Concepedia

Nephroangiosclerosis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Is NOTCH3 Mutation the Common Culprit?

Dominique Guerrot, Arnaud François, Jean‐Jacques Boffa, Nada Boulos, M. Hanoy, B. Legallicier, Aude Triquenot-Bagan, Lucie Guyant‐Maréchal, Annie Laquerrière, Caroline Fréguin-Bouilland,

American Journal of Kidney Diseases · 2008 · 18 citations · 19 references

DOI

Concepts

References

19

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Ryan M. McDaniell, Daniel M. Warthen, Pedro A. Sanchez‐Lara et al. · The American Journal of Human Genetics · 2006 · 743 citations · Full text

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Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

Anne Joutel, Katayoun Vahedi, Christophe Corpechot et al. · The Lancet · 1997 · 684 citations

, , +13

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

Anne Joutel, F. Andreux, Swann Gaulis et al. · Journal of Clinical Investigation · 2000 · 600 citations · Full text

, , +14

<i>Notch3</i> is required for arterial identity and maturation of vascular smooth muscle cells

Valérie Domenga, Peggy Fardoux, Pierre Lacombe et al. · Genes & Development · 2004 · 533 citations · Full text

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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

M M Ruchoux, Djelloul Guerouaou, B Vandenhaute et al. · Acta Neuropathologica · 1995 · 326 citations

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