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41.
Puk, O. et al.: Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype. Invest. Ophthalmol. Vis. Sci. 49, 1525-1532 (2008)
42.
den Hollander, A.I.* et al.: Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays. Invest. Ophthalmol. Vis. Sci. 48, 5690-5698 (2007)
43.
Prokisch, H. ; Hartig, M.B. ; Hellinger, R. ; Meitinger, T. & Rosenberg, T.*: A population-based epidemiological and genetic study of X-linked retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 48, 4012-4018 (2007)
44.
Graw, J. et al.: Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters. Invest. Ophthalmol. Vis. Sci. 46, 4671-4683 (2005)
45.
Dalke, C. et al.: Electroretinography as a screening method for mutations causing retinal dysfunction in mice. Invest. Ophthalmol. Vis. Sci. 45, 601-609 (2004)
46.
Graw, J. et al.: Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse. Invest. Ophthalmol. Vis. Sci. 45, 1202-1213 (2004)
47.
Santhiya, S.T.* et al.: Mutation analysis of congenital cataracts in Indian families: Identification of SNPs and a new causative allele in CRYBB2 gene. Invest. Ophthalmol. Vis. Sci. 45, 3599-3607 (2004)
48.
Alge, C.S.* et al.: Comparative proteome analysis of native differentiated and cultured dedifferentiated human RPE cells. Invest. Ophthalmol. Vis. Sci. 44, 3629-3641 (2003)
49.
Angeletti, B. et al.: An in Vivo Doxycycline-Controlled Expression System for Functional Studies of the Retina. Invest. Ophthalmol. Vis. Sci. 44, 755-760 (2003)
50.
Bader, I. et al.: X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequencxe stretch of exon ORF15. Invest. Ophthalmol. Vis. Sci. 44, 1458-1463 (2003)
51.
Graw, J. ; Neuhäuser-Klaus, A. ; Löster, J. & Favor, J.: A 6-bp Deletion in the Crygc Gene Leading to a Nuclear and Radial Cataract in the Mouse. Invest. Ophthalmol. Vis. Sci. 43, 236-240 (2002)
52.
Graw, J. ; Klopp, N. ; Neuhäuser-Klaus, A. ; Favor, J. & Löster, J.: CrygfRop : The First Mutation in the Crygf Gene Causing a Unique Radial Lens Opacity. Invest. Ophthalmol. Vis. Sci. 43, 2998-3002 (2002)
53.
Mosley, A.* ; Graw, J. & Delamaere, N.A.*: Altered Na,K-ATPase Pattern in y-Crystallin Mutant Mice. Invest. Ophthalmol. Vis. Sci. 43, 1517-1519 (2002)
54.
Graw, J. et al.: Aey2, a New Mutation in the ßB2-Crystallin-Encoding Gene of the Mouse. Invest. Ophthalmol. Vis. Sci. 42, 1574-1580 (2001)
55.
Graw, J. et al.: Characterization of a New, Dominant V124E Mutation in the Mouse alphaA-Crystallin-Encoding Gene. Invest. Ophthalmol. Vis. Sci. 42, 2909-2915 (2001)
56.
Klopp, N. ; Löster, J. & Graw, J.: Characterization of a 1-bp delection in the yE-Crystallin gene leading to a nuclear and zonular cataract in the mouse. Invest. Ophthalmol. Vis. Sci. 42, 183-187 (2001)
57.
Graw, J. et al.: Characterization of Cat-2t, a Radiation-induced Dominant Cataract Mutation in Mice. Invest. Ophthalmol. Vis. Sci. 31, 1353-1361 (1990)
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