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Development (Cambridge, England)|November 4, 2000
Asymmetric nodal signaling in the zebrafish diencephalon positions the pineal organJ O Liang, A Etheridge, L Hantsoo, et al.
European Journal of Biochemistry|June 26, 2001
Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscleC Thirion, R Stucka, B Mendel, et al.
The Journal of Biological Chemistry|May 10, 2011
Chromatin-modifying complex component Nurf55/p55 associates with histones H3 and H4 and polycomb repressive complex 2 subunit Su(z)12 through partially overlapping binding sitesAgnieszka J Nowak, Claudio Alfieri, Christian U Stirnimann, et al.
The Journal of Biological Chemistry|January 25, 2007
Epigenetic silencing of CYP24 in tumor-derived endothelial cells contributes to selective growth inhibition by calcitriolIvy Chung, Adam R Karpf, Josephia R Muindi, et al.
Immunohorizons|May 12, 2023
The Plasma Cell Infiltrate Populating the Muscle Tissue of Patients with Inclusion Body Myositis Features Distinct B Cell Receptor Repertoire PropertiesRoy Jiang, Bhaskar Roy, Qian Wu, et al.
Genes, Chromosomes & Cancer|August 14, 2012
Differential copy number aberrations in novel candidate genes associated with progression from in situ to invasive ductal carcinoma of the breastShaoxi Liao, Mohamed M Desouki, Daniel P Gaile, et al.
Cancer Genetics and Cytogenetics|February 14, 2009
Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18Huferesh K Darbary, Smitha S Dutt, Sheila J Sait, et al.
European Journal of Human Genetics : EJHG|December 20, 2024
Patients' perspectives regarding health professionals contacting their relatives about genetic risk directly (with patient consent)Jane Tiller, Keri Finlay, Evanthia O Madelli, et al.
Frontiers in Immunology|June 6, 2022
Acute Intoxication With Alcohol Reduces Trauma-Induced Proinflammatory Response and Barrier Breakdown in the Lung via the Wnt/β-Catenin Signaling PathwayLaurens Noack, Katrin Bundkirchen, Baolin Xu, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Smith-Magenis syndrome and Moyamoya disease in a patient with del(17)(p11.2p13.1)Santhosh Girirajan, Roberto Mendoza-Londono, Christopher N Vlangos, et al.
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