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Showing results (971-980 of 1,117) with videos related to
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BMJ Open
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March 19, 2021
Electronic clinical decision support tool for assessing stomach symptoms in primary care (ECASS): a feasibility study
Greg Rubin, Fiona M Walter, Jon Emery, et al.
Nature Genetics
|
July 1, 2026
U2AF1 mutations rescue deleterious exon skipping induced by KRAS mutations
David M Walter, Katherine Cho, Smruthy Sivakumar, et al.
BMJ Open
|
September 19, 2014
The Improving Rural Cancer Outcomes (IRCO) Trial: a factorial cluster-randomised controlled trial of a complex intervention to reduce time to diagnosis in rural patients with cancer in Western Australia: a study protocol
Jon D Emery, Victoria Gray, Fiona M Walter, et al.
Molecular Biology Reports
|
June 17, 2022
NTRK2 gene fusions are uncommon in pilocytic astrocytoma
Daniel Antunes Moreno, Aline Paixão Becker, Cristovam Scapulatempo-Neto, et al.
Cell Reports
|
May 3, 2018
Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses
Andreas Fulterer, Till F M Andlauer, Anatoli Ender, et al.
British Journal of Cancer
|
February 17, 2018
The Improving Rural Cancer Outcomes Trial: a cluster-randomised controlled trial of a complex intervention to reduce time to diagnosis in rural cancer patients in Western Australia
Jon D Emery, Victoria Gray, Fiona M Walter, et al.
BMJ (Clinical Research Ed.)
|
September 14, 2010
Acceptability and accuracy of a non-endoscopic screening test for Barrett's oesophagus in primary care: cohort study
Sudarshan R Kadri, Pierre Lao-Sirieix, Maria O'Donovan, et al.
The EMBO Journal
|
June 7, 2014
The SNARE protein vti1a functions in dense-core vesicle biogenesis
Alexander M Walter, Julia Kurps, Heidi de Wit, et al.
Nature Genetics
|
September 10, 1998
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy
S Rust, M Walter, H Funke, et al.
Human Molecular Genetics
|
July 10, 2020
Altered bone development with impaired cartilage formation precedes neuromuscular symptoms in spinal muscular atrophy
Niko Hensel, Hermann Brickwedde, Konstantinos Tsaknakis, et al.
Page
of 112
Search research articles
Search
Showing results (971-980 of 1,117) with videos related to
Sort By:
Page
of 112
BMJ Open
|
March 19, 2021
Electronic clinical decision support tool for assessing stomach symptoms in primary care (ECASS): a feasibility study
Greg Rubin, Fiona M Walter, Jon Emery, et al.
Nature Genetics
|
July 1, 2026
U2AF1 mutations rescue deleterious exon skipping induced by KRAS mutations
David M Walter, Katherine Cho, Smruthy Sivakumar, et al.
BMJ Open
|
September 19, 2014
The Improving Rural Cancer Outcomes (IRCO) Trial: a factorial cluster-randomised controlled trial of a complex intervention to reduce time to diagnosis in rural patients with cancer in Western Australia: a study protocol
Jon D Emery, Victoria Gray, Fiona M Walter, et al.
Molecular Biology Reports
|
June 17, 2022
NTRK2 gene fusions are uncommon in pilocytic astrocytoma
Daniel Antunes Moreno, Aline Paixão Becker, Cristovam Scapulatempo-Neto, et al.
Cell Reports
|
May 3, 2018
Active Zone Scaffold Protein Ratios Tune Functional Diversity across Brain Synapses
Andreas Fulterer, Till F M Andlauer, Anatoli Ender, et al.
British Journal of Cancer
|
February 17, 2018
The Improving Rural Cancer Outcomes Trial: a cluster-randomised controlled trial of a complex intervention to reduce time to diagnosis in rural cancer patients in Western Australia
Jon D Emery, Victoria Gray, Fiona M Walter, et al.
BMJ (Clinical Research Ed.)
|
September 14, 2010
Acceptability and accuracy of a non-endoscopic screening test for Barrett's oesophagus in primary care: cohort study
Sudarshan R Kadri, Pierre Lao-Sirieix, Maria O'Donovan, et al.
The EMBO Journal
|
June 7, 2014
The SNARE protein vti1a functions in dense-core vesicle biogenesis
Alexander M Walter, Julia Kurps, Heidi de Wit, et al.
Nature Genetics
|
September 10, 1998
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy
S Rust, M Walter, H Funke, et al.
Human Molecular Genetics
|
July 10, 2020
Altered bone development with impaired cartilage formation precedes neuromuscular symptoms in spinal muscular atrophy
Niko Hensel, Hermann Brickwedde, Konstantinos Tsaknakis, et al.
Page
of 112