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Items: 1 to 50 of 112

1.

Role of vitamin D and vitamin D receptor gene polymorphisms on residual beta cell function in children with type 1 diabetes mellitus.

Habibian N, Amoli MM, Abbasi F, Rabbani A, Alipour A, Sayarifard F, Rostami P, Dizaji SP, BabakSaadati, Setoodeh A.

Pharmacol Rep. 2018 Dec 28;71(2):282-288. doi: 10.1016/j.pharep.2018.12.012. [Epub ahead of print]

PMID:
30826568
2.

Comments on: "A Meta-Analysis of the Association between Microrna-196A2 and Risk of Ischemic Stroke and Coronary Artery Disease in Asian Population".

Gholami M, Amoli MM.

J Stroke Cerebrovasc Dis. 2019 Feb 13. pii: S1052-3057(19)30023-0. doi: 10.1016/j.jstrokecerebrovasdis.2019.01.014. [Epub ahead of print] No abstract available.

PMID:
30772165
3.

Competing endogenous RNA (ceRNA) cross talk and language in ceRNA regulatory networks: A new look at hallmarks of breast cancer.

Abdollahzadeh R, Daraei A, Mansoori Y, Sepahvand M, Amoli MM, Tavakkoly-Bazzaz J.

J Cell Physiol. 2018 Dec 10. doi: 10.1002/jcp.27941. [Epub ahead of print] Review.

PMID:
30537129
4.

MTHFR AND ApoE genetic variants association with sudden sensorineural hearing loss.

Hamidi AK, Yazdani N, Seyedjavadi KH, Ahrabi NZ, Tajdini A, Aghazadeh K, Amoli MM.

Am J Otolaryngol. 2019 Mar - Apr;40(2):260-264. doi: 10.1016/j.amjoto.2018.10.015. Epub 2018 Oct 29.

PMID:
30477909
5.

Over-expression of TGF-β1 gene in medication free Schizophrenia.

Amoli MM, Khatami F, Arzaghi SM, Enayati S, Nejatisafa AA.

Psychoneuroendocrinology. 2019 Jan;99:265-270. doi: 10.1016/j.psyneuen.2018.10.009. Epub 2018 Oct 21.

PMID:
30389222
6.

Haplotypes in vitamin D receptor gene encode risk in diabetic nephropathy.

Razi F, Meshkani MA, Zarrabi F, Sadr M, Asgarbeik S, Bandarian F, Forouzanfar K, Amoli MM.

Gene. 2019 Jan 30;683:149-152. doi: 10.1016/j.gene.2018.10.017. Epub 2018 Oct 11.

PMID:
30315926
7.

The p.Arg435His Variation of IgG3 With High Affinity to FcRn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts.

Recke A, Konitzer S, Lemcke S, Freitag M, Sommer NM, Abdelhady M, Amoli MM, Benoit S, El-Chennawy F, Eldarouti M, Eming R, Gläser R, Günther C, Hadaschik E, Homey B, Lieb W, Peitsch WK, Pföhler C, Robati RM, Saeedi M, Sárdy M, Sticherling M, Uzun S, Worm M, Zillikens D, Ibrahim S, Vidarsson G, Schmidt E; German AIBD Genetic Study Group.

Front Immunol. 2018 Aug 2;9:1788. doi: 10.3389/fimmu.2018.01788. eCollection 2018.

8.

SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

Hasani-Ranjbar S, Ejtahed HS, Amoli MM, Bitarafan F, Qorbani M, Soltani A, Yarjoo B.

J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):343-349. doi: 10.4274/jcrpe.0057. Epub 2018 May 29.

9.

Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity.

Dehghani MR, Mehrjardi MYV, Dilaver N, Tajamolian M, Enayati S, Ebrahimi P, Amoli MM, Farooqi S, Maroofian R.

Eur J Med Genet. 2018 Aug;61(8):465-467. doi: 10.1016/j.ejmg.2018.03.006. Epub 2018 Mar 12.

PMID:
29545012
10.

Association between MTHFR variant and diabetic neuropathy.

Kakavand Hamidi A, Radfar M, Amoli MM.

Pharmacol Rep. 2018 Feb;70(1):1-5. doi: 10.1016/j.pharep.2017.04.017. Epub 2017 Apr 26.

PMID:
29222982
11.

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes.

Abbasi F, Habibi M, Enayati S, Bitarafan F, Razzaghy-Azar M, Sotodeh A, Omran SP, Maroofian R, Amoli MM.

Can J Diabetes. 2018 Jun;42(3):272-275. doi: 10.1016/j.jcjd.2017.06.009. Epub 2017 Aug 23.

PMID:
28843469
12.

Evaluation of the presence of Epstein-Barr virus (EBV) in Iranian patients with thyroid papillary carcinoma.

Homayouni M, Mohammad Arabzadeh SA, Nili F, Razi F, Amoli MM.

Pathol Res Pract. 2017 Jul;213(7):854-856. doi: 10.1016/j.prp.2017.01.020. Epub 2017 Jan 28.

PMID:
28554750
13.

Influencing of antioxidants' gene variants on risk of diabetes mellitus and its complications: a systematic review.

Bitarafan F, Khodaeian M, Tabatabaei-Malazy O, Amoli MM.

Minerva Endocrinol. 2017 May 26. doi: 10.23736/S0391-1977.17.02632-3. [Epub ahead of print]

PMID:
28548478
14.

Association Between the Polymorphism of Glu298Asp in Exon 7 of the eNOS Gene With Foot Ulcer and Oxidative Stress in Adult Patients With Type 2 Diabetes.

Sadati SM, Radfar M, Hamidi AK, Abdollahi M, Qorbani M, Esfahani EN, Amoli MM.

Can J Diabetes. 2018 Feb;42(1):18-22. doi: 10.1016/j.jcjd.2017.03.001. Epub 2017 May 10.

PMID:
28499789
15.

Methylomics of breast cancer: Seeking epimarkers in peripheral blood of young subjects.

Khakpour G, Noruzinia M, Izadi P, Karami F, Ahmadvand M, Heshmat R, Amoli MM, Tavakkoly-Bazzaz J.

Tumour Biol. 2017 Mar;39(3):1010428317695040. doi: 10.1177/1010428317695040.

PMID:
28349825
16.

Liver alpha-amylase gene expression as an early obesity biomarker.

Mojbafan M, Afsartala Z, Amoli MM, Mahmoudi M, Yaghmaei P, Larijani B, Ebrahim-Habibi A.

Pharmacol Rep. 2017 Apr;69(2):229-234. doi: 10.1016/j.pharep.2016.11.001. Epub 2016 Nov 5.

PMID:
28095353
17.

Vitamin D receptor gene FokI variant in diabetic foot ulcer and its relation with oxidative stress.

Soroush N, Radfar M, Hamidi AK, Abdollahi M, Qorbani M, Razi F, Esfahani EN, Amoli MM.

Gene. 2017 Jan 30;599:87-91. doi: 10.1016/j.gene.2016.11.012. Epub 2016 Nov 9.

PMID:
27836663
18.

Adiponectin gene variants and abdominal obesity in an Iranian population.

Payab M, Amoli MM, Qorbani M, Hasani-Ranjbar S.

Eat Weight Disord. 2017 Mar;22(1):85-90. doi: 10.1007/s40519-016-0252-1. Epub 2016 Feb 22.

PMID:
26902743
19.

Prevalence of osteoporosis and vitamin D receptor gene polymorphisms (FokI) in an Iranian general population based study (Kurdistan) (IMOS).

Mohammadi Z, Keshtkar A, Fayyazbakhsh F, Ebrahimi M, Amoli MM, Ghorbani M, Khashayar P, Dini M, Ebrahimi-Rad M, Larijani B.

Med J Islam Repub Iran. 2015 Jul 20;29:238. eCollection 2015.

20.

Association between Genetic Variants and Diabetes Mellitus in Iranian Populations: A Systematic Review of Observational Studies.

Khodaeian M, Enayati S, Tabatabaei-Malazy O, Amoli MM.

J Diabetes Res. 2015;2015:585917. doi: 10.1155/2015/585917. Epub 2015 Oct 26. Review.

21.

Association between Macrophage Migration Inhibitory Factor Gene Variation and Response to Glucocorticoid Treatment in Sudden Sensorineural Hearing Loss.

Yazdani N, Kakavand Hamidi A, Ghazavi H, Rikhtegar MJ, Motesadi Zarandi M, Qorbani M, Amoli MM.

Audiol Neurootol. 2015;20(6):376-82. doi: 10.1159/000438741. Epub 2015 Oct 2.

PMID:
26426302
22.

Acarbose versus trans-chalcone: comparing the effect of two glycosidase inhibitors on obese mice.

Jalalvand F, Amoli MM, Yaghmaei P, Kimiagar M, Ebrahim-Habibi A.

Arch Endocrinol Metab. 2015 Jun;59(3):202-9. doi: 10.1590/2359-3997000000038.

23.

Epistatic interaction between adiponectin and survivin gene polymorphisms in endometrial carcinoma.

Aminimoghaddam S, Shahrabi-Farahani M, Mohajeri-Tehrani M, Amiri P, Fereidooni F, Larijani B, Shafiee G, Amoli MM.

Pathol Res Pract. 2015 Apr;211(4):293-7. doi: 10.1016/j.prp.2014.11.012. Epub 2014 Nov 27.

PMID:
25613698
24.

Association between vitamin D receptor gene polymorphisms (Fok1 and Bsm1) and osteoporosis: a systematic review.

Mohammadi Z, Fayyazbakhsh F, Ebrahimi M, Amoli MM, Khashayar P, Dini M, Zadeh RN, Keshtkar A, Barikani HR.

J Diabetes Metab Disord. 2014 Oct 17;13(1):98. doi: 10.1186/s40200-014-0098-x. eCollection 2014.

25.

Effects of extremely low frequency electromagnetic fields on paraoxonase serum activity and lipid peroxidation metabolites in rat.

Seifirad S, Farzampour S, Nourbakhsh M, Amoli MM, Razzaghy-Azar M, Larijani B.

J Diabetes Metab Disord. 2014 Aug 13;13(1):85. doi: 10.1186/s40200-014-0085-2. eCollection 2014.

26.

The antioxidants dilemma: are they potentially immunosuppressants and carcinogens?

Seifirad S, Ghaffari A, Amoli MM.

Front Physiol. 2014 Jul 14;5:245. doi: 10.3389/fphys.2014.00245. eCollection 2014. No abstract available.

27.

A novel missense mutation in oncostatin M receptor beta causing primary localized cutaneous amyloidosis.

Saeedi M, Ebrahim-Habibi A, Haghighi A, Zarrabi F, Amoli MM, Robati RM.

Biomed Res Int. 2014;2014:653724. doi: 10.1155/2014/653724. Epub 2014 Jun 26.

28.

Sex-specific association of RANTES gene -403 variant in Meniere's disease.

Yazdani N, Mojbafan M, Taleba M, Amiri P, Nejadian F, Ashtiani MK, Amoli MM.

Eur Arch Otorhinolaryngol. 2015 Sep;272(9):2221-5. doi: 10.1007/s00405-014-3151-y. Epub 2014 Jun 25.

PMID:
24961438
29.

A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations.

Hasani-Ranjbar S, Jouyandeh Z, Amoli MM, Soltani A, Arzaghi SM.

J Diabetes Metab Disord. 2014 May 22;13:56. doi: 10.1186/2251-6581-13-56. eCollection 2014.

30.

TNF-α and IFN-γ gene variation and genetic susceptibility to type 1 diabetes and its microangiopathic complications.

Bazzaz JT, Amoli MM, Taheri Z, Larijani B, Pravica V, Hutchinson IV.

J Diabetes Metab Disord. 2014 Apr 1;13:46. doi: 10.1186/2251-6581-13-46. eCollection 2014.

31.

TGF-β1 and IGF-I gene variations in type 1 diabetes microangiopathic complications.

Bazzaz JT, Amoli MM, Taheri Z, Larijani B, Pravica V, Hutchinson IV.

J Diabetes Metab Disord. 2014 Apr 1;13(1):45. doi: 10.1186/2251-6581-13-45.

32.

Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation.

Hasani-Ranjbar S, Rahmanian M, Ebrahim-Habibi A, Soltani A, Soltanzade A, Mahrampour E, Amoli MM.

Fam Cancer. 2014 Jun;13(2):267-72. doi: 10.1007/s10689-013-9692-1.

PMID:
24218143
33.

Association between MIF gene variation and Meniere's disease.

Yazdani N, Khorsandi Ashtiani MT, Zarandy MM, Mohammadi SJ, Ghazavi H, Mahrampour E, Amiri P, Amoli MM.

Int J Immunogenet. 2013 Dec;40(6):488-91. doi: 10.1111/iji.12058. Epub 2013 Apr 8.

PMID:
23566229
34.

eNOS Gene Variant in Patients with Coronary Artery Disease.

Abolhalaj M, Amoli MM, Amiri P.

J Biomark. 2013;2013:403783. doi: 10.1155/2013/403783. Epub 2012 Nov 28.

35.

Survivin gene polymorphism association with tongue squamous cell carcinoma.

Mostaan LV, Tabari A, Amiri P, Ashtiani MK, Mahdkhah A, Yazdani N, Khaniki M, Tabari A, Tavakkoly-Bazzaz J, Amoli MM.

Genet Test Mol Biomarkers. 2013 Jan;17(1):74-7. doi: 10.1089/gtmb.2012.0210. Epub 2012 Nov 23.

PMID:
23176035
36.

Association between the functional polymorphism C-159T in the CD14 promoter gene and nasal polyposis: potential role in asthma.

Yazdani N, Amoli MM, Naraghi M, Mersaghian A, Firouzi F, Sayyahpour F, Mokhtari Z.

J Investig Allergol Clin Immunol. 2012;22(6):406-11.

37.

IL-23 gene expression in PBMCs of patients with coronary artery disease.

Khojasteh-Fard M, Abolhalaj M, Amiri P, Zaki M, Taheri Z, Qorbani M, Bazzaz JT, Amoli MM.

Dis Markers. 2012;33(6):289-93. doi: 10.3233/DMA-2012-00933.

38.

Practical evaluation of late-night salivary cortisol: a real-life approach.

Hasani-Ranjbar S, Amoli MM.

Endocrine. 2012 Aug;42(1):220-1. No abstract available.

PMID:
22993753
39.

Macrophage migration inhibitory factor gene polymorphism is not associated with pemphigus vulgaris in Iranian patients.

Saeedi M, Amoli MM, Robati RM, Sayahpour F, Namazi N, Toossi P.

J Eur Acad Dermatol Venereol. 2013 Sep;27(9):1127-31. doi: 10.1111/j.1468-3083.2012.04676.x. Epub 2012 Aug 22.

PMID:
22909194
40.

VEGF gene mRNA expression in patients with coronary artery disease.

Amoli MM, Amiri P, Alborzi A, Larijani B, Saba S, Tavakkoly-Bazzaz J.

Mol Biol Rep. 2012 Sep;39(9):8595-9. doi: 10.1007/s11033-012-1713-x. Epub 2012 Jun 19.

PMID:
22711306
41.

SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuria.

Hasani-Ranjbar S, Amoli MM, Ebrahim-Habibi A, Dehghan E, Soltani A, Amiri P, Larijani B.

J Clin Res Pediatr Endocrinol. 2012 Jun;4(2):89-93. doi: 10.4274/jcrpe.601.

42.

Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus: implications for therapeutic management of family members with long-standing disease.

Abbasi F, Saba S, Ebrahim-Habibi A, Sayahpour FA, Amiri P, Larijani B, Amoli MM.

Mol Diagn Ther. 2012 Apr 1;16(2):109-14. doi: 10.2165/11599600-000000000-00000.

PMID:
22471336
43.

Survivin gene polymorphism association with papillary thyroid carcinoma.

Yazdani N, Sayahpour FA, Haghpanah V, Amiri P, Shahrabi-Farahani M, Moradi M, Mirmiran A, Khorsandi MT, Larijani B, Mostaan LV, Amoli MM.

Pathol Res Pract. 2012 Feb 15;208(2):100-3. doi: 10.1016/j.prp.2011.12.009. Epub 2012 Jan 30.

PMID:
22293278
44.
45.

Effect of adiponectin gene polymorphisms on waist circumference in patients with diabetes.

Hasani-Ranjbar S, Amoli MM, Tabatabaei-Malazy O, Rumi Y, Tavakkoly-Bazzaz J, Samimi H, Abbasifarid E.

J Diabetes Metab Disord. 2012 Sep 14;11(1):14. doi: 10.1186/2251-6581-11-14.

46.

Apolipoprotein E gene polymorphism and its effect on anthropometric measures in normoglycemic subjects and type 2 diabetes.

Tabatabaei-Malazy O, Fakhrzadeh H, Qorbani M, Amiri P, Larijani B, Tavakkoly-Bazzaz J, Amoli MM.

J Diabetes Metab Disord. 2012 Oct 8;11(1):18. doi: 10.1186/2251-6581-11-18.

47.

TGF-β and IL-23 gene expression in unstimulated PBMCs of patients with diabetes.

Abbasi F, Amiri P, Sayahpour FA, Pirmoradi S, Abolhalaj M, Larijani B, Bazzaz JT, Amoli MM.

Endocrine. 2012 Jun;41(3):430-4. doi: 10.1007/s12020-011-9578-7. Epub 2011 Dec 17.

PMID:
22180056
48.

Absence of kl-vs variant of klotho gene in Iranian cardiac patients (comparison to the world populations).

Tavakkoly-Bazzaz J, Tabatabaei-Malazy O, Tajmir-Riahi M, Javidi D, Izadi M, Shahrabi-Farahani M, Amiri P, Amoli MM.

Dis Markers. 2011;31(4):211-4. doi: 10.3233/DMA-2011-0818.

49.

Association of survivin gene polymorphism with endometrial cancer.

Zahedi P, Aminimoghaddam S, Sayahpour FA, Haghpanah V, Amiri P, Fereidoni F, Mahrampour E, Larijani B, Tavakkoly-Bazzaz J, Amoli MM.

Int J Gynecol Cancer. 2012 Jan;22(1):35-7. doi: 10.1097/IGC.0b013e318229902c.

PMID:
21897272
50.

RANTES gene mRNA expression and its -403 G/A promoter polymorphism in coronary artery disease.

Tavakkoly-Bazzaz J, Amiri P, Tajmir-Riahi M, Javidi D, Khojasteh-Fard M, Taheri Z, Tabrizi A, Keramatipour M, Amoli MM.

Gene. 2011 Nov 1;487(1):103-6. doi: 10.1016/j.gene.2011.07.019. Epub 2011 Aug 2.

PMID:
21839152

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