Pages that link to "Q59155620"
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The following pages link to Chava Kimchi-Sarfaty (Q59155620):
Displaying 50 items.
- A "silent" polymorphism in the MDR1 gene changes substrate specificity (Q29619435) (← links)
- Endogenous factor VIII synthesis from the intron 22-inverted F8 locus may modulate the immunogenicity of replacement therapy for hemophilia A (Q30585975) (← links)
- Multiple in silico tools predict phenotypic manifestations in congenital thrombotic thrombocytopenic purpura (Q33405479) (← links)
- A mechanistic investigation of thrombotic microangiopathy associated with IV abuse of Opana ER. (Q33436940) (← links)
- Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease (Q33490606) (← links)
- A gene-specific method for predicting hemophilia-causing point mutations (Q33642338) (← links)
- P-glycoprotein: from genomics to mechanism. (Q34272173) (← links)
- Characterization of coding synonymous and non-synonymous variants in ADAMTS13 using ex vivo and in silico approaches (Q34328026) (← links)
- Sensitive measurement of single-nucleotide polymorphism-induced changes of RNA conformation: application to disease studies (Q34466528) (← links)
- SV40 Pseudovirion gene delivery of a toxin to treat human adenocarcinomas in mice. (Q34695978) (← links)
- Inhibition of Multidrug Resistance by SV40 Pseudovirion Delivery of an Antigene Peptide Nucleic Acid (PNA) in Cultured Cells (Q34708277) (← links)
- Small ncRNA Expression-Profiling of Blood from Hemophilia A Patients Identifies miR-1246 as a Potential Regulator of Factor 8 Gene (Q35692013) (← links)
- Ethnicity-related polymorphisms and haplotypes in the human ABCB1 gene (Q35809516) (← links)
- SV40 pseudovirions as highly efficient vectors for gene transfer and their potential application in cancer therapy. (Q35950104) (← links)
- Cyclosporin A impairs the secretion and activity of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type 1 repeat). (Q36492812) (← links)
- MDR1 synonymous polymorphisms alter transporter specificity and protein stability in a stable epithelial monolayer (Q36669409) (← links)
- Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma (Q37104104) (← links)
- Detection of intracellular ADAMTS13, a secreted zinc-metalloprotease, via flow cytometry. (Q37424217) (← links)
- The development of gene therapy: from monogenic recessive disorders to complex diseases such as cancer. (Q37535778) (← links)
- Silent (synonymous) SNPs: should we care about them? (Q37600712) (← links)
- Understanding the contribution of synonymous mutations to human disease (Q37924093) (← links)
- Building better drugs: developing and regulating engineered therapeutic proteins. (Q38141225) (← links)
- Exposing synonymous mutations (Q38222377) (← links)
- Relative abundance of growth hormone receptor isoforms in rhesus monkey tissues and human transformed lymphocytes. (Q38356077) (← links)
- Single synonymous mutation in factor IX alters protein properties and underlies haemophilia B. (Q38779043) (← links)
- The importance of mRNA structure in determining the pathogenicity of synonymous and non-synonymous mutations in haemophilia (Q38785317) (← links)
- Recent advances in (therapeutic protein) drug development. (Q39148639) (← links)
- Cyclosporin A-dependent downregulation of the Na+/Ca2+ exchanger expression. (Q40143495) (← links)
- Transcriptional and translational regulation of the splicing isoforms of the growth hormone receptor by glucocorticoids. (Q40659509) (← links)
- High cloning capacity of in vitro packaged SV40 vectors with no SV40 virus sequences. (Q40667017) (← links)
- NCX1 surface expression: a tool to identify structural elements of functional importance. (Q40681085) (← links)
- In vitro-packaged SV40 pseudovirions as highly efficient vectors for gene transfer. (Q40754575) (← links)
- Transport activity and surface expression of the Na+-Ca2+ exchanger NCX1 are inhibited by the immunosuppressive agent cyclosporin A and by the nonimmunosuppressive agent PSC833. (Q40769608) (← links)
- A new and updated resource for codon usage tables (Q41597869) (← links)
- Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B. (Q41732261) (← links)
- Transduction of multiple cell types using improved conditions for gene delivery and expression of SV40 pseudovirions packaged in vitro. (Q44037086) (← links)
- Endoreduplication and polyploidy in fragile X cells induced by methotrexate and fluorodeoxyuridine: Implications for diagnosis (Q45227125) (← links)
- Functional characterization of coding polymorphisms in the human MDR1 gene using a vaccinia virus expression system. (Q45732147) (← links)
- Factor IX oligomerization underlies reduced activity upon disruption of physiological conditions. (Q45861473) (← links)
- Analysis of F9 point mutations and their correlation to severity of haemophilia B disease (Q45879366) (← links)
- Single-nucleotide variations defining previously unreported ADAMTS13 haplotypes are associated with differential expression and activity of the VWF-cleaving protease in a Salvadoran congenital thrombotic thrombocytopenic purpura family. (Q46027623) (← links)
- Elevated preoperative von Willebrand factor is associated with perioperative thrombosis in infants and neonates with congenital heart disease (Q47244753) (← links)
- Differences in rhodamine-123 efflux in B-type chronic lymphocytic leukemia suggest possible gender and stage variations in drug-resistance gene activity. (Q47815821) (← links)
- A splice variant of ADAMTS13 is expressed in human hepatic stellate cells and cancerous tissues. (Q49865252) (← links)
- Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females. (Q52019081) (← links)
- The sounds of silence: synonymous mutations affect function (Q80456034) (← links)
- Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels (Q89777008) (← links)
- A Single Synonymous Variant (c.354G>A [p.P118P]) in ADAMTS13 Confers Enhanced Specific Activity (Q91299302) (← links)
- Codon and Codon-Pair Usage Tables (CoCoPUTs): Facilitating Genetic Variation Analyses and Recombinant Gene Design (Q91567394) (← links)
- The Kazusa codon usage database, CoCoPUTs, and the value of up-to-date codon usage statistics (Q92115202) (← links)