Dung Vu
Overview
Explore the profile of Dung Vu including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
14
Citations
58
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0
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Recent Articles
11.
Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, et al.
Blood
. 2004 Jul;
104(12):3618-23.
PMID: 15284111
Congenital afibrinogenemia, the most severe form of fibrinogen deficiency, is characterized by the complete absence of fibrinogen. The disease is caused by mutations in 1 of the 3 fibrinogen genes...
12.
Vu D, Bolton-Maggs P, Parr J, Morris M, Moerloose P, Neerman-Arbez M
Blood
. 2003 Aug;
102(13):4413-5.
PMID: 12893758
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen. We previously identified the first causative mutations for this disease: a homozygous deletion of approximately...
13.
Vu D, Marin P, Walzer C, Cathieni M, Bianchi E, Saidji F, et al.
Brain Res Mol Brain Res
. 2003 Jul;
115(2):93-103.
PMID: 12877980
LMO4 is a transcription regulator interacting with proteins involved, among else, in tumorigenesis. Its function in the nervous system, and particularly in the adult nervous system, has however still to...
14.
Neerman-Arbez M, Vu D, Abu-Libdeh B, Bouchardy I, Morris M
Blood
. 2003 Jan;
101(9):3492-4.
PMID: 12511408
Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by the complete absence of detectable fibrinogen. We previously identified the first causative mutations for this disease, homozygous deletions of approximately...