Hashemi-Gorji F - Search Results

1

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. 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.

2

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.

3

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. 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.

4

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

5

Novel LAMA2 Gene Mutations Associated with Merosin-Deficient Congenital Muscular Dystrophy.

Hashemi-Gorji F, Yassaee VR, Dashti P, Miryounesi M. Hashemi-Gorji F, et al. Iran Biomed J. 2018 Nov;22(6):408-14. doi: 10.29252/.22.6.408. Epub 2018 Apr 30. Iran Biomed J. 2018. PMID: 29707938 Free PMC article.

6

A Novel Splice Site Mutation in HPS1 Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family.

Ghafouri-Fard S, Hashemi-Gorji F, Yassaee VR, Alipour N, Miryounesi M. Ghafouri-Fard S, et al. Int J Mol Cell Med. 2016 Summer;5(3):192-195. Epub 2016 Jul 3. Int J Mol Cell Med. 2016. PMID: 27942505 Free PMC article. No abstract available.

7

A novel SRD5A2 mutation in an Iranian family with sex development disorder.

Hashemi-Gorji F, Salehpour S, Miryounesi M, Mirfakhraie R, Yassaee VR. Hashemi-Gorji F, et al. Andrologia. 2021 Feb;53(1):e13847. doi: 10.1111/and.13847. Epub 2020 Oct 25. Andrologia. 2021. PMID: 33099786

8

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

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. 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

A Novel Nonsense Mutation in PANK2 Gene in Two Patients with Pantothenate Kinase-Associated Neurodegeneration.

Ghafouri-Fard S, Yassaee VR, Rezayi A, Hashemi-Gorji F, Alipour N, Miryounesi M. Ghafouri-Fard S, et al. Int J Mol Cell Med. 2016 Fall;5(4):255-259. Epub 2016 Oct 23. Int J Mol Cell Med. 2016. PMID: 28357202 Free PMC article.

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