J. Löster

发表

Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.

J Graw, H. Fuchs, E. Wolf, 2001, Investigative ophthalmology & visual science.

A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse.

J. Favor, J. Graw, J. Löster, 2002, Investigative ophthalmology & visual science.

Three murine cataract mutants (Cat2) are defective in different γ- crystallin genes

N. Klopp, A. Prescott, G. Vrensen, 1998 .

Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.

H. Fuchs, E. Wolf, R. Balling, 1999, Genomics.

Aey 2 , a New Mutation in the b B 2-Crystallin – Encoding Gene of the Mouse

H. Fuchs, M. Angelis, E. Wolf, 2001 .

Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity.

N. Klopp, J. Favor, J. Graw, 2002, Investigative ophthalmology & visual science.

Cat3vl and Cat3vao cataract mutations on mouse chromosome 10: phenotypic characterization, linkage studies and analysis of candidate genes

J. Graw, T. Schmitt-John, T. Immervoll, 1997, Molecular and General Genetics MGG.

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.

H. Fuchs, E. Wolf, M. D. de Angelis, 2008, Investigative ophthalmology & visual science.

Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion

J. Graw, T. Schmitt-John, W. Pretsch, 1996, Mammalian Genome.

Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.

J Graw, H. Fuchs, E. Wolf, 2001, Investigative ophthalmology & visual science.

Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse.

N. Klopp, P. Selby, J. Favor, 2004, Investigative ophthalmology & visual science.

Developmental genetics in ophthalmology

J. Graw, J. Löster, 2003, Ophthalmic genetics.

Electroretinography as a screening method for mutations causing retinal dysfunction in mice.

H. Fuchs, T. Meitinger, E. Zrenner, 2004, Investigative ophthalmology & visual science.

Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype

P. Gruss, L. Reneker, J. Graw, 2002, Proceedings of the National Academy of Sciences of the United States of America.

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.

J. Graw, W. Pretsch, J. Löster, 2003, Genetics.

Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.

Peter Nürnberg, Helmut Fuchs, Martin Hrabé de Angelis, 2005, Investigative ophthalmology & visual science.

Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts

P. M. Gopinath, J. Graw, P. Vijayalakshmi, 2002 .

Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.

N. Klopp, A. Prescott, G. Vrensen, 1998, Genomics.

Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.

H. Fuchs, E. Wolf, R. Balling, 2001, Genetics.

Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.

P. M. Gopinath, J. Graw, P. Vijayalakshmi, 2002, Journal of medical genetics.

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?

H. Fuchs, E. Wolf, P. Nürnberg, 2009, Investigative ophthalmology & visual science.

The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart

M. Biel, F. Hofmann, R. Feil, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.

H. Fuchs, M. Angelis, E. Wolf, 2001, Experimental eye research.

Sequence analysis of the beta B2-crystallin cDNA of hamster containing a domain conserved among vertebrates.

T. Werner, J. Graw, J. Löster, 1996, Gene.

Altered aggregation properties of mutant γ‐crystallins cause inherited cataract

C. Dobson, N. Klopp, C. MacPhee, 2002 .

V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice

Helmut Fuchs, André Reis, Eckhard Wolf, 2002, Mammalian Genome.

An in vivo doxycycline-controlled expression system for functional studies of the retina.

A. Ballabio, F. Gekeler, A. Auricchio, 2003, Investigative ophthalmology & visual science.

Altered aggregation properties of mutant gamma-crystallins cause inherited cataract.

C. Dobson, N. Klopp, C. MacPhee, 2002, The EMBO journal.

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.

N. Klopp, J. Favor, J. Graw, 2002, Genetics.

Characterization of a 1-bp deletion in the gammaE-crystallin gene leading to a nuclear and zonular cataract in the mouse.

N. Klopp, J. Graw, J. Löster, 2001, Investigative ophthalmology & visual science.

Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern.

N. Klopp, J. Favor, J. Graw, 1998, Developmental genetics.

Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1.

M. Lyon, J. Graw, T. Schmitt-John, 1994, Genomics.

Reduced levels of γ-crystallin transcripts during embryonic development of murine Cat2nop mutant lenses

J. Graw, J. Löster, S. Santhiya, 1995, Graefe's Archive for Clinical and Experimental Ophthalmology.

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.

H. Fuchs, E. Wolf, M. D. de Angelis, 2008, Investigative ophthalmology & visual science.