Results 141 to 150 of about 4,480 (203)

Enzymatic β-Mannosylation of Phenylethanoid Alcohols. [PDF]

Molecules
Černáková L, Haluz P, Mastihuba V, Košťálová Z, Karnišová Potocká E, Mastihubová M.   +5 more
europepmc   +1 more source

Trimmed <i>N</i>-glycans define aggressive gastric cancer and predict clinical outcomes. [PDF]

Theranostics
Ferreira D, Marinho-Santos B, Relvas-Santos M, Orr B, Brandão A, Afonso LP, Santos LL, Ferreira JA.   +7 more
europepmc   +1 more source

Deficient glycan extension and endoplasmic reticulum stresses in ALG3-CDG. [PDF]

J Inherit Metab Dis
Daniel EJP, Edmondson AC, Argon Y, Alsharhan H, Lam C, Freeze HH, He M.   +6 more
europepmc   +1 more source

Shaping the Glycan Landscape: Hidden Relationships between Linkage and Ring Distortions Induced by Carbohydrate-Active Enzymes. [PDF]

J Am Chem Soc
Grothaus IL, Spellerberg P, Rovira C, Colombi Ciacchi L.   +3 more
europepmc   +1 more source

Glycosylation in premature ovarian insufficiency: from genetic etiology to precision diagnostics. [PDF]

J Ovarian Res
Feng C, Qi N, Feng R, Liu Y, Yuan X.
europepmc   +1 more source

Elucidation of the late steps in the glycan-dependent ERAD of soluble misfolded glycoproteins. [PDF]

Plant J
Schoberer J, Vavra U, Shin YJ, Grünwald-Gruber C, Strasser R.   +4 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Microbial α-mannosidases

Enzyme and Microbial Technology, 1996
Microbial α-mannosidases are used in the analysis of glycopeptides and the developmental regulation of lysosomal enzymes. This survey presents comparison of properties of this high molecular weight, oligomeric protein from a number of microbial sources.
Sushama M Gaikwad
exaly   +2 more sources

Bovine β-mannosidase deficiency

Biochemical and Biophysical Research Communications, 1990
A fatal inherited glycoprotein storage disorder is described in Salers cattle which affects both sexes. Affected calves are unable to stand at birth, have a marked intention tremor, markedly enlarged kidneys, decreased white matter in all areas of the brain, and cytoplasmic vacuolation in multiple cell types of multiple tissues with nervous, renal ...
L, Bryan, S, Schmutz, S D, Hodges, F F, Snyder   +3 more
openaire   +2 more sources

Human β-Mannosidase Deficiency

New England Journal of Medicine, 1986
LYSOSOMAL disorders in humans due to deficiencies of lysosomal enzymes or effector proteins (activator or protector proteins) have been described for most steps in the catabolism of glycoproteins, ...
D A, Wenger, E, Sujansky, P V, Fennessey, J N, Thompson   +3 more
openaire   +2 more sources

Insight into microbial mannosidases: a review

Critical Reviews in Biotechnology, 2016
Mannan is the major constituent of hemicelluloses in softwoods. Mannan hydrolyzing enzymes cleave the 1,4-β-mannopyranosyl linkages of the hetero-1,4-β-d-mannans to yield mannose. β-Mannosidases are mandatory for the complete depolymerization of mannan, these are exo-acting enzymes, which acts on non-reducing end of mannooligomers and on mannobiose ...
Prakram Singh, Chauhan, Naveen, Gupta
openaire   +2 more sources