نتائج البحث - "Kevin Wojta"

1

دورية أكاديمية

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

المصدر: Molecular Neurodegeneration, Vol 13, Iss 1, Pp 1-11 (2018)

مصطلحات موضوعية: Genome-wide association study, Progressive supranuclear palsy, Neurodegeneration, Neurology. Diseases of the nervous system, RC346-429, Geriatrics, RC952-954.6

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13024-018-0270-8; https://doaj.org/toc/1750-1326

URL الوصول: https://doaj.org/article/38fd283c780d47908af18442210dfcca

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دورية أكاديمية

GATA4 Is Sufficient to Establish Jejunal Versus Ileal Identity in the Small IntestineSummary

المؤلفون: Cayla A. Thompson, Kevin Wojta, Kirthi Pulakanti, Sridhar Rao, Paul Dawson, Michele A. Battle

المصدر: Cellular and Molecular Gastroenterology and Hepatology, Vol 3, Iss 3, Pp 422-446 (2017)

مصطلحات موضوعية: Diseases of the digestive system. Gastroenterology, RC799-869

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2352345X17300140; https://doaj.org/toc/2352-345X

URL الوصول: https://doaj.org/article/488e9aef8b914428a34d3b7fc2a0770e

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A novel temporal‐predominant neuro‐astroglial tauopathy associated with TMEM106B gene polymorphism in FTLD/ALS‐TDP

المصدر: Brain Pathol

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a22478d31c0809a72a5a7b3dd7df5b8
https://doi.org/10.1111/bpa.12924

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4

Sex-related differences in the relationship between β-amyloid and cognitive trajectories in older adults

المؤلفون: Michelle You, Renaud La Joie, Jessica E. Rexach, Samantha M Walters, Lauren Edwards, Fanny M. Elahi, Alexandra C. Apple, Joel H. Kramer, John Neuhaus, Kaitlin B. Casaletto, Devyn Cotter, Breton M Asken, Leonardo Iaccarino, Elena Tsoy, Cutter A. Lindbergh, Gil D. Rabinovici, Adam M. Staffaroni, Kevin Wojta

المصدر: Neuropsychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7165a9d0c38506cf8144b9e7066d5927
https://doi.org/10.1037/neu0000696

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Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders

المساهمون: Ayer, Ariane H, Wojta, Kevin, Ramos, Eliana Marisa, Dokuru, Deepika, Chen, Jason A, Karydas, Anna M, Papatriantafyllou, John D, Agiomyrgiannakis, Dimitrio, Kamtsadeli, Vasiliki, Tsinia, Niki, Sali, Dimitra, Gylys, Karen H, Agosta, Federica, Filippi, Massimo, Small, Gary W, Bennett, David A, Gearing, Marla, Juncos, Jorge L, Kramer, Joel, Lee, Suzee E, Yokoyama, Jennifer S, Mendez, Mario F, Chui, Helena, Zarow, Chri, Ringman, John M, Kilic, Ulkan, Babacan-Yildiz, Gülsen, Levey, Allan, Decarli, Charles S, Cotman, Carl W, Boxer, Adam L, Miller, Bruce L, Coppola, Giovanni, BABACAN YILDIZ, GÜLSEN

المصدر: Alzheimer disease and associated disorders, vol 33, iss 4
Alzheimer Dis Assoc Disord

مصطلحات موضوعية: Male, Oncology, Aging, amyotrophic lateral sclerosis, Internationality, Disease, Neurodegenerative, Alzheimer's Disease, frontotemporal dementia, Cohort Studies, 0302 clinical medicine, Immunologic, Receptors, TREM2, 2.1 Biological and endogenous factors, genetics, 030212 general & internal medicine, Receptors, Immunologic, Ayer A., Wojta K., Ramos E., Dokuru D., Chen J., Karydas A., Papatriantafyllou J., Agiomyrgiannakis D., Kamtsadeli V., Tsinia N., et al., -Frequency of the TREM2 R47H Variant in Various Neurodegenerative Disorders.-, Alzheimer disease and associated disorders, cilt.33, ss.327-330, 2019, Aetiology, Amyotrophic lateral sclerosis, Membrane Glycoproteins, Neurodegenerative Diseases, Psychiatry and Mental health, Clinical Psychology, Frontotemporal Dementia, Neurological, Cohort, Female, Cognitive Sciences, Alzheimer's disease, Frontotemporal dementia, Cohort study, medicine.medical_specialty, Genotype, Clinical Sciences, association study, Article, Progressive supranuclear palsy, 03 medical and health sciences, Rare Diseases, mild cognitive impairment, Alzheimer Disease, Clinical Research, Internal medicine, Acquired Cognitive Impairment, medicine, Humans, Genetic Predisposition to Disease, Cognitive Dysfunction, Aged, business.industry, Amyotrophic Lateral Sclerosis, Neurosciences, Genetic Variation, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), progressive supranuclear palsy, corticobasal syndrome, medicine.disease, Brain Disorders, Geriatrics, Dementia, Geriatrics and Gerontology, business, Gerontology, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18e58314e4fd2edda9efc8940be6b907
https://doi.org/10.1097/wad.0000000000000339

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Epigenetic clock and methylation studies in vervet monkeys

المؤلفون: Caesar Z. Li, Amin Haghani, Joseph DeYoung, Roger P. Woods, Julie A. Mattison, Andrew W. Rao, Oi-Wa Choi, Xinmin Li, Adriana Arneson, Jason Ernst, Joseph A. Zoller, Matthew J. Jorgensen, Giovanni Coppola, Kylie Kavanagh, Anna J. Jasinska, Steve Horvath, Nelson B. Freimer, Kevin Wojta

المصدر: GeroScience. 44(2)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f2090cae663304968edb31930134ca
https://pubmed.ncbi.nlm.nih.gov/34591235

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7

Epigenetic clock and methylation studies in vervet monkeys

المؤلفون: Andrew W. Rao, Adriana Arneson, Kevin Wojta, Caesar Z. Li, Joseph A. Zoller, Kylie Kavanagh, Nelson B. Freimer, Joseph DeYoung, Anna J. Jasinska, Matthew J. Jorgensen, Giovanni Coppola, Steve Horvath, Amin Haghani, Roger P. Woods, Oi-Wa Choi, Xinmin Li, Julie A. Mattison, Jason Ernst

مصطلحات موضوعية: biology, animal diseases, Methylation, biology.organism_classification, Rhesus macaque, CpG site, Biomarkers of aging, Evolutionary biology, biology.animal, parasitic diseases, DNA methylation, Primate, Vervet monkey, Epigenetics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2a4cc5670a9a709d92db0738a05e9818
https://doi.org/10.1101/2020.09.09.289801

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Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

المؤلفون: Deepika Dokuru, Victoria Van Berlo, Joanne Taylor, Bruce L. Miller, Giovanni Coppola, Jeremy Syrjanen, Madeline Potter, Alden Y. Huang, Rodney Pearlman, Jamie Fong, Joel H. Kramer, Peter A. Ljubenkov, Yue Qin, Codrin Lungu, Maria Carmela Tartaglia, Alexander Pantelyat, Marka van Blitterswijk, Sandeep Deverasetty, Hilary W. Heuer, Jazmyne L. Jackson, Edward D. Huey, Leah K. Forsberg, Daniel I. Kaufer, Kimiko Domoto-Reilly, Walter K. Kremers, John Q. Trojanowski, Bradford C. Dickerson, Zbigniew K. Wszolek, Katherine P. Rankin, Murray Grossman, Nadine Tatton, Chiadi U. Onyike, Kelley Faber, David S. Knopman, Tatiana Foroud, Erik D. Roberson, Nupur Ghoshal, Eliana Marisa Ramos, Jonathan Graff-Radford, Patrick Brannelly, Bonnie Wong, Mario F. Mendez, Ian R. A. Mackenzie, Brad F. Boeve, Ging-Yuek Robin Hsiung, Q. Wang, Rosa Rademakers, Adam L. Boxer, Neill R. Graff-Radford, David J. Irwin, John Kornak, Irene Litvan, Danielle Brushaber, Ralitza H. Gavrilova, Kejal Kantarci, Yvette Bordelon, Ian Grant, Anna Karydas, Arthur W. Toga, Leslie M. Shaw, Julie A. Fields, Emily Rogalski, Len Petrucelli, Kevin Wojta, Walter A. Kukull, Howard J. Rosen, Sandra Weintraub, Artfl, Brian S. Appleby, Jill Goldman, Diana R. Kerwin, Susan Dickinson, Katya Rascovsky

المساهمون: ARTFL LEFFTDS Consortium

المصدر: Alzheimer's & dementia : the journal of the Alzheimer's Association, vol 16, iss 1
Alzheimers Dement
Alzheimer's & dementia

مصطلحات موضوعية: 0301 basic medicine, Male, Aging, Epidemiology, Neurodegenerative, Alzheimer's Disease, frontotemporal dementia, 0302 clinical medicine, Progranulins, C9orf72, MAPT, 2.1 Biological and endogenous factors, Aetiology, Alzheimer's Disease Related Dementias (ADRD), Likely pathogenic, media_common, Health Policy, TAR DNA-BINDING PROTEIN, Large series, familial, Frontotemporal lobar degeneration, Art, Middle Aged, Psychiatry and Mental health, Grossman, Frontotemporal Dementia (FTD), Frontotemporal Dementia, Neurological, Female, GRN, Frontotemporal dementia, media_common.quotation_subject, Clinical Sciences, tau Proteins, TARDBP, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, Unknown Significance, Rare Diseases, Developmental Neuroscience, Clinical Research, mental disorders, medicine, Genetics, Acquired Cognitive Impairment, Humans, Genetic Predisposition to Disease, Genetic Testing, Biology, C9orf72 Protein, Prevention, Human Genome, Neurosciences, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), medicine.disease, Brain Disorders, 030104 developmental biology, Geriatrics, sporadic, Dementia, Neurology (clinical), Human medicine, Geriatrics and Gerontology, Humanities, 030217 neurology & neurosurgery, ARTFL/LEFFTDS consortium

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15460067b5e5fb265d5a2faa1a21d0c0
https://escholarship.org/uc/item/90d8d1rh

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Lack of association between the CCR5-delta32 polymorphism and neurodegenerative disorders

المؤلفون: Anna Karydas, Jennifer S. Yokoyama, Eliana Marisa Ramos, Ariane H. Ayer, Giovanni Coppola, Bruce L. Miller, Suzee E. Lee, Adam L. Boxer, Joel H. Kramer, Kevin Wojta, Peter D. Nguyen

المصدر: Alzheimer Dis Assoc Disord
Alzheimer disease and associated disorders, vol 34, iss 3

مصطلحات موضوعية: Aging, viruses, Disease, Neurodegenerative, Bioinformatics, California, Cohort Studies, neurodegenerative disease, 0302 clinical medicine, Receptors, 2.1 Biological and endogenous factors, 030212 general & internal medicine, Aetiology, Age of Onset, Receptor, Neurodegeneration, virus diseases, Neurodegenerative Diseases, Middle Aged, Psychiatry and Mental health, Clinical Psychology, Neurological, Cohort, Cognitive Sciences, Adult, Receptors, CCR5, Clinical Sciences, association study, Article, Frameshift mutation, 03 medical and health sciences, Genetic, Genetics, medicine, Humans, Polymorphism, Allele, Alleles, Polymorphism, Genetic, business.industry, genetic variants, Neurosciences, medicine.disease, Geriatrics, Synaptic plasticity, Geriatrics and Gerontology, Age of onset, business, CCR5, Gerontology, 030217 neurology & neurosurgery, dementia

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c96df13d42617ffa1efb3e346f89df9d
https://europepmc.org/articles/PMC7365743/

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Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

المساهمون: University of California [Los Angeles] (UCLA), University of California (UC), King‘s College London, Laboratoire de Biostatistique, Epidémiologie clinique, Santé Publique Innovation et Méthodologie [CHU Nîmes] (BESPIM), Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)-Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Université Pierre et Marie Curie - Paris 6 (UPMC), University of Sussex, Queen Mary University of London (QMUL), Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 (RID-AGE), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Universität Ulm - Ulm University [Ulm, Allemagne], This work was funded by grants from the Tau Consortium (D.H.G. and G.C.), the National Institutes of Health, F31 NS084556 (J.A.C.) UG3 NS104095 and P30 NS062691 from the National Institute of Neurological Disorders and Stroke (Informatics Center for Neurogenetics and Neurogenomics to G.C.), and the Fu-Hsing and Jyu-Yuan Chen family. Z.C. was supported by funding from the NIHR Academic Clinical Fellowship. Three academic institutions (Institute of Psychiatry, Psychology and Neuroscience, King’s College London, Assistance Publique-Hôpitaux de Paris and University of Ulm) were sponsors of the NNIPPS study in each country, and jointly own the data. The BBBIPPS study was supported by the French Health Ministry, Programme Hospitalier de Recherche Clinique (AOM04035). The Assistance Publique - Hôpitaux de Paris (France) was the sponsor of the study. The protocol and amendments were reviewed and approved by the Comité de Protection des Personnes of Pitié-Salpêtrière Hospital (France). The NNIPPS genotyping and analysis was supported under the aegis of JPND – (www.jpnd.eu, United Kingdom), Medical Research Council (MR/L501529/1, MR/R024804/1) and Economic and Social Research Council (ES/L008238/1). A.A.C. receives salary support from the National Institute for Health Research (NIHR) Dementia Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. The work leading up to this publication was funded by the European Community’s Health Seventh Framework Programme (FP7/2007–2013, grant agreement number 259867) and Horizon 2020 Programme (H2020-PHC-2014-two-stage, grant agreement number 633413). We thank the UCLA Neuroscience Genomics Core (www.semel.ucla.edu/ungc) for assistance with genotyping data generation. Samples from the National Cell Repository for Alzheimer’s Disease (NCRAD), which receives government support under a cooperative agreement grant (U24 AG021886) awarded by the National Institute on Aging (NIA), were used in this study. We thank contributors who collected samples used in this study, as well as patients and their families, whose help and participation made this work possible., European Project: 259867,EC:FP7:HEALTH,FP7-HEALTH-2010-two-stage,EURO-MOTOR(2011), European Project: 633413,H2020,H2020-PHC-2014-two-stage,MIROCALS(2015), University of California, Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)

المصدر: Molecular Neurodegeneration, Vol 13, Iss 1, Pp 1-11 (2018)
Molecular Neurodegeneration
Molecular Neurodegeneration, 2018, 13 (1), pp.41. ⟨10.1186/s13024-018-0270-8⟩
Molecular Neurodegeneration, BioMed Central, 2018, 13 (1), pp.41. ⟨10.1186/s13024-018-0270-8⟩
Molecular neurodegeneration, vol 13, iss 1
Chen, J A, Chen, Z, Won, H, Huang, A Y, Lowe, J K, Wojta, K, Yokoyama, J S, Bensimon, G, Leigh, P N, Payan, C, Shatunov, A, Jones, A R, Lewis, C M, Deloukas, P, Amouyel, P, Tzourio, C, Dartigues, J F, Ludolph, A, Boxer, A L, Bronstein, J M, Al-Chalabi, A, Geschwind, D H & Coppola, G 2018, ' Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases ', Molecular Neurodegeneration, vol. 13, no. 1, 41 . https://doi.org/10.1186/s13024-018-0270-8

مصطلحات موضوعية: 0301 basic medicine, Male, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Genome-wide association study, Neurodegenerative, lcsh:Geriatrics, lcsh:RC346-429, 0302 clinical medicine, Supranuclear Palsy, 2.1 Biological and endogenous factors, Amyotrophic lateral sclerosis, Aetiology, Genetics, Neurodegeneration, Neurodegenerative Diseases, Single Nucleotide, 3. Good health, RC0346, Neurological, Female, Supranuclear Palsy, Progressive, Research Article, Genotype, Clinical Trials and Supportive Activities, Clinical Sciences, Locus (genetics), Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Progressive supranuclear palsy, 03 medical and health sciences, Cellular and Molecular Neuroscience, Rare Diseases, Progressive, Clinical Research, medicine, SNP, Humans, Genetic Predisposition to Disease, Polymorphism, Molecular Biology, lcsh:Neurology. Diseases of the nervous system, Neurology & Neurosurgery, [SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE], Prevention, Human Genome, Neurosciences, medicine.disease, Genetic architecture, eye diseases, lcsh:RC952-954.6, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Neurology (clinical), 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f44a2739ff83eca11c71369fbba6d592
http://link.springer.com/article/10.1186/s13024-018-0270-8

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