Lingqian Wu Selected Research

X-Linked Chondrodysplasia Punctata 1

1/2021

Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in ARSE.

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Lingqian Wu Research Topics

Disease

4	Spinal Muscular Atrophy (Progressive Muscular Atrophy) 04/2022 - 02/2018
4	Hemophilia A (Haemophilia) 01/2022 - 09/2019
4	Neoplasms (Cancer) 01/2022 - 12/2004
4	Aneuploidy (Aneuploid) 01/2019 - 10/2008
2	Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker) 01/2021 - 12/2008
2	Hemophilia B (Haemophilia B) 01/2021 - 10/2018
2	Melanoma (Melanoma, Malignant) 01/2020 - 06/2017
1	Bruton type agammaglobulinemia 06/2022
1	Bacterial Infections (Bacterial Infection) 06/2022
1	Inborn Genetic Diseases (Disease, Hereditary) 04/2022
1	Acquired Immunodeficiency Syndrome (AIDS) 03/2022
1	Thalassemia 01/2021
1	Methylmalonic acidemia 01/2021
1	X-Linked Chondrodysplasia Punctata 1 01/2021
1	Hepatomegaly 01/2021
1	Perinatal Death 10/2020
1	Langer-Giedion Syndrome (Trichorhinophalangeal Syndrome Type II) 08/2020
1	Chromothripsis 08/2020
1	Androgen-Insensitivity Syndrome (Testicular Feminization) 07/2020
1	Giant Axonal Neuropathy 03/2020
1	Lysosomal Storage Diseases (Lysosomal Storage Disease) 10/2019
1	Oculocutaneous Albinism (Albinism, Yellow Mutant) 10/2019
1	Prader-Willi Syndrome (Syndrome, Prader-Willi) 06/2019
1	Angelman Syndrome (Syndrome, Angelman) 06/2019
1	Multiple Hereditary Exostoses (Hereditary Multiple Exostoses) 05/2019
1	Ventricular Heart Septal Defects (Ventricular Septal Defect) 03/2019
1	Chromosome Aberrations (Chromosome Abnormalities) 01/2019
1	DiGeorge Syndrome (Syndrome, DiGeorge) 01/2019
1	Severe Combined Immunodeficiency (Bare Lymphocyte Syndrome) 10/2018
1	Thoracic Aortic Aneurysm 09/2018
1	Idiopathic Hypogonadotropic Hypogonadism 08/2018
1	Beta-Hydroxyisobutyryl CoA Deacylase Deficiency 07/2018
1	Neurodegenerative Diseases (Neurodegenerative Disease) 02/2018
1	Cataract (Cataracts) 01/2018
1	Neurodevelopmental Disorders 01/2018
1	Autism Spectrum Disorder 04/2016
1	Xanthomatosis (Xanthoma) 09/2015
1	Hyperlipoproteinemia Type II (Familial Hypercholesterolemia) 09/2015
1	Type 1e Demyelinating Charcot-Marie-Tooth Disease 07/2015
1	Hypophosphatemic Rickets 07/2015
1	Norrie disease 05/2015
1	Trisomy (Trisomies) 01/2015
1	Hepatolenticular Degeneration (Wilson's Disease) 01/2015
1	Craniofacial Dysostosis (Crouzon Disease) 06/2014
1	Polycystic Ovary Syndrome (Syndrome, Stein-Leventhal) 07/2013
1	Herpes Simplex 12/2004
1	Nasopharyngeal Carcinoma 12/2004

Drug/Important Bio-Agent (IBA)

4	dichlorobis(azomycin)platinum IIIBA 01/2021 - 01/2015
4	Ribosomal DNA (rDNA)IBA 01/2021 - 06/2017
4	DNA (Deoxyribonucleic Acid)IBA 08/2020 - 05/2013
4	Proteins (Proteins, Gene)FDA Link 02/2018 - 05/2015
2	Factor VIII (Coagulation Factor VIII)IBA 01/2022 - 01/2020
2	DystrophinIBA 01/2021 - 12/2008
2	Complementary DNA (cDNA)IBA 01/2021 - 09/2019
1	Immunoglobulins (Immunoglobulin)IBA 06/2022
1	Agammaglobulinaemia Tyrosine KinaseIBA 06/2022
1	Nucleic AcidsIBA 04/2022
1	TubulinIBA 03/2022
1	TNF-Related Apoptosis-Inducing LigandIBA 01/2022
1	Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)IBA 01/2022
1	Therapeutic UsesIBA 01/2021
1	human ARSL proteinIBA 01/2021
1	locked nucleic acidIBA 01/2021
1	SolutionsIBA 01/2021
1	LipidsIBA 01/2021
1	Hemoglobins (Hemoglobin)IBA 01/2021
1	Systemic carnitine deficiencyIBA 10/2020
1	Fatty Acids (Saturated Fatty Acids)IBA 10/2020
1	Androgen Receptors (Androgen Receptor)IBA 07/2020
1	ElementsIBA 03/2020
1	interleukin-24 (ST16)IBA 01/2020
1	lysosomal proteinsIBA 10/2019
1	Melanins (Melanin)IBA 10/2019
1	snRNP Core ProteinsIBA 06/2019
1	N-(4-isothiocyanatophenethyl)spiperoneIBA 01/2019
1	OligodeoxyribonucleotidesIBA 11/2018
1	Transforming Growth Factor-beta Type II ReceptorIBA 09/2018
1	LHRH Receptors (Gonadotropin-Releasing Hormone Receptor)IBA 08/2018
1	GonadotropinsIBA 08/2018
1	Valine (L-Valine)FDA Link 07/2018
1	HydrolasesIBA 07/2018
1	Messenger RNA (mRNA)IBA 01/2018
1	DNA Transposable Elements (Element, IS)IBA 04/2016
1	CholesterolIBA 09/2015
1	oxidized low density lipoproteinIBA 09/2015
1	Myelin ProteinsIBA 07/2015
1	Nonsense Codon (Nonsense Mutation)IBA 07/2015
1	Genetic Markers (Genetic Marker)IBA 01/2015
1	Type 2 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 2)IBA 06/2014
1	MicroRNAs (MicroRNA)IBA 07/2013
1	DNA ProbesIBA 10/2008
1	Cytosine DeaminaseIBA 12/2004
1	Thymidine KinaseIBA 12/2004
1	ProdrugsIBA 12/2004

Therapy/Procedure

2	Therapeutics 01/2022 - 12/2004
2	Transplantation 01/2021 - 10/2018
1	Intravenous Infusions 01/2022
1	Intravenous Injections 01/2020
1	Ligation 05/2019
1	Cell- and Tissue-Based Therapy (Cell Therapy) 06/2017