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Publications

Found 13 results
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Vu M-AT, Adali T, Ba D, Buzsaki G, Carlson D, Heller K, Liston C, Rudin C, Sohal V, Widge AS et al..  2018.  A Shared Vision for Machine Learning in Neuroscience.. J Neurosci.
Vu LP, Pickering BF, Cheng Y, Zaccara S, Nguyen D, Minuesa G, Chou T, Chow A, Saletore Y, MacKay M et al..  2017.  The N6-methyladenosine (m6A)-forming enzyme METTL3 controls myeloid differentiation of normal hematopoietic and leukemia cells.. Nat Med. 23(11):1369-1376.
Vo ML, Levy T, Lakhani S, Wang C, M Ross E.  2022.  Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxia.. Mol Genet Genomic Med. :e1906.
Victor JD, Boie SD, Connor EG, Crimaldi JP, G Ermentrout B, Nagel KI.  2019.  Olfactory navigation and the receptor nonlinearity.. J Neurosci.
Victor JD, Rizvi SM, Conte MM.  2017.  Two representations of a high-dimensional perceptual space.. Vision Res. 137:1-23.
Victor JD, Rizvi SM, Conte MM.  2019.  Image segmentation driven by elements of form.. Vision Res.
Victor JD, Conte MM, Chubb CF.  2017.  Textures as Probes of Visual Processing.. Annu Rev Vis Sci. 3:275-296.
Vargas WS, Monohan E, Pandya S, Raj A, Vartanian T, Nguyen TD, RĂșa SMHurtado, Gauthier SA.  2015.  Measuring longitudinal myelin water fraction in new multiple sclerosis lesions.. Neuroimage Clin. 9:369-75.
Van Kempen TA, Narayan A, Waters EM, Marques-Lopes J, Iadecola C, Glass MJ, Pickel VM, Milner TA.  2016.  Alterations in the subcellular distribution of NADPH oxidase p47(phox) in hypothalamic paraventricular neurons following slow-pressor angiotensin II hypertension in female mice with accelerated ovarian failure.. J Comp Neurol. 524(11):2251-65.
Van Kempen TA, Dodos M, Woods C, Marques-Lopes J, Justice NJ, Iadecola C, Pickel VM, Glass MJ, Milner TA.  2015.  Sex differences in NMDA GluN1 plasticity in rostral ventrolateral medulla neurons containing corticotropin-releasing factor type 1 receptor following slow-pressor angiotensin II hypertension.. Neuroscience. 307:83-97.
Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet J-B, Carmignac V, Garret P et al..  2019.  Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.. Nat Genet.
Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet J-B, Carmignac V, Garret P et al..  2020.  Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.. Nat Genet.
Vabres P, Sorlin A, Kholmanskikh SS, Demeer B, St-Onge J, Duffourd Y, Kuentz P, Courcet J-B, Carmignac V, Garret P et al..  2019.  Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.. Nat Genet.