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J Cowley

Showing results (371-380 of 489) with videos related to

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Cerebellum (London, England)|May 20, 2019
Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome SequencingAryun Kim, Kishore R Kumar, Ryan L Davis, et al.
Cell Transplantation|March 13, 2012
Human islets express a marked proinflammatory molecular signature prior to transplantationMark J Cowley, Anita Weinberg, Nathan W Zammit, et al.
Frontiers in Pharmacology|May 15, 2023
Radiation therapy attenuates lymphatic vessel repair by reducing VEGFR-3 signallingVinochani Pillay, Lipi Shukla, Prad Herle, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 1, 2019
Aquaporin-4 IgG seropositivity is associated with worse visual outcomes after optic neuritis than MOG-IgG seropositivity and multiple sclerosis, independent of macular ganglion cell layer thinningElias S Sotirchos, Angeliki Filippatou, Kathryn C Fitzgerald, et al.
Science (New York, N.Y.)|March 26, 2026
Distinctive DNA sequence features define epigenetic longevity of inflammatory memoryChristopher J Cowley, Sairaj M Sajjath, Luis F Soto-Ugaldi, et al.
The British Journal of Surgery|March 1, 1979
A prospective randomized trial of vagotomy in chronic duodenal ulcerationC G Koffman, J B Elder, I E Gillespie, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
NPJ Precision Oncology|February 13, 2021
Efficacy of MEK inhibition in a recurrent malignant peripheral nerve sheath tumorSumanth Nagabushan, Loretta M S Lau, Paulette Barahona, et al.
Briefings in Bioinformatics|May 24, 2026
A scalable, multi-resolution consensus clustering approach for prioritizing robust signals from high-throughput screensShaine Chenxin Bao, Kathleen I Pishas, Karla J Cowley, et al.
NPJ Genomic Medicine|December 20, 2024
Somatic mutation in autosomal dominant polycystic kidney disease revealed by deep sequencing human kidney cystsAmali C Mallawaarachchi, Yvonne Hort, Laura Wedd, et al.
Pageof 49

Showing results (371-380 of 489) with videos related to

Sort By:
Pageof 49
Cerebellum (London, England)|May 20, 2019
Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome SequencingAryun Kim, Kishore R Kumar, Ryan L Davis, et al.
Cell Transplantation|March 13, 2012
Human islets express a marked proinflammatory molecular signature prior to transplantationMark J Cowley, Anita Weinberg, Nathan W Zammit, et al.
Frontiers in Pharmacology|May 15, 2023
Radiation therapy attenuates lymphatic vessel repair by reducing VEGFR-3 signallingVinochani Pillay, Lipi Shukla, Prad Herle, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 1, 2019
Aquaporin-4 IgG seropositivity is associated with worse visual outcomes after optic neuritis than MOG-IgG seropositivity and multiple sclerosis, independent of macular ganglion cell layer thinningElias S Sotirchos, Angeliki Filippatou, Kathryn C Fitzgerald, et al.
Science (New York, N.Y.)|March 26, 2026
Distinctive DNA sequence features define epigenetic longevity of inflammatory memoryChristopher J Cowley, Sairaj M Sajjath, Luis F Soto-Ugaldi, et al.
The British Journal of Surgery|March 1, 1979
A prospective randomized trial of vagotomy in chronic duodenal ulcerationC G Koffman, J B Elder, I E Gillespie, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
NPJ Precision Oncology|February 13, 2021
Efficacy of MEK inhibition in a recurrent malignant peripheral nerve sheath tumorSumanth Nagabushan, Loretta M S Lau, Paulette Barahona, et al.
Briefings in Bioinformatics|May 24, 2026
A scalable, multi-resolution consensus clustering approach for prioritizing robust signals from high-throughput screensShaine Chenxin Bao, Kathleen I Pishas, Karla J Cowley, et al.
NPJ Genomic Medicine|December 20, 2024
Somatic mutation in autosomal dominant polycystic kidney disease revealed by deep sequencing human kidney cystsAmali C Mallawaarachchi, Yvonne Hort, Laura Wedd, et al.
Pageof 49