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  • Global Medical Genetics: 2023, vol: 10, issue: 3
  • 1)- Yue Zhang, Xifeng Dong, Huaquan Wang. VEXAS Syndrome-Review. Global medical genetics. 2023, 10 (3): 133-143
    Cited : 2
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  • 2)- Juan He, Xin Zhang, Xi Chen, Zongyao Xu, Xiaoqi Chen, Jiangyan Xu. Shared Genes and Molecular Mechanisms between Nonalcoholic Fatty Liver Disease and Hepatocellular Carcinoma Established by WGCNA Analysis. Global medical genetics. 2023, 10 (3): 144-158
    Cited : 0
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  • 3)- Saba Ahmadi, Sandro Surmava, Eka Kvaratskhelia, Elene Abzianidze, Ketevani Kankava. IL-10 Polymorphism and Breast Cancer Risk in Georgian Women: A Case-Control Study. Global medical genetics. 2023, 10 (3): 159-163
    Cited : 1
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  • 4)- Fatemeh Fakhr, Vahid Shaygannejad, Mehdi Khorrami, Leila Saberi, Omid Mirmosayyeb, Erfan Sadeghi, Majid Kheirollahi. Expression and Single Nucleotide Variants in Multiple Sclerosis Patients Affect the Response to Interferon Beta Therapy. Global medical genetics. 2023, 10 (3): 164-171
    Cited : 0
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  • 5)- Alessandro Pancrazzi, Francesco Bloise, Alice Moncada, Roberta Perticucci, Stefania Vecchietti, Francesca Pompili, Francesca Ricciarini, Silvia Lenzi, Cristina Gatteschi, Sabrina Giusti, Maria Pia Rosito, Sabrina Del Buono, Paola Belardi, Alessandra Bruni, Filippo Borri, Andrea Campione, Lorella Laurini, Rossella Occhini, Loretta Presenti, Viviana Viticchi, Maja Rossi, Sara Bardi, Antonio D'Urso, Simona Dei, Duccio Venezia, Raffaele Scala, Carmelo Bengala, Nicola Libertà Decarli, Andrea Carneval. BL-MOL-AR Project, Preliminary Results about Liquid Biopsy: Molecular Approach Experience and Research Activity in Oncological Settings. Global medical genetics. 2023, 10 (3): 172-187
    Cited : 0
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  • 6)- Josef Finsterer. Strokelike Episodes in Carriers Differ from Those in Mitochondrial Disorders. Global medical genetics. 2023, 10 (3): 188-189
    Cited : 0
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  • 7)- N Sreedevi, N Swapna, Santosh Maruthy, T Jayakumar, Charles Sylvester. Molecular Evaluation of Joubert Syndrome and Hearing Impairment in a Patient with Ataxic Cerebral Palsy. Global medical genetics. 2023, 10 (3): 190-193
    Cited : 0
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  • 8)- Mengying Zhang, Gaochao Zhang, Fangfang Xu, Mengyuan Liu, Xifeng Dong, Weiwei Qi, Huaquan Wang. Identification of Plasma Thrombopoietin Level and Its Significance in Patients with Aplastic Anemia and Myelodysplastic Syndrome. Global medical genetics. 2023, 10 (3): 194-198
    Cited : 0
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  • 9)- Md Arifur Rahman, Md Monirul Islam, Md Eunus Ali, Mohammad Ariful Islam, Farhana Afroze, Mohammad Shamim Hossain, Ahmed Abu Rus'd. Molecular Epidemiology of HCV RNA Genotype-3 in Dhaka City, Bangladesh. Global medical genetics. 2023, 10 (3): 199-204
    Cited : 1
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  • 10)- Eskandar Qaed, Bandar Al-Hamyari, Ahmed Al-Maamari, Abdullah Qaid, Haneen Alademy, Marwan Almoiliqy, Jean Claude Munyemana, Murad Al-Nusaif, Jameel Alafifi, Eman Alyafeai, Mohammed Safi, Zhaohong Geng, Zeyao Tang, Xiaodong Ma. Fisetin's Promising Antitumor Effects: Uncovering Mechanisms and Targeting for Future Therapies. Global medical genetics. 2023, 10 (3): 205-220
    Cited : 5
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  • 11)- Loganathan Kavitha, Jayaseelan Vijayashree Priyadharsini, Deepthi Kattula, Umadevi Krishna Mohan Rao, Rajabather Balaji Srikanth, Manogaran Kuzhalmozhi, Kannan Ranganathan. Expression of CD44 in Head and Neck Squamous Cell Carcinoma-An Study. Global medical genetics. 2023, 10 (3): 221-228
    Cited : 2
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  • 12)- Yanmei Xu, Yunfei Chen, Lei Zhang. Review: Advances in the Pathogenesis and Treatment of Immune Thrombocytopenia Associated with Viral Hepatitis. Global medical genetics. 2023, 10 (3): 229-233
    Cited : 0
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  • 13)- Piero Pavone, Raffaele Falsaperla, Martino Ruggieri, Simona Domenica Marino, Enrico Parano, Xena Giada Pappalardo. A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report. Global medical genetics. 2023, 10 (3): 234-239
    Cited : 0
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  • 14)- Gulten Tuncel, Burcin Sanlıdag, Eray Dirik, Tugba Baris, Mahmut Cerkez Ergoren, Sehime Gulsun Temel. Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis. Global medical genetics. 2023, 10 (3): 240-246
    Cited : 0
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  • 15)- Xialin Zhang, Kun Chen, Sicheng Bian, Gang Wang, Xiuyu Qin, Ruijuan Zhang, Linhua Yang. Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China. Global medical genetics. 2023, 10 (3): 247-262
    Cited : 0
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  • 16)- Sumei Wang, Minglu Liang, Jiehui Ma, Sheng Huang, Lili Fan, Feng Zhu, Dan Sun. Possible Role of Mitochondrial Transfer RNA Gene 5816 A > G Genetic Polymorphism (m.5816A > G) in a 3-Year-Old Child with Dystonia: Report of a Case. Global medical genetics. 2023, 10 (3): 263-270
    Cited : 0
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