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Nucleic Acids Research|October 4, 2023
Compartmentalization of androgen receptors at endogenous genes in living cellsSelçuk Yavuz, Hélène Kabbech, Jente van Staalduinen, et al.
Science (New York, N.Y.)|January 31, 1998
Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patientsF W van Leeuwen, D P de Kleijn, H H van den Hurk, et al.
Nature|June 25, 2015
The core spliceosome as target and effector of non-canonical ATM signallingMaria Tresini, Daniël O Warmerdam, Petros Kolovos, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 1, 1997
TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significanceJ E Rubnitz, J R Downing, C H Pui, et al.
Development (Cambridge, England)|April 8, 2020
Multifaceted actions of Zeb2 in postnatal neurogenesis from the ventricular-subventricular zone to the olfactory bulbAstrid Deryckere, Elke Stappers, Ruben Dries, et al.
Neurobiology of Disease|June 23, 2004
Hearing loss following Gata3 haploinsufficiency is caused by cochlear disorderJacqueline van der Wees, Marjolein A J van Looij, M Martijn de Ruiter, et al.
Epigenetics & Chromatin|December 31, 2016
The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomesTobias A Knoch, Malte Wachsmuth, Nick Kepper, et al.
Nature Genetics|May 3, 2011
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromesErik Engelen, Umut Akinci, Jan Christian Bryne, et al.
American Journal of Human Genetics|September 4, 2012
RTTN mutations link primary cilia function to organization of the human cerebral cortexSima Kheradmand Kia, Elly Verbeek, Erik Engelen, et al.
Pharmacogenomics|October 13, 2012
KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patientsJoseph Borg, Marios Phylactides, Marina Bartsakoulia, et al.
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