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Biochimica Et Biophysica Acta|February 9, 2013
Control of mitogenic and motogenic pathways by miR-198, diminishing hepatoma cell growth and migrationNatalia Elfimova, Elisabeth Sievers, Hannah Eischeid, et al.
Circulation. Genomic and Precision Medicine|May 23, 2025
Thoracic Aortic Disease in Patients With Heterozygous Variants Outside the Central Region of <i>FBN2</i>Till Joscha Demal, Marco Sachse, Celia Metzlaff, et al.
Nature Genetics|May 29, 2012
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiencyEirini Meimaridou, Julia Kowalczyk, Leonardo Guasti, et al.
Oncogene|January 12, 2018
AATF suppresses apoptosis, promotes proliferation and is critical for Kras-driven lung cancerDaniela Welcker, Manaswita Jain, Safiya Khurshid, et al.
Cell Stem Cell|April 16, 2019
Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCsMagdalena Laugsch, Michaela Bartusel, Rizwan Rehimi, et al.
European Heart Journal|June 12, 2008
Role of balloon occlusion for mononuclear bone marrow cell deposition after intracoronary injection in pigs with reperfused myocardial infarctionPaschalis Tossios, Benjamin Krausgrill, Matthias Schmidt, et al.
BMC Genomics|December 31, 2013
The genome of Romanomermis culicivorax: revealing fundamental changes in the core developmental genetic toolkit in NematodaPhilipp H Schiffer, Michael Kroiher, Christopher Kraus, et al.
American Journal of Human Genetics|May 10, 2011
Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing lossAntje K Huebner, Marta Gandia, Peter Frommolt, et al.
Nature Cell Biology|February 23, 2016
Dicer1-miR-328-Bace1 signalling controls brown adipose tissue differentiation and functionMatteo Oliverio, Elena Schmidt, Jan Mauer, et al.
Human Molecular Genetics|August 7, 2013
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephalyMuhammad S Hussain, Shahid M Baig, Sascha Neumann, et al.
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