Research paperRuxolitinib for the management of myelofibrosis: Results of an international physician survey Fulltext Access 4 Pages 2017
Emergence of novel and dominant acquired EGFR solvent-front mutations at Gly796 (G796S/R) together with C797S/R and L792F/H mutations in one EGFR (L858R/T790M) NSCLC patient who progressed on osimertinib Fulltext Access 4 Pages 2017
Short communicationInvestigation of patterns of nodal metastases in BRAF mutant lung cancer Fulltext Access 4 Pages 2017
Which patients with ES-SCLC are most likely to benefit from more aggressive radiotherapy: A secondary analysis of the Phase III CREST trial Fulltext Access 4 Pages 2017
Quantitative cell-free circulating EGFR mutation concentration is correlated with tumor burden in advanced NSCLC patients Fulltext Access 4 Pages 2017
Heterogeneous resistance mechanisms in an EGFR exon 19-mutated non-small cell lung cancer patient treated with erlotinib: Persistent FGFR3-mutation, localized transformation to EGFR-mutated SCLC, and acquired T790M EGFR-mutation Fulltext Access 4 Pages 2017
Review articlePD-L1 IHC in NSCLC with a global and methodological perspective Fulltext Access 4 Pages 2017
A primary esophageal MALT lymphoma patient with Helicobacter pylori infection achieved complete remission after H. pylori eradication without anti-lymphoma treatment Fulltext Access 4 Pages 2017
Haptoglobin is frequently low in patients with myelofibrosis: Clinical relevance Fulltext Access 4 Pages 2017
The effects of azacitidine on the response and prognosis of myelodysplastic syndrome and acute myeloid leukemia involving a bone marrow erythroblast frequency of >50% Fulltext Access 4 Pages 2017
Incidences and outcomes of therapy-related chronic myeloid leukemia in the era of tyrosine kinase inhibitors: Surveillance of the CML Cooperative Study Group Fulltext Access 4 Pages 2017
Research paperQuantitative miR analysis in chronic lymphocytic leukaemia/small lymphocytic lymphoma - proliferation centres are characterized by high miR-92a and miR-155 and low miR-150 expression Fulltext Access 4 Pages 2017
Research paperRefractory macrocytic anemias in patients with clonal hematopoietic disorders and isolated mutations of the spliceosome gene ZRSR2 Fulltext Access 4 Pages 2017
Case reportSequential liquid biopsies reveal dynamic alterations of EGFR driver mutations and indicate EGFR amplification as a new mechanism of resistance to osimertinib in NSCLC Fulltext Access 4 Pages 2017
Research paperA rare e13a3 (b2a3) BCR-ABL1 fusion transcript with normal karyotype in chronic myeloid leukemia: The challenges in diagnosis and monitoring minimal residual disease (MRD) Fulltext Access 4 Pages 2017
Research paperSharing post-AML consolidation supportive therapy with local centers reduces patient travel burden without compromising outcomes Fulltext Access 4 Pages 2017
Research paperLow Protein Z levels in patients with plasma cell neoplasms are inversely correlated with IL-6 levels Fulltext Access 4 Pages 2017
A review of the mechanism of action and clinical applications of sorafenib in advanced osteosarcoma Fulltext Access 4 Pages 2017
EJC Biennial ReportEuropean Journal of Cancer's Biennial report on soft tissue and visceral sarcomas or the rapid evolution of treatment concepts in sarcomas Fulltext Access 4 Pages 2017
Regression of melanoma metastases and multiple non-melanoma skin cancers in xeroderma pigmentosum by the PD1-antibody pembrolizumab Fulltext Access 4 Pages 2017
Germline polymorphisms on RET proto-oncogene involved in medullary thyroid carcinoma in a Druze family Fulltext Access 4 Pages 2017
Identification of a novel CSF3R-SPTAN1 fusion gene in an atypical chronic myeloid leukemia patient with t(1;9)(p34;q34) by RNA-Seq Fulltext Access 4 Pages 2017
Stage IV colorectal cancer primary site and patterns of distant metastasis Fulltext Access 4 Pages 2017
A novel germline TP53 mutation p.Pro190Arg detected in a patient with lung and bilateral breast cancers Fulltext Access 4 Pages 2017
Microgranular acute promyelocytic leukemia presenting with leukopenia and an unusual immunophenotype Fulltext Access 4 Pages 2017
Successful medical management of a neonate with spontaneous splenic rupture and severe hemophilia A Fulltext Access 4 Pages 2017
Disseminated Mycobacterium chelonae infection in a patient with T-cell lymphoma Fulltext Access 4 Pages 2017
Characterization of a novel variant BCR-ABL1 fusion transcript in a patient with chronic myeloid leukemia: Implications for molecular monitoring Fulltext Access 4 Pages 2017
Immediate completion lymph node dissection in stage IIIA melanoma does not provide significant additional staging information beyond EORTC SN tumour burden criteria Fulltext Access 4 Pages 2017
Immune checkpoint inhibitor-associated CNS autoimmune disorder (ICICAD) following nivolumab treatment: A new entity of drug-induced autoimmune encephalitis? Fulltext Access 4 Pages 2017
Overexpression of ubiquitin carboxyl-terminal hydrolase L1 (UCHL1) in serum of children after thermal injury Fulltext Access 4 Pages 2017
Serum chemerin in children with excess body weight may be associated with ongoing metabolic complications - A pilot study Fulltext Access 4 Pages 2017
MDS classification is improving in an era of the WHO 2016 criteria of MDS: A population-based analysis among 9159 MDS patients diagnosed in the Netherlands Fulltext Access 4 Pages 2017
XPA is primarily cytoplasmic but is transported into the nucleus upon UV damage in a cell cycle dependent manner Fulltext Access 4 Pages 2017
High glucose derived endothelial microparticles increase active caspase-3 and reduce microRNA-Let-7a expression in endothelial cells Fulltext Access 4 Pages 2017
Electrical pulse stimulation decreases electrochemical Na+ and K+ gradients in C2C12 myotubes Fulltext Access 4 Pages 2017
Mutation spectrum resulting in M13mp2 phage DNA exposed to N-nitrosoproline with UVA irradiation Fulltext Access 4 Pages 2017
Lack of response to nivolumab in a patient with EGFR-mutant non-small cell lung cancer adenocarcinoma sub-type transformed to small cell lung cancer Fulltext Access 4 Pages 2017
Short communicationUniform and blinded cause of death verification of the NELSON lung cancer screening participants Fulltext Access 4 Pages 2017
Short communicationEmergence of EGFR G724S mutation in EGFR-mutant lung adenocarcinoma post progression on osimertinib Fulltext Access 4 Pages 2017
Emergence of FGFR3-TACC3 fusions as a potential by-pass resistance mechanism to EGFR tyrosine kinase inhibitors in EGFR mutated NSCLC patients Fulltext Access 4 Pages 2017
Induced pluripotent stem cells derived from Bernard-Soulier Syndrome patient's peripheral blood cells with a p.Phe55Ser mutation in the GPIX gene Fulltext Access 4 Pages 2017
Isolation and characterization of Sprague-Dawley and Wistar Kyoto GFP rat embryonic stem cells Fulltext Access 4 Pages 2017
Establishment of an induced pluripotent stem cell (iPSC) line from a 9-year old male with autism spectrum disorder (ASD) Fulltext Access 4 Pages 2017
Generation of induced pluripotent stem cell (iPSC) line from a 36-year-old Charcot-Marie-Tooth disease patient with GJB1 mutation (CMTX) Fulltext Access 4 Pages 2017
An integration-free, virus-free rhesus macaque induced pluripotent stem cell line (riPSC90) from embryonic fibroblasts Fulltext Access 4 Pages 2017
Generation of Macaca fascicularis iPS cell line ATCi-MF1 from adult skin fibroblasts using non-integrative Sendai viruses Fulltext Access 4 Pages 2017
Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring Fulltext Access 4 Pages 2017
Establishment of MUi009 - A human induced pluripotent stem cells from a 32 year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2 Fulltext Access 4 Pages 2017
Peripheral blood derived induced pluripotent stem cells (iPSCs) from a female with familial hypertrophic cardiomyopathy Fulltext Access 4 Pages 2017
Generation and characterization of two iPSC lines from human epicardium-derived cells Fulltext Access 4 Pages 2017
Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1 Fulltext Access 4 Pages 2017
A feeder- and xeno-free human induced pluripotent stem cell line obtained from primary human dermal fibroblasts with epigenetic repression of reprogramming factors expression: GPCCi001-A Fulltext Access 4 Pages 2017
Generation and characterization of a human iPSC cell line expressing inducible Cas9 in the “safe harbor” AAVS1 locus Fulltext Access 4 Pages 2017
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 13 (MODY13) with a the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) mutation Fulltext Access 4 Pages 2017
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with “highest risk” RET mutation Fulltext Access 4 Pages 2017
Generation of an OCT4 reporter human induced pluripotent stem cell line using CRISPR/SpCas9 Fulltext Access 4 Pages 2017
A Marfan syndrome human induced pluripotent stem cell line with a heterozygous FBN1 c.4082G > A mutation, ISMMSi002-B, for disease modeling Fulltext Access 4 Pages 2017
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient Fulltext Access 4 Pages 2017
Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblasts Fulltext Access 4 Pages 2017
Generation of an induced pluripotent stem cell line, IBMS-iPSC-014-05, from a female autosomal dominant polycystic kidney disease patient carrying a common mutation of R803X in PKD2 Fulltext Access 4 Pages 2017
Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B Fulltext Access 4 Pages 2017
Generation of human erythroblast-derived iPSC line using episomal reprogramming system Fulltext Access 4 Pages 2017
Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation Fulltext Access 4 Pages 2017
Generation of a human control PBMC derived iPS cell line TUSMi001-A from a healthy male donor of Han Chinese genetic background Fulltext Access 4 Pages 2017
Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi) Fulltext Access 4 Pages 2017
Horning cell self-digestion: Autophagy wins the 2016 Nobel Prize in Physiology or Medicine Fulltext Access 4 Pages 2017
Food for thought: Autophagy researcher wins 2016 Nobel Prize in Physiology or Medicine Fulltext Access 4 Pages 2017
Brief ArticlesTargeting Integrin α4β7 in Steroid-Refractory Intestinal Graft-versus-Host Disease Fulltext Access 4 Pages 2017
Pretransplantation Exercise and Hematopoietic Cell Transplantation Survival: A Secondary Analysis of Blood and Marrow Transplant Clinical Trials Network (BMT CTN 0902) Fulltext Access 4 Pages 2017
Allogeneic Hematopoietic Cell Transplantation for Aggressive NK Cell Leukemia. A Center for International Blood and Marrow Transplant Research Analysis Fulltext Access 4 Pages 2017
ReviewPP2A regulates signaling through hormonal receptors in breast cancer with important therapeutic implications Fulltext Access 4 Pages 2017
Derivation of mouse embryonic stem cell lines from tyrosine hydroxylase reporter mice crossed with a human SNCA transgenic mouse model of Parkinson's disease Fulltext Access 4 Pages 2017
Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi001-A) and non-demented control (ASUi002-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant Fulltext Access 4 Pages 2017
Establishment of a congenital tooth agenesis related gene MSX1 knockout human embryonic stem cell lines by CRISPR-Cas9 technology Fulltext Access 4 Pages 2017
Generation, genome edition and characterization of iPSC lines from a patient with coenzyme Q10 deficiency harboring a heterozygous mutation in COQ4 gene Fulltext Access 4 Pages 2017
Generation of induced pluripotent stem cell (iPSC) line from a patient with triple negative breast cancer with hereditary exon 17 deletion of BRCA1 gene Fulltext Access 4 Pages 2017
Derivation and characterization of integration-free iPSC line ISRM-UM51 derived from SIX2-positive renal cells isolated from urine of an African male expressing the CYP2D6 *4/*17 variant which confers intermediate drug metabolizing activity Fulltext Access 4 Pages 2017
Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene Fulltext Access 4 Pages 2017
Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C > A; p.Ser545Arg Fulltext Access 4 Pages 2017
Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene Fulltext Access 4 Pages 2017
Generation of induced pluripotent stem cells (ARO-iPSC1-11) from a patient with autosomal recessive osteopetrosis harboring the c.212 + 1G > T mutation in SNX10 gene Fulltext Access 4 Pages 2017
Induced pluripotent stem cells derived from a patient with familial idiopathic basal ganglia calcification (IBGC) caused by a mutation in SLC20A2 gene Fulltext Access 4 Pages 2017
Establishment of DYT5 patient-specific induced pluripotent stem cells with a GCH1 mutation Fulltext Access 4 Pages 2017
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation Fulltext Access 4 Pages 2017
Generation of a pig induced pluripotent stem cell (piPSC) line from embryonic fibroblasts by incorporating LIN28 to the four transcriptional factor-mediated reprogramming: VSMUi001-D Fulltext Access 4 Pages 2017
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation Fulltext Access 4 Pages 2017
Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene Fulltext Access 4 Pages 2017
Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using integration free Sendai virus technology Fulltext Access 4 Pages 2017