Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 776

1.

Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.

Louie RJ, Tan QK, Gilner JB, Rogers RC, Younge N, Wechsler SB, McDonald MT, Gordon B, Saski CA, Jones JR, Chapman SJ, Stevenson RE, Sleasman JW, Friez MJ.

Am J Med Genet A. 2017 May;173(5):1219-1225. doi: 10.1002/ajmg.a.38144. Epub 2017 Mar 20.

PMID:
28317311
2.

Eosinophils from eosinophilic oesophagitis patients have T cell suppressive capacity and express FOXP3.

Lingblom C, Wallander J, Ingelsten M, Bergquist H, Bove M, Saalman R, Welin A, Wennerås C.

Clin Exp Immunol. 2017 Mar;187(3):455-465. doi: 10.1111/cei.12898. Epub 2016 Dec 6.

PMID:
27921303
3.

Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis.

Eftekharian MM, Sayad A, Omrani MD, Ghannad MS, Noroozi R, Mazdeh M, Mirfakhraie R, Movafagh A, Roshanaei G, Azimi T, Inoko H, Taheri M.

Hum Antibodies. 2016;24(3-4):85-90. doi: 10.3233/HAB-160299.

PMID:
27792007
4.

Correlation between protein expression of FOXP3 and level of FOXP3 promoter methylation in recurrent spontaneous abortion.

Hou W, Li Z, Li Y, Fang L, Li J, Huang J, Li X, You Z.

J Obstet Gynaecol Res. 2016 Nov;42(11):1439-1444. doi: 10.1111/jog.13076.

PMID:
27785899
5.

FOXP3 gene variations and susceptibility to autism: A case-control study.

Safari MR, Ghafouri-Fard S, Noroozi R, Sayad A, Omrani MD, Komaki A, Eftekharian MM, Taheri M.

Gene. 2017 Jan 5;596:119-122. doi: 10.1016/j.gene.2016.10.019. Epub 2016 Oct 14.

PMID:
27751813
6.

FOXP3 rs3761548 polymorphism is associated with tacrolimus-induced acute nephrotoxicity in renal transplant patients.

Wu Z, Xu Q, Qiu X, Jiao Z, Zhang M, Zhong M.

Eur J Clin Pharmacol. 2017 Jan;73(1):39-47. doi: 10.1007/s00228-016-2140-z. Epub 2016 Oct 17.

PMID:
27747372
7.

Association of aplastic anemia and FoxP3 gene polymorphisms in Koreans.

In JW, Lee N, Roh EY, Shin S, Park KU, Song EY.

Hematology. 2017 Apr;22(3):149-154. doi: 10.1080/10245332.2016.1238645. Epub 2016 Oct 5.

PMID:
27702400
8.

FoxP3 gene promoter polymorphism affects susceptibility to preeclampsia.

Norouzian M, Rahimzadeh M, Rajaee M, Arabpour F, Naderi N.

Hum Immunol. 2016 Dec;77(12):1232-1238. doi: 10.1016/j.humimm.2016.09.001. Epub 2016 Sep 8.

PMID:
27614018
9.

Impact of FOXP3 Polymorphisms on the Blood Level of Tacrolimus in Renal Transplant Recipients.

Ge J, Wang J, Zhao H, Li K, Jing Y, Li G.

Transplant Proc. 2016 Jul-Aug;48(6):1962-7. doi: 10.1016/j.transproceed.2016.04.016.

PMID:
27569929
10.

Epigenetic features of FoxP3 in children with cow's milk allergy.

Paparo L, Nocerino R, Cosenza L, Aitoro R, D'Argenio V, Del Monaco V, Di Scala C, Amoroso A, Di Costanzo M, Salvatore F, Berni Canani R.

Clin Epigenetics. 2016 Aug 12;8:86. doi: 10.1186/s13148-016-0252-z. eCollection 2016.

11.

The Role of FOXP3 in Human Cancers.

Szylberg Ł, Karbownik D, Marszałek A.

Anticancer Res. 2016 Aug;36(8):3789-94. Review.

PMID:
27466478
12.

Amphiregulin Confers Regulatory T Cell Suppressive Function and Tumor Invasion via the EGFR/GSK-3β/Foxp3 Axis.

Wang S, Zhang Y, Wang Y, Ye P, Li J, Li H, Ding Q, Xia J.

J Biol Chem. 2016 Sep 30;291(40):21085-21095. Epub 2016 Jul 18.

PMID:
27432879
13.

Classical Hodgkin Lymphoma with Positive Epstein-Barr Virus Status is Associated with More FOXP3 Regulatory T Cells.

Pavlovic A, Glavina Durdov M, Capkun V, Jakelic Pitesa J, Bozic Sakic M.

Med Sci Monit. 2016 Jul 5;22:2340-6.

14.

Diminished levels of regulatory T cell subsets (CD8+Foxp3, CD4+Foxp3 and CD4+CD39+Foxp3) but increased Foxp3 expression in adipose tissue from overweight subjects.

Núñez Ruiz A, Cortés-Garcia JD, Cortez-Espinosa N, Herrera-Rojas PI, Ruíz-Rodríguez VM, Salgado-Bustamante M, García-Hernández MH, Reynaga-Hernández E, Martínez-Jimenez Vdel C, Portales-Pérez DP.

Nutrition. 2016 Sep;32(9):943-54. doi: 10.1016/j.nut.2016.02.006. Epub 2016 Mar 4.

PMID:
27160497
15.

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis.

Şıklar Z, Karataş D, Doğu F, Hacıhamdioğlu B, İkincioğulları A, Berberoğlu M.

J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):276-81. doi: 10.4274/jcrpe.2766. Epub 2016 Apr 18.

16.

Activation-dependent mitochondrial translocation of Foxp3 in human hepatocytes.

Rojas J, Teran-Angel G, Barbosa L, Peterson DL, Berrueta L, Salmen S.

Exp Cell Res. 2016 May 1;343(2):159-67. doi: 10.1016/j.yexcr.2016.04.008. Epub 2016 Apr 8.

PMID:
27068374
17.

Non-small-cell lung cancer-induced immunosuppression by increased human regulatory T cells via Foxp3 promoter demethylation.

Ke X, Zhang S, Xu J, Liu G, Zhang L, Xie E, Gao L, Li D, Sun R, Wang F, Pan S.

Cancer Immunol Immunother. 2016 May;65(5):587-99. doi: 10.1007/s00262-016-1825-6. Epub 2016 Mar 21.

PMID:
27000869
18.

Genetic variants and expression study of FOXP3 gene in acute coronary syndrome in Iranian patients.

Gholami M, Esfandiary A, Vatanparast M, Mirfakhraie R, Hosseini MM, Ghafouri-Fard S.

Cell Biochem Funct. 2016 Apr;34(3):158-62. doi: 10.1002/cbf.3174. Epub 2016 Feb 29.

PMID:
26931655
19.

Suppressor Properties of Human CD8(+)CD28(-) T Cells in Mixed Leukocyte Reaction are not Affected by CsA and RAPA.

Korecka-Polak A, Bocian K, Pachówka M, Jałbrzykowska A, Korczak-Kowalska G.

Arch Immunol Ther Exp (Warsz). 2016 Oct;64(5):409-16. doi: 10.1007/s00005-016-0388-8. Epub 2016 Feb 26.

PMID:
26921303
20.

A Single Nucleotide Polymorphism in the FOXP3 Gene Associated with Behçet's Disease in an Iranian Population.

Hosseini A, Shanehbandi D, Estiar MA, Gholizadeh S, Khabbazi A, Khodadadi H, Sakhinia E, Babaloo Z.

Clin Lab. 2015;61(12):1897-903.

PMID:
26882813

Supplemental Content

Support Center