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 32

1.
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families
Syeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, Adil u Rehman, Sher Alam Khan, Shamim Saleha, Yar Muhammad Khan, Noor Muhammad, Saadullah Khan, Naveed Wasif
BMC Med Genomics. 2024; 17: 176. Published online 2024 Jul 2. doi: 10.1186/s12920-024-01943-2
PMCID:
PMC11221130
AbstractArticlePDF–5.5M
2.
Early ependymal tumor with MN1-BEND2 fusion: a mostly cerebral tumor of female children with a good prognosis that is distinct from classical astroblastoma
Norman L. Lehman
J Neurooncol. 2023; 161(3): 425–439. Published online 2023 Jan 6. doi: 10.1007/s11060-022-04222-1
PMCID:
PMC9992034
AbstractArticlePDF–2.0M
3.
METTL14-mediated epitranscriptome modification of MN1 mRNA promote tumorigenicity and all-trans-retinoic acid resistance in osteosarcoma
Hong-Bo Li, Gang Huang, Jian Tu, Dong-Ming Lv, Qing-Lin Jin, Jun-Kai Chen, Yu-Tong Zou, Dung-Fang Lee, Jing-Nan Shen, Xian-Biao Xie
eBioMedicine. 2022 Aug; 82: 104142. Published online 2022 Jul 7. doi: 10.1016/j.ebiom.2022.104142
PMCID:
PMC9272358
AbstractArticlePDF–6.5M
4.
Intrinsically disordered Meningioma-1 stabilizes the BAF complex to cause AML.
Simone S. Riedel, Congcong Lu, Hongbo M. Xie, Kevin Nestler, Marit W. Vermunt, Alexandra Lenard, Laura Bennett, Nancy A. Speck, Ichiro Hanamura, Julie Lessard, Gerd A. Blobel, Benjamin A. Garcia, Kathrin M. Bernt
Mol Cell. Author manuscript; available in PMC 2022 Jun 3.
Published in final edited form as: Mol Cell. 2021 Jun 3; 81(11): 2332–2348.e9. Published online 2021 May 10. doi: 10.1016/j.molcel.2021.04.014
PMCID:
PMC8380056
AbstractArticlePDF–3.4M
5.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
6.
MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis
Christopher C Y Mak, Dan Doherty, Angela E Lin, Nancy Vegas, Megan T Cho, Géraldine Viot, Clémantine Dimartino, James D Weisfeld-Adams, Davor Lessel, Shelagh Joss, Chumei Li, Claudia Gonzaga-Jauregui, Yuri A Zarate, Nadja Ehmke, Denise Horn, Caitlin Troyer, Sarina G Kant, Youngha Lee, Gisele E Ishak, Gordon Leung, Amanda Barone Pritchard, Sandra Yang, Eric G Bend, Francesca Filippini, Chelsea Roadhouse, Nicolas Lebrun, Michele G Mehaffey, Pierre-Marie Martin, Benjamin Apple, Francisca Millan, Oliver Puk, Mariette J V Hoffer, Lindsay B Henderson, Ruth McGowan, Ingrid M Wentzensen, Steven Pei, Farah R Zahir, Mullin Yu, William T Gibson, Ann Seman, Marcie Steeves, Jill R Murrell, Sabine Luettgen, Elizabeth Francisco, Tim M Strom, Louise Amlie-Wolf, Angela M Kaindl, William G Wilson, Sara Halbach, Lina Basel-Salmon, Noa Lev-El, Jonas Denecke, Lisenka E L M Vissers, Kelly Radtke, Jamel Chelly, Elaine Zackai, Jan M Friedman, Michael J Bamshad, Deborah A Nickerson, University of Washington Center for Mendelian Genomics, Russell R Reid, Koenraad Devriendt, Jong-Hee Chae, Elliot Stolerman, Carey McDougall, Zöe Powis, Thierry Bienvenu, Tiong Y Tan, Naama Orenstein, William B Dobyns, Joseph T Shieh, Murim Choi, Darrel Waggoner, Karen W Gripp, Michael J Parker, Joan Stoler, Stanislas Lyonnet, Valérie Cormier-Daire, David Viskochil, Trevor L Hoffman, Jeanne Amiel, Brian H Y Chung, Christopher T Gordon
Brain. 2020 Jan; 143(1): 55–68. Published online 2019 Dec 13. doi: 10.1093/brain/awz379
Correction in:
Brain. 2020 Mar; 143(3): e24.
PMCID:
PMC7962909
AbstractArticlePDF–1.7M
7.
MN1 overexpression with varying tumor grade is a promising predictor of survival of glioma patients
Masum Saini, Ajaya Nand Jha, Rajiv Tangri, Md Qudratullah, Sher Ali
Hum Mol Genet. 2020 Nov 1; 29(21): 3532–3545. Published online 2020 Oct 26. doi: 10.1093/hmg/ddaa231
PMCID:
PMC7788295
AbstractArticlePDF–1.6M
8.
Allogeneic stem cell transplantation mitigates the adverse prognostic impact of high diagnostic BAALC and MN1 expression in AML
Madlen Jentzsch, Marius Bill, Juliane Grimm, Dominic Brauer, Donata Backhaus, Karoline Goldmann, Julia Schulz, Dietger Niederwieser, Uwe Platzbecker, Sebastian Schwind
Ann Hematol. 2020; 99(10): 2417–2427. Published online 2020 Aug 29. doi: 10.1007/s00277-020-04235-8
PMCID:
PMC7481166
AbstractArticlePDF–1.0M
9.
Meningioma 1 is indispensable for mixed lineage leukemia-rearranged acute myeloid leukemia
Amit Sharma, Nidhi Jyotsana, Razif Gabdoulline, Dirk Heckl, Florian Kuchenbauer, Robert K. Slany, Arnold Ganser, Michael Heuser
Haematologica. 2020 May; 105(5): 1294–1305. Prepublished online 2019 Aug 14. doi: 10.3324/haematol.2018.211201
PMCID:
PMC7193500
AbstractArticlePDF–2.4M
10.
Gain-of-Function MN1 Truncation Variants Cause a Recognizable Syndrome with Craniofacial and Brain Abnormalities
Noriko Miyake, Hidehisa Takahashi, Kazuyuki Nakamura, Bertrand Isidor, Yoko Hiraki, Eriko Koshimizu, Masaaki Shiina, Kazunori Sasaki, Hidefumi Suzuki, Ryota Abe, Yayoi Kimura, Tomoko Akiyama, Shin-ichi Tomizawa, Tomonori Hirose, Kohei Hamanaka, Satoko Miyatake, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Kazuyuki Obo, Mitsuhiro Kato, Kazuhiro Ogata, Naomichi Matsumoto
Am J Hum Genet. 2020 Jan 2; 106(1): 13–25. Published online 2019 Dec 12. doi: 10.1016/j.ajhg.2019.11.011
PMCID:
PMC7042485
AbstractArticlePDF–1.9M
11.
Genomic analysis demonstrates that histologically-defined astroblastomas are molecularly heterogeneous and that tumors with MN1 rearrangement exhibit the most favorable prognosis
Norman L. Lehman, Aisulu Usubalieva, Tong Lin, Sariah J. Allen, Quynh T. Tran, Bret C. Mobley, Roger E. McLendon, Matthew J. Schniederjan, Maria-Magdalena Georgescu, Marta Couce, Mohanpal S. Dulai, Jack M. Raisanen, Mousa Al Abbadi, Cheryl A. Palmer, Eyas M. Hattab, Brent A. Orr
Acta Neuropathol Commun. 2019; 7: 42. Published online 2019 Mar 15. doi: 10.1186/s40478-019-0689-3
PMCID:
PMC6419470
AbstractArticlePDF–2.4M
12.
VIRMA mediates preferential m6A mRNA methylation in 3′UTR and near stop codon and associates with alternative polyadenylation
Yanan Yue, Jun Liu, Xiaolong Cui, Jie Cao, Guanzheng Luo, Zezhou Zhang, Tao Cheng, Minsong Gao, Xiao Shu, Honghui Ma, Fengqin Wang, Xinxia Wang, Bin Shen, Yizhen Wang, Xinhua Feng, Chuan He, Jianzhao Liu
Cell Discov. 2018; 4: 10. Published online 2018 Feb 27. doi: 10.1038/s41421-018-0019-0
PMCID:
PMC5826926
AbstractArticlePDF–2.3M
13.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
14.
Variable but consistent pattern of Meningioma 1 gene (MN1) expression in different genetic subsets of acute myelogenous leukaemia and its potential use as a marker for minimal residual disease detection
Sonia Carturan, Jessica Petiti, Valentina Rosso, Chiara Calabrese, Elisabetta Signorino, Giada Bot-Sartor, Paolo Nicoli, Daniela Gallo, Enrico Bracco, Alessandro Morotti, Cristina Panuzzo, Enrico Gottardi, Francesco Frassoni, Giuseppe Saglio, Daniela Cilloni
Oncotarget. 2016 Nov 8; 7(45): 74082–74096. Published online 2016 Sep 27. doi: 10.18632/oncotarget.12269
PMCID:
PMC5342037
AbstractArticlePDF–2.5M
15.
High MN1 expression increases the in vitro clonogenic activity of primary mouse B-cells
Masashi Numata, Mehmet Deniz Yener, Sema Sırma Ekmekçi, Müge Aydın, Gerard Grosveld, Monica Cardone, Sabrina Terranova, Ramon Klein Geltink, Uğur Özbek, Emrah Özçelik, Çağrı Güleç, Sema Anak, Serap Karaman, Gülyüz Öztürk, Meral Akbıyık, Ayten Kandilci
Leuk Res. Author manuscript; available in PMC 2016 Dec 13.
Published in final edited form as: Leuk Res. 2015 Aug; 39(8): 906–912. Published online 2015 Jun 12. doi: 10.1016/j.leukres.2015.05.013
PMCID:
PMC5154248
AbstractArticlePDF–1.4M
16.
MLL1 and DOT1L cooperate with meningioma-1 to induce acute myeloid leukemia
Simone S. Riedel, Jessica N. Haladyna, Matthew Bezzant, Brett Stevens, Daniel A. Pollyea, Amit U. Sinha, Scott A. Armstrong, Qi Wei, Roy M. Pollock, Scott R. Daigle, Craig T. Jordan, Patricia Ernst, Tobias Neff, Kathrin M. Bernt
J Clin Invest. 2016 Apr 1; 126(4): 1438–1450. Published online 2016 Feb 29. doi: 10.1172/JCI80825
PMCID:
PMC4811120
AbstractArticlePDF–2.2M
17.
Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate
Jeroen Breckpot, Britt-Marie Anderlid, Yasemin Alanay, Moira Blyth, Afane Brahimi, Bénédicte Duban-Bedu, Odile Gozé, Helen Firth, Mustafa Cengiz Yakicier, Greet Hens, Maissa Rayyan, Eric Legius, Joris Robert Vermeesch, Koen Devriendt
Eur J Hum Genet. 2016 Jan; 24(1): 51–58. Published online 2015 May 6. doi: 10.1038/ejhg.2015.65
PMCID:
PMC4795238
AbstractArticlePDF–872K
18.
Exome Sequencing on Malignant Meningiomas Identified Mutations in Neurofibromatosis Type 2 (NF2) and Meningioma 1 (MN1) Genes
Xu Zhang, Haiying Jia, Yao Lu, Chengliang Dong, Jinghui Hou, Zheng Wang, Feng Wang, Hongbin Zhong, Lin Wang, Kai Wang
Discov Med. Author manuscript; available in PMC 2016 Jan 20.
Published in final edited form as: Discov Med. 2014 Dec; 18(101): 301–311.
PMCID:
PMC4720499
AbstractArticlePDF–524K
19.
Gene–Smoking Interactions Identify Several Novel Blood Pressure Loci in the Framingham Heart Study
Yun J. Sung, Lisa de las Fuentes, Karen L. Schwander, Jeannette Simino, Dabeeru C. Rao
Am J Hypertens. 2015 Mar; 28(3): 343–354. Published online 2014 Sep 3. doi: 10.1093/ajh/hpu149
PMCID:
PMC4402348
AbstractArticlePDF–38M
20.
Modeling de novo leukemogenesis from human cord blood with MN1 and NUP98HOXD13
Suzan Imren, Michael Heuser, Maura Gasparetto, Philip A. Beer, Gudmundur L. Norddahl, Ping Xiang, Ling Chen, Tobias Berg, Garrett W. Rhyasen, Patricia Rosten, Gyeongsin Park, Yeonsook Moon, Andrew P. Weng, Connie J. Eaves, R. Keith Humphries
Blood. 2014 Dec 4; 124(24): 3608–3612. Prepublished online 2014 Oct 22. doi: 10.1182/blood-2014-04-564666
PMCID:
PMC4256911
AbstractArticle

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

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