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Effect of MAOA rs1465108 polymorphism on susceptibility to substance/alcohol use disorder: a novel PCR-RFLP assay for the detection of MAOA rs1465108
Kaya-Akyüzlü, Dilek, Özkan-Kotiloğlu, Selin, Yıldırım, Sariye Aybüke, Danışman, Mustafa, Yıldırım, Mukaddes Asena, Özgür-İlhan, İnci
Published in Molecular biology reports (01.12.2024)
Published in Molecular biology reports (01.12.2024)
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Molecular and hematological characteristics of two different δ-globin promoter variants, δ −276(A>G) and δ −77(T >C) among Thai, Burmese, and Laotian subjects
Panyasai, Sitthichai, Prayalaw, Patcharawadee, Singha, Kritsada, Fucharoen, Supan
Published in PeerJ (San Francisco, CA) (03.07.2025)
Published in PeerJ (San Francisco, CA) (03.07.2025)
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CDH1 and DDR1 common variants confer risk to vitiligo and autoimmune comorbidities
Almasi-Nasrabadi, Mina, Amoli, Mahsa M., Robati, Reza M., Rajabi, Fateme, Ghalamkarpour, Fariba, Gauthier, Yvon
Published in Gene (05.06.2019)
Published in Gene (05.06.2019)
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IRS gene polymorphisms in Turkish patients with late-onset Alzheimer’s disease
Ozkan, Hulya, Yildiz, Mustafa, Ustundag, Ayten, Kara, Ismail, Guldiken, Baburhan, Sut, Necdet, Sipahi, Tammam
Published in Molecular biology reports (01.12.2025)
Published in Molecular biology reports (01.12.2025)
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The possible effects of the MTOR polymorphisms on preeclampsia susceptibility, severity, and onset: a case–control study and in silico analysis
Rezaei, Mahnaz, Ghasemi, Marzieh, Saravani, Mohsen, Ghahghayi, Fatemeh, Shahraki-Ghadim, Hossein, Salimi, Saeedeh
Published in Molecular biology reports (01.12.2024)
Published in Molecular biology reports (01.12.2024)
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Matrix Metalloproteases 1 and 3 Promoter Gene Polymorphism Is Associated With Rotator Cuff Tear
Assunção, Jorge H., Godoy-Santos, Alexandre L., dos Santos, Maria Cristina L. G., Malavolta, Eduardo A., Gracitelli, Mauro E. C., Ferreira Neto, Arnaldo A.
Published in Clinical orthopaedics and related research (01.07.2017)
Published in Clinical orthopaedics and related research (01.07.2017)
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Association of Matrix Metalloproteinase-9 rs3918242 Promoter Genotypes With Colorectal Cancer Risk
WU, MING-HSIEN, TZENG, HUEY-EN, WU, CHENG-NAN, YUEH, TE-CHENG, PENG, YEN-CHUN, TSAI, CHUN-HAO, WANG, YUN-CHI, KE, TAO-WEI, PEI, JEN-SHENG, CHANG, WEN-SHIN, TSAI, CHIA-WEN, BAU, DA-TIAN
Published in Anticancer research (01.12.2019)
Published in Anticancer research (01.12.2019)
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Detection and genetic characterisation of Toxoplasma gondii circulating in free-range chickens, pigs and seropositive pregnant women in Benue state, Nigeria
Nzelu, Ifeoma N., Kwaga, Jacob K. P., Kabir, Junaidu, Lawal, Idris A., Beazley, Christy, Evans, Laura, Blake, Damer P.
Published in PLoS neglected tropical diseases (01.06.2021)
Published in PLoS neglected tropical diseases (01.06.2021)
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CRISPLD1 rs12115090 polymorphisms alters antiplatelet potency of clopidogrel in coronary artery disease patients in Chinese Han
Wang, Jie-Ya, Zhang, Yan-Jiao, Li, He, Hu, Xiao-Lei, Li, Mu-Peng, Song, Pei-Yuan, Ma, Qi-Lin, Peng, Li-Ming, Chen, Xiao-Ping
Published in Gene (15.12.2018)
Published in Gene (15.12.2018)
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Polymorphism in the 3′-UTR of LIF but Not in the ATF6B Gene Associates with Schizophrenia Susceptibility: a Case-Control Study and In Silico Analyses
Moudi, Mahdiyeh, Sargazi, Saman, Heidari Nia, Milad, Saravani, Ramin, Shirvaliloo, Milad, Shakiba, Mansoor
Published in Journal of molecular neuroscience (01.12.2020)
Published in Journal of molecular neuroscience (01.12.2020)
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Association between the Trp64Arg polymorphism of the ADRB3 gene and overactive bladder
Çırakoğlu, Abdullah, Fejzullahu, Arta, Benli, Erdal, Yuce, Ahmet, Ayyıldız, Ali, Aynacıoğlu, A. Şükrü
Published in Neurourology and urodynamics (01.09.2021)
Published in Neurourology and urodynamics (01.09.2021)
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Effects of the MTOR and AKT1 genes polymorphisms on papillary thyroid cancer development
Maruei-Milan, Rostam, Saravani, Mohsen, Heidari, Zahra, Asadi-Tarani, Mina, Salimi, Saeedeh
Published in IUBMB life (01.12.2020)
Published in IUBMB life (01.12.2020)
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Association between vitamin D receptor gene FokI and TaqI variants with autism spectrum disorder predisposition in Iranian population
Mobasheri, Leila, Moossavi, Seyedeh Zahra, Esmaeili, Aliakbar, Mohammadoo-khorasani, Milad, Sarab, Gholamreza Anani
Published in Gene (10.01.2020)
Published in Gene (10.01.2020)
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Arg4810Lys mutation in RNF213 among Eastern Indian non-MMD ischemic stroke patients: a genotype–phenotype correlation
Sadhukhan, Dipanwita, Mitra, Parama, Mishra, Smriti, Roy, Arunima, Podder, Gargi, Ray, Biman Kanti, Biswas, Atanu, Hui, Subhra Prakash, Banerjee, Tapas Kumar, Biswas, Arindam
Published in Neurological sciences (01.01.2024)
Published in Neurological sciences (01.01.2024)
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