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Christopher T Esapa

Showing results (1-10 of 18) with videos related to

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Human Molecular Genetics|December 3, 2004
Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cellsChristopher T Esapa, R A Jeffrey McIlhinney, Derek J Blake
Advances in Experimental Medicine and Biology|January 13, 2006
Glycosylation defects and muscular dystrophyDerek J Blake, Christopher T Esapa, Enca Martin-Rendon, et al.
Current Protocols in Mouse Biology|June 13, 2015
Bone Mineral Content and DensityChristopher T Esapa, J H Duncan Bassett, Holly Evans, et al.
Human Molecular Genetics|January 4, 2007
SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinAChristopher T Esapa, Adrian Waite, Matthew Locke, et al.
Muscle & Nerve|June 8, 2007
Fukutin-related protein localizes to the Golgi apparatus and mutations lead to mislocalization in muscle in vivoElizabeth Keramaris-Vrantsis, Pei J Lu, Timothy Doran, et al.
Plos One|April 11, 2015
N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse modelsChristopher T Esapa, Fadil M Hannan, Valerie N Babinsky, et al.
Hormones & Cancer|February 26, 2013
GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasivenessKatherine U Gaynor, Irina V Grigorieva, Michael D Allen, et al.
The Journal of Biological Chemistry|July 3, 2003
The adenosine A2A receptor interacts with the actin-binding protein alpha-actininJavier Burgueño, Derek J Blake, Matthew A Benson, et al.
Diabetes|February 13, 2016
Haploinsufficiency of the Insulin Receptor in the Presence of a Splice-Site Mutation in Ppp2r2a Results in a Novel Digenic Mouse Model of Type 2 DiabetesMichelle Goldsworthy, Ying Bai, Chi-Ming Li, et al.
Plos One|December 14, 2016
Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling PathwayChristopher T Esapa, Sian E Piret, M Andrew Nesbit, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|December 3, 2004
Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cellsChristopher T Esapa, R A Jeffrey McIlhinney, Derek J Blake
Advances in Experimental Medicine and Biology|January 13, 2006
Glycosylation defects and muscular dystrophyDerek J Blake, Christopher T Esapa, Enca Martin-Rendon, et al.
Current Protocols in Mouse Biology|June 13, 2015
Bone Mineral Content and DensityChristopher T Esapa, J H Duncan Bassett, Holly Evans, et al.
Human Molecular Genetics|January 4, 2007
SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinAChristopher T Esapa, Adrian Waite, Matthew Locke, et al.
Muscle & Nerve|June 8, 2007
Fukutin-related protein localizes to the Golgi apparatus and mutations lead to mislocalization in muscle in vivoElizabeth Keramaris-Vrantsis, Pei J Lu, Timothy Doran, et al.
Plos One|April 11, 2015
N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse modelsChristopher T Esapa, Fadil M Hannan, Valerie N Babinsky, et al.
Hormones & Cancer|February 26, 2013
GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasivenessKatherine U Gaynor, Irina V Grigorieva, Michael D Allen, et al.
The Journal of Biological Chemistry|July 3, 2003
The adenosine A2A receptor interacts with the actin-binding protein alpha-actininJavier Burgueño, Derek J Blake, Matthew A Benson, et al.
Diabetes|February 13, 2016
Haploinsufficiency of the Insulin Receptor in the Presence of a Splice-Site Mutation in Ppp2r2a Results in a Novel Digenic Mouse Model of Type 2 DiabetesMichelle Goldsworthy, Ying Bai, Chi-Ming Li, et al.
Plos One|December 14, 2016
Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling PathwayChristopher T Esapa, Sian E Piret, M Andrew Nesbit, et al.
Pageof 2