Suchergebnisse - "FGA protein, human"

PubPharm (32)

1

FGA Controls VEGFA Secretion to Promote Angiogenesis by Activating the VEGFR2-FAK Signalling Pathway

enthalten in: Frontiers in endocrinology | 2022

von Li, H. | Cai, E. | Cheng, H. | +4

2

Serum Proteomic Analysis Identifies SAA1, FGA, SAP, and CETP as New Biomarkers for Eosinophilic Granulomatosis With Polyangiitis

enthalten in: Frontiers in immunology | 2022

von Xiao, J. | Lu, S. | Wang, X. | +12

3

Cardiac Amyloidosis Screening at Trigger Finger Release Surgery

enthalten in: The American journal of cardiology | 2021

von Sperry, B. | Khedraki, R. | Gabrovsek, A. | +9

4

Afibrinogenemia with two compound heterozygous mutations in FGA gene

enthalten in: Haemophilia : the official journal of the World Federation of Hemophilia | 2021

von Feugray, G. | Billoir, P. | Casini, A. | +5

5

Identification of a recurrent missense mutation in the FGA gene likely causing a congenital fibrinogen disorder

enthalten in: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2021

von Gao, R. | Bi, M. | Li, B. | +4

6

Identification of a novel mutation in congenital afibrinogenemia in Iranian patients

enthalten in: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2021

von Nojehdeh, S. | Mojbafan, M. | Masoodifard, M. | +2

7

An association between fibrinogen gene polymorphisms and diabetic peripheral neuropathy in young patients with type 1 diabetes

enthalten in: Molecular biology reports | 2021

von Vojtková, J. | Kolková, Z. | Motyková, K. | +4

8

Down-regulation of RBP4 indicates a poor prognosis and correlates with immune cell infiltration in hepatocellular carcinoma

enthalten in: Bioscience reports | 2021

von Li, M. | Wang, Z. | Zhu, L. | +3

9

Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls

enthalten in: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2021

von Marchi, R. | Neerman-Arbez, M. | Gay, V. | +6

10

Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders

enthalten in: Blood cells, molecules & diseases | 2021

von Zhou, P. | Yu, M. | Peng, Y. | +2