Ian C Gray - JoVE Visualize

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Comparative and Functional Genomics|July 17, 2008

Atypical CTSK transcripts and ARNT transcription read-through into CTSKFabienne S Giraudeau, Jean-Philippe Walhin, Paul R Murdock, et al.

BMC Research Notes|February 26, 2010

CCR2 and coronary artery disease: a woscops substudyDavid J Dow, Alex D McMahon, Ian C Gray, et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 3, 2004

Characterization of common genetic variants in cathepsin K and testing for association with bone mineral density in a large cohort of perimenopausal women from ScotlandFabienne S Giraudeau, Ralph E McGinnis, Ian C Gray, et al.

Current Biology : CB|July 5, 2003

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, 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 mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.

Comparative and Functional Genomics|July 17, 2008

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.

Chemmedchem|September 29, 2011

Silicon analogues of the nonpeptidic GnRH antagonist AG-045572: syntheses, crystal structure analyses, and pharmacological characterizationMatthew J Barnes, Christian Burschka, Matthias W Büttner, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002

Novel phenotypes identified by plasma biochemical screening in the mouseTertius A Hough, Patrick M Nolan, Vicky Tsipouri, et al.

Genetica|December 29, 2004

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disordersSohaila Rastan, Tertius Hough, Amy Kierman, et al.

Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:

Pageof 1

Comparative and Functional Genomics|July 17, 2008

Atypical CTSK transcripts and ARNT transcription read-through into CTSKFabienne S Giraudeau, Jean-Philippe Walhin, Paul R Murdock, et al.

BMC Research Notes|February 26, 2010

CCR2 and coronary artery disease: a woscops substudyDavid J Dow, Alex D McMahon, Ian C Gray, et al.

Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 3, 2004

Characterization of common genetic variants in cathepsin K and testing for association with bone mineral density in a large cohort of perimenopausal women from ScotlandFabienne S Giraudeau, Ralph E McGinnis, Ian C Gray, et al.

Current Biology : CB|July 5, 2003

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, 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 mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.

Comparative and Functional Genomics|July 17, 2008

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.

Chemmedchem|September 29, 2011

Silicon analogues of the nonpeptidic GnRH antagonist AG-045572: syntheses, crystal structure analyses, and pharmacological characterizationMatthew J Barnes, Christian Burschka, Matthias W Büttner, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002

Novel phenotypes identified by plasma biochemical screening in the mouseTertius A Hough, Patrick M Nolan, Vicky Tsipouri, et al.

Genetica|December 29, 2004

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disordersSohaila Rastan, Tertius Hough, Amy Kierman, et al.

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