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Patrick M Nolan

Showing results (61-70 of 71) with videos related to

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Physiological Genomics|May 29, 2008
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory studySilvia Mandillo, Valter Tucci, Sabine M Hölter, 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.
Cell|August 2, 2015
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven AxisMichael J Parsons, Marco Brancaccio, Siddharth Sethi, et al.
Current Biology : CB|March 11, 2008
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMatthias Groszer, David A Keays, Robert M J Deacon, et al.
Disease Models & Mechanisms|September 3, 2021
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypesEva Lana-Elola, Heather Cater, Sheona Watson-Scales, et al.
Human Molecular Genetics|December 4, 2014
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityPeter I Joyce, Philip Mcgoldrick, Rachele A Saccon, et al.
The Journal of Clinical Investigation|March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic featuresValter Tucci, Tjitske Kleefstra, Andrea Hardy, 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.
American Journal of Human Genetics|May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic EncephalopathyMarianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Nature Communications|August 19, 2016
Novel gene function revealed by mouse mutagenesis screens for models of age-related diseasePaul K Potter, Michael R Bowl, Prashanthini Jeyarajan, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Physiological Genomics|May 29, 2008
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory studySilvia Mandillo, Valter Tucci, Sabine M Hölter, 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.
Cell|August 2, 2015
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven AxisMichael J Parsons, Marco Brancaccio, Siddharth Sethi, et al.
Current Biology : CB|March 11, 2008
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMatthias Groszer, David A Keays, Robert M J Deacon, et al.
Disease Models & Mechanisms|September 3, 2021
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypesEva Lana-Elola, Heather Cater, Sheona Watson-Scales, et al.
Human Molecular Genetics|December 4, 2014
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicityPeter I Joyce, Philip Mcgoldrick, Rachele A Saccon, et al.
The Journal of Clinical Investigation|March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic featuresValter Tucci, Tjitske Kleefstra, Andrea Hardy, 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.
American Journal of Human Genetics|May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic EncephalopathyMarianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Nature Communications|August 19, 2016
Novel gene function revealed by mouse mutagenesis screens for models of age-related diseasePaul K Potter, Michael R Bowl, Prashanthini Jeyarajan, et al.
Pageof 8