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Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation

Turkish journal of haematology, 2024-03, Vol.41 (1), p.66-68

2024

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Analysis of an Inherited FXII Deficiency Pedigree Associated with Double Heterozygous Mutations in the F12 Gene

Indian journal of hematology & blood transfusion, 2023-10, Vol.39 (4), p.712-714

2023

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B and NK Cells Closely Correlate with the Condition of Patients with Acute Pancreatitis

Gastroenterology research and practice, 2019-01, Vol.2019, p.7568410-13

2019

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Decreased Programmed Death-1 Expression on the T Cells of Patients With Ankylosing Spondylitis

The American journal of the medical sciences, 2015-06, Vol.349 (6), p.488-492

2015

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Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency

Zhonghua yi xue yi chuan xue za zhi, 2015-12, Vol.32 (6), p.793

2015

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Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events

International journal of laboratory hematology, 2024-04, Vol.46 (2), p.415-418

2024

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Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency

Zhonghua yi xue yi chuan xue za zhi, 2014-02, Vol.31 (1), p.16

2014

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A novel mutation of SETBP1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

Clinical case reports, 2015-06, Vol.3 (6), p.448-452

2015

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A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family

Blood coagulation & fibrinolysis, 2020-12, Vol.31 (8), p.569

2020

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A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient

Blood coagulation & fibrinolysis, 2020-01, Vol.31 (1), p.71

2020

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Hyperactivated peripheral invariant natural killer T cells correlate with the progression of HBV‐relative liver cirrhosis

Scandinavian journal of immunology, 2019-08, Vol.90 (2), p.e12775-n/a

2019

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Dynamic Distribution and Clinical Value of Peripheral Lymphocyte Subsets in Children with Infectious Mononucleosis

Indian journal of pediatrics, 2021-02, Vol.88 (2), p.113-119

2021

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Expression of CD56 is a risk factor for acute lymphocytic leukemia with central nervous system involvement in adults

Hematology (Luxembourg), 2017-02, Vol.22 (2), p.81-87

2017

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Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide

Clinical laboratory (Heidelberg), 2016-01, Vol.62 (11), p.2253

2016

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Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families

Blood coagulation & fibrinolysis, 2014-12, Vol.25 (8), p.894-897

2014

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Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia

Blood coagulation & fibrinolysis, 2014-10, Vol.25 (7), p.780-782

2014

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A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese families

Blood coagulation & fibrinolysis, 2015-09, Vol.26 (6), p.687-690

2015

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A novel mutation of SETBP 1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

Clinical case reports, 2015-06, Vol.3 (6), p.448-452

2015

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A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia

Hamostaseologie, 2023-12, Vol.43 (6), p.426

2023

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A novel mutation of SETBP1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

Clinical case reports, 2015, Vol.3 (6), p.448-452

2015

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Design and construction of HYSY981

中国工程科学：英文版, 2011, Vol.9 (4), p.44-50

Xie Bin Lin Yaosheng Su Jing Zeng Hengyi Xie Wenhui Jiang Zhe

2011

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Concept and method of drought disaster risk measurement based on drought propagation level--a case study of AnHui Province

Ecological indicators, 2024-09, Vol.166, p.112286, Article 112286

2024

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Advances in the roles of ATF4 in osteoporosis

Biomedicine & pharmacotherapy, 2023-12, Vol.169, p.115864-115864, Article 115864

2023

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A deep investigation into the adipogenesis mechanism: profile of microRNAs regulating adipogenesis by modulating the canonical Wnt/beta-catenin signaling pathway

BMC genomics, 2010-05, Vol.11 (1), p.320-320, Article 320

2010

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TMF inhibits extracellular matrix degradation by regulating the C/EBPβ/ADAMTS5 signaling pathway in osteoarthritis

Biomedicine & pharmacotherapy, 2024-05, Vol.174, p.116501-116501, Article 116501

2024

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Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel Mutation

Analysis of an Inherited FXII Deficiency Pedigree Associated with Double Heterozygous Mutations in the F12 Gene

B and NK Cells Closely Correlate with the Condition of Patients with Acute Pancreatitis

Decreased Programmed Death-1 Expression on the T Cells of Patients With Ankylosing Spondylitis

Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency

Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events

Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency

A novel mutation of SETBP1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family

A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient

Hyperactivated peripheral invariant natural killer T cells correlate with the progression of HBV‐relative liver cirrhosis

Dynamic Distribution and Clinical Value of Peripheral Lymphocyte Subsets in Children with Infectious Mononucleosis

Expression of CD56 is a risk factor for acute lymphocytic leukemia with central nervous system involvement in adults

Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide

Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families

Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia

A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese families

A novel mutation of SETBP 1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia

A novel mutation of SETBP1 in atypical chronic myeloid leukemia transformed from acute myelomonocytic leukemia

Design and construction of HYSY981

Concept and method of drought disaster risk measurement based on drought propagation level--a case study of AnHui Province

Advances in the roles of ATF4 in osteoporosis

A deep investigation into the adipogenesis mechanism: profile of microRNAs regulating adipogenesis by modulating the canonical Wnt/beta-catenin signaling pathway

TMF inhibits extracellular matrix degradation by regulating the C/EBPβ/ADAMTS5 signaling pathway in osteoarthritis

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