Genetics

Eur Rev Med Pharmacol Sci 2023; 27 (10): 4688-4692

DOI: 10.26355/eurrev_202305_32480

Melatonin receptor 1A (MTNR1A) gene linkage and association to type 2 diabetes in Italian families

M. Amin, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2023; 27 (9): 4080-4084

DOI: 10.26355/eurrev_202305_32315

Novel implication of the prolactin (PRL) gene in the comorbidity of type 2 diabetes and depression

M. Amin, R. Wu, T.T. Postolache, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2023; 27 (6): 2634-2639

DOI: 10.26355/eurrev_202303_31800

Oxytocin receptor (OXTR) is a risk gene for polycystic ovarian syndrome

M. Amin, N. Horst, R. Wu, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2023; 27 (4): 1427-1435

DOI: 10.26355/eurrev_202302_31380

MTHFR C677T polymorphism, homocysteine, burden, and location of AMI and ACI

H.-M. Hou, X.-J. Qin, H.-Y. Zhao
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Eur Rev Med Pharmacol Sci 2023; 27 (3): 1051-1057

DOI: 10.26355/eurrev_202302_31201

The promoter methylations of the autoimmune regulator (AIRE) gene and matrix metalloproteinase-3 (MMP-3) gene may have a role in gestational diabetes mellitus

U. Coban, Z.B. Celik
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Eur Rev Med Pharmacol Sci 2023; 27 (3): 942-948

DOI: 10.26355/eurrev_202302_31187

The mineralocorticoid receptor gene (NR3C2) is linked to and associated with polycystic ovarian syndrome in Italian families

M. Amin, M. Perrelli, R. Wu, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2023; 27 (2): 694-703

DOI: 10.26355/eurrev_202301_31072

Novel TCF7L2 familial linkage and association with Type 2 diabetes, depression, and their comorbidity

L. del Bosque-Plata, M. Amin, R. Wu, T.T. Postolache, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2023; 27 (2): 687-693

DOI: 10.26355/eurrev_202301_31071

22q11.2 deletion syndrome complicated with pulmonary alveolar proteinosis in a child: a case report

Y. Zheng, Y. Li, G.-H. Mao, H.-C. Dai, G.-T. Li, C.-L. Yang, Y. Zhu
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Eur Rev Med Pharmacol Sci 2023; 27 (1): 395-403

DOI: 10.26355/eurrev_202301_30893

The effect of hereditary thrombotic factors and comorbidities on the severity of COVID-19 disease

M. Kose, N. Senkal, H. Konyaoglu, A. Emet, Y. Oyaci, S. Pehlivan, G.Y. Sayin
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Eur Rev Med Pharmacol Sci 2023; 27 (1): 166-171

DOI: 10.26355/eurrev_202301_30868

Association of MTHFR gene C677T polymorphism with pregnancy outcome

L.-L. Huang, J.-R. Tong, Y. Huang, Y.-N. Wei, H.-F. Chen, Y. Chen, J.-Y. Su, L. Deng
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Eur Rev Med Pharmacol Sci 2022; 26 (23): 8873-8878

DOI: 10.26355/eurrev_202212_30559

PSMD9 is linked to T2D age of onset, years of isolated and combined insulin therapy, irregular menses, and hot flashes

L. del Bosque-Plata, M. Amin, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2022; 26 (23): 8777-8787

DOI: 10.26355/eurrev_202212_30549

IFNG and IFNGR1 polymorphisms are associated with tuberculosis: a case-control study

S.-Q. Wu, X.-J. Ding, Q.-L. Yang, M.-G. Wang, J.-Q. He
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Eur Rev Med Pharmacol Sci 2022; 26 (22): 8370-8375

DOI: 10.26355/eurrev_202211_30372

Linkage and association of novel DRD2 variants to the comorbidity of type 2 diabetes and depression

M. Amin, R. Wu, T.T. Postolache, C. Gragnoli
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Eur Rev Med Pharmacol Sci 2022; 26 (21): 8073-8086

DOI: 10.26355/eurrev_202211_30161

A novel nomogram associated with regulatory T cells infiltration by weighted gene co-expression network analysis for predicting survival in patients with colon cancer

H.-J. Li, J.-K. Peng, Y.-Q. Wang, H.-W. Jiang, J. Wang
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Eur Rev Med Pharmacol Sci 2022; 26 (21): 7866-7882

DOI: 10.26355/eurrev_202211_30138

The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children

S. Alhazmi, B. Aljahdli, R. Farsi, M. Alharbi, K. Algothmi, N. Alburae, M. Ganash, S. Azhari, F. Basingab, A. Almuhammadi, A. Alqosaibi, H. Alkhatabi, A. Elaimi, M. Jan, H. Aldhalaan, R. Alyoubi, A. Alrafiah, A. Alrofaidi
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Eur Rev Med Pharmacol Sci 2022; 26 (21): 7813-7826

DOI: 10.26355/eurrev_202211_30130

Aberrantly high DEPDC1B expression leads to poor prognosis in patients with lower-grade gliomas

Z.-D. Liu, W.-J. Liang, X.-B. Cheng, R.-J. Qian, Y.-Z. Gao
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Eur Rev Med Pharmacol Sci 2022; 26 (18): 6754-6763

DOI: 10.26355/eurrev_202209_29774

Identification of ferroptosis-related genes for the prediction of prognosis and chemotherapy benefit of gastric cancer

J.-J. Zheng, J.-P. Wang
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Eur Rev Med Pharmacol Sci 2022; 26 (18): 6700-6724

DOI: 10.26355/eurrev_202209_29771

EMMPRIN is an emerging protein capable of regulating cancer hallmarks

B. de la Cruz Concepción, L.D. Bartolo-García, M.D. Tizapa-Méndez, M. Martínez-Vélez, J.J. Valerio-Diego, B. Illades-Aguiar, E.G. Salmerón-Bárcenas, J. Ortiz-Ortiz, F.I. Torres-Rojas, M.Á. Mendoza-Catalán, N. Navarro-Tito, A.E. Zacapala-Gómez
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Eur Rev Med Pharmacol Sci 2022; 26 (18): 6593-6599

DOI: 10.26355/eurrev_202209_29759

DNA repair gene (XRCC1 and XPD) polymorphism and risk of primary ovarian failure

Z. Kali, F.T. Cagiran, P. Kirici, C. Dogan, O. Celik
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Eur Rev Med Pharmacol Sci 2022; 26 (16): 5983-5990

DOI: 10.26355/eurrev_202208_29540

Monkeypox: epidemiology, mode of transmission, clinical features, genetic clades and molecular properties

S. Kannan, P. Shaik Syed Ali, A. Sheeza
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