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Rare Diseases Volume 1, 2013 - Issue 1

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Research Paper

Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease)

Zhihui Xie Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA

Vijayaraj Nagarajan Computational Biology Section; Bioinformatics and Computational Biosciences Branch; OCICB; NIAID/NIH; Bethesda, MD USA

Daniel E Sturdevant Genomics Unit, Research Technologies Section; Rocky Mountain Laboratories; NIAID/NIH, Hamilton, MT USA

Shoko Iwaki Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA

Eunice Chan Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA

Laura Wisch Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA

Michael Young Clinical Research Directorate/CMRP; SAIC-Frederick, Inc; Frederick National Laboratory for Clinical Research; Frederick, MD USA

Celeste M Nelson Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA

Stephen F Porcella Genomics Unit, Research Technologies Section; Rocky Mountain Laboratories; NIAID/NIH, Hamilton, MT USA

Kirk M Druey Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USACorrespondence[email protected]

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Article: e27445 | Received 07 Oct 2013, Accepted 05 Dec 2013, Published online: 12 Dec 2013

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https://doi.org/10.4161/rdis.27445

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Dehua Gao, Wen Zhong, Weiru Zhang, Xuan Wang, Weiping Li & Jun Liu. (2023) Chronic systemic capillary leak syndrome with lymphatic capillaries involvement and MYOF mutation: case report and literature review. Frontiers in Genetics 14.
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Ararat J. Ablooglu, Abhishek DesaiJin-San Yoo, Cheon Ho ParkEun-Ah Lee, Bu Yeon Kim, Hyunsun ParkYoung Ae LeeSang Ryeol Shim, Weon Sup LeeKirk M. Druey. (2023) A ligand-independent Tie2-activating antibody reduces vascular leakage in models of Clarkson disease. Science Advances 9:46.
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A. V. Meyer, M. V. Ulyanova, D. O. Imekina, A. D. Padyukova, T. A. Tolochko, E. A. Astafieva & M. B. Lavryashina. (2023) Analytical screening of polymorphic variants of 20S proteasome genes when planning a study of pathogenetic effects of modification of NFKB1 post-translational processing. Fundamental and Clinical Medicine 8:2, pages 53-66.
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Patricia C. Cheung, A. Robin Eisch, Noble Maleque, Derek M. Polly, Sara C. Auld & Kirk M. Druey. (2021) Fatal Exacerbations of Systemic Capillary Leak Syndrome Complicating Coronavirus Disease. Emerging Infectious Diseases 27:10, pages 2529-2534.
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Robert Beal, Ana Alonso-Carriazo Fernandez, Dimitris K. Grammatopoulos, Karl Matter & Maria S. Balda. (2021) ARHGEF18/p114RhoGEF Coordinates PKA/CREB Signaling and Actomyosin Remodeling to Promote Trophoblast Cell-Cell Fusion During Placenta Morphogenesis. Frontiers in Cell and Developmental Biology 9.
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Anna L Tyler, Abbas Raza, Dimitry N Krementsov, Laure K Case, Rui Huang, Runlin Z Ma, Elizabeth P Blankenhorn, Cory Teuscher & J Matthew Mahoney. (2019) Network-Based Functional Prediction Augments Genetic Association To Predict Candidate Genes for Histamine Hypersensitivity in Mice. G3 Genes|Genomes|Genetics 9:12, pages 4223-4233.
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Christoph Standfuß, Jonas Parczyk, Jerome Ruhnau & Andreas Klein. (2019) Genome reorganization in different cancer types: detection of cancer specific breakpoint regions. Molecular Cytogenetics 12:1.
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Karen Ka Yan Leung, Jaime Sou Rosa Duque, Kwong-Man Yu, Kai-Ning Cheong, Patrick Chun-Yin Chong, Marco Hok-Kung Ho & Pak-Cheong Chow. (2019) Myocardial oedema in an 8-year-old Chinese boy with Idiopathic systemic capillary leak syndrome. BMC Pediatrics 19:1.
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Abbas Raza, Zhihui Xie, Eunice C. Chan, Wei-Sheng Chen, Linda M. Scott, A. Robin Eisch, Dimitry N. Krementsov, Helene F. Rosenberg, Samir M. Parikh, Elizabeth P. Blankenhorn, Cory Teuscher & Kirk M. Druey. (2019) A natural mouse model reveals genetic determinants of systemic capillary leak syndrome (Clarkson disease). Communications Biology 2:1.
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Ding Li, Yan Sun, Xiaochao Kong, Changxing Luan, Youjia Yu, Feng Chen & Peng Chen. (2018) Association between a Single Nucleotide Polymorphism in the 3 -UTR of ARHGEF18 and the Risk of Nonidiopathic Pulmonary Arterial Hypertension in Chinese Population . Disease Markers 2018, pages 1-6.
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Lotte Ebdrup, Kirk Druey & Trine Hyrup Mogensen. (2018) Severe capillary leak syndrome with cardiac arrest triggered by influenza virus infection. BMJ Case Reports, pages bcr-2018-226108.
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Richard W. Pierce, Jonathan Merola, John Paul Lavik, Martin S. Kluger, Anita Huttner, Mustafa K. Khokha & Jordan S. Pober. (2017) A p190BRhoGAP mutation and prolonged RhoB activation in fatal systemic capillary leak syndrome. Journal of Experimental Medicine 214:12, pages 3497-3505.
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Kirk M. Druey & Samir M. Parikh. (2017) Idiopathic systemic capillary leak syndrome (Clarkson disease). Journal of Allergy and Clinical Immunology 140:3, pages 663-670.
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Alex Upton, Johan Karlsson, Oswaldo Trelles, Miguel Hernandez & Juan Elvira. 2017. Euro-Par 2016: Parallel Processing Workshops. Euro-Par 2016: Parallel Processing Workshops 433 444 .

Prashant Kapoor. 2017. Biology and Management of Unusual Plasma Cell Dyscrasias. Biology and Management of Unusual Plasma Cell Dyscrasias 143 161 .

Soushi Ibata, Tsutomu Sato, Kohichi Takada, Ayumi Tatekoshi, Akari Hashimoto, Yusuke Kamihara, Wataru Jomen, Hiroto Horiguchi, Kaoru Ono, Kazuyuki Murase, Satoshi Iyama, Koji Miyanishi, Yasushi Sato, Rishu Takimoto, Masayoshi Kobune & Junji Kato. (2016) Isoform D of vascular endothelial growth factor in systemic capillary leak syndrome: a case report. Journal of Medical Case Reports 10:1.
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Min Kyung LeeHyun Sub CheongYoungil KohKwang-Sung AhnSung-Soo YoonHyoung Doo Shin. (2016) Genetic Association of PARP15 Polymorphisms with Clinical Outcome of Acute Myeloid Leukemia in a Korean Population . Genetic Testing and Molecular Biomarkers 20:11, pages 696-701.
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Adrian Sousa, Oscar Len, Laura Escolà-Vergé, Bruno Magnifico, Chema Mora, Elisabeth Papiol, Eva Revilla & Benito Almirante. (2015) Influenza a Virus Infection is associated with Systemic Capillary Leak Syndrome: Case Report and Systematic Review of the Literature. Antiviral Therapy 21:2, pages 181-183.
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Cornelia Then, Katrin Ritzel, Christa Seibold, Johannes F. E. Mann & Martin Reincke. (2015) Multiglandular Hormone Deficiency in a Patient with Systemic Capillary Leak Syndrome. Case Reports in Medicine 2015, pages 1-6.
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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease)

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Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease)

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