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Items: 1 to 20 of 48

1.
FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia
Xiao-Na Zhu, Yu-Sheng Wei, Qian Yang, Hao-Ran Liu, Zhe Zhi, Di Zhu, Li Xia, Deng-Li Hong, Yun Yu, Guo-Qiang Chen
J Hematol Oncol. 2023; 16: 9. Published online 2023 Feb 11. doi: 10.1186/s13045-023-01400-0
PMCID:
PMC9922468
AbstractArticlePDF–4.9M
2.
Spectrum of paired‐like homeobox 2b immunoexpression in pediatric brain tumors with embryonal morphology
Murad Alturkustani, Adam D. Walker, Ivy Tran, Matija Snuderl, Jennifer A. Cotter
Pathol Int. 2022 Aug; 72(8): 402–410. Published online 2022 Jun 28. doi: 10.1111/pin.13255
PMCID:
PMC9544136
AbstractArticlePDF–1.9M
3.
Effects of transcription factors Phox2 on expression of norepinephrine transporter and dopamine β-hydroxylase in SK-N-BE(2)C cells
Yan Fan, Jingjing Huang, Niamh Kieran, Meng-Yang Zhu
J Neurochem. Author manuscript; available in PMC 2022 Jul 31.
Published in final edited form as: J Neurochem. 2009 Sep; 110(5): 1502–1513. Published online 2009 Jul 1. doi: 10.1111/j.1471-4159.2009.06260.x
PMCID:
PMC9339151
AbstractArticlePDF–1.1M
4.
Variable phenotypes in congenital central hypoventilation syndrome with PHOX2B nonpolyalanine repeat mutations
Ajay S. Kasi, Hong Li, Taryn J. Jurgensen, Lokesh Guglani, Thomas G. Keens, Iris A. Perez
J Clin Sleep Med. 2021 Oct 1; 17(10): 2049–2055. Published online 2021 Oct 1. doi: 10.5664/jcsm.9370
PMCID:
PMC8494081
AbstractArticlePDF–518K
5.
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations
Shio Mitsuzawa, Naoki Suzuki, Tetsuya Akiyama, Mitsuru Ishikawa, Takefumi Sone, Jiro Kawada, Ryo Funayama, Matsuyuki Shirota, Hiroaki Mitsuhashi, Satoru Morimoto, Kensuke Ikeda, Tomomi Shijo, Akiyuki Ohno, Naoko Nakamura, Hiroya Ono, Risako Ono, Shion Osana, Tadashi Nakagawa, Ayumi Nishiyama, Rumiko Izumi, Shohei Kaneda, Yoshiho Ikeuchi, Keiko Nakayama, Teruo Fujii, Hitoshi Warita, Hideyuki Okano, Masashi Aoki
Stem Cell Reports. 2021 Jun 8; 16(6): 1527–1541. Published online 2021 May 27. doi: 10.1016/j.stemcr.2021.04.021
PMCID:
PMC8190591
AbstractArticlePDF–4.4M
6.
Impact of cytosine methylation on DNA binding specificities of human transcription factors
Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale
Science. Author manuscript; available in PMC 2021 Mar 30.
Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239
PMCID:
PMC8009048
AbstractArticlePDF–2.6M
7.
A respiratory/Hirschsprung phenotype in a three‐generation family associated with a novel pathogenic PHOX2B splice donor mutation
Nikolai Paul Pace, Michael Pace Bardon, Isabella Borg
Mol Genet Genomic Med. 2020 Dec; 8(12): e1528. Published online 2020 Oct 13. doi: 10.1002/mgg3.1528
PMCID:
PMC7767558
AbstractArticlePDF–655K
8.
Neuroblastoma patient‐derived cultures are enriched for a mesenchymal gene signature and reflect individual drug response
Esther Hee, Meng Kang Wong, Sheng Hui Tan, Zhang’E Choo, Chik Hong Kuick, Sharon Ling, Min Hwee Yong, Sudhanshi Jain, Derrick W. Q. Lian, Eileen H. Q. Ng, Yvonne F. L. Yong, Mee Hiong Ren, Nurfarhanah Syed Sulaiman, Sharon Y. Y. Low, Yong Wei Chua, Muhammad Fahmy Syed, Tony K. H. Lim, Shui Yen Soh, Prasad Iyer, Michaela S. F. Seng, Joyce C. M. Lam, Enrica E. K. Tan, Mei Yoke Chan, Ah Moy Tan, Yong Chen, Zhixiong Chen, Kenneth T. E. Chang, Amos Hong Pheng Loh
Cancer Sci. 2020 Oct; 111(10): 3780–3792. Published online 2020 Aug 28. doi: 10.1111/cas.14610
PMCID:
PMC7540996
AbstractArticlePDF–1.1M
9.
AMPK Interactome Reveals New Function in Non-homologous End Joining DNA Repair
Zhen Chen, Chao Wang, Antrix Jain, Mrinal Srivastava, Mengfan Tang, Huimin Zhang, Xu Feng, Litong Nie, Dan Su, Yun Xiong, Sung Yun Jung, Jun Qin, Junjie Chen
Mol Cell Proteomics. 2020 Mar; 19(3): 467–477. Published online 2020 Jan 3. doi: 10.1074/mcp.RA119.001794
PMCID:
PMC7050103
AbstractArticlePDF–1.8M
10.
Association between PHOX2B gene rs28647582 T>C polymorphism and Wilms tumor susceptibility
Ao Lin, Wen Fu, Wenwen Wang, Jinhong Zhu, Jiabin Liu, Huimin Xia, Guochang Liu, Jing He
Biosci Rep. 2019 Oct 30; 39(10): BSR20192529. Published online 2019 Oct 18. doi: 10.1042/BSR20192529
PMCID:
PMC6822530
AbstractArticlePDF–312K
11.
Defective Respiratory Rhythmogenesis and Loss of Central Chemosensitivity in Phox2b Mutants Targeting Retrotrapezoid Nucleus Neurons
Véronique Dubreuil, Muriel Thoby-Brisson, Murielle Rallu, Karin Persson, Alexandre Pattyn, Carmen Birchmeier, Jean-François Brunet, Gilles Fortin, Christo Goridis
J Neurosci. 2009 Nov 25; 29(47): 14836–14846. doi: 10.1523/JNEUROSCI.2623-09.2009
PMCID:
PMC6665996
AbstractArticlePDF–3.4M
12.
Altered enteric expression of the homeobox transcription factor Phox2b in patients with diverticular disease
François Cossais, Christina Lange, Martina Barrenschee, Marie Möding, Michael Ebsen, Ilka Vogel, Martina Böttner, Thilo Wedel
United European Gastroenterol J. 2019 Apr; 7(3): 349–357. Published online 2019 Jan 16. doi: 10.1177/2050640618824913
PMCID:
PMC6466753
AbstractArticlePDF–1.0M
13.
Pleiotropic effect of common PHOX2B variants in Hirschsprung disease and neuroblastoma
Jinglu Zhao, Yun Zhu, Xiaoli Xie, Yuxiao Yao, Jiao Zhang, Ruizhong Zhang, Lihua Huang, Jiwen Cheng, Huimin Xia, Jing He, Yan Zhang
Aging (Albany NY) 2019 Feb 28; 11(4): 1252–1261. Published online 2019 Feb 22. doi: 10.18632/aging.101834
PMCID:
PMC6402522
AbstractArticlePDF–445K
14.
Adult With PHOX2B Mutation and Late-Onset Congenital Central Hypoventilation Syndrome
Ajay S. Kasi, Sheila S. Kun, Thomas G. Keens, Iris A. Perez
J Clin Sleep Med. 2018 Dec 15; 14(12): 2079–2081. Published online 2018 Dec 15. doi: 10.5664/jcsm.7542
PMCID:
PMC6287728
AbstractArticlePDF–521K
15.
Atypical presentations associated with non-polyalanine repeat PHOX2B mutations
Umakanth Katwa, Alissa M. D'Gama, Anita E. Qualls, Lucas M. Donovan, Jody Heffernan, Jiahai Shi, Pankaj B. Agrawal
Am J Med Genet A. Author manuscript; available in PMC 2018 Aug 31.
Published in final edited form as: Am J Med Genet A. 2018 Jul; 176(7): 1627–1631. Published online 2018 Apr 28. doi: 10.1002/ajmg.a.38720
PMCID:
PMC6117218
AbstractArticlePDF–350K
16.
An In Vitro Approach to Test the Possible Role of Candidate Factors in the Transcriptional Regulation of the RET Proto-Oncogene
Tiziana Bachetti, Silvia Borghini, Roberto Ravazzolo, Isabella Ceccherini
Gene Expr. 2005; 12(3): 137–149. Published online 2018 Jun 20. doi: 10.3727/000000005783992106
PMCID:
PMC6009117
AbstractArticlePDF–319K
17.
Expanding the Phenotype of Congenital Central Hypoventilation Syndrome Impacts Management Decisions
Heather M. Byers, Maida Chen, Andrew S. Gelfand, Bruce Ong, Marisa Jendras, Ian A. Glass
Am J Med Genet A. Author manuscript; available in PMC 2019 Jun 1.
Published in final edited form as: Am J Med Genet A. 2018 Jun; 176(6): 1398–1404. Published online 2018 Apr 25. doi: 10.1002/ajmg.a.38726
PMCID:
PMC5992090
AbstractArticlePDF–754K
18.
Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndrome
Simona Di Lascio, Roberta Benfante, Eleonora Di Zanni, Silvia Cardani, Annalisa Adamo, Diego Fornasari, Isabella Ceccherini, Tiziana Bachetti
Hum Mutat. 2018 Feb; 39(2): 219–236. Published online 2017 Nov 21. doi: 10.1002/humu.23365
PMCID:
PMC5846889
AbstractArticlePDF–2.3M
19.
Genetic susceptibility to neuroblastoma
Vanessa P. Tolbert, Grace E. Coggins, John M. Maris
Curr Opin Genet Dev. Author manuscript; available in PMC 2018 Apr 28.
Published in final edited form as: Curr Opin Genet Dev. 2017 Feb; 42: 81–90. Published online 2017 Apr 28. doi: 10.1016/j.gde.2017.03.008
PMCID:
PMC5604862
AbstractArticlePDF–493K
20.
Examination of PHOX2B in Adult Neuroendocrine Neoplasms Reveals Relatively Frequent Expression in Pheochromocytomas and Paragangliomas
John P Lee, Yin P Hung, Thomas M O’Dorisio, James R Howe, Jason L Hornick, Andrew M Bellizzi
Histopathology. Author manuscript; available in PMC 2018 Oct 1.
Published in final edited form as: Histopathology. 2017 Oct; 71(4): 503–510. Published online 2017 Jul 13. doi: 10.1111/his.13243
PMCID:
PMC5597462
AbstractArticlePDF–3.3M

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