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E H Moore

Showing results (61-70 of 68) with videos related to

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Molecules (Basel, Switzerland)|June 9, 2019
Bacterial Lipid II Analogs: Novel In Vitro Substrates for Mammalian Oligosaccharyl Diphosphodolichol Diphosphatase (DLODP) ActivitiesAhmad Massarweh, Michael Bosco, Isabelle Chantret, et al.
International Wound Journal|July 6, 2022
A Clinical Support App for routine wound management: reducing practice variation, improving clinician confidence and increasing formulary complianceZena E H Moore, Georgina E Aynge, Caryn G Carr, et al.
Plos One|July 24, 2010
The compartmentalisation of phosphorylated free oligosaccharides in cells from a CDG Ig patient reveals a novel ER-to-cytosol translocation processDelphine Peric, Christelle Durrant-Arico, Christophe Delenda, et al.
Radiology|February 1, 1992
Bronchogenic carcinoma: analysis of staging in the mediastinum with CT by correlative lymph node mapping and samplingT C McLoud, P M Bourgouin, R W Greenberg, et al.
JIMD Reports|February 28, 2016
Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle VariantsJuliette Bouchereau, Sandrine Vuillaumier Barrot, Thierry Dupré, et al.
The Journal of Biological Chemistry|May 2, 2002
Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferaseIsabelle Chantret, Thierry Dupré, Christophe Delenda, et al.
The Journal of Biological Chemistry|December 14, 2002
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylationIsabelle Chantret, Julia Dancourt, Thierry Dupré, et al.
Journal of Medical Genetics|August 4, 2010
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutationsT Dupré, S Vuillaumier-Barrot, I Chantret, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Molecules (Basel, Switzerland)|June 9, 2019
Bacterial Lipid II Analogs: Novel In Vitro Substrates for Mammalian Oligosaccharyl Diphosphodolichol Diphosphatase (DLODP) ActivitiesAhmad Massarweh, Michael Bosco, Isabelle Chantret, et al.
International Wound Journal|July 6, 2022
A Clinical Support App for routine wound management: reducing practice variation, improving clinician confidence and increasing formulary complianceZena E H Moore, Georgina E Aynge, Caryn G Carr, et al.
Plos One|July 24, 2010
The compartmentalisation of phosphorylated free oligosaccharides in cells from a CDG Ig patient reveals a novel ER-to-cytosol translocation processDelphine Peric, Christelle Durrant-Arico, Christophe Delenda, et al.
Radiology|February 1, 1992
Bronchogenic carcinoma: analysis of staging in the mediastinum with CT by correlative lymph node mapping and samplingT C McLoud, P M Bourgouin, R W Greenberg, et al.
JIMD Reports|February 28, 2016
Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle VariantsJuliette Bouchereau, Sandrine Vuillaumier Barrot, Thierry Dupré, et al.
The Journal of Biological Chemistry|May 2, 2002
Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferaseIsabelle Chantret, Thierry Dupré, Christophe Delenda, et al.
The Journal of Biological Chemistry|December 14, 2002
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylationIsabelle Chantret, Julia Dancourt, Thierry Dupré, et al.
Journal of Medical Genetics|August 4, 2010
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutationsT Dupré, S Vuillaumier-Barrot, I Chantret, et al.
Pageof 7