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Select item 70571231.

Modification effect of sex and obesity on the correlation of LEP polymorphisms with leptin levels in Taiwanese obese women

De‐Min Duan, Jing‐Yi Jhang, Semon Wu, Ming‐Sheng Teng, Lung‐An Hsu, Yu‐Lin Ko

Mol Genet Genomic Med. 2020 Mar; 8(3): e1113. Published online 2020 Jan 8. doi: 10.1002/mgg3.1113

PMCID:: PMC7057123

Abstract Article PDF–701K

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 69784023.

LncRNA DLX6‐AS1 increases the expression of HIF‐1α and promotes the malignant phenotypes of nasopharyngeal carcinoma cells via targeting MiR‐199a‐5p

Bin Yang, Lin Jia, Hui Ren, Caibao Jin, Qingrong Ren, Haiyuan Zhang, Desheng Hu, Hao Zhang, Liu Hu, Tao Xie

Mol Genet Genomic Med. 2020 Jan; 8(1): e1017. Published online 2019 Nov 29. doi: 10.1002/mgg3.1017

PMCID:: PMC6978402

Abstract Article PDF–1.2M

Select item 69782394.

Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing

Juan C. Zenteno, Leopoldo A. García‐Montaño, Marisa Cruz‐Aguilar, Josué Ronquillo, Agustín Rodas‐Serrano, Luis Aguilar‐Castul, Rodrigo Matsui, Carlos I. Vencedor‐Meraz, Rocío Arce‐González, Federico Graue‐Wiechers, Mario Gutiérrez‐Paz, Tatiana Urrea‐Victoria, Ulises de Dios Cuadras, Oscar F. Chacón‐Camacho

Mol Genet Genomic Med. 2020 Jan; 8(1): 10.1002/mgg3.1044. Published online 2019 Nov 17. doi: 10.1002/mgg3.1044

PMCID:: PMC6978239

Abstract Article PDF–1.3M

Select item 69777515.

Computational analysis of functional single nucleotide polymorphisms associated with SLC26A4 gene

Mirza Jawad Ul Hasnain, Muhammad Shoaib, Salman Qadri, Bakhtawar Afzal, Tehreem Anwar, Syed Hassan Abbas, Amina Sarwar, Hafiz Muhammad Talha Malik, Muhammad Tariq Pervez

PLoS One. 2020; 15(1): e0225368. Published online 2020 Jan 23. doi: 10.1371/journal.pone.0225368

PMCID:: PMC6977751

Abstract Article PDF–2.4M

Select item 69433546.

Compensatory upregulation of aldo-keto reductase 1B10 to protect hepatocytes against oxidative stress during hepatocarcinogenesis

Yongzhen Liu, Jing Zhang, Hui Liu, Guiwen Guan, Ting Zhang, Leijie Wang, Xuewei Qi, Huiling Zheng, Chia-Chen Chen, Jia Liu, Deliang Cao, Fengmin Lu, Xiangmei Chen

Am J Cancer Res. 2019; 9(12): 2730–2748. Published online 2019 Dec 1.

PMCID:: PMC6943354

Abstract Article PDF–6.9M

Select item 69001827.

Long non‐coding RNAs influence the transcriptome in pulmonary arterial hypertension: the role of PAXIP1‐AS1

Katharina Jandl, Helene Thekkekara Puthenparampil, Leigh M Marsh, Julia Hoffmann, Jochen Wilhelm, Christine Veith, Katharina Sinn, Walter Klepetko, Horst Olschewski, Andrea Olschewski, Matthias Brock, Grazyna Kwapiszewska

J Pathol. 2019 Mar; 247(3): 357–370. Published online 2019 Jan 16. doi: 10.1002/path.5195

PMCID:: PMC6900182

Abstract Article PDF–4.5M

Select item 68836278.

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

Abstract Article PDF–807K

Select item 68424979.

A novel missense in GLI3 possibly affecting one of the zinc finger domains may lead to postaxial synpolydactyly: case report

Qianqian Zou, Zhigang Tian, Jie Zheng, Xiufang Zhi, Xiaojie Du, Jianbo Shu, Chunquan Cai

BMC Med Genet. 2019; 20: 174. Published online 2019 Nov 9. doi: 10.1186/s12881-019-0889-5

PMCID:: PMC6842497

Abstract Article PDF–1.0M

Select item 683211010.

Validation and Classification of Atypical Splicing Variants Associated With Osteogenesis Imperfecta

Lulu Li, Yixuan Cao, Feiyue Zhao, Bin Mao, Xiuzhi Ren, Yanzhou Wang, Yun Guan, Yi You, Shan Li, Tao Yang, Xiuli Zhao

Front Genet. 2019; 10: 979. Published online 2019 Oct 18. doi: 10.3389/fgene.2019.00979

PMCID:: PMC6832110

Abstract Article PDF–5.1M

Select item 679189211.

Endogenous intronic antisense long non-coding RNA, MGAT3-AS1, and kidney transplantation

Subagini Nagarajah, Shengqiang Xia, Marianne Rasmussen, Martin Tepel

Sci Rep. 2019; 9: 14743. Published online 2019 Oct 14. doi: 10.1038/s41598-019-51409-0

PMCID:: PMC6791892

Abstract Article PDF–1.1M

Select item 675619112.

HPV DNA Associates With Breast Cancer Malignancy and It Is Transferred to Breast Cancer Stromal Cells by Extracellular Vesicles

Sabrina De Carolis, Gianluca Storci, Claudio Ceccarelli, Claudia Savini, Lara Gallucci, Pasquale Sansone, Donatella Santini, Renato Seracchioli, Mario Taffurelli, Francesco Fabbri, Fabrizio Romani, Gaetano Compagnone, Cristina Giuliani, Paolo Garagnani, Massimiliano Bonafè, Monica Cricca

Front Oncol. 2019; 9: 860. Published online 2019 Sep 16. doi: 10.3389/fonc.2019.00860

PMCID:: PMC6756191

Abstract Article PDF–2.7M

Select item 675132813.

Purification and Identification of miRNA Target Sites in Genome Using DNA Affinity Precipitation

Yu Xun, Yingxin Tang, Linmin Hu, Hui Xiao, Shengwen Long, Mengting Gong, Chenxi Wei, Ke Wei, Shuanglin Xiang

Front Genet. 2019; 10: 778. Published online 2019 Sep 12. doi: 10.3389/fgene.2019.00778

Correction in:: Front Genet. 2020; 11: 909.

PMCID:: PMC6751328

Abstract Article PDF–3.0M

Select item 673228214.

Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family

Evelina Siavrienė, Violeta Mikštienė, Darius Radzevičius, Živilė Maldžienė, Tautvydas Rančelis, Gunda Petraitytė, Giedrė Tamulytė, Ingrida Kavaliauskienė, Laurynas Šarkinas, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė

Mol Genet Genomic Med. 2019 Sep; 7(9): e878. Published online 2019 Jul 20. doi: 10.1002/mgg3.878

PMCID:: PMC6732282

Abstract Article PDF–632K

Select item 671201815.

CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan

Chun-Wei Chang, Peng-Wei Hsu, Kuo-Chen Wei, Chia-Wen Chang, Hon-Chung Fung, Mo-Song Hsih, Wen-Chuin Hsu, Long-Sun Ro, Chen-Nen Chang, Jiun-Jie Wang, Yih-Ru Wu, Sien-Tsong Chen

Sci Rep. 2019; 9: 12387. Published online 2019 Aug 27. doi: 10.1038/s41598-019-48448-y

PMCID:: PMC6712018

Abstract Article PDF–2.0M

Select item 671184816.

A 2x folic acid treatment affects epigenetics and dendritic spine densities in SHSY5Y cells

Rahaf Al Sayed, Whitnei Smith, Nicole Rogers, Nuri Smith, Daniel Clark, Gabriel Castillo, Hunter McLeod, Stewart Glenister, Kimberly R. Shorter

Biochem Biophys Rep. 2019 Dec; 20: 100681. Published online 2019 Aug 17. doi: 10.1016/j.bbrep.2019.100681

PMCID:: PMC6711848

Abstract Article PDF–1.0M

Select item 670268717.

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 666424318.

ACTB Variants Confer the Genetic Susceptibility to Diabetic Kidney Disease in a Han Chinese Population

Mengxia Li, Ming Wu, Yu Qin, Jinyi Zhou, Jian Su, Enchun Pan, Qin Zhang, Ning Zhang, Hongyan Sheng, Jiayi Dong, Ye Tong, Chong Shen

Front Genet. 2019; 10: 663. Published online 2019 Jul 23. doi: 10.3389/fgene.2019.00663

PMCID:: PMC6664243

Abstract Article PDF–828K

Select item 655683719.

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Anne H. O’Donnell-Luria, Lynn S. Pais, Víctor Faundes, Jordan C. Wood, Abigail Sveden, Victor Luria, Rami Abou Jamra, Andrea Accogli, Kimberly Amburgey, Britt Marie Anderlid, Silvia Azzarello-Burri, Alice A. Basinger, Claudia Bianchini, Lynne M. Bird, Rebecca Buchert, Wilfrid Carre, Sophia Ceulemans, Perrine Charles, Helen Cox, Lisa Culliton, Aurora Currò, Deciphering Developmental Disorders (DDD) Study, Florence Demurger, James J. Dowling, Benedicte Duban-Bedu, Christèle Dubourg, Saga Elise Eiset, Luis F. Escobar, Alessandra Ferrarini, Tobias B. Haack, Mona Hashim, Solveig Heide, Katherine L. Helbig, Ingo Helbig, Raul Heredia, Delphine Héron, Bertrand Isidor, Amy R. Jonasson, Pascal Joset, Boris Keren, Fernando Kok, Hester Y. Kroes, Alinoë Lavillaureix, Xin Lu, Saskia M. Maas, Gustavo H.B. Maegawa, Carlo L.M. Marcelis, Paul R. Mark, Marcelo R. Masruha, Heather M. McLaughlin, Kirsty McWalter, Esther U. Melchinger, Saadet Mercimek-Andrews, Caroline Nava, Manuela Pendziwiat, Richard Person, Gian Paolo Ramelli, Luiza L.P. Ramos, Anita Rauch, Caitlin Reavey, Alessandra Renieri, Angelika Rieß, Amarilis Sanchez-Valle, Shifteh Sattar, Carol Saunders, Niklas Schwarz, Thomas Smol, Myriam Srour, Katharina Steindl, Steffen Syrbe, Jenny C. Taylor, Aida Telegrafi, Isabelle Thiffault, Doris A. Trauner, Helio van der Linden, Jr., Silvana van Koningsbruggen, Laurent Villard, Ida Vogel, Julie Vogt, Yvonne G. Weber, Ingrid M. Wentzensen, Elysa Widjaja, Jaroslav Zak, Samantha Baxter, Siddharth Banka, Lance H. Rodan

Am J Hum Genet. 2019 Jun 6; 104(6): 1210–1222. Published online 2019 May 9. doi: 10.1016/j.ajhg.2019.03.021

PMCID:: PMC6556837

Abstract Article PDF–1.5M

Select item 650301320.

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

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