U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 117

1.
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
AbstractArticlePDF–701K
2.
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Laura M. Huckins, Amanda Dobbyn, Douglas M. Ruderfer, Gabriel Hoffman, Weiqing Wang, Antonio F. Pardiñas, Veera M Rajagopal, Thomas D. Als, Hoang Nguyen, Kiran Girdhar, James Boocock, Panos Roussos, Menachem Fromer, Robin Kramer, Enrico Domenici, Eric R. Gamazon, Shaun Purcell, CommonMind Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, iPSYCH-GEMS Schizophrenia Working Group, Ditte Demontis, Anders D. Børglum, James T.R. Walters, Michael C. O'Donovan, Patrick Sullivan, Michael J. Owen, Bernie Devlin, Solveig K. Sieberts, Nancy J. Cox, Hae Kyung Im, Pamela Sklar, Eli A. Stahl
Nat Genet. Author manuscript; available in PMC 2020 Feb 21.
Published in final edited form as: Nat Genet. 2019 Apr; 51(4): 659–674. Published online 2019 Mar 25. doi: 10.1038/s41588-019-0364-4
Correction in:
Nat Genet. 2019 May 13
PMCID:
PMC7034316
AbstractArticlePDF–1.3M
3.
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
4.
Complicated paroxysmal kinesigenic dyskinesia associated with SACS mutations
Qiang Lu, Liang Shang, Wo Tu Tian, Li Cao, Xue Zhang, Qing Liu
Ann Transl Med. 2020 Jan; 8(1): 8. doi: 10.21037/atm.2019.11.31
PMCID:
PMC6995733
AbstractArticlePDF–1.1M
5.
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
AbstractArticlePDF–1.2M
6.
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
AbstractArticlePDF–1.3M
7.
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
AbstractArticlePDF–2.4M
8.
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
AbstractArticlePDF–6.9M
9.
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
AbstractArticlePDF–4.5M
10.
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
AbstractArticlePDF–807K
11.
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
AbstractArticlePDF–1.0M
12.
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
AbstractArticlePDF–5.1M
13.
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
AbstractArticlePDF–1.1M
14.
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
AbstractArticlePDF–2.7M
15.
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
AbstractArticlePDF–3.0M
16.
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations
Robert Fragoza, Jishnu Das, Shayne D. Wierbowski, Jin Liang, Tina N. Tran, Siqi Liang, Juan F. Beltran, Christen A. Rivera-Erick, Kaixiong Ye, Ting-Yi Wang, Li Yao, Matthew Mort, Peter D. Stenson, David N. Cooper, Xiaomu Wei, Alon Keinan, John C. Schimenti, Andrew G. Clark, Haiyuan Yu
Nat Commun. 2019; 10: 4141. Published online 2019 Sep 12. doi: 10.1038/s41467-019-11959-3
PMCID:
PMC6742646
AbstractArticlePDF–1.2M
17.
ULK1 phosphorylates Mad1 to regulate spindle assembly checkpoint
Fengjie Yuan, Ximin Jin, Dan Li, Yuanshuai Song, Nan Zhang, Xin Yang, Lina Wang, Wei-Guo Zhu, Chan Tian, Ying Zhao
Nucleic Acids Res. 2019 Sep 5; 47(15): 8096–8110. Published online 2019 Jul 10. doi: 10.1093/nar/gkz602
PMCID:
PMC6736072
AbstractArticlePDF–3.6M
18.
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
AbstractArticlePDF–632K
19.
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
AbstractArticlePDF–2.0M
20.
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

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

You are here: NCBI > Literature > PubMed Central (PMC)
Support Center