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Simulation on thermal characteristics of high-speed motorized spindle

Case studies in thermal engineering, 2022-07, Vol.35, p.102144, Article 102144

2022

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Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

EBioMedicine, 2017-09, Vol.23 (C), p.150-159

2017

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Mechanism Investigation of Tagetes patula L. against Chronic Nonbacterial Prostatitis by Metabolomics and Network Pharmacology

Molecules (Basel, Switzerland), 2019-06, Vol.24 (12), p.2266

2019

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Relationship Between Polymorphism of Thrombin-Activatable Fibrinolysis Inhibitor Gene +1040C/T and a Cohort of Chinese Women With Recurrent Spontaneous Abortion

Clinical and applied thrombosis/hemostasis, 2021, Vol.27, p.10760296211029720-10760296211029720

2021

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Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders

International journal of oral science, 2018-09, Vol.10 (3), p.26-9, Article 26

2018

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Evaluation of plasma D-dimer for the diagnosis in Chinese patients with hepatocellular carcinoma: A meta-analysis

Medicine (Baltimore), 2020-03, Vol.99 (12), p.e19461-e19461

2020

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Akt phosphorylation and kinase activity are down-regulated during hibernation in the 13-lined ground squirrel

Brain research, 2004-07, Vol.1014 (1), p.14-21

2004

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A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis

Gene, 2020-02, Vol.726, p.144226-144226, Article 144226

2020

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A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita

Medicine (Baltimore), 2018-05, Vol.97 (19), p.e0724-e0724

2018

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VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis

Genesis (New York, N.Y. : 2000), 2021-04, Vol.59 (4), p.e23415-n/a

2021

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Mechanisms for Increased Levels of Phosphorylation of Elongation Factor-2 during Hibernation in Ground Squirrels

Biochemistry (Easton), 2001-09, Vol.40 (38), p.11565-11570

2001

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Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele

British journal of haematology, 2019-08, Vol.186 (4), p.620-624

2019

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Chemical Constituents of Tagetes patula and Their Neuroprotecting Action

Natural product communications, 2020-11, Vol.15 (11), p.1934578

2020

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Cloning and characterization of a forkhead transcription factor gene, FoxO1a, from thirteen-lined ground squirrel

Gene, 2004-12, Vol.343 (1), p.203-209

2004

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Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

Molecular genetics and genomics : MGG, 2016-06, Vol.291 (3), p.1443-1450

2016

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A combination of the (αα)GZ and ‐‐SEA deletions causing a severe form of hemoglobin H disease

International journal of laboratory hematology, 2020-04, Vol.42 (2), p.e80-e83

2020

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A novel 223 kb deletion in the beta‐globin gene cluster was identified in a Chinese thalassemia major patient

International journal of laboratory hematology, 2019-08, Vol.41 (4), p.456-460

2019

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Two novel copy number variations involving the [alpha]-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

Molecular genetics and genomics : MGG, 2016-06, Vol.291 (3), p.1443

2016

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Unusual survival of a twin with homozygous α 0 -thalassemia due to Chimerism

Haematologica (Roma), 2020-10, Vol.106 (5), p.1507

2020

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Anti-lymphoproliferative activity of alpha-2-macroglobulin in the plasma of hibernating 13-lined ground squirrels and woodchucks

Veterinary immunology and immunopathology, 2014-09, Vol.161 (1-2), p.1-11

2014

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Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders

国际口腔科学杂志（英文版）, 2018, Vol.10 (4), p.223-231

2018

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Elevated arylalkylamine- N-acetyltransferase ( AA-NAT) gene expression in medial habenular and suprachiasmatic nuclei of hibernating ground squirrels

Brain research. Molecular brain research., 2002-06, Vol.102 (1), p.9-17

2002

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Generation of Multiple mRNA Fingerprints Using Fluorescence-Based Differential Display and an Automated DNA Sequencer

BioTechniques, 1997-03, Vol.22 (3), p.536-543

1997

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Review on Icing Fault Prediction for Overhead Transmission Lines

2023 IEEE International Conference on Advanced Power System Automation and Protection (APAP), 2023, p.442-446

2023

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Review on Icing Growth Model for Overhead Transmission Lines

2023 3rd Power System and Green Energy Conference (PSGEC), 2023, p.975-979

2023

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Simulation on thermal characteristics of high-speed motorized spindle

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Mechanism Investigation of Tagetes patula L. against Chronic Nonbacterial Prostatitis by Metabolomics and Network Pharmacology

Relationship Between Polymorphism of Thrombin-Activatable Fibrinolysis Inhibitor Gene +1040C/T and a Cohort of Chinese Women With Recurrent Spontaneous Abortion

Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders

Evaluation of plasma D-dimer for the diagnosis in Chinese patients with hepatocellular carcinoma: A meta-analysis

Akt phosphorylation and kinase activity are down-regulated during hibernation in the 13-lined ground squirrel

A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis

A case report of heterozygous TINF2 gene mutation associated with pulmonary fibrosis in a patient with dyskeratosis congenita

VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis

Mechanisms for Increased Levels of Phosphorylation of Elongation Factor-2 during Hibernation in Ground Squirrels

Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele

Chemical Constituents of Tagetes patula and Their Neuroprotecting Action

Cloning and characterization of a forkhead transcription factor gene, FoxO1a, from thirteen-lined ground squirrel

Two novel copy number variations involving the α-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

A combination of the (αα)GZ and ‐‐SEA deletions causing a severe form of hemoglobin H disease

A novel 223 kb deletion in the beta‐globin gene cluster was identified in a Chinese thalassemia major patient

Two novel copy number variations involving the [alpha]-globin gene cluster on chromosome 16 cause thalassemia in two Chinese families

Unusual survival of a twin with homozygous α 0 -thalassemia due to Chimerism

Anti-lymphoproliferative activity of alpha-2-macroglobulin in the plasma of hibernating 13-lined ground squirrels and woodchucks

Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders

Elevated arylalkylamine- N-acetyltransferase ( AA-NAT) gene expression in medial habenular and suprachiasmatic nuclei of hibernating ground squirrels

Generation of Multiple mRNA Fingerprints Using Fluorescence-Based Differential Display and an Automated DNA Sequencer

Review on Icing Fault Prediction for Overhead Transmission Lines

Review on Icing Growth Model for Overhead Transmission Lines

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