听力与言语-语言病理学

行为科学

医学伦理学

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  • Mechanisms and impact of altered tumour mechanics.

    abstract::The physical characteristics of tumours are intricately linked to the tumour phenotype and difficulties during treatment. Many factors contribute to the increased stiffness of tumours; from increased matrix deposition, matrix remodelling by forces from cancer cells and stromal fibroblasts, matrix crosslinking, increas...

    journal_title:Nature cell biology

    pub_type: 杂志文章,评审

    doi:10.1038/s41556-018-0131-2

    authors: Mohammadi H,Sahai E

    更新日期:2018-07-01 00:00:00

  • Senescence-associated ribosome biogenesis defects contributes to cell cycle arrest through the Rb pathway.

    abstract::Cellular senescence is a tumour suppressor programme characterized by a stable cell cycle arrest. Here we report that cellular senescence triggered by a variety of stimuli leads to diminished ribosome biogenesis and the accumulation of both rRNA precursors and ribosomal proteins. These defects were associated with red...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-018-0127-y

    authors: Lessard F,Igelmann S,Trahan C,Huot G,Saint-Germain E,Mignacca L,Del Toro N,Lopes-Paciencia S,Le Calvé B,Montero M,Deschênes-Simard X,Bury M,Moiseeva O,Rowell MC,Zorca CE,Zenklusen D,Brakier-Gingras L,Bourdeau V,Oeffin

    更新日期:2018-07-01 00:00:00

  • CK1α suppresses lung tumour growth by stabilizing PTEN and inducing autophagy.

    abstract::The contribution of autophagy to cancer development remains controversial, largely owing to the fact that autophagy can be tumour suppressive or oncogenic in different biological contexts. Here, we show that in non-small-cell lung cancer (NSCLC), casein kinase 1 alpha 1 (CK1α) suppresses tumour growth by functioning a...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-018-0065-8

    authors: Cai J,Li R,Xu X,Zhang L,Lian R,Fang L,Huang Y,Feng X,Liu X,Li X,Zhu X,Zhang H,Wu J,Zeng M,Song E,He Y,Yin Y,Li J,Li M

    更新日期:2018-04-01 00:00:00

  • NCoR/SMRT co-repressors cooperate with c-MYC to create an epigenetic barrier to somatic cell reprogramming.

    abstract::Somatic cell reprogramming by exogenous factors requires cooperation with transcriptional co-activators and co-repressors to effectively remodel the epigenetic environment. How this interplay is regulated remains poorly understood. Here, we demonstrate that NCoR/SMRT co-repressors bind to pluripotency loci to create a...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-018-0047-x

    authors: Zhuang Q,Li W,Benda C,Huang Z,Ahmed T,Liu P,Guo X,Ibañez DP,Luo Z,Zhang M,Abdul MM,Yang Z,Yang J,Huang Y,Zhang H,Huang D,Zhou J,Zhong X,Zhu X,Fu X,Fan W,Liu Y,Xu Y,Ward C,Khan MJ,Kanwal S,Mirza B,Tor

    更新日期:2018-04-01 00:00:00

  • Identification of distinct nanoparticles and subsets of extracellular vesicles by asymmetric flow field-flow fractionation.

    abstract::The heterogeneity of exosomal populations has hindered our understanding of their biogenesis, molecular composition, biodistribution and functions. By employing asymmetric flow field-flow fractionation (AF4), we identified two exosome subpopulations (large exosome vesicles, Exo-L, 90-120 nm; small exosome vesicles, Ex...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-018-0040-4

    authors: Zhang H,Freitas D,Kim HS,Fabijanic K,Li Z,Chen H,Mark MT,Molina H,Martin AB,Bojmar L,Fang J,Rampersaud S,Hoshino A,Matei I,Kenific CM,Nakajima M,Mutvei AP,Sansone P,Buehring W,Wang H,Jimenez JP,Cohen-Gould L,P

    更新日期:2018-03-01 00:00:00

  • Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.

    abstract::Mitochondrial DNA (mtDNA) mutations cause inherited diseases and are implicated in the pathogenesis of common late-onset disorders, but how they arise is not clear1,2. Here we show that mtDNA mutations are present in primordial germ cells (PGCs) within healthy female human embryos. Isolated PGCs have a profound reduct...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-017-0017-8

    authors: Floros VI,Pyle A,Dietmann S,Wei W,Tang WCW,Irie N,Payne B,Capalbo A,Noli L,Coxhead J,Hudson G,Crosier M,Strahl H,Khalaf Y,Saitou M,Ilic D,Surani MA,Chinnery PF

    更新日期:2018-02-01 00:00:00

  • Unresolved recombination intermediates lead to ultra-fine anaphase bridges, chromosome breaks and aberrations.

    abstract::The resolution of joint molecules that link recombining sister chromatids is essential for chromosome segregation. Here, we determine the fate of unresolved recombination intermediates arising in cells lacking two nucleases required for resolution (GEN1 -/- knockout cells depleted of MUS81). We find that intermediates...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/s41556-017-0011-1

    authors: Chan YW,Fugger K,West SC

    更新日期:2018-01-01 00:00:00

  • A transient pool of nuclear F-actin at mitotic exit controls chromatin organization.

    abstract::Re-establishment of nuclear structure and chromatin organization after cell division is integral for genome regulation or development and is frequently altered during cancer progression. The mechanisms underlying chromatin expansion in daughter cells remain largely unclear. Here, we describe the transient formation of...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3641

    authors: Baarlink C,Plessner M,Sherrard A,Morita K,Misu S,Virant D,Kleinschnitz EM,Harniman R,Alibhai D,Baumeister S,Miyamoto K,Endesfelder U,Kaidi A,Grosse R

    更新日期:2017-12-01 00:00:00

  • RNA takes over control of DNA break repair.

    abstract::Small RNAs generated at DNA break sites are implicated in mammalian DNA repair. Now, a study shows that following the formation of DNA double-strand breaks, bidirectional transcription events adjacent to the break generate small RNAs that trigger the DNA damage response by local RNA:RNA interactions. ...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3645

    authors: Storici F,Tichon AE

    更新日期:2017-11-29 00:00:00

  • The impact of cellular metabolism on chromatin dynamics and epigenetics.

    abstract::The substrates used to modify nucleic acids and chromatin are affected by nutrient availability and the activity of metabolic pathways. Thus, cellular metabolism constitutes a fundamental component of chromatin status and thereby of genome regulation. Here we describe the biochemical and genetic principles of how meta...

    journal_title:Nature cell biology

    pub_type: 杂志文章,评审

    doi:10.1038/ncb3629

    authors: Reid MA,Dai Z,Locasale JW

    更新日期:2017-11-01 00:00:00

  • EZH2 promotes degradation of stalled replication forks by recruiting MUS81 through histone H3 trimethylation.

    abstract::The emergence of resistance to poly-ADP-ribose polymerase inhibitors (PARPi) poses a threat to the treatment of BRCA1 and BRCA2 (BRCA1/2)-deficient tumours. Stabilization of stalled DNA replication forks is a recently identified PARPi-resistance mechanism that promotes genomic stability in BRCA1/2-deficient cancers. D...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3626

    authors: Rondinelli B,Gogola E,Yücel H,Duarte AA,van de Ven M,van der Sluijs R,Konstantinopoulos PA,Jonkers J,Ceccaldi R,Rottenberg S,D'Andrea AD

    更新日期:2017-11-01 00:00:00

  • Differential effects on lung and bone metastasis of breast cancer by Wnt signalling inhibitor DKK1.

    abstract::Metastatic cancer is a systemic disease, and metastasis determinants might elicit completely different effects in various target organs. Here we show that tumour-secreted DKK1 is a serological marker of breast cancer metastasis organotropism and inhibits lung metastasis. DKK1 suppresses PTGS2-induced macrophage and ne...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3613

    authors: Zhuang X,Zhang H,Li X,Li X,Cong M,Peng F,Yu J,Zhang X,Yang Q,Hu G

    更新日期:2017-10-01 00:00:00

  • Cell plasticity in epithelial homeostasis and tumorigenesis.

    abstract::The adult organism is characterized by remarkable plasticity, which enables efficient regeneration and restoration of homeostasis after damage. When aberrantly activated, this plasticity contributes to tumour initiation and progression. Here we review recent advances in this field with a focus on cell fate changes and...

    journal_title:Nature cell biology

    pub_type: 杂志文章,评审

    doi:10.1038/ncb3611

    authors: Varga J,Greten FR

    更新日期:2017-10-01 00:00:00

  • MK2 balances inflammation and cell death.

    abstract::The cytokine tumour necrosis factor (TNF) and the toll-like receptors (TLRs) coordinate immune responses by activating inflammatory transcriptional programs, but these signals can also trigger cell death. Recent studies identify the MAP kinase substrate MK2 as a key player in determining whether cells live or die in r...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3619

    authors: Oberst A

    更新日期:2017-09-29 00:00:00

  • SMC complexes differentially compact mitotic chromosomes according to genomic context.

    abstract::Structural maintenance of chromosomes (SMC) protein complexes are key determinants of chromosome conformation. Using Hi-C and polymer modelling, we study how cohesin and condensin, two deeply conserved SMC complexes, organize chromosomes in the budding yeast Saccharomyces cerevisiae. The canonical role of cohesin is t...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3594

    authors: Schalbetter SA,Goloborodko A,Fudenberg G,Belton JM,Miles C,Yu M,Dekker J,Mirny L,Baxter J

    更新日期:2017-09-01 00:00:00

  • Lactate dehydrogenase activity drives hair follicle stem cell activation.

    abstract::Although normally dormant, hair follicle stem cells (HFSCs) quickly become activated to divide during a new hair cycle. The quiescence of HFSCs is known to be regulated by a number of intrinsic and extrinsic mechanisms. Here we provide several lines of evidence to demonstrate that HFSCs utilize glycolytic metabolism a...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3575

    authors: Flores A,Schell J,Krall AS,Jelinek D,Miranda M,Grigorian M,Braas D,White AC,Zhou JL,Graham NA,Graeber T,Seth P,Evseenko D,Coller HA,Rutter J,Christofk HR,Lowry WE

    更新日期:2017-09-01 00:00:00

  • Enhancing brown fat with NFIA.

    abstract::Brown adipose tissue is a key metabolic organ that oxidizes fatty acids and glucose to generate heat. Through epigenomic analyses of multiple adipose depots, the transcription factor nuclear factor I-A (NFIA) is now shown to drive the brown fat genetic program through binding to lineage-specific cis-regulatory element...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3591

    authors: Shapira SN,Seale P

    更新日期:2017-08-31 00:00:00

  • Tissue-specific CTCF-cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo.

    abstract::The genome is organized via CTCF-cohesin-binding sites, which partition chromosomes into 1-5 megabase (Mb) topologically associated domains (TADs), and further into smaller sub-domains (sub-TADs). Here we examined in vivo an ∼80 kb sub-TAD, containing the mouse α-globin gene cluster, lying within a ∼1 Mb TAD. We find ...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3573

    authors: Hanssen LLP,Kassouf MT,Oudelaar AM,Biggs D,Preece C,Downes DJ,Gosden M,Sharpe JA,Sloane-Stanley JA,Hughes JR,Davies B,Higgs DR

    更新日期:2017-08-01 00:00:00

  • Bone marrow adipocytes promote the regeneration of stem cells and haematopoiesis by secreting SCF.

    abstract::Endothelial cells and leptin receptor+ (LepR+) stromal cells are critical sources of haematopoietic stem cell (HSC) niche factors, including stem cell factor (SCF), in bone marrow. After irradiation or chemotherapy, these cells are depleted while adipocytes become abundant. We discovered that bone marrow adipocytes sy...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3570

    authors: Zhou BO,Yu H,Yue R,Zhao Z,Rios JJ,Naveiras O,Morrison SJ

    更新日期:2017-08-01 00:00:00

  • Endoglin prevents vascular malformation by regulating flow-induced cell migration and specification through VEGFR2 signalling.

    abstract::Loss-of-function (LOF) mutations in the endothelial cell (EC)-enriched gene endoglin (ENG) cause the human disease hereditary haemorrhagic telangiectasia-1, characterized by vascular malformations promoted by vascular endothelial growth factor A (VEGFA). How ENG deficiency alters EC behaviour to trigger these anomalie...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3534

    authors: Jin Y,Muhl L,Burmakin M,Wang Y,Duchez AC,Betsholtz C,Arthur HM,Jakobsson L

    更新日期:2017-06-01 00:00:00

  • Multiscale force sensing in development.

    abstract::The seminal observation that mechanical signals can elicit changes in biochemical signalling within cells, a process commonly termed mechanosensation and mechanotransduction, has revolutionized our understanding of the role of cell mechanics in various fundamental biological processes, such as cell motility, adhesion,...

    journal_title:Nature cell biology

    pub_type: 杂志文章,评审

    doi:10.1038/ncb3524

    authors: Petridou NI,Spiró Z,Heisenberg CP

    更新日期:2017-05-31 00:00:00

  • Endocytic proteins are partitioned at the edge of the clathrin lattice in mammalian cells.

    abstract::Dozens of proteins capture, polymerize and reshape the clathrin lattice during clathrin-mediated endocytosis (CME). How or if this ensemble of proteins is organized in relation to the clathrin coat is unknown. Here, we map key molecules involved in CME at the nanoscale using correlative super-resolution light and tran...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3498

    authors: Sochacki KA,Dickey AM,Strub MP,Taraska JW

    更新日期:2017-04-01 00:00:00

  • PARL mediates Smac proteolytic maturation in mitochondria to promote apoptosis.

    abstract::Mitochondria drive apoptosis by releasing pro-apoptotic proteins that promote caspase activation in the cytosol. The rhomboid protease PARL, an intramembrane cleaving peptidase in the inner membrane, regulates mitophagy and plays an ill-defined role in apoptosis. Here, we employed PARL-based proteomics to define its s...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3488

    authors: Saita S,Nolte H,Fiedler KU,Kashkar H,Venne AS,Zahedi RP,Krüger M,Langer T

    更新日期:2017-04-01 00:00:00

  • A mechanically active heterotypic E-cadherin/N-cadherin adhesion enables fibroblasts to drive cancer cell invasion.

    abstract::Cancer-associated fibroblasts (CAFs) promote tumour invasion and metastasis. We show that CAFs exert a physical force on cancer cells that enables their collective invasion. Force transmission is mediated by a heterophilic adhesion involving N-cadherin at the CAF membrane and E-cadherin at the cancer cell membrane. Th...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3478

    authors: Labernadie A,Kato T,Brugués A,Serra-Picamal X,Derzsi S,Arwert E,Weston A,González-Tarragó V,Elosegui-Artola A,Albertazzi L,Alcaraz J,Roca-Cusachs P,Sahai E,Trepat X

    更新日期:2017-03-01 00:00:00

  • Long-range self-organization of cytoskeletal myosin II filament stacks.

    abstract::Although myosin II filaments are known to exist in non-muscle cells, their dynamics and organization are incompletely understood. Here, we combined structured illumination microscopy with pharmacological and genetic perturbations, to study the process of actomyosin cytoskeleton self-organization into arcs and stress f...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3466

    authors: Hu S,Dasbiswas K,Guo Z,Tee YH,Thiagarajan V,Hersen P,Chew TL,Safran SA,Zaidel-Bar R,Bershadsky AD

    更新日期:2017-02-01 00:00:00

  • Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining.

    abstract::Chromosome missegregation into a micronucleus can cause complex and localized genomic rearrangements known as chromothripsis, but the underlying mechanisms remain unresolved. Here we developed an inducible Y centromere-selective inactivation strategy by exploiting a CENP-A/histone H3 chimaera to directly examine the f...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3450

    authors: Ly P,Teitz LS,Kim DH,Shoshani O,Skaletsky H,Fachinetti D,Page DC,Cleveland DW

    更新日期:2017-01-01 00:00:00

  • Clonal fate mapping quantifies the number of haematopoietic stem cells that arise during development.

    abstract::Haematopoietic stem cells (HSCs) arise in the developing aorta during embryogenesis. The number of HSC clones born has been estimated through transplantation, but experimental approaches to assess the absolute number of forming HSCs in a native setting have remained challenging. Here, we applied single-cell and clonal...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3444

    authors: Henninger J,Santoso B,Hans S,Durand E,Moore J,Mosimann C,Brand M,Traver D,Zon L

    更新日期:2017-01-01 00:00:00

  • Y chromothripsis?

    abstract::Micronucleation of missegregated chromatin can lead to substantial chromosome rearrangements via chromothripsis. However, the molecular details of micronucleus-based chromothripsis are still unclear. Now, an elegant system that specifically induces missegregation of the Y chromosome provides insight into this process,...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3458

    authors: Hatch EM

    更新日期:2016-12-23 00:00:00

  • Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors.

    abstract::Direct reprogramming by forced expression of transcription factors can convert one cell type into another. Thus, desired cell types can be generated bypassing pluripotency. However, direct reprogramming towards renal cells remains an unmet challenge. Here, we identify renal cell fate-inducing factors on the basis of t...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3437

    authors: Kaminski MM,Tosic J,Kresbach C,Engel H,Klockenbusch J,Müller AL,Pichler R,Grahammer F,Kretz O,Huber TB,Walz G,Arnold SJ,Lienkamp SS

    更新日期:2016-12-01 00:00:00

  • ETAA1 acts at stalled replication forks to maintain genome integrity.

    abstract::The ATR checkpoint kinase coordinates cellular responses to DNA replication stress. Budding yeast contain three activators of Mec1 (the ATR orthologue); however, only TOPBP1 is known to activate ATR in vertebrates. We identified ETAA1 as a replication stress response protein in two proteomic screens. ETAA1-deficient c...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3415

    authors: Bass TE,Luzwick JW,Kavanaugh G,Carroll C,Dungrawala H,Glick GG,Feldkamp MD,Putney R,Chazin WJ,Cortez D

    更新日期:2016-11-01 00:00:00

  • The actin cable is dispensable in directing dorsal closure dynamics but neutralizes mechanical stress to prevent scarring in the Drosophila embryo.

    abstract::The actin cable is a supracellular structure that embryonic epithelia produce to close gaps. However, the action of the cable remains debated. Here, we address the function of the cable using Drosophila dorsal closure, a paradigm to understand wound healing. First, we show that the actin cytoskeleton protein Zasp52 is...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3421

    authors: Ducuing A,Vincent S

    更新日期:2016-11-01 00:00:00

  • An interaction between Scribble and the NADPH oxidase complex controls M1 macrophage polarization and function.

    abstract::The polarity protein Scribble (SCRIB) regulates apical-basal polarity, directional migration and tumour suppression in Drosophila and mammals. Here we report that SCRIB is an important regulator of myeloid cell functions including bacterial infection and inflammation. SCRIB interacts directly with the NADPH oxidase (N...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3413

    authors: Zheng W,Umitsu M,Jagan I,Tran CW,Ishiyama N,BeGora M,Araki K,Ohashi PS,Ikura M,Muthuswamy SK

    更新日期:2016-11-01 00:00:00

  • Protein kinase C controls lysosome biogenesis independently of mTORC1.

    abstract::Lysosomes respond to environmental cues by controlling their own biogenesis, but the underlying mechanisms are poorly understood. Here we describe a protein kinase C (PKC)-dependent and mTORC1-independent mechanism for regulating lysosome biogenesis, which provides insights into previously reported effects of PKC on l...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3407

    authors: Li Y,Xu M,Ding X,Yan C,Song Z,Chen L,Huang X,Wang X,Jian Y,Tang G,Tang C,Di Y,Mu S,Liu X,Liu K,Li T,Wang Y,Miao L,Guo W,Hao X,Yang C

    更新日期:2016-10-01 00:00:00

  • NOTCH1 mediates a switch between two distinct secretomes during senescence.

    abstract::Senescence, a persistent form of cell-cycle arrest, is often associated with a diverse secretome, which provides complex functionality for senescent cells within the tissue microenvironment. We show that oncogene-induced senescence is accompanied by a dynamic fluctuation of NOTCH1 activity, which drives a TGF-β-rich s...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3397

    authors: Hoare M,Ito Y,Kang TW,Weekes MP,Matheson NJ,Patten DA,Shetty S,Parry AJ,Menon S,Salama R,Antrobus R,Tomimatsu K,Howat W,Lehner PJ,Zender L,Narita M

    更新日期:2016-09-01 00:00:00

  • Autophagosome-lysosome fusion triggers a lysosomal response mediated by TLR9 and controlled by OCRL.

    abstract::Phosphoinositides (PtdIns) control fundamental cell processes, and inherited defects of PtdIns kinases or phosphatases cause severe human diseases, including Lowe syndrome due to mutations in OCRL, which encodes a PtdIns(4,5)P2 5-phosphatase. Here we unveil a lysosomal response to the arrival of autophagosomal cargo i...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3386

    authors: De Leo MG,Staiano L,Vicinanza M,Luciani A,Carissimo A,Mutarelli M,Di Campli A,Polishchuk E,Di Tullio G,Morra V,Levtchenko E,Oltrabella F,Starborg T,Santoro M,Di Bernardo D,Devuyst O,Lowe M,Medina DL,Ballabio A,De Ma

    更新日期:2016-08-01 00:00:00

  • F-actin dismantling through a redox-driven synergy between Mical and cofilin.

    abstract::Numerous cellular functions depend on actin filament (F-actin) disassembly. The best-characterized disassembly proteins, the ADF (actin-depolymerizing factor)/cofilins (encoded by the twinstar gene in Drosophila), sever filaments and recycle monomers to promote actin assembly. Cofilin is also a relatively weak actin d...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3390

    authors: Grintsevich EE,Yesilyurt HG,Rich SK,Hung RJ,Terman JR,Reisler E

    更新日期:2016-08-01 00:00:00

  • p53 mutations promote proteasomal activity.

    abstract::p53 mutations occur very frequently in human cancer. Besides abrogating the tumour suppressive functions of wild-type p53, many of those mutations also acquire oncogenic gain-of-function activities. Augmentation of proteasome activity is now reported as a common gain-of-function mechanism shared by different p53 mutan...

    journal_title:Nature cell biology

    pub_type: 新闻

    doi:10.1038/ncb3392

    authors: Oren M,Kotler E

    更新日期:2016-07-27 00:00:00

  • Pten regulates spindle pole movement through Dlg1-mediated recruitment of Eg5 to centrosomes.

    abstract::Phosphatase and tensin homologue (Pten) suppresses neoplastic growth by negatively regulating PI(3)K signalling through its phosphatase activity. To gain insight into the actions of non-catalytic Pten domains in normal physiological processes and tumorigenesis, we engineered mice lacking the PDZ-binding domain (PDZ-BD...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3369

    authors: van Ree JH,Nam HJ,Jeganathan KB,Kanakkanthara A,van Deursen JM

    更新日期:2016-07-01 00:00:00

  • The metabolic co-regulator PGC1α suppresses prostate cancer metastasis.

    abstract::Cellular transformation and cancer progression is accompanied by changes in the metabolic landscape. Master co-regulators of metabolism orchestrate the modulation of multiple metabolic pathways through transcriptional programs, and hence constitute a probabilistically parsimonious mechanism for general metabolic rewir...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3357

    authors: Torrano V,Valcarcel-Jimenez L,Cortazar AR,Liu X,Urosevic J,Castillo-Martin M,Fernández-Ruiz S,Morciano G,Caro-Maldonado A,Guiu M,Zúñiga-García P,Graupera M,Bellmunt A,Pandya P,Lorente M,Martín-Martín N,Sutherland JD,San

    更新日期:2016-06-01 00:00:00

  • Medial HOXA genes demarcate haematopoietic stem cell fate during human development.

    abstract::Pluripotent stem cells (PSCs) may provide a potential source of haematopoietic stem/progenitor cells (HSPCs) for transplantation; however, unknown molecular barriers prevent the self-renewal of PSC-HSPCs. Using two-step differentiation, human embryonic stem cells (hESCs) differentiated in vitro into multipotent haemat...

    journal_title:Nature cell biology

    pub_type: 杂志文章

    doi:10.1038/ncb3354

    authors: Dou DR,Calvanese V,Sierra MI,Nguyen AT,Minasian A,Saarikoski P,Sasidharan R,Ramirez CM,Zack JA,Crooks GM,Galic Z,Mikkola HK

    更新日期:2016-06-01 00:00:00

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