Science is social

Science is social Science is social, Published online: 28 November 2018; doi:10.1038/s41588-018-0308-4 Well-designed science education via social media may help to reach a larger group of audiences with the aim of reducing the boundaries between researchers and the public. This

Complements from the Lung

Foreword. In this Journal feature, information about a real patient is presented in stages (boldface type) to an expert clinician, who responds to the information by sharing relevant background and reasoning with the reader (regular type). The authors’ commentary follows.

Investigation of clinically relevant germline variants detected by next-generation sequencing in patients with childhood cancer: a review of the literature

Genetic predisposition is an important underlying cause of childhood cancer, although the proportion of patients with childhood cancer carrying predisposing pathogenic germline variants is uncertain. This review considers the pathogenic or likely pathogenic germline variants reported by six studies that

In review

The end of the year is a conventional time to take stock and assess ones performance over the preceding 12-month period. Comparisons are invariably the currency of these evaluations. Both the notion of evaluation, and the use of comparisons as

Integrative Proteomic Profiling Reveals PRC2-Dependent Epigenetic Crosstalk Maintains Ground-State Pluripotency

Marks and colleagues use integrative mass spectrometry to profile post-translational histone modifications and the chromatin-associated proteome in ground-state pluripotency. This reveals H3K27me3 and PRC2 as widespread hallmarks on euchromatin and heterochromatin. They show that ubiquitous chromatin-associated PRC2 protects the epigenome

Retraction

Sato Y, Asoh T, Metoki N, et al. Efficacy of methylprednisolone pulse therapy on neuroleptic malignant syndrome in Parkinson’s disease. J Neurol Neurosurg Psychiatry 2003;74:574–576. This article has been retracted. The editor received a letter from Dr Yoshihiro Sato retracting this article

Risk classification in primary prevention of CVD according to QRISK2 and JBS3 ‘heart age, and prevalence of elevated high-sensitivity C reactive protein in the UK cohort of the EURIKA study

Objectives This study assessed cardiovascular disease (CVD) risk classification according to QRISK2, JBS3 ‘heart age’ and the prevalence of elevated high-sensitivity C reactive protein (hsCRP) in UK primary prevention patients. Method The European Study on Cardiovascular Prevention and Management in

Calprotectin is not independent from baseline erosion in predicting radiological progression in early rheumatoid arthritis. Comment on ‘Calprotectin as a marker of inflammation in patients with early rheumatoid arthritis by Jonsson et al

We have read with great interest the article by Jonsson et al that was recently published online in ARD,1 which suggested that calprotectin, also known as S100A8/S100A9 heterodimer, was associated with radiographic progression in early rheumatoid arthritis (RA). Calprotectin correlates

Personalized DNA methylomics

Personalized DNA methylomics Personalized DNA methylomics, Published online: 15 November 2018; doi:10.1038/s41576-018-0076-0 A study in Nature Medicine reports the DNA methylome and transcriptome of an individual, and suggests that changes in the methylome and transcriptome might be associated with chronic

Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome, Published online: 14 November 2018; doi:10.1038/s41588-018-0304-8

Cancer chromatin accessed

Cancer chromatin accessed Cancer chromatin accessed, Published online: 14 November 2018; doi:10.1038/s41576-018-0075-1 A study in Science reports the genome-wide chromatin accessibility profiles across 23 cancer types from The Cancer Genome Atlas and notably increases the number of known gene regulatory

Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L

Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L, Published online: 13 November 2018; doi:10.1038/s41588-018-0293-7 Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L

Author Correction: Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors

Author Correction: Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors Author Correction: Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors, Published online: 12 November 2018; doi:10.1038/s41588-018-0299-1 Author Correction: Reference component

Equitably improving outcomes for cancer survivors and supporting caregivers: A blueprint for care delivery, research, education, and policy

Abstract Cancer care delivery is being shaped by growing numbers of cancer survivors coupled with provider shortages, rising costs of primary treatment and follow‐up care, significant survivorship health disparities, increased reliance on informal caregivers, and the transition to value‐based care.

Author Correction: Distinguishing genetic correlation from causation across 52 diseases and complex traits

Author Correction: Distinguishing genetic correlation from causation across 52 diseases and complex traits Author Correction: Distinguishing genetic correlation from causation across 52 diseases and complex traits, Published online: 06 November 2018; doi:10.1038/s41588-018-0296-4 Author Correction: Distinguishing genetic correlation from causation across

Efficacy and safety of ramucirumab-containing chemotherapy in patients with pretreated metastatic gastric neuroendocrine carcinoma

Background Ramucirumab (RAM), a monoclonal antibody for vascular endothelial growth factor 2 (VEGFR2), has been effective for advanced gastric adenocarcinoma (AC). However, little is known about the efficacy of RAM-containing chemotherapy (RAM-CTx) in gastric neuroendocrine carcinoma (G-NEC). Methods We retrospectively

Diverticulitis

Foreword. This Journal feature begins with a case vignette highlighting a common clinical problem. Evidence supporting various strategies is then presented, followed by a review of formal guidelines, when they exist. The article ends with the author’s clinical recommendations. Stage.

WhatsApp WhatsApp'tan Bize Yazın