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Journal of Biomedical Science
|
August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 <sup>I27N</sup> mutant mice
Sudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome
Rachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Plos One
|
April 22, 2016
CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection
Christophe Côme, Anna Cvrljevic, Mohd Moin Khan, et al.
Nature Communications
|
July 21, 2011
Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells
Monika Raab, Sven Kappel, Andrea Krämer, et al.
Human Molecular Genetics
|
June 27, 2023
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
Marie Lucienne, Raffaele Gerlini, Birgit Rathkolb, et al.
Journal of Cell Science
|
March 17, 2011
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia
Juha Saarikangas, Pieta K Mattila, Markku Varjosalo, et al.
Disease Models & Mechanisms
|
December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Lillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 9, 2023
Knockout mouse models as a resource for the study of rare diseases
Patricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse
Caroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Arthritis and Rheumatism
|
February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model
Koichiro Abe, Helmut Fuchs, Auke Boersma, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 70) with videos related to
Sort By:
Page
of 7
Journal of Biomedical Science
|
August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 <sup>I27N</sup> mutant mice
Sudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome
Rachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Plos One
|
April 22, 2016
CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection
Christophe Côme, Anna Cvrljevic, Mohd Moin Khan, et al.
Nature Communications
|
July 21, 2011
Toxicity modelling of Plk1-targeted therapies in genetically engineered mice and cultured primary mammalian cells
Monika Raab, Sven Kappel, Andrea Krämer, et al.
Human Molecular Genetics
|
June 27, 2023
Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
Marie Lucienne, Raffaele Gerlini, Birgit Rathkolb, et al.
Journal of Cell Science
|
March 17, 2011
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia
Juha Saarikangas, Pieta K Mattila, Markku Varjosalo, et al.
Disease Models & Mechanisms
|
December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Lillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 9, 2023
Knockout mouse models as a resource for the study of rare diseases
Patricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouse
Caroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Arthritis and Rheumatism
|
February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine model
Koichiro Abe, Helmut Fuchs, Auke Boersma, et al.
Page
of 7