Search Results - "Park, Joseph K."
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Systematic literature review and meta-analysis on use of Thrombopoietic agents for chemotherapy-induced thrombocytopenia
Published in PloS one (09-06-2022)“…Currently, there are no approved options to prevent or treat chemotherapy-induced thrombocytopenia (CIT). We performed a systematic literature review and…”
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Protein competition switches the function of COP9 from self-renewal to differentiation
Published in Nature (London) (09-10-2014)“…Using biochemical and genetic approaches, a protein-competition-based mechanism that controls the balance between stem cell self-renewal and differentiation of…”
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Bam and Bgcn antagonize Nanos-dependent germ-line stem cell maintenance
Published in Proceedings of the National Academy of Sciences - PNAS (09-06-2009)“…The balance between germ-line stem cell (GSC) self-renewal and differentiation in Drosophila ovaries is mediated by the antagonistic relationship between the…”
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The miRNA Pathway Intrinsically Controls Self-Renewal of Drosophila Germline Stem Cells
Published in Current biology (20-03-2007)“…Stem cells uniquely self-renew and maintain tissue homoeostasis by differentiating into different cell types to replace aged or damaged cells [1]. During…”
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Stonewalling Drosophila stem cell differentiation by epigenetic controls
Published in Development (Cambridge) (01-04-2007)“…During Drosophila oogenesis, germline stem cell (GSC) identity is maintained largely by preventing the expression of factors that promote differentiation. This…”
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The incidence of thrombocytopenia in adult patients receiving chemotherapy for solid tumors or hematologic malignancies
Published in European journal of haematology (01-05-2021)“…Objectives To estimate the risk of thrombocytopenia in various cancers and chemotherapy regimens. Methods Structured patient‐level data from the Flatiron…”
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Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease
Published in American journal of human genetics (01-03-2003)“…Gaucher disease results from an autosomal recessive deficiency of the lysosomal enzyme glucocerebrosidase. The glucocerebrosidase gene is located in a…”
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Myoclonic epilepsy in Gaucher disease: Genotype-phenotype insights from a rare patient subgroup
Published in Pediatric research (01-03-2003)“…Gaucher disease, the inherited deficiency of lysosomal glucocerebrosidase, presents with a wide spectrum of manifestations. Although Gaucher disease has been…”
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Assessment of romiplostim immunogenicity in adult patients in clinical trials and in a global postmarketing registry
Published in British journal of haematology (01-09-2020)“…Summary Antibodies to first‐generation recombinant thrombopoietin (TPO) neutralized endogenous TPO and caused thrombocytopenia in some healthy subjects and…”
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A Randomized, Double-Blind, Placebo-Controlled, Phase III Noninferiority Study of the Long-Term Safety and Efficacy of Darbepoetin Alfa for Chemotherapy-Induced Anemia in Patients With Advanced NSCLC
Published in Journal of thoracic oncology (01-02-2020)“…This study evaluated noninferiority of darbepoetin alfa versus placebo for overall survival (OS) and progression-free survival (PFS) in anemic patients with…”
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Biology of the bone marrow microenvironment and myelodysplastic syndromes
Published in Molecular genetics and metabolism (01-09-2015)“…Myelodysplastic syndromes (MDS) are characterized by cytopenias resulting from ineffective hematopoiesis with a predisposition to transform to acute myeloid…”
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Dicer-1, but not Loquacious, is critical for assembly of miRNA-induced silencing complexes
Published in RNA (Cambridge) (01-12-2007)“…Double-stranded RNA-binding proteins (dsRBPs), such as R2D2 and Loquacious (Loqs), function in tandem with Dicer (Dcr) enzymes in RNA interference (RNAi). In…”
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Hepatoblastoma Arising in a Pigmented β-catenin-activated Hepatocellular Adenoma: Case Report and Review of the Literature
Published in The American journal of surgical pathology (01-07-2016)“…Hepatoblastoma is the most common malignant liver tumor in childhood. It has been associated with a variety of constitutional syndromes and gene mutations…”
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Phenotypic continuum in neuronopathic gaucher disease: an intermediate phenotype between type 2 and type 3
Published in The Journal of pediatrics (01-08-2003)“…Neuronopathic Gaucher disease, classically divided into two types, can have a continuum of phenotypes, often defying categorization. Nine children had an…”
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Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype
Published in Molecular genetics and metabolism (01-08-2002)“…Gaucher disease, the inherited deficiency of lysosomal glucocerebrosidase, presents with a wide spectrum of clinical manifestations including neuronopathic and…”
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VELOCITY-Lung: A phase (Ph) 2 study evaluating safety and efficacy of domvanalimab (dom) + zimberelimab (zim) + sacituzumab govitecan (SG), or etrumadenant (etruma) + dom + zim, or etruma + zim in patients (pts) with treatment-naïve metastatic non-small cell lung cancer (mNSCLC)
Published in Journal of clinical oncology (01-06-2023)“…TPS9155 Background: Current standard of care (SOC) for pts with mNSCLC lacking an actionable mutation includes checkpoint inhibitor (CPI), platinum (PT)-based…”
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Sotorasib for previously treated colorectal cancers with KRASG12C mutation (CodeBreaK100): a prespecified analysis of a single-arm, phase 2 trial
Published in The lancet oncology (01-01-2022)“…Sotorasib, a specific, irreversible KRASG12C protein inhibitor, has shown monotherapy clinical activity in KRASG12C-mutated solid tumours, including colorectal…”
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Sotorasib for previously treated colorectal cancers with KRAS G12C mutation (CodeBreaK100): a prespecified analysis of a single-arm, phase 2 trial
Published in The lancet oncology (01-01-2022)“…Sotorasib, a specific, irreversible KRAS protein inhibitor, has shown monotherapy clinical activity in KRAS -mutated solid tumours, including colorectal…”
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Analysis and Classification of 304 Mutant Alleles in Patients with Type 1 and Type 3 Gaucher Disease
Published in American journal of human genetics (01-06-2000)“…Gaucher disease results from the inherited deficiency of the enzyme glucocerebrosidase (EC 3.2.1.45). Although >100 mutations in the gene for human…”
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