听力与言语-语言病理学

行为科学

医学伦理学

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  • Bending the genome.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0270-1

    authors: Rusk N

    更新日期:2019-01-01 00:00:00

  • Imaging cellular ultrastructures using expansion microscopy (U-ExM).

    abstract::Determining the structure and composition of macromolecular assemblies is a major challenge in biology. Here we describe ultrastructure expansion microscopy (U-ExM), an extension of expansion microscopy that allows the visualization of preserved ultrastructures by optical microscopy. This method allows for near-native...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0238-1

    authors: Gambarotto D,Zwettler FU,Le Guennec M,Schmidt-Cernohorska M,Fortun D,Borgers S,Heine J,Schloetel JG,Reuss M,Unser M,Boyden ES,Sauer M,Hamel V,Guichard P

    更新日期:2019-01-01 00:00:00

  • fMRIPrep: a robust preprocessing pipeline for functional MRI.

    abstract::Preprocessing of functional magnetic resonance imaging (fMRI) involves numerous steps to clean and standardize the data before statistical analysis. Generally, researchers create ad hoc preprocessing workflows for each dataset, building upon a large inventory of available tools. The complexity of these workflows has s...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0235-4

    authors: Esteban O,Markiewicz CJ,Blair RW,Moodie CA,Isik AI,Erramuzpe A,Kent JD,Goncalves M,DuPre E,Snyder M,Oya H,Ghosh SS,Wright J,Durnez J,Poldrack RA,Gorgolewski KJ

    更新日期:2019-01-01 00:00:00

  • Identification of differentially methylated cell types in epigenome-wide association studies.

    abstract::An outstanding challenge of epigenome-wide association studies (EWASs) performed in complex tissues is the identification of the specific cell type(s) responsible for the observed differential DNA methylation. Here we present a statistical algorithm called CellDMC ( https://github.com/sjczheng/EpiDISH ), which can ide...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0213-x

    authors: Zheng SC,Breeze CE,Beck S,Teschendorff AE

    更新日期:2018-12-01 00:00:00

  • Enhanced antibody validation.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 评论,杂志文章

    doi:10.1038/s41592-018-0248-z

    authors: Doerr A

    更新日期:2018-12-01 00:00:00

  • Changes at Nature Methods.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 社论

    doi:10.1038/s41592-018-0257-y

    authors:

    更新日期:2018-12-01 00:00:00

  • Finding S-sulfinylated proteins.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 评论,杂志文章

    doi:10.1038/s41592-018-0200-2

    authors: Doerr A

    更新日期:2018-11-01 00:00:00

  • FLIRT: fast local infrared thermogenetics for subcellular control of protein function.

    abstract::FLIRT (fast local infrared thermogenetics) is a microscopy-based technology to locally and reversibly manipulate protein function while simultaneously monitoring the effects in vivo. FLIRT locally inactivates fast-acting temperature-sensitive mutant proteins. We demonstrate that FLIRT can control temperature-sensitive...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0168-y

    authors: Hirsch SM,Sundaramoorthy S,Davies T,Zhuravlev Y,Waters JC,Shirasu-Hiza M,Dumont J,Canman JC

    更新日期:2018-11-01 00:00:00

  • Anna Moroni.

    abstract:: ...

    journal_title:Nature methods

    pub_type: 评论,新闻

    doi:10.1038/s41592-018-0192-y

    authors: Marx V

    更新日期:2018-11-01 00:00:00

  • Terminal exon characterization with TECtool reveals an abundance of cell-specific isoforms.

    abstract::Sequencing of RNA 3' ends has uncovered numerous sites that do not correspond to the termination sites of known transcripts. Through their 3' untranslated regions, protein-coding RNAs interact with RNA-binding proteins and microRNAs, which regulate many properties, including RNA stability and subcellular localization....

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0114-z

    authors: Gruber AJ,Gypas F,Riba A,Schmidt R,Zavolan M

    更新日期:2018-10-01 00:00:00

  • Author Correction: Genetically engineered cerebral organoids model brain tumor formation.

    abstract::In the originally published paper, the "before" image for the afatinib condition in Fig. 6c was incorrect. Instead of an image displaying a GBM-3 neoplastic organoid before afatinib treatment, this panel showed an image from the GBM-2 control (DMSO) group before treatment. This error has now been corrected in the HTML...

    journal_title:Nature methods

    pub_type: 已发布勘误

    doi:10.1038/s41592-018-0118-8

    authors: Bian S,Repic M,Guo Z,Kavirayani A,Burkard T,Bagley JA,Krauditsch C,Knoblich JA

    更新日期:2018-09-01 00:00:00

  • CRISPR off-target analysis in genetically engineered rats and mice.

    abstract::Despite widespread use of CRISPR, comprehensive data on the frequency and impact of Cas9-mediated off-targets in modified rodents are limited. Here we present deep-sequencing data from 81 genome-editing projects on mouse and rat genomes at 1,423 predicted off-target sites, 32 of which were confirmed, and show that hig...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0011-5

    authors: Anderson KR,Haeussler M,Watanabe C,Janakiraman V,Lund J,Modrusan Z,Stinson J,Bei Q,Buechler A,Yu C,Thamminana SR,Tam L,Sowick MA,Alcantar T,O'Neil N,Li J,Ta L,Lima L,Roose-Girma M,Rairdan X,Durinck S,Warming S

    更新日期:2018-07-01 00:00:00

  • High-speed volumetric imaging of neuronal activity in freely moving rodents.

    abstract::Thus far, optical recording of neuronal activity in freely behaving animals has been limited to a thin axial range. We present a head-mounted miniaturized light-field microscope (MiniLFM) capable of capturing neuronal network activity within a volume of 700 × 600 × 360 µm3 at 16 Hz in the hippocampus of freely moving ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/s41592-018-0008-0

    authors: Skocek O,Nöbauer T,Weilguny L,Martínez Traub F,Xia CN,Molodtsov MI,Grama A,Yamagata M,Aharoni D,Cox DD,Golshani P,Vaziri A

    更新日期:2018-06-01 00:00:00

  • Cell-type specific sequencing of microRNAs from complex animal tissues.

    abstract::MicroRNAs (miRNAs) play an essential role in the post-transcriptional regulation of animal development and physiology. However, in vivo studies aimed at linking miRNA function to the biology of distinct cell types within complex tissues remain challenging, partly because in vivo miRNA-profiling methods lack cellular r...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4610

    authors: Alberti C,Manzenreither RA,Sowemimo I,Burkard TR,Wang J,Mahofsky K,Ameres SL,Cochella L

    更新日期:2018-04-01 00:00:00

  • Localization-based super-resolution imaging meets high-content screening.

    abstract::Single-molecule localization microscopy techniques have proven to be essential tools for quantitatively monitoring biological processes at unprecedented spatial resolution. However, these techniques are very low throughput and are not yet compatible with fully automated, multiparametric cellular assays. This shortcomi...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4486

    authors: Beghin A,Kechkar A,Butler C,Levet F,Cabillic M,Rossier O,Giannone G,Galland R,Choquet D,Sibarita JB

    更新日期:2017-12-01 00:00:00

  • Long-term expansion of alveolar stem cells derived from human iPS cells in organoids.

    abstract::The stable expansion of tissue-specific stem cells in vitro has contributed to research on several organs. Alveolar epithelial type II (AT2) cells function as tissue stem cells in the lung, but robust models for studying human AT2 cells are lacking. Here we report a method for the efficient generation and long-term ex...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4448

    authors: Yamamoto Y,Gotoh S,Korogi Y,Seki M,Konishi S,Ikeo S,Sone N,Nagasaki T,Matsumoto H,Muro S,Ito I,Hirai T,Kohno T,Suzuki Y,Mishima M

    更新日期:2017-11-01 00:00:00

  • An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues.

    abstract::We present Omni-ATAC, an improved ATAC-seq protocol for chromatin accessibility profiling that works across multiple applications with substantial improvement of signal-to-background ratio and information content. The Omni-ATAC protocol generates chromatin accessibility profiles from archival frozen tissue samples and...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4396

    authors: Corces MR,Trevino AE,Hamilton EG,Greenside PG,Sinnott-Armstrong NA,Vesuna S,Satpathy AT,Rubin AJ,Montine KS,Wu B,Kathiria A,Cho SW,Mumbach MR,Carter AC,Kasowski M,Orloff LA,Risca VI,Kundaje A,Khavari PA,Montine TJ,

    更新日期:2017-10-01 00:00:00

  • Nm-seq maps 2'-O-methylation sites in human mRNA with base precision.

    abstract::The ribose of RNA nucleotides can be 2'-O-methylated (Nm). Despite advances in high-throughput detection, the inert chemical nature of Nm still limits sensitivity and precludes mapping in mRNA. We leveraged the differential reactivity of 2'-O-methylated and 2'-hydroxylated nucleosides to periodate oxidation to develop...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4294

    authors: Dai Q,Moshitch-Moshkovitz S,Han D,Kol N,Amariglio N,Rechavi G,Dominissini D,He C

    更新日期:2017-07-01 00:00:00

  • SCnorm: robust normalization of single-cell RNA-seq data.

    abstract::The normalization of RNA-seq data is essential for accurate downstream inference, but the assumptions upon which most normalization methods are based are not applicable in the single-cell setting. Consequently, applying existing normalization methods to single-cell RNA-seq data introduces artifacts that bias downstrea...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4263

    authors: Bacher R,Chu LF,Leng N,Gasch AP,Thomson JA,Stewart RM,Newton M,Kendziorski C

    更新日期:2017-06-01 00:00:00

  • Structural modeling of protein-RNA complexes using crosslinking of segmentally isotope-labeled RNA and MS/MS.

    abstract::Ribonucleoproteins (RNPs) are key regulators of cellular function. We established an efficient approach, crosslinking of segmentally isotope-labeled RNA and tandem mass spectrometry (CLIR-MS/MS), to localize protein-RNA interactions simultaneously at amino acid and nucleotide resolution. The approach was tested on pol...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4235

    authors: Dorn G,Leitner A,Boudet J,Campagne S,von Schroetter C,Moursy A,Aebersold R,Allain FH

    更新日期:2017-05-01 00:00:00

  • In vivo three-photon imaging of activity of GCaMP6-labeled neurons deep in intact mouse brain.

    abstract::High-resolution optical imaging is critical to understanding brain function. We demonstrate that three-photon microscopy at 1,300-nm excitation enables functional imaging of GCaMP6s-labeled neurons beyond the depth limit of two-photon microscopy. We record spontaneous activity from up to 150 neurons in the hippocampal...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4183

    authors: Ouzounov DG,Wang T,Wang M,Feng DD,Horton NG,Cruz-Hernández JC,Cheng YT,Reimer J,Tolias AS,Nishimura N,Xu C

    更新日期:2017-04-01 00:00:00

  • Visualization and analysis of single-cell RNA-seq data by kernel-based similarity learning.

    abstract::We present single-cell interpretation via multikernel learning (SIMLR), an analytic framework and software which learns a similarity measure from single-cell RNA-seq data in order to perform dimension reduction, clustering and visualization. On seven published data sets, we benchmark SIMLR against state-of-the-art met...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4207

    authors: Wang B,Zhu J,Pierson E,Ramazzotti D,Batzoglou S

    更新日期:2017-04-01 00:00:00

  • Pooled CRISPR screening with single-cell transcriptome readout.

    abstract::CRISPR-based genetic screens are accelerating biological discovery, but current methods have inherent limitations. Widely used pooled screens are restricted to simple readouts including cell proliferation and sortable marker proteins. Arrayed screens allow for comprehensive molecular readouts such as transcriptome pro...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4177

    authors: Datlinger P,Rendeiro AF,Schmidl C,Krausgruber T,Traxler P,Klughammer J,Schuster LC,Kuchler A,Alpar D,Bock C

    更新日期:2017-03-01 00:00:00

  • Post-translational selective intracellular silencing of acetylated proteins with de novo selected intrabodies.

    abstract::The ability to selectively interfere with post-translationally modified proteins would have many biological and therapeutic applications. However, post-translational modifications cannot be selectively targeted by nucleic-acid-based interference approaches. Here we describe post-translational intracellular silencing a...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4144

    authors: Chirichella M,Lisi S,Fantini M,Goracci M,Calvello M,Brandi R,Arisi I,D'Onofrio M,Di Primio C,Cattaneo A

    更新日期:2017-03-01 00:00:00

  • A guide to designing germline-dependent epigenetic inheritance experiments in mammals.

    abstract::Recent work has demonstrated that environmental factors experienced by parents can affect their offspring across multiple generations, and that such transgenerational transmission can depend on the germline. Causal evidence for the involvement of germ cells is rare, however, and the underlying molecular mechanisms rem...

    journal_title:Nature methods

    pub_type: 杂志文章,评审

    doi:10.1038/nmeth.4181

    authors: Bohacek J,Mansuy IM

    更新日期:2017-02-28 00:00:00

  • Atomic-resolution structures from fragmented protein crystals with the cryoEM method MicroED.

    abstract::Traditionally, crystallographic analysis of macromolecules has depended on large, well-ordered crystals, which often require significant effort to obtain. Even sizable crystals sometimes suffer from pathologies that render them inappropriate for high-resolution structure determination. Here we show that fragmentation ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4178

    authors: de la Cruz MJ,Hattne J,Shi D,Seidler P,Rodriguez J,Reyes FE,Sawaya MR,Cascio D,Weiss SC,Kim SK,Hinck CS,Hinck AP,Calero G,Eisenberg D,Gonen T

    更新日期:2017-02-13 00:00:00

  • In vivo quantification of spatially varying mechanical properties in developing tissues.

    abstract::The mechanical properties of the cellular microenvironment and their spatiotemporal variations are thought to play a central role in sculpting embryonic tissues, maintaining organ architecture and controlling cell behavior, including cell differentiation. However, no direct in vivo and in situ measurement of mechanica...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4101

    authors: Serwane F,Mongera A,Rowghanian P,Kealhofer DA,Lucio AA,Hockenbery ZM,Campàs O

    更新日期:2017-02-01 00:00:00

  • RESA identifies mRNA-regulatory sequences at high resolution.

    abstract::Gene expression is extensively regulated at the levels of mRNA stability, localization and translation. However, decoding functional RNA-regulatory features remains a limitation to understanding post-transcriptional regulation in vivo. Here, we developed RNA-element selection assay (RESA), a method that selects RNA el...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4121

    authors: Yartseva V,Takacs CM,Vejnar CE,Lee MT,Giraldez AJ

    更新日期:2017-02-01 00:00:00

  • Robust statistical modeling improves sensitivity of high-throughput RNA structure probing experiments.

    abstract::Structure probing coupled with high-throughput sequencing could revolutionize our understanding of the role of RNA structure in regulation of gene expression. Despite recent technological advances, intrinsic noise and high sequence coverage requirements greatly limit the applicability of these techniques. Here we desc...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4068

    authors: Selega A,Sirocchi C,Iosub I,Granneman S,Sanguinetti G

    更新日期:2017-01-01 00:00:00

  • Atmospheric pressure MALDI mass spectrometry imaging of tissues and cells at 1.4-μm lateral resolution.

    abstract::We report an atmospheric pressure (AP) matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) setup with a lateral resolution of 1.4 μm, a mass resolution greater than 100,000, and accuracy below ±2 p.p.m. We achieved this by coupling a focusing objective with a numerical aperture (NA) of ...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4071

    authors: Kompauer M,Heiles S,Spengler B

    更新日期:2017-01-01 00:00:00

  • Fluorescent indicators for simultaneous reporting of all four cell cycle phases.

    abstract::A robust method for simultaneous visualization of all four cell cycle phases in living cells is highly desirable. We developed an intensiometric reporter of the transition from S to G2 phase and engineered a far-red fluorescent protein, mMaroon1, to visualize chromatin condensation in mitosis. We combined these new re...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.4045

    authors: Bajar BT,Lam AJ,Badiee RK,Oh YH,Chu J,Zhou XX,Kim N,Kim BB,Chung M,Yablonovitch AL,Cruz BF,Kulalert K,Tao JJ,Meyer T,Su XD,Lin MZ

    更新日期:2016-12-01 00:00:00

  • An in vivo multiplexed small-molecule screening platform.

    abstract::Phenotype-based small-molecule screening is a powerful method to identify molecules that regulate cellular functions. However, such screens are generally performed in vitro under conditions that do not necessarily model complex physiological conditions or disease states. Here, we use molecular cell barcoding to enable...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3992

    authors: Grüner BM,Schulze CJ,Yang D,Ogasawara D,Dix MM,Rogers ZN,Chuang CH,McFarland CD,Chiou SH,Brown JM,Cravatt BF,Bogyo M,Winslow MM

    更新日期:2016-10-01 00:00:00

  • Stable long-term chronic brain mapping at the single-neuron level.

    abstract::Stable in vivo mapping and modulation of the same neurons and brain circuits over extended periods is critical to both neuroscience and medicine. Current electrical implants offer single-neuron spatiotemporal resolution but are limited by such factors as relative shear motion and chronic immune responses during long-t...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3969

    authors: Fu TM,Hong G,Zhou T,Schuhmann TG,Viveros RD,Lieber CM

    更新日期:2016-10-01 00:00:00

  • Virtual microfluidics for digital quantification and single-cell sequencing.

    abstract::We have developed hydrogel-based virtual microfluidics as a simple and robust alternative to complex engineered microfluidic systems for the compartmentalization of nucleic acid amplification reactions. We applied in-gel digital multiple displacement amplification (dMDA) to purified DNA templates, cultured bacterial c...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3955

    authors: Xu L,Brito IL,Alm EJ,Blainey PC

    更新日期:2016-09-01 00:00:00

  • Nanoscale imaging of RNA with expansion microscopy.

    abstract::The ability to image RNA identity and location with nanoscale precision in intact tissues is of great interest for defining cell types and states in normal and pathological biological settings. Here, we present a strategy for expansion microscopy of RNA. We developed a small-molecule linker that enables RNA to be cova...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3899

    authors: Chen F,Wassie AT,Cote AJ,Sinha A,Alon S,Asano S,Daugharthy ER,Chang JB,Marblestone A,Church GM,Raj A,Boyden ES

    更新日期:2016-08-01 00:00:00

  • Varying label density allows artifact-free analysis of membrane-protein nanoclusters.

    abstract::We present a method to robustly discriminate clustered from randomly distributed molecules detected with techniques based on single-molecule localization microscopy, such as PALM and STORM. The approach is based on deliberate variation of labeling density, such as titration of fluorescent antibody, combined with quant...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3897

    authors: Baumgart F,Arnold AM,Leskovar K,Staszek K,Fölser M,Weghuber J,Stockinger H,Schütz GJ

    更新日期:2016-08-01 00:00:00

  • Automated mapping of phenotype space with single-cell data.

    abstract::Accurate identification of cell subsets in complex populations is key to discovering novelty in multidimensional single-cell experiments. We present X-shift (http://web.stanford.edu/~samusik/vortex/), an algorithm that processes data sets using fast k-nearest-neighbor estimation of cell event density and arranges popu...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3863

    authors: Samusik N,Good Z,Spitzer MH,Davis KL,Nolan GP

    更新日期:2016-06-01 00:00:00

  • Quantitative super-resolution imaging with qPAINT.

    abstract::Counting molecules in complexes is challenging, even with super-resolution microscopy. Here, we use the programmable and specific binding of dye-labeled DNA probes to count integer numbers of targets. This method, called quantitative points accumulation in nanoscale topography (qPAINT), works independently of dye phot...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3804

    authors: Jungmann R,Avendaño MS,Dai M,Woehrstein JB,Agasti SS,Feiger Z,Rodal A,Yin P

    更新日期:2016-05-01 00:00:00

  • High-resolution mass spectrometry of small molecules bound to membrane proteins.

    abstract::Small molecules are known to stabilize membrane proteins and to modulate their function and oligomeric state, but such interactions are often hard to precisely define. Here we develop and apply a high-resolution, Orbitrap mass spectrometry-based method for analyzing intact membrane protein-ligand complexes. Using this...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3771

    authors: Gault J,Donlan JA,Liko I,Hopper JT,Gupta K,Housden NG,Struwe WB,Marty MT,Mize T,Bechara C,Zhu Y,Wu B,Kleanthous C,Belov M,Damoc E,Makarov A,Robinson CV

    更新日期:2016-04-01 00:00:00

  • Highly multiplexed simultaneous detection of RNAs and proteins in single cells.

    abstract::To enable the detection of expression signatures specific to individual cells, we developed PLAYR (proximity ligation assay for RNA), a method for highly multiplexed transcript quantification by flow and mass cytometry that is compatible with standard antibody staining. When used with mass cytometry, PLAYR allowed for...

    journal_title:Nature methods

    pub_type: 杂志文章

    doi:10.1038/nmeth.3742

    authors: Frei AP,Bava FA,Zunder ER,Hsieh EW,Chen SY,Nolan GP,Gherardini PF

    更新日期:2016-03-01 00:00:00

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