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Peter L. Nagy
Peter L. Nagy
Praxis Genomics LLC
Dirección de correo verificada de praxisgenomics.com - Página principal
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Necroptosis drives motor neuron death in models of both sporadic and familial ALS
DB Re, V Le Verche, C Yu, MW Amoroso, KA Politi, S Phani, B Ikiz, ...
Neuron 81 (5), 1001-1008, 2014
4602014
A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3
PL Nagy, J Griesenbeck, RD Kornberg, ML Cleary
Proceedings of the national academy of sciences 99 (1), 90-94, 2002
3842002
Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regions
J Baleriola, CA Walker, YY Jean, JF Crary, CM Troy, PL Nagy, U Hengst
Cell 158 (5), 1159-1172, 2014
3292014
Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations
JA Oberg, JL Glade Bender, ML Sulis, D Pendrick, AN Sireci, SJ Hsiao, ...
Genome medicine 8, 1-19, 2016
1732016
Genomewide demarcation of RNA polymerase II transcription units revealed by physical fractionation of chromatin
PL Nagy, ML Cleary, PO Brown, JD Lieb
Proceedings of the National Academy of Sciences 100 (11), 6364-6369, 2003
1492003
Analysis of the ABCA4 genomic locus in Stargardt disease
J Zernant, Y Xie, C Ayuso, R Riveiro-Alvarez, MA Lopez-Martinez, ...
Human molecular genetics 23 (25), 6797-6806, 2014
1482014
Identification of the Bacillus subtilis pur operon repressor
M Weng, PL Nagy, H Zalkin
Proceedings of the National Academy of Sciences 92 (16), 7455-7459, 1995
1421995
The Glc7 phosphatase subunit of the cleavage and polyadenylation factor is essential for transcription termination on snoRNA genes
E Nedea, D Nalbant, D Xia, NT Theoharis, B Suter, CJ Richardson, ...
Molecular cell 29 (5), 577-587, 2008
1382008
LMNA cardiomyopathy: cell biology and genetics meet clinical medicine
JT Lu, A Muchir, PL Nagy, HJ Worman
Disease models & mechanisms 4 (5), 562-568, 2011
1152011
Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort
J Murphy, P Factor-Litvak, R Goetz, C Lomen-Hoerth, PL Nagy, J Hupf, ...
Neurology 86 (9), 813-820, 2016
1002016
Formyltetrahydrofolate hydrolase, a regulatory enzyme that functions to balance pools of tetrahydrofolate and one-carbon tetrahydrofolate adducts in Escherichia coli
PL Nagy, A Marolewski, SJ Benkovic, H Zalkin
Journal of Bacteriology 177 (5), 1292-1298, 1995
791995
Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1
R Firestein, PL Nagy, M Daly, P Huie, M Conti, ML Cleary
The Journal of clinical investigation 109 (9), 1165-1172, 2002
772002
The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy
CR Coughlin, MA Swanson, E Spector, NJL Meeks, KE Kronquist, ...
Journal of inherited metabolic disease 42 (2), 353-361, 2019
732019
Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72
JS Goldman, C Quinzii, J Dunning-Broadbent, C Waters, H Mitsumoto, ...
JAMA neurology 71 (6), 771-774, 2014
702014
A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder
Y Wang, U Lichter-Konecki, K Anyane-Yeboa, JE Shaw, JT Lu, C Östlund, ...
Journal of cell science 129 (10), 1975-1980, 2016
652016
DNA-like class R inhibitory oligonucleotides (INH-ODNs) preferentially block autoantigen-induced B-cell and dendritic cell activation in vitro and autoantibody production in …
P Lenert, K Yasuda, L Busconi, P Nelson, C Fleenor, RS Ratnabalasuriar, ...
Arthritis research & therapy 11, 1-16, 2009
642009
Phenotypic and molecular analyses of primary lateral sclerosis
H Mitsumoto, PL Nagy, C Gennings, J Murphy, H Andrews, R Goetz, ...
Neurology: Genetics 1 (1), e3, 2015
592015
purU, a source of formate for purT-dependent phosphoribosyl-N-formylglycinamide synthesis
PL Nagy, GM McCorkle, H Zalkin
Journal of Bacteriology 175 (21), 7066-7073, 1993
541993
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations
S Mercier, S Küry, E Salort-Campana, A Magot, U Agbim, T Besnard, ...
Orphanet journal of rare diseases 10, 1-16, 2015
532015
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle
G Dialynas, KM Flannery, LN Zirbel, PL Nagy, KD Mathews, SA Moore, ...
Human molecular genetics 21 (7), 1544-1556, 2012
512012
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20