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Analytical Chemistry
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May 22, 2024
Maximizing Glycoproteomics Results through an Integrated Parallel Accumulation Serial Fragmentation Workflow
Melissa Baerenfaenger, Merel A Post, Fokje Zijlstra, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2005
Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype
Lucie Guyant-Maréchal, Aad Verrips, Carole Girard, et al.
Journal of Human Genetics
|
April 22, 2020
Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability
Karen M Knapp, Rebecca Luu, Melissa Baerenfaenger, et al.
International Journal of Molecular Sciences
|
May 13, 2023
The GlycoPaSER Prototype as a Real-Time N-Glycopeptide Identification Tool Based on the PaSER Parallel Computing Platform
Gad Armony, Sven Brehmer, Tharan Srikumar, et al.
Journal of Inherited Metabolic Disease
|
May 23, 2020
Nucleotide sugar profiles throughout development in wildtype and galt knockout zebrafish
Minela Haskovic, Ana I Coelho, Martijn Lindhout, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Glycoproteomics in Cerebrospinal Fluid Reveals Brain-Specific Glycosylation Changes
Melissa Baerenfaenger, Merel A Post, Pieter Langerhorst, et al.
Journal of Inherited Metabolic Disease
|
June 20, 2020
Screening for abnormal glycosylation in a cohort of adult liver disease patients
Jos C Jansen, Bart van Hoek, Herold J Metselaar, et al.
Journal of Advanced Research
|
September 8, 2023
Plasma glycoproteomics delivers high-specificity disease biomarkers by detecting site-specific glycosylation abnormalities
Hans J C T Wessels, Purva Kulkarni, Maurice van Dael, et al.
Frontiers in Immunology
|
September 8, 2025
Glycoproteomics analysis of complement factor H and its complement-regulatory function during <i>Streptococcus pneumoniae</i>-associated hemolytic uremic syndrome
Laura M Baas, Kioa L Wijnsma, Fokje Zijlstra, et al.
Nature Communications
|
October 29, 2021
Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5
Peter T A Linders, Eveline C F Gerretsen, Angel Ashikov, et al.
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Analytical Chemistry
|
May 22, 2024
Maximizing Glycoproteomics Results through an Integrated Parallel Accumulation Serial Fragmentation Workflow
Melissa Baerenfaenger, Merel A Post, Fokje Zijlstra, et al.
American Journal of Medical Genetics. Part A
|
November 10, 2005
Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype
Lucie Guyant-Maréchal, Aad Verrips, Carole Girard, et al.
Journal of Human Genetics
|
April 22, 2020
Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability
Karen M Knapp, Rebecca Luu, Melissa Baerenfaenger, et al.
International Journal of Molecular Sciences
|
May 13, 2023
The GlycoPaSER Prototype as a Real-Time N-Glycopeptide Identification Tool Based on the PaSER Parallel Computing Platform
Gad Armony, Sven Brehmer, Tharan Srikumar, et al.
Journal of Inherited Metabolic Disease
|
May 23, 2020
Nucleotide sugar profiles throughout development in wildtype and galt knockout zebrafish
Minela Haskovic, Ana I Coelho, Martijn Lindhout, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Glycoproteomics in Cerebrospinal Fluid Reveals Brain-Specific Glycosylation Changes
Melissa Baerenfaenger, Merel A Post, Pieter Langerhorst, et al.
Journal of Inherited Metabolic Disease
|
June 20, 2020
Screening for abnormal glycosylation in a cohort of adult liver disease patients
Jos C Jansen, Bart van Hoek, Herold J Metselaar, et al.
Journal of Advanced Research
|
September 8, 2023
Plasma glycoproteomics delivers high-specificity disease biomarkers by detecting site-specific glycosylation abnormalities
Hans J C T Wessels, Purva Kulkarni, Maurice van Dael, et al.
Frontiers in Immunology
|
September 8, 2025
Glycoproteomics analysis of complement factor H and its complement-regulatory function during <i>Streptococcus pneumoniae</i>-associated hemolytic uremic syndrome
Laura M Baas, Kioa L Wijnsma, Fokje Zijlstra, et al.
Nature Communications
|
October 29, 2021
Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5
Peter T A Linders, Eveline C F Gerretsen, Angel Ashikov, et al.
Page
of 2