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EMBO Reports
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January 21, 2015
Glycolytic enzymes localize to ribonucleoprotein granules in Drosophila germ cells, bind Tudor and protect from transposable elements
Ming Gao, Travis C Thomson, T Michael Creed, et al.
Nature
|
November 23, 2012
Autism-related deficits via dysregulated eIF4E-dependent translational control
Christos G Gkogkas, Arkady Khoutorsky, Israeli Ran, et al.
Molecular Cell
|
November 5, 2021
Histone H3.3 K27M and K36M mutations de-repress transposable elements through perturbation of antagonistic chromatin marks
Amel Chaouch, Johannes Berlandi, Carol C L Chen, et al.
Clinical and Translational Science
|
August 11, 2017
Progress in Rare Diseases Research 2010-2016: An IRDiRC Perspective
Hugh J S Dawkins, Ruxandra Draghia-Akli, Paul Lasko, et al.
Clinical Genetics
|
October 21, 2021
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene
Servi J C Stevens, Constance T R M Stumpel, Karin E M Diderich, et al.
Lab Animal
|
June 24, 2024
Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)
Kornelia Ellwanger, Julie A Brill, Elke de Boer, et al.
American Journal of Human Genetics
|
September 23, 2022
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans
Margot J Wyrwoll, Channah M Gaasbeek, Ieva Golubickaite, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2017
Initiating an undiagnosed diseases program in the Western Australian public health system
Gareth Baynam, Stephanie Broley, Alicia Bauskis, et al.
Science Translational Medicine
|
June 5, 2015
Global implementation of genomic medicine: We are not alone
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, et al.
BMC Genomics
|
June 20, 2014
Relationship between genome and epigenome--challenges and requirements for future research
Geneviève Almouzni, Lucia Altucci, Bruno Amati, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
EMBO Reports
|
January 21, 2015
Glycolytic enzymes localize to ribonucleoprotein granules in Drosophila germ cells, bind Tudor and protect from transposable elements
Ming Gao, Travis C Thomson, T Michael Creed, et al.
Nature
|
November 23, 2012
Autism-related deficits via dysregulated eIF4E-dependent translational control
Christos G Gkogkas, Arkady Khoutorsky, Israeli Ran, et al.
Molecular Cell
|
November 5, 2021
Histone H3.3 K27M and K36M mutations de-repress transposable elements through perturbation of antagonistic chromatin marks
Amel Chaouch, Johannes Berlandi, Carol C L Chen, et al.
Clinical and Translational Science
|
August 11, 2017
Progress in Rare Diseases Research 2010-2016: An IRDiRC Perspective
Hugh J S Dawkins, Ruxandra Draghia-Akli, Paul Lasko, et al.
Clinical Genetics
|
October 21, 2021
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene
Servi J C Stevens, Constance T R M Stumpel, Karin E M Diderich, et al.
Lab Animal
|
June 24, 2024
Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)
Kornelia Ellwanger, Julie A Brill, Elke de Boer, et al.
American Journal of Human Genetics
|
September 23, 2022
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans
Margot J Wyrwoll, Channah M Gaasbeek, Ieva Golubickaite, et al.
Orphanet Journal of Rare Diseases
|
May 5, 2017
Initiating an undiagnosed diseases program in the Western Australian public health system
Gareth Baynam, Stephanie Broley, Alicia Bauskis, et al.
Science Translational Medicine
|
June 5, 2015
Global implementation of genomic medicine: We are not alone
Teri A Manolio, Marc Abramowicz, Fahd Al-Mulla, et al.
BMC Genomics
|
June 20, 2014
Relationship between genome and epigenome--challenges and requirements for future research
Geneviève Almouzni, Lucia Altucci, Bruno Amati, et al.
Page
of 11