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Nancy B. Spinner
Published in Volume 105, Issue 5
J Clin Invest. 2000; 105(5):561 doi:10.1172/JCI9511
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Total citations by year in CrossRef

Year: 2012 2010 2009 2008 2006 2004 2003 2002 2001 Total
Citations: 1 1 1 3 3 3 1 1 2 16

Citations to this article in CrossRef (16)

Title and authors Publication Year
Notch and Disease: a growing field
Angeliki Louvi, Spyros Artavanis-Tsakonas
Sem Cell Dev Biol 2012
Fisiopatología del CADASIL
Alberto del Río Espínola, Esther Solé, Joan Montaner
Medicina Clínica 2010
CADASIL management or what to do when there is little one can do
Alberto del Río-Espínola, Maite Mendióroz, Sophie Domingues-Montanari, Patricia Pozo-Rosich, Esther Solé, Jessica Fernández-Morales, Israel Fernández-Cadenas, Joan Montaner
Expert Rev Neurotherapeutics 2009
CADASIL: the most common hereditary subcortical vascular dementia
Hannu Kalimo, Qing Miao, Saara Tikka, Kati Mykkänen, Maija Junna, Susanna Roine, Matti Viitanen, Minna Pöyhönen, Marc Baumann
Future Neurology 2008
Indirubin-3′-monoxime, a derivative of a Chinese anti-leukemia medicine, inhibits Notch1 signaling
Mi-Jee Lee, Mi-Yeon Kim, Jung-Soon Mo, Eun-Jung Ann, Mi-Sun Seo, Ji-Ae Hong, Yong-Chul Kim, Hee-Sae Park
Cancer Letters 2008
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, Melanie Hanoy, Bruno Legallicier, Aude Triquenot-Bagan, Lucie Guyant-Marechal, Annie Laquerriere, Caroline Freguin-Bouilland, Pierre Ronco, Michel Godin
American Journal of Kidney Diseases 2008
Physiology and pathology of notch signalling system
Silvia Bianchi, Maria Teresa Dotti, Antonio Federico
J. Cell. Physiol. 2006
CADASIL: A Critical Look at a Notch Disease
Angeliki Louvi, Joseph F. Arboleda-Velasquez, Spyros Artavanis-Tsakonas
Dev Neurosci 2006
CADASIL: a Common Form of Hereditary Arteriopathy Causing Brain Infarcts and Dementia
Hannu Kalimo, Marie-Magdaleine Ruchoux, Matti Viitanen, Raj N. Kalaria
Brain Pathology 2006
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.
Anne Joutel, Marie Monet, Valérie Domenga, Florence Riant, Elisabeth Tournier-Lasserve
Am. J. Hum. Genet. 2004