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Institution

Laboratory of Molecular Biology

FacilityCambridge, Cambridgeshire, United Kingdom
About: Laboratory of Molecular Biology is a facility organization based out in Cambridge, Cambridgeshire, United Kingdom. It is known for research contribution in the topics: Gene & RNA. The organization has 19395 authors who have published 24236 publications receiving 2101480 citations.
Topics: Gene, RNA, DNA, Population, Receptor


Papers
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Journal ArticleDOI
TL;DR: The mechanism of action of this ligand-induced molecular switch, in which changes in the dynamic behaviour of the receptor play a key role, is revealed, which facilitated the evolution of a family of nuclear receptors with highly diverse ligand recognition and signalling properties.

385 citations

Journal ArticleDOI
05 Nov 1971-Nature
TL;DR: The model suggests that chromosomal DNA falls into two classes: globular DNA (containing unpaired regions for control) and a much smaller fraction consisting of fibrous DNA which alone codes for proteins.
Abstract: The model suggests that chromosomal DNA falls into two classes: globular DNA (containing unpaired regions for control) and a much smaller fraction consisting of fibrous DNA which alone codes for proteins.

385 citations

Journal ArticleDOI
TL;DR: A physiological and heretofore unrecognized role for mitochondrial oxidant release is described and it is suggested that although chronic oxidant production may have deleterious effects, mitochondrial oxidants can also function acutely as signaling molecules to provide communication between the mitochondria and the cytosol.
Abstract: Leakage of mitochondrial oxidants contributes to a variety of harmful conditions ranging from neurodegenerative diseases to cellular senescence. We describe here, however, a physiological and heretofore unrecognized role for mitochondrial oxidant release. Mitochondrial metabolism of pyruvate is demonstrated to activate the c-Jun N-terminal kinase (JNK). This metabolite-induced rise in cytosolic JNK1 activity is shown to be triggered by increased release of mitochondrial H2O2. We further demonstrate that in turn, the redox-dependent activation of JNK1 feeds back and inhibits the activity of the metabolic enzymes glycogen synthase kinase 3β and glycogen synthase. As such, these results demonstrate a novel metabolic regulatory pathway activated by mitochondrial oxidants. In addition, they suggest that although chronic oxidant production may have deleterious effects, mitochondrial oxidants can also function acutely as signaling molecules to provide communication between the mitochondria and the cytosol.

384 citations

Journal ArticleDOI
TL;DR: The conflicting findings on tetanus and botulinum toxins binding to neuronal membranes are reviewed and discussed in terms of a double receptor formed by both a G 1b ganglioside and a protein component.

384 citations


Authors

Showing all 19431 results

NameH-indexPapersCitations
Robert J. Lefkowitz214860147995
Ronald M. Evans199708166722
Tony Hunter175593124726
Marc G. Caron17367499802
Mark Gerstein168751149578
Timothy A. Springer167669122421
Harvey F. Lodish165782101124
Ira Pastan1601286110069
Bruce N. Ames158506129010
Philip Cohen154555110856
Gerald M. Rubin152382115248
Ashok Kumar1515654164086
Kim Nasmyth14229459231
Kenneth M. Yamada13944672136
Harold E. Varmus13749676320
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20239
202265
20211,222
20201,165
20191,082
2018945