المؤلفون: Kirk M. Druey, Daniel E. Sturdevant, Eunice Chan, Vijayaraj Nagarajan, Celeste M Nelson, Zhihui Xie, Shoko Iwaki, Laura Wisch, Michael Young, Stephen F. Porcella

المصدر: Rare Diseases

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Peripheral edema, Single-nucleotide polymorphism, Disease, Biology, 03 medical and health sciences, 0302 clinical medicine, medicine, Systemic capillary leak syndrome, SNP, vascular permeability, 030304 developmental biology, 0303 health sciences, General Engineering, genetics, genome-wide SNP study, cell adhesion, cytoskeleton, medicine.disease, 3. Good health, cell junction, genomic DNA, medicine.symptom, DNA microarray, 030217 neurology & neurosurgery, systemic capillary leak syndrome, SNP array, Research Paper

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6beedec04de4e67b675dec524b57c5b
https://pubmed.ncbi.nlm.nih.gov/24808988

المؤلفون: Xie Z; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA., Nagarajan V; Computational Biology Section; Bioinformatics and Computational Biosciences Branch; OCICB; NIAID/NIH; Bethesda, MD USA., Sturdevant DE; Genomics Unit, Research Technologies Section; Rocky Mountain Laboratories; NIAID/NIH, Hamilton, MT USA., Iwaki S; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA., Chan E; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA., Wisch L; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA., Young M; Clinical Research Directorate/CMRP; SAIC-Frederick, Inc; Frederick National Laboratory for Clinical Research; Frederick, MD USA., Nelson CM; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA., Porcella SF; Genomics Unit, Research Technologies Section; Rocky Mountain Laboratories; NIAID/NIH, Hamilton, MT USA., Druey KM; Molecular Signal Transduction Section; NIAID/NIH; Bethesda, MD USA.

المصدر: Rare diseases (Austin, Tex.) [Rare Dis] 2013 Dec 12; Vol. 1 (1).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 101603407 Publication Model: Print Cited Medium: Print ISSN: 2167-5511 (Print) Linking ISSN: 21675511 NLM ISO Abbreviation: Rare Dis Subsets: PubMed not MEDLINE