Zobrazeno 1 - 10
of 441
pro vyhledávání: '"E, TITUS"'
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-20 (2023)
Abstract Background Genomic complexity is a growing field of evolution, with case studies for comparative evolutionary analyses in model and emerging non-model systems. Understanding complexity and the functional components of the genome is an untapp
Externí odkaz:
https://doaj.org/article/9f571859f5c24c0e85b11355eb614495
Autor:
Haley E. Titus, Yanan Chen, Joseph R. Podojil, Andrew P. Robinson, Roumen Balabanov, Brian Popko, Stephen D. Miller
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Multiple Sclerosis (MS) is an immune-mediated neurological disorder, characterized by central nervous system (CNS) inflammation, oligodendrocyte loss, demyelination, and axonal degeneration. Although autoimmunity, inflammatory demyelination and neuro
Externí odkaz:
https://doaj.org/article/1ab37b89f5234467a7b645562874cd52
Autor:
Michael J. Gale, Hope E. Titus, Gareth A. Harman, Talal Alabduljalil, Anna Dennis, Jenny L. Wilson, David M. Koeller, Erika Finanger, Peter A. Blasco, Pei-Wen Chiang, Daniel J. Karr, Paul Yang
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 10, Iss , Pp 244-248 (2018)
Purpose: We present the first detailed ophthalmic description of a child with Helsmoortel-Van der Aa Syndrome (HVDAS), including longitudinal follow-up and analysis. Observations: After extensive workup, a young child with poor visual behavior, hypot
Externí odkaz:
https://doaj.org/article/5509eb93e5144c8faea09c0a6efe526d
Autor:
Alejandro López-Juárez, Haley E. Titus, Sadiq H. Silbak, Joshua W. Pressler, Tilat A. Rizvi, Madeleine Bogard, Michael R. Bennett, Georgianne Ciraolo, Michael T. Williams, Charles V. Vorhees, Nancy Ratner
Publikováno v:
Cell Reports, Vol 19, Iss 3, Pp 545-557 (2017)
Summary: The RASopathy neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant genetic disorders. In NF1 patients, neurological issues may result from damaged myelin, and mice with a neurofibromin gene (Nf1) mutation show white ma
Externí odkaz:
https://doaj.org/article/2f5953b491e84a8187532b2f7cc037bb
Autor:
Alondra M. Díaz-Lameiro, Catalina I. Villamil, Tony Gamble, Brendan J. Pinto, Alexandra Herrera-Martínez, Richard Thomas, Justin M. Bernstein, James E. Titus-McQuillan, Stuart V. Nielsen, Eliacim Agosto-Torres, Alberto R. Puente-Rolón, Fernando J. Bird-Picó, Taras K. Oleksyk, Juan Carlos Martínez-Cruzado, Juan D. Daza
Publikováno v:
Ichthyology & Herpetology. 110
Publikováno v:
2022 Second International Conference on Next Generation Intelligent Systems (ICNGIS).
Publikováno v:
Cytotherapy. 25:S186
Autor:
V. Rajan, R. Carpenedo, C. Zmurchok, A. Pallaoro, M. Thomas, H. Hoi, E. Yoshida, D. Kirouac, S. Joshi, L. Csaszar, S.M. Woodside, E. Titus
Publikováno v:
Cytotherapy. 25:S208
Autor:
Haley E. Titus, Huan Xu, Andrew P. Robinson, Priyam A. Patel, Yanan Chen, Damiano Fantini, Valerie Eaton, Molly Karl, Eric D. Garrison, Indigo V. L. Rose, Ming Yi Chiang, Joseph R. Podojil, Roumen Balabanov, Shane A. Liddelow, Robert H. Miller, Brian Popko, Stephen D. Miller
Publikováno v:
Glia. 70(10)
Multiple sclerosis (MS) is a central nervous system (CNS) autoimmune disease characterized by inflammation, demyelination, and neurodegeneration. The ideal MS therapy would both specifically inhibit the underlying autoimmune response and promote repa
Autor:
Caitlin E. Titus, Hilary L. DeShong
Publikováno v:
Journal of Affective Disorders. 266:349-355
Background Borderline Personality Disorder (BPD) is characterized by a pattern of instability in interpersonal relationships, affect, self-image and is marked by behavioral impulsivity including suicidal ideation and attempts. Additionally, individua