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 : |
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 : Treatment outcome of tacrine therapy depends on apolipoprotein genotype and gender of the subjects with Alzheimer's disease - Farlow_1998_Neurology_50_669 |
Author(s) : Farlow MR , Lahiri DK , Poirier J , Davignon J , Schneider L , Hui SL |
Ref : Neurology , 50 :669 , 1998 |
Abstract : |
PubMedSearch : Farlow_1998_Neurology_50_669 |
PubMedID: 9521254 |
Title : Apolipoprotein E genotype and gender influence response to tacrine therapy - Farlow_1996_Ann.N.Y.Acad.Sci_802_101 |
Author(s) : Farlow MR , Lahiri DK , Poirier J , Davignon J , Hui S |
Ref : Annals of the New York Academy of Sciences , 802 :101 , 1996 |
Abstract : |
PubMedSearch : Farlow_1996_Ann.N.Y.Acad.Sci_802_101 |
PubMedID: 8993489 |
Title : Two naturally occurring mutations at the first and second bases of codon aspartic acid 156 in the proposed catalytic triad of human lipoprotein lipase. In vivo evidence that aspartic acid 156 is essential for catalysis - Ma_1992_J.Biol.Chem_267_1918 |
Author(s) : Ma YH , Bruin T , Tuzgol S , Wilson BI , Roederer G , Liu MS , Davignon J , Kastelein JJ , Brunzell JD , Hayden MR |
Ref : Journal of Biological Chemistry , 267 :1918 , 1992 |
Abstract : |
PubMedSearch : Ma_1992_J.Biol.Chem_267_1918 |
PubMedID: 1730727 |
Gene_locus related to this paper: human-LPL |