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Human Molecular Genetics
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May 17, 2012
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms
Frank Thiele, Christian M Cohrs, Armando Flor, et al.
BMJ Global Health
|
August 22, 2025
A brief international screening tool for traumatic birth and childbirth-related PTSD: the city BiTS-short form
Susan Ayers, Dan Brooks Wright, Rafael A Caparros-Gonzalez, et al.
Plos One
|
October 28, 2016
Sphingomyelin Synthase 1 Is Essential for Male Fertility in Mice
Anke Wittmann, Marcus O W Grimm, Harry Scherthan, et al.
Journal of Inherited Metabolic Disease
|
July 9, 2017
A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients
Ewa Pronicka, Mariola Ropacka-Lesiak, Joanna Trubicka, et al.
Biomarkers in Medicine
|
March 24, 2022
Development and validation of a cell cycle progression signature for decentralized testing of men with prostate cancer
Vanessa Kuhl, Wyatt Clegg, Stephanie Meek, et al.
Plos One
|
November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice
Elisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2016
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice
Germaine Korner, Tanja Scherer, Dea Adamsen, et al.
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.
Iscience
|
October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism
Jean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Plos One
|
June 30, 2009
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes
Isabel Rubio-Aliaga, Gerhard K H Przemeck, Helmut Fuchs, et al.
Page
of 66
Search research articles
Search
Showing results (611-620 of 657) with videos related to
Sort By:
Page
of 66
Human Molecular Genetics
|
May 17, 2012
Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms
Frank Thiele, Christian M Cohrs, Armando Flor, et al.
BMJ Global Health
|
August 22, 2025
A brief international screening tool for traumatic birth and childbirth-related PTSD: the city BiTS-short form
Susan Ayers, Dan Brooks Wright, Rafael A Caparros-Gonzalez, et al.
Plos One
|
October 28, 2016
Sphingomyelin Synthase 1 Is Essential for Male Fertility in Mice
Anke Wittmann, Marcus O W Grimm, Harry Scherthan, et al.
Journal of Inherited Metabolic Disease
|
July 9, 2017
A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients
Ewa Pronicka, Mariola Ropacka-Lesiak, Joanna Trubicka, et al.
Biomarkers in Medicine
|
March 24, 2022
Development and validation of a cell cycle progression signature for decentralized testing of men with prostate cancer
Vanessa Kuhl, Wyatt Clegg, Stephanie Meek, et al.
Plos One
|
November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant mice
Elisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Journal of Inherited Metabolic Disease
|
February 3, 2016
Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice
Germaine Korner, Tanja Scherer, Dea Adamsen, et al.
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.
Iscience
|
October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism
Jean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Plos One
|
June 30, 2009
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes
Isabel Rubio-Aliaga, Gerhard K H Przemeck, Helmut Fuchs, et al.
Page
of 66