Yassaee VR - Search Results

1

Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.

Yassaee VR, Hashemi-Gorji F, Boosaliki S, Parvaneh N. Yassaee VR, et al. Hum Immunol. 2016 Feb;77(2):191-5. doi: 10.1016/j.humimm.2015.11.019. Epub 2015 Nov 27. Hum Immunol. 2016. PMID: 26639818

2

Mutation spectra of the AAAS gene in Iranian families with Allgrove Syndrome.

Yassaee VR, Soltani Z, Ardakani BM. Yassaee VR, et al. Arch Med Res. 2011 Feb;42(2):163-8. doi: 10.1016/j.arcmed.2011.02.006. Arch Med Res. 2011. PMID: 21565631

3

A new approach for molecular diagnosis of TAR syndrome.

Yassaee VR, Hashemi-Gorji F, Soltani Z, Poorhosseini SM. Yassaee VR, et al. Clin Biochem. 2014 Jun;47(9):835-9. doi: 10.1016/j.clinbiochem.2014.04.018. Epub 2014 Apr 24. Clin Biochem. 2014. PMID: 24769264

4

A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A.

Yassaee VR, Khojaste A, Hashemi-Gorji F, Ravesh Z, Toosi P. Yassaee VR, et al. Gene. 2016 Feb 10;577(1):8-13. doi: 10.1016/j.gene.2015.08.071. Epub 2015 Nov 19. Gene. 2016. PMID: 26602028

5

Mutation Spectra of BRCA Genes in Iranian Women with Early Onset Breast Cancer - 15 Years Experience.

Yassaee VR, Ravesh Z, Soltani Z, Hashemi-Gorji F, Poorhosseini SM, Anbiaee R, Joulaee A. Yassaee VR, et al. Asian Pac J Cancer Prev. 2016;17(S3):149-53. doi: 10.7314/apjcp.2016.17.s3.149. Asian Pac J Cancer Prev. 2016. PMID: 27165220 Free article.

6

New Gene Profiling in Determination of Breast Cancer Recurrence and Prognosis in Iranian Women.

Poorhosseini SM, Hashemi M, Alipour Olyaei N, Izadi A, Moslemi E, Ravesh Z, Hashemi-Gorji F, Kheiri HR, Yassaee VR. Poorhosseini SM, et al. Among authors: yassaee vr. Asian Pac J Cancer Prev. 2016;17(S3):155-60. doi: 10.7314/apjcp.2016.17.s3.155. Asian Pac J Cancer Prev. 2016. PMID: 27165221 Free article.

7

First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population.

Soltani Z, Karami F, Yassaee V, Hashemi Gorji F, Talebzadeh M, Miryounesi M. Soltani Z, et al. Iran Red Crescent Med J. 2016 Jan 1;18(2):e21633. doi: 10.5812/ircmj.21633. eCollection 2016 Feb. Iran Red Crescent Med J. 2016. PMID: 27175306 Free PMC article.

8

A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β.

Hashemi-Gorji F, Ghafouri-Fard S, Salehpour S, Yassaee VR, Miryounesi M. Hashemi-Gorji F, et al. Among authors: yassaee vr. J Pediatr Endocrinol Metab. 2016 Aug 1;29(8):991-3. doi: 10.1515/jpem-2016-0032. J Pediatr Endocrinol Metab. 2016. PMID: 27180337

9

Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI.

Seyedhassani SM, Hashemi-Gorji F, Yavari M, Harazi F, Yassaee VR. Seyedhassani SM, et al. Among authors: yassaee vr. Fetal Pediatr Pathol. 2016;35(5):353-358. doi: 10.1080/15513815.2016.1191567. Epub 2016 Jun 30. Fetal Pediatr Pathol. 2016. PMID: 27362741

10

Gene expression profiling of the 8q22-24 position in human breast cancer: TSPYL5, MTDH, ATAD2 and CCNE2 genes are implicated in oncogenesis, while WISP1 and EXT1 genes may predict a risk of metastasis.

Taghavi A, Akbari ME, Hashemi-Bahremani M, Nafissi N, Khalilnezhad A, Poorhosseini SM, Hashemi-Gorji F, Yassaee VR. Taghavi A, et al. Among authors: yassaee vr. Oncol Lett. 2016 Nov;12(5):3845-3855. doi: 10.3892/ol.2016.5218. Epub 2016 Sep 30. Oncol Lett. 2016. PMID: 27895739 Free PMC article.

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