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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.
Scientific Reports|August 18, 2023
The interleukin-11 receptor variant p.W307R results in craniosynostosis in humansIlyas Ahmad, Juliane Lokau, Birte Kespohl, et al.
American Journal of Human Genetics|January 27, 2015
A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndromeFrank Rutsch, Mary MacDougall, Changming Lu, et al.
The Journal of Pathology|October 10, 2019
Prekallikrein inhibits innate immune signaling in the lung and impairs host defense during pneumosepsis in miceChao Ding, Brendon P Scicluna, Ingrid Stroo, et al.
International Journal of Cancer|August 29, 2018
Capturing colorectal cancer inter-tumor heterogeneity in patient-derived xenograft (PDX) modelsPramudita R Prasetyanti, Sander R van Hooff, Tessa van Herwaarden, et al.
Molecular Genetics & Genomic Medicine|October 6, 2015
Mutations in CDK5RAP2 cause Seckel syndromeGökhan Yigit, Karen E Brown, Hülya Kayserili, et al.
Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.
European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (ECP)|September 14, 2016
The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancerGuido Neidhardt, Alexandra Becker, Jan Hauke, et al.
BMC Pulmonary Medicine|January 7, 2005
Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma familiesJanine Altmüller, Corinna Seidel, Young-Ae Lee, et al.
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