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Jane E Hewitt

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

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Stem Cells (Dayton, Ohio)|August 14, 2012
Defects in glycosylation impair satellite stem cell function and niche composition in the muscles of the dystrophic Large(myd) mouseJacob Ross, Abigail Benn, Jacqueline Jonuschies, et al.
Human Molecular Genetics|October 2, 2002
Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disordersPaul J Holzfeind, Prabhjit K Grewal, Herbert A Reitsamer, et al.
Biochemical Society Symposium|March 27, 2003
MS screening strategies: investigating the glycomes of knockout and myodystrophic mice and leukodystrophic human brainsMark Sutton-Smith, Howard R Morris, Prabhjit K Grewal, et al.
Glycobiology|January 14, 2012
Glycoproteomic characterization of recombinant mouse α-dystroglycanRebecca Harrison, Paul G Hitchen, Maria Panico, et al.
American Journal of Human Genetics|August 2, 2007
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophyJannine Clapp, Laura M Mitchell, Daniel J Bolland, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Neuromuscular Disorders : NMD|November 13, 2014
A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patientsEmma L Humphrey, Erica Lacey, Lam T Le, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonucleiPeter S Masny, On Ying A Chan, Jessica C de Greef, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35Renee F Badenhop, Melissa J Moses, Anna Scimone, et al.
Human Genetics|April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndromeJeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
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Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Stem Cells (Dayton, Ohio)|August 14, 2012
Defects in glycosylation impair satellite stem cell function and niche composition in the muscles of the dystrophic Large(myd) mouseJacob Ross, Abigail Benn, Jacqueline Jonuschies, et al.
Human Molecular Genetics|October 2, 2002
Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disordersPaul J Holzfeind, Prabhjit K Grewal, Herbert A Reitsamer, et al.
Biochemical Society Symposium|March 27, 2003
MS screening strategies: investigating the glycomes of knockout and myodystrophic mice and leukodystrophic human brainsMark Sutton-Smith, Howard R Morris, Prabhjit K Grewal, et al.
Glycobiology|January 14, 2012
Glycoproteomic characterization of recombinant mouse α-dystroglycanRebecca Harrison, Paul G Hitchen, Maria Panico, et al.
American Journal of Human Genetics|August 2, 2007
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophyJannine Clapp, Laura M Mitchell, Daniel J Bolland, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Neuromuscular Disorders : NMD|November 13, 2014
A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patientsEmma L Humphrey, Erica Lacey, Lam T Le, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonucleiPeter S Masny, On Ying A Chan, Jessica C de Greef, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2003
Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35Renee F Badenhop, Melissa J Moses, Anna Scimone, et al.
Human Genetics|April 17, 2007
Intragenic deletion in the LARGE gene causes Walker-Warburg syndromeJeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, et al.
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