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Morag Robertson

Showing results (11-20 of 16) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 18, 2006
Nanog retrotransposed genes with functionally conserved open reading framesMorag Robertson, Frances Stenhouse, Douglas Colby, et al.
Nature|December 22, 2007
Nanog safeguards pluripotency and mediates germline developmentIan Chambers, Jose Silva, Douglas Colby, et al.
The EMBO Journal|November 27, 2012
OCT4/SOX2-independent Nanog autorepression modulates heterogeneous Nanog gene expression in mouse ES cellsPablo Navarro, Nicola Festuccia, Douglas Colby, et al.
Investigative Ophthalmology & Visual Science|March 5, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunctionShalini Jadeja, Alun R Barnard, Lisa McKie, et al.
Plos Genetics|May 10, 2014
A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected]Sally H Cross, Danilo G Macalinao, Lisa McKie, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 18, 2006
Nanog retrotransposed genes with functionally conserved open reading framesMorag Robertson, Frances Stenhouse, Douglas Colby, et al.
Nature|December 22, 2007
Nanog safeguards pluripotency and mediates germline developmentIan Chambers, Jose Silva, Douglas Colby, et al.
The EMBO Journal|November 27, 2012
OCT4/SOX2-independent Nanog autorepression modulates heterogeneous Nanog gene expression in mouse ES cellsPablo Navarro, Nicola Festuccia, Douglas Colby, et al.
Investigative Ophthalmology & Visual Science|March 5, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunctionShalini Jadeja, Alun R Barnard, Lisa McKie, et al.
Plos Genetics|May 10, 2014
A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected]Sally H Cross, Danilo G Macalinao, Lisa McKie, et al.
Human Molecular Genetics|June 14, 2012
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODHJoe Rainger, Hemant Bengani, Leigh Campbell, et al.
Pageof 2