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J Saunders

Showing results (1031-1040 of 1,085) with videos related to

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Nature Communications|February 6, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidineVíctor Faundes, Martin D Jennings, Siobhan Crilly, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 15, 2016
A Promyelocytic Leukemia Protein-Thrombospondin-2 Axis and the Risk of Relapse in NeuroblastomaMaria Dvorkina, Valentina Nieddu, Shalini Chakelam, et al.
American Journal of Human Genetics|October 7, 2000
A major locus for myoclonus-dystonia maps to chromosome 7q in eight familiesC Klein, K Schilling, R J Saunders-Pullman, et al.
Nature Reviews. Microbiology|September 29, 2015
An updated evolutionary classification of CRISPR-Cas systemsKira S Makarova, Yuri I Wolf, Omer S Alkhnbashi, et al.
The Lancet. Respiratory Medicine|May 5, 2015
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findingsLaurel K Willig, Josh E Petrikin, Laurie D Smith, et al.
Nature Communications|September 29, 2019
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese populationRyo Takata, Atsushi Takahashi, Masashi Fujita, et al.
BJU International|July 2, 2021
The BARCODE1 Pilot: a feasibility study of using germline single nucleotide polymorphisms to target prostate cancer screeningSarah Benafif, Holly Ni Raghallaigh, Eva McGrowder, et al.
Cancer Discovery|August 7, 2023
Inhibition of METTL3 Results in a Cell-Intrinsic Interferon Response That Enhances Antitumor ImmunityAndrew A Guirguis, Yaara Ofir-Rosenfeld, Kathy Knezevic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2023
LHX2 haploinsufficiency causes a variable neurodevelopmental disorderCosima M Schmid, Anne Gregor, Gregory Costain, et al.
European Journal of Ophthalmology|December 13, 2023
Myopia management algorithm. Annexe to the article titled Update and guidance on management of myopia. European Society of Ophthalmology in cooperation with International Myopia InstituteBeáta Tapasztó, Daniel Ian Flitcroft, Wagih A Aclimandos, et al.
Pageof 109

Showing results (1031-1040 of 1,085) with videos related to

Sort By:
Pageof 109
Nature Communications|February 6, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidineVíctor Faundes, Martin D Jennings, Siobhan Crilly, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 15, 2016
A Promyelocytic Leukemia Protein-Thrombospondin-2 Axis and the Risk of Relapse in NeuroblastomaMaria Dvorkina, Valentina Nieddu, Shalini Chakelam, et al.
American Journal of Human Genetics|October 7, 2000
A major locus for myoclonus-dystonia maps to chromosome 7q in eight familiesC Klein, K Schilling, R J Saunders-Pullman, et al.
Nature Reviews. Microbiology|September 29, 2015
An updated evolutionary classification of CRISPR-Cas systemsKira S Makarova, Yuri I Wolf, Omer S Alkhnbashi, et al.
The Lancet. Respiratory Medicine|May 5, 2015
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findingsLaurel K Willig, Josh E Petrikin, Laurie D Smith, et al.
Nature Communications|September 29, 2019
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese populationRyo Takata, Atsushi Takahashi, Masashi Fujita, et al.
BJU International|July 2, 2021
The BARCODE1 Pilot: a feasibility study of using germline single nucleotide polymorphisms to target prostate cancer screeningSarah Benafif, Holly Ni Raghallaigh, Eva McGrowder, et al.
Cancer Discovery|August 7, 2023
Inhibition of METTL3 Results in a Cell-Intrinsic Interferon Response That Enhances Antitumor ImmunityAndrew A Guirguis, Yaara Ofir-Rosenfeld, Kathy Knezevic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2023
LHX2 haploinsufficiency causes a variable neurodevelopmental disorderCosima M Schmid, Anne Gregor, Gregory Costain, et al.
European Journal of Ophthalmology|December 13, 2023
Myopia management algorithm. Annexe to the article titled Update and guidance on management of myopia. European Society of Ophthalmology in cooperation with International Myopia InstituteBeáta Tapasztó, Daniel Ian Flitcroft, Wagih A Aclimandos, et al.
Pageof 109