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Items: 1 to 20 of 178

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.
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
ArticlePDF–1.1M
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.
NanoTouch: intracellular recording using transmembrane conductive nanoparticles
Mitsuyoshi L. Saito
J Neurophysiol. 2019 Nov 1; 122(5): 2016–2026. Published online 2019 Sep 4. doi: 10.1152/jn.00359.2019
PMCID:
PMC6879961
Article
8.
Functional Consequences of the SCN5A-p.Y1977N Mutation within the PY Ubiquitylation Motif: Discrepancy between HEK293 Cells and Transgenic Mice
Simona Casini, Maxime Albesa, Zizun Wang, Vincent Portero, Daniela Ross-Kaschitza, Jean-Sébastien Rougier, Gerard A. Marchal, Wendy K. Chung, Connie R. Bezzina, Hugues Abriel, Carol Ann Remme
Int J Mol Sci. 2019 Oct; 20(20): 5033. Published online 2019 Oct 11. doi: 10.3390/ijms20205033
PMCID:
PMC6829230
ArticlePDF–2.7M
9.
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
10.
Novel SCN5A p.W697X Nonsense Mutation Segregation in a Family with Brugada Syndrome
Emanuele Micaglio, Michelle M. Monasky, Nicoletta Resta, Rosanna Bagnulo, Giuseppe Ciconte, Luigi Gianelli, Emanuela T. Locati, Gabriele Vicedomini, Valeria Borrelli, Andrea Ghiroldi, Luigi Anastasia, Sara Benedetti, Chiara Di Resta, Maurizio Ferrari, Carlo Pappone
Int J Mol Sci. 2019 Oct; 20(19): 4920. Published online 2019 Oct 4. doi: 10.3390/ijms20194920
PMCID:
PMC6801452
ArticlePDF–1.6M
11.
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
12.
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
13.
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
14.
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
15.
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
16.
The cardiac sodium channel gene SCN5A and its gene product NaV1.5: role in physiology and pathophysiology
Christiaan C. Veerman, Arthur A.M. Wilde, Elisabeth M. Lodder
Gene. Author manuscript; available in PMC 2019 Jul 17.
Published in final edited form as: Gene. 2015 Dec 1; 573(2): 177–187. Published online 2015 Sep 8. doi: 10.1016/j.gene.2015.08.062
PMCID:
PMC6636349
ArticlePDF–749K
17.
Sporadic Erythromelalgia Associated with a Homozygous Carrier of Common Missense Polymorphism in SCN9A Gene Coding for NaV1.7 Voltage-gated Sodium Channel
Piotr K Janicki, Victor Ruiz-Velasco, Sanjib Adhikary
Cureus. 2019 May; 11(5): e4587. Published online 2019 May 2. doi: 10.7759/cureus.4587
PMCID:
PMC6609274
ArticlePDF–335K
18.
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
19.
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
20.
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

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