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Items: 1 to 20 of 111

1.
Differential sequences and single nucleotide polymorphism of exosomal SOX2 DNA in cancer
Manjusha Vaidya, Kiminobu Sugaya
PLoS One. 2020; 15(2): e0229309. Published online 2020 Feb 24. doi: 10.1371/journal.pone.0229309
PMCID:
PMC7039433
AbstractArticlePDF–3.9M
2.
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
3.
Computational determination of human PPARG gene: SNPs and prediction of their effect on protein functions of diabetic patients
Howeida Abdullah Mustafa, Afraa Mohamed Suliman Albkrye, Buthiena Mohamed AbdAlla, Mona AbdelRahman Mohammed Khair, Nidal Abdelwahid, Hind Abdelaziz Elnasri
Clin Transl Med. 2020; 9: 7. Published online 2020 Feb 17. doi: 10.1186/s40169-020-0258-1
PMCID:
PMC7024687
AbstractArticlePDF–3.2M
4.
Investigation of DNA variants specific to ROBO2 Isoform ‘a’ in Irish vesicoureteric reflux patients reveals marked CpG island variation
John M. Darlow, Mark G. Dobson, Andrew J. Green, Prem Puri, David E. Barton
Sci Rep. 2020; 10: 2265. Published online 2020 Feb 10. doi: 10.1038/s41598-020-58818-6
PMCID:
PMC7010700
AbstractArticlePDF–1.1M
5.
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci
Elisabeth Luisa Germer, Sophie Imhoff, Carles Vilariño-Güell, Meike Kasten, Philip Seibler, Norbert Brüggemann, International Parkinson’s Disease Genomics Consortium, Christine Klein, Joanne Trinh
Front Neurol. 2019; 10: 1284. Published online 2019 Dec 13. doi: 10.3389/fneur.2019.01284
PMCID:
PMC6923768
AbstractArticlePDF–390K
6.
Gene‐level genome‐wide association analysis of suicide attempt, a preliminary study in a psychiatric Mexican population
Thelma Beatriz González‐Castro, José Jaime Martínez‐Magaña, Carlos Alfonso Tovilla‐Zárate, Isela Esther Juárez‐Rojop, Emmanuel Sarmiento, Alma Delia Genis‐Mendoza, Humberto Nicolini
Mol Genet Genomic Med. 2019 Dec; 7(12): e983. Published online 2019 Oct 2. doi: 10.1002/mgg3.983
PMCID:
PMC6900393
AbstractArticlePDF–604K
7.
Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis
Karen H.Y. Wong, Michal Levy‐Sakin, Walfred Ma, Nina Gonzaludo, Angel C.Y. Mak, Dedeepya Vaka, Annie Poon, Catherine Chu, Richard Lao, Melek Balamir, Zoe Grenville, Nicolas Wong, John P. Kane, Pui‐Yan Kwok, Mary J. Malloy, Clive R. Pullinger
Mol Genet Genomic Med. 2019 Dec; 7(12): e1007. Published online 2019 Oct 16. doi: 10.1002/mgg3.1007
PMCID:
PMC6900368
AbstractArticlePDF–1.3M
8.
Rapid Screening for Deleted Form of β‐thalassemia by Real‐Time Quantitative PCR
Liang‐Yin Ke, Jan‐Gowth Chang, Chao‐Sung Chang, Li‐Ling Hsieh, Ta‐Chih Liu
J Clin Lab Anal. 2017 Jan; 31(1): e22019. Published online 2016 Aug 16. doi: 10.1002/jcla.22019
PMCID:
PMC6817179
AbstractArticlePDF–277K
9.
Effect of type 2 diabetes mellitus caveolin-3 K15N mutation on glycometabolism
Yiyuan Huang, Yufeng Deng, Lina Shang, Lihui Yang, Juanjuan Huang, Jing Ma, Xianshan Liao, Hui Zhou, Jing Xian, Guining Liang, Qin Huang
Exp Ther Med. 2019 Oct; 18(4): 2531–2539. Published online 2019 Aug 2. doi: 10.3892/etm.2019.7840
Correction in:
Exp Ther Med. 2020 Feb; 19(2): 1137.
PMCID:
PMC6755474
AbstractArticlePDF–2.5M
10.
A cross-sectional study on factors associated with hypertension and genetic polymorphisms of renin-angiotensin-aldosterone system in Chinese hui pilgrims to hajj
Yinxia Zhang, Fangfang Shi, Zhanbiao Yu, Aimin Yang, Maolan Zeng, Jiaoyue Wang, Haiping Yin, Benzhong Zhang, Xiao Ma
BMC Public Health. 2019; 19: 1223. Published online 2019 Sep 4. doi: 10.1186/s12889-019-7357-1
PMCID:
PMC6727391
AbstractArticlePDF–1.7M
11.
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
12.
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
13.
ERβ promotes Aβ degradation via the modulation of autophagy
Yong Wei, Jiawei Zhou, Jun Wu, Jian Huang
Cell Death Dis. 2019 Aug; 10(8): 565. Published online 2019 Jul 22. doi: 10.1038/s41419-019-1786-8
Correction in:
Cell Death Dis. 2019 Sep; 10(9): 634.
PMCID:
PMC6646346
AbstractArticlePDF–1.7M
14.
Urinary 8-hydroxydeoxyguanosine in relation to XRCC1 rs25487 G/A (Arg399Gln) and OGG1 rs1052133 C/G (Ser326Cys) DNA repair genes polymorphisms in patients with chronic hepatitis C and related hepatocellular carcinoma
Aida A Mahmoud, Mohammed H Hassan, Ali A Ghweil, Amany Abdelrahman, Asmaa N Mohammad, Hesham H Ameen
Cancer Manag Res. 2019; 11: 5343–5351. Published online 2019 Jun 10. doi: 10.2147/CMAR.S209112
PMCID:
PMC6572741
AbstractArticlePDF–1.0M
15.
Polymorphisms in the CCR5 promoter associated with cervical intraepithelial neoplasia in a Chinese Han population
Shuyuan Liu, Jun Chen, Zhiling Yan, Shuying Dai, Chuanyin Li, Yufeng Yao, Li Shi
BMC Cancer. 2019; 19: 525. Published online 2019 May 31. doi: 10.1186/s12885-019-5738-6
PMCID:
PMC6544959
AbstractArticlePDF–853K
16.
IRS1‐ rs10498210 G/A and CCR5‐59029 A/G polymorphisms in patients with type 2 diabetes in Kurdistan
Fatemeh Keshavarzi, Shadi Golsheh
Mol Genet Genomic Med. 2019 May; 7(5): e631. Published online 2019 Mar 18. doi: 10.1002/mgg3.631
PMCID:
PMC6503169
AbstractArticlePDF–490K
17.
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
AbstractArticlePDF–1.2M
18.
Low genetic heterogeneity of copy number variations (CNVs) in the genes encoding the human deoxyribonucleases 1-like 3 and II potentially relevant to autoimmunity
Misuzu Ueki, Junko Fujihara, Kaori Kimura-Kataoka, Kazuo Yamada, Yoshikazu Takinami, Haruo Takeshita, Reiko Iida, Toshihiro Yasuda
PLoS One. 2019; 14(4): e0215479. Published online 2019 Apr 25. doi: 10.1371/journal.pone.0215479
PMCID:
PMC6483174
AbstractArticlePDF–1.0M
19.
Identification of differentially expressed non-coding RNAs and mRNAs involved in Qi stagnation and blood stasis syndrome
Guang Chen, Jialiang Gao, Haoqiang He, Chao Liu, Yongmei Liu, Jun Li, Jie Wang
Exp Ther Med. 2019 Feb; 17(2): 1206–1223. Published online 2018 Dec 7. doi: 10.3892/etm.2018.7068
PMCID:
PMC6327641
AbstractArticlePDF–3.7M
20.
Functional variants of the ATG7 gene promoter in acute myocardial infarction
Pei Zhang, Jie Zhang, Yexin Zhang, Shuai Wang, Shuchao Pang, Bo Yan
Mol Genet Genomic Med. 2018 Nov; 6(6): 1209–1219. Published online 2018 Nov 8. doi: 10.1002/mgg3.508
PMCID:
PMC6305654
AbstractArticlePDF–1.0M

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