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G Herrmann

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Nature Communications|July 4, 2019
Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epitheliumRaphael Brandt, Thomas Sell, Mareen Lüthen, et al.
Nature Communications|November 3, 2023
The lncRNA Sweetheart regulates compensatory cardiac hypertrophy after myocardial injury in murine malesSandra Rogala, Tamer Ali, Maria-Theodora Melissari, et al.
Nature Communications|May 12, 2017
Tau association with synaptic vesicles causes presynaptic dysfunctionLujia Zhou, Joseph McInnes, Keimpe Wierda, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Acta Neuropathologica Communications|December 22, 2019
Comparative profiling of the synaptic proteome from Alzheimer's disease patients with focus on the APOE genotypeRaphael Hesse, Maica Llavero Hurtado, Rosemary J Jackson, et al.
Plos One|January 5, 2011
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysisBernd Timmermann, Martin Kerick, Christina Roehr, et al.
Acta Neuropathologica Communications|December 15, 2015
Erratum to: Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Acta Neuropathologica Communications|September 4, 2015
Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
Pageof 62

Showing results (561-570 of 613) with videos related to

Sort By:
Pageof 62
Nature Communications|July 4, 2019
Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epitheliumRaphael Brandt, Thomas Sell, Mareen Lüthen, et al.
Nature Communications|November 3, 2023
The lncRNA Sweetheart regulates compensatory cardiac hypertrophy after myocardial injury in murine malesSandra Rogala, Tamer Ali, Maria-Theodora Melissari, et al.
Nature Communications|May 12, 2017
Tau association with synaptic vesicles causes presynaptic dysfunctionLujia Zhou, Joseph McInnes, Keimpe Wierda, et al.
Birth Defects Research|February 2, 2018
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate geneValerie Weitensteiner, Rong Zhang, Julia Bungenberg, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
Acta Neuropathologica Communications|December 22, 2019
Comparative profiling of the synaptic proteome from Alzheimer's disease patients with focus on the APOE genotypeRaphael Hesse, Maica Llavero Hurtado, Rosemary J Jackson, et al.
Plos One|January 5, 2011
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysisBernd Timmermann, Martin Kerick, Christina Roehr, et al.
Acta Neuropathologica Communications|December 15, 2015
Erratum to: Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Acta Neuropathologica Communications|September 4, 2015
Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapseChristopher M Henstridge, Rosemary J Jackson, JeeSoo M Kim, et al.
Plos Genetics|March 13, 2015
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophyMarkus Draaken, Michael Knapp, Tracie Pennimpede, et al.
Pageof 62