Search research articles
Contact Us
Filters
Showing results (31-40 of 46) with videos related to
Page
of 5
Sort By:
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
The Journal of Biological Chemistry
|
April 27, 2013
High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner
Jamie E Kugler, Marion Horsch, Di Huang, et al.
The Journal of Biological Chemistry
|
April 7, 2011
Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice
Marion Horsch, Peter H Seeburg, Thure Adler, et al.
Plos One
|
August 12, 2014
Pleiotropic functions for transcription factor zscan10
Petra Kraus, Sivakamasundari V, Hong Bing Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 25, 2009
Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice
Michael Rosemann, Alesia Ivashkevich, Jack Favor, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes
Heike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
The Journal of Clinical Investigation
|
July 19, 2013
Rapamycin extends murine lifespan but has limited effects on aging
Frauke Neff, Diana Flores-Dominguez, Devon P Ryan, et al.
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 pathology
Maik Hüttemann, Icksoo Lee, Xiufeng Gao, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
March 7, 2009
Systemic first-line phenotyping
Valérie 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 gene
Lars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 46) with videos related to
Sort By:
Page
of 5
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
The Journal of Biological Chemistry
|
April 27, 2013
High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner
Jamie E Kugler, Marion Horsch, Di Huang, et al.
The Journal of Biological Chemistry
|
April 7, 2011
Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice
Marion Horsch, Peter H Seeburg, Thure Adler, et al.
Plos One
|
August 12, 2014
Pleiotropic functions for transcription factor zscan10
Petra Kraus, Sivakamasundari V, Hong Bing Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 25, 2009
Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice
Michael Rosemann, Alesia Ivashkevich, Jack Favor, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 16, 2020
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes
Heike Kollmus, Helmut Fuchs, Christoph Lengger, et al.
The Journal of Clinical Investigation
|
July 19, 2013
Rapamycin extends murine lifespan but has limited effects on aging
Frauke Neff, Diana Flores-Dominguez, Devon P Ryan, et al.
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 pathology
Maik Hüttemann, Icksoo Lee, Xiufeng Gao, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
March 7, 2009
Systemic first-line phenotyping
Valérie 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 gene
Lars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Page
of 5