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phosphomannomutase (148) 148
humans (106) 106
glycosylation (83) 83
index medicus (81) 81
biochemistry & molecular biology (79) 79
phosphotransferases - genetics (72) 72
phosphotransferases - metabolism (52) 52
phosphomannomutase deficiency (49) 49
female (48) 48
genetics & heredity (46) 46
mutation (46) 46
congenital disorders of glycosylation - genetics (42) 42
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gene (38) 38
phosphoglucomutase (37) 37
molecular sequence data (36) 36
mutations (36) 36
biosynthesis (35) 35
deficient glycoprotein syndrome (33) 33
phosphotransferases - deficiency (31) 31
amino acid sequence (30) 30
congenital disorders of glycosylation (30) 30
enzymes (30) 30
pmm2 (30) 30
analysis (29) 29
cdg-ia (29) 29
genetic disorders (29) 29
phosphoglucomutase - metabolism (29) 29
phosphotransferases - chemistry (28) 28
microbiology (27) 27
animals (26) 26
glucose (26) 26
pediatrics (26) 26
phosphates (26) 26
mannose (25) 25
phosphoglucomutase - genetics (24) 24
biophysics (23) 23
congenital disorders of glycosylation - diagnosis (23) 23
proteins (23) 23
escherichia-coli (22) 22
pseudomonas-aeruginosa (22) 22
child, preschool (21) 21
infant (21) 21
n-glycosylation (21) 21
phosphoglucomutase - chemistry (21) 21
syndrome type-i (21) 21
child (20) 20
identification (20) 20
congenital disorders of glycosylation - enzymology (19) 19
protein (19) 19
research (19) 19
transferrin (19) 19
expression (18) 18
models, molecular (18) 18
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sequence homology, amino acid (18) 18
base sequence (17) 17
cloning, molecular (17) 17
kinetics (17) 17
cell biology (16) 16
cloning (16) 16
disease (16) 16
gene expression (16) 16
lipopolysaccharide (16) 16
adult (15) 15
congenital disorders of glycosylation - metabolism (15) 15
medicine, research & experimental (15) 15
phosphomannomutase/phosphoglucomutase (15) 15
pseudomonas aeruginosa - enzymology (15) 15
adolescent (14) 14
article (14) 14
bacterial proteins - genetics (14) 14
biotechnology & applied microbiology (14) 14
cdg (14) 14
diagnosis (14) 14
genetic aspects (14) 14
phosphomannose isomerase (14) 14
physiological aspects (14) 14
pseudomonas aeruginosa (14) 14
recombinant proteins - metabolism (14) 14
virulence (14) 14
clinical neurology (13) 13
congenital diseases (13) 13
congenital disorder (13) 13
congenital disorders of glycosylation - pathology (13) 13
phosphomannomutase 2 (13) 13
protein glycosylation (13) 13
saccharomyces-cerevisiae (13) 13
catalysis (12) 12
congenital disorders (12) 12
dna mutational analysis (12) 12
enzyme (12) 12
genotype (12) 12
isoelectric focusing (12) 12
magnetic resonance imaging (12) 12
mice (12) 12
pmm2-cdg (12) 12
serum transferrin (12) 12
bacterial proteins - metabolism (11) 11
dextrose (11) 11
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Journal of Microbiology and Biotechnology, ISSN 1017-7825, 2018, Volume 28, Issue 8, p. 1293
Phosphomannomutase (ManB) converts mannose-6-phosphate (M-6-P) to mannose-1-phosphate (M-1-P), which is a key metabolic precursor for the production of... 
Lactococcus lactis | phosphomannomutase | mannose-1-phosphate | mannose-6-phosphate
Journal Article
DISEASE MODELS & MECHANISMS, ISSN 1754-8403, 11/2019, Volume 12, Issue 11, p. dmm040584
Phosphomannomutase 2 deficiency, or PMM2-CDG, is the most common congenital disorder of glycosylation and affects over 1000 patients globally. There are no... 
Epalrestat | PMM2-CDG | Drug repurposing | Aldose reductase inhibitor | FLAVONOIDS | MODEL | PATHOLOGY | PHOSPHOMANNOMUTASE | DEFICIENCY | Phosphomannomutase 2 deficiency | CELL BIOLOGY | GENE | DISEASE | Congenital disorder of glycosylation | HEME OXYGENASE-1 | MUTATIONS
Journal Article
New Phytologist, ISSN 0028-646X, 01/2016, Volume 209, Issue 2, pp. 664 - 678
Journal Article
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 08/2019, Volume 84, Issue 15, pp. 9627 - 9636
alpha-Phosphomannomutase/phosphoglucomutase (alpha PMM/PGM) from P. aeruginosa is involved in bacterial cell wall assembly and is implicated in P. aeruginosa... 
PHOSPHOGLUCOMUTASE | PATHOGENESIS | NEISSERIA | MECHANISM | STRUCTURAL BASIS | PHOSPHOMANNOMUTASE/PHOSPHOGLUCOMUTASE | MOUSE MODEL | PHOSPHATES | CHEMISTRY, ORGANIC | PHOSPHOHEXOMUTASE | LIPOOLIGOSACCHARIDE BIOSYNTHESIS
Journal Article
Parasitology, ISSN 0031-1820, 7/2009, Volume 136, Issue 8, pp. 833 - 840
SUMMARYVaccination remains the best hope for control of all forms of leishmaniasis, and the development of a safe and effective vaccine is a critical global... 
Vaccine | Glycoconjugate | Phosphomannomutase | Leishmania
Journal Article
Human Mutation, ISSN 1059-7794, 09/2015, Volume 36, Issue 9, pp. 851 - 860
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 10, p. e0165901
[This corrects the article DOI: 10.1371/journal.pone.0158863.]. 
Cytotoxicity | Receptors | T cell receptors | Natural killer cells | Phosphomannomutase
Journal Article
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, ISSN 0066-4804, 10/2019, Volume 63, Issue 10
Chagas' disease, which is caused by the Trypanosoma cruzi parasite, has become a global health problem that is currently treated with poorly tolerated drugs... 
LEISHMANIA-MEXICANA PHOSPHOMANNOMUTASE | mannose | screening | BRUCEI | MICROBIOLOGY | VIRULENCE | GLYCOSYLPHOSPHATIDYLINOSITOL | drug discovery | ROLES | BIOSYNTHESIS | ligandability | PHARMACOLOGY & PHARMACY | Chagas' disease | target based
Journal Article
G3: Genes, Genomes, Genetics, ISSN 2160-1836, 02/2019, Volume 9, Issue 2, pp. 413 - 423
Phosphomannomutase 2 Deficiency (PMM2-CDG) is the most common monogenic congenital disorder of glycosylation (CDG) affecting at least 800 patients globally.... 
2 Deficiency | Human disease | PMM2-CDG | Congenital | Disorders of | Glycosylation | Yeast models of | Phosphomannomutase | Drug screens | Phosphomannomutase 2 Deficiency | PMM2 | DEFECT | drug screens | HUMAN CDNA | IDENTIFICATION | congenital disorders of glycosylation | GENE | CLONING | N-LINKED GLYCOSYLATION | GENETICS & HEREDITY | MUTATIONS | yeast models of human disease | PROTEIN GLYCOSYLATION | EXPRESSION
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 09/2019, Volume 20, Issue 17, p. 4164
A large number of mutations causing PMM2-CDG, which is the most frequent disorder of glycosylation, destabilize phosphomannomutase2. We looked for a... 
PMM2-CDG | BIOCHEMISTRY & MOLECULAR BIOLOGY | CONGENITAL DISORDER | CDG-IA | CHEMISTRY, MULTIDISCIPLINARY | glucose-1 | PHOSPHOMANNOMUTASE 2 DEFICIENCY | pharmacological chaperone | 6-bisphosphate | MUTATIONS | INHIBITORS | DERIVATIVES | EXPRESSION | glucose-1,6-bisphosphate
Journal Article
Microbiology (United Kingdom), ISSN 1350-0872, 04/2018, Volume 164, Issue 4, pp. 614 - 624
Journal Article
Annals of Neurology, ISSN 0364-5134, 05/2019, Volume 85, Issue 5, pp. 740 - 751
Journal Article