Results 141 to 150 of about 25,056,579 (316)
Optimal bounds for a Gaussian Arithmetic-Geometric type mean by quadratic and contraharmonic means [PDF]
In this paper, we present the best possible parameters $\alpha_i, \beta_i\ (i=1,2,3)$ and $\alpha_4,\beta_4\in(1/2,1)$ such that the double inequalities \begin{align*} \alpha_1Q(a,b)+(1-\alpha_1)C(a,b)&
arxiv
Metachromatic leukodystrophy (MLD) is a lysosomal lipid storage disease caused by arylsulfatase A deficiency. In MLD patients the sphingolipid sulfatide increasingly accumulates leading to progressive demyelination.
K Saravanan+7 more
doaj
Mucopolysaccharidosis VI (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B leading to the accumulation of dermatan sulfate. Birth prevalence is between 1 in 43,261 and 1 in 1,
Harmatz Paul+3 more
doaj +1 more source
Maps between non-commutative spaces [PDF]
We examine maps between noncommutative projective spaces. A surjection of graded rings A-->A/J induces a closed immersion Proj(A/J)-->Proj(A). A homomorphism f:A-->B between graded rings induces an affine map U --> Proj(A) from a non-empty open subspace U of Proj(B). If A^{(n)} is the n-th Veronese subalgebra of a graded ring A there is a map Proj(A)-->
arxiv
Inactivation of Slow Reacting Substance of Anaphylaxis (SRS-A) by Arylsulfatases [PDF]
Robert P. Orange+2 more
openalex +1 more source
Measurement of arylsulfatase A activity in urine. [PDF]
L E Posey, L R Morgan
openalex +1 more source
A steady smooth Euler flow with support in the vicinity of a helix [PDF]
In this article we construct a smooth Euler flow supported in a neighborhood of a helix. It may be considered a generalization of a similar solution found by the author for a circle.
arxiv
Activity Of Soil Enzymes In Constructed Wetlands Treated With Swine Wastewater [PDF]
The objectives of this research were to investigate the activity of soil enzymes at different depths of CW treated with swine wastewater and to assess the relationship between the enzyme activity and nutrient concentration.
Baddam, Ramgopal
core +1 more source
Mucopoly saccharidosis type maroteaux-lamy, a case report [PDF]
Mucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine--4-sulfate sulfatase (arylsulfatase B).
A.R. Alaee+3 more
doaj