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Salih Tuna

Showing results (1-10 of 20) with videos related to

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Bioinformatics (Oxford, England)|March 10, 2010
Reducing the algorithmic variability in transcriptome-based inferenceSalih Tuna, Mahesan Niranjan
The Journal of Craniofacial Surgery|May 4, 2019
Craniometric Analysis of Skullbase With Magnetic Resonance Imaging in Patients With Chiari MalformationGonul Guvenc, Ali Firat Sarp, Ceren Kizmazoglu, et al.
BMC Cardiovascular Disorders|August 27, 2014
Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemiaIngrid Brænne, Benedikt Reiz, Anja Medack, et al.
Cell Reports|August 28, 2017
The Dnmt3L ADD Domain Controls Cytosine Methylation Establishment during SpermatogenesisGeorgios Vlachogiannis, Chad E Niederhuth, Salih Tuna, et al.
Cell Reports|February 17, 2015
The Dnmt3L ADD Domain Controls Cytosine Methylation Establishment during SpermatogenesisGeorgios Vlachogiannis, Chad E Niederhuth, Salih Tuna, et al.
Nature Communications|April 10, 2020
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Blood|June 23, 2017
Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleedingSarah K Westbury, Matthias Canault, Daniel Greene, et al.
Journal of the American Society of Nephrology : JASN|January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 GlomerulopathyAdam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
American Journal of Human Genetics|August 4, 2023
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disordersAlba Sanchis-Juan, Karyn Megy, Jonathan Stephens, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|March 10, 2010
Reducing the algorithmic variability in transcriptome-based inferenceSalih Tuna, Mahesan Niranjan
The Journal of Craniofacial Surgery|May 4, 2019
Craniometric Analysis of Skullbase With Magnetic Resonance Imaging in Patients With Chiari MalformationGonul Guvenc, Ali Firat Sarp, Ceren Kizmazoglu, et al.
BMC Cardiovascular Disorders|August 27, 2014
Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemiaIngrid Brænne, Benedikt Reiz, Anja Medack, et al.
Cell Reports|August 28, 2017
The Dnmt3L ADD Domain Controls Cytosine Methylation Establishment during SpermatogenesisGeorgios Vlachogiannis, Chad E Niederhuth, Salih Tuna, et al.
Cell Reports|February 17, 2015
The Dnmt3L ADD Domain Controls Cytosine Methylation Establishment during SpermatogenesisGeorgios Vlachogiannis, Chad E Niederhuth, Salih Tuna, et al.
Nature Communications|April 10, 2020
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Nature Communications|July 24, 2020
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humansWei Wei, Alistair T Pagnamenta, Nicholas Gleadall, et al.
Blood|June 23, 2017
Expanded repertoire of <i>RASGRP2</i> variants responsible for platelet dysfunction and severe bleedingSarah K Westbury, Matthias Canault, Daniel Greene, et al.
Journal of the American Society of Nephrology : JASN|January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 GlomerulopathyAdam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
American Journal of Human Genetics|August 4, 2023
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disordersAlba Sanchis-Juan, Karyn Megy, Jonathan Stephens, et al.
Pageof 2