Jochen Graw
Institute of Mammalian Genetics
GSF-National Research Center for Environment and Health
Neuherberg
Germany
Name/email consistency: high
- Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P. Graw, J., Klopp, N., Illig, T., Preising, M.N., Lorenz, B. Graefes Arch. Clin. Exp. Ophthalmol. (2006)
- Haemophilia A: from mutation analysis to new therapies. Graw, J., Brackmann, H.H., Oldenburg, J., Schneppenheim, R., Spannagl, M., Schwaab, R. Nat. Rev. Genet. (2005)
- Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters. Graw, J., Löster, J., Puk, O., Münster, D., Haubst, N., Soewarto, D., Fuchs, H., Meyer, B., Nürnberg, P., Pretsch, W., Selby, P., Favor, J., Wolf, E., Hrabé de Angelis, M. Invest. Ophthalmol. Vis. Sci. (2005)
- Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse. Graw, J., Neuhäuser-Klaus, A., Klopp, N., Selby, P.B., Löster, J., Favor, J. Invest. Ophthalmol. Vis. Sci. (2004)
- Congenital hereditary cataracts. Graw, J. Int. J. Dev. Biol. (2004)
- Developmental genetics in ophthalmology. Graw, J., Löster, J. Ophthalmic Genet. (2003)
- Mutation in intron 6 of the hamster Mitf gene leads to skipping of the subsequent exon and creates a novel animal model for the human Waardenburg syndrome type II. Graw, J., Pretsch, W., Löster, J. Genetics (2003)
- The genetic and molecular basis of congenital eye defects. Graw, J. Nat. Rev. Genet. (2003)
- A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse. Graw, J., Neuhäuser-Klaus, A., Löster, J., Favor, J. Invest. Ophthalmol. Vis. Sci. (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. Graw, J., Neuhäuser-Klaus, A., Löster, J., Klopp, N., Favor, J. Genetics (2002)
- Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity. Graw, J., Klopp, N., Neuhäuser-Klaus, A., Favor, J., Löster, J. Invest. Ophthalmol. Vis. Sci. (2002)
- V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice. Graw, J., Löster, J., Soewarto, D., Fuchs, H., Reis, A., Wolf, E., Balling, R., Hrabé de Angelis, M. Mamm. Genome (2002)
- Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts. Graw, J., Klopp, N., Löster, J., Soewarto, D., Fuchs, H., Becker-Follmann, J., Reis, A., Wolf, E., Balling, R., Habré de Angelis, M. Genetics (2001)
- 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)
- Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene. Graw, J., Löster, J., Soewarto, D., Fuchs, H., Meyer, B., Reis, A., Wolf, E., Balling, R., Hrabé de Angelis, M. Invest. Ophthalmol. Vis. Sci. (2001)
- Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract. Graw, J., Löster, J., Soewarto, D., Fuchs, H., Meyer, B., Reis, A., Wolf, E., Balling, R., Hrabé de Angelis, M. Exp. Eye Res. (2001)
- 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)
- Mouse models of congenital cataract. Graw, J. Eye. (Lond) (1999)
- Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype. Graw, J., Neuhäuser-Klaus, A., Pretsch, W. Mutat. Res. (1997)
