Works by Klaften, Matthias

Results: 12

Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.

Published in:

BioMetals, 2015, v. 28, n. 2, p. 293, doi. 10.1007/s10534-015-9824-1

By:

Rathkolb, Birgit;
Klempt, Martina;
Sabrautzki, Sibylle;
Michel, Dian;
Klaften, Matthias;
Laufs, Jürgen;
Sedlmeier, Reinhard;
Hans, Wolfgang;
Fuchs, Helmut;
Muckenthaler, Martina;
Horsch, Marion;
Campagna, Dean;
Fleming, Mark;
Hrabé de Angelis, Martin;
Wolf, Eckhard;
Aigner, Bernhard

Publication type:

Article

ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.

Published in:

Nucleic Acids Research, 2005, v. 33, n. suppl 2, p. w496, doi. 10.1093/nar/gki430

By:

Klaften, Matthias;
de Angelis, Martin Hrabé

Publication type:

Article

Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.

Published in:

European Journal of Oral Sciences, 2012, v. 120, n. 4, p. 269, doi. 10.1111/j.1600-0722.2012.00966.x

By:

Fuchs, Helmut;
Sabrautzki, Sibylle;
Seedorf, Hartwig;
Rathkolb, Birgit;
Rozman, Jan;
Hans, Wolfgang;
Schneider, Ralf;
Klaften, Matthias;
Hölter, Sabine M.;
Becker, Lore;
Klempt, Martina;
Elvert, Ralf;
Wurst, Wolfgang;
Klopstock, Thomas;
Klingenspor, Martin;
Wolf, Eckhard;
Gailus‐Durner, Valérie;
Angelis, Martin Hrabě

Publication type:

Article

Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe β-Cell Loss in Munich Ins2C95S Mutant Mice.

Published in:

Diabetes, 2007, v. 56, n. 5, p. 1268, doi. 10.2337/db06-0658

By:

Herbach, Nadja;
Rathkolb, Birgit;
Kemter, Elisabeth;
Pichl, Lisa;
Klaften, Matthias;
Hrabé de Angelis, Martin;
Halban, Philippe A.;
Wolf, Eckhard;
Aigner, Bernhard;
Wanke, Ruediger

Publication type:

Article

New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts.

Published in:

PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125304

By:

Kunze, Sarah;
Dalke, Claudia;
Fuchs, Helmut;
Klaften, Matthias;
Rössler, Ute;
Hornhardt, Sabine;
Gomolka, Maria;
Puk, Oliver;
Sabrautzki, Sibylle;
Kulka, Ulrike;
Hrabě de Angelis, Martin;
Graw, Jochen

Publication type:

Article

Morphologic and molecular characterization of two novel Krt71 ( Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13.

Published in:

Mammalian Genome, 2006, v. 17, n. 12, p. 1172, doi. 10.1007/s00335-006-0084-9

By:

Runkel, Fabian;
Klaften, Matthias;
Koch, Kerstin;
Böhnert, Volker;
Büssow, Heinrich;
Fuchs, Helmut;
Franz, Thomas;
de Angelis, Martin Hrabé

Publication type:

Article

A Genetic Screen for Modifiers of the Deltal-Dependent Notch Signaling Function in the Mouse.

Published in:

Genetics, 2007, v. 175, n. 3, p. 1451, doi. 10.1534/genetics.106.067298

By:

Rubio-Aliaga, Isabel;
Soewarto, Dian;
Wagner, Sibylle;
Klaften, Matthias;
Fuchs, Helmut;
Kalaydjiev, Svetoslav;
Busch, Dirk H.;
Klempt, Martina;
Rathkolb, Birgit;
Wolf, Eckhard;
Abe, Koichiro;
Zeiser, Stefan;
Przemeck, Gerhard K. H.;
Beckers, Johannes;
de Angelis, Martin Hrabé

Publication type:

Article

Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.

Published in:

Experimental Physiology, 2009, v. 94, n. 4, p. 412, doi. 10.1113/expphysiol.2008.045864

By:

Aigner, Bernhard;
Rathkolb, Birgit;
Klaften, Matthias;
Sedlmeier, Reinhard;
Klempt, Martina;
Wagner, Sibylle;
Michel, Dian;
Mayer, Ulrike;
Klopstock, Thomas;
Hrabé de Angelis, Martin;
Wolf, Eckhard

Publication type:

Article

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

Published in:

2014

By:

Sabrautzki, Sibylle;
Rubio-Aliaga, Isabel;
Hans, Wolfgang;
Fuchs, Helmut;
Rathkolb, Birgit;
Calzada-Wack, Julia;
Cohrs, Christian;
Klaften, Matthias;
Seedorf, Hartwig;
Eck, Sebastian;
Benet-Pagès, Ana;
Favor, Jack;
Esposito, Irene;
Strom, Tim;
Wolf, Eckhard;
Lorenz-Depiereux, Bettina;
Hrabĕ de Angelis, Martin

Publication type:

Erratum

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

Published in:

Mammalian Genome, 2012, v. 23, n. 7/8, p. 416, doi. 10.1007/s00335-012-9397-z

By:

Sabrautzki, Sibylle;
Rubio-Aliaga, Isabel;
Hans, Wolfgang;
Fuchs, Helmut;
Rathkolb, Birgit;
Calzada-Wack, Julia;
Cohrs, Christian;
Klaften, Matthias;
Seedorf, Hartwig;
Eck, Sebastian;
Benet-Pagès, Ana;
Favor, Jack;
Esposito, Irene;
Strom, Tim;
Wolf, Eckhard;
Lorenz-Depiereux, Bettina;
Hrabě de Angelis, Martin

Publication type:

Article

Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in hematological parameters.

Published in:

Mammalian Genome, 2011, v. 22, n. 9/10, p. 495, doi. 10.1007/s00335-011-9328-4

By:

Aigner, Bernhard;
Rathkolb, Birgit;
Klempt, Martina;
Wagner, Sibylle;
Michel, Dian;
Klaften, Matthias;
Laufs, Jürgen;
Schneider, Boris;
Sedlmeier, Reinhard;
Hrabé de Angelis, Martin;
Wolf, Eckhard

Publication type:

Article

Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice.

Published in:

Mammalian Genome, 2009, v. 20, n. 3, p. 152, doi. 10.1007/s00335-009-9170-0

By:

Abe, Koichiro;
Klaften, Matthias;
Narita, Akira;
Kimura, Tetsuaki;
Imai, Kenji;
Kimura, Minoru;
Rubio-Aliaga, Isabel;
Wagner, Sibylle;
Jakob, Thilo;
de Angelis, Martin Hrabé

Publication type:

Article

Works by Klaften, Matthias

Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.

ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.

Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.

Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe β-Cell Loss in Munich Ins2<sup>C95S</sup> Mutant Mice.

New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts.

Morphologic and molecular characterization of two novel Krt71 ( Krt2-6g) mutations: Krt71 <sup>rco12</sup> and Krt71 <sup>rco13</sup>.

A Genetic Screen for Modifiers of the Deltal-Dependent Notch Signaling Function in the Mouse.

Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.

Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in hematological parameters.

Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice.