DNA DIAGNOSTICS AND MUTATION SPECTRUM OF THE GENE FBN1 IN MARFAN’S SYNDROME by Yu. A. Rogozhina, V. A. Rumyantseva, A. A. Bukaeva, E. V. Zaklyazminskaya

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Metformin's impact on asprosin and FBN1 expression: Potential mechanisms beyond insulin sensitivity in type 2 diabetes in rats by Ali Dashtkar, Mansour Karajibani, Mohsen Saravani, Roya zanganeh, Hamed Fanaei

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Urinary Proteomic Shifts over Time and Their Associations with eGFR Decline in Chronic Kidney Disease by Zhalaliddin Makhammajanov, Kamila Nurlybayeva, Zikrillo Artikov, Pavel Tarlykov, Mohamad Aljofan, Rostislav Bukasov, Duman Turebekov, Syed Hani Abidi, Mehmet Kanbay, Abduzhappar Gaipov

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A novel missense variant of FBN1 gene in a Sardinian family with Marfan syndrome: a case report by Marina Marsan, Mattia Brutti, F. Meloni, M. Marica, C. Soddu, F. Lai, D. Martorana, S. Savasta

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Functional analysis of a novel FBN1 deep intronic variant causing Marfan syndrome in a Chinese patient by Qingming Wang, Fang Zhang, Xinlong Zhou, Hui Li, Juan Zhao, Haiming Yuan

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Dysregulation of cell migration by matrix metalloproteinases in geleophysic dysplasia by Alejo A. Morales, Vladimir Camarena, LéShon Peart, Sarah Smithson, Lindsay Shaw, Lucy Webber, Jose M. Negron, Juan E. Sola, Ann-Christina Brady, Katherina Walz, Gaofeng Wang, Mustafa Tekin

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Interpretation and classification of FBN1 variants associated with Marfan syndrome: consensus recommendations from the Clinical Genome Resource’s FBN1 variant curation expert panel... by A. Drackley, C. Somerville, P. Arnaud, L. M. Baudhuin, N. Hanna, M. L. Kluge, K. Kotzer, C. Boileau, L. Bronicki, B. Callewaert, A. Cecchi, H. Dietz, D. Guo, S. Harris, O. Jarinova, M. Lindsay, L. Little, B. Loeys, G. MacCarrick, J. Meester, D. Milewicz, T. Morisaki, H. Morisaki, D. Murdock, M. Renard, J. Richer, L. Robert, M. Ouzounian, L. Van Laer, J. De Backer, L. Muiño-Mosquera

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Case Report: A case of severe pulmonary hypertension combined with FBN1 mutation associated geleophysic dysplasia by Ze-yang Chen, Yuan Cao, Jie Yang, Xue-hua He, Li-ping Liu, Yong-hua Yuan

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Phenotypic Diversity of Marfan Syndrome by Zixiang Xu, MD, Zhenghong Li, MD, Long Xiang, MD, Tao Chen, MD, Wang Lu, MD, Chang’e Guo, MD, Jinmiao Chen, MD, PhD, Bi’ang Kang, MD, PhD, Zesi Liu, MD, Daokang Xiang, MD, PhD, Liqun Sun, MD, PhD, Kui Hu, MD, PhD

Subjects: “…FBN1 gene…”
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REGULAR GENETIC COUNSELING AND DNA-DIAGNOSTICS OF MARFAN SYNDROME IN THE WORK OF FEDERAL SURGERY INSTITUTION by V. A. Rumyantseva, Yu. A. Rogozhina, A. A. Bukaeva, D. V. Bazarov, E. R. Charchyan, E. V. Zaklyazminskaya

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Case Report: FBN1 mutation screening in South African patients with Marfan syndrome by F. Mhlongo, C. Feben, A. Krause, N. Carstens, N. Carstens

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Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts by Rio Miyadai, Shiori Hinata, Yuya Amemiya, Satori Shigematsu, Kazuhiro Umeyama, Hiroshi Nagashima, Kenji Yamatoya, Jun Ohgane

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Unraveling a novel FBN1 variant in Marfan syndrome with dilated aortic root manifestation by Amirreza Sabahizadeh, Amir Askarinejad, Saranaz Seyed AliAkbar, Mahdieh Soveizi, Golnaz Houshmand, Hojjat Mortezaeian, Amin Elahifar, Majid Maleki, Samira Kalayinia

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