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Human Molecular Genetics
|
April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye disease
Caroline Thaung, Katrine West, Brian J Clark, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2
Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse
Adrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Plos Genetics
|
October 13, 2006
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media
Nicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, et al.
Psychopharmacology
|
June 19, 2004
Localisation of NMU1R and NMU2R in human and rat central nervous system and effects of neuromedin-U following central administration in rats
Jane Gartlon, Philip Szekeres, Mark Pullen, et al.
Comparative and Functional Genomics
|
July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse
Vicky Tsipouri, John A Curtin, Pat M Nolan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 1, 2004
A gene-driven ENU-based approach to generating an allelic series in any gene
Mohamed Mohideen Quwailid, Alison Hugill, Neil Dear, et al.
Neuropharmacology
|
October 5, 2014
First-in-class thyrotropin-releasing hormone (TRH)-based compound binds to a pharmacologically distinct TRH receptor subtype in human brain and is effective in neurodegenerative models
Julie A Kelly, Noreen T Boyle, Natalie Cole, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Human Molecular Genetics
|
April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye disease
Caroline Thaung, Katrine West, Brian J Clark, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2
Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse
Adrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
Plos Genetics
|
October 13, 2006
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media
Nicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, et al.
Psychopharmacology
|
June 19, 2004
Localisation of NMU1R and NMU2R in human and rat central nervous system and effects of neuromedin-U following central administration in rats
Jane Gartlon, Philip Szekeres, Mark Pullen, et al.
Comparative and Functional Genomics
|
July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse
Vicky Tsipouri, John A Curtin, Pat M Nolan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
October 1, 2004
A gene-driven ENU-based approach to generating an allelic series in any gene
Mohamed Mohideen Quwailid, Alison Hugill, Neil Dear, et al.
Neuropharmacology
|
October 5, 2014
First-in-class thyrotropin-releasing hormone (TRH)-based compound binds to a pharmacologically distinct TRH receptor subtype in human brain and is effective in neurodegenerative models
Julie A Kelly, Noreen T Boyle, Natalie Cole, et al.
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of 3