受强制性开放获取政策约束的文章 - Deeann Wallis了解详情
可在其他位置公开访问的文章：20 篇
Tryptophan biosynthesis protects mycobacteria from CD4 T-cell-mediated killing
YJ Zhang, MC Reddy, TR Ioerger, AC Rothchild, V Dartois, BM Schuster, ...
Cell 155 (6), 1296-1308, 2013
强制性开放获取政策： US National Institutes of Health
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, MT Acosta, S Shively, H Stanescu, D Wallis, ...
Molecular psychiatry 15 (11), 1053-1066, 2010
强制性开放获取政策： US National Institutes of Health, German Research Foundation
Development of a novel lead that targets M. tuberculosis polyketide synthase 13
A Aggarwal, MK Parai, N Shetty, D Wallis, L Woolhiser, C Hastings, ...
Cell 170 (2), 249-259. e25, 2017
强制性开放获取政策： Bill & Melinda Gates Foundation, US National Institutes of Health, Wellcome …
Initial characterization of mice null for Lphn3, a gene implicated in ADHD and addiction
D Wallis, DS Hill, IA Mendez, LC Abbott, RH Finnell, PJ Wellman, ...
Brain research 1463, 85-92, 2012
强制性开放获取政策： US National Institutes of Health
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility
S Domené, H Stanescu, D Wallis, B Tinloy, DE Pineda, R Kleta, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 …, 2011
强制性开放获取政策： US National Institutes of Health
Autism‐Like Behavior and Epigenetic Changes Associated with Autism as Consequences of In Utero Exposure to Environmental Pollutants in a Mouse Model
DS Hill, R Cabrera, D Wallis Schultz, H Zhu, W Lu, RH Finnell, ...
Behavioural Neurology 2015 (1), 426263, 2015
强制性开放获取政策： US National Institutes of Health
Behavioral and transcriptomic profiling of mice null for Lphn3, a gene implicated in ADHD and addiction
CA Orsini, B Setlow, M DeJesus, S Galaviz, K Loesch, T Ioerger, D Wallis
Molecular genetics & genomic medicine 4 (3), 322-343, 2016
强制性开放获取政策： US National Institutes of Health
Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response
F Larroquette, L Seto, PL Gaub, B Kamal, D Wallis, R Larivière, J Vallée, ...
Human molecular genetics 24 (22), 6515-6529, 2015
强制性开放获取政策： Canadian Institutes of Health Research
ADGRL3 (LPHN3) variants predict substance use disorder
M Arcos-Burgos, JI Vélez, AF Martinez, M Ribasés, JA Ramos-Quiroga, ...
Translational psychiatry 9 (1), 42, 2019
强制性开放获取政策： US National Institutes of Health, US Department of Education, European …
Additional EFNB1 mutations in craniofrontonasal syndrome
D Wallis, F Lacbawan, M Jain, VM Der Kaloustian, CE Steiner, ...
American Journal of Medical Genetics Part A 146 (15), 2008-2012, 2008
强制性开放获取政策： US National Institutes of Health
Affinity purification of NF1 protein–protein interactors identifies keratins and neurofibromin itself as binding partners
RM Carnes, RA Kesterson, BR Korf, JA Mobley, D Wallis
Genes 10 (9), 650, 2019
强制性开放获取政策： US National Institutes of Health
Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I
A Leier, M Moore, H Liu, M Daniel, AM Hyde, L Messiaen, BR Korf, ...
Molecular Therapy-Nucleic Acids 28, 261-278, 2022
强制性开放获取政策： US National Institutes of Health
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
M Jain, D Wallis, NH Robin, FW De Vrieze, JA Hardy, M Ghadami, ...
American journal of medical genetics. Part A 146 (17), 2308, 2008
强制性开放获取政策： US National Institutes of Health
Functional genomics screening utilizing mutant mouse embryonic stem cells identifies novel radiation-response genes
K Loesch, S Galaviz, Z Hamoui, R Clanton, G Akabani, M Deveau, ...
PLoS One 10 (4), e0120534, 2015
强制性开放获取政策： US National Institutes of Health
Restoration of normal NF1 function with antisense morpholino treatment of recurrent pathogenic patient-specific variant c. 1466A> G; p. Y489C
EK Awad, M Moore, H Liu, L Ciszewski, L Lambert, BR Korf, L Popplewell, ...
Journal of Personalized Medicine 11 (12), 1320, 2021
强制性开放获取政策： US National Institutes of Health
Status and recommendations for incorporating biomarkers for cutaneous neurofibromas into clinical research
D Wallis, A Stemmer-Rachamimov, S Adsit, B Korf, D Pichard, J Blakeley, ...
Neurology 97 (7_Supplement_1), S42-S49, 2021
强制性开放获取政策： US National Institutes of Health, Damon Runyon Cancer Research Foundation …
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies
A Long, A Crouse, RA Kesterson, M Might, D Wallis
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 189 …, 2022
强制性开放获取政策： US National Institutes of Health
Exhaustive non-synonymous variants functionality prediction enables high resolution characterization of the neurofibromin architecture
O Isakov, D Wallis, DG Evans, S Ben-Shachar
EBioMedicine 36, 508-516, 2018
强制性开放获取政策： National Institute for Health Research, UK
Folate transport and folate responsive developmental disorders
EB Gorman, D Wallis, JL Ballard, RP Goin-Kochel, RH Finnell
Pteridines 20, 156-162, 2010
强制性开放获取政策： US National Institutes of Health
Exon Skipping as a Therapeutic for Neurofibromatosis Type I
D Wallis, A Leier, M Moore, M Daniel, H Liu, A Hyde, L Messiaen, ...
强制性开放获取政策： US National Institutes of Health
出版信息和资助信息由计算机程序自动确定