• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
MRC Laboratory of Molecular Biology

MRC Laboratory of Molecular Biology

One of the world's leading research institutes, our scientists are working to advance understanding of biological processes at the molecular level - providing the knowledge needed to solve key problems in human health.

  • Home
  • About LMB
  • Research
  • Research Groups
  • Students
  • Recruitment
  • Life at the LMB
  • Achievements
  • News & Events

Insight on Research

First RNAi meiosis screen in mammals reveals genes essential to generate eggs

Published on 7 July, 2015

During fertilisation, an egg and a sperm fuse to form a new embryo. To create the egg, a precursor cell called an oocyte undergoes meiosis: a specialised form of cell division in which half the chromosomes are separated away leaving exactly the right number of chromosomes in the egg. Meiosis in human oocytes is highly […]

Revealing how GPCRs activate Gα proteins.

Published on 7 July, 2015

G protein coupled receptor (GPCR) mediated signalling is one of the largest and the most diverse signalling pathways in cellular systems. Human GPCRs sense various signals and activate different Gα proteins to trigger distinct cellular responses. This signalling pathway is important for a broad range of processes such as regulation of the immune system, neurotransmission, […]

Structure of the human 20S proteasome with a ligand revealed by cryo-EM

Published on 3 July, 2015

The proteasome is a protein recycling complex that plays a critical role in the smooth running of our cells. It is present in all multicellular organisms and facilitates cell renewal and the controlled death of damaged cells. Paula da Fonseca, from the LMB’s Structural Studies Division, and Edward Morris, from the Institute of Cancer Research, […]

Spliceosome U4/U6.U5 tri-snRNP structure revealed by cryo-EM

Published on 25 June, 2015

Genes in eukaryotic organisms are frequently interrupted by non-coding segments called introns. Before the protein can be produced, the entire length of each gene including the introns, is transcribed to produce precursor messenger RNA (pre-mRNA). An immense and dynamic molecular machine known as the spliceosome then removes the introns and splices the coding segments together […]

Atomic structure of the anaphase-promoting complex (APC/C)

Published on 15 June, 2015

The anaphase-promoting complex (APC/C) is an unusually large multi-subunit complex that has a key role in cell division, controlling chromosome segregation and the cell cycle. Using electron cryo-microscopy (cryo-EM), David Barford and his group in the LMB’s Structural Studies Division have solved the first atomic structure of the APC/C, revealing its molecular architecture in unprecedented […]

Human egg defects caused by error-prone spindle assembly

Published on 5 June, 2015

Miscarriages and genetic disorders, such as Down’s syndrome, are often caused by errors when an egg develops from its progenitor cell, the oocyte. Most defects occur during meiosis, a specialised form of cell division that leads to the formation of an egg. To ensure the egg cell has exactly the right number of chromosomes, an […]

  • « Go to Previous Page
  • Page 1
  • Interim pages omitted …
  • Page 44
  • Page 45
  • Page 46
  • Page 47
  • Page 48
  • Interim pages omitted …
  • Page 62
  • Go to Next Page »

Primary Sidebar

Search

  • Privacy & Cookies
  • Contact Directory
  • Freedom of Information
  • Site Map
Find Us
©2025 MRC Laboratory of Molecular Biology,
Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK. 01223 267000

The MRC is part of UK Research and Innovation

Contact Us

This site uses cookies. The LMB may use cookies to analyse how you use our website. We use external analysis systems which may set additional cookies to perform their analysis. These cookies (and any others in use) are detailed in our Privacy and Cookies Policy and are integral to our website. You can delete or disable these cookies in your web browser if you wish, but then our site may not work as it is designed. Ok