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David Grynspan

Showing results (51-60 of 61) with videos related to

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 21, 2023
Synoptic Reporting in Clinical Placental Pathology: A Preliminary Investigation Into Report Findings and Interobserver AgreementSonia R Dancey, Samantha J Benton, Anthea J Lafreniere, et al.
Pediatric Blood & Cancer|May 17, 2017
H3.1 K36M mutation in a congenital-onset soft tissue neoplasmKristin D Kernohan, David Grynspan, Raveena Ramphal, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencingHao Liu, Sarah L Sawyer, Monika Gos, et al.
JIMD Reports|August 1, 2013
Infantile Sialic Acid Storage Disease: Two Unrelated Inuit Cases Homozygous for a Common Novel SLC17A5 MutationMatthew A Lines, C Anthony Rupar, Jack W Rip, et al.
International Journal of Molecular Sciences|October 14, 2022
Proteomics Profiling of Stool Samples from Preterm Neonates with SWATH/DIA Mass Spectrometry for Predicting Necrotizing EnterocolitisDavid Gagné, Elmira Shajari, Marie-Pier Thibault, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 15, 2015
The Placental Distal Villous Hypoplasia Pattern: Interobserver Agreement and Automated Fractal Dimension as an Objective MetricAnika Mukherjee, Adrian D C Chan, Sarah Keating, et al.
BMC Medical Genomics|January 24, 2016
Gene expression profiling in necrotizing enterocolitis reveals pathways common to those reported in Crohn's diseaseÉric Tremblay, Marie-Pier Thibault, Emanuela Ferretti, et al.
Placenta|May 31, 2016
Placental growth factor as a marker of fetal growth restriction caused by placental dysfunctionSamantha J Benton, Lesley M McCowan, Alexander E P Heazell, et al.
American Journal of Human Genetics|November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality DefectsSerge Bonnefoy, Christopher M Watson, Kristin D Kernohan, et al.
Science (New York, N.Y.)|May 14, 2016
Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscapeChao Lu, Siddhant U Jain, Dominik Hoelper, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 21, 2023
Synoptic Reporting in Clinical Placental Pathology: A Preliminary Investigation Into Report Findings and Interobserver AgreementSonia R Dancey, Samantha J Benton, Anthea J Lafreniere, et al.
Pediatric Blood & Cancer|May 17, 2017
H3.1 K36M mutation in a congenital-onset soft tissue neoplasmKristin D Kernohan, David Grynspan, Raveena Ramphal, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencingHao Liu, Sarah L Sawyer, Monika Gos, et al.
JIMD Reports|August 1, 2013
Infantile Sialic Acid Storage Disease: Two Unrelated Inuit Cases Homozygous for a Common Novel SLC17A5 MutationMatthew A Lines, C Anthony Rupar, Jack W Rip, et al.
International Journal of Molecular Sciences|October 14, 2022
Proteomics Profiling of Stool Samples from Preterm Neonates with SWATH/DIA Mass Spectrometry for Predicting Necrotizing EnterocolitisDavid Gagné, Elmira Shajari, Marie-Pier Thibault, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 15, 2015
The Placental Distal Villous Hypoplasia Pattern: Interobserver Agreement and Automated Fractal Dimension as an Objective MetricAnika Mukherjee, Adrian D C Chan, Sarah Keating, et al.
BMC Medical Genomics|January 24, 2016
Gene expression profiling in necrotizing enterocolitis reveals pathways common to those reported in Crohn's diseaseÉric Tremblay, Marie-Pier Thibault, Emanuela Ferretti, et al.
Placenta|May 31, 2016
Placental growth factor as a marker of fetal growth restriction caused by placental dysfunctionSamantha J Benton, Lesley M McCowan, Alexander E P Heazell, et al.
American Journal of Human Genetics|November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality DefectsSerge Bonnefoy, Christopher M Watson, Kristin D Kernohan, et al.
Science (New York, N.Y.)|May 14, 2016
Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscapeChao Lu, Siddhant U Jain, Dominik Hoelper, et al.
Pageof 7