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JBMR Plus
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February 27, 2018
N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (<i>Ap2s1</i>) Mutations Establish <i>Ap2s1</i> Loss-of-Function Mice
Caroline M Gorvin, Angela Rogers, Michelle Stewart, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 27, 2009
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract
Laura M Pastorelli, Sara Wells, Martin Fray, et al.
Biogerontology
|
October 3, 2013
Shared Ageing Research Models (ShARM): a new facility to support ageing research
Adele L Duran, Paul Potter, Sara Wells, et al.
Plos Genetics
|
January 31, 2022
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing
Sherylanne Newton, Fanbo Kong, Adam J Carlton, et al.
Nature Genetics
|
November 16, 2010
Overexpression of Fto leads to increased food intake and results in obesity
Chris Church, Lee Moir, Fiona McMurray, et al.
Development (Cambridge, England)
|
December 4, 2024
Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice
Raissa G G Kay, Richard Reeves, Pam Siggers, et al.
Human Molecular Genetics
|
March 17, 2021
Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2
Fadil M Hannan, Mark Stevenson, Asha L Bayliss, et al.
Scientific Reports
|
January 15, 2021
Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring
Renato S Gaspar, Amanda J Unsworth, Alaa Al-Dibouni, et al.
BMC Developmental Biology
|
August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear
Anju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Physiological Genomics
|
November 8, 2007
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda
Ivana Barbaric, Mark J Perry, T Neil Dear, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 154) with videos related to
Sort By:
Page
of 16
JBMR Plus
|
February 27, 2018
N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (<i>Ap2s1</i>) Mutations Establish <i>Ap2s1</i> Loss-of-Function Mice
Caroline M Gorvin, Angela Rogers, Michelle Stewart, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 27, 2009
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract
Laura M Pastorelli, Sara Wells, Martin Fray, et al.
Biogerontology
|
October 3, 2013
Shared Ageing Research Models (ShARM): a new facility to support ageing research
Adele L Duran, Paul Potter, Sara Wells, et al.
Plos Genetics
|
January 31, 2022
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing
Sherylanne Newton, Fanbo Kong, Adam J Carlton, et al.
Nature Genetics
|
November 16, 2010
Overexpression of Fto leads to increased food intake and results in obesity
Chris Church, Lee Moir, Fiona McMurray, et al.
Development (Cambridge, England)
|
December 4, 2024
Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice
Raissa G G Kay, Richard Reeves, Pam Siggers, et al.
Human Molecular Genetics
|
March 17, 2021
Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2
Fadil M Hannan, Mark Stevenson, Asha L Bayliss, et al.
Scientific Reports
|
January 15, 2021
Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring
Renato S Gaspar, Amanda J Unsworth, Alaa Al-Dibouni, et al.
BMC Developmental Biology
|
August 14, 2010
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear
Anju Paudyal, Christine Damrau, Victoria L Patterson, et al.
Physiological Genomics
|
November 8, 2007
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda
Ivana Barbaric, Mark J Perry, T Neil Dear, et al.
Page
of 16