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Oliver Puk

Showing results (41-50 of 51) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 26, 2012
Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathologyMaik Hüttemann, Icksoo Lee, Xiufeng Gao, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Systemic first-line phenotypingValérie Gailus-Durner, Helmut Fuchs, Thure Adler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, et al.
American Journal of Medical Genetics. Part A|February 1, 2021
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesKevin E Glinton, Anna C E Hurst, Kevin M Bowling, et al.
Methods (San Diego, Calif.)|August 17, 2010
Mouse phenotypingHelmut Fuchs, Valérie Gailus-Durner, Thure Adler, et al.
G3 (Bethesda, Md.)|November 6, 2016
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic AlterationsHelmut Fuchs, Sibylle Sabrautzki, Gerhard K H Przemeck, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.
Genome Biology|August 2, 2013
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strainsMichelle M Simon, Simon Greenaway, Jacqueline K White, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 26, 2012
Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathologyMaik Hüttemann, Icksoo Lee, Xiufeng Gao, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 7, 2009
Systemic first-line phenotypingValérie Gailus-Durner, Helmut Fuchs, Thure Adler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, et al.
American Journal of Medical Genetics. Part A|February 1, 2021
Phenotypic expansion of the BPTF-related neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesKevin E Glinton, Anna C E Hurst, Kevin M Bowling, et al.
Methods (San Diego, Calif.)|August 17, 2010
Mouse phenotypingHelmut Fuchs, Valérie Gailus-Durner, Thure Adler, et al.
G3 (Bethesda, Md.)|November 6, 2016
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic AlterationsHelmut Fuchs, Sibylle Sabrautzki, Gerhard K H Przemeck, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 29, 2012
Innovations in phenotyping of mouse models in the German Mouse ClinicHelmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, et al.
Genome Biology|August 2, 2013
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strainsMichelle M Simon, Simon Greenaway, Jacqueline K White, et al.
Brain : a Journal of Neurology|December 14, 2019
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsisChristopher C Y Mak, Dan Doherty, Angela E Lin, et al.
Pageof 6