Results 61 to 70 of about 6,281 (181)

Oleoylethanolamide regulates intestinal stem cell activity and villus size via PPARα signaling pathway

iMetaOmics, Volume 3, Issue 1, March 2026.
First use of a natural swine model with lipid metabolism to directly link lipid differences to a quantifiable intestinal villus height phenotype. Identified the phospholipid‐derived oleoylethanolamide, rather than canonical fatty acids, as the endogenous primary ligand that activates peroxisome proliferator‐activated receptors α (PPARα) to enlarge ...
Qianqian Wang, Lanmei Yin, Zhaobin Wang, Jun Li, Xianglin Zeng, Qiye Wang, Jianzhong Li, Kang Xu, Huansheng Yang, Yulong Yin   +9 more
wiley   +1 more source

Air-drying pretreatment effect on soil enzymatic activity

Plant, Soil and Environment, 2017
Air-drying of soil samples is a common practice for all-purpose soil testing. However, it may cause the cessation of microbial activity changing the biochemical attributes.
Rodrigo Santos MOREIRA, Marcio Koiti CHIBA, Stefany Batista NUNES, Isabella Clerici de MARIA   +3 more
doaj   +1 more source

Arylsulfatase LvArs2 regulates glycosaminoglycan sulfation and modulates white spot syndrome virus burden in Litopenaeus vannamei

Aquaculture Reports
Glycosaminoglycans (GAGs) and their sulfation patterns are pivotal in determining barrier tissue homeostasis and pathogen interactions in crustaceans. However, the underlying enzymatic regulators remain to be fully elucidated.
Chuhang Cheng, Tianyi Shen, Shella Li, Huteng He, Fajun Jiang   +4 more
doaj   +1 more source

Glycosylation and phosphorylation of arylsulfatase A.

Journal of Biological Chemistry, 1994
The glycosylation and phosphorylation of the lysosomal enzyme arylsulfatase A was analyzed by a combination of metabolic labeling, tryptic fragmentation, mass spectrometry, and radiosequencing. The results demonstrate that all three potential N-glycosylation sites at Asn residues 158, 184, and 350 are utilized in arylsufatase A and carry high mannose ...
H J, Sommerlade, T, Selmer, A, Ingendoh, V, Gieselmann, K, von Figura, K, Neifer, B, Schmidt   +6 more
openaire   +2 more sources

Arylsulfatase A deficiency causes seminolipid accumulation and a lysosomal storage disorder in Sertoli cells[S]

Journal of Lipid Research, 2011
Sulfogalactosylglycerolipid (SGG) is the major sulfoglycolipid of male germ cells. During spermatogenesis, apoptosis occurs in >50% of total germ cells.
Hongbin Xu, Kessiri Kongmanas, Suraj Kadunganattil, Charles E. Smith, Tony Rupar, Naoko Goto-Inoue, Louis Hermo, Kym F. Faull, Nongnuj Tanphaichitr   +8 more
doaj   +1 more source

Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B.

Journal of Biological Chemistry, 1990
A 2.2-kilobase cDNA clone for human arylsulfatase B (ASB) and several genomic clones were isolated and sequenced. The deduced amino acid sequence of 533 amino acids contains a 41-amino acid N-terminal signal peptide and a mature polypeptide of 492 amino acid residues.
C, Peters, B, Schmidt, W, Rommerskirch, K, Rupp, M, Zühlsdorf, M, Vingron, H E, Meyer, R, Pohlmann, K, von Figura   +8 more
openaire   +2 more sources

Newborn Screening for Metachromatic Leukodystrophy in Tuscany: The Paradigm of a Successful Preventive Medicine Program

International Journal of Neonatal Screening
Metachromatic leukodystrophy (MLD) is a rare inherited disorder of lysosomal storage, caused by a deficiency in the arylsulfatase A (ARSA) enzyme, leading to toxic accumulation of sulfatides, which progressively impair motor and cognitive function.
Sabrina Malvagia, Alessandra Bettiol, Margherita Porcaro, Massimo Mura, Silvia Funghini, Daniela Ombrone, Giulia Forni, Emanuela Scolamiero, Filippo Coppi, Roberta Damiano, Cristina Cereda, Simonetta Simonetti, Annalisa Lonetti, Marta Daniotti, Anna Caciotti, Amelia Morrone, Valeria Calbi, Francesca Fumagalli, Alessandro Aiuti, Elena Procopio, Renzo Guerrini, Giancarlo la Marca   +21 more
doaj   +1 more source

Metachromatic Leucodystrophy: A Case Report

Journal of Karnali Academy of Health Sciences, 2021
Metachromatic leukodystrophy (MLD) is a rare autosomal recessive inherited disease, which is caused by a deficiency in the enzyme activity of Arylsulfatase A (ARSA). Deficiency of this enzyme results in intralysosomal storage of sphingolipid cerebroside
Ramchandra Bastola, Shree Krishna Shrestha, Amrita Ghimire, Sunita Ghimire   +3 more
doaj  

Biochar-Based Granular Fertilizers with Agro-Industrial Binders Enhance Enzymatic Activity and Nutrient Cycling in Tropical Oxisols

Agronomy
The low fertility of tropical Oxisols challenges sustainable agriculture. While biochar-based granular fertilizers (BBGFs) offer a solution, the influence of different organic binders is unclear. This study investigated how BBGFs formulated with bio-oil (
José Mendes dos Santos Júnior, Luiz Arnaldo Fernandes, Fernando Colen, Leidivan Almeida Frazão, Rodinei Facco Pegoraro   +4 more
doaj   +1 more source

Mucopoly saccharidosis type maroteaux-lamy, a case report [PDF]

Journal of Mazandaran University of Medical Sciences, 2007
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, F. Rashidi ghader, F. Mojtahedzadeh, A. Tale   +3 more
doaj