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Cell|January 22, 2021
p53 is a central regulator driving neurodegeneration caused by C9orf72 poly(PR)Maya Maor-Nof, Zohar Shipony, Rodrigo Lopez-Gonzalez, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Transplantation Direct|March 11, 2024
Single-center Outcomes After Liver Transplantation With SARS-CoV-2-Positive Donors: An Argument for Increased UtilizationAshton A Connor, Max W Adelman, Constance M Mobley, et al.
Nature Methods|May 29, 2024
A bistable inhibitory optoGPCR for multiplexed optogenetic control of neural circuitsJonas Wietek, Adrianna Nozownik, Mauro Pulin, et al.
Human Genetics|January 9, 2016
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeElisabeth E Mlynarski, Michael Xie, Deanne Taylor, et al.
Bioorganic & Medicinal Chemistry Letters|July 22, 2015
Methyl-substitution of an iminohydantoin spiropiperidine β-secretase (BACE-1) inhibitor has a profound effect on its potencyMelissa Egbertson, Georgia B McGaughey, Steven M Pitzenberger, et al.
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