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European Journal of Human Genetics : EJHG|May 28, 2015
A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this fieldRajae El Malti, Hui Liu, Bérénice Doray, et al.
Nature Communications|March 29, 2025
PD-L1<sup>+</sup> plasma cells suppress T lymphocyte responses in patients with sepsis and mouse sepsis modelsMorgane Gossez, Clara Vigneron, Alexandra Vandermoeten, et al.
Annals of Surgical Oncology|April 2, 2026
Enhanced Recovery After Liver Surgery: Does Compliance Impact Survival?Martina Mariatti, Francesca Venza, Alessandra Cristaudi, et al.
Magnetic Resonance in Medicine|June 6, 2020
Tensor image enhancement and optimal multichannel receiver combination analyses for human hyperpolarized <sup>13</sup> C MRSIHsin-Yu Chen, Adam W Autry, Jeffrey R Brender, et al.
BMC Cancer|July 2, 2025
Homologous recombination deficiency (HRD) tests for ovarian cancer: a multicenter French phase II study (HERO)Raphaël Leman, François Cherifi, Marianne Leheurteur, et al.
Journal of Medicinal Chemistry|February 19, 2026
Large Library Docking for PolypharmacologyYujin Wu, Seth Vigneron, Joao Braz, et al.
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