|
🐜
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Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
11 auth.
S. Rust,
Marie Rosier,
H. Funke,
J. Real,
Z. Amoura,
J. Piette,
...
J. Deleuze,
H. Brewer,
N. Duverger,
P. Denéfle,
G. Assmann
|
10 |
1999 |
10
🐜
|
|
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Association between early-onset Parkinson's disease and mutations in the parkin gene.
13 auth.
C. B. Lücking,
A. Durr,
Bonifati,
J. Vaughan,
G. Michele,
T. Gasser,
B. Harhangi,
G. Meco,
P. Denéfle,
N. Wood,
...
Y. Agid,
A. Brice,
French Parkinsons Dis Genetics Stu
|
10 |
2000 |
10
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|
|
🐜
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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
23 auth.
N. Abbas,
Christoph B. Lü,
S. Ricard,
A. Dürr,
V. Bonifati,
G. Michele,
S. Bouley,
Jenny R. Va ughan,
T. Gasser,
R. Marconi,
...
E. Broussolle,
C. Brefel‐Courbon,
B. Harhangi,
B. Oostra,
Edito Fabr izio,
G. Böhme,
L. Pradier,
N. Wood,
Alessandro F illa,
G. Meco,
P. Denéfle,
Y. Agid,
Alexis Br ice
|
9 |
1999 |
9
🐜
|
|
🐜
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Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.
27 auth.
J. Itier,
P. Ibáñez,
M. Mena,
N. Abbas,
C. Cohen-Salmon,
G. Bohme,
M. Laville,
J. Pratt,
O. Corti,
L. Pradier,
G. Ret,
C. Joubert,
Magali Periquet,
F. Araujo,
J. Negroni,
...
M. Casarejos,
S. Canals,
R. Solano,
A. Serrano,
E. Gallego,
Marina P Sánchez,
P. Denéfle,
J. Benavides,
G. Tremp,
T. Rooney,
A. Brice,
J. García de Yébenes
|
8 |
2003 |
8
🐜
|
|
🐜
|
Brain macrophages synthesize interleukin‐1 and interleukin‐1 mRNAs in vitro
7 auth.
E. Hetier,
J. Ayala,
P. Denéfle,
A. Bousseau,
P. Rouget,
M. Mallat,
...
A. Prochiantz
|
8 |
1988 |
8
🐜
|
|
🐜
|
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
10 auth.
B. V. D. Warrenburg,
M. Lammens,
C. B. Lücking,
P. Denéfle,
P. Wesseling,
J. Booij,
...
P. Praamstra,
N. Quinn,
A. Brice,
M. Horstink
|
8 |
2001 |
8
🐜
|
|
🐜
|
Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred.
20 auth.
A. Remaley,
S. Rust,
M. Rosier,
C. Knapper,
L. Naudin,
C. Broccardo,
K. Peterson,
C. Koch,
I. Arnould,
C. Prades,
...
N. Duverger,
H. Funke,
G. Assman,
M. Dinger,
M. Dean,
G. Chimini,
S. Santamarina-Fojo,
D. Fredrickson,
P. Denéfle,
H. Brewer
|
8 |
1999 |
8
🐜
|
|
🐜
|
Opposite regulation of human versus mouse apolipoprotein A-I by fibrates in human apolipoprotein A-I transgenic mice.
11 auth.
L. Berthou,
N. Duverger,
F. Emmanuel,
S. Langouët,
J. Auwerx,
A. Guillouzo,
...
J. Fruchart,
E. Rubin,
P. Denéfle,
B. Staels,
D. Branellec
|
8 |
1996 |
8
🐜
|
|
🐢
|
Protection Against Atherogenesis in Mice Mediated by Human Apolipoprotein A-IV
8 auth.
N. Duverger,
G. Tremp,
J. Caillaud,
F. Emmanuel,
G. Castro,
J. Fruchart,
...
A. Steinmetz,
P. Denéfle
|
8 |
1996 |
8
🐢
|
|
🐢
|
Inhibition of atherosclerosis development in cholesterol-fed human apolipoprotein A-I-transgenic rabbits.
11 auth.
N. Duverger,
H. Kruth,
F. Emmanuel,
J. Caillaud,
C. Viglietta,
G. Castro,
...
A. Tailleux,
C. Fiévet,
J. Fruchart,
L. Houdebine,
P. Denéfle
|
7 |
1996 |
7
🐢
|
|
🐜
|
Complete genomic sequence of the human ABCA1 gene: analysis of the human and mouse ATP-binding cassette A promoter.
20 auth.
S. Santamarina-Fojo,
K. Peterson,
C. Knapper,
Yang Qiu,
L. Freeman,
Jan-Fang Cheng,
J. Osorio,
A. Remaley,
Xiaoping Yang,
Changting Haudenschild,
...
C. Prades,
G. Chimini,
Eunice Blackmon,
Teena L. Francois,
N. Duverger,
E. Rubin,
Marie Rosier,
P. Denéfle,
D. Fredrickson,
H. Brewer
|
7 |
2000 |
7
🐜
|
|
🐜
|
p21CIP1-mediated inhibition of cell proliferation by overexpression of the gax homeodomain gene.
11 auth.
Roy C. Smith,
D. Branellec,
D. Gorski,
K. Guo,
H. Perlman,
J. Dedieu,
...
Christopher Pastore,
A. Mahfoudi,
P. Denéfle,
J. Isner,
K. Walsh
|
7 |
1997 |
7
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|
