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Items: 1 to 20 of 130

1.

Structural Basis of Highly Specific Interaction between Nephrin and MAGI1 in Slit Diaphragm Assembly and Signaling.

Weng Z, Shang Y, Ji Z, Ye F, Lin L, Zhang R, Zhu J.

J Am Soc Nephrol. 2018 Jul 13. pii: ASN.2017121275. doi: 10.1681/ASN.2017121275. [Epub ahead of print]

PMID:
30006415
2.

LncRNAs and EGFRvIII sequestered in TEPs enable blood-based NSCLC diagnosis.

Luo CL, Xu ZG, Chen H, Ji J, Wang YH, Hu W, Wang K, Zhang WW, Yuan CH, Wang FB.

Cancer Manag Res. 2018 Jun 8;10:1449-1459. doi: 10.2147/CMAR.S164227. eCollection 2018.

3.

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.

Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A, Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F.

Nat Commun. 2018 May 17;9(1):1960. doi: 10.1038/s41467-018-04193-w.

4.

Long non-coding RNA (lncRNA) MAGI2-AS3 inhibits breast cancer cell growth by targeting the Fas/FasL signalling pathway.

Yang Y, Yang H, Xu M, Zhang H, Sun M, Mu P, Dong T, Du S, Liu K.

Hum Cell. 2018 Jul;31(3):232-241. doi: 10.1007/s13577-018-0206-1. Epub 2018 Apr 20.

PMID:
29679339
5.

MAGI2 is an independent predictor of biochemical recurrence in prostate cancer.

David SN, Arnold Egloff SA, Goyal R, Clark PE, Phillips S, Gellert LL, Hameed O, Giannico GA.

Prostate. 2018 Jun;78(8):616-622. doi: 10.1002/pros.23506. Epub 2018 Mar 14.

PMID:
29542165
6.

Genetic Variation and Gene Expression Levels of Tight Junction Genes Indicates Relationships Between PTEN as well as MAGI1 and Microscopic Colitis.

Norén E, Mellander MR, Almer S, Söderman J.

Dig Dis Sci. 2018 Jan;63(1):105-112. doi: 10.1007/s10620-017-4857-7. Epub 2017 Dec 4.

7.

The feasibility of detecting endometrial and ovarian cancer using DNA methylation biomarkers in cervical scrapings.

Chang CC, Wang HC, Liao YP, Chen YC, Weng YC, Yu MH, Lai HC.

J Gynecol Oncol. 2018 Jan;29(1):e17. doi: 10.3802/jgo.2018.29.e17.

8.

Genetic variation and expression levels of tight junction genes identifies association between MAGI3 and inflammatory bowel disease.

Norén E, Almer S, Söderman J.

BMC Gastroenterol. 2017 May 25;17(1):68. doi: 10.1186/s12876-017-0620-y.

9.

Glomerulosclerosis Induced by Deficiency of Membrane-Associated Guanylate Kinase Inverted 2 in Kidney Podocytes.

Shirata N, Ihara KI, Yamamoto-Nonaka K, Seki T, Makino SI, Oliva Trejo JA, Miyake T, Yamada H, Campbell KN, Nakagawa T, Mori K, Yanagita M, Mundel P, Nishimori K, Asanuma K.

J Am Soc Nephrol. 2017 Sep;28(9):2654-2669. doi: 10.1681/ASN.2016121356. Epub 2017 May 24.

PMID:
28539383
10.

Genetic predictors of antipsychotic response to lurasidone identified in a genome wide association study and by schizophrenia risk genes.

Li J, Yoshikawa A, Brennan MD, Ramsey TL, Meltzer HY.

Schizophr Res. 2018 Feb;192:194-204. doi: 10.1016/j.schres.2017.04.009. Epub 2017 Apr 19.

PMID:
28431800
11.

Deep sequencing of a candidate region harboring the SOX9 gene for the canine XX disorder of sex development.

Nowacka-Woszuk J, Szczerbal I, Pausch H, Hundi S, Hytönen MK, Grzemski A, Flisikowski K, Lohi H, Switonski M, Szydlowski M.

Anim Genet. 2017 Jun;48(3):330-337. doi: 10.1111/age.12538. Epub 2017 Jan 17.

PMID:
28094446
12.

MAGI2 Mutations Cause Congenital Nephrotic Syndrome.

Bierzynska A, Soderquest K, Dean P, Colby E, Rollason R, Jones C, Inward CD, McCarthy HJ, Simpson MA, Lord GM, Williams M, Welsh GI, Koziell AB, Saleem MA; NephroS; UK study of Nephrotic Syndrome.

J Am Soc Nephrol. 2017 May;28(5):1614-1621. doi: 10.1681/ASN.2016040387. Epub 2016 Dec 8.

13.

MAGI-2 Is a Sensitive and Specific Marker of Prostatic Adenocarcinoma:  A Comparison With AMACR.

Goldstein J, Goyal R, Roland JT, Gellert LL, Clark PE, Hameed O, Giannico GA.

Am J Clin Pathol. 2016 Sep;146(3):294-302. doi: 10.1093/ajcp/aqw111.

PMID:
27543977
14.

MiR-487a Promotes TGF-β1-induced EMT, the Migration and Invasion of Breast Cancer Cells by Directly Targeting MAGI2.

Ma M, He M, Jiang Q, Yan Y, Guan S, Zhang J, Yu Z, Chen Q, Sun M, Yao W, Zhao H, Jin F, Wei M.

Int J Biol Sci. 2016 Feb 5;12(4):397-408. doi: 10.7150/ijbs.13475. eCollection 2016.

15.

MAGI-2 in prostate cancer: an immunohistochemical study.

Goldstein J, Borowsky AD, Goyal R, Roland JT, Arnold SA, Gellert LL, Clark PE, Hameed O, Giannico GA.

Hum Pathol. 2016 Jun;52:83-91. doi: 10.1016/j.humpath.2016.01.003. Epub 2016 Feb 4.

PMID:
26980016
16.

Comparative Transcriptomic Analysis of Primary Duck Hepatocytes Provides Insight into Differential Susceptibility to DHBV Infection.

Yan L, Qu S, Liu G, Liu L, Yu Y, Ding G, Zhao Y, Li Y, Xie Y, Zhang J, Qu D.

PLoS One. 2016 Feb 22;11(2):e0149702. doi: 10.1371/journal.pone.0149702. eCollection 2016.

17.

Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity.

Gadelha A, Coleman J, Breen G, Mazzoti DR, Yonamine CM, Pellegrino R, Ota VK, Belangero SI, Glessner J, Sleiman P, Hakonarson H, Hayashi MA, Bressan RA.

Schizophr Res. 2016 Apr;172(1-3):60-7. doi: 10.1016/j.schres.2016.01.043. Epub 2016 Feb 2.

PMID:
26851141
18.

Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins.

Elboudwarej E, Cole M, Briggs FB, Fouts A, Fain PR, Quach H, Quach D, Sinclair E, Criswell LA, Lane JA, Steck AK, Barcellos LF, Noble JA.

J Autoimmun. 2016 Apr;68:23-9. doi: 10.1016/j.jaut.2015.12.003. Epub 2016 Jan 9.

19.

CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids.

Dahlin A, Denny J, Roden DM, Brilliant MH, Ingram C, Kitchner TE, Linneman JG, Shaffer CM, Weeke P, Xu H, Kubo M, Tamari M, Clemmer GL, Ziniti J, McGeachie MJ, Tantisira KG, Weiss ST, Wu AC.

Immun Inflamm Dis. 2015 Jul 14;3(4):350-9. doi: 10.1002/iid3.73. eCollection 2015 Dec.

20.

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.

Nicita F, Garone G, Spalice A, Savasta S, Striano P, Pantaleoni C, Spartà MV, Kluger G, Capovilla G, Pruna D, Freri E, D'Arrigo S, Verrotti A.

Am J Med Genet A. 2016 Jan;170A(1):148-55. doi: 10.1002/ajmg.a.37410. Epub 2015 Oct 5.

PMID:
26437767

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