-
1
-
-
2542496696
-
An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice
-
AHITUV, N., ERVEN, A., FUCHS, H., GUY, K., ASHERY-PADAN, R., WILLIAMS, T., DE ANGELIS, M.H., AVRAHAM, K.B. & STEEL, K.P. (2004). An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice. Mammalian Genome 15, 424-432.
-
(2004)
Mammalian Genome
, vol.15
, pp. 424-432
-
-
Ahituv, N.1
Erven, A.2
Fuchs, H.3
Guy, K.4
Ashery-Padan, R.5
Williams, T.6
De Angelis, M.H.7
Avraham, K.B.8
Steel, K.P.9
-
2
-
-
0038708118
-
Age-related macular degeneration: Etiology, pathogenesis, and therapeutic strategies
-
AMBATI, J., AMBATI, B.K., YOO, S.H., IANCHULEV, S. & ADAMIS, A.P. (2003). Age-related macular degeneration: Etiology, pathogenesis, and therapeutic strategies. Survey Ophthalmologyl 48, 257-293.
-
(2003)
Survey Ophthalmologyl
, vol.48
, pp. 257-293
-
-
Ambati, J.1
Ambati, B.K.2
Yoo, S.H.3
Ianchulev, S.4
Adamis, A.P.5
-
3
-
-
2942619095
-
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice
-
ANDERSON, M.G., SMITH, R.S., SAVINOVA, O.V., HAWES, N.L., CHANG, B., ZABALETA, A., WILPAN, R., HECKENLIVELY, J.R., DAVISSON, M. & JOHN, S.W. (2001). Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice. Biomedical Central Genetics 2, 1.
-
(2001)
Biomedical Central Genetics
, vol.2
, pp. 1
-
-
Anderson, M.G.1
Smith, R.S.2
Savinova, O.V.3
Hawes, N.L.4
Chang, B.5
Zabaleta, A.6
Wilpan, R.7
Heckenlively, J.R.8
Davisson, M.9
John, S.W.10
-
4
-
-
2942513045
-
MuTrack: A genome analysis system for large-scale mutagenesis in the mouse
-
BAKER, E.J., GALLOWAY, L., JACKSON, B., SCHMOYER, D. & SNODDY, J. (2004). MuTrack: A genome analysis system for large-scale mutagenesis in the mouse. BMC Bioinformatics 3, 11.
-
(2004)
BMC Bioinformatics
, vol.3
, pp. 11
-
-
Baker, E.J.1
Galloway, L.2
Jackson, B.3
Schmoyer, D.4
Snoddy, J.5
-
5
-
-
12144288188
-
Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice
-
DU, X., TABETA, K., HOEBE, K., LIU, H., MANN, N., MUDD, S., CROZAT, K., SOVATH, S., GONG, X. & BEUTLER, B. (2004). Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice. Genetics 166, 331-340.
-
(2004)
Genetics
, vol.166
, pp. 331-340
-
-
Du, X.1
Tabeta, K.2
Hoebe, K.3
Liu, H.4
Mann, N.5
Mudd, S.6
Crozat, K.7
Sovath, S.8
Gong, X.9
Beutler, B.10
-
6
-
-
9944236320
-
Large-scale mutagenesis of the mouse to understand the genetic bases of nervous system structure and function
-
GOLDOWITZ, D., FRANKEL, W.N., TAKAHASHI, J.S., HOLTZ-VITATERNA, M., BULT, C., KIBBE, W.A., SNODDY, J., LI, Y., PRETEL, S., YATES, J. & SWANSON, D.J. (2004). Large-scale mutagenesis of the mouse to understand the genetic bases of nervous system structure and function. Molecular Brain Research 132, 105.
-
(2004)
Molecular Brain Research
, vol.132
, pp. 105
-
-
Goldowitz, D.1
Frankel, W.N.2
Takahashi, J.S.3
Holtz-Vitaterna, M.4
Bult, C.5
Kibbe, W.A.6
Snoddy, J.7
Li, Y.8
Pretel, S.9
Yates, J.10
Swanson, D.J.11
-
7
-
-
0036672646
-
Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract
-
GRAW, J., NEUHAUSER-KLAUS, A., LOSTER, J., KLOPP, N. & FAVOR, J. (2002). Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract. Genetics 161, 1633-1640.
-
(2002)
Genetics
, vol.161
, pp. 1633-1640
-
-
Graw, J.1
Neuhauser-Klaus, A.2
Loster, J.3
Klopp, N.4
Favor, J.5
-
8
-
-
0033520641
-
Histopathology of age-related macular degeneration
-
GREEN, W. (1999). Histopathology of age-related macular degeneration. Molecular Vision 5, 27.
-
(1999)
Molecular Vision
, vol.5
, pp. 27
-
-
Green, W.1
-
9
-
-
0031968397
-
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice
-
JOHN, S.W., SMITH, R.S., SAVINOVA, O.V., HAWES, N.L., CHANG, B., TURNBULL, D., DAVISSON, M., RODERICK, T.H. & HECKENLIVELY, J.R. (1998). Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. Investigative Ophthalmology and Visual Science 39, 951-962.
-
(1998)
Investigative Ophthalmology and Visual Science
, vol.39
, pp. 951-962
-
-
John, S.W.1
Smith, R.S.2
Savinova, O.V.3
Hawes, N.L.4
Chang, B.5
Turnbull, D.6
Davisson, M.7
Roderick, T.H.8
Heckenlively, J.R.9
-
10
-
-
26244463713
-
Phenotype screening for genetically-determined age-onset disorders and increased longevity in ENU-mutagenized mice
-
JOHNSON, D.K., RINCHIK, E.M., MOUSTAID-MOUSSA, N., MILLER, D.R., WILLIAMS, R.W., MICHAUD, E.J., JABLONSKI, M.M., ELBERGER, A., HAMRE, K., SMEYNE, R. & GOLDOWITZ, D. (2005). Phenotype screening for genetically-determined age-onset disorders and increased longevity in ENU-mutagenized mice. Age 27, 75-90.
-
(2005)
Age
, vol.27
, pp. 75-90
-
-
Johnson, D.K.1
Rinchik, E.M.2
Moustaid-Moussa, N.3
Miller, D.R.4
Williams, R.W.5
Michaud, E.J.6
Jablonski, M.M.7
Elberger, A.8
Hamre, K.9
Smeyne, R.10
Goldowitz, D.11
-
11
-
-
4644344753
-
Pathogenesis of persistent hyperplastic primary vitreous in mice lacking the arf tumor suppressor gene
-
MARTIN, A.C., THORNTON, J.D., LIU, J., WANG, X., ZUO, J., JABLONSKI, M.M., CHAUM, E., ZINDY, F. & SKAPEK, S.X. (2004). Pathogenesis of persistent hyperplastic primary vitreous in mice lacking the arf tumor suppressor gene. Investigative Ophthalmology and Visual Science 45, 3387-3396.
-
(2004)
Investigative Ophthalmology and Visual Science
, vol.45
, pp. 3387-3396
-
-
Martin, A.C.1
Thornton, J.D.2
Liu, J.3
Wang, X.4
Zuo, J.5
Jablonski, M.M.6
Chaum, E.7
Zindy, F.8
Skapek, S.X.9
-
12
-
-
0037377962
-
Quick-freeze/deep-etch visualization of age-related lipid accumulation in Bruch's membrane
-
RUBERTI, J.W., CURCIO, C.A., MILLICAN, C.L., MENCO, B.P., HUANG, J.D. & JOHNSON, M. (2003). Quick-freeze/deep-etch visualization of age-related lipid accumulation in Bruch's membrane. Investigative Ophthalmology and Visual Science 44, 1753-1759.
-
(2003)
Investigative Ophthalmology and Visual Science
, vol.44
, pp. 1753-1759
-
-
Ruberti, J.W.1
Curcio, C.A.2
Millican, C.L.3
Menco, B.P.4
Huang, J.D.5
Johnson, M.6
-
13
-
-
0038683341
-
An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina
-
SEMENOVA, E., WANG, X.F., JABLONSKI, M.M., LEVORSE, J. & TILGHMAN, S.M. (2003). An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina. Human Molecular Genetics 12, 1301-1312.
-
(2003)
Human Molecular Genetics
, vol.12
, pp. 1301-1312
-
-
Semenova, E.1
Wang, X.F.2
Jablonski, M.M.3
Levorse, J.4
Tilghman, S.M.5
-
14
-
-
0036538038
-
Novel ENU-induced eye mutations in the mouse: Models for human eye disease
-
THAUNG, C., WEST, K., CLARK, B.J., MCKIE, L., MORGAN, J.E., ARNOLD, K., NOLAN, P.M., PETERS, J., HUNTER, A.J., BROWN, S.D., JACKSON, I.J. & CROSS, S.H. (2002). Novel ENU-induced eye mutations in the mouse: Models for human eye disease. Human Molecular Genetics 11, 755-767.
-
(2002)
Human Molecular Genetics
, vol.11
, pp. 755-767
-
-
Thaung, C.1
West, K.2
Clark, B.J.3
McKie, L.4
Morgan, J.E.5
Arnold, K.6
Nolan, P.M.7
Peters, J.8
Hunter, A.J.9
Brown, S.D.10
Jackson, I.J.11
Cross, S.H.12
-
15
-
-
0028241271
-
Mutagenesis and mapping of a mouse gene, clock, essential for circadian behavior
-
VITATERNA, M.H., KING, D.P., CHANG, A.M., KORNHAUSER, J.M., LOWREY, P.L., MCDONALD, J.D., DOVE, W.F., PINTO, L.H., TUREK, F.W. & TAKAHASHI, J.S. (1994). Mutagenesis and mapping of a mouse gene, clock, essential for circadian behavior. Science 264, 719-725.
-
(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
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