239 related articles for article (PubMed ID: 19578028)
1. Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse.
Puk O; Dalke C; Calzada-Wack J; Ahmad N; Klaften M; Wagner S; de Angelis MH; Graw J
Invest Ophthalmol Vis Sci; 2009 Dec; 50(12):5653-61. PubMed ID: 19578028
[TBL] [Abstract][Full Text] [Related]
2. A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk O; Esposito I; Söker T; Löster J; Budde B; Nürnberg P; Michel-Soewarto D; Fuchs H; Wolf E; Hrabé de Angelis M; Graw J
Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4311-8. PubMed ID: 19407009
[TBL] [Abstract][Full Text] [Related]
3. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
Jablonski MM; Dalke C; Wang X; Lu L; Manly KF; Pretsch W; Favor J; Pardue MT; Rinchik EM; Williams RW; Goldowitz D; Graw J
Mol Vis; 2005 Jul; 11():569-81. PubMed ID: 16088326
[TBL] [Abstract][Full Text] [Related]
4. In vivo biometry in the mouse eye with low coherence interferometry.
Schmucker C; Schaeffel F
Vision Res; 2004; 44(21):2445-56. PubMed ID: 15358080
[TBL] [Abstract][Full Text] [Related]
5. Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Puk O; Löster J; Dalke C; Soewarto D; Fuchs H; Budde B; Nürnberg P; Wolf E; de Angelis MH; Graw J
Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1525-32. PubMed ID: 18385072
[TBL] [Abstract][Full Text] [Related]
6. Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye.
Hopfer U; Fukai N; Hopfer H; Wolf G; Joyce N; Li E; Olsen BR
FASEB J; 2005 Aug; 19(10):1232-44. PubMed ID: 16051690
[TBL] [Abstract][Full Text] [Related]
7. First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts.
Puk O; Ahmad N; Wagner S; Hrabé de Angelis M; Graw J
Invest Ophthalmol Vis Sci; 2011 Apr; 52(5):2571-6. PubMed ID: 21212184
[TBL] [Abstract][Full Text] [Related]
8. Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.
Graw J; Jung M; Löster J; Klopp N; Soewarto D; Fella C; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Genomics; 1999 Nov; 62(1):67-73. PubMed ID: 10585769
[TBL] [Abstract][Full Text] [Related]
9. Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene.
Gottsch JD; Zhang C; Sundin OH; Bell WR; Stark WJ; Green WR
Invest Ophthalmol Vis Sci; 2005 Dec; 46(12):4504-11. PubMed ID: 16303941
[TBL] [Abstract][Full Text] [Related]
10. Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
Graw J; Löster J; Soewarto D; Fuchs H; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1574-80. PubMed ID: 11381063
[TBL] [Abstract][Full Text] [Related]
11. Genotype-phenotype correlation of mouse pde6b mutations.
Hart AW; McKie L; Morgan JE; Gautier P; West K; Jackson IJ; Cross SH
Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3443-50. PubMed ID: 16123450
[TBL] [Abstract][Full Text] [Related]
12. Relative axial myopia in Egr-1 (ZENK) knockout mice.
Schippert R; Burkhardt E; Feldkaemper M; Schaeffel F
Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):11-7. PubMed ID: 17197510
[TBL] [Abstract][Full Text] [Related]
13. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.
Grimes PA; Koeberlein B; Favor J; Neuhäuser-Klaus A; Stambolian D
Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1863-9. PubMed ID: 9727409
[TBL] [Abstract][Full Text] [Related]
14. Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy.
Gottsch JD; Sundin OH; Liu SH; Jun AS; Broman KW; Stark WJ; Vito EC; Narang AK; Thompson JM; Magovern M
Invest Ophthalmol Vis Sci; 2005 Jun; 46(6):1934-9. PubMed ID: 15914606
[TBL] [Abstract][Full Text] [Related]
15. Androgen-dependent hereditary mouse keratoconus: linkage to an MHC region.
Tachibana M; Adachi W; Kinoshita S; Kobayashi Y; Honma Y; Hiai H; Matsushima Y
Invest Ophthalmol Vis Sci; 2002 Jan; 43(1):51-7. PubMed ID: 11773012
[TBL] [Abstract][Full Text] [Related]
16. The Tennessee Mouse Genome Consortium: identification of ocular mutants.
Jablonski MM; Wang X; Lu L; Miller DR; Rinchik EM; Williams RW; Goldowitz D
Vis Neurosci; 2005; 22(5):595-604. PubMed ID: 16332270
[TBL] [Abstract][Full Text] [Related]
17. A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.
Masuya H; Sezutsu H; Sakuraba Y; Sagai T; Hosoya M; Kaneda H; Miura I; Kobayashi K; Sumiyama K; Shimizu A; Nagano J; Yokoyama H; Kaneko S; Sakurai N; Okagaki Y; Noda T; Wakana S; Gondo Y; Shiroishi T
Genomics; 2007 Feb; 89(2):207-14. PubMed ID: 17049204
[TBL] [Abstract][Full Text] [Related]
18. Two kinds of ENU-induced scant hair mice and mapping of the mutant genes.
Wu BJ; Shao YX; Mao HH; Tang D; Liu J; Xue ZF; Li HD
J Dermatol Sci; 2004 Dec; 36(3):149-56. PubMed ID: 15541636
[TBL] [Abstract][Full Text] [Related]
19. Keratoconus is not associated with mutations in COL8A1 and COL8A2.
Aldave AJ; Bourla N; Yellore VS; Rayner SA; Khan MA; Salem AK; Sonmez B
Cornea; 2007 Sep; 26(8):963-5. PubMed ID: 17721297
[TBL] [Abstract][Full Text] [Related]
20. Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice.
Michaud EJ; Culiat CT; Klebig ML; Barker PE; Cain KT; Carpenter DJ; Easter LL; Foster CM; Gardner AW; Guo ZY; Houser KJ; Hughes LA; Kerley MK; Liu Z; Olszewski RE; Pinn I; Shaw GD; Shinpock SG; Wymore AM; Rinchik EM; Johnson DK
BMC Genomics; 2005 Nov; 6():164. PubMed ID: 16300676
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]