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Items: 1 to 20 of 222

1.

[The analysis of association between ENPP1 K121Q polymorphism and risk factors of type 2 diabetes mellitus in ukrainian population].

Marchenko IV, Dubovyk YI, Matlai OI, Biesiedina AA, Kniazkova PV, Harbuzova YA.

Wiad Lek. 2018;71(4):815-820. Russian.

PMID:
30099416
2.

ENPP1 K121Q (rs1044498 C > A) genetic polymorphism confers a high risk of susceptibility to coronary heart disease: A PRISMA-compliant article.

Di JY, Dai ML, Zhang ZX.

Medicine (Baltimore). 2018 Jul;97(27):e11236. doi: 10.1097/MD.0000000000011236. Review.

3.

Association and in silico studies of ENPP1 gene variants with type 2 diabetes mellitus in a Northern Iranian population.

Sharafshah A, Keshavarz P, Rezaei S, Farhadian N.

Gene. 2018 Oct 30;675:225-232. doi: 10.1016/j.gene.2018.06.006. Epub 2018 Jun 26.

PMID:
29958952
4.

[The association between enpp1 rs997509 polymorphism and type 2 diabetes mellitus development in ukrainian population].

Marchenko IV, Dubovyk YI, Tkach GF, Maksymova OS, Matlai OI, Ataman AV, Harbuzova VY.

Wiad Lek. 2018;71(3 pt 1):490-495. Russian.

PMID:
29783211
5.

Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population.

Chen L, Qin Y, Liang D, Liang X, Liang Y, Li L, Xian J, Zhang L, Tong L, Li H, Zhang H.

Gene. 2017 Dec 30;637:190-195. doi: 10.1016/j.gene.2017.09.052. Epub 2017 Sep 23.

PMID:
28951309
6.

The ENPP1 K121Q polymorphism modulates developing of bone disorders in type 2 diabetes: A cross sectional study.

Neamati N, Hosseini SR, Hajiahmadi M, Halalkhor S, Nooreddini H, Niaki HA, Korani B, Parsian H.

Gene. 2017 Dec 30;637:100-107. doi: 10.1016/j.gene.2017.09.042. Epub 2017 Sep 21.

PMID:
28942038
7.

Condylar geometry variation is associated with ENPP1 variant in a population of patients with dento-facial deformities.

Constant M, Nicot R, Vieira AR, Raoul G, Sciote JJ, Ferri J.

J Craniomaxillofac Surg. 2017 Jun;45(6):826-830. doi: 10.1016/j.jcms.2017.02.020. Epub 2017 Mar 8.

8.

The promiscuous ectonucleotidase NPP1: molecular insights into substrate binding and hydrolysis.

Namasivayam V, Lee SY, Müller CE.

Biochim Biophys Acta Gen Subj. 2017 Mar;1861(3):603-614. doi: 10.1016/j.bbagen.2016.12.019. Epub 2016 Dec 21. No abstract available.

PMID:
28011303
9.

The ENPP1 K121Q polymorphism is associated with type 2 diabetes and related metabolic phenotypes in a Taiwanese population.

Hsiao TJ, Lin E.

Mol Cell Endocrinol. 2016 Sep 15;433:20-5. doi: 10.1016/j.mce.2016.05.020. Epub 2016 May 26.

PMID:
27238374
10.

Association of K121Q Polymorphism in Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 with Clinical Characteristics of Metabolic Syndrom.

Li N, Pan H, Cui M, Li Q.

Exp Clin Endocrinol Diabetes. 2016 May;124(5):313-7. doi: 10.1055/s-0042-104498. Epub 2016 May 24.

PMID:
27219689
11.

Plasma cell alloantigen ENPP1 is expressed by a subset of human B cells with potential regulatory functions.

Yoon J, Wang H, Kim YC, Yoshimoto M, Abbasi S, Morse Iii HC.

Immunol Cell Biol. 2016 Sep;94(8):719-28. doi: 10.1038/icb.2016.31. Epub 2016 Mar 31.

PMID:
27029896
12.

[Molecular biology as a diagnostic tool in the newborn Emergency department: a rare case of idiopathic infantile arterial calcification].

Borromini A, Rossi G, Maggi P, Speciale D, Mirri G, Cogliardi A, Addis C, Dainese E, Bonoldi E, Marando A.

G Ital Cardiol (Rome). 2016 Mar;17(3):234-6. doi: 10.1714/2190.23670. Italian.

PMID:
27029882
13.

Association of Cole disease with novel heterozygous mutations in the somatomedin-B domains of the ENPP1 gene: necessary, but not always sufficient.

Schlipf NA, Traupe H, Gilaberte Y, Peitsch WK, Hausser I, Oji V, Schmieder A, Schneider SW, Demmer P, Rösler B, Fischer J.

Br J Dermatol. 2016 May;174(5):1152-6. doi: 10.1111/bjd.14328. Epub 2016 Feb 18. No abstract available.

PMID:
26617416
14.

Decreased expression of ectonucleotidase E-NPP1 in leukocytes from subjects with severe asthma exacerbation.

Montaño LM, Vargas MH, Díaz-Hernández V, De Ita M, Kazakova R, Barajas-López C.

Allergy. 2016 Jan;71(1):124-8. doi: 10.1111/all.12772. Epub 2015 Oct 20.

PMID:
26405014
15.

Association between the ENPP1 K121Q polymorphism and risk of diabetic kidney disease: a systematic review and meta-analysis.

Sortica DA, Buffon MP, Souza BM, Nicoletto BB, Santer A, Assmann TS, Crispim D, Canani LH.

PLoS One. 2015 Mar 20;10(3):e0118416. doi: 10.1371/journal.pone.0118416. eCollection 2015. Review.

16.

Early onset hearing loss in autosomal recessive hypophosphatemic rickets caused by loss of function mutation in ENPP1.

Steichen-Gersdorf E, Lorenz-Depiereux B, Strom TM, Shaw NJ.

J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):967-70. doi: 10.1515/jpem-2014-0531.

PMID:
25741938
17.

Impact of ENPP1 K121Q on change of insulin resistance after web-based intervention in Korean men with diabetes and impaired fasting glucose.

Kang JY, Sung SH, Lee YJ, Choi TI, Choi SJ.

J Korean Med Sci. 2014 Oct;29(10):1353-9. doi: 10.3346/jkms.2014.29.10.1353. Epub 2014 Oct 8.

18.

Body mass index associated to rs2021966 ENPP1 polymorphism increases the risk for gestational diabetes mellitus.

Tarquini F, Picchiassi E, Centra M, Pennacchi L, Bini V, Cappuccini B, Torlone E, Coata G, Di Renzo G, Brancorsini S.

Gynecol Endocrinol. 2015 Jan;31(1):83-6. doi: 10.3109/09513590.2014.958994. Epub 2014 Sep 15.

PMID:
25222839
19.

Association of the ENPP1 K121Q polymorphism with susceptibility to type 2 diabetes in different populations: evidence based on 40 studies.

Tang ST, Shen XR, Tang HQ, Wang CJ, Wei W, Zhang Q, Wang Y.

Endocr J. 2014;61(11):1093-103. Epub 2014 Aug 8.

20.

Stem cell characteristics in glioblastoma are maintained by the ecto-nucleotidase E-NPP1.

Bageritz J, Puccio L, Piro RM, Hovestadt V, Phillips E, Pankert T, Lohr J, Herold-Mende C, Lichter P, Goidts V.

Cell Death Differ. 2014 Jun;21(6):929-40. doi: 10.1038/cdd.2014.12. Epub 2014 Feb 14.

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