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Items: 1 to 20 of 52

1.
Investigating the ID3/SLC22A4 as immune-related signatures in ischemic stroke
Dading Lu, Heng Cai, Yugang Li, Wenyuan Chang, Xiu Liu, Qiwei Dai, Wanning Yu, Wangli Chen, Guomin Qiao, Haojie Xie, Xiong Xiao, Zhiqing Li
Aging (Albany NY) 2023 Dec 31; 15(24): 14803–14829. Published online 2023 Dec 14. doi: 10.18632/aging.205308
PMCID:
PMC10781493
AbstractArticlePDF–2.4M
2.
Localization of Xenobiotic Transporters Expressed at the Human Blood-Testis Barrier
Raymond K. Hau, Robert R. Klein, Stephen H. Wright, Nathan J. Cherrington
Drug Metab Dispos. 2022 Jun; 50(6): 770–780. Published online 2022 Jun. doi: 10.1124/dmd.121.000748
PMCID:
PMC9190233
AbstractArticlePDF–2.8M
3.
Tooth loss and adiposity: possible role of carnitine transporter (OCTN1/2) polymorphisms in women but not in men
Peter Meisel, Stefanie Pagels, Markus Grube, Gabriele Jedlitschky, Henry Völzke, Thomas Kocher
Clin Oral Investig. 2021; 25(2): 701–709. Published online 2020 Sep 22. doi: 10.1007/s00784-020-03594-w
Correction in:
Clin Oral Investig. 2021; 25(8): 5119.
PMCID:
PMC8208909
AbstractArticlePDF–405K
4.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
5.
DNA Methylation‐Based Epigenetic Repression of SLC22A4 Promotes Resistance to Cytarabine in Acute Myeloid Leukemia
Daelynn R. Buelow, Jason T. Anderson, Stanley B. Pounds, Lei Shi, Jatinder K. Lamba, Shuiying Hu, Alice A. Gibson, Emily A. Goodwin, Alex Sparreboom, Sharyn D. Baker
Clin Transl Sci. 2021 Jan; 14(1): 137–142. Published online 2020 Sep 9. doi: 10.1111/cts.12861
PMCID:
PMC7877866
AbstractArticlePDF–396K
6.
Deorphaning a Solute Carrier 22 family member, SLC22A15, through functional genomic studies
Sook Wah Yee, Dina Buitrago, Adrian Stecula, Huy X. Ngo, Huan-Chieh Chien, Ling Zou, Megan L. Koleske, Kathleen M. Giacomini
FASEB J. Author manuscript; available in PMC 2021 Jan 27.
Published in final edited form as: FASEB J. 2020 Dec; 34(12): 15734–15752. Published online 2020 Oct 30. doi: 10.1096/fj.202001497R
PMCID:
PMC7839234
AbstractArticlePDF–1.2M
7.
Hypermethylation of UCHL1 Promotes Metastasis of Nasopharyngeal Carcinoma by Suppressing Degradation of Cortactin (CTTN)
Yin Zhao, Yuan Lei, Shi-Wei He, Ying-Qin Li, Ya-Qin Wang, Xiao-Hong Hong, Ye-Lin Liang, Jun-Yan Li, Yang Chen, Wei-Jie Luo, Pan-Pan Zhang, Xiao-Jing Yang, Qing-Mei He, Jun Ma, Na Liu, Ling-Long Tang
Cells. 2020 Mar; 9(3): 559. Published online 2020 Feb 27. doi: 10.3390/cells9030559
Correction in:
Cells. 2024 May; 13(10): 816.
PMCID:
PMC7140450
AbstractArticlePDF–4.3M
8.
The Functional Proximal Proteome of Oncogenic Ras Includes mTORC2
Joanna R. Kovalski, Aparna Bhaduri, Ashley M. Zehnder, Poornima H. Neela, Yonglu Che, Glenn G. Wozniak, Paul A. Khavari
Mol Cell. Author manuscript; available in PMC 2020 Feb 21.
Published in final edited form as: Mol Cell. 2019 Feb 21; 73(4): 830–844.e12. Published online 2019 Jan 10. doi: 10.1016/j.molcel.2018.12.001
PMCID:
PMC6386588
AbstractArticlePDF–1.7M
9.
Screening genes associated with elevated neutrophil-to-lymphocyte ratio in chronic heart failure
Guoxing Wan, Lihua Ji, Wenbin Xia, Lan Cheng, Yonggang Zhang
Mol Med Rep. 2018 Aug; 18(2): 1415–1422. Published online 2018 Jun 5. doi: 10.3892/mmr.2018.9132
PMCID:
PMC6072186
AbstractArticlePDF–1.3M
10.
OCTN1 is a high-affinity carrier of nucleoside analogs
Christina D. Drenberg, Alice A. Gibson, Stanley B. Pounds, Lei Shi, Dena P. Rhinehart, Lie Li, Shuiying Hu, Guoqing Du, Anne T. Nies, Matthias Schwab, Navjotsingh Pabla, William Blum, Tanja A. Gruber, Sharyn D. Baker, Alex Sparreboom
Cancer Res. Author manuscript; available in PMC 2018 Apr 15.
Published in final edited form as: Cancer Res. 2017 Apr 15; 77(8): 2102–2111. Published online 2017 Feb 16. doi: 10.1158/0008-5472.CAN-16-2548
PMCID:
PMC5419029
AbstractArticlePDF–1.2M
11.
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
Mariem Ben Said, M’hamed Grati, Takahiro Ishimoto, Bing Zou, Imen Chakchouk, Qi Ma, Qi Yao, Bouthaina Hammami, Denise Yan, Rahul Mittal, Noritaka Nakamichi, Abdelmonem Ghorbel, Lingling Neng, Mustafa Tekin, Xiao Rui Shi, Yukio Kato, Saber Masmoudi, Zhongmin Lu, Mounira Hmani, Xuezhong Liu
Hum Genet. Author manuscript; available in PMC 2017 May 1.
Published in final edited form as: Hum Genet. 2016 May; 135(5): 513–524. Published online 2016 Mar 29. doi: 10.1007/s00439-016-1657-7
PMCID:
PMC4836961
AbstractArticlePDF–1.3M
12.
Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn’s disease
Maria Gazouli, Gerassimos Mantzaris, Athanassios J Archimandritis, George Nasioulas, Nicholas P Anagnou
World J Gastroenterol. 2005 Dec 21; 11(47): 7525–7530. Published online 2005 Dec 21. doi: 10.3748/wjg.v11.i47.7525
PMCID:
PMC4725165
AbstractArticlePDF–726K
13.
Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population
Xin Hou, Jinyuan Mao, Yushu Li, Jia Li, Weiwei Wang, Chenling Fan, Hong Wang, Hongmei Zhang, Zhongyan Shan, Weiping Teng
BMC Med Genet. 2015; 16: 76. Published online 2015 Sep 2. doi: 10.1186/s12881-015-0222-x
PMCID:
PMC4557484
AbstractArticlePDF–375K
14.
Genome-wide interaction studies reveal sex-specific asthma risk alleles
Rachel A. Myers, Nicole M. Scott, W. James Gauderman, Weiliang Qiu, Rasika A. Mathias, Isabelle Romieu, Albert M. Levin, Maria Pino-Yanes, Penelope E. Graves, Albino Barraza Villarreal, Terri H. Beaty, Vincent J. Carey, Damien C. Croteau-Chonka, Blanca del Rio Navarro, Christopher Edlund, Leticia Hernandez-Cadena, Efrain Navarro-Olivos, Badri Padhukasahasram, Muhammad T. Salam, Dara G. Torgerson, David J. Van den Berg, Hita Vora, Eugene R. Bleecker, Deborah A. Meyers, L. Keoki Williams, Fernando D. Martinez, Esteban G. Burchard, Kathleen C. Barnes, Frank D. Gilliland, Scott T. Weiss, Stephanie J. London, Benjamin A. Raby, Carole Ober, Dan L. Nicolae
Hum Mol Genet. 2014 Oct 1; 23(19): 5251–5259. Published online 2014 May 13. doi: 10.1093/hmg/ddu222
PMCID:
PMC4159149
AbstractArticlePDF–222K
15.
Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases
S Cucchiara, A Latiano, O Palmieri, AM Staiano, R D’Incà, G Guariso, G Vieni, V Rutigliano, O Borrelli, MR Valvano, V Annese
World J Gastroenterol. 2007 Feb 28; 13(8): 1221–1229. Published online 2007 Feb 28. doi: 10.3748/wjg.v13.i8.1221
PMCID:
PMC4146997
AbstractArticlePDF–850K
16.
Metabolic Heritability at Birth: Implications for Chronic Disease Research
Kelli K. Ryckman, Caitlin J. Smith, Laura L Jelliffe-Pawlowski, Allison M. Momany, Stanton L. Berberich, Jeffrey C. Murray
Hum Genet. Author manuscript; available in PMC 2015 Aug 1.
Published in final edited form as: Hum Genet. 2014 Aug; 133(8): 1049–1057. Published online 2014 May 22. doi: 10.1007/s00439-014-1450-4
PMCID:
PMC4102629
AbstractArticlePDF–193K
17.
Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn’s disease
Judit Bene, Lili Magyari, Gábor Talián, Katalin Komlósi, Beáta Gasztonyi, Beáta Tari, Ágnes Várkonyi, Gyula Mózsik, Béla Melegh
World J Gastroenterol. 2006 Sep 14; 12(34): 5550–5553. Published online 2006 Sep 14. doi: 10.3748/wjg.v12.i34.5550
PMCID:
PMC4088243
AbstractArticlePDF–622K
18.
OCTNs: Will the real IBD5 gene please stand up?
Mark S Silverberg
World J Gastroenterol. 2006 Jun 21; 12(23): 3678–3681. Published online 2006 Jun 21. doi: 10.3748/wjg.v12.i23.3678
PMCID:
PMC4087460
AbstractArticlePDF–661K
19.
An atlas of genetic influences on human blood metabolites
So-Youn Shin, Eric B. Fauman, Ann-Kristin Petersen, Jan Krumsiek, Rita Santos, Jie Huang, Matthias Arnold, Idil Erte, Vincenzo Forgetta, Tsun-Po Yang, Klaudia Walter, Cristina Menni, Lu Chen, Louella Vasquez, Ana M. Valdes, Craig L. Hyde, Vicky Wang, Daniel Ziemek, Phoebe Roberts, Li Xi, Elin Grundberg, The Multiple Tissue Human Expression Resource (MuTHER) Consortium, Melanie Waldenberger, J. Brent Richards, Robert P. Mohney, Michael V. Milburn, Sally L. John, Jeff Trimmer, Fabian J. Theis, John P. Overington, Karsten Suhre, M. Julia Brosnan, Christian Gieger, Gabi Kastenmüller, Tim D Spector, Nicole Soranzo
Nat Genet. Author manuscript; available in PMC 2014 Dec 1.
Published in final edited form as: Nat Genet. 2014 Jun; 46(6): 543–550. Published online 2014 May 11. doi: 10.1038/ng.2982
PMCID:
PMC4064254
AbstractArticlePDF–2.4M
20.
Human metabolic individuality in biomedical and pharmaceutical research
Karsten Suhre, So-Youn Shin, Ann-Kristin Petersen, Robert P. Mohney, David Meredith, Brigitte Wägele, Elisabeth Altmaier, CARDIoGRAM, Panos Deloukas, Jeanette Erdmann, Elin Grundberg, Christopher J. Hammond, Martin Hrabé de Angelis, Gabi Kastenmüller, Anna Köttgen, Florian Kronenberg, Massimo Mangino, Christa Meisinger, Thomas Meitinger, Hans-Werner Mewes, Michael V. Milburn, Cornelia Prehn, Johannes Raffler, Janina S. Ried, Werner Römisch-Margl, Nilesh J. Samani, Kerrin S. Small, H.-Erich Wichmann, Guangju Zhai, Thomas Illig, Tim D. Spector, Jerzy Adamski, Nicole Soranzo, Christian Gieger
Nature. Author manuscript; available in PMC 2013 Nov 19.
Published in final edited form as: Nature. 2011 Aug 31; 477(7362): 10.1038/nature10354. Published online 2011 Aug 31. doi: 10.1038/nature10354
PMCID:
PMC3832838
AbstractArticlePDF–839K

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