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Showing results (641-650 of 1,048) with videos related to

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Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.
Cancer Research|December 16, 1998
MUC1 synthetic peptide inhibition of intercellular adhesion molecule-1 and MUC1 binding requires six tandem repeatsJ L Kam, L H Regimbald, J H Hilgers, et al.
American Journal of Medical Genetics|February 1, 1983
Search for a red cell enzyme or serum protein marker in amyotrophic lateral sclerosis and parkinsonism-dementia of GuamN M Blake, R L Kirk, S R Wilson, et al.
Pediatric Research|May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequenciesR Ziadeh, E P Hoffman, D N Finegold, et al.
The Journal of Trauma|September 11, 1992
Associated aortic rupture-pelvic fracture: an alert for orthopedic and general surgeonsM G Ochsner, A P Hoffman, D DiPasquale, et al.
Developmental Biology|July 3, 2007
Laminin alpha5 is necessary for submandibular gland epithelial morphogenesis and influences FGFR expression through beta1 integrin signalingIvan T Rebustini, Vaishali N Patel, Julian S Stewart, et al.
Bioinformatics (Oxford, England)|December 30, 2008
Differential dependency network analysis to identify condition-specific topological changes in biological networksBai Zhang, Huai Li, Rebecca B Riggins, et al.
Plos Currents|November 17, 2018
Neurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DNHS)Mathula Thangarajh, Christopher F Spurney, Heather Gordish-Dressman, et al.
Developmental Cell|June 25, 2014
Hs3st3-modified heparan sulfate controls KIT+ progenitor expansion by regulating 3-O-sulfotransferasesVaishali N Patel, Isabelle M A Lombaert, Samuel N Cowherd, et al.
The Journal of Clinical Endocrinology and Metabolism|August 3, 2024
Adrenal Suppression From Vamorolone and Prednisone in Duchenne Muscular Dystrophy: Results From the Phase 2b Clinical TrialAlexandra Ahmet, Rebecca Tobin, Utkarsh J Dang, et al.
Pageof 105

Showing results (641-650 of 1,048) with videos related to

Sort By:
Pageof 105
Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.
Cancer Research|December 16, 1998
MUC1 synthetic peptide inhibition of intercellular adhesion molecule-1 and MUC1 binding requires six tandem repeatsJ L Kam, L H Regimbald, J H Hilgers, et al.
American Journal of Medical Genetics|February 1, 1983
Search for a red cell enzyme or serum protein marker in amyotrophic lateral sclerosis and parkinsonism-dementia of GuamN M Blake, R L Kirk, S R Wilson, et al.
Pediatric Research|May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequenciesR Ziadeh, E P Hoffman, D N Finegold, et al.
The Journal of Trauma|September 11, 1992
Associated aortic rupture-pelvic fracture: an alert for orthopedic and general surgeonsM G Ochsner, A P Hoffman, D DiPasquale, et al.
Developmental Biology|July 3, 2007
Laminin alpha5 is necessary for submandibular gland epithelial morphogenesis and influences FGFR expression through beta1 integrin signalingIvan T Rebustini, Vaishali N Patel, Julian S Stewart, et al.
Bioinformatics (Oxford, England)|December 30, 2008
Differential dependency network analysis to identify condition-specific topological changes in biological networksBai Zhang, Huai Li, Rebecca B Riggins, et al.
Plos Currents|November 17, 2018
Neurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural History Study (DNHS)Mathula Thangarajh, Christopher F Spurney, Heather Gordish-Dressman, et al.
Developmental Cell|June 25, 2014
Hs3st3-modified heparan sulfate controls KIT+ progenitor expansion by regulating 3-O-sulfotransferasesVaishali N Patel, Isabelle M A Lombaert, Samuel N Cowherd, et al.
The Journal of Clinical Endocrinology and Metabolism|August 3, 2024
Adrenal Suppression From Vamorolone and Prednisone in Duchenne Muscular Dystrophy: Results From the Phase 2b Clinical TrialAlexandra Ahmet, Rebecca Tobin, Utkarsh J Dang, et al.
Pageof 105