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Material Type: Artigo
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Relative expression of vascular endothelial growth factor isoforms in squamous cell carcinoma of the head and neckWilkie, Mark D. ; Emmett, Maxine S. ; Santosh, Shilpa ; Lightbody, Kathryn A. ; Lane, Steven ; Goodyear, Paul W. ; Sheard, Jon D. ; Boyd, Mark T. ; Pritchard-Jones, Rowan O. ; Jones, Terence M.Head & neck, 2016-05, Vol.38 (5), p.775-781 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromesShaffer, Lisa G. ; Coppinger, Justine ; Morton, S. Annie ; Alliman, Sarah ; Burleson, Jessica ; Traylor, Ryan ; Walker, Cathryn ; Byerly, Steve ; Lamb, Allen N. ; Schultz, Roger ; Ravnan, J. Britt ; Kashork, Catherine D. ; Torchia, Beth S. ; Sulpizio, Scott ; Sundin, Kyle ; Schermer, Mack ; Adler, Karl ; Dallaire, Stephanie ; Ballif, Blake C.Prenatal diagnosis, 2011-08, Vol.31 (8), p.778-787 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Asymptotics of solutions to periodic problem for the Korteweg–de Vries–Burgers equationNaumkin, Pavel I. ; Villela‐Aguilar, José de JesúsStudies in applied mathematics (Cambridge), 2022-08, Vol.149 (2), p.523-536 [Periódico revisado por pares]Cambridge: Blackwell Publishing LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Differential expression of osteoblast-specific factor 2 and polymeric immunoglobulin receptor genes in nasopharyngeal carcinomaChang, Yao ; Lee, Tso-Ching ; Li, Jian-Chiuan ; Lai, Ting-Lung ; Chua, Huey-Huey ; Chen, Chi-Long ; Doong, Shin-Lian ; Chou, Chen-Kung ; Sheen, Tzung-Shiahn ; Tsai, Ching-HwaHead & neck, 2005-10, Vol.27 (10), p.873-882 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Diagnostic utility of microarray testing in pregnancy lossRosenfeld, J. A. ; Tucker, M. E. ; Escobar, L. F. ; Neill, N. J. ; Torchia, B. S. ; McDaniel, L. D. ; Schultz, R. A. ; Chong, K. ; Chitayat, D.Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.478-486 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Coamplification of Myc/Pvt1 and homozygous deletion of Nlrp1 locus are frequent genetics changes in mouse osteosarcomaRao, Pulivarthi H. ; Zhao, Shuying ; Zhao, Yi-Jue ; Yu, Alexander ; Rainusso, Nino ; Trucco, Matteo ; Allen-Rhoades, Wendy ; Satterfield, Laura ; Fuja, Daniel ; Borra, Vishnupriya J. ; Man, Tsz-Kwong ; Donehower, Lawrence A. ; Yustein, Jason T.Genes chromosomes & cancer, 2015-12, Vol.54 (12), p.796-808 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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7 |
Material Type: Artigo
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SRSF‐1 and microvessel density immunohistochemical analysis by semi‐automated tissue microarray in prostate cancer patients with diabetes (DIAMOND study)Broggi, Giuseppe ; Lo Giudice, Arturo ; Di Mauro, Marina ; Asmundo, Maria Giovanna ; Pricoco, Elisabetta ; Piombino, Eliana ; Caltabiano, Rosario ; Morgia, Giuseppe ; Russo, Giorgio IvanThe Prostate, 2021-09, Vol.81 (12), p.882-892 [Periódico revisado por pares]United States: Wiley Subscription Services, IncTexto completo disponível |
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8 |
Material Type: Artigo
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Different Hierarchies of Anti–Modified Protein Autoantibody Reactivities in Rheumatoid ArthritisSahlström, Peter ; Hansson, Monika ; Steen, Johanna ; Amara, Khaled ; Titcombe, Philip J. ; Forsström, Björn ; Stålesen, Ragnhild ; Israelsson, Lena ; Piccoli, Luca ; Lundberg, Karin ; Klareskog, Lars ; Mueller, Daniel L. ; Catrina, Anca I. ; Skriner, Karl ; Malmström, Vivianne ; Grönwall, CarolineArthritis & rheumatology (Hoboken, N.J.), 2020-10, Vol.72 (10), p.1643-1657 [Periódico revisado por pares]United States: Wiley Subscription Services, IncTexto completo disponível |
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9 |
Material Type: Artigo
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Turner syndrome: New insights from prenatal genomics and transcriptomicsBianchi, Diana W.American journal of medical genetics. Part C, Seminars in medical genetics, 2019-03, Vol.181 (1), p.29-33Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disordersMikhail, Fady M. ; Lose, Edward J. ; Robin, Nathaniel H. ; Descartes, Maria D. ; Rutledge, Katherine D. ; Rutledge, S. Lane ; Korf, Bruce R. ; Carroll, Andrew J.American journal of medical genetics. Part A, 2011-10, Vol.155A (10), p.2386-2396 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |