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Items: 1 to 20 of 95

1.
A Strategy for Precise and Large Scale Identification of Core Fucosylated Glycoproteins
Wei Jia, Zhuang Lu, Yan Fu, Hai-Peng Wang, Le-Heng Wang, Hao Chi, Zuo-Fei Yuan, Zhao-Bin Zheng, Li-Na Song, Huan-Huan Han, Yi-Min Liang, Jing-Lan Wang, Yun Cai, Yu-Kui Zhang, Yu-Lin Deng, Wan-Tao Ying, Si-Min He, Xiao-Hong Qian
Mol Cell Proteomics. 2009 May; 8(5): 913–923. doi: 10.1074/mcp.M800504-MCP200
PMCID:
PMC2689764
AbstractArticlePDF–352K
2.
Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr).
M C Iannuzzi, N Hidaka, M Boehnke, M E Bruck, W T Hanna, F S Collins, D Ginsburg
Am J Hum Genet. 1991 Apr; 48(4): 757–763.
PMCID:
PMC1682950
SummaryPage BrowsePDF–1.1M
3.
Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.
E W Murray, A R Giles, D Lillicrap
Am J Hum Genet. 1992 Jan; 50(1): 199–207.
PMCID:
PMC1682529
SummaryPage BrowsePDF–1.7M
4.
Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit.
C L Verweij, P J Diergaarde, M Hart, H Pannekoek
EMBO J. 1986 Aug; 5(8): 1839–1847. doi: 10.1002/j.1460-2075.1986.tb04435.x
Correction in:
EMBO J. 1986 Nov; 5(11): 3074.
PMCID:
PMC1167049
SummaryPage BrowsePDF–1.9M
5.
The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)
Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504
Correction in:
Genome Res. 2006 Jun; 16(6): 804.
PMCID:
PMC528928
AbstractArticlePDF–140K
6.
Cloning and characterization of two cDNAs coding for human von Willebrand factor.
J E Sadler, B B Shelton-Inloes, J M Sorace, J M Harlan, K Titani, E W Davie
Proc Natl Acad Sci U S A. 1985 Oct; 82(19): 6394–6398. doi: 10.1073/pnas.82.19.6394
PMCID:
PMC390722
SummaryPage BrowsePDF–1.1M
7.
Construction of cDNA coding for human von Willebrand factor using antibody probes for colony-screening and mapping of the chromosomal gene.
C L Verweij, C J de Vries, B Distel, A J van Zonneveld, A G van Kessel, J A van Mourik, H Pannekoek
Nucleic Acids Res. 1985 Jul 11; 13(13): 4699–4717. doi: 10.1093/nar/13.13.4699
PMCID:
PMC321821
SummaryPage BrowsePDF–2.0M
8.
Nucleotide sequence of pre-pro-von Willebrand factor cDNA.
D Bonthron, E C Orr, L M Mitsock, D Ginsburg, R I Handin, S H Orkin
Nucleic Acids Res. 1986 Sep 11; 14(17): 7125–7127. doi: 10.1093/nar/14.17.7125
PMCID:
PMC311723
SummaryPage BrowsePDF–469K
9.
Molecular cloning of the human gene for von Willebrand factor and identification of the transcription initiation site.
C J Collins, J P Underdahl, R B Levene, C P Ravera, M J Morin, M J Dombalagian, G Ricca, D M Livingston, D C Lynch
Proc Natl Acad Sci U S A. 1987 Jul; 84(13): 4393–4397. doi: 10.1073/pnas.84.13.4393
PMCID:
PMC305095
SummaryPage BrowsePDF–1.2M
10.
The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.
K A Cooney, W C Nichols, M E Bruck, W F Bahou, A D Shapiro, E J Bowie, H R Gralnick, D Ginsburg
J Clin Invest. 1991 Apr; 87(4): 1227–1233. doi: 10.1172/JCI115123
PMCID:
PMC295141
SummaryPage BrowsePDF–1.8M
11.
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences.
A M Randi, I Rabinowitz, D J Mancuso, P M Mannucci, J E Sadler
J Clin Invest. 1991 Apr; 87(4): 1220–1226. doi: 10.1172/JCI115122
PMCID:
PMC295140
SummaryPage BrowsePDF–1.6M
12.
von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.
L Holmberg, J A Dent, R Schneppenheim, U Budde, J Ware, Z M Ruggeri
J Clin Invest. 1993 May; 91(5): 2169–2177. doi: 10.1172/JCI116443
PMCID:
PMC288219
SummaryPage BrowsePDF–2.0M
13.
Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.
D Ginsburg, B A Konkle, J C Gill, R R Montgomery, P L Bockenstedt, T A Johnson, A Y Yang
Proc Natl Acad Sci U S A. 1989 May; 86(10): 3723–3727. doi: 10.1073/pnas.86.10.3723
PMCID:
PMC287212
SummaryPage BrowsePDF–1.4M
14.
Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A.
E A Tuley, C Gaucher, S Jorieux, N K Worrall, J E Sadler, C Mazurier
Proc Natl Acad Sci U S A. 1991 Jul 15; 88(14): 6377–6381. doi: 10.1073/pnas.88.14.6377
PMCID:
PMC52086
SummaryPage BrowsePDF–1.1M
15.
Identification of a point mutation in type IIB von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor.
J Ware, J A Dent, H Azuma, M Sugimoto, P A Kyrle, A Yoshioka, Z M Ruggeri
Proc Natl Acad Sci U S A. 1991 Apr 1; 88(7): 2946–2950. doi: 10.1073/pnas.88.7.2946
PMCID:
PMC51357
SummaryPage BrowsePDF–1.2M
16.
von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.
I Rabinowitz, E A Tuley, D J Mancuso, A M Randi, B G Firkin, M A Howard, J E Sadler
Proc Natl Acad Sci U S A. 1992 Oct 15; 89(20): 9846–9849. doi: 10.1073/pnas.89.20.9846
PMCID:
PMC50230
SummaryPage BrowsePDF–1.0M
17.
Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.
R Schneppenheim, J Brassard, S Krey, U Budde, T J Kunicki, L Holmberg, J Ware, Z M Ruggeri
Proc Natl Acad Sci U S A. 1996 Apr 16; 93(8): 3581–3586. doi: 10.1073/pnas.93.8.3581
PMCID:
PMC39653
SummaryPage BrowsePDF–1.7M
18.
Serum proteomics study reveals candidate biomarkers for systemic lupus erythematosus
Lijun Zhong, Jiao Liu, Juntuo Zhou, Lin Sun, Changhong Li, Xinyi Li, Rui Liu, Jinxia Zhao, Bin Yang, Xiangyuan Liu, Xiaoli Deng
Int J Clin Exp Pathol. 2017; 10(10): 10681–10694. Published online 2017 Oct 1.
PMCID:
PMC6965801
AbstractArticlePDF–3.0M
19.
Plasma CAMK2A predicts chemotherapy resistance in metastatic triple negative breast cancer
Bin Shao, Zhihua Tian, Huirong Ding, Qingsong Wang, Guohong Song, Lijun Di, Hong Zhang, Huiping Li, Jing Shen
Int J Clin Exp Pathol. 2018; 11(2): 650–663. Published online 2018 Feb 1.
PMCID:
PMC6958019
AbstractArticlePDF–913K
20.
Quantitative iTRAQ-based proteomic analysis of differentially expressed proteins in aging in human and monkey
Hao Wang, Xiaoqi Zhu, Junyan Shen, En-Feng Zhao, Dajun He, Haitao Shen, Hailiang Liu, Yongxin Zhou
BMC Genomics. 2019; 20: 725. Published online 2019 Oct 11. doi: 10.1186/s12864-019-6089-z
PMCID:
PMC6788010
AbstractArticlePDF–1.5M

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