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Briefings in Functional Genomics & Proteomics
|
July 9, 2004
Genomic analysis of facioscapulohumeral muscular dystrophy
Jannine Clapp, Daniel J Bolland, Jane E Hewitt
Genomics
|
July 18, 2008
Genes required for functional glycosylation of dystroglycan are conserved in zebrafish
Christopher J Moore, Huey Tse Goh, Jane E Hewitt
Plos One
|
March 8, 2013
Formation of the embryonic organizer is restricted by the competitive influences of Fgf signaling and the SoxB1 transcription factors
Cheng-Liang Kuo, Chi Man Lam, Jane E Hewitt, et al.
Neuromuscular Disorders : NMD
|
April 19, 2005
A rapid PCR method for genotyping the Large(myd) mouse, a model of glycosylation-deficient congenital muscular dystrophy
Claudia A Browning, Prabhjit K Grewal, Christopher J Moore, et al.
European Journal of Human Genetics : EJHG
|
March 2, 2012
Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis
Andreas Leidenroth, Hanne Sørmo Sorte, Gregor Gilfillan, et al.
Human Molecular Genetics
|
August 22, 2002
Identification of the autoantigen SART-1 as a candidate gene for the development of atopy
Amanda P Wheatley, Daniel J Bolland, Jane E Hewitt, et al.
Glycobiology
|
June 17, 2005
Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies
Prabhjit K Grewal, Jennifer M McLaughlan, Christopher J Moore, et al.
The Journal of Biological Chemistry
|
November 14, 2012
Re-evaluation of the role of calcium homeostasis endoplasmic reticulum protein (CHERP) in cellular calcium signaling
Yaping Lin-Moshier, Peter J Sebastian, Leeann Higgins, et al.
Chromosoma
|
August 21, 2012
Evolution of DUX gene macrosatellites in placental mammals
Andreas Leidenroth, Jannine Clapp, Laura M Mitchell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 27, 2009
A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments
Felipe A Court, Jane E Hewitt, Kay Davies, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Briefings in Functional Genomics & Proteomics
|
July 9, 2004
Genomic analysis of facioscapulohumeral muscular dystrophy
Jannine Clapp, Daniel J Bolland, Jane E Hewitt
Genomics
|
July 18, 2008
Genes required for functional glycosylation of dystroglycan are conserved in zebrafish
Christopher J Moore, Huey Tse Goh, Jane E Hewitt
Plos One
|
March 8, 2013
Formation of the embryonic organizer is restricted by the competitive influences of Fgf signaling and the SoxB1 transcription factors
Cheng-Liang Kuo, Chi Man Lam, Jane E Hewitt, et al.
Neuromuscular Disorders : NMD
|
April 19, 2005
A rapid PCR method for genotyping the Large(myd) mouse, a model of glycosylation-deficient congenital muscular dystrophy
Claudia A Browning, Prabhjit K Grewal, Christopher J Moore, et al.
European Journal of Human Genetics : EJHG
|
March 2, 2012
Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis
Andreas Leidenroth, Hanne Sørmo Sorte, Gregor Gilfillan, et al.
Human Molecular Genetics
|
August 22, 2002
Identification of the autoantigen SART-1 as a candidate gene for the development of atopy
Amanda P Wheatley, Daniel J Bolland, Jane E Hewitt, et al.
Glycobiology
|
June 17, 2005
Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies
Prabhjit K Grewal, Jennifer M McLaughlan, Christopher J Moore, et al.
The Journal of Biological Chemistry
|
November 14, 2012
Re-evaluation of the role of calcium homeostasis endoplasmic reticulum protein (CHERP) in cellular calcium signaling
Yaping Lin-Moshier, Peter J Sebastian, Leeann Higgins, et al.
Chromosoma
|
August 21, 2012
Evolution of DUX gene macrosatellites in placental mammals
Andreas Leidenroth, Jannine Clapp, Laura M Mitchell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 27, 2009
A laminin-2, dystroglycan, utrophin axis is required for compartmentalization and elongation of myelin segments
Felipe A Court, Jane E Hewitt, Kay Davies, et al.
Page
of 3