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Frontiers in Cellular Neuroscience|February 7, 2024
Human iPSC-derived retinal organoids develop robust Alzheimer's disease neuropathologyEthan James, Anne Vielle, Karen Cusato, et al.BMC Medical Genetics|April 9, 2004
Molecular epidemiology of DFNB1 deafness in FranceAnne-Françoise Roux, Nathalie Pallares-Ruiz, Anne Vielle, et al.Science Advances|February 4, 2021
A single-nucleotide change underlies the genetic assimilation of a plastic traitPaul Vigne, Clotilde Gimond, Céline Ferrari, et al.Human Mutation|April 4, 2007
Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patientsDavid Baux, Lise Larrieu, Catherine Blanchet, et al.Plos Genetics|October 3, 2012
H4K20me1 contributes to downregulation of X-linked genes for C. elegans dosage compensationAnne Vielle, Jackie Lang, Yan Dong, et al.The Journal of Clinical Endocrinology and Metabolism|September 13, 2007
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotypeFrancesca Lombardi, Francesca Gullotta, Marta Columbaro, et al.Genome Research|December 24, 2010
Broad chromosomal domains of histone modification patterns in C. elegansTao Liu, Andreas Rechtsteiner, Thea A Egelhofer, et al.Nature Structural & Molecular Biology|December 7, 2010
An assessment of histone-modification antibody qualityThea A Egelhofer, Aki Minoda, Sarit Klugman, et al.Nature|August 29, 2014
Comparative analysis of metazoan chromatin organizationJoshua W K Ho, Youngsook L Jung, Tao Liu, et al.Science (New York, N.Y.)|December 24, 2010
Integrative analysis of the Caenorhabditis elegans genome by the modENCODE projectMark B Gerstein, Zhi John Lu, Eric L Van Nostrand, et al.Pageof 2