Showing results (301-310 of 310) with videos related to

Sort By:
Pageof 31
You have reached the last page of results.This site can display upto 310 results.
International Journal of Cancer|October 10, 2022
Proteomic signature for detection of high-grade ovarian cancer in germline BRCA mutation carriersKeren Bahar-Shany, Georgina D Barnabas, Lisa Deutsch, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Clinical Kidney Journal|February 10, 2025
Multiethnic prevalence of the APOL1 G1 and G2 variants among the Israeli dialysis populationDror Ben-Ruby, Danit Atias-Varon, Maayan Kagan, et al.
Brain : a Journal of Neurology|April 2, 2017
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathyOrtal Barel, May Christine V Malicdan, Bruria Ben-Zeev, et al.
Pediatric Nephrology (Berlin, Germany)|January 7, 2022
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insightsBen Pode-Shakked, Yishay Ben-Moshe, Ortal Barel, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 23, 2016
Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair DeficiencyEric Bouffet, Valérie Larouche, Brittany B Campbell, et al.
Nature Communications|June 4, 2014
Genome-wide adaptive complexes to underground stresses in blind mole rats SpalaxXiaodong Fang, Eviatar Nevo, Lijuan Han, et al.
RNA Biology|April 20, 2018
Positioning Europe for the EPITRANSCRIPTOMICS challengeMichael F Jantsch, Alessandro Quattrone, Mary O'Connell, et al.
Cell|October 24, 2017
Comprehensive Analysis of Hypermutation in Human CancerBrittany B Campbell, Nicholas Light, David Fabrizio, et al.
American Journal of Human Genetics|July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndromeDmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Pageof 31