Search Results - "Molecular Genetics"

Evaluation of HER2 immunohistochemistry expression in non-standard solid tumors from a Single-Institution Prospective Cohort by Saurav Verma, Amanda Chapman, Lee-Anne Pickard, Danielle Porplycia, Haley McConkey, Patricia Jarosz, James Sinfield, Carolyn Lauzon-Young, Matthew J Cecchini, Christopher Howlett, Natalie Grindrod, Bekim Sadikovic, Stephen A Welch, Daniel Breadner

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Atypical hemolytic uremic syndrome: a pediatric case report by K.K. Hodiatska, T.K. Mavropulo, T.A. Bordii, S.V. Alifanova, V.F. Doroshenko, L.M. Cherhinets

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OPRM1 A118G Polymorphisms and Its Role in Opioid Addiction: Implication on Severity and Treatment Approaches by Taqi MM, Faisal M, Zaman H

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Identification of genes with a correlation between copy number and expression in gastric cancer by Cheng Lei, Wang Ping, Yang Sheng, Yang Yanqing, Zhang Qing, Zhang Wen, Xiao Huasheng, Gao Hengjun, Zhang Qinghua

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BRAF status in сito-morphological diagnosis of thyroid nodules by Yu. M. Tarashchenko, A. Ye. Kovalenko, M. V. Ostafiichuk, K. A. Nekrasov

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Mathematical modeling of pregnancy loss with normal embryo karyotype in the first trimester by N. N. Potapov, E. V. Kudryavtseva, V. V. Kovalev

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Ellis-Van Creveld Syndrome: Prenatal Diagnosis, Molecular Analysis and Genetic Counseling by Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Po-Tsang Chen, Wayseen Wang

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Can expelled cells/debris from a developing embryo be used for PGT? by Adva Aizer, Noa Harel-Inbar, Hagit Shani, Raoul Orvieto

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COMBINED TREATMENT OF PATIENTS WITH NON-SMALL CELL LUNG CANCER WITH PERSONALIZED PRESCRIPTION OF ADJUVANT CHEMOTHERAPY by E.O. RODIONOV, S.V. MILLER, L.A. EFTEEV, S.A. TUZIKOV, M.M. TSYGANOV, I.V. DERYUSHEVA, N.V. LITVYAKOV, V.A. MARKOVICH, U.B. URMONOV

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Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report by Lukas Varga, Daniel Danis, Martina Skopkova, Ivica Masindova, Zuzana Slobodova, Lucia Demesova, Milan Profant, Daniela Gasperikova

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Tumor molecular profiling of responders and non-responders following pembrolizumab monotherapy in chemotherapy resistant advanced cervical cancer by N.Y.L. Ngoi, V. Heong, X.W. Lee, Y.Q. Huang, Y.L. Thian, B.A. Choo, D. Lim, Y.W. Lim, S.E. Lim, A. Ilancheran, R. Soong, D.S.P. Tan

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Frequency of Fabry disease in a juvenile idiopathic arthritis cohort by Luciana Paim-Marques, Amanda Virginia Cavalcante, Islane Verçosa, Paula Carneiro, Marcia Souto-Maior, Erlane Marques, Simone Appenzeller

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Clinical Masks of Neurofibromatosis Type 1 by R. N. Mustafin

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A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss by Bai Yan, Wang Zhengmin, Dai Wenjia, Li Qingzhong, Chen Guoling, Cong Ning, Guan Minxin, Li Huawei

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Comprehensive Approach to Developing Baseline Reference Ranges for Platelet Function by Olga B. Gordeeva, Maria S. Karaseva, Vasily A. Lastovka, Nato D. Vashakmadze, Margarita A. Soloshenko, Gregory V. Revunenkov, Kirill A. Valyalov, Viktor V. Altunin

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MANIFESTATION OF POLYMORPHISM OF LIPID METABOLISM GENES TO IDENTIFY THEIR ROLE IN THE DEVELOPMENT OF VASCULAR DISEASES IN CHILDREN BORN OF MOTHERS WITH METABOLIC SYNDROME by V.V. NIKITINA, О.P. ZHUKHAREVA, I.L. IVANENKO, G.P. GLADILIN, E.V. VOLODKO

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Breeding, Genetics and Safety Production of Dairy Cattle

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Poultry: Breeding, Health, Nutrition, and Management

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Features prevalence of polymorphism lle50Val gene IL4RA in patients with bronchial asthma and healthy children school age Vinnichina by V. M. Dudnyk, O. V. Kutsak

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Case report: a rare case of Hunter syndrome (type II mucopolysaccharidosis) in a girl by A. N. Semyachkina, E. Y. Voskoboeva, E. Y. Zakharova, E. A. Nikolaeva, I. V. Kanivets, A. D. Kolotii, G. V. Baydakova, M. N. Kharabadze, R. G. Kuramagomedova, N. V. Melnikova

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