Journal Cover Nature Reviews Molecular Cell Biology
  [SJR: 32.928]   [H-I: 324]   [381 followers]  Follow
    
   Full-text available via subscription Subscription journal
   ISSN (Print) 1471-0072 - ISSN (Online) 1471-0080
   Published by NPG Homepage  [142 journals]
  • Why does biopolymer condensation matter'
    • Why does biopolymer condensation matter?

      Why does biopolymer condensation matter?, Published online: 16 May 2018; doi:10.1038/s41580-018-0023-0

      Biomolecules can phase separate and form condensates that have roles in diverse cellular processes and contexts. Michnick and Bergeron-Sandoval comment on this rapidly progressing field and envisage that the study of biological phase separation will bring new understanding of cell and developmental biology.Why does biopolymer condensation matter?, Published online: 2018-05-16; doi:10.1038/s41580-018-0023-02018-05-16
      DOI: 10.1038/s41580-018-0023-0
       
  • Overcoming obstacles to progression
    • Overcoming obstacles to progression

      Overcoming obstacles to progression, Published online: 16 May 2018; doi:10.1038/s41580-018-0027-9

      The spindle checkpoint complex BUB3–BUB1 facilitates telomere replication through recruitment of the helicase BLM, and the telomere capping protein TRF2 promotes replication at pericentromeres by recruiting the helicase RTEL1; both helicases resolve G-quadruplex structures.Overcoming obstacles to progression, Published online: 2018-05-16; doi:10.1038/s41580-018-0027-92018-05-16
      DOI: 10.1038/s41580-018-0027-9
       
  • Stepping outside the comfort zone of membrane contact site research
    • Stepping outside the comfort zone of membrane contact site research

      Stepping outside the comfort zone of membrane contact site research, Published online: 15 May 2018; doi:10.1038/s41580-018-0022-1

      Cellular organelles extensively communicate with each other by close interactions, known as membrane contact sites. Schuldiner and Bohnert comment on the progress of this rapidly developing field, highlighting that the complexity of interactions at membrane contact sites is only now starting to emerge.Stepping outside the comfort zone of membrane contact site research, Published online: 2018-05-15; doi:10.1038/s41580-018-0022-12018-05-15
      DOI: 10.1038/s41580-018-0022-1
       
  • Roadblocks and resolutions in eukaryotic translation
    • Roadblocks and resolutions in eukaryotic translation

      Roadblocks and resolutions in eukaryotic translation, Published online: 14 May 2018; doi:10.1038/s41580-018-0011-4

      Ribosomes encounter obstacles during translation elongation that cause their stalling and can have a profound impact on protein yield. Ribosome stalling depends on the genetic code, amino acid availability, regulatory elements and mRNA context and can be resolved by resumption of translation or by ribosome rescue and recycling.Roadblocks and resolutions in eukaryotic translation, Published online: 2018-05-14; doi:10.1038/s41580-018-0011-42018-05-14
      DOI: 10.1038/s41580-018-0011-4
       
  • The beginning of totipotency
    • The beginning of totipotency

      The beginning of totipotency, Published online: 11 May 2018; doi:10.1038/s41580-018-0017-y

      The beginning of totipotencyThe beginning of totipotency, Published online: 2018-05-11; doi:10.1038/s41580-018-0017-y2018-05-11
      DOI: 10.1038/s41580-018-0017-y
       
  • Born to run: control of transcription elongation by RNA polymerase II
    • Born to run: control of transcription elongation by RNA polymerase II

      Born to run: control of transcription elongation by RNA polymerase II, Published online: 08 May 2018; doi:10.1038/s41580-018-0010-5

      Transcription elongation by RNA polymerase II (Pol II) involves pausing of Pol II at promoter-proximal regions. Pol II release into gene bodies (productive elongation) is controlled by many transcription-specific factors, enhancers and factors that are canonically associated with genome maintenance.Born to run: control of transcription elongation by RNA polymerase II, Published online: 2018-05-08; doi:10.1038/s41580-018-0010-52018-05-08
      DOI: 10.1038/s41580-018-0010-5
       
  • Publisher Correction: Contextual determinants of TGFβ action in
           development, immunity and cancer
    • Publisher Correction: Contextual determinants of TGFβ action in development, immunity and cancer

      Publisher Correction: Contextual determinants of TGFβ action in development, immunity and cancer, Published online: 08 May 2018; doi:10.1038/s41580-018-0018-x

      Publisher Correction: Contextual determinants of TGFβ action in development, immunity and cancerPublisher Correction: Contextual determinants of TGFβ action in development, immunity and cancer, Published online: 2018-05-08; doi:10.1038/s41580-018-0018-x2018-05-08
      DOI: 10.1038/s41580-018-0018-x
       
  • Publisher Correction: The cytoplasmic dynein transport machinery and its
           many cargoes
    • Publisher Correction: The cytoplasmic dynein transport machinery and its many cargoes

      Publisher Correction: The cytoplasmic dynein transport machinery and its many cargoes, Published online: 08 May 2018; doi:10.1038/s41580-018-0021-2

      Publisher Correction: The cytoplasmic dynein transport machinery and its many cargoesPublisher Correction: The cytoplasmic dynein transport machinery and its many cargoes, Published online: 2018-05-08; doi:10.1038/s41580-018-0021-22018-05-08
      DOI: 10.1038/s41580-018-0021-2
       
 
 
JournalTOCs
School of Mathematical and Computer Sciences
Heriot-Watt University
Edinburgh, EH14 4AS, UK
Email: journaltocs@hw.ac.uk
Tel: +00 44 (0)131 4513762
Fax: +00 44 (0)131 4513327
 
Home (Search)
Subjects A-Z
Publishers A-Z
Customise
APIs
Your IP address: 54.166.212.152
 
About JournalTOCs
API
Help
News (blog, publications)
JournalTOCs on Twitter   JournalTOCs on Facebook

JournalTOCs © 2009-