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Ian Smyth

Showing results (21-30 of 29) with videos related to

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Plos Genetics|September 20, 2008
A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasisIan Smyth, Douglas F Hacking, Adrienne A Hilton, et al.
Nature Genetics|April 20, 2005
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebsShalini Jadeja, Ian Smyth, Jolanta E Pitera, et al.
Cell Reports|April 27, 2022
Interferons limit autoantigen-specific CD8<sup>+</sup> T-cell expansion in the non-obese diabetic mouseGaurang Jhala, Balasubramanian Krishnamurthy, Thomas C Brodnicki, et al.
Plos Genetics|October 27, 2010
Dual functions of ASCIZ in the DNA base damage response and pulmonary organogenesisSabine Jurado, Ian Smyth, Bryce van Denderen, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Journal of Medical Genetics|April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
Nature Communications|September 4, 2019
Attenuated palmitoylation of serotonin receptor 5-HT1A affects receptor function and contributes to depression-like behaviorsNataliya Gorinski, Monika Bijata, Sonal Prasad, et al.
BMC Nephrology|February 3, 2025
Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocolAmali Mallawaarachchi, Hugh McCarthy, Thomas A Forbes, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Plos Genetics|September 20, 2008
A mouse model of harlequin ichthyosis delineates a key role for Abca12 in lipid homeostasisIan Smyth, Douglas F Hacking, Adrienne A Hilton, et al.
Nature Genetics|April 20, 2005
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebsShalini Jadeja, Ian Smyth, Jolanta E Pitera, et al.
Cell Reports|April 27, 2022
Interferons limit autoantigen-specific CD8<sup>+</sup> T-cell expansion in the non-obese diabetic mouseGaurang Jhala, Balasubramanian Krishnamurthy, Thomas C Brodnicki, et al.
Plos Genetics|October 27, 2010
Dual functions of ASCIZ in the DNA base damage response and pulmonary organogenesisSabine Jurado, Ian Smyth, Bryce van Denderen, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Journal of Medical Genetics|April 22, 2011
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, et al.
Nature Communications|September 4, 2019
Attenuated palmitoylation of serotonin receptor 5-HT1A affects receptor function and contributes to depression-like behaviorsNataliya Gorinski, Monika Bijata, Sonal Prasad, et al.
BMC Nephrology|February 3, 2025
Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocolAmali Mallawaarachchi, Hugh McCarthy, Thomas A Forbes, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Pageof 3