-
8
-
-
0028241271
-
Mutagenesis and mapping of a mouse gene, clock, essential for circadian behavior
-
(1994)
Science
, vol.264
, pp. 719-725
-
-
Vitaterna, M.H.1
King, D.P.2
Chang, A.-M.3
Kornhauser, J.M.4
Lowrey, P.L.5
McDonald, J.D.6
Dove, W.F.7
Pinto, L.H.8
Turek, F.W.9
Takahashi, J.S.10
-
13
-
-
0031717379
-
Inducible gene targeting in mice using the Cre/lox system
-
(1998)
Methods
, vol.14
, pp. 381-392
-
-
Sauer, B.1
-
18
-
-
0027363063
-
Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
-
(1993)
Cell
, vol.75
, pp. 631-639
-
-
Dietrich, W.F.1
Lander, E.S.2
Smith, J.S.3
Moser, A.R.4
Gould, K.A.5
Luongo, C.6
Borenstein, N.7
Dove, W.8
-
21
-
-
0029005278
-
Disruption of the adenosine deaminase gene causes hepatocellular impairment and perinatal lethality in mice
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3673-3677
-
-
Wakamiya, M.1
Blackburn, M.R.2
Jurecic, R.3
McArthur, M.J.4
Geske, R.S.5
Cartwright, J.J.6
Mtani, K.7
Vaishnav, S.8
Belmont, J.W.9
Kellems, R.E.10
Finegold, M.J.11
Montgomery, C.A.J.12
Bradley, A.13
Caskey, C.T.14
-
22
-
-
0028158177
-
Aku, A mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16
-
(1994)
Genomics
, vol.19
, pp. 9-11
-
-
Montagutelli, X.1
Lalouette, A.2
Coude, M.3
Kamoun, P.4
Forest, M.5
Guenet, J.L.6
-
28
-
-
0026778029
-
Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene
-
(1992)
Nature
, vol.357
, pp. 407-410
-
-
Tybulewicz, V.L.J.1
Tremblay, M.L.2
LaMarca, M.E.3
Willemsen, R.4
Stubblefield, B.K.5
Winfield, S.6
Zablocka, B.7
Sidransky, E.8
Martin, B.M.9
Huang, S.P.10
Mintzer, K.A.11
Westphal, H.12
Mulligan, R.C.13
Ginns, E.I.14
-
29
-
-
0030977130
-
Mice with genetic γ-glutamyl transpeptidase deficiency exhibit glutathionuria, severe growth failure, reduced life spans, and infertility
-
(1997)
J Biol Chem
, vol.272
, pp. 12560-12567
-
-
Harding, C.O.1
Williams, P.2
Wagner, E.3
Chang, D.S.4
Wild, K.5
Colwell, R.E.6
Wolff, J.A.7
-
31
-
-
0001376313
-
HFE gene knockout produces mouse model of hereditary hemochromatosis
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 2492-2497
-
-
Zhou, X.Y.1
Tomatsu, S.2
Gfleming, R.E.3
Parkkila, S.4
Waheed, A.5
Jiang, J.6
Fei, Y.7
Brunt, E.M.8
Ruddy, D.A.9
Prass, C.E.10
Schatzman, R.C.11
O'Neill, R.O.12
Britton, R.S.13
Bacon, B.R.14
Sly, W.A.S.15
-
34
-
-
0028819754
-
Severe hypertriglyceridemia, reduced high density lipoprotein, and neonatal death in lipoprotein lipase knockout mice: Mild hypertriglyceridemia with impaired very low density lipoprotein clearance in heterozygotes
-
(1995)
J Clin Invest
, vol.96
, pp. 2555-2568
-
-
Weinstock, P.H.1
Bisgaier, C.L.2
Aalto-Setala, K.3
Radner, H.4
Ramakrishnan, R.5
Levak-Frank, S.6
Essenburg, A.D.7
Zechner, R.8
Breslow, J.L.9
-
35
-
-
13044277575
-
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 15592-15597
-
-
Kurtz, D.M.1
Rinaldo, P.2
Rhead, W.J.3
Tian, L.4
Millington, D.S.5
Vockley, J.6
Hamm, D.A.7
Brix, A.E.8
Lindsey, J.R.9
Pinkert, C.A.10
O'Brien, W.E.11
Wood, P.A.12
-
36
-
-
0029738625
-
Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8214-8219
-
-
Evers, M.1
Saftig, P.2
Schmidt, P.3
Hafner, A.4
McLoghlin, D.B.5
Schmahl, W.6
Hess, B.7
Von Figura, K.8
Peters, C.9
-
37
-
-
0029014350
-
Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease)
-
(1995)
Cell
, vol.81
, pp. 1053-1061
-
-
Otterbach, B.1
Stoffel, W.2
|