Lysosomal enzyme replacement therapies: Historical development, clinical outcomes, and future perspectives
Lysosomes and lysosomal enzymes play a central role in numerous cellular processes,
including cellular nutrition, recycling, signaling, defense, and cell death. Genetic deficiencies …
including cellular nutrition, recycling, signaling, defense, and cell death. Genetic deficiencies …
A molecular genetics view on Mucopolysaccharidosis Type II
S Verma, S Pantoom, J Petters, AK Pandey… - … Research/Reviews in …, 2021 - Elsevier
Abstract Mucopolysaccharidosis Type II (MPS II) is an X-linked recessive genetic disorder
that primarily affects male patients. With an incidence of 1 in 100,000 male live births, the …
that primarily affects male patients. With an incidence of 1 in 100,000 male live births, the …
A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia
MA Puentes-Tellez, PA Lerma-Barbosa… - Heliyon, 2020 - cell.com
Lysosomal storage diseases (LSDs) are a group of about 50 inborn errors of metabolism
characterized by the lysosomal accumulation of partially or non-degraded molecules due to …
characterized by the lysosomal accumulation of partially or non-degraded molecules due to …
[HTML][HTML] Characteristics of two lysis-related proteins from a Shewanella putrefaciens phage with high lytic activity and wide Spectrum
Y Zhang, H Lin, J Wang, M Li - Journal of Food Protection, 2018 - Elsevier
Although Shewanella putrefaciens is the specific spoilage organism in most seafood, only
seven Shewanella phages have been sequenced and their endolysins have not been …
seven Shewanella phages have been sequenced and their endolysins have not been …