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Nucleic Acids Research|December 24, 2023
The BRCA2 R2645G variant increases DNA binding and induces hyper-recombinationLucia Alvaro-Aranda, Ambre Petitalot, Yasmina Djeghmoum, et al.
Nature Communications|July 9, 2026
Eight-qubit operation of a 300 mm SiMOS foundry-fabricated deviceAndreas Nickl, Nard Dumoulin Stuyck, Paul Steinacker, et al.
Journal of Medical Genetics|April 16, 2005
Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancerT Frebourg, C Oliveira, P Hochain, et al.
Brain : a Journal of Neurology|October 11, 2019
Exacerbation of C1q dysregulation, synaptic loss and memory deficits in tau pathology linked to neuronal adenosine A2A receptorKevin Carvalho, Emilie Faivre, Marie J Pietrowski, et al.
Clinical Pharmacology and Therapeutics|May 27, 2025
Folinic Acid Prophylaxis and Dose Adjustments Enable Safe Treatment with Pemetrexed in Patients with Renal ImpairmentNikki de Rouw, Leila-Sophie Otten, Mart P Kicken, et al.
BMJ (Clinical Research Ed.)|November 26, 2015
Long term trends in prevalence of neural tube defects in Europe: population based studyBabak Khoshnood, Maria Loane, Hermien de Walle, et al.
Nature|April 29, 2026
Spatial atlas of diabetic kidney disease reveals a B cell-rich subgroupBernhard Dumoulin, Jonathan Levinsohn, Konstantin A Klötzer, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
BMC Pediatrics|October 22, 2010
Long term costs and effects of reducing the number of twin pregnancies in IVF by single embryo transfer: the TwinSing studyMirjam M J van Heesch, Gouke J Bonsel, John C M Dumoulin, et al.
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