The mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion
Favor, J., Grimes, P., Neuhäuser-Klaus, A., Pretsch, W., Stambolian, D.
Published in Mammalian genome (01.05.2008)
Published in Mammalian genome (01.05.2008)
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Journal Article
mouse Cat4 locus maps to Chromosome 8 and mutants express lens-corneal adhesion
Favor, J, Grimes, P, Neuhäuser-Klaus, A, Pretsch, W, Stambolian, D
Published in Mammalian genome (01.06.1997)
Published in Mammalian genome (01.06.1997)
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Journal Article
Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4
Zhou, E, Grimes, P, Favor, J, Koeberlein, B, Pretsch, W, Neuhauser-Klaus, A, Sidjanin, D, Stambolian, D
Published in Mammalian genome (01.03.1997)
Published in Mammalian genome (01.03.1997)
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Journal Article
Molecular analysis of four lactate dehydrogenase-A mutants in the mouse
Sandulache, R, Pretsch, W, Chatterjee, B, Gimbel, W, Graw, J, Favor, J
Published in Mammalian genome (01.12.1994)
Published in Mammalian genome (01.12.1994)
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Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion
Graw, J, Löster, J, Neuhäuser-Klaus, A, Pretsch, W, Schmitt-John, T
Published in Mammalian genome (01.11.1996)
Published in Mammalian genome (01.11.1996)
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The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney
Favor, J, Sandulache, R, Neuhäuser-Klaus, A, Pretsch, W, Chatterjee, B, Senft, E, Wurst, W, Blanquet, V, Grimes, P, Spörle, R, Schughart, K
Published in Proceedings of the National Academy of Sciences - PNAS (26.11.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (26.11.1996)
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Mechanisms of compensation of hemolytic anemia in a lactate dehydrogenase mouse mutant
Kremer, J P, Datta, T, Pretsch, W, Charles, D J, Dörmer, P
Published in Experimental hematology (01.07.1987)
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Published in Experimental hematology (01.07.1987)
Journal Article
Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters
Graw, Jochen, Loster, Jana, Puk, Oliver, Munster, Doris, Haubst, Nicole, Soewarto, Dian, Fuchs, Helmut, Meyer, Birgit, Nurnberg, Peter, Pretsch, Walter, Selby, Paul, Favor, Jack, Wolf, Eckhard, de Angelis, Martin Hrabe
Published in Investigative ophthalmology & visual science (01.12.2005)
Published in Investigative ophthalmology & visual science (01.12.2005)
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Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice
Dalke, Claudia, Loster, Jana, Fuchs, Helmut, Gailus-Durner, Valerie, Soewarto, Dian, Favor, Jack, Neuhauser-Klaus, Angelika, Pretsch, Walter, Gekeler, Florian, Shinoda, Kei, Zrenner, Eberhart, Meitinger, Thomas, de Angelis, Martin Hrabe, Graw, Jochen
Published in Investigative ophthalmology & visual science (01.02.2004)
Published in Investigative ophthalmology & visual science (01.02.2004)
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Journal Article
An ENU-induced mutation in Rs1h causes disruption of retinal structure and function
Jablonski, Monica M, Dalke, Claudia, Wang, XiaoFei, Lu, Lu, Manly, Kenneth F, Pretsch, Walter, Favor, Jack, Pardue, Machelle T, Rinchik, Eugene M, Williams, Robert W, Goldowitz, Daniel, Graw, Jochen
Published in Molecular vision (27.07.2005)
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Published in Molecular vision (27.07.2005)
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