U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO Profiles

Items: 1 to 20 of 24

1.
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population
Mohammad AlMuhaizea, Omar Dabbagh, Hanan AlQudairy, Aljouhra AlHargan, Wafa Alotaibi, Ruba Sami, Rahaf AlOtaibi, Mariam Mahmoud Ali, Hindi AlHindi, Dilek Colak, Namik Kaya
Genes (Basel) 2021 Nov; 12(11): 1783. Published online 2021 Nov 10. doi: 10.3390/genes12111783
PMCID:
PMC8620084
AbstractArticlePDF–2.1M
2.
Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy
Madhurima Saha, Skylar A Rizzo, Manashwi Ramanathan, Rylie M Hightower, Katherine E Santostefano, Naohiro Terada, Richard S Finkel, Jonathan S Berg, Nizar Chahin, Christina A Pacak, Richard E Wagner, Matthew S Alexander, Isabelle Draper, Peter B Kang
Hum Mol Genet. 2019 Jul 15; 28(14): 2365–2377. Published online 2019 Apr 2. doi: 10.1093/hmg/ddz064
PMCID:
PMC6606856
AbstractArticlePDF–36M
3.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
4.
Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions
Madhurima Saha, Satomi Mitsuhashi, Michael D. Jones, Kelsey Manko, Hemakumar M. Reddy, Christine C. Bruels, Kyung-Ah Cho, Christina A. Pacak, Isabelle Draper, Peter B. Kang
Hum Mol Genet. 2017 Aug 1; 26(15): 2984–3000. Published online 2017 May 11. doi: 10.1093/hmg/ddx189
PMCID:
PMC6075367
AbstractArticlePDF–2.7M
5.
MEGF10, a Glioma Survival-Associated Molecular Signature, Predicts IDH Mutation Status
Guanzhang Li, Zhiliang Wang, Chuanbao Zhang, Xing Liu, Fuqiang Yang, Lihua Sun, Jingshan Liang, Huimin Hu, Yanwei Liu, Gan You, Zhaoshi Bao, Wei Zhang, Zheng Wang, Tao Jiang
Dis Markers. 2018; 2018: 5975216. Published online 2018 May 20. doi: 10.1155/2018/5975216
PMCID:
PMC5985127
AbstractArticlePDF–2.1M
6.
Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population
Zhiliu Wu, Jian Qin, Yang You, Yuanlin Ma, Meixiang Jia, Linyan Wang, Tianlan Lu, Weihua Yue, Yanyan Ruan, Dai Zhang, Jun Li, Lifang Wang
Sci Rep. 2017; 7: 2292. Published online 2017 May 23. doi: 10.1038/s41598-017-02348-1
PMCID:
PMC5442155
AbstractArticlePDF–1.5M
7.
Genome‐wide DNA methylation analysis identifies MEGF10 as a novel epigenetically repressed candidate tumor suppressor gene in neuroblastoma
Jessica Charlet, Ayumi Tomari, Anthony R. Dallosso, Marianna Szemes, Martina Kaselova, Thomas J. Curry, Bader Almutairi, Heather C. Etchevers, Carmel McConville, Karim T. A. Malik, Keith W. Brown
Mol Carcinog. 2017 Apr; 56(4): 1290–1301. Published online 2016 Nov 29. doi: 10.1002/mc.22591
PMCID:
PMC5396313
AbstractArticlePDF–1.4M
8.
Megf10 Is a Receptor for C1Q That Mediates Clearance of Apoptotic Cells by Astrocytes
Tal Iram, Zaida Ramirez-Ortiz, Michael H. Byrne, Uwanda A. Coleman, Nathan D. Kingery, Terry K. Means, Dan Frenkel, Joseph El Khoury
J Neurosci. 2016 May 11; 36(19): 5185–5192. doi: 10.1523/JNEUROSCI.3850-15.2016
PMCID:
PMC4863057
AbstractArticlePDF–1.7M
9.
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Tyler Mark Pierson, Thomas Markello, John Accardi, Lynne Wolfe, David Adams, Murat Sincan, Noor M. Tarazi, Karin Fuentes Fajardo, Praveen F. Cherukuri, Ilda Bajraktari, Katy G. Meilleur, Sandra Donkervoort, Mina Jain, Ying Hu, Tanya J. Lehky, Pedro Cruz, James C. Mullikin, Carsten Bonnemann, William A. Gahl, Cornelius F. Boerkoel, Cynthia J. Tifft
Neuromuscul Disord. Author manuscript; available in PMC 2014 Jun 1.
Published in final edited form as: Neuromuscul Disord. 2013 Jun; 23(6): 483–488. Published online 2013 Mar 1. doi: 10.1016/j.nmd.2013.01.013
PMCID:
PMC3940074
AbstractArticlePDF–1.0M
10.
Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy
Satomi Mitsuhashi, Hiroaki Mitsuhashi, Matthew S Alexander, Hiroyuki Sugimoto, Peter B Kang
FEBS Lett. Author manuscript; available in PMC 2014 Sep 17.
Published in final edited form as: FEBS Lett. 2013 Sep 17; 587(18): 2952–2957. Published online 2013 Aug 15. doi: 10.1016/j.febslet.2013.08.002
PMCID:
PMC3791867
AbstractArticlePDF–1.6M
11.
Genome Wide Association Study of the Rate of Cognitive Decline in Alzheimer’s Disease
Richard Sherva, Yorghos Tripodis, David Bennett, Lori B. Chibnik, Paul K. Crane, Philip de Jager, Lindsay A. Farrer, Andrew J. Saykin, Joshua Shulman, Robert C. Green, the Alzheimer’s Disease Neuroimaging Initiative
Alzheimers Dement. Author manuscript; available in PMC 2015 Jan 1.
Published in final edited form as: Alzheimers Dement. 2014 Jan; 10(1): 10.1016/j.jalz.2013.01.008. Published online 2013 Mar 25. doi: 10.1016/j.jalz.2013.01.008
PMCID:
PMC3760995
AbstractArticlePDF–589K
12.
Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
Gordan Lauc, Jennifer E. Huffman, Maja Pučić, Lina Zgaga, Barbara Adamczyk, Ana Mužinić, Mislav Novokmet, Ozren Polašek, Olga Gornik, Jasminka Krištić, Toma Keser, Veronique Vitart, Blanca Scheijen, Hae-Won Uh, Mariam Molokhia, Alan Leslie Patrick, Paul McKeigue, Ivana Kolčić, Ivan Krešimir Lukić, Olivia Swann, Frank N. van Leeuwen, L. Renee Ruhaak, Jeanine J. Houwing-Duistermaat, P. Eline Slagboom, Marian Beekman, Anton J. M. de Craen, André M. Deelder, Qiang Zeng, Wei Wang, Nicholas D. Hastie, Ulf Gyllensten, James F. Wilson, Manfred Wuhrer, Alan F. Wright, Pauline M. Rudd, Caroline Hayward, Yurii Aulchenko, Harry Campbell, Igor Rudan
PLoS Genet. 2013 Jan; 9(1): e1003225. Published online 2013 Jan 31. doi: 10.1371/journal.pgen.1003225
PMCID:
PMC3561084
AbstractArticlePDF–1.0M
13.
Jedi-1 and MEGF10 Signal Engulfment of Apoptotic Neurons through the Tyrosine Kinase Syk
Jami L. Scheib, Chelsea S. Sullivan, Bruce D. Carter
J Neurosci. 2012 Sep 19; 32(38): 13022–13031. doi: 10.1523/JNEUROSCI.6350-11.2012
PMCID:
PMC3464495
AbstractArticlePDF–1.9M
14.
Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores
Steven E. Boyden, Lane J. Mahoney, Genri Kawahara, Jennifer A. Myers, Satomi Mitsuhashi, Elicia A. Estrella, Anna R. Duncan, Friederike Dey, Elizabeth T. DeChene, Jessica M. Blasko-Goehringer, Carsten G. Bönnemann, Basil T. Darras, Jerry R. Mendell, Hart G. W. Lidov, Ichizo Nishino, Alan H. Beggs, Louis M. Kunkel, Peter B. Kang
Neurogenetics. 2012; 13(2): 115–124. Published online 2012 Feb 28. doi: 10.1007/s10048-012-0315-z
PMCID:
PMC3332380
AbstractArticlePDF–502K
15.
MEGF10 AND 11 MEDIATE HOMOTYPIC INTERACTIONS REQUIRED FOR MOSAIC SPACING OF RETINAL NEURONS
Jeremy N. Kay, Monica W. Chu, Joshua R. Sanes
Nature. Author manuscript; available in PMC 2012 Sep 22.
Published in final edited form as: Nature. 2012 Mar 22; 483(7390): 465–469. Published online 2012 Mar 11. doi: 10.1038/nature10877
PMCID:
PMC3310952
AbstractArticlePDF–965K
16.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
17.
Protein interactome reveals converging molecular pathways among autism disorders
Yasunari Sakai, Chad A. Shaw, Brian C. Dawson, Diana V. Dugas, Zaina Al-Mohtaseb, David E. Hill, Huda Y. Zoghbi
Sci Transl Med. Author manuscript; available in PMC 2011 Dec 8.
Published in final edited form as: Sci Transl Med. 2011 Jun 8; 3(86): 86ra49. doi: 10.1126/scitranslmed.3002166
PMCID:
PMC3169432
AbstractArticlePDF–6.0M
18.
Personalized Smoking Cessation: Interactions between Nicotine Dose, Dependence and Quit-Success Genotype Score
Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl
Mol Med. 2010 Jul-Aug; 16(7-8): 247–253. Published online 2010 Mar 17. doi: 10.2119/molmed.2009.00159
Correction in:
Mol Med. 2012; 18(1): 729.
PMCID:
PMC2896464
AbstractArticlePDF–2.4M
19.
Apoptotic Engulfment Pathway and Schizophrenia
Xiangning Chen, Cuie Sun, Qi Chen, F. Anthony O'Neill, Dermot Walsh, Ayman H. Fanous, Kodavali V. Chowdari, Vishwajit L. Nimgaonkar, Adrian Scott, Sibylle G. Schwab, Dieter B. Wildenauer, Ronglin Che, Wei Tang, Yongyong Shi, Lin He, Xiong-jian Luo, Bing Su, Todd L. Edwards, Zhongming Zhao, Kenneth S. Kendler
PLoS One. 2009; 4(9): e6875. Published online 2009 Sep 1. doi: 10.1371/journal.pone.0006875
PMCID:
PMC2731162
AbstractArticlePDF–156K
20.
MEGF10 Association with Schizophrenia
Xiangning Chen, Xu Wang, Qi Chen, Vernell Williamson, Edwin van den Oord, Brion S. Maher, F. Anthony O’Neill, Dermot Walsh, Kenneth S. Kendler
Biol Psychiatry. Author manuscript; available in PMC 2009 Mar 1.
Published in final edited form as: Biol Psychiatry. 2008 Mar 1; 63(5): 441–448. Published online 2008 Jan 7. doi: 10.1016/j.biopsych.2007.11.003
PMCID:
PMC2268016
AbstractArticlePDF–1.2M

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

You are here: NCBI > Literature > PubMed Central (PMC)
Support Center