Report for Bernier L

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References (4)

Title : Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype - Baass_2009_Atherosclerosis_207_452
Author(s) : Baass A , Wassef H , Tremblay M , Bernier L , Dufour R , Davignon J
Ref : Atherosclerosis , 207 :452 , 2009
Abstract : Baass_2009_Atherosclerosis_207_452
ESTHER : Baass_2009_Atherosclerosis_207_452
PubMedSearch : Baass_2009_Atherosclerosis_207_452
PubMedID: 19515369

Title : Severe oily ichthyosis in monozygotic twins mimicking Chanarin-Dorfman syndrome but not associated with a mutation of the CGI58 gene -
Author(s) : Solomon C , Bernier L , Germain L , Dufour R , Davignon J
Ref : Arch Dermatol , 142 :402 , 2006
PubMedID: 16549731
Gene_locus related to this paper: human-ABHD5

Title : What molecular steps determine the time course of the memory for short-term sensitization in Aplysia? -
Author(s) : Schwartz JH , Bernier L , Castellucci VF , Palazzolo M , Saitoh T , Stapleton A , Kandel ER
Ref : Cold Spring Harbor Symposium on Quantitative Biology , 48 Pt 2 :811 , 1983
PubMedID: 6327177

Title : Classical conditioning and sensitization share aspects of the same molecular cascade in Aplysia -
Author(s) : Kandel ER , Abrams T , Bernier L , Carew TJ , Hawkins RD , Schwartz JH
Ref : Cold Spring Harbor Symposium on Quantitative Biology , 48 Pt 2 :821 , 1983
PubMedID: 6327178