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Items: 1 to 20 of 92

1.
Systematic Nucleotide Exchange Analysis of ESTs From the Human Cancer Genome Project Report: Origins of 347 Unknown ESTs Indicate Putative Transcription of Non-Coding Genomic Regions
Ganesh Warthi, Pierre-Edouard Fournier, Hervé Seligmann
Front Genet. 2020; 11: 42. Published online 2020 Feb 11. doi: 10.3389/fgene.2020.00042
PMCID:
PMC7027195
AbstractArticlePDF–1.2M
2.
Candidate modifier genes for immune function in 22q11.2 deletion syndrome
Catherina T. Pinnaro, Travis Henry, Heather J. Major, Mrutyunjaya Parida, Lucy E. DesJardin, John R. Manak, Benjamin W. Darbro
Mol Genet Genomic Med. 2020 Jan; 8(1): e1057. Published online 2019 Dec 12. doi: 10.1002/mgg3.1057
PMCID:
PMC6978229
AbstractArticlePDF–761K
3.
Identification and validation of mRNA 3′untranslated regions of DNMT3B and TET3 as novel competing endogenous RNAs of the tumor suppressor PTEN
Kenneth Anthony R. Roquid, Krizelle Mae M. Alcantara, Reynaldo L. Garcia
Int J Oncol. 2020 Feb; 56(2): 544–558. Published online 2019 Dec 20. doi: 10.3892/ijo.2019.4947
PMCID:
PMC6959461
AbstractArticlePDF–1.5M
4.
Frequencies of clinically important CYP2C19 and CYP2D6 alleles are graded across Europe
Jelena Petrović, Vesna Pešić, Volker M. Lauschke
Eur J Hum Genet. 2020 Jan; 28(1): 88–94. Published online 2019 Jul 29. doi: 10.1038/s41431-019-0480-8
PMCID:
PMC6906321
AbstractArticlePDF–3.6M
5.
Frequency of Germline Mutations in Cancer Susceptibility Genes in Malignant Mesothelioma
Vasiliki Panou, Meghana Gadiraju, Arthur Wolin, Caroline M. Weipert, Emily Skarda, Aliya N. Husain, Jyoti D. Patel, Buerkley Rose, Shannon R. Zhang, Madison Weatherly, Viswateja Nelakuditi, Amy Knight Johnson, Maria Helgeson, David Fischer, Arpita Desai, Nanna Sulai, Lauren Ritterhouse, Oluf D. Røe, Kiran K. Turaga, Dezheng Huo, Jeremy Segal, Sabah Kadri, Zejuan Li, Hedy L. Kindler, Jane E. Churpek
J Clin Oncol. 2018 Oct 1; 36(28): 2863–2871. Published online 2018 Aug 16. doi: 10.1200/JCO.2018.78.5204
PMCID:
PMC6804864
AbstractArticlePDF–709K
6.
Parvalbumin Promoter Methylation Altered in Major Depressive Disorder
Benjamard Thaweethee-Sukjai, Sirijit Suttajit, Samur Thanoi, Caroline F. Dalton, Gavin P. Reynolds, Sutisa Nudmamud-Thanoi
Int J Med Sci. 2019; 16(9): 1207–1214. Published online 2019 Aug 14. doi: 10.7150/ijms.36131
PMCID:
PMC6775273
AbstractArticlePDF–918K
7.
The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling
Yan Cui, Susann Groth, Scott Troutman, Annemarie Carlstedt, Tobias Sperka, Lars Björn Riecken, Joseph L. Kissil, Hongchuan Jin, Helen Morrison
Oncogene. 2019; 38(36): 6370–6381. Published online 2019 Jul 16. doi: 10.1038/s41388-019-0883-6
PMCID:
PMC6756068
AbstractArticlePDF–1.8M
8.
Different gene expression profiles in subcutaneous & visceral adipose tissues from Mexican patients with obesity
María D. Ronquillo, Alla Mellnyk, Noemí Cárdenas-Rodríguez, Emmanuel Martínez, David A. Comoto, Liliana Carmona-Aparicio, Norma E. Herrera, Eleazar Lara, Armando Pereyra, Esaú Floriano-Sánchez
Indian J Med Res. 2019 May; 149(5): 616–626. doi: 10.4103/ijmr.IJMR_1165_17
PMCID:
PMC6702687
AbstractArticlePDF–1.3M
9.
Computational analysis of high-risk SNPs in human CHK2 gene responsible for hereditary breast cancer: A functional and structural impact
Nutan V. Badgujar, Bhoomi V. Tarapara, Franky D. Shah
PLoS One. 2019; 14(8): e0220711. Published online 2019 Aug 9. doi: 10.1371/journal.pone.0220711
PMCID:
PMC6688789
AbstractArticlePDF–1.0M
10.
Association of BCR/ABL transcript variants with different blood parameters and demographic features in Iraqi chronic myeloid leukemia patients
Mahmood S. Khazaal, Farqad B. Hamdan, Qasim S. Al‐Mayah
Mol Genet Genomic Med. 2019 Aug; 7(8): e809. Published online 2019 Jun 17. doi: 10.1002/mgg3.809
PMCID:
PMC6687619
AbstractArticlePDF–541K
11.
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing
Ye Cao, Mari J. Tokita, Edward S. Chen, Rajarshi Ghosh, Tiansheng Chen, Yanming Feng, Elizabeth Gorman, Federica Gibellini, Patricia A. Ward, Alicia Braxton, Xia Wang, Linyan Meng, Rui Xiao, Weimin Bi, Fan Xia, Christine M. Eng, Yaping Yang, Tomasz Gambin, Chad Shaw, Pengfei Liu, Pawel Stankiewicz
Genome Med. 2019; 11: 48. Published online 2019 Jul 26. doi: 10.1186/s13073-019-0658-2
PMCID:
PMC6660700
AbstractArticlePDF–980K
12.
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins
Amira Jaballah-Gabteni, Haifa Tounsi, Maria Kabbage, Yosr Hamdi, Sahar Elouej, Ines Ben Ayed, Mouna Medhioub, Moufida Mahmoudi, Hamza Dallali, Hamza Yaiche, Nadia Ben Jemii, Afifa Maaloul, Najla Mezghani, Sonia Abdelhak, Lamine Hamzaoui, Mousaddak Azzouz, Samir Boubaker
J Transl Med. 2019; 17: 212. Published online 2019 Jun 27. doi: 10.1186/s12967-019-1961-9
PMCID:
PMC6598283
AbstractArticlePDF–1.8M
13.
Two Sides of the Coin: Ezrin/Radixin/Moesin and Merlin Control Membrane Structure and Contact Inhibition
Katharine A. Michie, Adam Bermeister, Neil O. Robertson, Sophia C. Goodchild, Paul M. G. Curmi
Int J Mol Sci. 2019 Apr; 20(8): 1996. Published online 2019 Apr 23. doi: 10.3390/ijms20081996
PMCID:
PMC6515277
AbstractArticlePDF–6.7M
14.
Genetic analysis of pharmacogenomic VIP variants in the Blang population from Yunnan Province of China
Chan Zhang, Weiwei Guo, Yujing Cheng, Qi Li, Xin Yang, Run Dai, Linhao Zhu, Wanlu Chen
Mol Genet Genomic Med. 2019 May; 7(5): e574. Published online 2019 Apr 5. doi: 10.1002/mgg3.574
PMCID:
PMC6503013
AbstractArticlePDF–1.2M
15.
A proteasome-resistant fragment of NIK mediates oncogenic NF-κB signaling in schwannomas
Jeffrey R Gehlhausen, Eric Hawley, Benjamin Mark Wahle, Yongzheng He, Donna Edwards, Steven D Rhodes, Jacquelyn D Lajiness, Karl Staser, Shi Chen, Xianlin Yang, Jin Yuan, Xiaohong Li, Li Jiang, Abbi Smith, Waylan Bessler, George Sandusky, Anat Stemmer-Rachamimov, Timothy J Stuhlmiller, Steven P Angus, Gary L Johnson, Grzegorz Nalepa, Charles W Yates, D Wade Clapp, Su-Jung Park
Hum Mol Genet. 2019 Feb 15; 28(4): 572–583. Published online 2018 Oct 17. doi: 10.1093/hmg/ddy361
PMCID:
PMC6489415
AbstractArticlePDF–11M
16.
MicroRNA-92a promotes cell proliferation, migration and survival by directly targeting the tumor suppressor gene NF2 in colorectal and lung cancer cells
Krizelle Mae M. Alcantara, Reynaldo L. Garcia
Oncol Rep. 2019 Apr; 41(4): 2103–2116. Published online 2019 Feb 19. doi: 10.3892/or.2019.7020
PMCID:
PMC6412542
AbstractArticlePDF–2.4M
17.
PES1 promotes the occurrence and development of papillary thyroid cancer by upregulating the ERα/ERβ protein ratio
Yi-Bo Qiu, Ling-Yao Liao, Rong Jiang, Man Xu, Lin-Wan Xu, George G. Chen, Zhi-Min Liu
Sci Rep. 2019; 9: 1032. Published online 2019 Jan 31. doi: 10.1038/s41598-018-37648-7
PMCID:
PMC6355968
AbstractArticlePDF–2.0M
18.
Establishment and characterization of CRISPR/Cas9‐mediated NF2−/− human mesothelial cell line: Molecular insight into fibroblast growth factor receptor 2 in malignant pleural mesothelioma
Md Wahiduzzaman, Sivasundaram Karnan, Akinobu Ota, Ichiro Hanamura, Hideki Murakami, Akihito Inoko, Md Lutfur Rahman, Toshinori Hyodo, Hiroyuki Konishi, Shinobu Tsuzuki, Yoshitaka Hosokawa
Cancer Sci. 2019 Jan; 110(1): 180–193. Published online 2018 Dec 14. doi: 10.1111/cas.13871
PMCID:
PMC6317947
AbstractArticlePDF–1.5M
19.
V-ATPases and osteoclasts: ambiguous future of V-ATPases inhibitors in osteoporosis
Xiaohong Duan, Shaoqing Yang, Lei Zhang, Tielin Yang
Theranostics. 2018; 8(19): 5379–5399. Published online 2018 Oct 26. doi: 10.7150/thno.28391
PMCID:
PMC6276090
AbstractArticlePDF–1.2M
20.
SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences
Enzo Rucci, Carlos Garcia, Guillermo Botella, Armando De Giusti, Marcelo Naiouf, Manuel Prieto-Matias
BMC Syst Biol. 2018; 12(Suppl 5): 96. Published online 2018 Nov 20. doi: 10.1186/s12918-018-0614-6
PMCID:
PMC6245597
AbstractArticlePDF–746K

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