R Bruzzone
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Explore the profile of R Bruzzone including associated specialties, affiliations and a list of published articles.
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103
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2366
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Recent Articles
11.
Fugazza G, Miglino M, Bruzzone R, Quintino S, Gatti A, Grasso R, et al.
J Exp Clin Cancer Res
. 2004 Sep;
23(2):295-9.
PMID: 15354415
Imatinib mesylate determines a favorable clinical course in most Ph positive Chronic Myeloid Leukemia (CML) patients in the chronic phase. Cytogenetic response is usually evaluated by analyzing 20-25 bone marrow...
12.
Bruzzone R, Veronesi V, Gomes D, Bicego M, Duval N, Marlin S, et al.
FEBS Lett
. 2002 Dec;
533(1-3):79-88.
PMID: 12505163
Connexins are the protein subunits of gap junction channels that allow a direct signaling pathway between networks of cells. The specific role of connexin channels in the homeostasis of different...
13.
Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness
Bruzzone R, Gomes D, Denoyelle E, Duval N, Perea J, Veronesi V, et al.
Cell Commun Adhes
. 2002 Jun;
8(4-6):425-31.
PMID: 12064630
Cx26 has been implicated in dominant (DFNA3) and recessive (DFNB1) forms of nonsyndromic sensorineural deafness. While most homozygous DFNB1 Cx26 mutations result in a simple loss of channel activity, it...
14.
Belluardo N, White T, Srinivas M, Trovato-Salinaro A, Ripps H, Mudo G, et al.
Cell Commun Adhes
. 2002 Jun;
8(4-6):173-8.
PMID: 12064584
By combining in silico and bench molecular biology methods we have identified a novel human gap junction gene that encodes a protein designated HCx31.9. We have determined its human chromosomal...
15.
Bruzzone R
Genome Biol
. 2001 Dec;
2(11):REPORTS4027.
PMID: 11737941
A report on the Ninth International Gap Junction Conference, Honolulu, USA, 4-9 August 2001.
16.
Nicholson S, Gomes D, de Nechaud B, Bruzzone R
J Neurosci Res
. 2001 Oct;
66(1):23-36.
PMID: 11598999
The discovery that the dominant X-linked form of Charcot-Marie-Tooth disease (CMTX), a genetic disease of the peripheral nervous system (PNS), is associated with mutations in connexin32 (Cx32) has brought attention...
17.
Baulac S, Huberfeld G, Gourfinkel-An I, Mitropoulou G, Beranger A, Prudhomme J, et al.
Nat Genet
. 2001 Apr;
28(1):46-8.
PMID: 11326274
Major advances in the identification of genes implicated in idiopathic epilepsy have been made. Generalized epilepsy with febrile seizures plus (GEFS+), benign familial neonatal convulsions and nocturnal frontal lobe epilepsy,...
18.
White T, Ripps H, Srinivas M, Bruzzone R
Biol Bull
. 2000 Nov;
199(2):165-8.
PMID: 11081716
No abstract available.
19.
Dermietzel R, Kremer M, Paputsoglu G, Stang A, Skerrett I, Gomes D, et al.
J Neurosci
. 2000 Nov;
20(22):8331-43.
PMID: 11069940
Electrical synapses (gap junctions) in neuronal circuits have become a major focus in the study of network properties such as synchronization and oscillation (Galarreta and Hestrin, 1999; Gibson et al.,...
20.
White T, Bruzzone R
Curr Biol
. 2000 Sep;
10(18):R685-8.
PMID: 10996812
The reasons for the molecular heterogeneity of connexin channels in vivo remain unclear. Functional replacement of one connexin gene with another has now revealed unexpected phenotypes and shows that cellular...