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Select item 70271951.

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

Abstract Article PDF–1.2M

Select item 69782292.

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

Abstract Article PDF–761K

Select item 69063213.

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

Abstract Article PDF–3.6M

Select item 67752734.

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

Abstract Article PDF–918K

Select item 67026875.

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

Abstract Article PDF–1.3M

Select item 66887896.

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

Abstract Article PDF–1.0M

Select item 66876197.

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

Abstract Article PDF–541K

Select item 65030138.

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

Abstract Article PDF–1.2M

Select item 63559689.

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

Abstract Article PDF–2.0M

Select item 627609010.

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

Abstract Article PDF–1.2M

Select item 624559711.

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

Abstract Article PDF–746K

Select item 624549312.

DNA sequences alignment in multi-GPUs: acceleration and energy payoff

Jesús Pérez-Serrano, Edans Sandes, Alba Cristina Magalhaes Alves de Melo, Manuel Ujaldón

BMC Bioinformatics. 2018; 19(Suppl 14): 421. Published online 2018 Nov 20. doi: 10.1186/s12859-018-2389-6

PMCID:: PMC6245493

Abstract Article PDF–2.9M

Select item 621112613.

Genetic Polymorphisms and In Silico Mutagenesis Analyses of CYP2C9, CYP2D6, and CYPOR Genes in the Pakistani Population

Shabbir Ahmed, Jie Zhou, Zhan Zhou, Shu-Qing Chen

Genes (Basel) 2018 Oct; 9(10): 514. Published online 2018 Oct 22. doi: 10.3390/genes9100514

PMCID:: PMC6211126

Abstract Article PDF–3.4M

Select item 617617714.

Altered expression pattern of circular RNAs in metastatic oral mucosal melanoma

Houyu Ju, Liming Zhang, Lu Mao, Shuli Liu, Weiya Xia, Jingzhou Hu, Min Ruan, Guoxin Ren

Am J Cancer Res. 2018; 8(9): 1788–1800. Published online 2018 Sep 1.

PMCID:: PMC6176177

Abstract Article PDF–2.0M

Select item 616167315.

MiRNA-BD: an evidence-based bioinformatics model and software tool for microRNA biomarker discovery

Yuxin Lin, Wentao Wu, Zhandong Sun, Li Shen, Bairong Shen

RNA Biol. 2018; 15(8): 1093–1105. Published online 2018 Sep 17. doi: 10.1080/15476286.2018.1502590

PMCID:: PMC6161673

Abstract Article PDF–2.4M

Select item 607306416.

Novel heterozygous mutation in TBX1 in an infant with hypocalcemic seizures

Kosei Hasegawa, Hiroyuki Tanaka, Yousuke Higuchi, Yumiko Hayashi, Katsuhiro Kobayashi, Hirokazu Tsukahara

Clin Pediatr Endocrinol. 2018; 27(3): 159–164. Published online 2018 Jul 31. doi: 10.1297/cpe.27.159

PMCID:: PMC6073064

Abstract Article PDF–1.7M

Select item 601357117.

Differentiation-Dependent Regulation of Human Endogenous Retrovirus K Sequences and Neighboring Genes in Germ Cell Tumor Cells

Thomas Mueller, Claudia Hantsch, Ines Volkmer, Martin S. Staege

Front Microbiol. 2018; 9: 1253. Published online 2018 Jun 15. doi: 10.3389/fmicb.2018.01253

PMCID:: PMC6013571

Abstract Article PDF–2.0M

Select item 590601718.

A family of long intergenic non-coding RNA genes in human chromosomal region 22q11.2 carry a DNA translocation breakpoint/AT-rich sequence

Nicholas Delihas

PLoS One. 2018; 13(4): e0195702. Published online 2018 Apr 18. doi: 10.1371/journal.pone.0195702

PMCID:: PMC5906017

Abstract Article PDF–3.7M

Select item 586945919.

Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

Nehir Kurtas, Filippo Arrigoni, Edoardo Errichiello, Claudio Zucca, Cristina Maghini, Maria Grazia D’Angelo, Silvana Beri, Roberto Giorda, Sara Bertuzzo, Massimo Delledonne, Luciano Xumerle, Marzia Rossato, Orsetta Zuffardi, Maria Clara Bonaglia

J Med Genet. 2018 Apr; 55(4): 269–277. Published online 2018 Jan 29. doi: 10.1136/jmedgenet-2017-105125