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P Hoffman

Showing results (1001-1010 of 1,048) with videos related to

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Brain : a Journal of Neurology|February 16, 2006
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regenerationMarina Bakay, Zuyi Wang, Gisela Melcon, et al.
Clinical Colorectal Cancer|September 2, 2006
Isolation and characterization of circulating tumor cells in patients with metastatic colorectal cancerSteven J Cohen, R Katherine Alpaugh, Steve Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2015
Large-scale serum protein biomarker discovery in Duchenne muscular dystrophyYetrib Hathout, Edward Brody, Paula R Clemens, et al.
Journal of Translational Medicine|May 6, 2016
Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlationsJ K Poninska, Z T Bilinska, M Franaszczyk, et al.
JAMA Surgery|June 9, 2016
Preoperative Modified FOLFIRINOX Treatment Followed by Capecitabine-Based Chemoradiation for Borderline Resectable Pancreatic Cancer: Alliance for Clinical Trials in Oncology Trial A021101Matthew H G Katz, Qian Shi, Syed A Ahmad, et al.
Skeletal Muscle|December 4, 2015
Elusive sources of variability of dystrophin rescue by exon skippingMaria Candida Vila, Margaret Benny Klimek, James S Novak, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 6, 2012
Canine models of Duchenne muscular dystrophy and their use in therapeutic strategiesJoe N Kornegay, Janet R Bogan, Daniel J Bogan, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophyPietro Spitali, Irina Zaharieva, Stefan Bohringer, et al.
Journal of Child Neurology|February 12, 2008
Genetic and clinical heterogeneity in eIF2B-related disorderJelena Maletkovic, Raphael Schiffmann, J Rafael Gorospe, et al.
Science (New York, N.Y.)|January 18, 2020
Correlative three-dimensional super-resolution and block-face electron microscopy of whole vitreously frozen cellsDavid P Hoffman, Gleb Shtengel, C Shan Xu, et al.
Pageof 105

Showing results (1001-1010 of 1,048) with videos related to

Sort By:
Pageof 105
Brain : a Journal of Neurology|February 16, 2006
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regenerationMarina Bakay, Zuyi Wang, Gisela Melcon, et al.
Clinical Colorectal Cancer|September 2, 2006
Isolation and characterization of circulating tumor cells in patients with metastatic colorectal cancerSteven J Cohen, R Katherine Alpaugh, Steve Gross, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2015
Large-scale serum protein biomarker discovery in Duchenne muscular dystrophyYetrib Hathout, Edward Brody, Paula R Clemens, et al.
Journal of Translational Medicine|May 6, 2016
Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlationsJ K Poninska, Z T Bilinska, M Franaszczyk, et al.
JAMA Surgery|June 9, 2016
Preoperative Modified FOLFIRINOX Treatment Followed by Capecitabine-Based Chemoradiation for Borderline Resectable Pancreatic Cancer: Alliance for Clinical Trials in Oncology Trial A021101Matthew H G Katz, Qian Shi, Syed A Ahmad, et al.
Skeletal Muscle|December 4, 2015
Elusive sources of variability of dystrophin rescue by exon skippingMaria Candida Vila, Margaret Benny Klimek, James S Novak, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 6, 2012
Canine models of Duchenne muscular dystrophy and their use in therapeutic strategiesJoe N Kornegay, Janet R Bogan, Daniel J Bogan, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophyPietro Spitali, Irina Zaharieva, Stefan Bohringer, et al.
Journal of Child Neurology|February 12, 2008
Genetic and clinical heterogeneity in eIF2B-related disorderJelena Maletkovic, Raphael Schiffmann, J Rafael Gorospe, et al.
Science (New York, N.Y.)|January 18, 2020
Correlative three-dimensional super-resolution and block-face electron microscopy of whole vitreously frozen cellsDavid P Hoffman, Gleb Shtengel, C Shan Xu, et al.
Pageof 105