Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Salih Tuna

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
The Journal of Allergy and Clinical Immunology|February 26, 2018
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in EuropeansPaul Tuijnenburg, Hana Lango Allen, Siobhan O Burns, et al.
Blood|May 9, 2019
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disordersKate Downes, Karyn Megy, Daniel Duarte, et al.
The Journal of Experimental Medicine|June 26, 2019
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responsesSarah Spencer, Sevgi Köstel Bal, William Egner, et al.
Blood Advances|August 5, 2020
Development and validation of a universal blood donor genotyping platform: a multinational prospective studyNicholas S Gleadall, Barbera Veldhuisen, Jeremy Gollub, et al.
Science (New York, N.Y.)|May 25, 2019
Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.
Blood|February 26, 2016
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing lossSimon Stritt, Paquita Nurden, Ernest Turro, et al.
Nature Communications|July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancersRomina Petersen, John J Lambourne, Biola M Javierre, et al.
Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.
Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.
Blood|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
The Journal of Allergy and Clinical Immunology|February 26, 2018
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in EuropeansPaul Tuijnenburg, Hana Lango Allen, Siobhan O Burns, et al.
Blood|May 9, 2019
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disordersKate Downes, Karyn Megy, Daniel Duarte, et al.
The Journal of Experimental Medicine|June 26, 2019
Loss of the interleukin-6 receptor causes immunodeficiency, atopy, and abnormal inflammatory responsesSarah Spencer, Sevgi Köstel Bal, William Egner, et al.
Blood Advances|August 5, 2020
Development and validation of a universal blood donor genotyping platform: a multinational prospective studyNicholas S Gleadall, Barbera Veldhuisen, Jeremy Gollub, et al.
Science (New York, N.Y.)|May 25, 2019
Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.
Blood|February 26, 2016
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing lossSimon Stritt, Paquita Nurden, Ernest Turro, et al.
Nature Communications|July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancersRomina Petersen, John J Lambourne, Biola M Javierre, et al.
Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.
Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.
Blood|April 17, 2016
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersIlenia Simeoni, Jonathan C Stephens, Fengyuan Hu, et al.
Pageof 2