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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

Article PDF–1.2M

Select item 69930582.

Targeted Sequencing and RNA Assay Reveal a Noncanonical JAG1 Splicing Variant Causing Alagille Syndrome

Yiyao Chen, Xueli Liu, Songchang Chen, Junyu Zhang, Chenming Xu

Front Genet. 2019; 10: 1363. Published online 2020 Jan 24. doi: 10.3389/fgene.2019.01363

PMCID:: PMC6993058

Article PDF–3.7M

Select item 69408403.

Novel JAG1 Deletion Variant in Patient with Atypical Alagille Syndrome

Emanuele Micaglio, Andreea Alina Andronache, Paola Carrera, Michelle M. Monasky, Emanuela T. Locati, Barbara Pirola, Silvia Presi, Mario Carminati, Maurizio Ferrari, Alessandro Giamberti, Carlo Pappone

Int J Mol Sci. 2019 Dec; 20(24): 6247. Published online 2019 Dec 11. doi: 10.3390/ijms20246247

PMCID:: PMC6940840

Article PDF–2.2M

Select item 69174944.

Coronary arterial development is regulated by a Dll4-Jag1-EphrinB2 signaling cascade

Stanislao Igor Travisano, Vera Lucia Oliveira, Belén Prados, Joaquim Grego-Bessa, Rebeca Piñeiro-Sabarís, Vanesa Bou, Manuel J Gómez, Fátima Sánchez-Cabo, Donal MacGrogan, José Luis de la Pompa

eLife. 2019; 8: e49977. Published online 2019 Dec 4. doi: 10.7554/eLife.49977

PMCID:: PMC6917494

Article PDF–19M

Select item 68836275.

Validation of an epigenetic field of susceptibility to detect significant prostate cancer from non-tumor biopsies

Bing Yang, Tyler Etheridge, Johnathon McCormick, Adam Schultz, Tariq A. Khemees, Nathan Damaschke, Glen Leverson, Kaitlin Woo, Geoffrey A. Sonn, Eric A. Klein, Mike Fumo, Wei Huang, David F. Jarrard

Clin Epigenetics. 2019; 11: 168. Published online 2019 Nov 28. doi: 10.1186/s13148-019-0771-5

PMCID:: PMC6883627

Article PDF–807K

Select item 68521366.

Association of JAG1 gene polymorphism with systemic blood pressure in patients with obstructive sleep apnea: a prospective cohort study

Ivana Paraničová, Viera Habalová, Lucia Klimčáková, Ivana Trojová, Jozef Židzik, Ivan Tkáč, Ružena Tkáčová, Pavol Joppa

Croat Med J. 2019 Oct; 60(5): 421–430. doi: 10.3325/cmj.2019.60.421

PMCID:: PMC6852136

Article PDF–285K

Select item 68312027.

Anisomycin inhibits angiogenesis in ovarian cancer by attenuating the molecular sponge effect of the lncRNA-Meg3/miR-421/PDGFRA axis

Weiping Ye, Zhentian Ni, Shen Yicheng, Hao Pan, Yongyi Huang, Ying Xiong, Te Liu

Int J Oncol. 2019 Dec; 55(6): 1296–1312. Published online 2019 Sep 30. doi: 10.3892/ijo.2019.4887

PMCID:: PMC6831202

Article PDF–4.1M

Select item 67773558.

Knockdown of HE4 suppresses aggressive cell growth and malignant progression of ovarian cancer by inhibiting the JAK/STAT3 pathway

Aihong Wang, Canhui Jin, Xiaoyu Tian, Ying Wang, Hongyu Li

Biol Open. 2019 Sep 15; 8(9): bio043570. Published online 2019 Sep 15. doi: 10.1242/bio.043570

PMCID:: PMC6777355

Article PDF–6.6M

Select item 67756149.

Heavy-Ion Carbon Radiation Regulates Long Non-Coding RNAs in Cervical Cancer HeLa Cells

Zhi Yang, Qingying Gu, Ying Wang, Bo Liu, Guangming Zhou, Chunlin Shao, Jing Ruan, Renbing Jia, Shengfang Ge

J Cancer. 2019; 10(21): 5022–5030. Published online 2019 Aug 28. doi: 10.7150/jca.30846

PMCID:: PMC6775614

Article PDF–1.1M

Select item 677426710.

Mechanisms of IFNalpha-1a-Induced Apoptosis in a Laryngeal Cancer Cell Line

Xiao-Lei Xin, Ran Zhang, Xiao-Mei Yuan, Li Liu

Med Sci Monit. 2019; 25: 7100–7114. Published online 2019 Sep 22. doi: 10.12659/MSM.917097

PMCID:: PMC6774267

Article PDF–2.4M

Select item 675965611.

Evaluation of the Possibility to Detect Circulating Tumor DNA From Pituitary Adenoma

Kaspars Megnis, Raitis Peculis, Vita Rovite, Pola Laksa, Helvijs Niedra, Inga Balcere, Olivija Caune, Austra Breiksa, Jurijs Nazarovs, Janis Stukens, Ilze Konrade, Valdis Pirags, Janis Klovins

Front Endocrinol (Lausanne) 2019; 10: 615. Published online 2019 Sep 18. doi: 10.3389/fendo.2019.00615

PMCID:: PMC6759656

Article PDF–354K

Select item 668394912.

Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt–Jakob disease

Eva Bagyinszky, YoungSoon Yang, Vo Van Giau, Young Chul Youn, Seong Soo A An, SangYun Kim

Clin Interv Aging. 2019; 14: 1387–1397. Published online 2019 Aug 2. doi: 10.2147/CIA.S210909

PMCID:: PMC6683949

Article PDF–4.2M

Select item 667828313.

Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review

Livia Bernardi, Amalia C. Bruni

Int J Mol Sci. 2019 Jul; 20(14): 3606. Published online 2019 Jul 23. doi: 10.3390/ijms20143606

PMCID:: PMC6678283

Article PDF–589K

Select item 656554614.

Clinical utility in infants with suspected monogenic conditions through next‐generation sequencing

Sha Hong, Li Wang, Dongying Zhao, Yonghong Zhang, Yan Chen, Jintong Tan, Lili Liang, Tianwen Zhu

Mol Genet Genomic Med. 2019 Jun; 7(6): e684. Published online 2019 Apr 9. doi: 10.1002/mgg3.684

PMCID:: PMC6565546

Article PDF–931K

Select item 654907215.

Gene expression alterations of human liver cancer cells following borax exposure

Lun Wu, Ying Wei, Wen-Bo Zhou, You-Shun Zhang, Qin-Hua Chen, Ming-Xing Liu, Zheng-Peng Zhu, Jiao Zhou, Li-Hua Yang, Hong-Mei Wang, Guang-Min Wei, Sheng Wang, Zhi-Gang Tang

Oncol Rep. 2019 Jul; 42(1): 115–130. Published online 2019 May 23. doi: 10.3892/or.2019.7169

PMCID:: PMC6549072

Article PDF–852K

Select item 652984316.

Alagille Syndrome: A Novel Mutation in JAG1 Gene

Rita Fischetto, Viviana V. Palmieri, Maria E. Tripaldi, Alberto Gaeta, Angela Michelucci, Maurizio Delvecchio, Ruggiero Francavilla, Paola Giordano

Front Pediatr. 2019; 7: 199. Published online 2019 May 15. doi: 10.3389/fped.2019.00199

PMCID:: PMC6529843

Article PDF–1.1M

Select item 650301317.

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

Article PDF–1.2M

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

PMCID:: PMC6418363

Article PDF–1.8M

Select item 641341019.

NOTCH Signaling Is Activated through Mechanical Strain in Human Bone Marrow-Derived Mesenchymal Stromal Cells

Fani Ziouti, Regina Ebert, Maximilian Rummler, Melanie Krug, Sigrid Müller-Deubert, Martin Lüdemann, Franz Jakob, Bettina M. Willie, Franziska Jundt

Stem Cells Int. 2019; 2019: 5150634. Published online 2019 Feb 26. doi: 10.1155/2019/5150634

PMCID:: PMC6413410

Article PDF–1.4M

Select item 639843820.

Nonsyndromic Craniosynostosis: Novel Coding Variants

Anshuman Sewda, Sierra R. White, Monica Erazo, Ke Hao, Gemma García-Fructuoso, Ivette Fernández-Rodriguez, Yann Heuzé, Joan T. Richtsmeier, Paul A. Romitti, Boris Reva, Ethylin Wang Jabs, Inga Peter

Pediatr Res. Author manuscript; available in PMC 2019 Jul 14.

Published in final edited form as: Pediatr Res. 2019 Mar; 85(4): 463–468. Published online 2019 Jan 14. doi: 10.1038/s41390-019-0274-2