메뉴 건너뛰기




Volumn 354, Issue 14, 2006, Pages 1489-1496

Role of COL4A1 in small-vessel disease and hemorrhagic stroke

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 4; PROTEIN COL4A1; UNCLASSIFIED DRUG;

EID: 33645498692     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMoa053727     Document Type: Article
Times cited : (466)

References (12)
  • 3
    • 21044442223 scopus 로고    scopus 로고
    • Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly
    • Gould DB, Phalan FC, Breedveld GJ, et al. Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly. Science 2005;308:1167-71.
    • (2005) Science , vol.308 , pp. 1167-1171
    • Gould, D.B.1    Phalan, F.C.2    Breedveld, G.J.3
  • 4
    • 33645533307 scopus 로고    scopus 로고
    • Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
    • in press
    • Breedveld G, de Coo RF, Lequin MH, et al. Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly. J Med Genet (in press).
    • J Med Genet
    • Breedveld, G.1    De Coo, R.F.2    Lequin, M.H.3
  • 6
    • 0037067391 scopus 로고    scopus 로고
    • QTL associated with blood pressure, heart rate, and heart weight in CBA/CaJ and BALB/cJ mice
    • Sugiyama F, Churchill GA, Li R, et al. QTL associated with blood pressure, heart rate, and heart weight in CBA/CaJ and BALB/cJ mice. Physiol Genomics 2002;10:5-12.
    • (2002) Physiol Genomics , vol.10 , pp. 5-12
    • Sugiyama, F.1    Churchill, G.A.2    Li, R.3
  • 7
    • 0037435523 scopus 로고    scopus 로고
    • Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
    • Vahedi K, Massin P, Guichard JP, et al. Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy. Neurology 2003;60:57-63.
    • (2003) Neurology , vol.60 , pp. 57-63
    • Vahedi, K.1    Massin, P.2    Guichard, J.P.3
  • 8
    • 0030712287 scopus 로고    scopus 로고
    • Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
    • Jen J, Cohen AH, Yue Q, et al. Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS). Neurology 1997;49:1322-30.
    • (1997) Neurology , vol.49 , pp. 1322-1330
    • Jen, J.1    Cohen, A.H.2    Yue, Q.3
  • 9
    • 23044454428 scopus 로고    scopus 로고
    • Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: A novel syndrome
    • Plaisier E, Alamowitch S, Gribouval O, et al. Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: a novel syndrome. Kidney Int 2005;67:2354-60.
    • (2005) Kidney Int , vol.67 , pp. 2354-2360
    • Plaisier, E.1    Alamowitch, S.2    Gribouval, O.3
  • 10
    • 0030612084 scopus 로고    scopus 로고
    • Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution
    • Gupta MC, Graham PL, Kramer JM. Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution. J Cell Biol 1997;137:1185-96.
    • (1997) J Cell Biol , vol.137 , pp. 1185-1196
    • Gupta, M.C.1    Graham, P.L.2    Kramer, J.M.3
  • 12
    • 0034920305 scopus 로고    scopus 로고
    • Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3
    • Ophoff RA, DeYoung J, Service SK, et al. Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 2001;69:447-53.
    • (2001) Am J Hum Genet , vol.69 , pp. 447-453
    • Ophoff, R.A.1    DeYoung, J.2    Service, S.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.