Sakae N; Yamada N; Yamanaka H; Fujii N; Nakashima Y
Rinsho Shinkeigaku; 2001 Jun; 41(6):306-9. PubMed ID: 11771160
[TBL] [Abstract][Full Text] [Related]
11. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) characteristics in Japan: variety of clinical features.
Adachi Y; Nakashima K
Intern Med; 2000 Sep; 39(9):681-2. PubMed ID: 10969895
[No Abstract] [Full Text] [Related]
12. Diverse requirements for Notch signalling in mammals.
Sparrow DB; Clements M; Withington SL; Scott AN; Novotny J; Sillence D; Kusumi K; Beddington RS; Dunwoodie SL
Int J Dev Biol; 2002; 46(4):365-74. PubMed ID: 12141422
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigree.
Grigg R; Lea R; Sullivan AA; Curtain R; MacMillian J; Griffiths L
Hum Mutat; 2000 Nov; 16(5):449-50. PubMed ID: 11058919
[No Abstract] [Full Text] [Related]
14. Screening British CADASIL families for mutations in the NOTCH3 gene.
de Lange RP; Bolt J; Reid E; da Silva R; Shaw DJ; St Clair DM
J Med Genet; 2000 Mar; 37(3):224-5. PubMed ID: 10777367
[No Abstract] [Full Text] [Related]
15. [Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].
Yamada H; Yasuda T; Kotorii S; Takahashi K; Tabira T; Sunada Y
Rinsho Shinkeigaku; 2001; 41(2-3):144-6. PubMed ID: 11481859
[TBL] [Abstract][Full Text] [Related]
16. [Atypical CADASIL phenotypes and pathological findings in two new French families].
Mikol J; Hénin D; Baudrimont M; Gaulier A; Bacri D; Tillier JN; Davous P
Rev Neurol (Paris); 2001 Jul; 157(6-7):655-67. PubMed ID: 11458185
[TBL] [Abstract][Full Text] [Related]
17. [Familial non-Alzheimer dementia].
Tabira T
Rinsho Shinkeigaku; 2003 Nov; 43(11):775-8. PubMed ID: 15152461
[TBL] [Abstract][Full Text] [Related]
18. Screening for CADASIL mutations.
Inzitari D; Sarti C
Stroke; 2003 Jan; 34(1):205-6. PubMed ID: 12557863
[No Abstract] [Full Text] [Related]
19. Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL.
Joutel A; Chabriat H; Vahedi K; Domenga V; Vayssière C; Ruchoux MM; Lucas C; Leys D; Bousser MG; Tournier-Lasserve E
Neurology; 2000 May; 54(9):1874-5. PubMed ID: 10802807
[No Abstract] [Full Text] [Related]
20. [CADASIL: clinical analysis of CADASIL and CADASIL-like disorders in Japan].
Uchino M; Uyama E; Maeda Y; Hirano T; Suenaga A; Yamada H; Hashimoto Y; Kotorii S; Takahashi K; Tabira T
Rinsho Shinkeigaku; 2000 Dec; 40(12):1247-50. PubMed ID: 11464469
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]