G
Graeme Bilbe
Researcher at Drugs for Neglected Diseases Initiative
Publications - 70
Citations - 5753
Graeme Bilbe is an academic researcher from Drugs for Neglected Diseases Initiative. The author has contributed to research in topics: Receptor & Agonist. The author has an hindex of 38, co-authored 70 publications receiving 5427 citations. Previous affiliations of Graeme Bilbe include Novartis.
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Journal ArticleDOI
Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056
Sébastien Jacquemont,Aurore Curie,Vincent des Portes,Maria Giulia Torrioli,Elizabeth Berry-Kravis,Randi J Hagerman,Feliciano J. Ramos,Kim Cornish,Yunsheng He,Charles Paulding,Giovanni Neri,Fei Chen,Fei Chen,Nouchine Hadjikhani,Nouchine Hadjikhani,Danielle Martinet,Joanne M. Meyer,Jacques S. Beckmann,Karine Delange,Amandine Brun,Gérald Bussy,Fabrizio Gasparini,Talita Hilse,Annette Floesser,Janice Branson,Graeme Bilbe,Donald Johns,Baltazar Gomez-Mancilla +27 more
TL;DR: An antagonist for the metabotropic glutamate receptor may improve symptoms in patients with fragile X syndrome whose FMR1 promoters are fully methylated, a sign that gene expression is completely silenced, and provides the basis for a larger study to test whether methylation can serve as a predictor of a positive antagonist response in a population of patients with Fragile X syndrome.
Journal ArticleDOI
Neuropathology in Mice Expressing Human α-Synuclein
Herman van der Putten,Karl-Heinz Wiederhold,Alphonse Probst,Samuel Barbieri,Claudia Mistl,Simone Danner,Sabine Kauffmann,Katja Hofele,Will P.J.M Spooren,Markus A. Rüegg,Shuo Lin,Pico Caroni,Bernd Sommer,Markus Tolnay,Graeme Bilbe +14 more
TL;DR: Thy1 transgene expression of wild-type human α-synuclein resulted in similar pathological changes, thus supporting a central role for mutant and wild- type α- Synuclein in familial and idiotypic forms of diseases with neuronal α- synucleinopathy and Lewy pathology.
Journal ArticleDOI
Molecular Cloning of Human cDNA for Cathepsin K: Novel Cysteine Proteinase Predominantly Expressed in Bone
TL;DR: Northern blot analysis showed that cathepsin K mRNA is expressed at high levels in some osteoarthritic hip bones and at a very high level in osteoclastoma compared to very low levels in other tissues, suggesting that cat hepsinK is closely involved in human osteoclastic bone resorption.
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Differential expression of TGF beta 1, beta 2 and beta 3 genes during mouse embryogenesis.
TL;DR: All three isoforms were expressed in bone tissues but showed distinct patterns of expression both spatially and temporally, and TGF beta 3 was strongest in prevertebral tissue, in some mesothelia and in lung epithelia.
Journal Article
The osteoclast-associated protease cathepsin K is expressed in human breast carcinoma.
Amanda Littlewood-Evans,Graeme Bilbe,W.B. Bowler,David Farley,Brenda Wlodarski,Toshio Kokubo,Tetsuya Inaoka,John Sloane,Dean B. Evans,James A. Gallagher +9 more
TL;DR: Human cathepsin K is a novel cysteine protease previously reported to be restricted in its expression to osteoclasts that may contribute to the invasive potential of breast cancer cells, including those that metastasize to bone.