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Select item 70282781.

Aberrant DNA methylation of the toll-like receptors 2 and 6 genes in patients with obstructive sleep apnea

Kuo-Tung Huang, Yung-Che Chen, Chia-Cheng Tseng, Huang-Chih Chang, Mao-Chang Su, Ting-Ya Wang, Yong-Yong Lin, Yi-Xin Zheng, Jen-Chieh Chang, Chien-Hung Chin, Chang-Chun Hsiao, Meng-Chih Lin

PLoS One. 2020; 15(2): e0228958. Published online 2020 Feb 18. doi: 10.1371/journal.pone.0228958

PMCID:: PMC7028278

Abstract Article PDF–1.6M

Select item 70271952.

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 70168903.

HIF1α/TET1 Pathway Mediates Hypoxia-Induced Adipocytokine Promoter Hypomethylation in Human Adipocytes

Mohamed M. Ali, Shane A. Phillips, Abeer M. Mahmoud

Cells. 2020 Jan; 9(1): 134. Published online 2020 Jan 6. doi: 10.3390/cells9010134

PMCID:: PMC7016890

Abstract Article PDF–2.2M

Select item 69883204.

NFкB is a critical transcriptional regulator of atypical cadherin FAT1 in glioma

Chitrangda Srivastava, Khushboo Irshad, Yakhlesh Gupta, Chitra Sarkar, Ashish Suri, Parthaprasad Chattopadhyay, Subrata Sinha, Kunzang Chosdol

BMC Cancer. 2020; 20: 62. Published online 2020 Jan 28. doi: 10.1186/s12885-019-6435-1

PMCID:: PMC6988320

Abstract Article PDF–3.3M

Select item 69614065.

Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report

Maryam Sobhani, Mohammad Amin Tabatabaiefar, Soudeh Ghafouri-Fard, Asadollah Rajab, Asal Hojjat, Abdol-Mohammad Kajbafzadeh, Mohammad Reza Noori-Daloii

BMC Med Genet. 2020; 21: 13. Published online 2020 Jan 14. doi: 10.1186/s12881-020-0950-4

Correction in:: BMC Med Genet. 2020; 21: 58.

PMCID:: PMC6961406

Abstract Article PDF–1.1M

Select item 69356246.

A novel detrimental homozygous mutation in the WFS1 gene in two sisters from nonconsanguineous parents with untreated diabetes insipidus

Dimitrios T. Papadimitriou, Kleanthis Kleanthous, Emmanouil Manolakos, Anatoly Tiulpakov, Thomas Nikolopoulos, Alexandros Delides, Gerasimos Voros, Argyrios Dinopoulos, George Zoupanos, Anastasios Papadimitriou, Georgios Mastorakos, Fumihiko Urano

Clin Case Rep. 2019 Dec; 7(12): 2355–2357. Published online 2019 Oct 23. doi: 10.1002/ccr3.2494

PMCID:: PMC6935624

Abstract Article PDF–113K

Select item 68876517.

The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing

Dan-Dan Wang, Fang-Yuan Hu, Feng-Juan Gao, Sheng-Hai Zhang, Ping Xu, Guo-Hong Tian, Ji-Hong Wu

Front Genet. 2019; 10: 1217. Published online 2019 Nov 26. doi: 10.3389/fgene.2019.01217

PMCID:: PMC6887651

Abstract Article PDF–1.6M

Select item 68583428.

Comprehensive Analysis of the Expression Profiles of Long Non-Coding RNAs with Associated ceRNA Network Involved in the Colon Cancer Staging and Progression

Meini Wu, Wenliang Li, Fengchang Huang, Jing Sun, Kang ping Li, Jiandong Shi, Jingyu Yang, Jianfang Li, Yanhan Li, Ningzhu Hu, YunZhang Hu

Sci Rep. 2019; 9: 16910. Published online 2019 Nov 15. doi: 10.1038/s41598-019-52883-2

PMCID:: PMC6858342

Abstract Article PDF–4.1M

Select item 68310709.

Compound heterozygous mutations in WFS1 cause atypical Wolfram syndrome

Yun-Di Pan, Jun-Ling Fu, Xin-Hua Xiao

Chin Med J (Engl) 2019 Oct 20; 132(20): 2508–2509. Published online 2019 Oct 20. doi: 10.1097/CM9.0000000000000464

PMCID:: PMC6831070

Article PDF–277K

Select item 678593410.

Circ-SMARCA5 suppresses progression of multiple myeloma by targeting miR-767-5p

Haiyan Liu, Yan Wu, Shunye Wang, Jie Jiang, Chenlu Zhang, Yijing Jiang, Xingfeng Wang, Lewen Hong, Hongming Huang

BMC Cancer. 2019; 19: 937. Published online 2019 Oct 10. doi: 10.1186/s12885-019-6088-0

PMCID:: PMC6785934

Abstract Article PDF–7.6M

Select item 673447411.

CALCA and TRPV1 genes polymorphisms are related to a good outcome in female chronic migraine patients treated with OnabotulinumtoxinA

R. Moreno-Mayordomo, M. Ruiz, J. Pascual, M. Gallego de la Sacristana, I. Vidriales, M. Sobrado, E. Cernuda-Morollon, A. B. Gago-Veiga, D. Garcia-Azorin, J. J. Telleria, A. L. Guerrero

J Headache Pain. 2019; 20(1): 39. Published online 2019 Apr 23. doi: 10.1186/s10194-019-0989-9

PMCID:: PMC6734474

Abstract Article PDF–623K

Select item 673233912.

Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort

Amjad Khan, Shirui Han, Rongrong Wang, Muhammad Ansar, Wasim Ahmad, Xue Zhang

Mol Genet Genomic Med. 2019 Sep; 7(9): e917. Published online 2019 Aug 6. doi: 10.1002/mgg3.917

PMCID:: PMC6732339

Abstract Article PDF–876K

Select item 670132813.

GNPDA2 Gene Affects Adipogenesis and Alters the Transcriptome Profile of Human Adipose-Derived Mesenchymal Stem Cells

Lijun Wu, Feifei Ma, Xiaoyuan Zhao, Mei-Xian Zhang, Jianxin Wu, Jie Mi

Int J Endocrinol. 2019; 2019: 9145452. Published online 2019 Aug 1. doi: 10.1155/2019/9145452

PMCID:: PMC6701328

Abstract Article PDF–4.0M

Select item 662996414.

Latrophilins: A Neuro-Centric View of an Evolutionary Conserved Adhesion G Protein-Coupled Receptor Subfamily

Ana L. Moreno-Salinas, Monserrat Avila-Zozaya, Paul Ugalde-Silva, David A. Hernández-Guzmán, Fanis Missirlis, Antony A. Boucard

Front Neurosci. 2019; 13: 700. Published online 2019 Jul 9. doi: 10.3389/fnins.2019.00700

PMCID:: PMC6629964

Abstract Article PDF–5.8M

Select item 654957515.

A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants

Jianling Ji, Lishuang Shen, Moiz Bootwalla, Catherine Quindipan, Tatiana Tatarinova, Dennis T. Maglinte, Jonathan Buckley, Gordana Raca, Sulagna C. Saitta, Jaclyn A. Biegel, Xiaowu Gai

Cold Spring Harb Mol Case Stud. 2019 Apr; 5(2): a003756. doi: 10.1101/mcs.a003756

PMCID:: PMC6549575

Abstract Article PDF–3.3M

Select item 650301316.

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 646565717.

Integrated bioinformatics analysis of key genes involved in progress of colon cancer

Haojie Yang, Jiong Wu, Jingjing Zhang, Zhigang Yang, Wei Jin, Ying Li, Lei Jin, Lu Yin, Hua Liu, Zhenyi Wang

Mol Genet Genomic Med. 2019 Apr; 7(4): e00588. Published online 2019 Feb 11. doi: 10.1002/mgg3.588

PMCID:: PMC6465657

Abstract Article PDF–1017K

Select item 641836318.

Interaction of germline variants in a family with a history of early‐onset clear cell renal cell carcinoma

Emmanuelle Nicolas, Elena V. Demidova, Waleed Iqbal, Ilya G. Serebriiskii, Ramilia Vlasenkova, Pooja Ghatalia, Yan Zhou, Kim Rainey, Andrea F. Forman, Roland L. Dunbrack, Jr, Erica A. Golemis, Michael J. Hall, Mary B. Daly, Sanjeevani Arora

Mol Genet Genomic Med. 2019 Mar; 7(3): e556. Published online 2019 Jan 24. doi: 10.1002/mgg3.556