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Journal of Pharmacological and Toxicological Methods|October 2, 2010
A multi-species assay for siRNA-mediated mRNA knockdown analysis without the need for RNA purificationZhibin Wang, Stephen J Pacchione, Zhutian Niu, et al.
Microbiology (Reading, England)|October 28, 1999
Two fatty acid delta9-desaturase genes, ole1 and ole2, from Mortierella alpina complement the yeast ole1 mutationP Wongwathanarat, L V Michaelson, A T Carter, et al.
The Journal of Cell Biology|December 1, 1994
Localization of the Lys, Asp, Glu, Leu tetrapeptide receptor to the Golgi complex and the intermediate compartment in mammalian cellsG Griffiths, M Ericsson, J Krijnse-Locker, et al.
The EMBO Journal|January 19, 2000
Involvement of ezrin/moesin in de novo actin assembly on phagosomal membranesH Defacque, M Egeberg, A Habermann, et al.
Leukemia|September 1, 1989
A mutant RAS gene acts through protein kinase C to augment interleukin-3 dependent proliferation in a fastidious immortal myeloid cell lineH S Boswell, M A Harrington, G S Burgess, et al.
Journal of Neurosurgery. Spine|March 18, 2017
Cervical disc arthroplasty with the Prestige LP disc versus anterior cervical discectomy and fusion, at 2 levels: results of a prospective, multicenter randomized controlled clinical trial at 24 monthsMatthew F Gornet, Todd H Lanman, J Kenneth Burkus, et al.
International Journal of Spine Surgery|March 11, 2022
Impact of Cervical Disc Arthroplasty vs Anterior Cervical Discectomy and Fusion on Driving Disability: Post Hoc Analysis of a Randomized Controlled Trial With 10-Year Follow-UpDeeptee Jain, Michael P Kelly, Matthew F Gornet, et al.
Nature|May 22, 2024
Adhesive anti-fibrotic interfaces on diverse organsJingjing Wu, Jue Deng, Georgios Theocharidis, et al.
Human Molecular Genetics|July 27, 2001
Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye developmentL C Bibb, J K Holt, E E Tarttelin, et al.
Molecular Vision|January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathyGavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
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