Search research articles
Contact Us
Filters
Showing results (11-20 of 16) with videos related to
Page
of 2
Sort By:
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 frames
Morag Robertson, Frances Stenhouse, Douglas Colby, et al.
Nature
|
December 22, 2007
Nanog safeguards pluripotency and mediates germline development
Ian 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 cells
Pablo 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 dysfunction
Shalini 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 DHODH
Joe Rainger, Hemant Bengani, Leigh Campbell, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 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 frames
Morag Robertson, Frances Stenhouse, Douglas Colby, et al.
Nature
|
December 22, 2007
Nanog safeguards pluripotency and mediates germline development
Ian 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 cells
Pablo 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 dysfunction
Shalini 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 DHODH
Joe Rainger, Hemant Bengani, Leigh Campbell, et al.
Page
of 2