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Frontiers in Cardiovascular Medicine
|
March 11, 2026
Correction: Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
Manuela A Oestereicher, Christopher S Ward, Elida Schneltzer, et al.
JBMR Plus
|
June 7, 2023
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (<i>NFIX</i>) Gene Has Phenotypic Features of Marshall-Smith Syndrome
Kreepa G Kooblall, Mark Stevenson, Michelle Stewart, et al.
Neuroscience Applied
|
July 14, 2025
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
Lillian Garrett, Dietrich Trümbach, Donghyung Lee, et al.
Med (New York, N.Y.)
|
October 20, 2023
Shiga toxin targets the podocyte causing hemolytic uremic syndrome through endothelial complement activation
Emily E Bowen, Jennifer A Hurcombe, Fern Barrington, et al.
EMBO Molecular Medicine
|
August 27, 2019
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function
Lucy A Dunbar, Pranav Patni, Carlos Aguilar, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 11, 2012
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project
Abdel Ayadi, Marie-Christine Birling, Joanna Bottomley, et al.
Plos Biology
|
May 21, 2015
Applying the ARRIVE Guidelines to an In Vivo Database
Natasha A Karp, Terry F Meehan, Hugh Morgan, et al.
Genome Medicine
|
October 13, 2022
Mendelian gene identification through mouse embryo viability screening
Pilar Cacheiro, Carl Henrik Westerberg, Jesse Mager, et al.
The Journal of Clinical Investigation
|
March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features
Valter Tucci, Tjitske Kleefstra, Andrea Hardy, et al.
American Journal of Human Genetics
|
May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy
Marianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 154) with videos related to
Sort By:
Page
of 16
Frontiers in Cardiovascular Medicine
|
March 11, 2026
Correction: Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
Manuela A Oestereicher, Christopher S Ward, Elida Schneltzer, et al.
JBMR Plus
|
June 7, 2023
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (<i>NFIX</i>) Gene Has Phenotypic Features of Marshall-Smith Syndrome
Kreepa G Kooblall, Mark Stevenson, Michelle Stewart, et al.
Neuroscience Applied
|
July 14, 2025
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
Lillian Garrett, Dietrich Trümbach, Donghyung Lee, et al.
Med (New York, N.Y.)
|
October 20, 2023
Shiga toxin targets the podocyte causing hemolytic uremic syndrome through endothelial complement activation
Emily E Bowen, Jennifer A Hurcombe, Fern Barrington, et al.
EMBO Molecular Medicine
|
August 27, 2019
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function
Lucy A Dunbar, Pranav Patni, Carlos Aguilar, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 11, 2012
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project
Abdel Ayadi, Marie-Christine Birling, Joanna Bottomley, et al.
Plos Biology
|
May 21, 2015
Applying the ARRIVE Guidelines to an In Vivo Database
Natasha A Karp, Terry F Meehan, Hugh Morgan, et al.
Genome Medicine
|
October 13, 2022
Mendelian gene identification through mouse embryo viability screening
Pilar Cacheiro, Carl Henrik Westerberg, Jesse Mager, et al.
The Journal of Clinical Investigation
|
March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features
Valter Tucci, Tjitske Kleefstra, Andrea Hardy, et al.
American Journal of Human Genetics
|
May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy
Marianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Page
of 16