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Showing results (891-900 of 1,048) with videos related to

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American Journal of Human Genetics|January 9, 2008
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophyJuliane Ramser, Mary Ellen Ahearn, Claus Lenski, et al.
Journal of the American Academy of Orthopaedic Surgeons. Global Research & Reviews|April 4, 2025
Rating the Efficacy of Diagnostic Imaging Studies Conducted for the Workup of Musculoskeletal TumorsWilliam T Li, Sumail Bhogal, Matthew F Gong, et al.
Medicine and Science in Sports and Exercise|July 6, 2004
Functional polymorphisms associated with human muscle size and strengthPaul D Thompson, Niall Moyna, Richard Seip, et al.
Cell Metabolism|October 11, 2005
Elevated stearoyl-CoA desaturase-1 expression in skeletal muscle contributes to abnormal fatty acid partitioning in obese humansMatthew W Hulver, Jason R Berggren, Michael J Carper, et al.
Diabetologia|August 6, 2014
Metabolite signatures of exercise training in human skeletal muscle relate to mitochondrial remodelling and cardiometabolic fitnessKim M Huffman, Timothy R Koves, Monica J Hubal, et al.
Urology|July 5, 2011
Clinical Stage T1 micropapillary urothelial carcinoma presenting with metastasis to the pancreasDaniel Canter, Jay Simhan, Marc C Smaldone, et al.
International Journal of Radiation Oncology, Biology, Physics|January 5, 2016
RECQ1 A159C Polymorphism Is Associated With Overall Survival of Patients With Resected Pancreatic Cancer: A Replication Study in NRG Oncology Radiation Therapy Oncology Group 9704Donghui Li, Jennifer Moughan, Christopher Crane, et al.
Cancer|June 22, 1999
The evaluation and treatment of patients receiving radiation therapy for carcinoma of the esophagus: results of the 1992-1994 Patterns of Care StudyL R Coia, B D Minsky, M J John, et al.
Neurology|June 13, 2001
MeCP2 mutations in children with and without the phenotype of Rett syndromeK Hoffbuhr, J M Devaney, B LaFleur, et al.
Frontiers in Molecular Neuroscience|January 27, 2025
Serum metabolomic signatures of patients with rare neurogenetic diseases: an insight into potential biomarkers and treatment targetsNalaka Wijekoon, Lakmal Gonawala, Pyara Ratnayake, et al.
Pageof 105

Showing results (891-900 of 1,048) with videos related to

Sort By:
Pageof 105
American Journal of Human Genetics|January 9, 2008
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophyJuliane Ramser, Mary Ellen Ahearn, Claus Lenski, et al.
Journal of the American Academy of Orthopaedic Surgeons. Global Research & Reviews|April 4, 2025
Rating the Efficacy of Diagnostic Imaging Studies Conducted for the Workup of Musculoskeletal TumorsWilliam T Li, Sumail Bhogal, Matthew F Gong, et al.
Medicine and Science in Sports and Exercise|July 6, 2004
Functional polymorphisms associated with human muscle size and strengthPaul D Thompson, Niall Moyna, Richard Seip, et al.
Cell Metabolism|October 11, 2005
Elevated stearoyl-CoA desaturase-1 expression in skeletal muscle contributes to abnormal fatty acid partitioning in obese humansMatthew W Hulver, Jason R Berggren, Michael J Carper, et al.
Diabetologia|August 6, 2014
Metabolite signatures of exercise training in human skeletal muscle relate to mitochondrial remodelling and cardiometabolic fitnessKim M Huffman, Timothy R Koves, Monica J Hubal, et al.
Urology|July 5, 2011
Clinical Stage T1 micropapillary urothelial carcinoma presenting with metastasis to the pancreasDaniel Canter, Jay Simhan, Marc C Smaldone, et al.
International Journal of Radiation Oncology, Biology, Physics|January 5, 2016
RECQ1 A159C Polymorphism Is Associated With Overall Survival of Patients With Resected Pancreatic Cancer: A Replication Study in NRG Oncology Radiation Therapy Oncology Group 9704Donghui Li, Jennifer Moughan, Christopher Crane, et al.
Cancer|June 22, 1999
The evaluation and treatment of patients receiving radiation therapy for carcinoma of the esophagus: results of the 1992-1994 Patterns of Care StudyL R Coia, B D Minsky, M J John, et al.
Neurology|June 13, 2001
MeCP2 mutations in children with and without the phenotype of Rett syndromeK Hoffbuhr, J M Devaney, B LaFleur, et al.
Frontiers in Molecular Neuroscience|January 27, 2025
Serum metabolomic signatures of patients with rare neurogenetic diseases: an insight into potential biomarkers and treatment targetsNalaka Wijekoon, Lakmal Gonawala, Pyara Ratnayake, et al.
Pageof 105