Published in Blood Coagul Fibrinolysis on September 01, 2015
Store-independent activation of Orai1 by SPCA2 in mammary tumors. Cell (2010) 2.29
Anti-HMGB1 neutralizing antibody ameliorates gut barrier dysfunction and improves survival after hemorrhagic shock. Mol Med (2006) 2.27
Hypothermia protects the brain from transient global ischemia/reperfusion by attenuating endoplasmic reticulum response-induced apoptosis through CHOP. PLoS One (2013) 0.90
Changes of tumor necrosis factor-alpha and the effects of ulinastatin injection during cardiopulmonary cerebral resuscitation. J Huazhong Univ Sci Technolog Med Sci (2004) 0.81
[Expression and its Clinical Significance of NOK, EGFR in NSCLC.]. Zhongguo Fei Ai Za Zhi (2009) 0.77
Twenty-one novel mutations identified in the COL4A5 gene in Chinese patients with X-linked Alport's syndrome confirmed by skin biopsy. Nephrol Dial Transplant (2011) 0.77
Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivation. Blood Coagul Fibrinolysis (2015) 0.77
Decreased programmed death-1 expression on the T cells of patients with ankylosing spondylitis. Am J Med Sci (2015) 0.76
[Impacts on oxidative stress in the patients with cardiac valve replacement treated with electroacupuncture at Neiguan (PC 6)]. Zhongguo Zhen Jiu (2015) 0.76
Adaptive and regulatory mechanisms in aged rats with postoperative cognitive dysfunction. Neural Regen Res (2014) 0.75
Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency. Blood Coagul Fibrinolysis (2019) 0.75
[Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2014) 0.75
[Impacts of transcutaneous acupoint electric stimulation on the postoperative nausea and vomiting and plasma 5-HT concentration after cesarean section]. Zhongguo Zhen Jiu (2015) 0.75
Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese Patients. Acta Haematol (2016) 0.75
Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s. Blood Coagul Fibrinolysis (2016) 0.75
[Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2015) 0.75
Factor V deficiency caused by a novel nonsense mutation (Gln2031stop) in a Chinese patient. Blood Coagul Fibrinolysis (2014) 0.75
Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide. Clin Lab (2016) 0.75
A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families. Blood Coagul Fibrinolysis (2016) 0.75
[Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2013) 0.75
A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family. Blood Coagul Fibrinolysis (2013) 0.75
Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiency. Blood Coagul Fibrinolysis (2013) 0.75
Removal of low concentrations of ammonium and humic acid from simulated groundwater by Vermiculite/Palygorskite mixture. Water Environ Res (2012) 0.75
Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication. Thromb Haemost (2011) 0.75
Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families. Blood Coagul Fibrinolysis (2014) 0.75
[Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2015) 0.75
[Genetic analysis of a pedigree with hereditary coagulation factor Ⅶ deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2015) 0.75
[Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2017) 0.75
[Expression of nitric oxide synthase and its significance in nasal polyps]. Lin Chuang Er Bi Yan Hou Ke Za Zhi (2004) 0.75
[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2015) 0.75
[Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2016) 0.75
[FCM detection and pathology observation of 5 mm cutting-edge of laryngocarcinoma]. Lin Chuang Er Bi Yan Hou Ke Za Zhi (2003) 0.75
[Phenotypic and genetic analysis of two pedigrees affected with hereditary antithrombin deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2016) 0.75
Occurence of haemophilia A and B in a Chinese family with mosaicism of the F9 gene mutation in the HB index's maternal grandfather. Thromb Haemost (2010) 0.75
Molecular Characterization of a Novel Missense Mutation (Asp538Asn) in a Chinese Patient with Factor XII Deficiency. Clin Lab (2015) 0.75
Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia. Blood Coagul Fibrinolysis (2014) 0.75