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Results: 1-12 |
Results: 12
Comparative analysis of the promoter structure and genomic organization ofthe human and mouse ABCA7 gene encoding a novel ABCA transporter
Authors: Broccardo, C Osorio, J Luciani, MF Schriml, LM Prades, C Shulenin, S Arnould, I Naudin, L Lafargue, C Rosier, M Jordan, B Mattei, M Dean, M Denefle, P Chimini, G
Citation: C. Broccardo et al., Comparative analysis of the promoter structure and genomic organization ofthe human and mouse ABCA7 gene encoding a novel ABCA transporter, CYTOG C GEN, 92(3-4), 2001, pp. 264-270
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
Authors: van de Warrenburg, BPC Lammens, M Lucking, CB Denefle, P Wesseling, P Booij, J Praamstra, P Quinn, N Brice, A Horstink, MWIM
Citation: Bpc. Van De Warrenburg et al., Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations, NEUROLOGY, 56(4), 2001, pp. 555-557
Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects
Authors: Periquet, M Lucking, CB Vaughan, JR Bonifati, V Durr, A De Michele, G Horstink, MW Farrer, M Illarioshkin, SN Pollak, P Borg, M Brefel-Courbon, C Denefle, P Meco, G Gasser, T Breteler, MMB Wood, NW Agid, Y Brice, A
Citation: M. Periquet et al., Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects, AM J HU GEN, 68(3), 2001, pp. 617-626
Association between early-onset Parkinson's disease and mutations in the parkin gene
Authors: Lucking, CB Durr, A Bonifati, V Vaughan, J De Michele, G Gasser, T Harhangi, BS Meco, G Denefle, P Wood, NW Agid, Y Brice, A
Citation: Cb. Lucking et al., Association between early-onset Parkinson's disease and mutations in the parkin gene, N ENG J MED, 342(21), 2000, pp. 1560-1567
Complete genomic sequence of the human ABCA1 gene: Analysis of the human and mouse ATP-binding cassette A promoter
Authors: Santamarina-Fojo, S Peterson, K Knapper, C Qiu, Y Freeman, L Cheng, JF Osorio, J Remaley, A Yang, XP Haudenschild, C Prades, C Chimini, G Blackmon, E Francois, T Duverger, N Rubin, EM Rosier, M Denefle, P Fredrickson, DS Brewer, HB
Citation: S. Santamarina-fojo et al., Complete genomic sequence of the human ABCA1 gene: Analysis of the human and mouse ATP-binding cassette A promoter, P NAS US, 97(14), 2000, pp. 7987-7992
Structure and interfacial properties of chicken apolipoprotein A-IV
Authors: Weinberg, RB Anderson, RA Cook, VR Emmanuel, F Denefle, P Hermann, M Steinmetz, A
Citation: Rb. Weinberg et al., Structure and interfacial properties of chicken apolipoprotein A-IV, J LIPID RES, 41(9), 2000, pp. 1410-1418
Functional screening of an asthma QTL in YAC transgenic mice
Authors: Symula, DJ Frazer, KA Ueda, Y Denefle, P Stevens, ME Wang, ZE Locksley, R Rubin, EM
Citation: Dj. Symula et al., Functional screening of an asthma QTL in YAC transgenic mice, NAT GENET, 23(2), 1999, pp. 241-244
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
Authors: Rust, S Rosier, M Funke, H Real, J Amoura, Z Piette, JC Deleuze, JF Brewer, HB Duverger, N Denefle, P Assmann, G
Citation: S. Rust et al., Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1, NAT GENET, 22(4), 1999, pp. 352-355
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
Authors: Abbas, N Lucking, CB Ricard, S Durr, A Bonifati, V De Michele, G Bouley, S Vaughan, JR Gasser, T Marconi, R Broussolle, E Brefel-Courbon, C Harhangi, BS Oostra, AB Fabrizio, E Bohme, GA Pradier, L Wood, NW Filla, A Meco, G Denefle, P Agid, Y Brice, A
Citation: N. Abbas et al., A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe, HUM MOL GEN, 8(4), 1999, pp. 567-574
Apolipoprotein A-I(R151C)(Paris) is defective in activation of lecithin : cholesterol acyltransferase but not in initial lipid binding, formation of reconstituted lipoproteins, or promotion of cholesterol efflux
Authors: Daum, U Langer, C Duverger, N Emmanuel, F Benoit, P Denefle, P Chirazi, A Cullen, P Pritchard, PH Bruckert, E Assmann, G von Eckardstein, A
Citation: U. Daum et al., Apolipoprotein A-I(R151C)(Paris) is defective in activation of lecithin : cholesterol acyltransferase but not in initial lipid binding, formation of reconstituted lipoproteins, or promotion of cholesterol efflux, J MOL MED-J, 77(8), 1999, pp. 614-622
Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred
Authors: Remaley, AT Rust, S Rosier, M Knapper, C Naudin, L Broccardo, C Peterson, KM Koch, C Arnould, I Prades, C Duverger, N Funke, H Assman, G Dinger, M Dean, M Chimini, G Santamarina-Fojo, S Fredrickson, DS Denefle, P Brewer, HB
Citation: At. Remaley et al., Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred, P NAS US, 96(22), 1999, pp. 12685-12690
Somatic gene transfer of human apoA-I inhibits atherosclerosis progressionin mouse models
Authors: Benoit, P Emmanuel, F Caillaud, JM Bassinet, L Castro, G Gallix, P Fruchart, JC Branellec, D Denefle, P Duverger, N
Citation: P. Benoit et al., Somatic gene transfer of human apoA-I inhibits atherosclerosis progressionin mouse models, CIRCULATION, 99(1), 1999, pp. 105-110
Risultati: 1-12 |