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Bryan Krock

Showing results (1-10 of 15) with videos related to

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Clinics in Laboratory Medicine|July 26, 2021
Molecular Genetics of Pediatric Acute Myeloid LeukemiaBryan Krock, Matthew J Oberley
Cell Metabolism|January 4, 2011
The tumor suppressor LKB1 emerges as a critical factor in hematopoietic stem cell biologyBryan Krock, Nicolas Skuli, M Celeste Simon
Expert Review of Molecular Diagnostics|July 9, 2016
Sequencing-based diagnostics for pediatric genetic diseases: progress and potentialAhmad N Abou Tayoun, Bryan Krock, Nancy B Spinner
Cytopathology : Official Journal of the British Society for Clinical Cytology|March 24, 2022
Cytological features of NUT-carcinoma harbouring an NSD3-NUTM1 fusionKimon V Argyropoulos, Lawrence Hsu Lin, Andre L Moreira, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2018
Congenital Hyperinsulinism and Hypopituitarism Attributable to a Mutation in FOXA2Mary Ellen Vajravelu, Jinghua Chai, Bryan Krock, et al.
Child Neurology Open|July 27, 2018
Novel <i>PLP1</i> Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical PhenotypesRebecca L Margraf, Jacob Durtschi, Bryan Krock, et al.
American Journal of Medical Genetics. Part A|March 6, 2020
Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndromeAmanda Barone Pritchard, Stanley M Kanai, Bryan Krock, et al.
Acta Neuropathologica|May 30, 2015
Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degenerationEunRan Suh, Edward B Lee, Donald Neal, et al.
Radiology|March 3, 2017
Ischemia Induces Quiescence and Autophagy Dependence in Hepatocellular CarcinomaTerence P F Gade, Elizabeth Tucker, Michael S Nakazawa, et al.
American Journal of Human Genetics|November 26, 2018
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating DefectsNiki T Loges, Dinu Antony, Ales Maver, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Clinics in Laboratory Medicine|July 26, 2021
Molecular Genetics of Pediatric Acute Myeloid LeukemiaBryan Krock, Matthew J Oberley
Cell Metabolism|January 4, 2011
The tumor suppressor LKB1 emerges as a critical factor in hematopoietic stem cell biologyBryan Krock, Nicolas Skuli, M Celeste Simon
Expert Review of Molecular Diagnostics|July 9, 2016
Sequencing-based diagnostics for pediatric genetic diseases: progress and potentialAhmad N Abou Tayoun, Bryan Krock, Nancy B Spinner
Cytopathology : Official Journal of the British Society for Clinical Cytology|March 24, 2022
Cytological features of NUT-carcinoma harbouring an NSD3-NUTM1 fusionKimon V Argyropoulos, Lawrence Hsu Lin, Andre L Moreira, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2018
Congenital Hyperinsulinism and Hypopituitarism Attributable to a Mutation in FOXA2Mary Ellen Vajravelu, Jinghua Chai, Bryan Krock, et al.
Child Neurology Open|July 27, 2018
Novel <i>PLP1</i> Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical PhenotypesRebecca L Margraf, Jacob Durtschi, Bryan Krock, et al.
American Journal of Medical Genetics. Part A|March 6, 2020
Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndromeAmanda Barone Pritchard, Stanley M Kanai, Bryan Krock, et al.
Acta Neuropathologica|May 30, 2015
Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degenerationEunRan Suh, Edward B Lee, Donald Neal, et al.
Radiology|March 3, 2017
Ischemia Induces Quiescence and Autophagy Dependence in Hepatocellular CarcinomaTerence P F Gade, Elizabeth Tucker, Michael S Nakazawa, et al.
American Journal of Human Genetics|November 26, 2018
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating DefectsNiki T Loges, Dinu Antony, Ales Maver, et al.
Pageof 2