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Select item 48067671.

AA-PMe, a novel asiatic acid derivative, induces apoptosis and suppresses proliferation, migration, and invasion of gastric cancer cells

Yue Jing, Gang Wang, Ying Ge, Minjie Xu, Shuainan Tang, Zhunan Gong

Onco Targets Ther. 2016; 9: 1605–1621. Published online 2016 Mar 17. doi: 10.2147/OTT.S98849

PMCID:: PMC4806767

Abstract Article PDF–4.6M

Select item 87416432.

Halogen Dance-Based Synthesis of Phosphonomethoxyethyl (PME) Substituted 2-Aminothiazoles as Potent Inhibitors of Bacterial Adenylate Cyclases

Dr. Michal Česnek, Michal Šafránek, Dr. Martin Dračínský, Eva Tloušťová, Dr. Helena Mertlíková-Kaiserová, Michael P. Hayes, Dr. Val J. Watts, Dr. Zlatko Janeba

ChemMedChem. Author manuscript; available in PMC 2023 Jan 5.

Published in final edited form as: ChemMedChem. 2022 Jan 5; 17(1): e202100568. Published online 2021 Oct 22. doi: 10.1002/cmdc.202100568

PMCID:: PMC8741643

Abstract Article PDF–774K

Select item 87151413.

Effect of different microwave power levels on inactivation of PPO and PME and also on quality changes of peach puree

Linyan Zhou, Chia Ying Tey, Gokhan Bingol, Murat O. Balaban, Shengbao Cai

Curr Res Food Sci. 2022; 5: 41–48. Published online 2021 Dec 20. doi: 10.1016/j.crfs.2021.12.006

PMCID:: PMC8715141

Abstract Article PDF–3.3M

Select item 86703204.

Adult‐onset rapidly worsening progressive myoclonic epilepsy caused by a novel variant in DHDDS

Seondeuk Kim, Man Jin Kim, Hyoshin Son, Sungeun Hwang, Mi‐Kyoung Kang, Kon Chu, Sang Kun Lee, Jangsup Moon

Ann Clin Transl Neurol. 2021 Dec; 8(12): 2319–2326. Published online 2021 Nov 27. doi: 10.1002/acn3.51483

PMCID:: PMC8670320

Abstract Article PDF–1.1M

Select item 86656455.

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

Laura C Bott, Mitra Forouhan, Maria Lieto, Ambre J Sala, Ruth Ellerington, Janel O Johnson, Alfina A Speciale, Chiara Criscuolo, Alessandro Filla, David Chitayat, Ebba Alkhunaizi, Patrick Shannon, Andrea H Nemeth, Italian Undiagnosed Diseases Network , Francesco Angelucci, Wooi Fang Lim, Pasquale Striano, Federico Zara, Ingo Helbig, Mikko Muona, Carolina Courage, Anna-Elina Lehesjoki, Samuel F Berkovic, ATPase Consortium , Kenneth H Fischbeck, Francesco Brancati, Richard I Morimoto, Matthew J A Wood, Carlo Rinaldi

Brain Commun. 2021; 3(4): fcab245. Published online 2021 Oct 18. doi: 10.1093/braincomms/fcab245

PMCID:: PMC8665645

Abstract Article PDF–1.2M

Select item 86474936.

Genome-wide identification of PME genes, evolution and expression analyses in soybean (Glycine max L.)

Liang Wang, Yingqi Gao, Songming Wang, Qiqi Zhang, Shouping Yang

BMC Plant Biol. 2021; 21: 578. Published online 2021 Dec 6. doi: 10.1186/s12870-021-03355-1

PMCID:: PMC8647493

Abstract Article PDF–11M

Select item 62516927.

Protein Phosphatase 2A and Its Methylation Modulating Enzymes LCMT-1 and PME-1 Are Dysregulated in Tauopathies of Progressive Supranuclear Palsy and Alzheimer Disease

Hye-Jin Park, Kang-Woo Lee, Stephanie Oh, Run Yan, Jie Zhang, Thomas G Beach, Charles H Adler, Michael Voronkov, Steven P Braithwaite, Jeffry B Stock, M Maral Mouradian

J Neuropathol Exp Neurol. 2018 Feb; 77(2): 139–148. Published online 2017 Dec 21. doi: 10.1093/jnen/nlx110

PMCID:: PMC6251692

Abstract Article PDF–873K

Select item 31542848.

Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism

Philippe Couarch, Santiago Vernia, Isabelle Gourfinkel-An, Gaëtan Lesca, Svetlana Gataullina, Estelle Fedirko, Oriane Trouillard, Christel Depienne, Olivier Dulac, Dominique Steschenko, Eric Leguern, Pascual Sanz, Stéphanie Baulac

J Mol Med (Berl) 2011; 89(9): 915–925. Published online 2011 Apr 20. doi: 10.1007/s00109-011-0758-y

PMCID:: PMC3154284

Abstract Article PDF–624K

Select item 85771219.

Bilateral Representation of Sensorimotor Responses in Benign Adult Familial Myoclonus Epilepsy: An MEG Study

Teppei Matsubara, Seppo P. Ahlfors, Tatsuya Mima, Koichi Hagiwara, Hiroshi Shigeto, Shozo Tobimatsu, Yoshinobu Goto, Steven Stufflebeam

Front Neurol. 2021; 12: 759866. Published online 2021 Oct 26. doi: 10.3389/fneur.2021.759866

PMCID:: PMC8577121

Abstract Article PDF–2.8M

Select item 856270310.

A novel deletion mutation in EPM2A underlies progressive myoclonic epilepsy (Lafora body disease) in a Pakistani family

Fizza Orooj, Umm-e-Kalsoom, XiaoChu Zhao, Arsalan Ahmad, Imran Nazir Ahmed, Muhammad Faheem, Muhammad Jawad Hassan, Berge A. Minasian

Neurol Asia. Author manuscript; available in PMC 2021 Nov 2.

Published in final edited form as: Neurol Asia. 2021 Jun; 26(2): 427–433.

PMCID:: PMC8562703

Abstract Article PDF–960K

Select item 628134711.

Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia

John A. Damiano, Zaid Afawi, Melanie Bahlo, Monika Mauermann, Adel Misk, Todor Arsov, Karen L. Oliver, Hans-Henrik M. Dahl, A. Eliot Shearer, Richard J.H. Smith, Nathan E. Hall, Khalid Mahmood, Richard J. Leventer, Ingrid E. Scheffer, Mikko Muona, Anna-Elina Lehesjoki, Amos D. Korczyn, Harald Herrmann, Samuel F. Berkovic, Michael S. Hildebrand

Hum Mol Genet. 2015 Aug 15; 24(16): 4483–4490. Published online 2015 May 7. doi: 10.1093/hmg/ddv171

PMCID:: PMC6281347

Abstract Article PDF–557K

Select item 314672012.

A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia

Mark A. Corbett, Michael Schwake, Melanie Bahlo, Leanne M. Dibbens, Meng Lin, Luke C. Gandolfo, Danya F. Vears, John D. O'Sullivan, Thomas Robertson, Marta A. Bayly, Alison E. Gardner, Annemarie M. Vlaar, G. Christoph Korenke, Bastiaan R. Bloem, Irenaeus F. de Coo, Judith M.A. Verhagen, Anna-Elina Lehesjoki, Jozef Gecz, Samuel F. Berkovic

Am J Hum Genet. 2011 May 13; 88(5): 657–663. doi: 10.1016/j.ajhg.2011.04.011

PMCID:: PMC3146720

Abstract Article PDF–577K

Select item 843676813.

Progressive myoclonus epilepsy KCNC1 variant causes a developmental dendritopathy

Jenna C. Carpenter, Roope Männikkö, Catherine Heffner, Jana Heneine, Marisol Sampedro‐Castañeda, Gabriele Lignani, Stephanie Schorge

Epilepsia. 2021 May; 62(5): 1256–1267. Published online 2021 Mar 18. doi: 10.1111/epi.16867

PMCID:: PMC8436768

Abstract Article PDF–1.8M

Select item 630566114.

Sleep is associated with reduction of epileptiform discharges in benign adult familial myoclonus epilepsy

Takefumi Hitomi, Morito Inouchi, Hirofumi Takeyama, Katsuya Kobayashi, Shamima Sultana, Takeshi Inoue, Yuko Nakayama, Akihiro Shimotake, Masao Matsuhashi, Riki Matsumoto, Kazuo Chin, Ryosuke Takahashi, Akio Ikeda

Epilepsy Behav Case Rep. 2019; 11: 18–21. Published online 2018 Oct 16. doi: 10.1016/j.ebcr.2018.09.010

PMCID:: PMC6305661

Abstract Article PDF–1.0M

Select item 630654015.

Falling After Starting Running in a Case of Myoclonus Epilepsy Associated with Ragged-red Fibers with a 8344A>G mtDNA Mutation

Noriyuki Miyaue, Yuki Yamanishi, Satoshi Tada, Rina Ando, Masahiro Nagai, Masahiro Nomoto

Intern Med. 2018 Dec 1; 57(23): 3439–3443. Published online 2018 Jul 6. doi: 10.2169/internalmedicine.1210-18

PMCID:: PMC6306540

Abstract Article PDF–1.2M

Select item 838175416.

A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy

Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi

Clin Case Rep. 2021 Aug; 9(8): e04520. Published online 2021 Aug 23. doi: 10.1002/ccr3.4520

PMCID:: PMC8381754

Abstract Article PDF–618K

Select item 468303217.

Protein Phosphatase Methyl-Esterase PME-1 Protects Protein Phosphatase 2A from Ubiquitin/Proteasome Degradation

Ryotaro Yabe, Akane Miura, Tatsuya Usui, Ingrid Mudrak, Egon Ogris, Takashi Ohama, Koichi Sato

PLoS One. 2015; 10(12): e0145226. Published online 2015 Dec 17. doi: 10.1371/journal.pone.0145226

PMCID:: PMC4683032

Abstract Article PDF–2.6M

Select item 634286818.

Progressive myoclonus epilepsy in Gaucher Disease due to a new Gly–Gly mutation causing loss of an Exonic Splicing Enhancer

Rodolfo Tonin, Serena Catarzi, Anna Caciotti, Elena Procopio, Carla Marini, Renzo Guerrini, Amelia Morrone

J Neurol. 2019; 266(1): 92–101. Published online 2018 Oct 31. doi: 10.1007/s00415-018-9084-4

PMCID:: PMC6342868

Abstract Article PDF–1.5M

Select item 832733119.

Juvenile Huntington’s disease masquerading as progressive myoclonus epilepsy

Bina Thakor, Sujit A. Jagtap, Aniruddha Joshi

Epilepsy Behav Rep. 2021; 16: 100470. Published online 2021 Jul 15. doi: 10.1016/j.ebr.2021.100470

PMCID:: PMC8327331

Abstract Article PDF–2.1M

Select item 635341420.

Deep Brain Stimulation in Three Related Cases of North Sea Progressive Myoclonic Epilepsy from South Africa

David G. Anderson, Andrea H. Németh, Katherine A. Fawcett, David Sims, Jack Miller, Amanda Krause

Mov Disord Clin Pract. 2017 Mar-Apr; 4(2): 249–253. Published online 2016 Jun 16. doi: 10.1002/mdc3.12372

PMCID:: PMC6353414

Abstract Article PDF–181K

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Synergus erinacei isolate 602-003-1A cytochrome c oxidase subunit I (COX1) gene,...
Synergus erinacei isolate 602-003-1A cytochrome c oxidase subunit I (COX1) gene, partial cds; mitochondrial
gi|1815523995|gb|MT124868.1|

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