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232 related items for PubMed ID: 23267103
1. Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, Mirel DB, Kim Y, Cropp CD, Molloy AM, Kirke PN, Bailey-Wilson JE, Wilson AF, Mills JL, Scott JM, Brody LC, Li JZ, Ginsburg D. Proc Natl Acad Sci U S A; 2013 Jan 08; 110(2):588-93. PubMed ID: 23267103 [Abstract] [Full Text] [Related]
2. Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance. Ozel AB, McGee B, Siemieniak D, Jacobi PM, Haberichter SL, Brody LC, Mills JL, Molloy AM, Ginsburg D, Li JZ, Desch KC. J Thromb Haemost; 2016 Sep 08; 14(9):1888-98. PubMed ID: 27359253 [Abstract] [Full Text] [Related]
3. Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project. Souto JC, Almasy L, Soria JM, Buil A, Stone W, Lathrop M, Blangero J, Fontcuberta J. Thromb Haemost; 2003 Mar 08; 89(3):468-74. PubMed ID: 12624629 [Abstract] [Full Text] [Related]
4. Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci. De Visser MC, Sandkuijl LA, Lensen RP, Vos HL, Rosendaal FR, Bertina RM. J Thromb Haemost; 2003 Aug 08; 1(8):1771-6. PubMed ID: 12911592 [Abstract] [Full Text] [Related]
5. Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke. Williams SR, Hsu FC, Keene KL, Chen WM, Dzhivhuho G, Rowles JL, Southerland AM, Furie KL, Rich SS, Worrall BB, Sale MM, GARNET (The Genomics and Randomized Trials Network) Collaborative Research Group. Stroke; 2017 Jun 08; 48(6):1444-1450. PubMed ID: 28495826 [Abstract] [Full Text] [Related]
6. Genome-wide association studies identify genetic loci for low von Willebrand factor levels. van Loon J, Dehghan A, Weihong T, Trompet S, McArdle WL, Asselbergs FW, Chen MH, Lopez LM, Huffman JE, Leebeek FW, Basu S, Stott DJ, Rumley A, Gansevoort RT, Davies G, Wilson JJ, Witteman JC, Cao X, de Craen AJ, Bakker SJ, Psaty BM, Starr JM, Hofman A, Wouter Jukema J, Deary IJ, Hayward C, van der Harst P, Lowe GD, Folsom AR, Strachan DP, Smith N, de Maat MP, O'Donnell C. Eur J Hum Genet; 2016 Jul 08; 24(7):1035-40. PubMed ID: 26486471 [Abstract] [Full Text] [Related]
7. Genome-wide linkage analysis of von Willebrand factor plasma levels implicates the ABO locus as a principal determinant: should we overlook ADAMTS13? Bowen DJ. Thromb Haemost; 2003 Nov 08; 90(5):961; author reply 962. PubMed ID: 14597995 [No Abstract] [Full Text] [Related]
8. Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions. Daidone V, Cattini MG, Pontara E, Sartorello F, Gallinaro L, Marotti A, Scaroni C, Pagnan A, Casonato A. Thromb Haemost; 2009 Feb 08; 101(2):298-304. PubMed ID: 19190813 [Abstract] [Full Text] [Related]
9. Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor gene. Casaña P, Martínez F, Haya S, Espinós C, Aznar JA. Br J Haematol; 2001 Dec 08; 115(3):692-700. PubMed ID: 11736956 [Abstract] [Full Text] [Related]
10. Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes. Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B. Thromb Haemost; 2008 Jun 08; 99(6):1013-8. PubMed ID: 18521502 [Abstract] [Full Text] [Related]
11. Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time. Souto JC, Almasy L, Muñiz-Diaz E, Soria JM, Borrell M, Bayén L, Mateo J, Madoz P, Stone W, Blangero J, Fontcuberta J. Arterioscler Thromb Vasc Biol; 2000 Aug 08; 20(8):2024-8. PubMed ID: 10938027 [Abstract] [Full Text] [Related]
12. Genome-Wide Association Study Identifies That the ABO Blood Group System Influences Interleukin-10 Levels and the Risk of Clinical Events in Patients with Acute Coronary Syndrome. Johansson Å, Alfredsson J, Eriksson N, Wallentin L, Siegbahn A. PLoS One; 2015 Aug 08; 10(11):e0142518. PubMed ID: 26600159 [Abstract] [Full Text] [Related]
13. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Smith NL, Chen MH, Dehghan A, Strachan DP, Basu S, Soranzo N, Hayward C, Rudan I, Sabater-Lleal M, Bis JC, de Maat MP, Rumley A, Kong X, Yang Q, Williams FM, Vitart V, Campbell H, Mälarstig A, Wiggins KL, Van Duijn CM, McArdle WL, Pankow JS, Johnson AD, Silveira A, McKnight B, Uitterlinden AG, Wellcome Trust Case Control Consortium;, Aleksic N, Meigs JB, Peters A, Koenig W, Cushman M, Kathiresan S, Rotter JI, Bovill EG, Hofman A, Boerwinkle E, Tofler GH, Peden JF, Psaty BM, Leebeek F, Folsom AR, Larson MG, Spector TD, Wright AF, Wilson JF, Hamsten A, Lumley T, Witteman JC, Tang W, O'Donnell CJ. Circulation; 2010 Mar 30; 121(12):1382-92. PubMed ID: 20231535 [Abstract] [Full Text] [Related]
14. Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes. Pujol-Moix N, Martinez-Perez A, Sabater-Lleal M, Llobet D, Vilalta N, Hamsten A, Souto JC, Soria JM. Int J Mol Sci; 2019 Jun 30; 20(13):. PubMed ID: 31262040 [Abstract] [Full Text] [Related]
15. Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort. Borràs N, Garcia-Martínez I, Batlle J, Pérez-Rodríguez A, Parra R, Altisent C, López-Fernández MF, Costa Pinto J, Batlle-López F, Cid AR, Bonanad S, Cabrera N, Moret A, Mingot-Castellano ME, Navarro N, Pérez-Montes R, Marcellini S, Moreto A, Herrero S, Soto I, Fernández-Mosteirín N, Jiménez-Yuste V, Alonso N, de Andrés-Jacob A, Fontanes E, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Castro Quismondo N, Iñigo B, Del Mar Nieto M, Vidal R, Martínez MP, Aguinaco R, Tenorio M, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Dobón M, Aguilar C, Corrales I, Vidal F. Thromb Haemost; 2020 Mar 30; 120(3):437-448. PubMed ID: 32135566 [Abstract] [Full Text] [Related]
16. Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip. Zabaneh D, Gaunt TR, Kumari M, Drenos F, Shah S, Berry D, Power C, Hypponen E, Shah T, Palmen J, Pallas J, Talmud PJ, Casas JP, Sofat R, Lowe G, Rumley A, Morris RW, Whincup PH, Rodriguez S, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Kivimaki M, Whittaker J, Hingorani AD, Day IN, Humphries SE. Ann Hum Genet; 2011 Jul 30; 75(4):456-67. PubMed ID: 21534939 [Abstract] [Full Text] [Related]
17. Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter. Keightley AM, Lam YM, Brady JN, Cameron CL, Lillicrap D. Blood; 1999 Jun 15; 93(12):4277-83. PubMed ID: 10361125 [Abstract] [Full Text] [Related]
18. ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens. Morelli VM, de Visser MC, van Tilburg NH, Vos HL, Eikenboom JC, Rosendaal FR, Bertina RM. Thromb Haemost; 2007 Apr 15; 97(4):534-41. PubMed ID: 17393014 [Abstract] [Full Text] [Related]
19. A multi-stage multi-design strategy provides strong evidence that the BAI3 locus is associated with early-onset venous thromboembolism. Antoni G, Morange PE, Luo Y, Saut N, Burgos G, Heath S, Germain M, Biron-Andreani C, Schved JF, Pernod G, Galan P, Zelenika D, Alessi MC, Drouet L, Visvikis-Siest S, Wells PS, Lathrop M, Emmerich J, Tregouet DA, Gagnon F. J Thromb Haemost; 2010 Dec 15; 8(12):2671-9. PubMed ID: 20946148 [Abstract] [Full Text] [Related]
20. Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels. Ma Q, Jacobi PM, Emmer BT, Kretz CA, Ozel AB, McGee B, Kimchi-Sarfaty C, Ginsburg D, Li JZ, Desch KC. Blood Adv; 2017 Jun 27; 1(15):1037-1046. PubMed ID: 29296746 [Abstract] [Full Text] [Related] Page: [Next] [New Search]