Wenman Wu
Overview
Explore the profile of Wenman Wu including associated specialties, affiliations and a list of published articles.
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51
Citations
226
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Recent Articles
11.
Lou C, Jiang J, Chen W, Zhang Z, Xu G, Liu Y, et al.
Br J Haematol
. 2023 Mar;
202(3):623-635.
PMID: 36951360
Hereditary factor VII (FVII) deficiency is a rare recessive bleeding disorder with an estimated prevalence of 1/500 000. We had investigated 50 unrelated Chinese patients with FVII deficiency and identified,...
12.
Liu G, Sun J, Li Z, Chen Z, Wu W, Wu R
Blood
. 2022 Nov;
141(6):677-680.
PMID: 36347023
No abstract available.
13.
Wu W, Zhou X, Jiang Z, Zhang D, Yu F, Zhang L, et al.
Hum Genomics
. 2022 Jul;
16(1):28.
PMID: 35897115
Background: High-cost, time-consuming and complex processes of several current approaches limit the use of noninvasive prenatal diagnosis (NIPD) for monogenic disorders in clinical application. Thus, a more cost-effective and easily...
14.
Ettingshausen C, Yang R, Wu W, Meeks S
Haemophilia
. 2022 May;
28 Suppl 4:111-118.
PMID: 35521731
Factor (F) VIII inhibitors develop in around 30% of previously untreated patients (PUPs) with severe haemophilia, to a lesser extend in moderate and mild haemophilia A and in up to...
15.
Zhang H, Chen C, Wu X, Lou C, Liang Q, Wu W, et al.
Hum Mutat
. 2022 Apr;
43(7):928-939.
PMID: 35391506
There is growing evidence that synonymous codon variants (SCVs) can cause disease through the disruption of different processes of protein production. The aim of the study is to investigate whether...
16.
Zeng J, Shu Z, Liang Q, Zhang J, Wu W, Wang X, et al.
Blood
. 2022 Feb;
139(22):3314-3324.
PMID: 35148377
The von Willebrand factor (VWF) propeptide (domains D1D2) is essential for the assembly of VWF multimers and its tubular storage in Weibel-Palade bodies. However, detailed molecular mechanism underlying this propeptide...
17.
Liang Q, Lin X, Wu X, Shao Y, Chen C, Dai J, et al.
Hum Mutat
. 2021 Dec;
43(2):215-227.
PMID: 34882887
Approximately 10% of von Willebrand factor (VWF) gene variants are suspected to disrupt messenger RNA (mRNA) processing, the number of which might be underestimated due to the lack of transcript...
18.
Liu G, Chen Z, Wu W, Wu R
Int J Immunopathol Pharmacol
. 2021 Feb;
35:2058738420980259.
PMID: 33626954
Neutralizing antibodies (inhibitors) against factor VIII/IX (FVIII/FIX) poses a serious and challenging complication in the hemophilia treatment. Allergic reaction is more common in hemophilia B and always companion with FIX...
19.
Cao W, Dong B, Horling F, Firrman J, Lengler J, Klugmann M, et al.
Mol Ther Methods Clin Dev
. 2020 Dec;
19:486-495.
PMID: 33313336
One important limitation for achieving therapeutic expression of human factor VIII (FVIII) in hemophilia A gene therapy is inefficient secretion of the FVIII protein. Substitution of five amino acids in...
20.
Lu Z, Zhang H, Chen C, Wu W, Wei H
Thromb Res
. 2020 Nov;
198:23-25.
PMID: 33249248
No abstract available.