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PMM1
Annual Report DDUV 2009
Articles Catalytic Cycling in Β-Phosphoglucomutase: a Kinetic
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Transcriptomic and Proteomic Profiling Provides Insight Into
The Analysis of Variants in the General Population Reveals That PMM2 Is Extremely Tolerant to Missense Mutations and That Diagno
Supplemental Table S1. Primers for Sybrgreen Quantitative RT-PCR Assays
Successes and Challenges in Functional Assignment in a Superfamily of Phosphatases
The Effects of Genetic Variants on Protein Structure and Their Associations with Preeclampsia
Induction of Therapeutic Tissue Tolerance Foxp3 Expression Is
University of Oklahoma Graduate College
Supplemental Figures 04 12 2017
Supplemental Tables.Pdf
A Mutant of Phosphomannomutase1 Retains Full Enzymatic Activity, but Is Not Activated by IMP: Possible Implications for the Disease PMM2-CDG
Phophomannomutase2 Mutants in Vitro and Represents [0.9]
Lack of Homozygotes for the Most Frequent Disease Allele In
The X-Ray Crystal Structures of Human
Work Towards the Isolation and Characterization of the Muscle Isoform of Glucose 1,6-Bisphosphatase
University of Groningen Engineering of Sugar Metabolism in Lactococcus
Top View
Molecular and Evolutionary Investigation of the Phosphoglucomutase Gene Family
Nrf2 Activation Attenuates Genetic Endoplasmic Reticulum Stress Induced by a Mutation in the Phosphomannomutase 2 Gene in Zebrafish
Generated by SRI International Pathway Tools Version 25.0 on Mon
Quantitative 1H NMR Metabolomics Reveal Distinct Metabolic Adaptations in Human Macrophages Following Differential Activation
Functional Significance of PMM2 Mutations in Mildly Affected Patients
Carbohydrate-Deficient Glycoprotein Syndrome Type 1A: Expression and Characterisation of Wild Type and Mutant PMM2 in E. Coli
Supplementary Table 2
Mutations in PMM2 That Cause Congenital Disorders of Glycosylation, Type Ia (CDG-Ia)
Supplemental Material
Generated by SRI International Pathway Tools Version 24.0 on Thu