SIX1 overexpression in diffuse-type and grade III gastric tumors: Features that are associated with poor prognosis

Por Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Emadi-Andani, Elaheh
Publicado no Adv Biomed Res (2015)

Augmented expression levels of lncRNAs ecCEBPA and UCA1 in gastric cancer tissues and their clinical significance

Por Nasrollahzadeh-Khakiani, Mojdeh, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh
Publicado no Iran J Basic Med Sci (2017)

Gene Expression Analysis of Two Epithelial-mesenchymal Transition-related Genes: Long Noncoding RNA-ATB and SETD8 in Gastric Cancer Tissues

Por Nourbakhsh, Nooshin, Emadi-Baygi, Modjtaba, Salehi, Rasoul, Nikpour, Parvaneh
Publicado no Adv Biomed Res (2018)

Association of HOTAIR expression in gastric carcinoma with invasion and distant metastasis

Por Emadi-Andani, Elaheh, Nikpour, Parvaneh, Emadi-Baygi, Modjtaba, Bidmeshkipour, Ali
Publicado em 2014

Expression profile of ZFX isoform3/variant 5 in gastric cancer tissues and its association with tumor size

Por Rahmati, Shima, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Emadi-Andani, Elaheh
Publicado no Iran J Basic Med Sci (2014)

Absence of association between –286C>A>T polymorphism in the CRP gene and metabolic syndrome in Iranian pediatric

Por Nikpour, Parvaneh, Emadi-Baygi, Modjtaba, Fatemi, Sayedeh Ghazaleh, Kelishadi, Roya
Publicado no Adv Biomed Res (2015)

Association Study Between Metabolic Syndrome and rs8066560 Polymorphism in the Promoter Region of Sterol Regulatory Element-binding Transcription Factor 1 Gene in Iranian Children...

Por Miranzadeh-Mahabadi, Hajar, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Kelishadi, Roya
Publicado no Int J Prev Med (2016)

Expression of ZFX gene correlated with the central features of the neoplastic phenotype in human brain tumors with distinct phenotypes

Por Afzali, Azita, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Nazemroaya, Fatemehe, Kheirollahi, Majid
Publicado no Adv Biomed Res (2015)

Identification of a New Single-nucleotide Polymorphism within the Apolipoprotein A5 Gene, Which is Associated with Metabolic Syndrome

Por Salehi, Samaneh, Emadi-Baygi, Modjtaba, Rezaei, Majdaddin, Kelishadi, Roya, Nikpour, Parvaneh
Publicado no Adv Biomed Res (2017)

Lack of Evidence of the Role of APOA5 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome

Por Salehi, Samaneh, Emadi-Baygi, Modjtaba, Rezaei, Majdaddin, Kelishadi, Roya, Nikpour, Parvaneh
Publicado no Diabetes Metab J (2018)

Absence of Association between -1131T>C Polymorphism in the Apolipoprotein APOA5 Gene and Pediatric Metabolic Syndrome

Por Fatemi, Sayedeh Ghazaleh, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Kelishadi, Roya, Hashemipour, Mahin
Publicado no Iran J Pediatr (2014)

Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis

Por Miranzadeh-Mahabadi, Hajar, Emadi-Baygi, Modjtaba, Nikpour, Parvaneh, Mostofizade, Neda, Hovsepian, Silva, Hashemipour, Mahin
Publicado no Adv Biomed Res (2016)

The G395R Mutation of the Sodium/Iodide Symporter (NIS) Gene in Patients with Dyshormonogenetic Congenital Hypothyroidism

Por Mostofizade, Neda, Nikpour, Parvaneh, Javanmard, Shaghayegh Haghjooy, Emadi-Baygi, Modjtaba, Miranzadeh-Mahabadi, Hajar, Hovsepian, Silva, Hashemipour, Mahin
Publicado em 2013