Zobrazeno 1 - 10
of 284
pro vyhledávání: '"A. Neuhäuser-Klaus"'
Publikováno v:
Environmental Health Perspectives, 1985 Oct 01. 62, 163-169.
Externí odkaz:
https://www.jstor.org/stable/3430108
Autor:
Sidjanin, D.J., Parker-Wilson, Devonne M., Neuhäuser-Klaus, Angelika, Pretsch, Walter, Favor, Jack, Deen, Peter M.T., Ohtaka-Maruyama, Chiaki, Lu, Yun, Bragin, Alvina, Skach, William R., Chepelinsky, Ana B., Grimes, Patricia A., Stambolian, Dwight E.
Publikováno v:
In Genomics 15 June 2001 74(3):313-319
Autor:
Walter Pretsch, Angelika Neuhäuser-Klaus, Rodica Sandulache, Irmgard Zaus, Jack Favor, Christian Johannes Gloeckner, Simon Saule
Publikováno v:
Genetics 179, 1345-1355 (2008)
In this study we extend the mouse Pax6 mutant allelic series to include a homozygous and hemizygous viable hypomorph allele. The Pax6132-14Neu allele is a Phe272Ile missense mutation within the third helix of the homeodomain. The mutant Pax6 homeodom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5844a53f06b95940d01f3ed2f3e1e812
https://doi.org/10.1534/genetics.108.088591
https://doi.org/10.1534/genetics.108.088591
Autor:
Martina Klempt, Wolfgang W. Schmahl, Christian Johannes Gloeckner, Jack Favor, Dirk Janik, Walter Pretsch, Angelika Neuhäuser-Klaus, Leticia Quintanilla-Fend
Publikováno v:
Genetics. 175:725-736
The basement membrane is important for proper tissue development, stability, and physiology. Major components of the basement membrane include laminins and type IV collagens. The type IV procollagens Col4a1 and Col4a2 form the heterotrimer [α1(IV)]2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db439511e1cd505cd2bc81146b2cec12
https://doi.org/10.1534/genetics.106.064733
https://doi.org/10.1534/genetics.106.064733
Autor:
Martin Hrabé de Angelis, Angelika Neuhäuser-Klaus, Karen Pálsdóttir, John Favor, Eiríkur Steingrímsson, Adalheidur Gı́gja Hansdottir, Helmut Fuchs
Publikováno v:
Genomics. 83:932-935
Mutations in the microphthalmia-associated transcription factor (Mitf) gene affect the development of different cell types, including melanocytes, osteoclasts, and retinal pigmented epithelial cells of the eye. Many different mutations at the locus a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::802e85d44d13de4c7385400fa86b0ea2
https://doi.org/10.1016/j.ygeno.2003.10.013
https://doi.org/10.1016/j.ygeno.2003.10.013
Publikováno v:
Scopus-Elsevier
A novel ENU-induced mutation in the mouse leading to a nuclear and cortical opacity of the eye lens (ENU418) was mapped to proximal chromosome 1 by a genome-wide mapping approach. It suggests that the cluster of γ-crystallin encoding genes (Cryg) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6030e3bc20371f30cd73abbe66cbdd1
https://doi.org/10.1093/genetics/161.4.1633
https://doi.org/10.1093/genetics/161.4.1633
Autor:
Angelika Neuhäuser-Klaus, Jack Favor, Bimal Chatterjee, Thomas Hermann, Wolfgang W. Schmahl, Heiko Peters, Rodica Sandulache
Publikováno v:
Genetics. 159:1689-1700
Phenotype-based mutagenesis experiments will increase the mouse mutant resource, generating mutations at previously unmarked loci as well as extending the allelic series at known loci. Mapping, molecular characterization, and phenotypic analysis of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d30721865ded2561f638076af93abc61
https://doi.org/10.1093/genetics/159.4.1689
https://doi.org/10.1093/genetics/159.4.1689
Autor:
Angelika Neuhäuser-Klaus, Chiaki Ohtaka-Maruyama, Patricia A. Grimes, William R. Skach, Walter Pretsch, Dwight Stambolian, Yun Lu, Ana B. Chepelinsky, Peter M.T. Deen, Alvina Bragin, Jack Favor, D.J. Sidjanin, Devonne M. Parker-Wilson
Publikováno v:
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 74, 313--9
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 74, 3, pp. 313--9
Genomics : International Journal of Gene Mapping and Nucleotide Sequencing Emphasizing Analyses of the Human and Other Complex Genomes, 74, 3, pp. 313--9
Item does not contain fulltext Hfi is a dominant cataract mutation where heterozygotes show hydropic lens fibers and homozygotes show total lens opacity. The Hfi locus was mapped to the distal part of mouse chromosome 10 close to the major intrinsic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08fcf0f03ac203c4d8371abd3afbd946
https://doi.org/10.1006/geno.2001.6509
https://doi.org/10.1006/geno.2001.6509
Publikováno v:
Genetical Research. 72:177-183
Ifosfamide induced dominant lethal mutations in spermatozoa of mice at doses of 200 and 300 mg/kg and in spermatids and spermatocytes at 600 mg/kg. The highest dose also induced specific-locus mutations in post-spermatogonial germ-cell stages of mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c540b61b1fd961444658ffc00d5c126c
https://doi.org/10.1017/s0016672398003413
https://doi.org/10.1017/s0016672398003413
Autor:
Angelika Neuhäuser-Klaus, Jack Favor
Publikováno v:
Genetical Research. 72:199-204
The occurrence of homozygous-viable dilute–short ear (Myo5a–Bmp5) double mutants in mouse specific locus mutation experiments has generally been assumed to be the result of double non- disjunction such that the mutant inherits two copies of chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c2df2ec1f6f3b9fa85655ba3823d16
https://doi.org/10.1017/s001667239800353x
https://doi.org/10.1017/s001667239800353x