Related Experiment Videos
Gaucher type I (Ashkenazi) disease: considerations for heterozygote detection and prenatal diagnosis
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation.
The pharmacogenomics journal·2012
Enzyme replacement therapy for lysosomal diseases: lessons from 20 years of experience and remaining challenges.
Annual review of genomics and human genetics·2012
Multi-ethnic distribution of clinically relevant CYP2C genotypes and haplotypes.
The pharmacogenomics journal·2012
Identification of CYP2C19*4B: pharmacogenetic implications for drug metabolism including clopidogrel responsiveness.
The pharmacogenomics journal·2011
Accumulation and distribution of α-synuclein and ubiquitin in the CNS of Gaucher disease mouse models.
Molecular genetics and metabolism·2011
DNA homology and chromosome stability: a sensitive yeast genetic system for identifying double-stranded DNA damage.
Progress in clinical and biological research·2018
Interaction of lipopolysaccharide with a mammalian lyso-phosphatidate acyltransferase (LPAAT) transfected into E. coli, and effect of lisofylline on LPAAT transfected into mammalian cells.
Progress in clinical and biological research·1998
The molecular basis for therapeutic concepts utilizing CD14.
Progress in clinical and biological research·1998
Endotoxin tolerance alters macrophage membrane regulatory G proteins.
Progress in clinical and biological research·1998
Molecular mechanisms responsible for endotoxin tolerance.
Progress in clinical and biological research·1998
Antibiotic-mediated release of endotoxin and the pathogenesis of gram-negative sepsis.
Progress in clinical and biological research·1998
Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.
The Journal of allergy and clinical immunology·2026
CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.
Molecular genetics and genomics : MGG·2026
Congenital Hyperinsulinism With Paternally Inherited ABCC8 Variants: A Single Center Experience Over a Decade in Singapore.
Journal of the ASEAN Federation of Endocrine Societies·2026