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Items: 1 to 20 of 123

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
ArticlePDF–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
ArticlePDF–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
ArticlePDF–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
ArticlePDF–1.1M
5.
Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia
Avani Solanki, Aruna Rajendran, Sheila Mohan, Revathy Raj, Babu Rao Vundinti
PLoS One. 2020; 15(1): e0227603. Published online 2020 Jan 15. doi: 10.1371/journal.pone.0227603
PMCID:
PMC6961948
ArticlePDF–772K
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
ArticlePDF–604K
7.
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
ArticlePDF–277K
8.
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
ArticlePDF–2.5M
9.
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
ArticlePDF–1.7M
10.
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
ArticlePDF–2.0M
11.
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
ArticlePDF–1.3M
12.
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
ArticlePDF–1.7M
13.
FANCD2 Binding to H4K20me2 via a Methyl-Binding Domain Is Essential for Efficient DNA Cross-Link Repair
Karissa L. Paquin, Nicholas E. Mamrak, Jada L. Garzon, Juan A. Cantres-Velez, Paul A. Azzinaro, Elizabeth A. Vuono, Kevin E. Lima, Jodi L. Camberg, Niall G. Howlett
Mol Cell Biol. 2019 Aug 1; 39(15): e00194-19. Prepublished online 2019 May 13. Published online 2019 Jul 16. doi: 10.1128/MCB.00194-19
PMCID:
PMC6639249
ArticlePDF–3.2M
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
ArticlePDF–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
ArticlePDF–853K
16.
Malignant Transformation of Fanconi Anemia Complementation Group D2-deficient (Fancd2−/−) Hematopoietic Progenitor Cells by a Single HPV16 Oncogene
XICHEN ZHANG, RENEE FISHER, DONNA SHIELDS, WEN HOU, DARCY FRANICOLA, HONG WANG, MICHAEL W. EPPERLY, LORA RIGATTI, JOEL S. GREENBERGER
In Vivo. 2019 Mar-Apr; 33(2): 303–311. Published online 2019 Mar 3. doi: 10.21873/invivo.11476
PMCID:
PMC6506306
ArticlePDF–740K
17.
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
ArticlePDF–490K
18.
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
ArticlePDF–1.2M
19.
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
ArticlePDF–1.0M
20.
High-risk human papillomavirus oncogenes disrupt the Fanconi anemia DNA repair pathway by impairing localization and de-ubiquitination of FancD2
Sujita Khanal, Denise A. Galloway
PLoS Pathog. 2019 Feb; 15(2): e1007442. Published online 2019 Feb 28. doi: 10.1371/journal.ppat.1007442
PMCID:
PMC6413947
ArticlePDF–2.9M

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