Noori-Daloii MR - Search Results

1

Transforming growth factor-beta1 codon 10 polymorphism is associated with acute GVHD after allogenic BMT in Iranian population.

Noori-Daloii MR, Rashidi-Nezhad A, Izadi P, Hossein-Nezhad A, Sobhani M, Derakhshandeh-Peykar P, Alimoghaddam K, Ghavamzadeh A. Noori-Daloii MR, et al. Ann Transplant. 2007;12(4):5-10. Ann Transplant. 2007. PMID: 18344931 Free article.

2

TGF-Beta codon 25 polymorphism and the risk of graft-versus-host disease after allogenic hematopoietic stem cell transplantation.

Rashidi-Nezhad A, Azimi C, Alimoghaddam K, Ghavamzadeh A, Hossein-Nezhad A, Izadi P, Sobhani M, Noori-Daloii AR, Noori-Daloii MR. Rashidi-Nezhad A, et al. Iran J Allergy Asthma Immunol. 2010 Mar;9(1):1-6. Iran J Allergy Asthma Immunol. 2010. PMID: 20548127 Free article.

3

Cytokine gene polymorphism and graft-versus-host disease: a survey in Iranian bone marrow transplanted patients.

Noori-Daloii MR, Jalilian N, Izadi P, Sobhani M, Rabii-Gilani Z, Yekaninejad MS. Noori-Daloii MR, et al. Mol Biol Rep. 2013 Aug;40(8):4861-7. doi: 10.1007/s11033-013-2585-4. Epub 2013 May 6. Mol Biol Rep. 2013. PMID: 23645090

4

Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Gene. 2013 Oct 10;528(2):309-13. doi: 10.1016/j.gene.2013.06.040. Epub 2013 Jul 8. Gene. 2013. PMID: 23845777

5

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.

Pourreza MR, Sobhani M, Rahimi A, Aramideh M, Kajbafzadeh AM, Noori-Daloii MR, Tabatabaiefar MA. Pourreza MR, et al. Among authors: noori daloii mr. Acta Diabetol. 2020 Jan;57(1):81-87. doi: 10.1007/s00592-019-01381-y. Epub 2019 Jul 15. Acta Diabetol. 2020. PMID: 31309279

6

Significant expressivity of Wolfram syndrome: phenotypic assessment of two known and one novel mutation in the WFS1 gene in three Iranian families.

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Mol Biol Rep. 2014 Nov;41(11):7499-505. doi: 10.1007/s11033-014-3642-3. Epub 2014 Aug 31. Mol Biol Rep. 2014. PMID: 25173644

7

Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Sobhani M, Amin Tabatabaiefar M, Ghafouri-Fard S, Rajab A, Mozafarpour S, Nasrniya S, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Among authors: noori daloii mr. Endocrine. 2019 Nov;66(2):185-191. doi: 10.1007/s12020-019-02004-w. Epub 2019 Jul 16. Endocrine. 2019. PMID: 31313226

8

Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.

Sobhani M, Tabatabaiefar MA, Ghafouri-Fard S, Rajab A, Hojjat A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Among authors: noori daloii mr. BMC Med Genet. 2020 Jan 14;21(1):13. doi: 10.1186/s12881-020-0950-4. BMC Med Genet. 2020. PMID: 31937257 Free PMC article.

9

Use of siRNA in knocking down of dopamine receptors, a possible therapeutic option in neuropsychiatric disorders.

Noori-Daloii MR, Mojarrad M, Rashidi-Nezhad A, Kheirollahi M, Shahbazi A, Khaksari M, Korzebor A, Goodarzi A, Ebrahimi M, Noori-Daloii AR. Noori-Daloii MR, et al. Mol Biol Rep. 2012 Feb;39(2):2003-10. doi: 10.1007/s11033-011-0947-3. Epub 2011 Jun 3. Mol Biol Rep. 2012. PMID: 21633887

10

Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.

Sobhani M, Tabatabaiefar MA, Ghafouri-Fard S, Rajab A, Hojjat A, Kajbafzadeh AM, Noori-Daloii MR. Sobhani M, et al. Among authors: noori daloii mr. BMC Med Genet. 2020 Mar 20;21(1):58. doi: 10.1186/s12881-020-0980-y. BMC Med Genet. 2020. PMID: 32197577 Free PMC article.

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