Alessandro D Mori
Overview
Explore the profile of Alessandro D Mori including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
535
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Recent Articles
1.
Franklin S, Chow V, Mori A, Wong N
J Hypertens
. 2011 Apr;
29(6):1101-8.
PMID: 21478753
Objectives: To determine the features of isolated systolic hypertension (ISH), the most common hypertensive subtype in persons at least age 50, associated with greater cardiovascular disease (CVD) risk when accompanied...
2.
Takeuchi J, Lou X, Alexander J, Sugizaki H, Delgado-Olguin P, Holloway A, et al.
Nat Commun
. 2011 Feb;
2:187.
PMID: 21304516
Dominant mutations in cardiac transcription factor genes cause human inherited congenital heart defects (CHDs); however, their molecular basis is not understood. Interactions between transcription factors and the Brg1/Brm-associated factor (BAF)...
3.
Puskaric S, Schmitteckert S, Mori A, Glaser A, Schneider K, Bruneau B, et al.
Hum Mol Genet
. 2010 Sep;
19(23):4625-33.
PMID: 20858598
Heart formation requires a highly balanced network of transcriptional activation of genes. The homeodomain transcription factor, Shox2, is essential for the formation of the sinoatrial valves and for the development...
4.
Koshiba-Takeuchi K, Mori A, Kaynak B, Cebra-Thomas J, Sukonnik T, Georges R, et al.
Nature
. 2009 Sep;
461(7260):95-8.
PMID: 19727199
The emergence of terrestrial life witnessed the need for more sophisticated circulatory systems. This has evolved in birds, mammals and crocodilians into complete septation of the heart into left and...
5.
Mori A, Zhu Y, Vahora I, Nieman B, Koshiba-Takeuchi K, Davidson L, et al.
Dev Biol
. 2006 Jul;
297(2):566-86.
PMID: 16870172
Dominant mutations in the T-box transcription factor gene TBX5 cause Holt-Oram syndrome (HOS), an inherited human disease characterized by upper limb malformations and congenital heart defects (CHDs) of variable severity....
6.
Takeuchi J, Mileikovskaia M, Koshiba-Takeuchi K, Heidt A, Mori A, Arruda E, et al.
Development
. 2005 Apr;
132(10):2463-74.
PMID: 15843409
To elucidate the function of the T-box transcription factor Tbx20 in mammalian development, we generated a graded loss-of-function series by transgenic RNA interference in entirely embryonic stem cell-derived mouse embryos....
7.
Mori A, Bruneau B
Curr Opin Cardiol
. 2004 Apr;
19(3):211-5.
PMID: 15096952
Purpose Of Review: Mutations in the T-box transcription factor TBX5 cause Holt-Oram syndrome (HOS), an autosomal-dominant condition characterized by a familial history of congenital heart defects and preaxial radial ray...