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Nature Methods|March 27, 2024
The multimodality cell segmentation challenge: toward universal solutionsJun Ma, Ronald Xie, Shamini Ayyadhury, et al.
Brain : a Journal of Neurology|March 1, 2024
HLA-DQB1*05 subtypes and not DRB1*10:01 mediates risk in anti-IgLON5 diseaseSelina M Yogeshwar, Sergio Muñiz-Castrillo, Lidia Sabater, et al.
NPJ Genomic Medicine|November 9, 2021
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodMichael A Levy, David B Beck, Kay Metcalfe, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 19, 2021
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the <i>TRANK1</i> gene lociAditya Ambati, Ryan Hillary, Smaranda Leu-Semenescu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2022
Highlighting the Dystonic Phenotype Related to GNAO1Thomas Wirth, Giacomo Garone, Manju A Kurian, et al.
Nature|July 31, 2020
North Atlantic climate far more predictable than models implyD M Smith, A A Scaife, R Eade, et al.
Annals of Neurology|November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body DiseaseMarios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2020
Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineationSolveig Heide, Myrtille Spentchian, Stéphanie Valence, et al.
American Journal of Medical Genetics. Part A|November 12, 2022
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patientsClémence Jacquin, Emilie Landais, Céline Poirsier, et al.
American Journal of Human Genetics|November 27, 2012
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegiaChristelle Tesson, Magdalena Nawara, Mustafa A M Salih, et al.
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