Pu Dai Selected Research

Nonsyndromic Deafness

1/2018	A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.
12/2017	A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations.
11/2013	Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing.
8/2012	Rapid screening for the mitochondrial DNA C1494T mutation in a deaf population in China using real-time quantitative PCR.
7/2011	Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.
12/2010	Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.
9/2009	Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.
11/2007	[Mutation screening of the COCH gene in familial and sporadic patients with late onset nonsyndromic sensorineural hearing loss among Chinese population].
6/2007	The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.
5/2007	The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.

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Pu Dai Research Topics

Disease

42	Hearing Loss (Hearing Impairment) 02/2022 - 02/2005
27	Deafness (Deaf Mutism) 02/2022 - 02/2006
12	Nonsyndromic Deafness 01/2018 - 10/2006
8	Sensorineural Hearing Loss 10/2020 - 02/2006
4	Ototoxicity 07/2015 - 02/2005
4	Mitochondrial Diseases (Mitochondrial Disease) 02/2014 - 10/2006
3	Autosomal Recessive 4 Deafness 11/2008 - 07/2006
2	Bilateral Hearing Loss 11/2009 - 10/2007
1	Cholesteatoma 06/2022
1	Zimmerman Laband syndrome 04/2022
1	Waardenburg Syndrome (Klein Syndrome) 01/2022
1	Autosomal Recessive 77 Deafness 01/2022
1	Diabetes Complications 01/2022
1	Dementia (Dementias) 10/2020
1	Intellectual Disability (Idiocy) 07/2019
1	Autosomal Dominant 15 Deafness 01/2018
1	Necrosis 01/2017
1	Infections 01/2017
1	Autosomal Recessive 10 Deafness 01/2017
1	Cerebrospinal Fluid Leak 01/2017
1	Wounds and Injuries (Trauma) 01/2017
1	Inflammation (Inflammations) 07/2016
1	Hepatitis B 06/2016
1	Foreign Bodies (Foreign Body) 04/2013
1	Congenital Abnormalities (Deformity) 09/2012
1	Neoplasms (Cancer) 03/2012
1	Facial Nerve Injuries 12/2011
1	Noise-Induced Hearing Loss (Acoustic Trauma) 05/2010
1	Neoplasm Metastasis (Metastasis) 06/2009
1	Palmoplantar Keratoderma (Keratosis Palmaris et Plantaris) 02/2009
1	Aminoglycoside-Induced Deafness 06/2008
1	Breast Neoplasms (Breast Cancer) 05/2006
1	Lactic Acidosis 05/2005
1	Cardiomyopathies (Cardiomyopathy) 05/2005
1	Genetic Predisposition to Disease (Genetic Predisposition) 02/2005
1	Hypoxia (Hypoxemia) 03/2004
1	Presbycusis 09/2002

Drug/Important Bio-Agent (IBA)

29	Mitochondrial DNA (mtDNA)IBA 01/2022 - 09/2002
13	12S ribosomal RNAIBA 01/2022 - 02/2006
11	AminoglycosidesIBA 07/2015 - 02/2005
10	DNA (Deoxyribonucleic Acid)IBA 01/2020 - 05/2007
4	Pharmaceutical PreparationsIBA 01/2021 - 07/2012
3	Anti-Bacterial Agents (Antibiotics)IBA 07/2015 - 05/2006
2	Nonsense Codon (Nonsense Mutation)IBA 01/2014 - 12/2010
2	Proteins (Proteins, Gene)FDA Link 07/2011 - 09/2006
2	Connexin 26IBA 02/2009 - 02/2009
2	Thyroid HormonesIBA 11/2008 - 07/2006
2	Ser Transfer RNAIBA 09/2008 - 10/2007
2	NucleotidesIBA 05/2007 - 05/2006
1	Potassium Channels (Potassium Channel)IBA 04/2022
1	CRISPR-Cas Systems Guide RNAIBA 02/2022
1	N-acetyltalosaminuronic acid (NAT)IBA 02/2022
1	Terpenes (Terpenoids)IBA 01/2022
1	CytokinesIBA 01/2022
1	Cytokine Receptors (Cytokine Receptor)IBA 01/2022
1	Retroelements (Retrotransposon)IBA 01/2022
1	Lipoxygenase (Lipoxygenase-1)IBA 01/2022
1	AdipokinesIBA 01/2022
1	SteroidsIBA 01/2022
1	Protons (Proton)IBA 01/2021
1	Adenosine Monophosphate (AMP)IBA 01/2020
1	Adenosine Triphosphatases (ATPase)IBA 07/2019
1	Transcription Factor 4IBA 01/2018
1	Interferon LambdaIBA 01/2018
1	Transcription Factor 3IBA 01/2018
1	MorpholinosIBA 01/2018
1	N-(4-isothiocyanatophenethyl)spiperoneIBA 12/2017
1	Serine Proteases (Serine Protease)IBA 01/2017
1	Hepatitis B Core AntigensIBA 06/2016
1	AnionsIBA 11/2012
1	Glycine (Aminoacetic Acid)FDA LinkGeneric 12/2010
1	Glutamic Acid (Glutamate)FDA Link 12/2010
1	ConnexinsIBA 02/2009
1	human GJB3 proteinIBA 02/2009
1	RNA Precursors (Precursor, mRNA)IBA 09/2008
1	Blood Coagulation Factors (Coagulation Factor)IBA 11/2007
1	Transfer RNA (tRNA)IBA 06/2007
1	Ala Transfer RNAIBA 06/2007
1	Connexin 30IBA 01/2007
1	Arg Transfer RNAIBA 10/2006
1	Thr Transfer RNAIBA 10/2006
1	Glu Transfer RNAIBA 10/2006
1	16S Ribosomal RNAIBA 09/2006
1	Amantadine (Aman)FDA LinkGeneric 05/2006
1	polyglutamineIBA 05/2006
1	EnzymesIBA 05/2005

Therapy/Procedure

5	Cochlear Implantation 01/2022 - 10/2010
4	Therapeutics 10/2020 - 02/2006
3	Electrodes (Electrode) 01/2022 - 09/2012
3	Cochlear Implants (Cochlear Implant) 10/2020 - 10/2010
2	Mastoidectomy 11/2018 - 12/2011
1	Endoscopes 06/2022
1	Hearing Aids (Hearing Aid) 10/2020
1	Replantation 01/2017
1	General Anesthesia 04/2013
1	Adjuvant Radiotherapy 03/2012
1	Radiotherapy 06/2009